| geneid | 92241 |
|---|---|
| ensemblid | ENSG00000198771.11 |
| hgncid | 28310 |
| symbol | RCSD1 |
| name | RCSD domain containing 1 |
| refseq_nuc | NM_052862.4 |
| refseq_prot | NP_443094.3 |
| ensembl_nuc | ENST00000367854.8 |
| ensembl_prot | ENSP00000356828.3 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 167630232 |
| end | 167708696 |
| strand | + |
| ver | v1.2 |
| region | chr1:167630232-167708696 |
| region5000 | chr1:167625232-167713696 |
| regionname0 | RCSD1_chr1_167630232_167708696 |
| regionname5000 | RCSD1_chr1_167625232_167713696 |
| 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 | 416 | 342 | 85 | 55 | 148 | 14 | 38 | 112 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| a0002 | 0/0 | 416 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| a0003 | 0/0 | 416 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| a0004 | 0/0 | 416 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| a0005 | 0/0 | 416 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| a0006 | 0/0 | 416 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| 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 | 1/1 | 1251 | 335 | 81 | 53 | 147 | 14 | 38 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| c0002 | 0/0 | 1251 | 3 | 3 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| c0003 | 0/0 | 1251 | 2 | 1 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| c0004 | 0/0 | 1251 | 2 | 2 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| c0005 | 0/0 | 1251 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| c0006 | 0/0 | 1251 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| c0007 | 0/0 | 1251 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| c0008 | 0/0 | 1251 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| c0009 | 0/0 | 1251 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| c0010 | 0/0 | 1251 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| c0011 | 0/0 | 1251 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| c0012 | 0/0 | 1251 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| 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 | 4193 | 127 | 24 | 21 | 51 | 6 | 24 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| t0002 | 0/0 | 4193 | 38 | 2 | 11 | 23 | 1 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| t0003 | 0/0 | 4181 | 36 | 4 | 5 | 20 | 2 | 5 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| t0004 | 0/0 | 4193 | 25 | 0 | 3 | 17 | 2 | 3 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| t0005 | 0/0 | 4193 | 11 | 11 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| t0006 | 0/0 | 4182 | 8 | 4 | 3 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| t0007 | 0/0 | 4181 | 7 | 1 | 1 | 3 | 1 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| t0008 | 0/0 | 4197 | 7 | 7 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| t0009 | 0/0 | 4193 | 7 | 7 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| t0010 | 0/0 | 4181 | 7 | 0 | 0 | 5 | 1 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| t0011 | 0/0 | 4181 | 6 | 1 | 3 | 2 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| t0012 | 0/0 | 4193 | 5 | 0 | 0 | 5 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| t0013 | 0/0 | 4193 | 4 | 0 | 1 | 3 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| t0014 | 0/0 | 4181 | 4 | 0 | 1 | 3 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| t0015 | 0/0 | 4197 | 4 | 4 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| t0016 | 0/0 | 4198 | 3 | 3 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| t0017 | 0/0 | 4198 | 3 | 3 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| t0018 | 0/0 | 4197 | 3 | 3 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| t0019 | 0/0 | 4182 | 3 | 1 | 1 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| t0020 | 0/0 | 4193 | 2 | 1 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| t0021 | 0/0 | 4197 | 2 | 2 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| t0022 | 0/0 | 4197 | 2 | 2 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| t0023 | 0/0 | 4193 | 2 | 2 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| t0024 | 1/0 | 4193 | 2 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| t0025 | 0/0 | 4197 | 2 | 2 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| t0026 | 0/0 | 4193 | 2 | 1 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| t0027 | 0/0 | 4193 | 2 | 0 | 0 | 2 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| t0028 | 0/0 | 4197 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| t0029 | 0/0 | 4192 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| t0030 | 0/0 | 4193 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| t0031 | 0/0 | 4193 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| t0032 | 0/0 | 4181 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| t0033 | 0/0 | 4182 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| t0034 | 0/0 | 4181 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| t0035 | 0/0 | 4179 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| t0036 | 0/0 | 4193 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| t0037 | 0/0 | 4193 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| t0038 | 0/0 | 4193 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| t0039 | 0/0 | 4193 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| t0040 | 0/0 | 4193 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| t0041 | 0/0 | 4197 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| t0042 | 0/0 | 4197 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| t0043 | 0/0 | 4193 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| t0044 | 0/0 | 4193 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| t0045 | 0/0 | 4193 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| t0046 | 0/0 | 4197 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| t0047 | 0/0 | 4181 | 1 | 0 | 0 | 0 | 1 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| t0048 | 0/0 | 4182 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| t0049 | 0/0 | 4181 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| t0050 | 0/0 | 4193 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| t0051 | 0/0 | 4197 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| t0052 | 0/0 | 4193 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| t0053 | 0/0 | 4181 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| 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 | 2 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0074 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0233 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0333 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| 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 | 1/1 | 1251 | 335 | 81 | 53 | 147 | 14 | 38 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| a0001c0003 | 0/0 | 1251 | 2 | 1 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| a0001c0005 | 0/0 | 1251 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| a0001c0008 | 0/0 | 1251 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| a0001c0009 | 0/0 | 1251 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| a0001c0010 | 0/0 | 1251 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| a0001c0011 | 0/0 | 1251 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| a0002c0002 | 0/0 | 1251 | 3 | 3 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| a0003c0004 | 0/0 | 1251 | 2 | 2 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| a0004c0006 | 0/0 | 1251 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| a0005c0007 | 0/0 | 1251 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| a0006c0012 | 0/0 | 1251 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 5443 | 126 | 24 | 20 | 51 | 6 | 24 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| a0001c0001t0002 | 0/0 | 5443 | 37 | 2 | 10 | 23 | 1 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| a0001c0001t0003 | 0/0 | 5431 | 36 | 4 | 5 | 20 | 2 | 5 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| a0001c0001t0004 | 0/0 | 5443 | 24 | 0 | 3 | 16 | 2 | 3 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| a0001c0001t0005 | 0/0 | 5443 | 10 | 10 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| a0001c0001t0006 | 0/0 | 5432 | 8 | 4 | 3 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| a0001c0001t0007 | 0/0 | 5431 | 7 | 1 | 1 | 3 | 1 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| a0001c0001t0008 | 0/0 | 5447 | 6 | 6 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| a0001c0001t0009 | 0/0 | 5443 | 4 | 4 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| a0001c0001t0010 | 0/0 | 5431 | 7 | 0 | 0 | 5 | 1 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| a0001c0001t0011 | 0/0 | 5431 | 5 | 0 | 3 | 2 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| a0001c0001t0012 | 0/0 | 5443 | 5 | 0 | 0 | 5 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| a0001c0001t0013 | 0/0 | 5443 | 4 | 0 | 1 | 3 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| a0001c0001t0014 | 0/0 | 5431 | 4 | 0 | 1 | 3 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| a0001c0001t0015 | 0/0 | 5447 | 4 | 4 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| a0001c0001t0016 | 0/0 | 5448 | 3 | 3 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| a0001c0001t0017 | 0/0 | 5448 | 2 | 2 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| a0001c0001t0018 | 0/0 | 5447 | 3 | 3 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| a0001c0001t0019 | 0/0 | 5432 | 3 | 1 | 1 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| a0001c0001t0020 | 0/0 | 5443 | 2 | 1 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| a0001c0001t0021 | 0/0 | 5447 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| a0001c0001t0022 | 0/0 | 5447 | 2 | 2 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| a0001c0001t0023 | 0/0 | 5443 | 2 | 2 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| a0001c0001t0024 | 1/0 | 5443 | 2 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| a0001c0001t0027 | 0/0 | 5443 | 2 | 0 | 0 | 2 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| a0001c0001t0028 | 0/0 | 5447 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| a0001c0001t0029 | 0/0 | 5442 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| a0001c0001t0030 | 0/0 | 5443 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| a0001c0001t0031 | 0/0 | 5443 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| a0001c0001t0032 | 0/0 | 5431 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| a0001c0001t0033 | 0/0 | 5432 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| a0001c0001t0034 | 0/0 | 5431 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| a0001c0001t0035 | 0/0 | 5429 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| a0001c0001t0036 | 0/0 | 5443 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| a0001c0001t0037 | 0/0 | 5443 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| a0001c0001t0038 | 0/0 | 5443 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| a0001c0001t0039 | 0/0 | 5443 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| a0001c0001t0040 | 0/0 | 5443 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| a0001c0001t0041 | 0/0 | 5447 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| a0001c0001t0042 | 0/0 | 5447 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| a0001c0001t0043 | 0/0 | 5443 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| a0001c0001t0044 | 0/0 | 5443 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| a0001c0001t0045 | 0/0 | 5443 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| a0001c0001t0046 | 0/0 | 5447 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| a0001c0001t0047 | 0/0 | 5431 | 1 | 0 | 0 | 0 | 1 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| a0001c0001t0048 | 0/0 | 5432 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| a0001c0001t0049 | 0/0 | 5431 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| a0001c0001t0050 | 0/0 | 5443 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| a0001c0001t0051 | 0/0 | 5447 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| a0001c0001t0052 | 0/0 | 5443 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| a0001c0001t0053 | 0/0 | 5431 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| a0001c0003t0026 | 0/0 | 5443 | 2 | 1 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| a0001c0005t0008 | 0/0 | 5447 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| a0001c0008t0021 | 0/0 | 5447 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| a0001c0009t0005 | 0/0 | 5443 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| a0001c0010t0001 | 0/0 | 5443 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| a0001c0011t0004 | 0/0 | 5443 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| a0002c0002t0009 | 0/0 | 5443 | 3 | 3 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| a0003c0004t0025 | 0/0 | 5447 | 2 | 2 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| a0004c0006t0002 | 0/0 | 5443 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| a0005c0007t0017 | 0/0 | 5448 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| a0006c0012t0011 | 0/0 | 5431 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | copy fasta | chr1 | 167625232 | 167713696 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0074 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0001g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0003g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0003g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0003g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0003g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0003g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0003g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0003g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0003g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0003g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0003g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0003g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0003g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0003g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0003g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0003g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0003g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0003g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0003g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0003g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0003g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0003g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0003g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0003g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0003g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0003g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0003g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0003g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0003g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0004g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0004g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0004g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0004g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0004g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0004g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0004g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0004g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0004g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0004g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0004g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0004g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0004g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0004g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0004g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0004g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0004g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0004g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0004g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0004g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0004g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0004g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0004g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0004g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0005g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0005g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0005g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0005g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0005g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0005g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0005g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0005g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0005g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0005g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0006g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0006g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0006g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0006g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0006g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0006g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0006g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0006g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0007g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0007g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0007g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0007g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0007g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0007g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0007g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0008g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0008g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0008g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0008g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0008g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0008g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0009g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0009g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0009g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0009g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0010g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0010g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0010g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0010g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0010g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0010g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0010g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0011g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0011g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0011g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0011g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0011g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0012g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0012g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0012g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0012g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0012g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0013g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0013g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0013g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0013g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0014g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0014g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0014g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0014g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0015g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0015g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0015g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0015g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0016g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0016g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0016g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0017g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0017g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0018g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0018g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0018g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0019g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0019g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0019g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0020g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0020g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0021g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0022g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0022g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0023g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0023g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0024g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0024g0233 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0027g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0027g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0028g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0029g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0030g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0031g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0032g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0033g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0034g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0035g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0036g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0037g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0038g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0039g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0040g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0041g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0042g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0043g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0044g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0045g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0046g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0047g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0048g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0049g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0050g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0051g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0052g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0001t0053g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0003t0026g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0003t0026g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0005t0008g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0008t0021g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0009t0005g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0010t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0001c0011t0004g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0002c0002t0009g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0002c0002t0009g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0002c0002t0009g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0003c0004t0025g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0003c0004t0025g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0004c0006t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0005c0007t0017g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| a0006c0012t0011g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0049 | EUR | GBR | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG00099 | hp2 | a0001 | c0001 | t0003 | g0286 | EUR | GBR | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0285 | EUR | GBR | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0209 | EUR | GBR | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0139 | EUR | FIN | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG00280 | hp2 | a0001 | c0001 | t0047 | g0065 | EUR | FIN | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG00323 | hp1 | a0001 | c0001 | t0004 | g0127 | EUR | FIN | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG00323 | hp2 | a0001 | c0001 | t0004 | g0126 | EUR | FIN | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG00408 | hp1 | a0001 | c0001 | t0051 | g0117 | EAS | CHS | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | CHS | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG00423 | hp1 | a0001 | c0001 | t0050 | g0119 | EAS | CHS | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG00423 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | CHS | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | CHS | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG00438 | hp2 | a0001 | c0001 | t0011 | g0042 | EAS | CHS | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG00544 | hp1 | a0001 | c0001 | t0012 | g0315 | EAS | CHS | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG00544 | hp2 | a0001 | c0001 | t0004 | g0122 | EAS | CHS | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | CHS | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG00558 | hp2 | a0001 | c0001 | t0012 | g0008 | EAS | CHS | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | CHS | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0178 | EAS | CHS | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0149 | EAS | CHS | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0208 | AMR | PUR | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG00673 | hp1 | a0001 | c0001 | t0004 | g0088 | EAS | CHS | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG00673 | hp2 | a0001 | c0001 | t0004 | g0124 | EAS | CHS | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0133 | AMR | PUR | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG00741 | hp1 | a0001 | c0001 | t0007 | g0182 | AMR | PUR | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG01070 | hp1 | a0001 | c0001 | t0034 | g0183 | AMR | PUR | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG01074 | hp1 | a0001 | c0001 | t0004 | g0125 | AMR | PUR | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG01074 | hp2 | a0001 | c0001 | t0014 | g0314 | AMR | PUR | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG01081 | hp2 | a0001 | c0001 | t0028 | g0335 | AMR | PUR | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0210 | AMR | PUR | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG01109 | hp1 | a0001 | c0001 | t0024 | g0159 | AMR | PUR | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG01109 | hp2 | a0001 | c0003 | t0026 | g0218 | AMR | PUR | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0287 | AMR | PUR | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0151 | AMR | PUR | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG01175 | hp2 | a0001 | c0001 | t0011 | g0043 | AMR | PUR | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | PUR | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG01192 | hp2 | a0004 | c0006 | t0002 | g0207 | AMR | PUR | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG01243 | hp1 | a0001 | c0001 | t0020 | g0301 | AMR | PUR | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG01243 | hp2 | a0001 | c0001 | t0011 | g0067 | AMR | PUR | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG01255 | hp1 | a0001 | c0001 | t0004 | g0080 | AMR | CLM | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG01255 | hp2 | a0001 | c0001 | t0033 | g0180 | AMR | CLM | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0163 | AMR | CLM | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0164 | AMR | CLM | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | CLM | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG01361 | hp2 | a0001 | c0001 | t0003 | g0245 | AMR | CLM | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0273 | AMR | CLM | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG01433 | hp2 | a0001 | c0001 | t0006 | g0223 | AMR | CLM | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG01496 | hp1 | a0001 | c0010 | t0001 | g0012 | AMR | CLM | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0175 | AMR | CLM | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG01515 | hp1 | a0001 | c0001 | t0007 | g0057 | EUR | IBS | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0333 | EUR | IBS | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG01516 | hp1 | a0001 | c0001 | t0003 | g0161 | EUR | IBS | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG01516 | hp2 | a0001 | c0001 | t0010 | g0248 | EUR | IBS | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG01884 | hp1 | a0001 | c0001 | t0040 | g0156 | AFR | ACB | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG01884 | hp2 | a0001 | c0001 | t0018 | g0339 | AFR | ACB | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG01891 | hp1 | a0001 | c0001 | t0008 | g0331 | AFR | ACB | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG01891 | hp2 | a0001 | c0001 | t0044 | g0217 | AFR | ACB | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG01928 | hp1 | a0001 | c0001 | t0004 | g0097 | AMR | PEL | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG01928 | hp2 | a0001 | c0001 | t0019 | g0099 | AMR | PEL | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG01934 | hp1 | a0001 | c0001 | t0011 | g0274 | AMR | PEL | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PEL | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PEL | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0045 | AMR | PEL | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG01981 | hp2 | a0001 | c0001 | t0006 | g0098 | AMR | PEL | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG01993 | hp1 | a0001 | c0001 | t0003 | g0224 | AMR | PEL | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0272 | AMR | PEL | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0165 | AMR | PEL | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG02004 | hp2 | a0001 | c0001 | t0003 | g0018 | AMR | PEL | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0197 | EAS | KHV | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | KHV | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | KHV | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0166 | EAS | KHV | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | KHV | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG02040 | hp2 | a0001 | c0011 | t0004 | g0250 | EAS | KHV | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG02055 | hp1 | a0001 | c0001 | t0005 | g0020 | AFR | ACB | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG02055 | hp2 | a0001 | c0001 | t0005 | g0326 | AFR | ACB | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG02056 | hp1 | a0001 | c0001 | t0004 | g0094 | EAS | KHV | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0323 | EAS | KHV | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG02074 | hp1 | a0001 | c0001 | t0004 | g0246 | EAS | KHV | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | KHV | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG02080 | hp2 | a0001 | c0001 | t0007 | g0173 | EAS | KHV | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG02083 | hp1 | a0001 | c0001 | t0003 | g0024 | EAS | KHV | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG02083 | hp2 | a0001 | c0001 | t0037 | g0325 | EAS | KHV | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0346 | AFR | ACB | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG02145 | hp2 | a0001 | c0001 | t0005 | g0069 | AFR | ACB | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG02148 | hp1 | a0001 | c0001 | t0006 | g0153 | AMR | PEL | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0147 | AMR | PEL | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | CDX | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG02155 | hp2 | a0001 | c0001 | t0004 | g0120 | EAS | CDX | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0324 | EAS | CDX | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | CDX | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG02257 | hp1 | a0001 | c0001 | t0009 | g0334 | AFR | ACB | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG02257 | hp2 | a0001 | c0001 | t0007 | g0036 | AFR | ACB | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG02258 | hp1 | a0001 | c0001 | t0005 | g0030 | AFR | ACB | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG02258 | hp2 | a0001 | c0001 | t0016 | g0112 | AFR | ACB | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG02280 | hp1 | a0003 | c0004 | t0025 | g0034 | AFR | ACB | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | ACB | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG02293 | hp1 | a0001 | c0001 | t0013 | g0148 | AMR | PEL | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG02293 | hp2 | a0001 | c0001 | t0003 | g0041 | AMR | PEL | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG02451 | hp1 | a0002 | c0002 | t0009 | g0269 | AFR | ACB | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0268 | AFR | ACB | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0121 | EAS | KHV | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | KHV | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG02572 | hp1 | a0001 | c0001 | t0005 | g0111 | AFR | GWD | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG02572 | hp2 | a0001 | c0001 | t0009 | g0213 | AFR | GWD | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0051 | SAS | PJL | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG02602 | hp2 | a0001 | c0001 | t0042 | g0215 | SAS | PJL | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG02622 | hp1 | a0001 | c0001 | t0008 | g0329 | AFR | GWD | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG02622 | hp2 | a0001 | c0001 | t0039 | g0337 | AFR | GWD | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0307 | AFR | GWD | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0206 | AFR | GWD | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG02647 | hp1 | a0001 | c0001 | t0006 | g0271 | AFR | GWD | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0302 | AFR | GWD | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG02698 | hp1 | a0001 | c0001 | t0003 | g0267 | SAS | PJL | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG02698 | hp2 | a0001 | c0001 | t0003 | g0039 | SAS | PJL | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG02717 | hp1 | a0001 | c0001 | t0009 | g0128 | AFR | GWD | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG02717 | hp2 | a0001 | c0001 | t0008 | g0300 | AFR | GWD | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG02723 | hp1 | a0001 | c0001 | t0046 | g0058 | AFR | GWD | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG02723 | hp2 | a0001 | c0001 | t0015 | g0239 | AFR | GWD | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0231 | SAS | PJL | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0054 | SAS | PJL | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0297 | SAS | PJL | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0048 | SAS | PJL | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG02818 | hp1 | a0001 | c0001 | t0015 | g0052 | AFR | GWD | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG02818 | hp2 | a0001 | c0001 | t0022 | g0242 | AFR | GWD | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG02886 | hp1 | a0006 | c0012 | t0011 | g0234 | AFR | GWD | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG02886 | hp2 | a0001 | c0001 | t0005 | g0244 | AFR | GWD | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG02895 | hp1 | a0001 | c0009 | t0005 | g0062 | AFR | GWD | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG02895 | hp2 | a0001 | c0001 | t0015 | g0304 | AFR | GWD | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG02896 | hp1 | a0001 | c0001 | t0006 | g0226 | AFR | GWD | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0236 | AFR | GWD | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG02897 | hp1 | a0001 | c0001 | t0015 | g0305 | AFR | GWD | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG02897 | hp2 | a0001 | c0001 | t0006 | g0225 | AFR | GWD | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG02922 | hp1 | a0001 | c0003 | t0026 | g0303 | AFR | ESN | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG02922 | hp2 | a0001 | c0001 | t0016 | g0327 | AFR | ESN | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG02965 | hp1 | a0002 | c0002 | t0009 | g0318 | AFR | ESN | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG02965 | hp2 | a0001 | c0001 | t0005 | g0061 | AFR | ESN | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG02976 | hp1 | a0001 | c0008 | t0021 | g0185 | AFR | ESN | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG02976 | hp2 | a0003 | c0004 | t0025 | g0240 | AFR | ESN | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG03017 | hp1 | a0001 | c0001 | t0010 | g0073 | SAS | PJL | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0347 | SAS | PJL | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG03041 | hp1 | a0001 | c0001 | t0052 | g0158 | AFR | GWD | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG03041 | hp2 | a0001 | c0001 | t0020 | g0317 | AFR | GWD | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG03098 | hp1 | a0001 | c0001 | t0008 | g0219 | AFR | MSL | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0308 | AFR | MSL | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG03130 | hp1 | a0001 | c0001 | t0018 | g0340 | AFR | ESN | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0299 | AFR | ESN | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG03139 | hp2 | a0001 | c0001 | t0016 | g0253 | AFR | ESN | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0289 | AFR | ESN | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0319 | AFR | ESN | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0004 | AFR | MSL | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG03209 | hp2 | a0001 | c0001 | t0017 | g0341 | AFR | MSL | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG03225 | hp1 | a0001 | c0001 | t0041 | g0311 | AFR | MSL | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | MSL | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0265 | SAS | PJL | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG03239 | hp2 | a0001 | c0001 | t0003 | g0345 | SAS | PJL | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG03453 | hp1 | a0001 | c0001 | t0008 | g0310 | AFR | MSL | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG03453 | hp2 | a0001 | c0001 | t0023 | g0227 | AFR | MSL | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0336 | AFR | MSL | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0238 | AFR | MSL | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG03491 | hp2 | a0001 | c0001 | t0004 | g0087 | SAS | PJL | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0282 | SAS | PJL | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG03516 | hp1 | a0001 | c0001 | t0005 | g0288 | AFR | ESN | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0279 | AFR | ESN | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG03540 | hp1 | a0005 | c0007 | t0017 | g0243 | AFR | GWD | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG03579 | hp1 | a0001 | c0001 | t0003 | g0306 | AFR | MSL | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG03579 | hp2 | a0001 | c0001 | t0022 | g0342 | AFR | MSL | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0059 | SAS | PJL | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG03669 | hp2 | a0001 | c0001 | t0003 | g0037 | SAS | PJL | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0222 | SAS | STU | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | STU | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0264 | SAS | PJL | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG03831 | hp1 | a0001 | c0001 | t0004 | g0118 | SAS | BEB | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0216 | SAS | BEB | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | BEB | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG03834 | hp2 | a0001 | c0001 | t0045 | g0109 | SAS | BEB | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG03927 | hp1 | a0001 | c0001 | t0007 | g0142 | SAS | BEB | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG03927 | hp2 | a0001 | c0001 | t0004 | g0091 | SAS | BEB | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0266 | SAS | BEB | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG03942 | hp2 | a0001 | c0001 | t0003 | g0053 | SAS | BEB | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0258 | SAS | STU | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0316 | SAS | STU | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0291 | SAS | BEB | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG04184 | hp2 | a0001 | c0001 | t0038 | g0343 | SAS | BEB | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0023 | SAS | STU | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0046 | SAS | STU | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0344 | SAS | STU | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0176 | SAS | STU | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0313 | AFR | YRI | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA18522 | hp2 | a0001 | c0001 | t0019 | g0157 | AFR | YRI | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | YRI | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA18906 | hp2 | a0002 | c0002 | t0009 | g0212 | AFR | YRI | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA18939 | hp1 | a0001 | c0001 | t0003 | g0284 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA18942 | hp1 | a0001 | c0001 | t0004 | g0092 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA18942 | hp2 | a0001 | c0001 | t0012 | g0277 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA18945 | hp1 | a0001 | c0001 | t0003 | g0214 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA18945 | hp2 | a0001 | c0001 | t0004 | g0076 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA18947 | hp1 | a0001 | c0001 | t0027 | g0089 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA18947 | hp2 | a0001 | c0001 | t0036 | g0280 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA18950 | hp2 | a0001 | c0001 | t0004 | g0095 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA18951 | hp2 | a0001 | c0001 | t0004 | g0086 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA18952 | hp1 | a0001 | c0001 | t0010 | g0068 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA18956 | hp1 | a0001 | c0001 | t0010 | g0071 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA18957 | hp2 | a0001 | c0001 | t0003 | g0134 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA18959 | hp1 | a0001 | c0001 | t0003 | g0135 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA18961 | hp1 | a0001 | c0001 | t0013 | g0199 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA18961 | hp2 | a0001 | c0001 | t0049 | g0211 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA18968 | hp1 | a0001 | c0001 | t0003 | g0084 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA18968 | hp2 | a0001 | c0001 | t0003 | g0283 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA18969 | hp1 | a0001 | c0001 | t0003 | g0130 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA18970 | hp1 | a0001 | c0001 | t0035 | g0198 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA18970 | hp2 | a0001 | c0001 | t0007 | g0192 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA18972 | hp1 | a0001 | c0001 | t0003 | g0026 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA18972 | hp2 | a0001 | c0001 | t0006 | g0257 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA18974 | hp1 | a0001 | c0001 | t0003 | g0322 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA18977 | hp1 | a0001 | c0001 | t0004 | g0075 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA18977 | hp2 | a0001 | c0001 | t0019 | g0093 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA18979 | hp1 | a0001 | c0001 | t0014 | g0177 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA18982 | hp1 | a0001 | c0001 | t0004 | g0123 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA18983 | hp1 | a0001 | c0001 | t0013 | g0200 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA18984 | hp2 | a0001 | c0001 | t0012 | g0251 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA18985 | hp1 | a0001 | c0001 | t0004 | g0056 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA18985 | hp2 | a0001 | c0001 | t0014 | g0181 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA18989 | hp2 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA18990 | hp2 | a0001 | c0001 | t0010 | g0249 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA18994 | hp2 | a0001 | c0001 | t0011 | g0100 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA18995 | hp2 | a0001 | c0001 | t0003 | g0321 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA19000 | hp1 | a0001 | c0001 | t0003 | g0256 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA19001 | hp2 | a0001 | c0001 | t0048 | g0102 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA19002 | hp1 | a0001 | c0001 | t0032 | g0167 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA19002 | hp2 | a0001 | c0001 | t0010 | g0077 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA19003 | hp1 | a0001 | c0001 | t0013 | g0204 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA19003 | hp2 | a0001 | c0001 | t0007 | g0174 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA19005 | hp1 | a0001 | c0001 | t0043 | g0015 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA19009 | hp2 | a0001 | c0001 | t0031 | g0172 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA19011 | hp1 | a0001 | c0001 | t0003 | g0255 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | LWK | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA19030 | hp2 | a0001 | c0001 | t0009 | g0290 | AFR | LWK | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA19043 | hp1 | a0001 | c0001 | t0053 | g0096 | AFR | LWK | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA19043 | hp2 | a0001 | c0001 | t0017 | g0338 | AFR | LWK | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA19056 | hp1 | a0001 | c0001 | t0014 | g0202 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA19057 | hp1 | a0001 | c0001 | t0010 | g0079 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA19058 | hp2 | a0001 | c0001 | t0030 | g0191 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA19063 | hp2 | a0001 | c0001 | t0012 | g0312 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA19064 | hp1 | a0001 | c0001 | t0004 | g0090 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA19064 | hp2 | a0001 | c0001 | t0003 | g0230 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0162 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA19066 | hp2 | a0001 | c0001 | t0004 | g0072 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA19067 | hp1 | a0001 | c0001 | t0029 | g0179 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA19067 | hp2 | a0001 | c0001 | t0027 | g0078 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA19070 | hp1 | a0001 | c0001 | t0004 | g0247 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA19070 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA19081 | hp1 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA19087 | hp1 | a0001 | c0001 | t0003 | g0060 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA19091 | hp2 | a0001 | c0001 | t0003 | g0140 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0261 | AFR | YRI | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA19240 | hp2 | a0001 | c0001 | t0008 | g0262 | AFR | YRI | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0047 | EUR | TSI | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0070 | EUR | TSI | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0184 | AMR | CLM | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | CLM | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG02109 | hp1 | a0001 | c0001 | t0005 | g0237 | AFR | ACB | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0281 | AFR | ACB | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG02486 | hp1 | a0001 | c0001 | t0023 | g0259 | AFR | ACB | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0328 | AFR | ACB | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0270 | AFR | ACB | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG02559 | hp2 | a0001 | c0005 | t0008 | g0296 | AFR | ACB | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG03471 | hp1 | a0001 | c0001 | t0021 | g0005 | AFR | MSL | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG03471 | hp2 | a0001 | c0001 | t0018 | g0330 | AFR | MSL | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | USA | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0040 | AFR | USA | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | USA | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA20300 | hp2 | a0001 | c0001 | t0005 | g0332 | AFR | USA | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA21309 | hp1 | a0001 | c0001 | t0006 | g0295 | AFR | LWK | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0309 | AFR | LWK | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0074 | REF | REF | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0024 | g0233 | REF | REF | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:167683906
|
C | T | 1 | a0006 | 1 | HG02886.hp1 | missense_variant | MODERATE | c.13C>T | p.Pro5Ser | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 2/7 | 205/5443 | 13/1251 | 5/416 | chr1 | 167683906 | ||
| chr1:167697313
|
C | A | 1 | a0004 | 1 | HG01192.hp2 | missense_variant | MODERATE | c.689C>A | p.Thr230Asn | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/7 | 881/5443 | 689/1251 | 230/416 | chr1 | 167697313 | ||
| chr1:167697469
|
C | T | 1 | a0003 | 2 | HG02280.hp1 HG02976.hp2 |
missense_variant | MODERATE | c.845C>T | p.Pro282Leu | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/7 | 1037/5443 | 845/1251 | 282/416 | chr1 | 167697469 | ||
| chr1:167697572
|
G | C | 2 | a0003a0005 | 3 | HG02280.hp1 HG02976.hp2 HG03540.hp1 |
missense_variant | MODERATE | c.948G>C | p.Glu316Asp | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/7 | 1140/5443 | 948/1251 | 316/416 | chr1 | 167697572 | ||
| chr1:167697775
|
A | G | 1 | a0002 | 3 | HG02451.hp1 HG02965.hp1 NA18906.hp2 |
missense_variant | MODERATE | c.1151A>G | p.Gln384Arg | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/7 | 1343/5443 | 1151/1251 | 384/416 | chr1 | 167697775 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:167694122
|
T | C | 1 | a0001c0003 | 2 | HG01109.hp2 HG02922.hp1 |
synonymous_variant | LOW | c.294T>C | p.Ala98Ala | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 5/7 | 486/5443 | 294/1251 | 98/416 | chr1 | 167694122 | ||
| chr1:167694161
|
C | T | 1 | a0001c0011 | 1 | HG02040.hp2 | synonymous_variant | LOW | c.333C>T | p.Leu111Leu | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 5/7 | 525/5443 | 333/1251 | 111/416 | chr1 | 167694161 | ||
| chr1:167694239
|
A | G | 1 | a0001c0010 | 1 | HG01496.hp1 | synonymous_variant | LOW | c.411A>G | p.Ala137Ala | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 5/7 | 603/5443 | 411/1251 | 137/416 | chr1 | 167694239 | ||
| chr1:167697296
|
G | A | 1 | a0001c0005 | 1 | HG02559.hp2 | synonymous_variant | LOW | c.672G>A | p.Ala224Ala | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/7 | 864/5443 | 672/1251 | 224/416 | chr1 | 167697296 | ||
| chr1:167697404
|
C | T | 1 | a0001c0009 | 1 | HG02895.hp1 | synonymous_variant | LOW | c.780C>T | p.Asn260Asn | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/7 | 972/5443 | 780/1251 | 260/416 | chr1 | 167697404 | ||
| chr1:167697821
|
G | A | 1 | a0001c0008 | 1 | HG02976.hp1 | synonymous_variant | LOW | c.1197G>A | p.Glu399Glu | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/7 | 1389/5443 | 1197/1251 | 399/416 | chr1 | 167697821 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:167630289
|
G | C | 1 | a0001c0001t0028 | 1 | HG01081.hp2 | 5_prime_UTR_variant | MODIFIER | c.-135G>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/7 | 135 | chr1 | 167630289 | |||||
| chr1:167630296
|
C | T | 9 | a0001c0001t0004a0001c0001t0010a0001c0001t0019others(6): Show | 41 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(38): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-128C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/7 | chr1 | 167630296 | ||||||
| chr1:167630346
|
G | A | 12 | a0001c0001t0002a0001c0001t0007a0001c0001t0013others(9): Show | 60 | HG00140.hp2 HG00609.hp2 HG00621.hp1 others(57): Show |
5_prime_UTR_variant | MODIFIER | c.-78G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/7 | 78 | chr1 | 167630346 | |||||
| chr1:167630371
|
G | A | 1 | a0001c0001t0036 | 1 | NA18947.hp2 | 5_prime_UTR_variant | MODIFIER | c.-53G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/7 | 53 | chr1 | 167630371 | |||||
| chr1:167630408
|
T | G | 1 | a0001c0001t0013 | 4 | HG02293.hp1 NA18961.hp1 NA18983.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-16T>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/7 | 16 | chr1 | 167630408 | |||||
| chr1:167704779
|
C | T | 1 | a0001c0003t0026 | 2 | HG01109.hp2 HG02922.hp1 |
3_prime_UTR_variant | MODIFIER | c.*83C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 7/7 | 83 | chr1 | 167704779 | |||||
| chr1:167704867
|
G | A | 1 | a0001c0001t0037 | 1 | HG02083.hp2 | 3_prime_UTR_variant | MODIFIER | c.*171G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 7/7 | 171 | chr1 | 167704867 | |||||
| chr1:167704906
|
C | T | 1 | a0003c0004t0025 | 2 | HG02280.hp1 HG02976.hp2 |
3_prime_UTR_variant | MODIFIER | c.*210C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 7/7 | 210 | chr1 | 167704906 | |||||
| chr1:167705050
|
CAGCTAAT others(2): Show |
C | 16 | a0001c0001t0003a0001c0001t0006a0001c0001t0007others(13): Show | 79 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*359_*367delAATTTA others(3): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 7/7 | 359 | INFO_REALIGN_3_PRIME | chr1 | 167705050 | ||||
| chr1:167705066
|
T | C | 16 | a0001c0001t0003a0001c0001t0006a0001c0001t0007others(13): Show | 79 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*370T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 7/7 | 370 | chr1 | 167705066 | |||||
| chr1:167705069
|
CTAAT | C | 16 | a0001c0001t0003a0001c0001t0006a0001c0001t0007others(13): Show | 79 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*375_*378delAATT | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 7/7 | 375 | INFO_REALIGN_3_PRIME | chr1 | 167705069 | ||||
| chr1:167705074
|
T | C | 16 | a0001c0001t0003a0001c0001t0006a0001c0001t0007others(13): Show | 79 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*378T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 7/7 | 378 | chr1 | 167705074 | |||||
| chr1:167705075
|
T | G | 16 | a0001c0001t0003a0001c0001t0006a0001c0001t0007others(13): Show | 79 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*379T>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 7/7 | 379 | chr1 | 167705075 | |||||
| chr1:167705179
|
G | C | 1 | a0001c0001t0038 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*483G>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 7/7 | 483 | chr1 | 167705179 | |||||
| chr1:167705332
|
T | TAA | 15 | a0001c0001t0003a0001c0001t0006a0001c0001t0007others(12): Show | 78 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*646_*647dupAA | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 7/7 | 648 | INFO_REALIGN_3_PRIME | chr1 | 167705332 | ||||
| chr1:167705351
|
A | T | 3 | a0001c0001t0015a0001c0001t0018a0001c0001t0046 | 8 | HG01884.hp2 HG02723.hp1 HG02723.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*655A>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 7/7 | 655 | chr1 | 167705351 | |||||
| chr1:167705416
|
C | G | 15 | a0001c0001t0003a0001c0001t0006a0001c0001t0007others(12): Show | 78 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*720C>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 7/7 | 720 | chr1 | 167705416 | |||||
| chr1:167705432
|
C | G | 1 | a0001c0001t0018 | 3 | HG01884.hp2 HG03130.hp1 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*736C>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 7/7 | 736 | chr1 | 167705432 | |||||
| chr1:167705480
|
G | A | 2 | a0001c0001t0020a0001c0001t0039 | 3 | HG01243.hp1 HG02622.hp2 HG03041.hp2 |
3_prime_UTR_variant | MODIFIER | c.*784G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 7/7 | 784 | chr1 | 167705480 | |||||
| chr1:167705540
|
G | A | 4 | a0001c0001t0005a0001c0001t0040a0001c0003t0026others(1): Show | 14 | HG01109.hp2 HG01884.hp1 HG02055.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*844G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 7/7 | 844 | chr1 | 167705540 | |||||
| chr1:167705650
|
T | C | 2 | a0001c0001t0008a0001c0005t0008 | 7 | HG01891.hp1 HG02559.hp2 HG02622.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*954T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 7/7 | 954 | chr1 | 167705650 | |||||
| chr1:167705720
|
C | T | 1 | a0001c0001t0053 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1024C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 7/7 | 1024 | chr1 | 167705720 | |||||
| chr1:167705755
|
T | C | 1 | a0001c0003t0026 | 2 | HG01109.hp2 HG02922.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1059T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 7/7 | 1059 | chr1 | 167705755 | |||||
| chr1:167706172
|
T | C | 1 | a0001c0001t0050 | 1 | HG00423.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1476T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 7/7 | 1476 | chr1 | 167706172 | |||||
| chr1:167706298
|
A | G | 16 | a0001c0001t0003a0001c0001t0006a0001c0001t0007others(13): Show | 79 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*1602A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 7/7 | 1602 | chr1 | 167706298 | |||||
| chr1:167706378
|
T | C | 3 | a0001c0001t0011a0001c0001t0014a0006c0012t0011 | 10 | HG00438.hp2 HG01074.hp2 HG01175.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1682T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 7/7 | 1682 | chr1 | 167706378 | |||||
| chr1:167706412
|
T | C | 32 | a0001c0001t0003a0001c0001t0006a0001c0001t0007others(29): Show | 110 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(107): Show |
3_prime_UTR_variant | MODIFIER | c.*1716T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 7/7 | 1716 | chr1 | 167706412 | |||||
| chr1:167706448
|
T | C | 2 | a0001c0001t0027a0001c0001t0043 | 3 | NA18947.hp1 NA19005.hp1 NA19067.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1752T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 7/7 | 1752 | chr1 | 167706448 | |||||
| chr1:167706476
|
A | ACTTTT | 16 | a0001c0001t0008a0001c0001t0015a0001c0001t0016others(13): Show | 31 | HG00408.hp1 HG01081.hp2 HG01884.hp2 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*1784_*1785insTCTT others(1): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 7/7 | 1785 | INFO_REALIGN_3_PRIME | chr1 | 167706476 | ||||
| chr1:167706509
|
T | C | 5 | a0001c0001t0016a0001c0001t0017a0001c0001t0021others(2): Show | 8 | HG02258.hp2 HG02922.hp2 HG02976.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1813T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 7/7 | 1813 | chr1 | 167706509 | |||||
| chr1:167706892
|
C | T | 1 | a0001c0001t0045 | 1 | HG03834.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2196C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 7/7 | 2196 | chr1 | 167706892 | |||||
| chr1:167706955
|
T | C | 4 | a0001c0001t0008a0001c0001t0022a0001c0001t0028others(1): Show | 10 | HG01081.hp2 HG01891.hp1 HG02559.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2259T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 7/7 | 2259 | chr1 | 167706955 | |||||
| chr1:167706981
|
G | A | 1 | a0001c0001t0016 | 3 | HG02258.hp2 HG02922.hp2 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2285G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 7/7 | 2285 | chr1 | 167706981 | |||||
| chr1:167707084
|
G | A | 5 | a0001c0001t0008a0001c0001t0022a0001c0001t0028others(2): Show | 11 | HG01081.hp2 HG01891.hp1 HG02559.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2388G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 7/7 | 2388 | chr1 | 167707084 | |||||
| chr1:167707102
|
A | C | 1 | a0001c0001t0049 | 1 | NA18961.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2406A>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 7/7 | 2406 | chr1 | 167707102 | |||||
| chr1:167707127
|
C | A | 29 | a0001c0001t0003a0001c0001t0006a0001c0001t0007others(26): Show | 104 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(101): Show |
3_prime_UTR_variant | MODIFIER | c.*2431C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 7/7 | 2431 | chr1 | 167707127 | |||||
| chr1:167707174
|
T | C | 7 | a0001c0001t0005a0001c0001t0016a0001c0001t0017others(4): Show | 20 | HG01109.hp2 HG01884.hp1 HG02055.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*2478T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 7/7 | 2478 | chr1 | 167707174 | |||||
| chr1:167707383
|
G | A | 1 | a0001c0001t0039 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2687G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 7/7 | 2687 | chr1 | 167707383 | |||||
| chr1:167707481
|
C | T | 29 | a0001c0001t0003a0001c0001t0006a0001c0001t0007others(26): Show | 104 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(101): Show |
3_prime_UTR_variant | MODIFIER | c.*2785C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 7/7 | 2785 | chr1 | 167707481 | |||||
| chr1:167707493
|
G | GA | 3 | a0001c0001t0006a0001c0001t0019a0001c0001t0033 | 12 | HG01255.hp2 HG01433.hp2 HG01928.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2804dupA | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 7/7 | 2805 | INFO_REALIGN_3_PRIME | chr1 | 167707493 | ||||
| chr1:167707507
|
T | C | 1 | a0001c0001t0023 | 2 | HG02486.hp1 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2811T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 7/7 | 2811 | chr1 | 167707507 | |||||
| chr1:167707564
|
C | T | 4 | a0001c0001t0012a0001c0001t0027a0001c0001t0031others(1): Show | 9 | HG00544.hp1 HG00558.hp2 NA18942.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2868C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 7/7 | 2868 | chr1 | 167707564 | |||||
| chr1:167707631
|
T | C | 32 | a0001c0001t0003a0001c0001t0006a0001c0001t0007others(29): Show | 110 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(107): Show |
3_prime_UTR_variant | MODIFIER | c.*2935T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 7/7 | 2935 | chr1 | 167707631 | |||||
| chr1:167707671
|
CT | C | 29 | a0001c0001t0003a0001c0001t0006a0001c0001t0007others(26): Show | 104 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(101): Show |
3_prime_UTR_variant | MODIFIER | c.*2984delT | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 7/7 | 2984 | INFO_REALIGN_3_PRIME | chr1 | 167707671 | ||||
| chr1:167707776
|
C | T | 3 | a0001c0001t0009a0001c0001t0052a0002c0002t0009 | 8 | HG02257.hp1 HG02451.hp1 HG02572.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3080C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 7/7 | 3080 | chr1 | 167707776 | |||||
| chr1:167708054
|
A | C | 61 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(58): Show | 348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
3_prime_UTR_variant | MODIFIER | c.*3358A>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 7/7 | 3358 | chr1 | 167708054 | |||||
| chr1:167708121
|
C | T | 8 | a0001c0001t0003a0001c0001t0007a0001c0001t0010others(5): Show | 55 | HG00099.hp2 HG00423.hp2 HG00735.hp2 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*3425C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 7/7 | 3425 | chr1 | 167708121 | |||||
| chr1:167708265
|
G | A | 1 | a0003c0004t0025 | 2 | HG02280.hp1 HG02976.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3569G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 7/7 | 3569 | chr1 | 167708265 | |||||
| chr1:167708312
|
C | T | 1 | a0001c0001t0044 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3616C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 7/7 | 3616 | chr1 | 167708312 | |||||
| chr1:167708334
|
C | T | 1 | a0001c0001t0030 | 1 | NA19058.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3638C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 7/7 | 3638 | chr1 | 167708334 | |||||
| chr1:167708380
|
C | T | 3 | a0001c0001t0015a0001c0001t0018a0001c0001t0046 | 8 | HG01884.hp2 HG02723.hp1 HG02723.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3684C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 7/7 | 3684 | chr1 | 167708380 | |||||
| chr1:167708388
|
A | T | 1 | a0001c0001t0042 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3692A>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 7/7 | 3692 | chr1 | 167708388 | |||||
| chr1:167708407
|
C | T | 2 | a0001c0001t0005a0001c0009t0005 | 11 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*3711C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 7/7 | 3711 | chr1 | 167708407 | |||||
| chr1:167708410
|
G | A | 1 | a0001c0001t0015 | 4 | HG02723.hp2 HG02818.hp1 HG02895.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3714G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 7/7 | 3714 | chr1 | 167708410 | |||||
| chr1:167708448
|
A | C | 3 | a0001c0001t0006a0001c0001t0019a0001c0001t0033 | 12 | HG01255.hp2 HG01433.hp2 HG01928.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*3752A>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 7/7 | 3752 | chr1 | 167708448 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:167630452
|
G | A | 2 | a0001c0001t0003g0004a0001c0001t0021g0005 | 2 | HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.6+23G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167630452 | ||||||
| chr1:167630684
|
C | T | 1 | a0001c0001t0001g0347 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.6+255C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167630684 | ||||||
| chr1:167630721
|
T | TA | 10 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0222others(7): Show | 10 | HG01169.hp1 HG01433.hp2 HG01993.hp1 others(7): Show |
intron_variant | MODIFIER | c.6+324dupA | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167630721 | |||||
| chr1:167630721
|
T | TAA | 6 | a0001c0001t0001g0216a0001c0001t0003g0214a0001c0001t0009g0213others(3): Show | 6 | HG01109.hp2 HG01891.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.6+323_6+324dupAA | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167630721 | |||||
| chr1:167630721
|
T | TAAA | 22 | a0001c0001t0002g0193a0001c0001t0002g0194a0001c0001t0002g0195others(19): Show | 22 | HG00140.hp2 HG00639.hp1 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.6+322_6+324dupAAA | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167630721 | |||||
| chr1:167630721
|
T | TAAAA | 29 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(26): Show | 29 | HG00609.hp2 HG00741.hp1 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.6+321_6+324dupAAAA | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167630721 | |||||
| chr1:167630721
|
T | TAAAAA | 22 | a0001c0001t0001g0001a0001c0001t0001g0152a0001c0001t0001g0154others(19): Show | 23 | HG00621.hp1 HG00639.hp2 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.6+320_6+324dupAAAA others(1): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167630721 | |||||
| chr1:167630721
|
T | TAAAAAA | 32 | a0001c0001t0001g0110a0001c0001t0001g0113a0001c0001t0001g0114others(29): Show | 32 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(29): Show |
intron_variant | MODIFIER | c.6+319_6+324dupAAAA others(2): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167630721 | |||||
| chr1:167630721
|
T | TAAAAAAA | 28 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0083others(25): Show | 28 | HG00408.hp2 HG00438.hp1 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.6+318_6+324dupAAAA others(3): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167630721 | |||||
| chr1:167630721
|
T | TAAAAAAA others(1): Show |
6 | a0001c0001t0004g0075a0001c0001t0004g0076a0001c0001t0004g0080others(3): Show | 6 | HG01255.hp1 NA18945.hp2 NA18977.hp1 others(3): Show |
intron_variant | MODIFIER | c.6+317_6+324dupAAAA others(4): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167630721 | |||||
| chr1:167630721
|
T | TAAAAAAA others(3): Show |
6 | a0001c0001t0001g0070a0001c0001t0001g0074a0001c0001t0004g0072others(3): Show | 6 | HG02145.hp2 HG03017.hp1 NA18956.hp1 others(3): Show |
intron_variant | MODIFIER | c.6+315_6+324dupAAAA others(6): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167630721 | |||||
| chr1:167630721
|
T | TAAAAAAA others(4): Show |
3 | a0001c0001t0001g0066a0001c0001t0010g0068a0001c0001t0011g0067 | 3 | HG01243.hp2 NA18946.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.6+314_6+324dupAAAA others(7): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167630721 | |||||
| chr1:167630721
|
T | TAAAAAAA others(5): Show |
5 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0005g0061others(2): Show | 5 | HG00280.hp2 HG00735.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.6+313_6+324dupAAAA others(8): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167630721 | |||||
| chr1:167630721
|
T | TAAAAAAA others(6): Show |
4 | a0001c0001t0001g0059a0001c0001t0003g0060a0001c0001t0007g0057others(1): Show | 4 | HG01515.hp1 HG02723.hp1 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.6+312_6+324dupAAAA others(9): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167630721 | |||||
| chr1:167630721
|
T | TAAAAAAA others(7): Show |
5 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0003g0053others(2): Show | 5 | HG02735.hp2 HG02818.hp1 HG03942.hp2 others(2): Show |
intron_variant | MODIFIER | c.6+311_6+324dupAAAA others(10): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167630721 | |||||
| chr1:167630721
|
T | TAAAAAAA others(8): Show |
7 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(4): Show | 7 | HG00099.hp1 HG01981.hp1 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.6+310_6+324dupAAAA others(11): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167630721 | |||||
| chr1:167630721
|
T | TAAAAAAA others(9): Show |
1 | a0001c0001t0001g0044 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.6+309_6+324dupAAAA others(12): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167630721 | |||||
| chr1:167630721
|
T | TAAAAAAA others(10): Show |
4 | a0001c0001t0002g0040a0001c0001t0003g0041a0001c0001t0011g0042others(1): Show | 4 | HG00438.hp2 HG01175.hp2 HG02293.hp2 others(1): Show |
intron_variant | MODIFIER | c.6+308_6+324dupAAAA others(13): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167630721 | |||||
| chr1:167630721
|
T | TAAAAAAA others(11): Show |
4 | a0001c0001t0001g0038a0001c0001t0003g0037a0001c0001t0003g0039others(1): Show | 4 | HG02257.hp2 HG02698.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.6+307_6+324dupAAAA others(14): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167630721 | |||||
| chr1:167630721
|
T | TAAAAAAA others(12): Show |
2 | a0001c0001t0001g0035a0003c0004t0025g0034 | 2 | HG02280.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.6+306_6+324dupAAAA others(15): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167630721 | |||||
| chr1:167630721
|
T | TAAAAAAA others(13): Show |
1 | a0001c0001t0001g0033 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.6+305_6+324dupAAAA others(16): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167630721 | |||||
| chr1:167630721
|
T | TAAAAAAA others(14): Show |
1 | a0001c0001t0001g0032 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.6+304_6+324dupAAAA others(17): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167630721 | |||||
| chr1:167630721
|
T | TAAAAAAA others(15): Show |
2 | a0001c0001t0001g0031a0001c0001t0005g0030 | 2 | HG02258.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.6+303_6+324dupAAAA others(18): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167630721 | |||||
| chr1:167630721
|
T | TAAAAAAA others(16): Show |
1 | a0001c0001t0001g0029 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.6+302_6+324dupAAAA others(19): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167630721 | |||||
| chr1:167630721
|
T | TAAAAAAA others(17): Show |
2 | a0001c0001t0001g0027a0001c0001t0001g0028 | 2 | NA18962.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.6+301_6+324dupAAAA others(20): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167630721 | |||||
| chr1:167630721
|
T | TAAAAAAA others(18): Show |
7 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(4): Show | 7 | HG02055.hp1 HG02083.hp1 HG03834.hp1 others(4): Show |
intron_variant | MODIFIER | c.6+300_6+324dupAAAA others(21): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167630721 | |||||
| chr1:167630721
|
T | TAAAAAAA others(19): Show |
3 | a0001c0001t0001g0017a0001c0001t0003g0018a0001c0001t0003g0019 | 3 | HG02004.hp2 NA18950.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.6+299_6+324dupAAAA others(22): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167630721 | |||||
| chr1:167630721
|
T | TAAAAAAA others(20): Show |
3 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0043g0015 | 3 | HG01099.hp1 HG01978.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.6+298_6+324dupAAAA others(23): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167630721 | |||||
| chr1:167630721
|
T | TAAAAAAA others(21): Show |
5 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0013others(2): Show | 5 | HG00621.hp2 HG01081.hp1 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.6+297_6+324dupAAAA others(24): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167630721 | |||||
| chr1:167630721
|
T | TAAAAAAA others(22): Show |
1 | a0001c0001t0012g0008 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.6+296_6+324dupAAAA others(25): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167630721 | |||||
| chr1:167630721
|
T | TAAAAAAA others(23): Show |
1 | a0001c0001t0003g0007 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.6+295_6+324dupAAAA others(26): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167630721 | |||||
| chr1:167630721
|
T | TAAAAAAA others(24): Show |
1 | a0001c0001t0003g0006 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.6+294_6+324dupAAAA others(27): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167630721 | |||||
| chr1:167630721
|
TA | T | 23 | a0001c0001t0001g0002a0001c0001t0001g0254a0001c0001t0001g0258others(20): Show | 24 | HG01433.hp1 HG01934.hp1 HG01993.hp2 others(21): Show |
intron_variant | MODIFIER | c.6+324delA | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167630721 | |||||
| chr1:167630721
|
TAA | T | 23 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0278others(20): Show | 23 | HG00099.hp2 HG00140.hp1 HG00558.hp1 others(20): Show |
intron_variant | MODIFIER | c.6+323_6+324delAA | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167630721 | |||||
| chr1:167630721
|
TAAA | T | 16 | a0001c0001t0001g0298a0001c0001t0001g0299a0001c0001t0001g0302others(13): Show | 16 | HG01243.hp1 HG02630.hp1 HG02647.hp2 others(13): Show |
intron_variant | MODIFIER | c.6+322_6+324delAAA | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167630721 | |||||
| chr1:167630721
|
TAAAAAA | T | 6 | a0001c0001t0001g0003a0001c0001t0001g0316a0001c0001t0012g0315others(3): Show | 7 | HG00544.hp1 HG01074.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.6+319_6+324delAAAA others(2): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167630721 | |||||
| chr1:167630721
|
TAAAAAAA others(1): Show |
T | 8 | a0001c0001t0001g0319a0001c0001t0001g0320a0001c0001t0001g0323others(5): Show | 8 | HG02055.hp2 HG02056.hp2 HG02083.hp2 others(5): Show |
intron_variant | MODIFIER | c.6+317_6+324delAAAA others(4): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167630721 | |||||
| chr1:167630721
|
TAAAAAAA others(2): Show |
T | 6 | a0001c0001t0001g0328a0001c0001t0005g0332a0001c0001t0008g0329others(3): Show | 6 | HG01891.hp1 HG02486.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.6+316_6+324delAAAA others(5): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167630721 | |||||
| chr1:167630721
|
TAAAAAAA others(3): Show |
T | 12 | a0001c0001t0001g0333a0001c0001t0001g0336a0001c0001t0003g0004others(9): Show | 12 | HG01081.hp2 HG01515.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.6+315_6+324delAAAA others(6): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167630721 | |||||
| chr1:167630721
|
TAAAAAAA others(8): Show |
T | 3 | a0001c0001t0001g0344a0001c0001t0003g0345a0001c0001t0038g0343 | 3 | HG03239.hp2 HG04184.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.6+310_6+324delAAAA others(11): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167630721 | |||||
| chr1:167630721
|
TAAAAAAA others(9): Show |
T | 1 | a0001c0001t0001g0346 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.6+309_6+324delAAAA others(12): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167630721 | |||||
| chr1:167630736
|
A | AAAAAAAA others(17): Show |
1 | a0001c0001t0003g0140 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.6+324_6+325insAAAA others(20): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167630736 | |||||
| chr1:167630983
|
T | C | 59 | a0001c0001t0002g0040a0001c0001t0002g0045a0001c0001t0002g0141others(56): Show | 59 | HG00140.hp2 HG00609.hp2 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.6+554T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167630983 | ||||||
| chr1:167631139
|
C | T | 1 | a0001c0001t0003g0313 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.6+710C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167631139 | ||||||
| chr1:167631179
|
T | C | 2 | a0001c0001t0001g0229a0001c0001t0012g0315 | 2 | HG00544.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.6+750T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167631179 | ||||||
| chr1:167631320
|
G | A | 3 | a0001c0001t0001g0319a0001c0001t0001g0328a0001c0001t0016g0327 | 3 | HG02486.hp2 HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.6+891G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167631320 | ||||||
| chr1:167631453
|
G | A | 11 | a0001c0001t0001g0229a0001c0001t0001g0320a0001c0001t0003g0321others(8): Show | 11 | HG00544.hp1 HG02165.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.6+1024G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167631453 | ||||||
| chr1:167631571
|
G | T | 5 | a0001c0001t0001g0228a0001c0001t0001g0252a0001c0001t0001g0272others(2): Show | 5 | HG01169.hp1 HG01192.hp1 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.6+1142G>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167631571 | ||||||
| chr1:167631581
|
C | T | 18 | a0001c0001t0001g0003a0001c0001t0001g0336a0001c0001t0003g0004others(15): Show | 19 | HG01081.hp2 HG01884.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.6+1152C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167631581 | ||||||
| chr1:167631605
|
C | T | 85 | a0001c0001t0001g0074a0001c0001t0001g0101a0001c0001t0001g0103others(82): Show | 85 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.6+1176C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167631605 | ||||||
| chr1:167631627
|
A | G | 157 | a0001c0001t0001g0003a0001c0001t0001g0074a0001c0001t0001g0101others(154): Show | 158 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.6+1198A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167631627 | ||||||
| chr1:167631783
|
T | C | 45 | a0001c0001t0002g0121a0001c0001t0004g0056a0001c0001t0004g0072others(42): Show | 45 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(42): Show |
intron_variant | MODIFIER | c.6+1354T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167631783 | ||||||
| chr1:167631824
|
G | A | 127 | a0001c0001t0001g0074a0001c0001t0001g0101a0001c0001t0001g0103others(124): Show | 127 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.6+1395G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167631824 | ||||||
| chr1:167632209
|
G | A | 18 | a0001c0001t0001g0003a0001c0001t0001g0336a0001c0001t0003g0004others(15): Show | 19 | HG01081.hp2 HG01884.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.6+1780G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167632209 | ||||||
| chr1:167632269
|
G | A | 1 | a0001c0001t0016g0253 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.6+1840G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167632269 | ||||||
| chr1:167632316
|
A | C | 254 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(251): Show | 256 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.6+1887A>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167632316 | ||||||
| chr1:167632317
|
G | A | 2 | a0001c0001t0001g0319a0001c0001t0016g0327 | 2 | HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.6+1888G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167632317 | ||||||
| chr1:167632450
|
A | T | 9 | a0001c0001t0002g0151a0001c0001t0002g0184a0001c0001t0002g0206others(6): Show | 9 | HG00140.hp2 HG00639.hp1 HG00741.hp1 others(6): Show |
intron_variant | MODIFIER | c.6+2021A>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167632450 | ||||||
| chr1:167632485
|
A | G | 1 | a0001c0001t0016g0253 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.6+2056A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167632485 | ||||||
| chr1:167632553
|
C | G | 5 | a0001c0001t0001g0229a0001c0001t0001g0320a0001c0001t0003g0321others(2): Show | 5 | HG00544.hp1 HG02165.hp2 NA18971.hp2 others(2): Show |
intron_variant | MODIFIER | c.6+2124C>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167632553 | ||||||
| chr1:167632580
|
G | A | 1 | a0001c0001t0001g0059 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.6+2151G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167632580 | ||||||
| chr1:167632647
|
A | C | 273 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(270): Show | 275 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.6+2218A>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167632647 | ||||||
| chr1:167632657
|
G | T | 1 | a0001c0001t0004g0127 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.6+2228G>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167632657 | ||||||
| chr1:167632686
|
TCAC | T | 270 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(267): Show | 272 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.6+2258_6+2260delCA others(1): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167632686 | ||||||
| chr1:167632691
|
TCCAGTAG others(7): Show |
T | 270 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(267): Show | 272 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.6+2263_6+2276delCC others(12): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167632691 | ||||||
| chr1:167632697
|
A | T | 2 | a0001c0001t0001g0229a0001c0001t0012g0315 | 2 | HG00544.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.6+2268A>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167632697 | ||||||
| chr1:167632698
|
GGTCACTA others(4): Show |
G | 2 | a0001c0001t0001g0229a0001c0001t0012g0315 | 2 | HG00544.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.6+2270_6+2280delGT others(9): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167632698 | ||||||
| chr1:167632706
|
A | T | 270 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(267): Show | 272 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.6+2277A>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167632706 | ||||||
| chr1:167632708
|
CCT | C | 270 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(267): Show | 272 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.6+2280_6+2281delCT | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167632708 | ||||||
| chr1:167632710
|
T | C | 2 | a0001c0001t0001g0229a0001c0001t0012g0315 | 2 | HG00544.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.6+2281T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167632710 | ||||||
| chr1:167632713
|
T | G | 272 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(269): Show | 274 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.6+2284T>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167632713 | ||||||
| chr1:167632714
|
C | G | 272 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(269): Show | 274 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.6+2285C>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167632714 | ||||||
| chr1:167632793
|
T | C | 254 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(251): Show | 256 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.6+2364T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167632793 | ||||||
| chr1:167632921
|
A | G | 1 | a0001c0001t0005g0069 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.6+2492A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167632921 | ||||||
| chr1:167633025
|
A | G | 21 | a0001c0001t0001g0003a0001c0001t0001g0319a0001c0001t0001g0328others(18): Show | 22 | HG01081.hp2 HG01884.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.6+2596A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167633025 | ||||||
| chr1:167633067
|
A | C | 254 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(251): Show | 256 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.6+2638A>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167633067 | ||||||
| chr1:167633101
|
C | T | 3 | a0001c0001t0001g0031a0001c0001t0003g0039a0001c0005t0008g0296 | 3 | HG02559.hp2 HG02698.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.6+2672C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167633101 | ||||||
| chr1:167633404
|
G | A | 272 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(269): Show | 274 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.6+2975G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167633404 | ||||||
| chr1:167633429
|
C | A | 3 | a0001c0001t0001g0049a0001c0001t0001g0063a0001c0001t0001g0070 | 3 | HG00099.hp1 HG00735.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.6+3000C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167633429 | ||||||
| chr1:167633650
|
G | A | 5 | a0001c0001t0001g0229a0001c0001t0001g0320a0001c0001t0003g0321others(2): Show | 5 | HG00544.hp1 HG02165.hp2 NA18971.hp2 others(2): Show |
intron_variant | MODIFIER | c.6+3221G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167633650 | ||||||
| chr1:167633716
|
A | G | 2 | a0001c0001t0003g0245a0001c0001t0006g0271 | 2 | HG01361.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.6+3287A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167633716 | ||||||
| chr1:167633824
|
C | T | 9 | a0001c0001t0001g0003a0001c0001t0005g0332a0001c0001t0008g0329others(6): Show | 10 | HG01891.hp1 HG02622.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.6+3395C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167633824 | ||||||
| chr1:167633825
|
C | G | 334 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(331): Show | 337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.6+3396C>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167633825 | ||||||
| chr1:167633966
|
A | G | 2 | a0001c0001t0004g0125a0001c0001t0004g0126 | 2 | HG00323.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.6+3537A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167633966 | ||||||
| chr1:167634012
|
T | G | 2 | a0001c0001t0001g0229a0001c0001t0012g0315 | 2 | HG00544.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.6+3583T>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167634012 | ||||||
| chr1:167634045
|
C | T | 4 | a0001c0001t0001g0038a0001c0001t0001g0085a0001c0001t0001g0116others(1): Show | 4 | HG03704.hp2 NA18968.hp1 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.6+3616C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167634045 | ||||||
| chr1:167634147
|
G | A | 2 | a0001c0001t0001g0229a0001c0001t0012g0315 | 2 | HG00544.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.6+3718G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167634147 | ||||||
| chr1:167634379
|
G | GT | 6 | a0001c0001t0001g0013a0001c0001t0001g0309a0001c0001t0001g0346others(3): Show | 6 | HG02074.hp2 HG02145.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.6+3961dupT | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167634379 | |||||
| chr1:167634379
|
G | GTT | 8 | a0001c0001t0005g0061a0001c0001t0008g0219a0001c0001t0008g0310others(5): Show | 8 | HG02257.hp1 HG02717.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.6+3960_6+3961dupTT | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167634379 | |||||
| chr1:167634379
|
G | GTTT | 25 | a0001c0001t0001g0074a0001c0001t0001g0101a0001c0001t0001g0103others(22): Show | 25 | HG00280.hp1 HG00438.hp1 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.6+3959_6+3961dupTT others(1): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167634379 | |||||
| chr1:167634397
|
C | A | 3 | a0001c0001t0001g0229a0001c0001t0012g0315a0001c0001t0045g0109 | 3 | HG00544.hp1 HG02165.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.6+3968C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167634397 | ||||||
| chr1:167634520
|
T | C | 55 | a0001c0001t0001g0129a0001c0001t0001g0254a0001c0001t0001g0272others(52): Show | 55 | HG00609.hp2 HG00621.hp1 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.6+4091T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167634520 | ||||||
| chr1:167634571
|
T | G | 346 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(343): Show | 349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.6+4142T>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167634571 | ||||||
| chr1:167634658
|
T | C | 2 | a0001c0001t0001g0238a0001c0001t0028g0335 | 2 | HG01081.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.6+4229T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167634658 | ||||||
| chr1:167634692
|
C | G | 7 | a0001c0001t0001g0108a0001c0001t0001g0232a0001c0001t0001g0276others(4): Show | 7 | HG02040.hp2 NA18942.hp2 NA18945.hp1 others(4): Show |
intron_variant | MODIFIER | c.6+4263C>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167634692 | ||||||
| chr1:167634726
|
G | A | 253 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(250): Show | 255 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(252): Show |
intron_variant | MODIFIER | c.6+4297G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167634726 | ||||||
| chr1:167634773
|
C | G | 211 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(208): Show | 213 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.6+4344C>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167634773 | ||||||
| chr1:167634937
|
TGA | T | 30 | a0001c0001t0001g0254a0001c0001t0001g0272a0001c0001t0002g0040others(27): Show | 30 | HG01074.hp2 HG01515.hp1 HG01981.hp1 others(27): Show |
intron_variant | MODIFIER | c.6+4512_6+4513delAG | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167634937 | |||||
| chr1:167634939
|
AGAGT | A | 7 | a0001c0001t0001g0129a0001c0001t0002g0141a0001c0001t0002g0162others(4): Show | 7 | HG00642.hp1 HG01257.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.6+4512_6+4515delAG others(2): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167634939 | |||||
| chr1:167634941
|
A | AGT | 21 | a0001c0001t0001g0279a0001c0001t0001g0346a0001c0001t0002g0151others(18): Show | 21 | HG00140.hp2 HG00639.hp1 HG00673.hp2 others(18): Show |
intron_variant | MODIFIER | c.6+4541_6+4542dupGT | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167634941 | |||||
| chr1:167634941
|
A | AGTGT | 5 | a0001c0001t0002g0210a0001c0001t0006g0295a0001c0001t0008g0310others(2): Show | 5 | HG01099.hp2 HG02895.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.6+4539_6+4542dupGT others(2): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167634941 | |||||
| chr1:167634941
|
AGT | A | 11 | a0001c0001t0001g0033a0001c0001t0001g0302a0001c0001t0005g0332others(8): Show | 11 | HG01891.hp1 HG02280.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.6+4541_6+4542delGT | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167634941 | |||||
| chr1:167634941
|
AGTGT | A | 36 | a0001c0001t0001g0074a0001c0001t0001g0101a0001c0001t0001g0103others(33): Show | 36 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(33): Show |
intron_variant | MODIFIER | c.6+4539_6+4542delGT others(2): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167634941 | |||||
| chr1:167634941
|
AGTGTGTG others(3): Show |
A | 166 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(163): Show | 168 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(165): Show |
intron_variant | MODIFIER | c.6+4533_6+4542delGT others(8): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167634941 | |||||
| chr1:167634947
|
T | A | 1 | a0001c0001t0003g0130 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.6+4518T>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167634947 | ||||||
| chr1:167635078
|
G | T | 2 | a0001c0001t0002g0146a0001c0001t0014g0181 | 2 | NA18949.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.6+4649G>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167635078 | ||||||
| chr1:167635402
|
CAG | C | 5 | a0001c0001t0001g0139a0001c0001t0001g0229a0001c0001t0001g0294others(2): Show | 5 | HG00280.hp1 HG00544.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.6+4974_6+4975delAG | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167635402 | ||||||
| chr1:167635751
|
A | G | 1 | a0001c0001t0001g0264 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.6+5322A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167635751 | ||||||
| chr1:167635957
|
C | T | 2 | a0001c0001t0044g0217a0001c0001t0053g0096 | 2 | HG01891.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.6+5528C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167635957 | ||||||
| chr1:167636022
|
A | T | 1 | a0001c0001t0001g0013 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.6+5593A>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167636022 | ||||||
| chr1:167636099
|
T | C | 2 | a0001c0001t0001g0281a0001c0001t0023g0259 | 2 | HG02109.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.6+5670T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167636099 | ||||||
| chr1:167636492
|
G | A | 1 | a0001c0001t0001g0114 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.6+6063G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167636492 | ||||||
| chr1:167636548
|
A | G | 4 | a0001c0001t0001g0263a0001c0001t0001g0292a0001c0001t0001g0293others(1): Show | 4 | NA18947.hp2 NA18952.hp2 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.6+6119A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167636548 | ||||||
| chr1:167636580
|
G | GTT | 7 | a0001c0001t0001g0033a0001c0001t0001g0139a0001c0001t0001g0229others(4): Show | 7 | HG00280.hp1 HG00544.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.6+6159_6+6160dupTT | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167636580 | |||||
| chr1:167636586
|
T | G | 3 | a0001c0001t0003g0004a0001c0001t0015g0304a0001c0001t0015g0305 | 3 | HG02895.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.6+6157T>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167636586 | ||||||
| chr1:167636590
|
G | T | 2 | a0001c0001t0001g0107a0001c0001t0003g0011 | 2 | NA18954.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.6+6161G>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167636590 | ||||||
| chr1:167636747
|
C | T | 1 | a0001c0001t0008g0300 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.6+6318C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167636747 | ||||||
| chr1:167636772
|
G | A | 1 | a0001c0001t0001g0328 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.6+6343G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167636772 | ||||||
| chr1:167636872
|
G | A | 9 | a0001c0001t0001g0139a0001c0001t0001g0229a0001c0001t0001g0294others(6): Show | 9 | HG00280.hp1 HG00544.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.6+6443G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167636872 | ||||||
| chr1:167637014
|
C | A | 21 | a0001c0001t0002g0147a0001c0001t0002g0149a0001c0001t0002g0150others(18): Show | 21 | HG00609.hp2 HG00621.hp1 HG01496.hp2 others(18): Show |
intron_variant | MODIFIER | c.6+6585C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167637014 | ||||||
| chr1:167637154
|
A | G | 1 | a0001c0001t0001g0232 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.6+6725A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167637154 | ||||||
| chr1:167637156
|
G | A | 1 | a0001c0001t0001g0232 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.6+6727G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167637156 | ||||||
| chr1:167637313
|
G | A | 2 | a0001c0001t0044g0217a0001c0001t0053g0096 | 2 | HG01891.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.6+6884G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167637313 | ||||||
| chr1:167637503
|
G | A | 1 | a0001c0001t0002g0162 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.6+7074G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167637503 | ||||||
| chr1:167637660
|
T | G | 345 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(342): Show | 348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.6+7231T>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167637660 | ||||||
| chr1:167637730
|
C | CCA | 12 | a0001c0001t0001g0231a0001c0001t0001g0263a0001c0001t0001g0282others(9): Show | 12 | HG02074.hp1 HG02109.hp1 HG02735.hp1 others(9): Show |
intron_variant | MODIFIER | c.6+7335_6+7336dupAC | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167637730 | |||||
| chr1:167637730
|
C | CCACACAC others(1): Show |
8 | a0001c0001t0001g0279a0001c0001t0001g0328a0001c0001t0001g0346others(5): Show | 8 | HG01243.hp1 HG02145.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.6+7329_6+7336dupAC others(6): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167637730 | |||||
| chr1:167637730
|
C | CCACACAC others(3): Show |
1 | a0001c0001t0005g0326 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.6+7327_6+7336dupAC others(8): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167637730 | |||||
| chr1:167637730
|
CCA | C | 200 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0010others(197): Show | 201 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.6+7335_6+7336delAC | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167637730 | |||||
| chr1:167637730
|
CCACA | C | 12 | a0001c0001t0001g0139a0001c0001t0001g0229a0001c0001t0001g0270others(9): Show | 12 | HG00280.hp1 HG00544.hp1 HG02040.hp1 others(9): Show |
intron_variant | MODIFIER | c.6+7333_6+7336delAC others(2): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167637730 | |||||
| chr1:167637972
|
G | C | 1 | a0001c0001t0005g0237 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.6+7543G>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167637972 | ||||||
| chr1:167638103
|
C | T | 255 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(252): Show | 257 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(254): Show |
intron_variant | MODIFIER | c.6+7674C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167638103 | ||||||
| chr1:167638252
|
A | T | 22 | a0001c0001t0001g0101a0001c0001t0001g0103a0001c0001t0001g0104others(19): Show | 22 | HG00438.hp1 HG00639.hp2 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.6+7823A>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167638252 | ||||||
| chr1:167638634
|
A | T | 1 | a0001c0001t0002g0151 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.6+8205A>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167638634 | ||||||
| chr1:167638730
|
G | A | 1 | a0001c0001t0015g0239 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.6+8301G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167638730 | ||||||
| chr1:167638872
|
A | G | 271 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(268): Show | 274 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(271): Show |
intron_variant | MODIFIER | c.6+8443A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167638872 | ||||||
| chr1:167638988
|
A | T | 1 | a0001c0001t0001g0138 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.6+8559A>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167638988 | ||||||
| chr1:167639013
|
T | C | 1 | a0001c0001t0001g0101 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.6+8584T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167639013 | ||||||
| chr1:167639019
|
C | G | 66 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0016others(63): Show | 66 | HG00099.hp1 HG00735.hp1 HG01074.hp2 others(63): Show |
intron_variant | MODIFIER | c.6+8590C>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167639019 | ||||||
| chr1:167639045
|
A | G | 3 | a0001c0001t0001g0032a0001c0001t0001g0051a0001c0001t0047g0065 | 3 | HG00280.hp2 HG01070.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.6+8616A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167639045 | ||||||
| chr1:167639086
|
A | G | 1 | a0001c0001t0001g0136 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.6+8657A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167639086 | ||||||
| chr1:167639140
|
C | A | 4 | a0001c0001t0008g0329a0001c0001t0008g0331a0001c0001t0018g0330others(1): Show | 4 | HG01891.hp1 HG02622.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.6+8711C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167639140 | ||||||
| chr1:167639153
|
G | C | 1 | a0001c0001t0001g0270 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.6+8724G>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167639153 | ||||||
| chr1:167639165
|
A | C | 1 | a0001c0001t0001g0328 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.6+8736A>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167639165 | ||||||
| chr1:167639165
|
A | G | 273 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(270): Show | 276 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(273): Show |
intron_variant | MODIFIER | c.6+8736A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167639165 | ||||||
| chr1:167639165
|
A | T | 4 | a0001c0001t0005g0111a0001c0001t0016g0112a0001c0001t0040g0156others(1): Show | 4 | HG01884.hp1 HG02258.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.6+8736A>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167639165 | ||||||
| chr1:167639173
|
C | T | 2 | a0001c0001t0015g0304a0001c0001t0015g0305 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.6+8744C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167639173 | ||||||
| chr1:167639195
|
T | C | 1 | a0001c0001t0001g0293 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.6+8766T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167639195 | ||||||
| chr1:167639233
|
C | A | 61 | a0001c0001t0001g0035a0001c0001t0001g0046a0001c0001t0001g0047others(58): Show | 61 | HG00438.hp1 HG00438.hp2 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.6+8804C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167639233 | ||||||
| chr1:167639234
|
A | AGC | 61 | a0001c0001t0001g0035a0001c0001t0001g0046a0001c0001t0001g0047others(58): Show | 61 | HG00438.hp1 HG00438.hp2 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.6+8805_6+8806insGC | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167639234 | ||||||
| chr1:167639239
|
G | A | 61 | a0001c0001t0001g0035a0001c0001t0001g0046a0001c0001t0001g0047others(58): Show | 61 | HG00438.hp1 HG00438.hp2 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.6+8810G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167639239 | ||||||
| chr1:167639246
|
CAA | C | 61 | a0001c0001t0001g0035a0001c0001t0001g0046a0001c0001t0001g0047others(58): Show | 61 | HG00438.hp1 HG00438.hp2 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.6+8821_6+8822delAA | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167639246 | |||||
| chr1:167639248
|
A | AAAAC | 214 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(211): Show | 217 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.6+8831_6+8834dupCA others(2): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167639248 | |||||
| chr1:167639452
|
G | A | 3 | a0001c0001t0015g0304a0001c0001t0015g0305a0001c0001t0028g0335 | 3 | HG01081.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.6+9023G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167639452 | ||||||
| chr1:167639658
|
A | G | 1 | a0001c0001t0001g0114 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.6+9229A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167639658 | ||||||
| chr1:167639776
|
G | A | 47 | a0001c0001t0001g0101a0001c0001t0001g0103a0001c0001t0001g0104others(44): Show | 47 | HG00323.hp1 HG00438.hp1 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.6+9347G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167639776 | ||||||
| chr1:167639790
|
G | A | 26 | a0001c0001t0001g0101a0001c0001t0001g0103a0001c0001t0001g0104others(23): Show | 26 | HG00438.hp1 HG00639.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.6+9361G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167639790 | ||||||
| chr1:167639883
|
A | C | 14 | a0001c0001t0001g0137a0001c0001t0001g0152a0001c0001t0001g0254others(11): Show | 14 | HG01934.hp2 HG01978.hp2 HG01981.hp2 others(11): Show |
intron_variant | MODIFIER | c.6+9454A>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167639883 | ||||||
| chr1:167640050
|
G | A | 1 | a0001c0001t0019g0157 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.6+9621G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167640050 | ||||||
| chr1:167640080
|
G | A | 1 | a0001c0001t0051g0117 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.6+9651G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167640080 | ||||||
| chr1:167640112
|
G | A | 14 | a0001c0001t0001g0137a0001c0001t0001g0152a0001c0001t0001g0254others(11): Show | 14 | HG01934.hp2 HG01978.hp2 HG01981.hp2 others(11): Show |
intron_variant | MODIFIER | c.6+9683G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167640112 | ||||||
| chr1:167640236
|
G | A | 7 | a0001c0001t0001g0289a0001c0001t0001g0302a0001c0001t0005g0288others(4): Show | 7 | HG02559.hp2 HG02572.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.6+9807G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167640236 | ||||||
| chr1:167640237
|
G | A | 203 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(200): Show | 206 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.6+9808G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167640237 | ||||||
| chr1:167640288
|
G | A | 6 | a0001c0001t0001g0346a0001c0001t0003g0313a0001c0001t0004g0127others(3): Show | 6 | HG00323.hp1 HG02145.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.6+9859G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167640288 | ||||||
| chr1:167640438
|
G | A | 2 | a0001c0001t0001g0129a0001c0001t0033g0180 | 2 | HG00642.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.6+10009G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167640438 | ||||||
| chr1:167640560
|
T | C | 1 | a0001c0001t0005g0069 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.6+10131T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167640560 | ||||||
| chr1:167640605
|
A | G | 25 | a0001c0001t0001g0003a0001c0001t0001g0050a0001c0001t0001g0064others(22): Show | 26 | HG00609.hp1 HG01361.hp2 HG01433.hp2 others(23): Show |
intron_variant | MODIFIER | c.6+10176A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167640605 | ||||||
| chr1:167640693
|
G | A | 3 | a0001c0001t0001g0221a0001c0001t0003g0236a0001c0001t0052g0158 | 3 | HG02896.hp2 HG03041.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.6+10264G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167640693 | ||||||
| chr1:167640713
|
G | A | 5 | a0001c0001t0001g0346a0001c0001t0003g0313a0001c0001t0004g0127others(2): Show | 5 | HG00323.hp1 HG02145.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.6+10284G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167640713 | ||||||
| chr1:167640895
|
C | T | 1 | a0001c0001t0009g0290 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.6+10466C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167640895 | ||||||
| chr1:167640963
|
G | A | 15 | a0001c0001t0001g0046a0001c0001t0001g0048a0001c0001t0001g0054others(12): Show | 15 | HG00438.hp2 HG01175.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.6+10534G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167640963 | ||||||
| chr1:167640981
|
C | T | 18 | a0001c0001t0001g0046a0001c0001t0001g0048a0001c0001t0001g0054others(15): Show | 18 | HG00438.hp2 HG01081.hp2 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.6+10552C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167640981 | ||||||
| chr1:167640988
|
C | T | 40 | a0001c0001t0001g0101a0001c0001t0001g0103a0001c0001t0001g0104others(37): Show | 40 | HG00438.hp1 HG00639.hp2 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.6+10559C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167640988 | ||||||
| chr1:167640996
|
C | G | 1 | a0001c0001t0013g0204 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.6+10567C>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167640996 | ||||||
| chr1:167641030
|
T | C | 1 | a0001c0001t0001g0347 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.6+10601T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167641030 | ||||||
| chr1:167641125
|
A | G | 5 | a0001c0001t0001g0035a0001c0001t0001g0221a0001c0001t0003g0236others(2): Show | 5 | HG02896.hp2 HG02922.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.6+10696A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167641125 | ||||||
| chr1:167641205
|
A | C | 1 | a0001c0001t0008g0310 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.6+10776A>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167641205 | ||||||
| chr1:167641262
|
G | T | 1 | a0001c0001t0001g0059 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.6+10833G>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167641262 | ||||||
| chr1:167641278
|
C | A | 1 | a0003c0004t0025g0240 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.6+10849C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167641278 | ||||||
| chr1:167641419
|
A | G | 1 | a0001c0001t0004g0122 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.6+10990A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167641419 | ||||||
| chr1:167641506
|
G | C | 197 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(194): Show | 200 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.6+11077G>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167641506 | ||||||
| chr1:167641524
|
C | G | 1 | a0001c0001t0008g0310 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.6+11095C>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167641524 | ||||||
| chr1:167641617
|
C | G | 1 | a0001c0001t0003g0345 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.6+11188C>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167641617 | ||||||
| chr1:167641725
|
A | G | 7 | a0001c0001t0001g0346a0001c0001t0003g0313a0001c0001t0004g0127others(4): Show | 7 | HG00323.hp1 HG02145.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.6+11296A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167641725 | ||||||
| chr1:167641748
|
C | A | 1 | a0001c0001t0019g0157 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.6+11319C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167641748 | ||||||
| chr1:167641801
|
G | A | 281 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(278): Show | 284 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(281): Show |
intron_variant | MODIFIER | c.6+11372G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167641801 | ||||||
| chr1:167641948
|
G | A | 7 | a0001c0001t0005g0020a0001c0001t0005g0030a0001c0001t0005g0061others(4): Show | 7 | HG01884.hp1 HG02055.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.6+11519G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167641948 | ||||||
| chr1:167641950
|
C | A | 3 | a0001c0001t0001g0033a0001c0001t0041g0311a0001c0003t0026g0303 | 3 | HG02922.hp1 HG03225.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.6+11521C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167641950 | ||||||
| chr1:167641984
|
C | T | 183 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(180): Show | 186 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.6+11555C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167641984 | ||||||
| chr1:167642133
|
A | C | 257 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(254): Show | 260 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(257): Show |
intron_variant | MODIFIER | c.6+11704A>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167642133 | ||||||
| chr1:167642171
|
C | A | 7 | a0001c0001t0001g0035a0001c0001t0001g0221a0001c0001t0003g0236others(4): Show | 7 | HG02572.hp2 HG02896.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.6+11742C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167642171 | ||||||
| chr1:167642171
|
C | T | 3 | a0001c0001t0015g0304a0001c0001t0015g0305a0001c0001t0028g0335 | 3 | HG01081.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.6+11742C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167642171 | ||||||
| chr1:167642251
|
C | T | 1 | a0001c0001t0003g0313 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.6+11822C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167642251 | ||||||
| chr1:167642314
|
G | A | 183 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(180): Show | 186 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.6+11885G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167642314 | ||||||
| chr1:167642324
|
GTGTTTA | G | 183 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(180): Show | 186 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.6+11897_6+11902del others(6): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167642324 | |||||
| chr1:167642331
|
T | C | 183 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(180): Show | 186 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.6+11902T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167642331 | ||||||
| chr1:167642522
|
C | T | 1 | a0001c0001t0014g0181 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.6+12093C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167642522 | ||||||
| chr1:167642589
|
T | C | 254 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(251): Show | 257 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(254): Show |
intron_variant | MODIFIER | c.6+12160T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167642589 | ||||||
| chr1:167642645
|
T | C | 1 | a0001c0001t0001g0221 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.6+12216T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167642645 | ||||||
| chr1:167642672
|
C | T | 27 | a0001c0001t0001g0101a0001c0001t0001g0103a0001c0001t0001g0104others(24): Show | 27 | HG00438.hp1 HG00639.hp2 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.6+12243C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167642672 | ||||||
| chr1:167642673
|
G | A | 2 | a0001c0001t0001g0033a0001c0003t0026g0303 | 2 | HG02922.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.6+12244G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167642673 | ||||||
| chr1:167642715
|
T | G | 17 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(14): Show | 17 | HG00438.hp2 HG01175.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.6+12286T>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167642715 | ||||||
| chr1:167642735
|
C | A | 7 | a0001c0001t0001g0346a0001c0001t0003g0313a0001c0001t0004g0127others(4): Show | 7 | HG00323.hp1 HG02145.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.6+12306C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167642735 | ||||||
| chr1:167642754
|
T | A | 3 | a0001c0001t0015g0304a0001c0001t0015g0305a0001c0001t0028g0335 | 3 | HG01081.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.6+12325T>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167642754 | ||||||
| chr1:167642808
|
A | G | 6 | a0001c0001t0001g0289a0001c0001t0001g0302a0001c0001t0001g0328others(3): Show | 6 | HG02486.hp2 HG02559.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.6+12379A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167642808 | ||||||
| chr1:167642925
|
C | T | 21 | a0001c0001t0001g0101a0001c0001t0001g0103a0001c0001t0001g0104others(18): Show | 21 | HG00438.hp1 HG00639.hp2 HG00642.hp1 others(18): Show |
intron_variant | MODIFIER | c.6+12496C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167642925 | ||||||
| chr1:167642940
|
G | T | 3 | a0001c0001t0001g0074a0001c0001t0001g0287a0001c0010t0001g0012 | 3 | HG01169.hp2 HG01496.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.6+12511G>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167642940 | ||||||
| chr1:167642962
|
T | A | 195 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(192): Show | 198 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(195): Show |
intron_variant | MODIFIER | c.6+12533T>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167642962 | ||||||
| chr1:167642978
|
G | A | 1 | a0001c0001t0003g0313 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.6+12549G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167642978 | ||||||
| chr1:167643049
|
C | T | 2 | a0001c0001t0015g0304a0001c0001t0015g0305 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.6+12620C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167643049 | ||||||
| chr1:167643051
|
C | T | 1 | a0001c0001t0001g0046 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.6+12622C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167643051 | ||||||
| chr1:167643460
|
C | G | 73 | a0001c0001t0001g0001a0001c0001t0001g0025a0001c0001t0001g0081others(70): Show | 74 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.6+13031C>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167643460 | ||||||
| chr1:167643645
|
ATGGC | A | 15 | a0001c0001t0001g0107a0001c0001t0001g0137a0001c0001t0001g0152others(12): Show | 15 | HG01934.hp2 HG01978.hp2 HG01981.hp2 others(12): Show |
intron_variant | MODIFIER | c.6+13220_6+13223del others(4): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167643645 | |||||
| chr1:167643775
|
G | A | 42 | a0001c0001t0001g0101a0001c0001t0001g0103a0001c0001t0001g0104others(39): Show | 42 | HG00438.hp1 HG00639.hp2 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.6+13346G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167643775 | ||||||
| chr1:167643800
|
G | A | 6 | a0001c0001t0001g0035a0001c0001t0001g0221a0001c0001t0003g0236others(3): Show | 6 | HG02572.hp2 HG02896.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.6+13371G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167643800 | ||||||
| chr1:167643800
|
G | T | 1 | a0001c0001t0016g0327 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.6+13371G>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167643800 | ||||||
| chr1:167643912
|
G | A | 3 | a0001c0001t0015g0304a0001c0001t0015g0305a0001c0001t0028g0335 | 3 | HG01081.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.6+13483G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167643912 | ||||||
| chr1:167643994
|
C | T | 1 | a0001c0001t0003g0130 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.6+13565C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167643994 | ||||||
| chr1:167644182
|
T | C | 68 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0074others(65): Show | 68 | HG00323.hp1 HG00438.hp1 HG00639.hp2 others(65): Show |
intron_variant | MODIFIER | c.6+13753T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167644182 | ||||||
| chr1:167644246
|
G | A | 6 | a0001c0001t0001g0289a0001c0001t0001g0302a0001c0001t0001g0328others(3): Show | 6 | HG02486.hp2 HG02559.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.6+13817G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167644246 | ||||||
| chr1:167644347
|
T | C | 7 | a0001c0001t0001g0035a0001c0001t0001g0221a0001c0001t0003g0236others(4): Show | 7 | HG02572.hp2 HG02896.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.6+13918T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167644347 | ||||||
| chr1:167644366
|
C | T | 3 | a0001c0001t0015g0304a0001c0001t0015g0305a0001c0001t0028g0335 | 3 | HG01081.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.6+13937C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167644366 | ||||||
| chr1:167644401
|
C | T | 2 | a0001c0001t0002g0045a0001c0001t0007g0057 | 2 | HG01515.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.6+13972C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167644401 | ||||||
| chr1:167644482
|
A | AAAAT | 11 | a0001c0001t0001g0035a0001c0001t0001g0132a0001c0001t0001g0221others(8): Show | 11 | HG02155.hp1 HG02280.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.6+14059_6+14062dup others(4): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167644482 | |||||
| chr1:167644482
|
A | AAAATAAA others(1): Show |
9 | a0001c0001t0001g0254a0001c0001t0002g0195a0001c0001t0003g0230others(6): Show | 9 | HG01981.hp2 HG03491.hp2 NA18977.hp1 others(6): Show |
intron_variant | MODIFIER | c.6+14055_6+14062dup others(8): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167644482 | |||||
| chr1:167644488
|
A | AATAAATA others(5): Show |
5 | a0001c0001t0001g0107a0001c0001t0001g0137a0001c0001t0001g0152others(2): Show | 5 | HG01934.hp2 HG01978.hp2 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.6+14062_6+14063ins others(12): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167644488 | |||||
| chr1:167644488
|
AATAC | A | 95 | a0001c0001t0001g0013a0001c0001t0001g0023a0001c0001t0001g0046others(92): Show | 95 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(92): Show |
intron_variant | MODIFIER | c.6+14106_6+14109del others(4): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167644488 | |||||
| chr1:167644488
|
AATACATA others(1): Show |
A | 181 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(178): Show | 184 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.6+14102_6+14109del others(8): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167644488 | |||||
| chr1:167644488
|
AATACATA others(5): Show |
A | 1 | a0001c0001t0001g0328 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.6+14098_6+14109del others(12): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167644488 | |||||
| chr1:167644488
|
AATACATA others(13): Show |
A | 1 | a0001c0001t0001g0216 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.6+14090_6+14109del others(20): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167644488 | |||||
| chr1:167644492
|
C | A | 31 | a0001c0001t0001g0101a0001c0001t0001g0103a0001c0001t0001g0104others(28): Show | 31 | HG00323.hp1 HG00438.hp1 HG00639.hp2 others(28): Show |
intron_variant | MODIFIER | c.6+14063C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167644492 | ||||||
| chr1:167644496
|
C | A | 43 | a0001c0001t0001g0101a0001c0001t0001g0103a0001c0001t0001g0104others(40): Show | 43 | HG00438.hp1 HG00639.hp2 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.6+14067C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167644496 | ||||||
| chr1:167644500
|
C | A | 192 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(189): Show | 195 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(192): Show |
intron_variant | MODIFIER | c.6+14071C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167644500 | ||||||
| chr1:167644504
|
C | A | 173 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(170): Show | 176 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(173): Show |
intron_variant | MODIFIER | c.6+14075C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167644504 | ||||||
| chr1:167644508
|
C | A | 1 | a0001c0001t0001g0344 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.6+14079C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167644508 | ||||||
| chr1:167644512
|
C | A | 1 | a0001c0001t0001g0216 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.6+14083C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167644512 | ||||||
| chr1:167644516
|
C | A | 1 | a0001c0001t0001g0216 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.6+14087C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167644516 | ||||||
| chr1:167644523
|
A | G | 7 | a0001c0001t0001g0035a0001c0001t0001g0221a0001c0001t0003g0236others(4): Show | 7 | HG02572.hp2 HG02896.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.6+14094A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167644523 | ||||||
| chr1:167644912
|
A | T | 2 | a0001c0001t0002g0045a0001c0001t0007g0057 | 2 | HG01515.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.6+14483A>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167644912 | ||||||
| chr1:167644914
|
G | A | 3 | a0001c0001t0015g0304a0001c0001t0015g0305a0001c0001t0028g0335 | 3 | HG01081.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.6+14485G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167644914 | ||||||
| chr1:167645082
|
TG | T | 12 | a0001c0001t0001g0046a0001c0001t0001g0048a0001c0001t0001g0054others(9): Show | 12 | HG00438.hp2 HG01175.hp2 HG02735.hp2 others(9): Show |
intron_variant | MODIFIER | c.6+14654delG | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167645082 | ||||||
| chr1:167645301
|
C | G | 3 | a0001c0001t0008g0219a0001c0001t0015g0052a0001c0001t0046g0058 | 3 | HG02723.hp1 HG02818.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.6+14872C>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167645301 | ||||||
| chr1:167645404
|
G | A | 16 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(13): Show | 16 | HG00438.hp2 HG01175.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.6+14975G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167645404 | ||||||
| chr1:167645405
|
A | C | 1 | a0001c0001t0003g0039 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.6+14976A>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167645405 | ||||||
| chr1:167645405
|
A | G | 16 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(13): Show | 16 | HG00438.hp2 HG01175.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.6+14976A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167645405 | ||||||
| chr1:167645438
|
A | G | 285 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(282): Show | 288 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(285): Show |
intron_variant | MODIFIER | c.6+15009A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167645438 | ||||||
| chr1:167645441
|
T | C | 246 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(243): Show | 249 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(246): Show |
intron_variant | MODIFIER | c.6+15012T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167645441 | ||||||
| chr1:167645508
|
G | A | 20 | a0001c0001t0001g0101a0001c0001t0001g0103a0001c0001t0001g0104others(17): Show | 20 | HG00438.hp1 HG00639.hp2 HG00642.hp1 others(17): Show |
intron_variant | MODIFIER | c.6+15079G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167645508 | ||||||
| chr1:167645515
|
A | G | 20 | a0001c0001t0001g0101a0001c0001t0001g0103a0001c0001t0001g0104others(17): Show | 20 | HG00438.hp1 HG00639.hp2 HG00642.hp1 others(17): Show |
intron_variant | MODIFIER | c.6+15086A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167645515 | ||||||
| chr1:167645536
|
C | T | 1 | a0001c0001t0008g0310 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.6+15107C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167645536 | ||||||
| chr1:167645700
|
C | A | 1 | a0001c0001t0009g0128 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.6+15271C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167645700 | ||||||
| chr1:167645716
|
C | T | 285 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(282): Show | 288 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(285): Show |
intron_variant | MODIFIER | c.6+15287C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167645716 | ||||||
| chr1:167645764
|
C | T | 1 | a0001c0001t0001g0189 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.6+15335C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167645764 | ||||||
| chr1:167645841
|
G | A | 20 | a0001c0001t0001g0101a0001c0001t0001g0103a0001c0001t0001g0104others(17): Show | 20 | HG00438.hp1 HG00639.hp2 HG00642.hp1 others(17): Show |
intron_variant | MODIFIER | c.6+15412G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167645841 | ||||||
| chr1:167645965
|
C | T | 1 | a0001c0001t0002g0166 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.6+15536C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167645965 | ||||||
| chr1:167646047
|
G | A | 10 | a0001c0001t0001g0074a0001c0001t0001g0279a0001c0001t0001g0287others(7): Show | 10 | HG01169.hp2 HG01243.hp1 HG01496.hp1 others(7): Show |
intron_variant | MODIFIER | c.6+15618G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167646047 | ||||||
| chr1:167646131
|
T | C | 285 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(282): Show | 288 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(285): Show |
intron_variant | MODIFIER | c.6+15702T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167646131 | ||||||
| chr1:167646256
|
C | G | 1 | a0001c0001t0006g0295 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.6+15827C>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167646256 | ||||||
| chr1:167646281
|
C | T | 1 | a0001c0001t0001g0023 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.6+15852C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167646281 | ||||||
| chr1:167646298
|
A | G | 4 | a0001c0001t0003g0004a0001c0001t0015g0304a0001c0001t0015g0305others(1): Show | 4 | HG01081.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.6+15869A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167646298 | ||||||
| chr1:167646446
|
TA | T | 56 | a0001c0001t0001g0013a0001c0001t0001g0023a0001c0001t0001g0108others(53): Show | 56 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(53): Show |
intron_variant | MODIFIER | c.6+16037delA | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167646446 | |||||
| chr1:167646446
|
TAA | T | 25 | a0001c0001t0001g0139a0001c0001t0001g0336a0001c0001t0001g0346others(22): Show | 25 | HG00280.hp1 HG01081.hp2 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.6+16036_6+16037del others(2): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167646446 | |||||
| chr1:167646446
|
TAAA | T | 253 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(250): Show | 256 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(253): Show |
intron_variant | MODIFIER | c.6+16035_6+16037del others(3): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167646446 | |||||
| chr1:167646446
|
TAAAA | T | 11 | a0001c0001t0001g0032a0001c0001t0001g0287a0001c0001t0001g0289others(8): Show | 11 | HG01070.hp2 HG01169.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.6+16034_6+16037del others(4): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167646446 | |||||
| chr1:167646464
|
A | G | 1 | a0001c0001t0012g0277 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.6+16035A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167646464 | ||||||
| chr1:167646505
|
TTTTTTC | T | 279 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(276): Show | 282 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(279): Show |
intron_variant | MODIFIER | c.6+16100_6+16105del others(6): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167646505 | |||||
| chr1:167646566
|
C | T | 5 | a0001c0001t0003g0236a0001c0001t0052g0158a0001c0003t0026g0218others(2): Show | 5 | HG01109.hp2 HG02451.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.6+16137C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167646566 | ||||||
| chr1:167646594
|
C | T | 6 | a0001c0001t0008g0329a0001c0001t0008g0331a0001c0001t0015g0239others(3): Show | 6 | HG01891.hp1 HG02622.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.6+16165C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167646594 | ||||||
| chr1:167646649
|
A | C | 4 | a0001c0001t0001g0220a0001c0001t0001g0275a0001c0001t0003g0256others(1): Show | 4 | HG00558.hp1 HG00673.hp2 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.6+16220A>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167646649 | ||||||
| chr1:167646661
|
C | T | 1 | a0001c0001t0008g0310 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.6+16232C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167646661 | ||||||
| chr1:167646786
|
C | T | 1 | a0001c0001t0019g0093 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.6+16357C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167646786 | ||||||
| chr1:167646795
|
T | C | 283 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(280): Show | 286 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(283): Show |
intron_variant | MODIFIER | c.6+16366T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167646795 | ||||||
| chr1:167646796
|
G | A | 1 | a0001c0001t0005g0326 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.6+16367G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167646796 | ||||||
| chr1:167646928
|
A | G | 21 | a0001c0001t0001g0033a0001c0001t0001g0107a0001c0001t0001g0137others(18): Show | 21 | HG01934.hp2 HG01978.hp2 HG01981.hp2 others(18): Show |
intron_variant | MODIFIER | c.6+16499A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167646928 | ||||||
| chr1:167647072
|
G | A | 103 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(100): Show | 105 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.6+16643G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167647072 | ||||||
| chr1:167647130
|
C | CAAAAAAA others(3): Show |
28 | a0001c0001t0001g0028a0001c0001t0001g0055a0001c0001t0001g0101others(25): Show | 28 | HG00438.hp1 HG00639.hp2 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.6+16710_6+16711ins others(10): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167647130 | |||||
| chr1:167647130
|
C | CAAAAAAA others(4): Show |
232 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(229): Show | 234 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(231): Show |
intron_variant | MODIFIER | c.6+16710_6+16711ins others(11): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167647130 | |||||
| chr1:167647130
|
C | CAAAAAAA others(5): Show |
21 | a0001c0001t0001g0003a0001c0001t0001g0035a0001c0001t0001g0074others(18): Show | 22 | HG01109.hp2 HG01169.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.6+16710_6+16711ins others(12): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167647130 | |||||
| chr1:167647130
|
C | CAAAAAAA others(6): Show |
1 | a0001c0001t0003g0255 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.6+16710_6+16711ins others(13): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167647130 | |||||
| chr1:167647264
|
T | C | 1 | a0001c0001t0001g0050 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.6+16835T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167647264 | ||||||
| chr1:167647317
|
A | G | 289 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(286): Show | 292 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(289): Show |
intron_variant | MODIFIER | c.6+16888A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167647317 | ||||||
| chr1:167647372
|
T | A | 1 | a0001c0001t0001g0282 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.6+16943T>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167647372 | ||||||
| chr1:167647420
|
C | A | 2 | a0001c0001t0001g0241a0001c0001t0006g0223 | 2 | HG01433.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.6+16991C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167647420 | ||||||
| chr1:167647425
|
C | CA | 50 | a0001c0001t0001g0035a0001c0001t0001g0074a0001c0001t0001g0101others(47): Show | 50 | HG00438.hp1 HG00438.hp2 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.6+17010dupA | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167647425 | |||||
| chr1:167647483
|
G | T | 3 | a0001c0001t0001g0139a0001c0001t0004g0127a0001c0001t0045g0109 | 3 | HG00280.hp1 HG00323.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.6+17054G>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167647483 | ||||||
| chr1:167647601
|
C | A | 44 | a0001c0001t0001g0035a0001c0001t0001g0074a0001c0001t0001g0101others(41): Show | 44 | HG00438.hp1 HG00639.hp2 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.6+17172C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167647601 | ||||||
| chr1:167647788
|
T | C | 3 | a0001c0001t0001g0279a0001c0001t0020g0301a0001c0001t0039g0337 | 3 | HG01243.hp1 HG02622.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.6+17359T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167647788 | ||||||
| chr1:167647850
|
C | T | 285 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(282): Show | 288 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(285): Show |
intron_variant | MODIFIER | c.6+17421C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167647850 | ||||||
| chr1:167647877
|
A | T | 1 | a0001c0001t0021g0005 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.6+17448A>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167647877 | ||||||
| chr1:167647903
|
A | T | 1 | a0001c0001t0001g0287 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.6+17474A>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167647903 | ||||||
| chr1:167648029
|
CA | C | 3 | a0001c0001t0001g0346a0001c0001t0016g0253a0003c0004t0025g0034 | 3 | HG02145.hp1 HG02280.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.6+17601delA | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167648029 | ||||||
| chr1:167648088
|
T | C | 21 | a0001c0001t0001g0101a0001c0001t0001g0103a0001c0001t0001g0104others(18): Show | 21 | HG00438.hp1 HG00639.hp2 HG00642.hp1 others(18): Show |
intron_variant | MODIFIER | c.6+17659T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167648088 | ||||||
| chr1:167648146
|
C | T | 18 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0021others(15): Show | 18 | HG00408.hp2 HG00423.hp2 HG00558.hp2 others(15): Show |
intron_variant | MODIFIER | c.6+17717C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167648146 | ||||||
| chr1:167648201
|
A | G | 10 | a0001c0001t0001g0035a0001c0001t0003g0236a0001c0001t0008g0262others(7): Show | 10 | HG01109.hp2 HG02451.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.6+17772A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167648201 | ||||||
| chr1:167648254
|
T | G | 1 | a0001c0001t0001g0316 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.6+17825T>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167648254 | ||||||
| chr1:167648298
|
T | C | 285 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(282): Show | 288 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(285): Show |
intron_variant | MODIFIER | c.6+17869T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167648298 | ||||||
| chr1:167648462
|
A | G | 41 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0107others(38): Show | 41 | HG01109.hp2 HG01934.hp2 HG01978.hp2 others(38): Show |
intron_variant | MODIFIER | c.6+18033A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167648462 | ||||||
| chr1:167648512
|
G | A | 5 | a0001c0001t0001g0346a0001c0001t0003g0313a0001c0001t0016g0253others(2): Show | 5 | HG02145.hp1 HG02280.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.6+18083G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167648512 | ||||||
| chr1:167648523
|
G | C | 3 | a0001c0001t0001g0139a0001c0001t0004g0127a0001c0001t0045g0109 | 3 | HG00280.hp1 HG00323.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.6+18094G>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167648523 | ||||||
| chr1:167648540
|
G | T | 285 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(282): Show | 288 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(285): Show |
intron_variant | MODIFIER | c.6+18111G>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167648540 | ||||||
| chr1:167648585
|
G | A | 4 | a0001c0001t0001g0232a0001c0001t0001g0235a0001c0001t0002g0168others(1): Show | 4 | NA18945.hp1 NA18973.hp2 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.6+18156G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167648585 | ||||||
| chr1:167648621
|
C | T | 9 | a0001c0001t0001g0035a0001c0001t0003g0236a0001c0001t0008g0262others(6): Show | 9 | HG01109.hp2 HG02451.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.6+18192C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167648621 | ||||||
| chr1:167648688
|
C | T | 1 | a0001c0001t0003g0286 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.6+18259C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167648688 | ||||||
| chr1:167648694
|
TG | T | 21 | a0001c0001t0001g0101a0001c0001t0001g0103a0001c0001t0001g0104others(18): Show | 21 | HG00438.hp1 HG00639.hp2 HG00642.hp1 others(18): Show |
intron_variant | MODIFIER | c.6+18269delG | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167648694 | |||||
| chr1:167648710
|
G | C | 1 | a0001c0001t0004g0087 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.6+18281G>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167648710 | ||||||
| chr1:167648803
|
G | A | 6 | a0001c0001t0008g0329a0001c0001t0008g0331a0001c0001t0015g0239others(3): Show | 6 | HG01891.hp1 HG02622.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.6+18374G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167648803 | ||||||
| chr1:167648819
|
A | G | 10 | a0001c0001t0001g0025a0001c0001t0002g0149a0001c0001t0002g0150others(7): Show | 10 | HG00609.hp2 HG00621.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.6+18390A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167648819 | ||||||
| chr1:167648827
|
C | T | 1 | a0001c0001t0001g0282 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.6+18398C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167648827 | ||||||
| chr1:167648845
|
G | C | 1 | a0001c0001t0012g0008 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.6+18416G>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167648845 | ||||||
| chr1:167648883
|
C | T | 14 | a0001c0001t0001g0107a0001c0001t0001g0137a0001c0001t0001g0254others(11): Show | 14 | HG01934.hp2 HG01981.hp2 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.6+18454C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167648883 | ||||||
| chr1:167648933
|
T | C | 74 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0074others(71): Show | 74 | HG00438.hp1 HG00639.hp2 HG00642.hp1 others(71): Show |
intron_variant | MODIFIER | c.6+18504T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167648933 | ||||||
| chr1:167648979
|
A | C | 2 | a0001c0001t0002g0193a0001c0001t0002g0194 | 2 | NA18951.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.6+18550A>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167648979 | ||||||
| chr1:167649038
|
T | A | 2 | a0001c0001t0001g0033a0001c0003t0026g0303 | 2 | HG02922.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.6+18609T>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167649038 | ||||||
| chr1:167649045
|
T | G | 4 | a0001c0001t0001g0003a0001c0001t0001g0319a0001c0001t0020g0317others(1): Show | 5 | HG02965.hp1 HG03041.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.6+18616T>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167649045 | ||||||
| chr1:167649123
|
A | G | 4 | a0001c0001t0003g0004a0001c0001t0015g0304a0001c0001t0015g0305others(1): Show | 4 | HG01081.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.6+18694A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167649123 | ||||||
| chr1:167649231
|
G | A | 4 | a0001c0001t0001g0328a0001c0001t0005g0237a0001c0001t0005g0244others(1): Show | 4 | HG02109.hp1 HG02486.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.6+18802G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167649231 | ||||||
| chr1:167649269
|
T | C | 4 | a0001c0001t0003g0004a0001c0001t0015g0304a0001c0001t0015g0305others(1): Show | 4 | HG01081.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.6+18840T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167649269 | ||||||
| chr1:167649330
|
T | C | 15 | a0001c0001t0001g0107a0001c0001t0001g0137a0001c0001t0001g0152others(12): Show | 15 | HG01934.hp2 HG01978.hp2 HG01981.hp2 others(12): Show |
intron_variant | MODIFIER | c.6+18901T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167649330 | ||||||
| chr1:167649380
|
C | T | 1 | a0001c0001t0008g0310 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.6+18951C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167649380 | ||||||
| chr1:167649538
|
G | A | 9 | a0001c0001t0001g0221a0001c0001t0001g0238a0001c0001t0005g0332others(6): Show | 9 | HG02723.hp1 HG02818.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.6+19109G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167649538 | ||||||
| chr1:167649587
|
C | T | 5 | a0001c0001t0001g0289a0001c0001t0001g0302a0001c0001t0005g0288others(2): Show | 5 | HG02559.hp2 HG02647.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.6+19158C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167649587 | ||||||
| chr1:167649588
|
G | A | 1 | a0001c0001t0001g0014 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.6+19159G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167649588 | ||||||
| chr1:167649634
|
G | A | 21 | a0001c0001t0001g0101a0001c0001t0001g0103a0001c0001t0001g0104others(18): Show | 21 | HG00438.hp1 HG00639.hp2 HG00642.hp1 others(18): Show |
intron_variant | MODIFIER | c.6+19205G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167649634 | ||||||
| chr1:167649715
|
G | T | 6 | a0001c0001t0001g0033a0001c0001t0001g0328a0001c0001t0005g0237others(3): Show | 6 | HG02109.hp1 HG02486.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.6+19286G>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167649715 | ||||||
| chr1:167649724
|
G | A | 1 | a0001c0001t0003g0161 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.6+19295G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167649724 | ||||||
| chr1:167649792
|
G | A | 1 | a0001c0001t0014g0314 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.6+19363G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167649792 | ||||||
| chr1:167649904
|
C | T | 1 | a0001c0001t0051g0117 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.6+19475C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167649904 | ||||||
| chr1:167650089
|
T | C | 1 | a0001c0001t0009g0128 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.6+19660T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167650089 | ||||||
| chr1:167650096
|
C | T | 35 | a0001c0001t0001g0074a0001c0001t0001g0101a0001c0001t0001g0103others(32): Show | 35 | HG00438.hp1 HG00639.hp2 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.6+19667C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167650096 | ||||||
| chr1:167650153
|
A | C | 4 | a0001c0001t0001g0074a0001c0001t0001g0287a0001c0001t0023g0227others(1): Show | 4 | HG01169.hp2 HG01496.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.6+19724A>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167650153 | ||||||
| chr1:167650339
|
G | A | 1 | a0001c0001t0008g0310 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.6+19910G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167650339 | ||||||
| chr1:167650514
|
G | T | 1 | a0001c0001t0005g0237 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.6+20085G>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167650514 | ||||||
| chr1:167650745
|
C | T | 191 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(188): Show | 194 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.6+20316C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167650745 | ||||||
| chr1:167650782
|
C | T | 26 | a0001c0001t0001g0035a0001c0001t0001g0101a0001c0001t0001g0103others(23): Show | 26 | HG00438.hp1 HG00639.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.6+20353C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167650782 | ||||||
| chr1:167650972
|
G | A | 2 | a0001c0001t0001g0033a0001c0003t0026g0303 | 2 | HG02922.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.6+20543G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167650972 | ||||||
| chr1:167651056
|
C | G | 4 | a0001c0001t0001g0074a0001c0001t0001g0287a0001c0001t0023g0227others(1): Show | 4 | HG01169.hp2 HG01496.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.6+20627C>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167651056 | ||||||
| chr1:167651122
|
G | A | 71 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0074others(68): Show | 71 | HG00280.hp1 HG00438.hp1 HG00639.hp2 others(68): Show |
intron_variant | MODIFIER | c.6+20693G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167651122 | ||||||
| chr1:167651136
|
T | G | 6 | a0001c0001t0008g0329a0001c0001t0008g0331a0001c0001t0015g0239others(3): Show | 6 | HG01891.hp1 HG02622.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.6+20707T>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167651136 | ||||||
| chr1:167651237
|
T | C | 6 | a0001c0001t0001g0033a0001c0001t0001g0328a0001c0001t0005g0237others(3): Show | 6 | HG02109.hp1 HG02486.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.6+20808T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167651237 | ||||||
| chr1:167651367
|
C | T | 5 | a0001c0001t0008g0310a0001c0001t0008g0329a0001c0001t0008g0331others(2): Show | 5 | HG01891.hp1 HG02622.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.6+20938C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167651367 | ||||||
| chr1:167651422
|
A | C | 1 | a0001c0001t0004g0094 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.6+20993A>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167651422 | ||||||
| chr1:167651472
|
C | A | 8 | a0001c0001t0001g0035a0001c0001t0003g0004a0001c0001t0003g0236others(5): Show | 8 | HG02886.hp2 HG02895.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.6+21043C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167651472 | ||||||
| chr1:167651494
|
C | T | 5 | a0001c0001t0001g0033a0001c0001t0001g0328a0001c0001t0005g0237others(2): Show | 5 | HG02109.hp1 HG02486.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.6+21065C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167651494 | ||||||
| chr1:167651666
|
G | C | 73 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0074others(70): Show | 73 | HG00280.hp1 HG00438.hp1 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.6+21237G>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167651666 | ||||||
| chr1:167651702
|
G | A | 1 | a0001c0001t0001g0048 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.6+21273G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167651702 | ||||||
| chr1:167651791
|
C | T | 1 | a0001c0001t0002g0203 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.6+21362C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167651791 | ||||||
| chr1:167651801
|
A | T | 9 | a0001c0001t0001g0221a0001c0001t0001g0238a0001c0001t0005g0332others(6): Show | 9 | HG02723.hp1 HG02818.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.6+21372A>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167651801 | ||||||
| chr1:167651837
|
C | A | 1 | a0001c0001t0005g0326 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.6+21408C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167651837 | ||||||
| chr1:167651859
|
G | A | 1 | a0001c0001t0019g0157 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.6+21430G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167651859 | ||||||
| chr1:167651907
|
T | C | 74 | a0001c0001t0001g0023a0001c0001t0001g0033a0001c0001t0001g0035others(71): Show | 74 | HG00280.hp1 HG00438.hp1 HG00639.hp2 others(71): Show |
intron_variant | MODIFIER | c.6+21478T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167651907 | ||||||
| chr1:167651956
|
C | T | 4 | a0001c0001t0017g0338a0001c0001t0018g0339a0001c0001t0018g0340others(1): Show | 4 | HG01081.hp2 HG01884.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.6+21527C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167651956 | ||||||
| chr1:167652018
|
C | CTT | 12 | a0001c0001t0001g0287a0001c0001t0001g0289a0001c0001t0003g0134others(9): Show | 12 | HG01169.hp2 HG01891.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.6+21609_6+21610dup others(2): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167652018 | |||||
| chr1:167652018
|
C | CTTT | 33 | a0001c0001t0001g0035a0001c0001t0001g0074a0001c0001t0001g0101others(30): Show | 33 | HG00280.hp1 HG00438.hp1 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.6+21608_6+21610dup others(3): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167652018 | |||||
| chr1:167652018
|
C | CTTTT | 21 | a0001c0001t0001g0023a0001c0001t0001g0107a0001c0001t0001g0137others(18): Show | 21 | HG01884.hp2 HG01934.hp2 HG01978.hp2 others(18): Show |
intron_variant | MODIFIER | c.6+21607_6+21610dup others(4): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167652018 | |||||
| chr1:167652018
|
C | T | 1 | a0001c0001t0022g0342 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.6+21589C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167652018 | ||||||
| chr1:167652018
|
CT | C | 185 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(182): Show | 188 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.6+21610delT | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167652018 | |||||
| chr1:167652123
|
G | A | 2 | a0001c0001t0002g0045a0001c0001t0007g0057 | 2 | HG01515.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.6+21694G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167652123 | ||||||
| chr1:167652170
|
C | T | 1 | a0001c0001t0005g0237 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.6+21741C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167652170 | ||||||
| chr1:167652177
|
A | G | 2 | a0001c0001t0003g0283a0001c0001t0003g0284 | 2 | NA18939.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.6+21748A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167652177 | ||||||
| chr1:167652194
|
G | A | 5 | a0001c0001t0001g0033a0001c0001t0001g0328a0001c0001t0005g0237others(2): Show | 5 | HG02109.hp1 HG02486.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.6+21765G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167652194 | ||||||
| chr1:167652301
|
C | T | 3 | a0001c0001t0017g0338a0001c0001t0018g0339a0001c0001t0018g0340 | 3 | HG01884.hp2 HG03130.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.6+21872C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167652301 | ||||||
| chr1:167652445
|
A | G | 8 | a0001c0001t0001g0035a0001c0001t0003g0004a0001c0001t0003g0236others(5): Show | 8 | HG02886.hp2 HG02895.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.6+22016A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167652445 | ||||||
| chr1:167652599
|
A | G | 1 | a0001c0001t0022g0342 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.6+22170A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167652599 | ||||||
| chr1:167652633
|
A | G | 74 | a0001c0001t0001g0023a0001c0001t0001g0033a0001c0001t0001g0035others(71): Show | 74 | HG00280.hp1 HG00438.hp1 HG00639.hp2 others(71): Show |
intron_variant | MODIFIER | c.6+22204A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167652633 | ||||||
| chr1:167652663
|
G | C | 18 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0328others(15): Show | 18 | HG01891.hp1 HG02109.hp1 HG02486.hp2 others(15): Show |
intron_variant | MODIFIER | c.6+22234G>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167652663 | ||||||
| chr1:167652712
|
A | AT | 16 | a0001c0001t0001g0017a0001c0001t0001g0021a0001c0001t0001g0022others(13): Show | 16 | HG00408.hp2 HG00423.hp2 HG00558.hp2 others(13): Show |
intron_variant | MODIFIER | c.6+22292dupT | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167652712 | |||||
| chr1:167652727
|
T | C | 1 | a0001c0001t0021g0005 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.6+22298T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167652727 | ||||||
| chr1:167652762
|
A | G | 2 | a0001c0001t0001g0033a0001c0003t0026g0303 | 2 | HG02922.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.6+22333A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167652762 | ||||||
| chr1:167652766
|
T | A | 15 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(12): Show | 15 | HG00438.hp2 HG00544.hp2 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.6+22337T>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167652766 | ||||||
| chr1:167652767
|
G | A | 15 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(12): Show | 15 | HG00438.hp2 HG00544.hp2 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.6+22338G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167652767 | ||||||
| chr1:167652775
|
G | A | 1 | a0001c0001t0022g0342 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.6+22346G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167652775 | ||||||
| chr1:167652882
|
T | G | 44 | a0001c0001t0001g0023a0001c0001t0001g0033a0001c0001t0001g0035others(41): Show | 44 | HG00280.hp1 HG01081.hp2 HG01884.hp2 others(41): Show |
intron_variant | MODIFIER | c.6+22453T>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167652882 | ||||||
| chr1:167652933
|
A | G | 1 | a0001c0001t0001g0022 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.6+22504A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167652933 | ||||||
| chr1:167652952
|
T | G | 8 | a0001c0001t0001g0074a0001c0001t0001g0287a0001c0001t0001g0289others(5): Show | 8 | HG01169.hp2 HG01496.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.6+22523T>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167652952 | ||||||
| chr1:167652953
|
A | T | 8 | a0001c0001t0001g0074a0001c0001t0001g0287a0001c0001t0001g0289others(5): Show | 8 | HG01169.hp2 HG01496.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.6+22524A>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167652953 | ||||||
| chr1:167652985
|
G | A | 2 | a0001c0001t0001g0229a0001c0001t0001g0294 | 2 | HG02040.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.6+22556G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167652985 | ||||||
| chr1:167653334
|
C | T | 5 | a0001c0001t0008g0310a0001c0001t0008g0329a0001c0001t0008g0331others(2): Show | 5 | HG01891.hp1 HG02622.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.6+22905C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167653334 | ||||||
| chr1:167653381
|
T | C | 5 | a0001c0001t0008g0310a0001c0001t0008g0329a0001c0001t0008g0331others(2): Show | 5 | HG01891.hp1 HG02622.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.6+22952T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167653381 | ||||||
| chr1:167653494
|
T | C | 1 | a0001c0001t0023g0227 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.6+23065T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167653494 | ||||||
| chr1:167653818
|
T | C | 6 | a0001c0001t0001g0082a0001c0001t0001g0106a0001c0001t0010g0077others(3): Show | 6 | HG02523.hp2 NA18947.hp1 NA19002.hp2 others(3): Show |
intron_variant | MODIFIER | c.6+23389T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167653818 | ||||||
| chr1:167653983
|
G | A | 1 | a0001c0001t0015g0239 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.6+23554G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167653983 | ||||||
| chr1:167654045
|
G | A | 2 | a0001c0001t0001g0216a0001c0001t0003g0267 | 2 | HG02698.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.6+23616G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167654045 | ||||||
| chr1:167654050
|
A | T | 1 | a0001c0001t0011g0042 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.6+23621A>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167654050 | ||||||
| chr1:167654083
|
G | A | 181 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(178): Show | 184 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.6+23654G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167654083 | ||||||
| chr1:167654151
|
T | C | 34 | a0001c0001t0001g0023a0001c0001t0001g0033a0001c0001t0001g0107others(31): Show | 34 | HG00280.hp1 HG01081.hp2 HG01884.hp2 others(31): Show |
intron_variant | MODIFIER | c.6+23722T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167654151 | ||||||
| chr1:167654165
|
G | A | 8 | a0001c0001t0001g0035a0001c0001t0003g0004a0001c0001t0003g0236others(5): Show | 8 | HG02886.hp2 HG02895.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.6+23736G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167654165 | ||||||
| chr1:167654184
|
G | T | 8 | a0001c0001t0001g0035a0001c0001t0003g0004a0001c0001t0003g0236others(5): Show | 8 | HG02886.hp2 HG02895.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.6+23755G>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167654184 | ||||||
| chr1:167654226
|
G | T | 3 | a0001c0003t0026g0218a0002c0002t0009g0212a0002c0002t0009g0269 | 3 | HG01109.hp2 HG02451.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.6+23797G>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167654226 | ||||||
| chr1:167654376
|
A | G | 8 | a0001c0001t0005g0020a0001c0001t0005g0030a0001c0001t0005g0061others(5): Show | 8 | HG01884.hp1 HG02055.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.6+23947A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167654376 | ||||||
| chr1:167654547
|
T | C | 1 | a0001c0001t0015g0239 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.6+24118T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167654547 | ||||||
| chr1:167654775
|
C | T | 8 | a0001c0001t0005g0020a0001c0001t0005g0030a0001c0001t0005g0061others(5): Show | 8 | HG01884.hp1 HG02055.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.6+24346C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167654775 | ||||||
| chr1:167655113
|
C | T | 2 | a0001c0001t0001g0139a0001c0001t0045g0109 | 2 | HG00280.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.6+24684C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167655113 | ||||||
| chr1:167655114
|
G | T | 16 | a0001c0001t0001g0152a0001c0001t0001g0272a0001c0001t0002g0141others(13): Show | 16 | HG01255.hp1 HG01257.hp2 HG01258.hp1 others(13): Show |
intron_variant | MODIFIER | c.6+24685G>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167655114 | ||||||
| chr1:167655240
|
G | A | 2 | a0001c0001t0001g0139a0001c0001t0045g0109 | 2 | HG00280.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.6+24811G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167655240 | ||||||
| chr1:167655327
|
C | T | 2 | a0001c0001t0004g0091a0001c0001t0010g0073 | 2 | HG03017.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.6+24898C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167655327 | ||||||
| chr1:167655362
|
AT | A | 8 | a0001c0001t0001g0035a0001c0001t0003g0004a0001c0001t0003g0236others(5): Show | 8 | HG02886.hp2 HG02895.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.6+24940delT | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167655362 | |||||
| chr1:167655533
|
C | T | 4 | a0001c0001t0017g0338a0001c0001t0018g0339a0001c0001t0018g0340others(1): Show | 4 | HG01081.hp2 HG01884.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.6+25104C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167655533 | ||||||
| chr1:167655534
|
G | A | 1 | a0001c0001t0001g0292 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.6+25105G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167655534 | ||||||
| chr1:167655555
|
C | A | 9 | a0001c0001t0001g0074a0001c0001t0001g0287a0001c0001t0001g0289others(6): Show | 9 | HG01169.hp2 HG01496.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.6+25126C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167655555 | ||||||
| chr1:167655818
|
G | A | 19 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0139others(16): Show | 19 | HG00280.hp1 HG01081.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.6+25389G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167655818 | ||||||
| chr1:167656101
|
A | G | 2 | a0001c0001t0006g0225a0001c0001t0006g0226 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.6+25672A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167656101 | ||||||
| chr1:167656134
|
T | G | 1 | a0001c0001t0005g0030 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.6+25705T>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167656134 | ||||||
| chr1:167656177
|
A | G | 1 | a0001c0001t0039g0337 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.6+25748A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167656177 | ||||||
| chr1:167656207
|
G | A | 1 | a0001c0001t0037g0325 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.6+25778G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167656207 | ||||||
| chr1:167656208
|
C | T | 8 | a0001c0001t0001g0035a0001c0001t0003g0004a0001c0001t0003g0236others(5): Show | 8 | HG02886.hp2 HG02895.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.6+25779C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167656208 | ||||||
| chr1:167656258
|
A | T | 19 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0139others(16): Show | 19 | HG00280.hp1 HG01081.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.6+25829A>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167656258 | ||||||
| chr1:167656328
|
G | A | 1 | a0001c0001t0023g0259 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.6+25899G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167656328 | ||||||
| chr1:167656415
|
C | T | 73 | a0001c0001t0001g0023a0001c0001t0001g0033a0001c0001t0001g0035others(70): Show | 73 | HG00280.hp1 HG00438.hp1 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.6+25986C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167656415 | ||||||
| chr1:167656595
|
C | G | 1 | a0001c0001t0001g0333 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.6+26166C>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167656595 | ||||||
| chr1:167656659
|
G | A | 4 | a0001c0001t0001g0074a0001c0001t0001g0287a0001c0001t0023g0227others(1): Show | 4 | HG01169.hp2 HG01496.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.6+26230G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167656659 | ||||||
| chr1:167656851
|
A | G | 1 | a0001c0001t0003g0256 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.6+26422A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167656851 | ||||||
| chr1:167656993
|
C | T | 2 | a0001c0001t0009g0334a0001c0001t0015g0239 | 2 | HG02257.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.6+26564C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167656993 | ||||||
| chr1:167657077
|
A | C | 8 | a0001c0001t0001g0035a0001c0001t0003g0004a0001c0001t0003g0236others(5): Show | 8 | HG02886.hp2 HG02895.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.6+26648A>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167657077 | ||||||
| chr1:167657466
|
A | G | 1 | a0001c0001t0003g0245 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.7-26434A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167657466 | ||||||
| chr1:167657548
|
G | A | 1 | a0001c0001t0001g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.7-26352G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167657548 | ||||||
| chr1:167657588
|
T | C | 23 | a0001c0001t0001g0023a0001c0001t0001g0074a0001c0001t0001g0107others(20): Show | 23 | HG01169.hp2 HG01496.hp1 HG01934.hp2 others(20): Show |
intron_variant | MODIFIER | c.7-26312T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167657588 | ||||||
| chr1:167657694
|
G | A | 1 | a0001c0001t0008g0310 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.7-26206G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167657694 | ||||||
| chr1:167657780
|
A | T | 7 | a0001c0001t0002g0149a0001c0001t0002g0178a0001c0001t0002g0197others(4): Show | 7 | HG00609.hp2 HG00621.hp1 HG02015.hp1 others(4): Show |
intron_variant | MODIFIER | c.7-26120A>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167657780 | ||||||
| chr1:167657854
|
G | A | 1 | a0001c0001t0007g0182 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.7-26046G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167657854 | ||||||
| chr1:167657891
|
G | GCA | 7 | a0001c0001t0001g0131a0001c0001t0001g0222a0001c0001t0002g0040others(4): Show | 7 | HG01074.hp2 HG01515.hp1 HG01981.hp1 others(4): Show |
intron_variant | MODIFIER | c.7-25986_7-25985dup others(2): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167657891 | |||||
| chr1:167657891
|
GCA | G | 29 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0074others(26): Show | 29 | HG00280.hp1 HG01169.hp2 HG01361.hp2 others(26): Show |
intron_variant | MODIFIER | c.7-25986_7-25985del others(2): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167657891 | |||||
| chr1:167657891
|
GCACA | G | 5 | a0001c0001t0001g0324a0001c0001t0008g0329a0001c0001t0008g0331others(2): Show | 5 | HG01891.hp1 HG02165.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.7-25988_7-25985del others(4): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167657891 | |||||
| chr1:167658031
|
G | A | 3 | a0001c0001t0017g0338a0001c0001t0018g0339a0001c0001t0018g0340 | 3 | HG01884.hp2 HG03130.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.7-25869G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167658031 | ||||||
| chr1:167658062
|
G | C | 1 | a0001c0005t0008g0296 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.7-25838G>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167658062 | ||||||
| chr1:167658235
|
A | T | 3 | a0001c0001t0001g0328a0001c0001t0005g0237a0001c0001t0041g0311 | 3 | HG02109.hp1 HG02486.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.7-25665A>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167658235 | ||||||
| chr1:167658242
|
A | T | 8 | a0001c0001t0001g0035a0001c0001t0003g0004a0001c0001t0003g0236others(5): Show | 8 | HG02886.hp2 HG02895.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.7-25658A>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167658242 | ||||||
| chr1:167658416
|
G | T | 2 | a0001c0001t0001g0139a0001c0001t0045g0109 | 2 | HG00280.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.7-25484G>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167658416 | ||||||
| chr1:167658471
|
A | G | 23 | a0001c0001t0001g0023a0001c0001t0001g0074a0001c0001t0001g0107others(20): Show | 23 | HG01169.hp2 HG01496.hp1 HG01934.hp2 others(20): Show |
intron_variant | MODIFIER | c.7-25429A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167658471 | ||||||
| chr1:167658528
|
C | T | 2 | a0001c0001t0001g0139a0001c0001t0045g0109 | 2 | HG00280.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.7-25372C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167658528 | ||||||
| chr1:167658556
|
A | G | 23 | a0001c0001t0001g0023a0001c0001t0001g0074a0001c0001t0001g0107others(20): Show | 23 | HG01169.hp2 HG01496.hp1 HG01934.hp2 others(20): Show |
intron_variant | MODIFIER | c.7-25344A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167658556 | ||||||
| chr1:167658582
|
C | T | 7 | a0001c0001t0001g0033a0001c0001t0001g0139a0001c0001t0001g0328others(4): Show | 7 | HG00280.hp1 HG02109.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.7-25318C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167658582 | ||||||
| chr1:167658602
|
T | C | 21 | a0001c0001t0001g0101a0001c0001t0001g0103a0001c0001t0001g0104others(18): Show | 21 | HG00438.hp1 HG00639.hp2 HG00642.hp1 others(18): Show |
intron_variant | MODIFIER | c.7-25298T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167658602 | ||||||
| chr1:167658603
|
C | T | 21 | a0001c0001t0001g0101a0001c0001t0001g0103a0001c0001t0001g0104others(18): Show | 21 | HG00438.hp1 HG00639.hp2 HG00642.hp1 others(18): Show |
intron_variant | MODIFIER | c.7-25297C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167658603 | ||||||
| chr1:167658615
|
G | T | 19 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0139others(16): Show | 19 | HG00280.hp1 HG01081.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.7-25285G>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167658615 | ||||||
| chr1:167658619
|
C | T | 4 | a0001c0001t0017g0338a0001c0001t0018g0339a0001c0001t0018g0340others(1): Show | 4 | HG01081.hp2 HG01884.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.7-25281C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167658619 | ||||||
| chr1:167658729
|
C | A | 1 | a0001c0001t0011g0043 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.7-25171C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167658729 | ||||||
| chr1:167658943
|
T | G | 3 | a0001c0001t0001g0238a0001c0001t0006g0225a0001c0001t0006g0226 | 3 | HG02896.hp1 HG02897.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.7-24957T>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167658943 | ||||||
| chr1:167658998
|
C | A | 5 | a0001c0001t0001g0289a0001c0001t0005g0288a0001c0001t0008g0310others(2): Show | 5 | HG02559.hp2 HG03195.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.7-24902C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167658998 | ||||||
| chr1:167659054
|
C | T | 21 | a0001c0001t0001g0101a0001c0001t0001g0103a0001c0001t0001g0104others(18): Show | 21 | HG00438.hp1 HG00639.hp2 HG00642.hp1 others(18): Show |
intron_variant | MODIFIER | c.7-24846C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167659054 | ||||||
| chr1:167659163
|
C | A | 8 | a0001c0001t0001g0035a0001c0001t0003g0004a0001c0001t0003g0236others(5): Show | 8 | HG02886.hp2 HG02895.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.7-24737C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167659163 | ||||||
| chr1:167659222
|
G | A | 14 | a0001c0001t0001g0017a0001c0001t0001g0021a0001c0001t0001g0022others(11): Show | 14 | HG00408.hp2 HG00423.hp2 HG00558.hp2 others(11): Show |
intron_variant | MODIFIER | c.7-24678G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167659222 | ||||||
| chr1:167659366
|
T | C | 2 | a0001c0001t0002g0206a0001c0001t0034g0183 | 2 | HG01070.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.7-24534T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167659366 | ||||||
| chr1:167659554
|
C | T | 8 | a0001c0001t0001g0035a0001c0001t0003g0004a0001c0001t0003g0236others(5): Show | 8 | HG02886.hp2 HG02895.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.7-24346C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167659554 | ||||||
| chr1:167659638
|
G | A | 4 | a0001c0001t0008g0329a0001c0001t0008g0331a0001c0001t0017g0341others(1): Show | 4 | HG01891.hp1 HG02622.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.7-24262G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167659638 | ||||||
| chr1:167659713
|
A | G | 1 | a0001c0001t0001g0285 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.7-24187A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167659713 | ||||||
| chr1:167659727
|
T | G | 1 | a0001c0001t0004g0127 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.7-24173T>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167659727 | ||||||
| chr1:167659858
|
C | T | 1 | a0001c0001t0022g0342 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.7-24042C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167659858 | ||||||
| chr1:167659880
|
G | A | 1 | a0001c0001t0028g0335 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.7-24020G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167659880 | ||||||
| chr1:167660007
|
G | A | 1 | a0001c0001t0002g0165 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.7-23893G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167660007 | ||||||
| chr1:167660122
|
C | T | 16 | a0001c0001t0001g0033a0001c0001t0001g0074a0001c0001t0001g0139others(13): Show | 16 | HG00280.hp1 HG01081.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.7-23778C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167660122 | ||||||
| chr1:167660248
|
G | A | 16 | a0001c0001t0001g0033a0001c0001t0001g0074a0001c0001t0001g0139others(13): Show | 16 | HG00280.hp1 HG01081.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.7-23652G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167660248 | ||||||
| chr1:167660254
|
C | T | 5 | a0001c0001t0001g0074a0001c0001t0001g0287a0001c0001t0022g0342others(2): Show | 5 | HG01169.hp2 HG01496.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.7-23646C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167660254 | ||||||
| chr1:167660305
|
G | A | 1 | a0001c0001t0003g0004 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.7-23595G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167660305 | ||||||
| chr1:167660432
|
G | C | 37 | a0001c0001t0001g0023a0001c0001t0001g0033a0001c0001t0001g0035others(34): Show | 37 | HG00280.hp1 HG01081.hp2 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.7-23468G>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167660432 | ||||||
| chr1:167660471
|
T | TTG | 7 | a0001c0001t0003g0004a0001c0001t0003g0236a0001c0001t0005g0244others(4): Show | 7 | HG02886.hp2 HG02895.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.7-23428_7-23427ins others(2): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167660471 | |||||
| chr1:167660472
|
T | TG | 19 | a0001c0001t0001g0023a0001c0001t0001g0035a0001c0001t0001g0107others(16): Show | 19 | HG01934.hp2 HG01981.hp2 HG02027.hp2 others(16): Show |
intron_variant | MODIFIER | c.7-23428_7-23427ins others(1): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167660472 | ||||||
| chr1:167660473
|
T | G | 11 | a0001c0001t0001g0033a0001c0001t0001g0139a0001c0001t0001g0328others(8): Show | 11 | HG00280.hp1 HG01081.hp2 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.7-23427T>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167660473 | ||||||
| chr1:167660475
|
G | GT | 6 | a0001c0001t0001g0139a0001c0001t0017g0338a0001c0001t0018g0339others(3): Show | 6 | HG00280.hp1 HG01081.hp2 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.7-23412dupT | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167660475 | |||||
| chr1:167660475
|
G | T | 26 | a0001c0001t0001g0023a0001c0001t0001g0035a0001c0001t0001g0107others(23): Show | 26 | HG01934.hp2 HG01981.hp2 HG02027.hp2 others(23): Show |
intron_variant | MODIFIER | c.7-23425G>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167660475 | ||||||
| chr1:167660480
|
T | G | 2 | a0001c0001t0012g0251a0001c0001t0012g0312 | 2 | NA18984.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.7-23420T>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167660480 | ||||||
| chr1:167660608
|
G | T | 4 | a0001c0001t0017g0338a0001c0001t0018g0339a0001c0001t0018g0340others(1): Show | 4 | HG01081.hp2 HG01884.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.7-23292G>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167660608 | ||||||
| chr1:167660691
|
C | T | 4 | a0001c0001t0001g0074a0001c0001t0001g0287a0001c0001t0023g0227others(1): Show | 4 | HG01169.hp2 HG01496.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.7-23209C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167660691 | ||||||
| chr1:167661076
|
C | T | 36 | a0001c0001t0001g0013a0001c0001t0001g0023a0001c0001t0001g0033others(33): Show | 36 | HG01081.hp2 HG01884.hp2 HG01934.hp2 others(33): Show |
intron_variant | MODIFIER | c.7-22824C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167661076 | ||||||
| chr1:167661197
|
T | C | 9 | a0001c0001t0001g0328a0001c0001t0005g0237a0001c0001t0017g0338others(6): Show | 9 | HG01081.hp2 HG01884.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.7-22703T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167661197 | ||||||
| chr1:167661276
|
C | T | 1 | a0001c0001t0001g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.7-22624C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167661276 | ||||||
| chr1:167661615
|
G | C | 1 | a0001c0001t0001g0333 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.7-22285G>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167661615 | ||||||
| chr1:167661688
|
C | T | 1 | a0001c0001t0019g0157 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.7-22212C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167661688 | ||||||
| chr1:167661754
|
T | A | 5 | a0001c0001t0001g0033a0001c0001t0005g0237a0001c0001t0016g0327others(2): Show | 5 | HG02109.hp1 HG02922.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.7-22146T>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167661754 | ||||||
| chr1:167661908
|
A | G | 1 | a0001c0001t0001g0155 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.7-21992A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167661908 | ||||||
| chr1:167661949
|
G | C | 1 | a0001c0001t0009g0334 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.7-21951G>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167661949 | ||||||
| chr1:167661997
|
G | C | 1 | a0001c0001t0001g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.7-21903G>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167661997 | ||||||
| chr1:167662070
|
G | A | 28 | a0001c0001t0001g0101a0001c0001t0001g0103a0001c0001t0001g0104others(25): Show | 28 | HG00280.hp2 HG00438.hp1 HG00639.hp2 others(25): Show |
intron_variant | MODIFIER | c.7-21830G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167662070 | ||||||
| chr1:167662112
|
T | C | 9 | a0001c0001t0001g0035a0001c0001t0003g0004a0001c0001t0003g0236others(6): Show | 9 | HG01109.hp2 HG02257.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.7-21788T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167662112 | ||||||
| chr1:167662427
|
G | A | 30 | a0001c0001t0001g0023a0001c0001t0001g0031a0001c0001t0001g0032others(27): Show | 30 | HG00558.hp1 HG01070.hp2 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.7-21473G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167662427 | ||||||
| chr1:167662569
|
C | T | 20 | a0001c0001t0001g0101a0001c0001t0001g0103a0001c0001t0001g0104others(17): Show | 20 | HG00280.hp2 HG00438.hp1 HG00639.hp2 others(17): Show |
intron_variant | MODIFIER | c.7-21331C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167662569 | ||||||
| chr1:167662677
|
T | C | 1 | a0001c0001t0001g0328 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.7-21223T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167662677 | ||||||
| chr1:167662760
|
T | C | 1 | a0001c0001t0001g0014 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.7-21140T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167662760 | ||||||
| chr1:167662796
|
C | T | 1 | a0001c0001t0017g0341 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.7-21104C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167662796 | ||||||
| chr1:167662800
|
C | G | 5 | a0001c0001t0001g0033a0001c0001t0005g0237a0001c0001t0016g0327others(2): Show | 5 | HG02109.hp1 HG02922.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.7-21100C>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167662800 | ||||||
| chr1:167662800
|
C | T | 67 | a0001c0001t0001g0023a0001c0001t0001g0031a0001c0001t0001g0032others(64): Show | 67 | HG00280.hp2 HG00438.hp1 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.7-21100C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167662800 | ||||||
| chr1:167662801
|
G | A | 1 | a0001c0001t0007g0182 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.7-21099G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167662801 | ||||||
| chr1:167662810
|
G | T | 1 | a0001c0001t0001g0263 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.7-21090G>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167662810 | ||||||
| chr1:167662845
|
G | C | 37 | a0001c0001t0001g0059a0001c0001t0001g0074a0001c0001t0001g0101others(34): Show | 37 | HG00280.hp2 HG00438.hp1 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.7-21055G>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167662845 | ||||||
| chr1:167662864
|
T | A | 37 | a0001c0001t0001g0059a0001c0001t0001g0074a0001c0001t0001g0101others(34): Show | 37 | HG00280.hp2 HG00438.hp1 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.7-21036T>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167662864 | ||||||
| chr1:167662974
|
T | A | 4 | a0001c0001t0005g0326a0001c0001t0020g0301a0001c0001t0021g0005others(1): Show | 4 | HG01243.hp1 HG02055.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.7-20926T>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167662974 | ||||||
| chr1:167663034
|
A | G | 70 | a0001c0001t0001g0023a0001c0001t0001g0031a0001c0001t0001g0032others(67): Show | 70 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.7-20866A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167663034 | ||||||
| chr1:167663124
|
G | T | 30 | a0001c0001t0001g0023a0001c0001t0001g0031a0001c0001t0001g0032others(27): Show | 30 | HG00558.hp1 HG01070.hp2 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.7-20776G>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167663124 | ||||||
| chr1:167663179
|
G | A | 1 | a0001c0001t0012g0277 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.7-20721G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167663179 | ||||||
| chr1:167663239
|
G | C | 2 | a0001c0001t0001g0252a0004c0006t0002g0207 | 2 | HG01192.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.7-20661G>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167663239 | ||||||
| chr1:167663242
|
G | A | 1 | a0001c0001t0001g0320 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.7-20658G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167663242 | ||||||
| chr1:167663381
|
G | A | 70 | a0001c0001t0001g0023a0001c0001t0001g0031a0001c0001t0001g0032others(67): Show | 70 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.7-20519G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167663381 | ||||||
| chr1:167663408
|
CG | C | 70 | a0001c0001t0001g0023a0001c0001t0001g0031a0001c0001t0001g0032others(67): Show | 70 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.7-20490delG | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167663408 | |||||
| chr1:167663409
|
G | A | 9 | a0001c0001t0001g0035a0001c0001t0003g0004a0001c0001t0003g0236others(6): Show | 9 | HG01109.hp2 HG02257.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.7-20491G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167663409 | ||||||
| chr1:167663417
|
C | A | 4 | a0001c0001t0005g0326a0001c0001t0020g0301a0001c0001t0021g0005others(1): Show | 4 | HG01243.hp1 HG02055.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.7-20483C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167663417 | ||||||
| chr1:167663451
|
C | T | 23 | a0001c0001t0001g0101a0001c0001t0001g0103a0001c0001t0001g0104others(20): Show | 23 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(20): Show |
intron_variant | MODIFIER | c.7-20449C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167663451 | ||||||
| chr1:167663539
|
A | T | 70 | a0001c0001t0001g0023a0001c0001t0001g0031a0001c0001t0001g0032others(67): Show | 70 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.7-20361A>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167663539 | ||||||
| chr1:167663585
|
T | C | 70 | a0001c0001t0001g0023a0001c0001t0001g0031a0001c0001t0001g0032others(67): Show | 70 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.7-20315T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167663585 | ||||||
| chr1:167663620
|
C | T | 1 | a0001c0001t0022g0342 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.7-20280C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167663620 | ||||||
| chr1:167663621
|
G | A | 1 | a0001c0001t0009g0334 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.7-20279G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167663621 | ||||||
| chr1:167663811
|
T | C | 2 | a0001c0001t0012g0251a0001c0001t0012g0312 | 2 | NA18984.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.7-20089T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167663811 | ||||||
| chr1:167663827
|
C | A | 6 | a0001c0001t0001g0139a0001c0001t0001g0231a0001c0001t0017g0338others(3): Show | 6 | HG00280.hp1 HG01884.hp2 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.7-20073C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167663827 | ||||||
| chr1:167663942
|
A | G | 2 | a0001c0001t0001g0132a0001c0001t0004g0088 | 2 | HG00673.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.7-19958A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167663942 | ||||||
| chr1:167664033
|
G | T | 6 | a0001c0001t0001g0139a0001c0001t0001g0231a0001c0001t0017g0338others(3): Show | 6 | HG00280.hp1 HG01884.hp2 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.7-19867G>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167664033 | ||||||
| chr1:167664355
|
G | C | 7 | a0001c0001t0001g0107a0001c0001t0002g0170a0001c0001t0002g0195others(4): Show | 7 | NA18954.hp2 NA18983.hp2 NA18985.hp2 others(4): Show |
intron_variant | MODIFIER | c.7-19545G>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167664355 | ||||||
| chr1:167664359
|
C | A | 1 | a0001c0001t0001g0328 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.7-19541C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167664359 | ||||||
| chr1:167664365
|
G | A | 1 | a0001c0001t0004g0056 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.7-19535G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167664365 | ||||||
| chr1:167664595
|
G | A | 1 | a0001c0001t0015g0239 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.7-19305G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167664595 | ||||||
| chr1:167664606
|
A | C | 9 | a0001c0001t0001g0035a0001c0001t0003g0004a0001c0001t0003g0236others(6): Show | 9 | HG01109.hp2 HG02257.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.7-19294A>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167664606 | ||||||
| chr1:167664624
|
G | A | 4 | a0001c0001t0001g0059a0001c0001t0001g0074a0001c0001t0023g0227others(1): Show | 4 | HG01496.hp1 HG03453.hp2 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.7-19276G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167664624 | ||||||
| chr1:167664740
|
A | G | 4 | a0001c0001t0001g0289a0001c0001t0005g0288a0001c0001t0009g0290others(1): Show | 4 | HG02559.hp2 HG03195.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.7-19160A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167664740 | ||||||
| chr1:167664808
|
G | A | 2 | a0001c0001t0002g0151a0001c0001t0002g0208 | 2 | HG00639.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.7-19092G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167664808 | ||||||
| chr1:167664830
|
A | G | 72 | a0001c0001t0001g0023a0001c0001t0001g0031a0001c0001t0001g0032others(69): Show | 72 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.7-19070A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167664830 | ||||||
| chr1:167664835
|
T | G | 1 | a0001c0001t0010g0077 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.7-19065T>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167664835 | ||||||
| chr1:167664881
|
A | C | 9 | a0001c0001t0001g0035a0001c0001t0003g0004a0001c0001t0003g0236others(6): Show | 9 | HG01109.hp2 HG02257.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.7-19019A>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167664881 | ||||||
| chr1:167664993
|
G | A | 35 | a0001c0001t0001g0023a0001c0001t0001g0031a0001c0001t0001g0038others(32): Show | 35 | HG00558.hp1 HG01081.hp2 HG01169.hp2 others(32): Show |
intron_variant | MODIFIER | c.7-18907G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167664993 | ||||||
| chr1:167665040
|
C | CAA | 23 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0038others(20): Show | 23 | HG01070.hp2 HG01081.hp2 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.7-18844_7-18843dup others(2): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167665040 | |||||
| chr1:167665055
|
A | AAG | 14 | a0001c0001t0001g0137a0001c0001t0001g0275a0001c0001t0001g0289others(11): Show | 14 | HG00558.hp1 HG01891.hp1 HG01934.hp2 others(11): Show |
intron_variant | MODIFIER | c.7-18844_7-18843ins others(2): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167665055 | |||||
| chr1:167665055
|
A | AG | 8 | a0001c0001t0001g0035a0001c0001t0003g0004a0001c0001t0003g0236others(5): Show | 8 | HG01109.hp2 HG02451.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.7-18845_7-18844ins others(1): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167665055 | ||||||
| chr1:167665055
|
A | G | 1 | a0001c0001t0007g0182 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.7-18845A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167665055 | ||||||
| chr1:167665335
|
G | A | 36 | a0001c0001t0001g0059a0001c0001t0001g0074a0001c0001t0001g0101others(33): Show | 36 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(33): Show |
intron_variant | MODIFIER | c.7-18565G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167665335 | ||||||
| chr1:167665347
|
TTGTC | T | 23 | a0001c0001t0001g0101a0001c0001t0001g0103a0001c0001t0001g0104others(20): Show | 23 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(20): Show |
intron_variant | MODIFIER | c.7-18547_7-18544del others(4): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167665347 | |||||
| chr1:167665408
|
A | G | 7 | a0001c0001t0001g0059a0001c0001t0001g0074a0001c0001t0005g0326others(4): Show | 7 | HG01243.hp1 HG01496.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.7-18492A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167665408 | ||||||
| chr1:167665481
|
A | G | 9 | a0001c0001t0001g0035a0001c0001t0003g0004a0001c0001t0003g0236others(6): Show | 9 | HG01109.hp2 HG02257.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.7-18419A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167665481 | ||||||
| chr1:167665488
|
T | C | 1 | a0001c0001t0041g0311 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.7-18412T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167665488 | ||||||
| chr1:167665498
|
G | A | 1 | a0001c0001t0002g0195 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.7-18402G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167665498 | ||||||
| chr1:167665635
|
A | G | 7 | a0001c0001t0001g0289a0001c0001t0005g0288a0001c0001t0008g0329others(4): Show | 7 | HG01891.hp1 HG02559.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.7-18265A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167665635 | ||||||
| chr1:167665668
|
G | A | 1 | a0001c0001t0001g0264 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.7-18232G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167665668 | ||||||
| chr1:167665817
|
C | CT | 30 | a0001c0001t0001g0023a0001c0001t0001g0031a0001c0001t0001g0032others(27): Show | 30 | HG00558.hp1 HG01070.hp2 HG01169.hp2 others(27): Show |
intron_variant | MODIFIER | c.7-18071dupT | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167665817 | |||||
| chr1:167665857
|
T | A | 3 | a0001c0001t0002g0170a0001c0001t0003g0230a0001c0001t0003g0255 | 3 | NA19011.hp1 NA19056.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.7-18043T>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167665857 | ||||||
| chr1:167665867
|
G | A | 1 | a0001c0001t0001g0021 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.7-18033G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167665867 | ||||||
| chr1:167665881
|
C | T | 1 | a0001c0001t0001g0328 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.7-18019C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167665881 | ||||||
| chr1:167665894
|
C | A | 1 | a0001c0001t0002g0146 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.7-18006C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167665894 | ||||||
| chr1:167665950
|
T | C | 9 | a0001c0001t0001g0059a0001c0001t0001g0074a0001c0001t0001g0289others(6): Show | 9 | HG01496.hp1 HG02559.hp2 HG03195.hp1 others(6): Show |
intron_variant | MODIFIER | c.7-17950T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167665950 | ||||||
| chr1:167665957
|
G | A | 9 | a0001c0001t0001g0035a0001c0001t0003g0004a0001c0001t0003g0236others(6): Show | 9 | HG01109.hp2 HG02257.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.7-17943G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167665957 | ||||||
| chr1:167665973
|
G | A | 3 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0129 | 3 | HG00642.hp1 NA19000.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.7-17927G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167665973 | ||||||
| chr1:167665977
|
A | T | 1 | a0001c0001t0005g0237 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.7-17923A>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167665977 | ||||||
| chr1:167666014
|
G | A | 2 | a0001c0001t0004g0091a0001c0001t0010g0073 | 2 | HG03017.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.7-17886G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167666014 | ||||||
| chr1:167666094
|
A | G | 91 | a0001c0001t0001g0023a0001c0001t0001g0031a0001c0001t0001g0032others(88): Show | 91 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.7-17806A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167666094 | ||||||
| chr1:167666267
|
T | C | 3 | a0001c0001t0001g0059a0001c0001t0001g0074a0001c0010t0001g0012 | 3 | HG01496.hp1 HG03669.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.7-17633T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167666267 | ||||||
| chr1:167666320
|
C | T | 2 | a0001c0001t0004g0126a0001c0001t0010g0248 | 2 | HG00323.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.7-17580C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167666320 | ||||||
| chr1:167666338
|
A | G | 91 | a0001c0001t0001g0023a0001c0001t0001g0031a0001c0001t0001g0032others(88): Show | 91 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.7-17562A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167666338 | ||||||
| chr1:167666508
|
G | C | 1 | a0001c0001t0001g0328 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.7-17392G>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167666508 | ||||||
| chr1:167666534
|
A | G | 9 | a0001c0001t0005g0020a0001c0001t0005g0030a0001c0001t0005g0061others(6): Show | 9 | HG01884.hp1 HG02055.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.7-17366A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167666534 | ||||||
| chr1:167666585
|
C | T | 5 | a0001c0001t0005g0326a0001c0001t0017g0341a0001c0001t0020g0301others(2): Show | 5 | HG01243.hp1 HG02055.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.7-17315C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167666585 | ||||||
| chr1:167666592
|
C | G | 3 | a0001c0001t0001g0263a0001c0001t0001g0293a0001c0001t0036g0280 | 3 | NA18947.hp2 NA18952.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.7-17308C>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167666592 | ||||||
| chr1:167666727
|
C | T | 3 | a0001c0001t0008g0329a0001c0001t0008g0331a0001c0001t0018g0330 | 3 | HG01891.hp1 HG02622.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.7-17173C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167666727 | ||||||
| chr1:167666879
|
A | G | 1 | a0001c0001t0001g0328 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.7-17021A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167666879 | ||||||
| chr1:167667103
|
C | CCATTGTA others(31): Show |
3 | a0001c0001t0003g0306a0001c0001t0044g0217a0001c0001t0053g0096 | 3 | HG01891.hp2 HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.7-16763_7-16726dup others(38): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167667103 | |||||
| chr1:167667103
|
CCATTGTA others(31): Show |
C | 1 | a0001c0001t0009g0334 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.7-16763_7-16726del others(38): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167667103 | |||||
| chr1:167667210
|
T | C | 1 | a0001c0001t0003g0135 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.7-16690T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167667210 | ||||||
| chr1:167667323
|
C | T | 8 | a0001c0001t0001g0033a0001c0001t0001g0221a0001c0001t0005g0237others(5): Show | 8 | HG02109.hp1 HG02922.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.7-16577C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167667323 | ||||||
| chr1:167667324
|
G | A | 1 | a0001c0001t0017g0341 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.7-16576G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167667324 | ||||||
| chr1:167667383
|
A | G | 1 | a0001c0001t0001g0328 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.7-16517A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167667383 | ||||||
| chr1:167667422
|
A | G | 47 | a0001c0001t0001g0003a0001c0001t0001g0035a0001c0001t0001g0046others(44): Show | 48 | HG00438.hp2 HG00639.hp1 HG01074.hp1 others(45): Show |
intron_variant | MODIFIER | c.7-16478A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167667422 | ||||||
| chr1:167667423
|
A | G | 1 | a0001c0001t0001g0282 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.7-16477A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167667423 | ||||||
| chr1:167667470
|
A | T | 1 | a0001c0001t0001g0308 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.7-16430A>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167667470 | ||||||
| chr1:167667577
|
T | C | 1 | a0001c0001t0001g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.7-16323T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167667577 | ||||||
| chr1:167667769
|
A | G | 44 | a0001c0001t0001g0003a0001c0001t0001g0035a0001c0001t0001g0046others(41): Show | 45 | HG00438.hp2 HG00639.hp1 HG01074.hp1 others(42): Show |
intron_variant | MODIFIER | c.7-16131A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167667769 | ||||||
| chr1:167667813
|
A | G | 4 | a0001c0001t0001g0328a0001c0001t0017g0338a0001c0001t0018g0339others(1): Show | 4 | HG01884.hp2 HG02486.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.7-16087A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167667813 | ||||||
| chr1:167667835
|
T | C | 2 | a0001c0001t0001g0307a0001c0001t0001g0308 | 2 | HG02630.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.7-16065T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167667835 | ||||||
| chr1:167668018
|
T | C | 280 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(277): Show | 283 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.7-15882T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167668018 | ||||||
| chr1:167668083
|
G | C | 1 | a0001c0001t0028g0335 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.7-15817G>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167668083 | ||||||
| chr1:167668120
|
C | T | 2 | a0001c0001t0001g0336a0001c0001t0023g0227 | 2 | HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.7-15780C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167668120 | ||||||
| chr1:167668178
|
G | A | 1 | a0001c0001t0001g0009 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.7-15722G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167668178 | ||||||
| chr1:167668178
|
G | T | 1 | a0001c0001t0004g0126 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.7-15722G>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167668178 | ||||||
| chr1:167668287
|
G | A | 20 | a0001c0001t0001g0033a0001c0001t0001g0221a0001c0001t0001g0328others(17): Show | 20 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.7-15613G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167668287 | ||||||
| chr1:167668396
|
G | A | 228 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(225): Show | 230 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.7-15504G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167668396 | ||||||
| chr1:167668487
|
A | T | 9 | a0001c0001t0005g0020a0001c0001t0005g0030a0001c0001t0005g0061others(6): Show | 9 | HG01884.hp1 HG02055.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.7-15413A>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167668487 | ||||||
| chr1:167668526
|
A | G | 283 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(280): Show | 286 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.7-15374A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167668526 | ||||||
| chr1:167668530
|
C | A | 5 | a0001c0001t0001g0320a0001c0001t0003g0321a0001c0001t0003g0322others(2): Show | 5 | HG02040.hp2 NA18971.hp2 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.7-15370C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167668530 | ||||||
| chr1:167668705
|
T | TAATG | 4 | a0001c0001t0003g0019a0001c0001t0003g0026a0001c0001t0010g0249others(1): Show | 4 | NA18970.hp1 NA18972.hp1 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.7-15183_7-15180dup others(4): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167668705 | |||||
| chr1:167668731
|
T | C | 4 | a0001c0001t0005g0237a0001c0001t0008g0310a0001c0001t0016g0327others(1): Show | 4 | HG02109.hp1 HG02922.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.7-15169T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167668731 | ||||||
| chr1:167668736
|
TA | T | 179 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(176): Show | 181 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.7-15147delA | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167668736 | |||||
| chr1:167668736
|
TAAA | T | 20 | a0001c0001t0001g0017a0001c0001t0001g0021a0001c0001t0001g0022others(17): Show | 20 | HG00408.hp2 HG00558.hp2 HG02056.hp2 others(17): Show |
intron_variant | MODIFIER | c.7-15149_7-15147del others(3): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167668736 | |||||
| chr1:167668816
|
G | A | 1 | a0001c0001t0001g0347 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.7-15084G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167668816 | ||||||
| chr1:167668887
|
G | A | 173 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(170): Show | 175 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.7-15013G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167668887 | ||||||
| chr1:167668966
|
T | C | 283 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(280): Show | 286 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.7-14934T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167668966 | ||||||
| chr1:167669014
|
T | G | 283 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(280): Show | 286 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.7-14886T>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167669014 | ||||||
| chr1:167669051
|
T | C | 25 | a0001c0001t0001g0003a0001c0001t0001g0046a0001c0001t0001g0048others(22): Show | 26 | HG00438.hp2 HG00639.hp1 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.7-14849T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167669051 | ||||||
| chr1:167669186
|
C | T | 18 | a0001c0001t0001g0033a0001c0001t0001g0221a0001c0001t0003g0236others(15): Show | 18 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.7-14714C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167669186 | ||||||
| chr1:167669202
|
A | G | 1 | a0001c0001t0001g0328 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.7-14698A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167669202 | ||||||
| chr1:167669214
|
C | T | 173 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(170): Show | 175 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.7-14686C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167669214 | ||||||
| chr1:167669224
|
T | C | 160 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(157): Show | 162 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(159): Show |
intron_variant | MODIFIER | c.7-14676T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167669224 | ||||||
| chr1:167669320
|
G | A | 166 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(163): Show | 168 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.7-14580G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167669320 | ||||||
| chr1:167669380
|
G | C | 1 | a0001c0001t0001g0047 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.7-14520G>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167669380 | ||||||
| chr1:167669454
|
G | C | 1 | a0001c0001t0002g0195 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.7-14446G>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167669454 | ||||||
| chr1:167669779
|
A | G | 3 | a0001c0001t0001g0027a0001c0001t0001g0188a0001c0001t0012g0008 | 3 | HG00558.hp2 NA18960.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.7-14121A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167669779 | ||||||
| chr1:167669833
|
G | C | 106 | a0001c0001t0001g0003a0001c0001t0001g0031a0001c0001t0001g0032others(103): Show | 107 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.7-14067G>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167669833 | ||||||
| chr1:167669902
|
T | A | 106 | a0001c0001t0001g0003a0001c0001t0001g0031a0001c0001t0001g0032others(103): Show | 107 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.7-13998T>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167669902 | ||||||
| chr1:167669987
|
ACACACG | A | 278 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(275): Show | 281 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(278): Show |
intron_variant | MODIFIER | c.7-13901_7-13896del others(6): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167669987 | |||||
| chr1:167669999
|
G | T | 2 | a0001c0001t0001g0025a0001c0001t0002g0143 | 2 | NA18990.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.7-13901G>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167669999 | ||||||
| chr1:167670072
|
C | T | 7 | a0001c0001t0001g0289a0001c0001t0005g0288a0001c0001t0017g0338others(4): Show | 7 | HG01884.hp2 HG02559.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.7-13828C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167670072 | ||||||
| chr1:167670094
|
C | T | 7 | a0001c0001t0001g0003a0001c0001t0001g0319a0001c0001t0020g0301others(4): Show | 8 | HG01243.hp1 HG02622.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.7-13806C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167670094 | ||||||
| chr1:167670160
|
C | G | 8 | a0001c0001t0001g0238a0001c0001t0006g0225a0001c0001t0006g0226others(5): Show | 8 | HG02717.hp1 HG02895.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.7-13740C>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167670160 | ||||||
| chr1:167670261
|
G | A | 3 | a0001c0001t0001g0307a0001c0001t0001g0308a0001c0001t0001g0309 | 3 | HG02630.hp1 HG03098.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.7-13639G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167670261 | ||||||
| chr1:167670327
|
A | G | 1 | a0001c0001t0001g0336 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.7-13573A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167670327 | ||||||
| chr1:167670357
|
G | GA | 22 | a0001c0001t0001g0033a0001c0001t0001g0155a0001c0001t0001g0221others(19): Show | 22 | HG01884.hp2 HG01891.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.7-13527dupA | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167670357 | |||||
| chr1:167670357
|
G | GAA | 183 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(180): Show | 185 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(182): Show |
intron_variant | MODIFIER | c.7-13528_7-13527dup others(2): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167670357 | |||||
| chr1:167670357
|
G | GAAA | 70 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0048others(67): Show | 71 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.7-13529_7-13527dup others(3): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167670357 | |||||
| chr1:167670357
|
G | GAAAA | 6 | a0001c0001t0001g0103a0001c0001t0001g0105a0001c0001t0001g0139others(3): Show | 6 | HG00280.hp1 HG00438.hp1 HG00673.hp1 others(3): Show |
intron_variant | MODIFIER | c.7-13530_7-13527dup others(4): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167670357 | |||||
| chr1:167670422
|
C | T | 1 | a0001c0001t0021g0005 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.7-13478C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167670422 | ||||||
| chr1:167670549
|
C | T | 3 | a0001c0001t0001g0328a0001c0001t0008g0310a0001c0001t0016g0327 | 3 | HG02486.hp2 HG02922.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.7-13351C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167670549 | ||||||
| chr1:167670618
|
C | T | 174 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0013others(171): Show | 176 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.7-13282C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167670618 | ||||||
| chr1:167670719
|
C | T | 1 | a0001c0001t0001g0302 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.7-13181C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167670719 | ||||||
| chr1:167670737
|
C | G | 4 | a0001c0001t0005g0326a0001c0001t0006g0225a0001c0001t0006g0226others(1): Show | 4 | HG02055.hp2 HG02257.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.7-13163C>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167670737 | ||||||
| chr1:167670738
|
C | T | 1 | a0001c0001t0001g0328 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.7-13162C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167670738 | ||||||
| chr1:167670783
|
A | C | 36 | a0001c0001t0001g0046a0001c0001t0001g0054a0001c0001t0001g0101others(33): Show | 36 | HG00280.hp2 HG00438.hp1 HG00558.hp2 others(33): Show |
intron_variant | MODIFIER | c.7-13117A>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167670783 | ||||||
| chr1:167670885
|
C | T | 37 | a0001c0001t0001g0046a0001c0001t0001g0070a0001c0001t0001g0101others(34): Show | 37 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(34): Show |
intron_variant | MODIFIER | c.7-13015C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167670885 | ||||||
| chr1:167670949
|
C | T | 1 | a0001c0001t0009g0334 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.7-12951C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167670949 | ||||||
| chr1:167670996
|
C | T | 41 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0038others(38): Show | 41 | HG00408.hp1 HG00423.hp2 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.7-12904C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167670996 | ||||||
| chr1:167671076
|
G | A | 5 | a0001c0001t0002g0040a0001c0001t0002g0045a0001c0001t0003g0286others(2): Show | 5 | HG00099.hp2 HG01515.hp1 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.7-12824G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167671076 | ||||||
| chr1:167671375
|
T | C | 1 | a0001c0001t0023g0259 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.7-12525T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167671375 | ||||||
| chr1:167671407
|
G | A | 2 | a0001c0001t0004g0072a0001c0001t0004g0092 | 2 | NA18942.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.7-12493G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167671407 | ||||||
| chr1:167671433
|
C | T | 1 | a0001c0001t0023g0227 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.7-12467C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167671433 | ||||||
| chr1:167671474
|
T | A | 225 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0013others(222): Show | 227 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.7-12426T>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167671474 | ||||||
| chr1:167671590
|
A | G | 226 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0013others(223): Show | 228 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.7-12310A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167671590 | ||||||
| chr1:167671602
|
T | C | 226 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0013others(223): Show | 228 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.7-12298T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167671602 | ||||||
| chr1:167671881
|
C | T | 3 | a0001c0003t0026g0218a0002c0002t0009g0212a0002c0002t0009g0269 | 3 | HG01109.hp2 HG02451.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.7-12019C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167671881 | ||||||
| chr1:167671917
|
G | A | 1 | a0001c0001t0001g0048 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.7-11983G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167671917 | ||||||
| chr1:167672042
|
A | G | 3 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0004g0127 | 3 | HG00323.hp1 HG01081.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.7-11858A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167672042 | ||||||
| chr1:167672055
|
A | G | 229 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0013others(226): Show | 231 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.7-11845A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167672055 | ||||||
| chr1:167672132
|
G | A | 5 | a0001c0001t0001g0035a0001c0001t0017g0341a0001c0001t0022g0242others(2): Show | 5 | HG02818.hp2 HG03209.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.7-11768G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167672132 | ||||||
| chr1:167672142
|
A | G | 6 | a0001c0001t0001g0070a0001c0001t0001g0139a0001c0001t0002g0151others(3): Show | 6 | HG00280.hp1 HG00639.hp1 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.7-11758A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167672142 | ||||||
| chr1:167672174
|
C | T | 3 | a0001c0001t0001g0289a0001c0001t0005g0288a0001c0005t0008g0296 | 3 | HG02559.hp2 HG03195.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.7-11726C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167672174 | ||||||
| chr1:167672541
|
T | C | 27 | a0001c0001t0001g0046a0001c0001t0001g0054a0001c0001t0001g0101others(24): Show | 27 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(24): Show |
intron_variant | MODIFIER | c.7-11359T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167672541 | ||||||
| chr1:167672707
|
C | A | 228 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0013others(225): Show | 230 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.7-11193C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167672707 | ||||||
| chr1:167672786
|
A | G | 5 | a0001c0001t0001g0035a0001c0001t0017g0341a0001c0001t0022g0242others(2): Show | 5 | HG02818.hp2 HG03209.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.7-11114A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167672786 | ||||||
| chr1:167672873
|
A | G | 227 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0013others(224): Show | 229 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.7-11027A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167672873 | ||||||
| chr1:167672884
|
T | C | 6 | a0001c0001t0001g0070a0001c0001t0001g0139a0001c0001t0002g0151others(3): Show | 6 | HG00280.hp1 HG00639.hp1 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.7-11016T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167672884 | ||||||
| chr1:167672889
|
C | T | 3 | a0001c0001t0001g0328a0001c0001t0003g0004a0001c0001t0016g0327 | 3 | HG02486.hp2 HG02922.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.7-11011C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167672889 | ||||||
| chr1:167672951
|
C | T | 1 | a0001c0001t0023g0259 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.7-10949C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167672951 | ||||||
| chr1:167672959
|
C | T | 3 | a0001c0001t0001g0289a0001c0001t0005g0288a0001c0005t0008g0296 | 3 | HG02559.hp2 HG03195.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.7-10941C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167672959 | ||||||
| chr1:167673080
|
G | A | 224 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0013others(221): Show | 226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.7-10820G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167673080 | ||||||
| chr1:167673094
|
G | A | 1 | a0001c0001t0001g0336 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.7-10806G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167673094 | ||||||
| chr1:167673200
|
G | C | 25 | a0001c0001t0001g0044a0001c0001t0001g0047a0001c0001t0001g0064others(22): Show | 25 | HG01361.hp2 HG01884.hp2 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.7-10700G>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167673200 | ||||||
| chr1:167673257
|
T | C | 86 | a0001c0001t0001g0013a0001c0001t0001g0033a0001c0001t0001g0044others(83): Show | 86 | HG00099.hp1 HG00280.hp1 HG00639.hp1 others(83): Show |
intron_variant | MODIFIER | c.7-10643T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167673257 | ||||||
| chr1:167673288
|
T | C | 3 | a0001c0001t0003g0306a0001c0001t0044g0217a0001c0001t0053g0096 | 3 | HG01891.hp2 HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.7-10612T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167673288 | ||||||
| chr1:167673330
|
C | T | 1 | a0001c0001t0001g0282 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.7-10570C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167673330 | ||||||
| chr1:167673483
|
G | A | 1 | a0001c0001t0019g0157 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.7-10417G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167673483 | ||||||
| chr1:167673527
|
T | A | 5 | a0001c0001t0005g0020a0001c0001t0005g0030a0001c0001t0005g0061others(2): Show | 5 | HG01884.hp1 HG02055.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.7-10373T>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167673527 | ||||||
| chr1:167673570
|
C | G | 279 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(276): Show | 282 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(279): Show |
intron_variant | MODIFIER | c.7-10330C>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167673570 | ||||||
| chr1:167673629
|
A | T | 1 | a0001c0001t0004g0247 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.7-10271A>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167673629 | ||||||
| chr1:167673699
|
C | G | 38 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0016others(35): Show | 39 | HG00323.hp1 HG00609.hp2 HG01070.hp2 others(36): Show |
intron_variant | MODIFIER | c.7-10201C>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167673699 | ||||||
| chr1:167673755
|
C | T | 37 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0044others(34): Show | 37 | HG00099.hp1 HG00735.hp1 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.7-10145C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167673755 | ||||||
| chr1:167673800
|
C | T | 1 | a0001c0001t0003g0140 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.7-10100C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167673800 | ||||||
| chr1:167673805
|
G | C | 4 | a0001c0001t0001g0186a0001c0001t0001g0276a0001c0001t0003g0130others(1): Show | 4 | NA18952.hp1 NA18960.hp1 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.7-10095G>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167673805 | ||||||
| chr1:167673892
|
A | G | 257 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(254): Show | 258 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(255): Show |
intron_variant | MODIFIER | c.7-10008A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167673892 | ||||||
| chr1:167673941
|
T | C | 1 | a0001c0001t0004g0118 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.7-9959T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167673941 | ||||||
| chr1:167673947
|
T | C | 14 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0254others(11): Show | 14 | HG00099.hp1 HG00280.hp2 HG02165.hp1 others(11): Show |
intron_variant | MODIFIER | c.7-9953T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167673947 | ||||||
| chr1:167673981
|
C | T | 43 | a0001c0001t0001g0003a0001c0001t0001g0032a0001c0001t0001g0054others(40): Show | 44 | HG00140.hp2 HG00544.hp1 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.7-9919C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167673981 | ||||||
| chr1:167674003
|
T | C | 2 | a0001c0001t0010g0077a0001c0001t0049g0211 | 2 | NA18961.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.7-9897T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167674003 | ||||||
| chr1:167674044
|
G | C | 1 | a0001c0001t0001g0289 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.7-9856G>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167674044 | ||||||
| chr1:167674118
|
A | G | 2 | a0001c0001t0001g0023a0001c0001t0045g0109 | 2 | HG03834.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.7-9782A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167674118 | ||||||
| chr1:167674176
|
G | C | 199 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0021others(196): Show | 199 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.7-9724G>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167674176 | ||||||
| chr1:167674224
|
C | T | 66 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0038others(63): Show | 67 | HG00099.hp1 HG00735.hp1 HG01070.hp1 others(64): Show |
intron_variant | MODIFIER | c.7-9676C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167674224 | ||||||
| chr1:167674227
|
G | A | 5 | a0001c0001t0001g0038a0001c0001t0002g0206a0001c0001t0005g0237others(2): Show | 5 | HG01070.hp1 HG02109.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.7-9673G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167674227 | ||||||
| chr1:167674249
|
C | G | 6 | a0001c0001t0008g0219a0001c0001t0015g0052a0001c0001t0015g0239others(3): Show | 6 | HG02723.hp1 HG02723.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.7-9651C>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167674249 | ||||||
| chr1:167674444
|
C | T | 39 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0270others(36): Show | 40 | HG01081.hp2 HG01175.hp2 HG02074.hp2 others(37): Show |
intron_variant | MODIFIER | c.7-9456C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167674444 | ||||||
| chr1:167674455
|
TA | T | 35 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0270others(32): Show | 36 | HG01081.hp2 HG01175.hp2 HG02074.hp2 others(33): Show |
intron_variant | MODIFIER | c.7-9440delA | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167674455 | |||||
| chr1:167674482
|
G | A | 1 | a0001c0001t0001g0268 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.7-9418G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167674482 | ||||||
| chr1:167674559
|
A | G | 7 | a0001c0001t0001g0261a0001c0001t0001g0270a0001c0001t0009g0128others(4): Show | 7 | HG02257.hp1 HG02559.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.7-9341A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167674559 | ||||||
| chr1:167674620
|
C | T | 1 | a0001c0001t0001g0294 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.7-9280C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167674620 | ||||||
| chr1:167674779
|
A | G | 19 | a0001c0001t0001g0038a0001c0001t0001g0221a0001c0001t0001g0238others(16): Show | 19 | HG01070.hp1 HG01109.hp2 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.7-9121A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167674779 | ||||||
| chr1:167674928
|
C | T | 4 | a0001c0001t0002g0166a0001c0001t0004g0056a0001c0001t0014g0177others(1): Show | 4 | HG02027.hp2 NA18979.hp1 NA18985.hp1 others(1): Show |
intron_variant | MODIFIER | c.7-8972C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167674928 | ||||||
| chr1:167674932
|
T | C | 1 | a0001c0001t0001g0046 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.7-8968T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167674932 | ||||||
| chr1:167674934
|
C | T | 5 | a0001c0001t0002g0166a0001c0001t0004g0056a0001c0001t0014g0177others(2): Show | 5 | HG02027.hp2 HG02486.hp1 NA18979.hp1 others(2): Show |
intron_variant | MODIFIER | c.7-8966C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167674934 | ||||||
| chr1:167674935
|
G | A | 1 | a0001c0001t0051g0117 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.7-8965G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167674935 | ||||||
| chr1:167674940
|
C | T | 140 | a0001c0001t0001g0014a0001c0001t0001g0021a0001c0001t0001g0023others(137): Show | 140 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.7-8960C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167674940 | ||||||
| chr1:167674981
|
T | C | 8 | a0001c0001t0003g0004a0001c0001t0008g0219a0001c0001t0015g0052others(5): Show | 8 | HG02723.hp1 HG02723.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.7-8919T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167674981 | ||||||
| chr1:167674983
|
A | G | 7 | a0001c0001t0003g0004a0001c0001t0008g0219a0001c0001t0015g0052others(4): Show | 7 | HG02723.hp1 HG02723.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.7-8917A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167674983 | ||||||
| chr1:167674989
|
A | G | 7 | a0001c0001t0003g0004a0001c0001t0008g0219a0001c0001t0015g0052others(4): Show | 7 | HG02723.hp1 HG02723.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.7-8911A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167674989 | ||||||
| chr1:167674991
|
A | G | 7 | a0001c0001t0003g0004a0001c0001t0008g0219a0001c0001t0015g0052others(4): Show | 7 | HG02723.hp1 HG02723.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.7-8909A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167674991 | ||||||
| chr1:167675000
|
A | T | 1 | a0001c0001t0024g0159 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.7-8900A>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167675000 | ||||||
| chr1:167675002
|
C | G | 5 | a0001c0001t0001g0238a0001c0001t0017g0338a0001c0001t0017g0341others(2): Show | 5 | HG01109.hp2 HG02922.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.7-8898C>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167675002 | ||||||
| chr1:167675003
|
A | G | 111 | a0001c0001t0001g0017a0001c0001t0001g0022a0001c0001t0001g0023others(108): Show | 111 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.7-8897A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167675003 | ||||||
| chr1:167675018
|
A | G | 3 | a0001c0001t0001g0082a0001c0001t0001g0266a0001c0001t0003g0134 | 3 | HG03942.hp1 NA18957.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.7-8882A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167675018 | ||||||
| chr1:167675023
|
A | G | 1 | a0001c0001t0001g0266 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.7-8877A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167675023 | ||||||
| chr1:167675030
|
C | T | 1 | a0001c0001t0001g0266 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.7-8870C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167675030 | ||||||
| chr1:167675099
|
C | T | 38 | a0001c0001t0001g0003a0001c0001t0001g0038a0001c0001t0001g0105others(35): Show | 39 | HG00438.hp1 HG01070.hp1 HG01081.hp2 others(36): Show |
intron_variant | MODIFIER | c.7-8801C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167675099 | ||||||
| chr1:167675119
|
C | T | 66 | a0001c0001t0001g0003a0001c0001t0001g0038a0001c0001t0001g0101others(63): Show | 67 | HG00099.hp2 HG00438.hp1 HG00741.hp1 others(64): Show |
intron_variant | MODIFIER | c.7-8781C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167675119 | ||||||
| chr1:167675207
|
G | GA | 74 | a0001c0001t0001g0021a0001c0001t0001g0027a0001c0001t0001g0038others(71): Show | 74 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.7-8668dupA | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167675207 | |||||
| chr1:167675207
|
G | GAA | 9 | a0001c0001t0002g0149a0001c0001t0002g0151a0001c0001t0005g0111others(6): Show | 9 | HG00621.hp1 HG00741.hp1 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.7-8669_7-8668dupAA | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167675207 | |||||
| chr1:167675207
|
G | GGA | 6 | a0001c0001t0001g0328a0001c0001t0022g0342a0001c0001t0028g0335others(3): Show | 6 | HG01081.hp2 HG02451.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.7-8693_7-8692insGA | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167675207 | ||||||
| chr1:167675207
|
G | GGAA | 12 | a0001c0001t0001g0003a0001c0001t0001g0281a0001c0001t0001g0289others(9): Show | 13 | HG02109.hp2 HG02723.hp1 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.7-8693_7-8692insGA others(1): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167675207 | ||||||
| chr1:167675207
|
G | GGAAA | 6 | a0001c0001t0001g0279a0001c0001t0003g0004a0001c0001t0005g0326others(3): Show | 6 | HG01891.hp1 HG02055.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.7-8693_7-8692insGA others(2): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167675207 | ||||||
| chr1:167675207
|
GA | G | 31 | a0001c0001t0001g0023a0001c0001t0001g0048a0001c0001t0001g0049others(28): Show | 31 | HG00099.hp1 HG00735.hp1 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.7-8668delA | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167675207 | |||||
| chr1:167675356
|
G | A | 2 | a0001c0001t0001g0252a0004c0006t0002g0207 | 2 | HG01192.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.7-8544G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167675356 | ||||||
| chr1:167675358
|
G | A | 24 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0105others(21): Show | 25 | HG00438.hp1 HG01081.hp2 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.7-8542G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167675358 | ||||||
| chr1:167675430
|
C | T | 49 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0221others(46): Show | 50 | HG01074.hp2 HG01081.hp2 HG01175.hp2 others(47): Show |
intron_variant | MODIFIER | c.7-8470C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167675430 | ||||||
| chr1:167675487
|
C | G | 8 | a0001c0001t0001g0003a0001c0001t0001g0279a0001c0001t0001g0281others(5): Show | 9 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.7-8413C>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167675487 | ||||||
| chr1:167675493
|
T | C | 45 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0101others(42): Show | 46 | HG00280.hp2 HG00741.hp1 HG01074.hp2 others(43): Show |
intron_variant | MODIFIER | c.7-8407T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167675493 | ||||||
| chr1:167675512
|
T | G | 45 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0101others(42): Show | 46 | HG00280.hp2 HG00741.hp1 HG01074.hp2 others(43): Show |
intron_variant | MODIFIER | c.7-8388T>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167675512 | ||||||
| chr1:167675639
|
C | T | 5 | a0001c0001t0005g0244a0001c0001t0018g0330a0001c0001t0018g0339others(2): Show | 5 | HG01884.hp2 HG02886.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.7-8261C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167675639 | ||||||
| chr1:167675651
|
C | T | 2 | a0001c0001t0001g0017a0001c0001t0001g0022 | 2 | NA18950.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.7-8249C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167675651 | ||||||
| chr1:167675674
|
G | A | 5 | a0001c0001t0001g0038a0001c0001t0005g0237a0001c0001t0023g0227others(2): Show | 5 | HG01070.hp1 HG02109.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.7-8226G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167675674 | ||||||
| chr1:167675855
|
C | G | 1 | a0001c0001t0001g0013 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.7-8045C>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167675855 | ||||||
| chr1:167676429
|
A | G | 3 | a0001c0001t0001g0221a0001c0001t0001g0302a0001c0001t0005g0069 | 3 | HG02145.hp2 HG02647.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.7-7471A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167676429 | ||||||
| chr1:167676491
|
T | C | 1 | a0001c0001t0001g0055 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.7-7409T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167676491 | ||||||
| chr1:167676638
|
G | C | 1 | a0001c0001t0032g0167 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.7-7262G>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167676638 | ||||||
| chr1:167676736
|
C | A | 30 | a0001c0001t0001g0003a0001c0001t0001g0221a0001c0001t0001g0279others(27): Show | 31 | HG00280.hp2 HG00741.hp1 HG01433.hp2 others(28): Show |
intron_variant | MODIFIER | c.7-7164C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167676736 | ||||||
| chr1:167676866
|
G | A | 1 | a0001c0001t0001g0013 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.7-7034G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167676866 | ||||||
| chr1:167676871
|
A | G | 4 | a0001c0001t0003g0019a0001c0001t0003g0026a0001c0001t0010g0249others(1): Show | 4 | NA18970.hp1 NA18972.hp1 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.7-7029A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167676871 | ||||||
| chr1:167676880
|
T | C | 1 | a0001c0001t0002g0175 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.7-7020T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167676880 | ||||||
| chr1:167676969
|
A | T | 1 | a0001c0001t0003g0006 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.7-6931A>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167676969 | ||||||
| chr1:167676985
|
C | G | 30 | a0001c0001t0001g0003a0001c0001t0001g0221a0001c0001t0001g0279others(27): Show | 31 | HG00280.hp2 HG00741.hp1 HG01433.hp2 others(28): Show |
intron_variant | MODIFIER | c.7-6915C>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167676985 | ||||||
| chr1:167677194
|
GA | G | 9 | a0001c0001t0011g0042a0001c0001t0011g0043a0001c0001t0011g0067others(6): Show | 9 | HG00438.hp2 HG01074.hp2 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.7-6701delA | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167677194 | |||||
| chr1:167677222
|
G | A | 1 | a0001c0001t0001g0268 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.7-6678G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167677222 | ||||||
| chr1:167677226
|
C | T | 1 | a0001c0001t0001g0046 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.7-6674C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167677226 | ||||||
| chr1:167677237
|
A | G | 23 | a0001c0001t0001g0021a0001c0001t0001g0027a0001c0001t0001g0028others(20): Show | 23 | HG00099.hp1 HG00609.hp1 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.7-6663A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167677237 | ||||||
| chr1:167677337
|
T | C | 1 | a0001c0001t0050g0119 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.7-6563T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167677337 | ||||||
| chr1:167677477
|
G | T | 29 | a0001c0001t0001g0003a0001c0001t0001g0221a0001c0001t0001g0279others(26): Show | 30 | HG00741.hp1 HG01433.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.7-6423G>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167677477 | ||||||
| chr1:167677774
|
C | T | 1 | a0001c0001t0004g0118 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.7-6126C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167677774 | ||||||
| chr1:167677935
|
G | T | 5 | a0001c0001t0015g0052a0001c0001t0015g0239a0001c0001t0015g0304others(2): Show | 5 | HG02723.hp1 HG02723.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.7-5965G>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167677935 | ||||||
| chr1:167677957
|
G | A | 2 | a0001c0001t0001g0002a0001c0001t0001g0059 | 3 | HG03491.hp1 HG03492.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.7-5943G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167677957 | ||||||
| chr1:167677971
|
C | A | 10 | a0001c0001t0001g0013a0001c0001t0011g0042a0001c0001t0011g0043others(7): Show | 10 | HG00438.hp2 HG01074.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.7-5929C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167677971 | ||||||
| chr1:167678158
|
T | C | 4 | a0001c0001t0005g0237a0001c0001t0023g0227a0001c0001t0023g0259others(1): Show | 4 | HG01070.hp1 HG02109.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.7-5742T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167678158 | ||||||
| chr1:167678262
|
A | G | 8 | a0001c0001t0001g0003a0001c0001t0001g0279a0001c0001t0001g0281others(5): Show | 9 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.7-5638A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167678262 | ||||||
| chr1:167678323
|
C | T | 1 | a0001c0001t0001g0049 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.7-5577C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167678323 | ||||||
| chr1:167678324
|
G | A | 4 | a0001c0001t0003g0019a0001c0001t0003g0026a0001c0001t0010g0249others(1): Show | 4 | NA18970.hp1 NA18972.hp1 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.7-5576G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167678324 | ||||||
| chr1:167678336
|
T | G | 1 | a0001c0001t0004g0126 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.7-5564T>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167678336 | ||||||
| chr1:167678402
|
CCAACATG others(5): Show |
C | 16 | a0001c0001t0001g0003a0001c0001t0001g0221a0001c0001t0001g0279others(13): Show | 17 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.7-5493_7-5482delAT others(10): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167678402 | |||||
| chr1:167678573
|
C | T | 4 | a0001c0001t0005g0244a0001c0001t0018g0330a0001c0001t0018g0339others(1): Show | 4 | HG01884.hp2 HG02886.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.7-5327C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167678573 | ||||||
| chr1:167678606
|
C | A | 1 | a0002c0002t0009g0318 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.7-5294C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167678606 | ||||||
| chr1:167678695
|
T | C | 1 | a0001c0001t0001g0268 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.7-5205T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167678695 | ||||||
| chr1:167678738
|
C | T | 16 | a0001c0001t0001g0003a0001c0001t0001g0221a0001c0001t0001g0279others(13): Show | 17 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.7-5162C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167678738 | ||||||
| chr1:167678785
|
G | T | 3 | a0001c0001t0027g0078a0001c0001t0027g0089a0001c0001t0043g0015 | 3 | NA18947.hp1 NA19005.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.7-5115G>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167678785 | ||||||
| chr1:167678797
|
C | A | 2 | a0001c0001t0009g0213a0001c0001t0052g0158 | 2 | HG02572.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.7-5103C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167678797 | ||||||
| chr1:167678861
|
C | A | 13 | a0001c0001t0001g0003a0001c0001t0001g0279a0001c0001t0001g0281others(10): Show | 14 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.7-5039C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167678861 | ||||||
| chr1:167678911
|
C | T | 13 | a0001c0001t0001g0003a0001c0001t0001g0279a0001c0001t0001g0281others(10): Show | 14 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.7-4989C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167678911 | ||||||
| chr1:167679011
|
G | A | 1 | a0001c0001t0001g0264 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.7-4889G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167679011 | ||||||
| chr1:167679156
|
A | G | 14 | a0001c0001t0001g0328a0001c0001t0003g0004a0001c0001t0009g0128others(11): Show | 14 | HG01081.hp2 HG02257.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.7-4744A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167679156 | ||||||
| chr1:167679232
|
CT | C | 9 | a0001c0001t0011g0042a0001c0001t0011g0043a0001c0001t0011g0067others(6): Show | 9 | HG00438.hp2 HG01074.hp2 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.7-4666delT | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167679232 | |||||
| chr1:167679316
|
C | G | 1 | a0001c0001t0017g0341 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.7-4584C>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167679316 | ||||||
| chr1:167679403
|
T | A | 21 | a0001c0001t0001g0021a0001c0001t0001g0027a0001c0001t0001g0028others(18): Show | 21 | HG00099.hp1 HG00609.hp1 HG00621.hp1 others(18): Show |
intron_variant | MODIFIER | c.7-4497T>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167679403 | ||||||
| chr1:167679410
|
C | A | 1 | a0001c0001t0004g0246 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.7-4490C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167679410 | ||||||
| chr1:167679528
|
G | A | 1 | a0001c0001t0001g0268 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.7-4372G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167679528 | ||||||
| chr1:167679567
|
G | T | 1 | a0001c0001t0007g0182 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.7-4333G>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167679567 | ||||||
| chr1:167679632
|
G | A | 1 | a0001c0001t0011g0042 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.7-4268G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167679632 | ||||||
| chr1:167679674
|
C | T | 1 | a0001c0001t0050g0119 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.7-4226C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167679674 | ||||||
| chr1:167679827
|
G | T | 1 | a0001c0001t0003g0053 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.7-4073G>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167679827 | ||||||
| chr1:167679921
|
A | G | 1 | a0001c0001t0019g0099 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.7-3979A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167679921 | ||||||
| chr1:167680060
|
T | A | 13 | a0001c0001t0001g0003a0001c0001t0001g0279a0001c0001t0001g0281others(10): Show | 14 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.7-3840T>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167680060 | ||||||
| chr1:167680098
|
G | A | 3 | a0001c0001t0001g0221a0001c0001t0001g0302a0001c0001t0005g0069 | 3 | HG02145.hp2 HG02647.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.7-3802G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167680098 | ||||||
| chr1:167680409
|
G | A | 3 | a0001c0001t0002g0176a0001c0001t0002g0197a0001c0001t0004g0124 | 3 | HG00673.hp2 HG02015.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.7-3491G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167680409 | ||||||
| chr1:167680448
|
C | CTGTTTT | 49 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0027others(46): Show | 50 | HG00099.hp1 HG00280.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.7-3414_7-3409dupGT others(4): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167680448 | |||||
| chr1:167680448
|
C | CTGTTTTT others(5): Show |
4 | a0001c0001t0001g0187a0001c0001t0006g0223a0001c0001t0006g0257others(1): Show | 4 | HG00741.hp1 HG01433.hp2 NA18972.hp2 others(1): Show |
intron_variant | MODIFIER | c.7-3420_7-3409dupGT others(10): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167680448 | |||||
| chr1:167680448
|
C | CTGTTTTT others(11): Show |
2 | a0001c0001t0001g0033a0001c0001t0001g0064 | 2 | HG03225.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.7-3426_7-3409dupGT others(16): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167680448 | |||||
| chr1:167680448
|
CTGTTTT | C | 24 | a0001c0001t0001g0013a0001c0001t0001g0221a0001c0001t0001g0282others(21): Show | 24 | HG00438.hp2 HG01074.hp2 HG01175.hp2 others(21): Show |
intron_variant | MODIFIER | c.7-3414_7-3409delGT others(4): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167680448 | |||||
| chr1:167680448
|
CTGTTTTT others(5): Show |
C | 9 | a0001c0001t0001g0003a0001c0001t0001g0279a0001c0001t0001g0281others(6): Show | 10 | HG00423.hp1 HG01891.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.7-3420_7-3409delGT others(10): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167680448 | |||||
| chr1:167680566
|
G | A | 14 | a0001c0001t0001g0328a0001c0001t0003g0004a0001c0001t0009g0128others(11): Show | 14 | HG01081.hp2 HG02257.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.7-3334G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167680566 | ||||||
| chr1:167680629
|
C | T | 1 | a0001c0001t0001g0264 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.7-3271C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167680629 | ||||||
| chr1:167680692
|
C | T | 87 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0025others(84): Show | 87 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.7-3208C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167680692 | ||||||
| chr1:167680820
|
C | T | 3 | a0001c0001t0018g0330a0001c0001t0018g0339a0001c0001t0018g0340 | 3 | HG01884.hp2 HG03130.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.7-3080C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167680820 | ||||||
| chr1:167680969
|
A | G | 17 | a0001c0001t0001g0003a0001c0001t0001g0279a0001c0001t0001g0281others(14): Show | 18 | HG01070.hp1 HG01891.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.7-2931A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167680969 | ||||||
| chr1:167680999
|
T | C | 13 | a0001c0001t0001g0003a0001c0001t0001g0279a0001c0001t0001g0281others(10): Show | 14 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.7-2901T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167680999 | ||||||
| chr1:167681170
|
G | T | 1 | a0001c0001t0012g0277 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.7-2730G>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167681170 | ||||||
| chr1:167681260
|
T | C | 13 | a0001c0001t0001g0003a0001c0001t0001g0279a0001c0001t0001g0281others(10): Show | 14 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.7-2640T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167681260 | ||||||
| chr1:167681370
|
A | G | 8 | a0001c0001t0001g0003a0001c0001t0001g0279a0001c0001t0001g0281others(5): Show | 9 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.7-2530A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167681370 | ||||||
| chr1:167681414
|
G | A | 8 | a0001c0001t0001g0238a0001c0001t0001g0241a0001c0001t0008g0219others(5): Show | 8 | HG01109.hp2 HG02280.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.7-2486G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167681414 | ||||||
| chr1:167681465
|
G | A | 5 | a0001c0001t0015g0052a0001c0001t0015g0239a0001c0001t0015g0304others(2): Show | 5 | HG02723.hp1 HG02723.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.7-2435G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167681465 | ||||||
| chr1:167681490
|
T | A | 8 | a0001c0001t0001g0003a0001c0001t0001g0279a0001c0001t0001g0281others(5): Show | 9 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.7-2410T>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167681490 | ||||||
| chr1:167681666
|
C | T | 13 | a0001c0001t0001g0003a0001c0001t0001g0279a0001c0001t0001g0281others(10): Show | 14 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.7-2234C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167681666 | ||||||
| chr1:167681668
|
C | A | 1 | a0001c0001t0001g0013 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.7-2232C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167681668 | ||||||
| chr1:167681890
|
G | A | 1 | a0001c0001t0001g0013 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.7-2010G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167681890 | ||||||
| chr1:167681951
|
G | A | 2 | a0001c0001t0001g0027a0001c0001t0013g0199 | 2 | NA18961.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.7-1949G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167681951 | ||||||
| chr1:167681955
|
T | C | 4 | a0001c0001t0005g0237a0001c0001t0023g0227a0001c0001t0023g0259others(1): Show | 4 | HG01070.hp1 HG02109.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.7-1945T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167681955 | ||||||
| chr1:167682131
|
G | A | 5 | a0001c0001t0001g0241a0001c0001t0008g0219a0001c0001t0008g0262others(2): Show | 5 | HG02280.hp2 HG02717.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.7-1769G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167682131 | ||||||
| chr1:167682172
|
C | CT | 23 | a0001c0001t0001g0291a0001c0001t0001g0328a0001c0001t0003g0004others(20): Show | 23 | HG01081.hp2 HG01884.hp2 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.7-1713dupT | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167682172 | |||||
| chr1:167682172
|
C | CTTT | 14 | a0001c0001t0001g0003a0001c0001t0001g0268a0001c0001t0001g0279others(11): Show | 15 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.7-1715_7-1713dupTT others(1): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167682172 | |||||
| chr1:167682212
|
C | G | 3 | a0001c0001t0018g0330a0001c0001t0018g0339a0001c0001t0018g0340 | 3 | HG01884.hp2 HG03130.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.7-1688C>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167682212 | ||||||
| chr1:167682295
|
A | G | 8 | a0001c0001t0001g0003a0001c0001t0001g0279a0001c0001t0001g0281others(5): Show | 9 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.7-1605A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167682295 | ||||||
| chr1:167682378
|
A | T | 3 | a0001c0001t0001g0238a0001c0003t0026g0218a0001c0003t0026g0303 | 3 | HG01109.hp2 HG02922.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.7-1522A>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167682378 | ||||||
| chr1:167682388
|
C | T | 1 | a0001c0001t0039g0337 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.7-1512C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167682388 | ||||||
| chr1:167682406
|
T | A | 2 | a0001c0001t0015g0304a0001c0001t0015g0305 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.7-1494T>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167682406 | ||||||
| chr1:167682419
|
C | T | 20 | a0001c0001t0001g0241a0001c0001t0001g0328a0001c0001t0003g0004others(17): Show | 20 | HG01081.hp2 HG02257.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.7-1481C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167682419 | ||||||
| chr1:167682476
|
C | G | 1 | a0001c0001t0001g0241 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.7-1424C>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167682476 | ||||||
| chr1:167682577
|
T | C | 3 | a0001c0001t0002g0176a0001c0001t0002g0197a0001c0001t0004g0124 | 3 | HG00673.hp2 HG02015.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.7-1323T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167682577 | ||||||
| chr1:167682668
|
A | AGT | 78 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0017others(75): Show | 79 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.7-1191_7-1190dupGT | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167682668 | |||||
| chr1:167682668
|
A | AGTGT | 42 | a0001c0001t0001g0033a0001c0001t0001g0051a0001c0001t0001g0228others(39): Show | 42 | HG00140.hp1 HG00323.hp2 HG01169.hp1 others(39): Show |
intron_variant | MODIFIER | c.7-1193_7-1190dupGT others(2): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167682668 | |||||
| chr1:167682668
|
A | AGTGTGT | 20 | a0001c0001t0001g0035a0001c0001t0001g0081a0001c0001t0001g0116others(17): Show | 20 | HG00423.hp2 HG01109.hp2 HG01993.hp1 others(17): Show |
intron_variant | MODIFIER | c.7-1195_7-1190dupGT others(4): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167682668 | |||||
| chr1:167682668
|
A | AGTGTGTG others(3): Show |
1 | a0001c0001t0001g0032 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.7-1199_7-1190dupGT others(8): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167682668 | |||||
| chr1:167682668
|
AGT | A | 51 | a0001c0001t0001g0021a0001c0001t0001g0027a0001c0001t0001g0028others(48): Show | 51 | HG00621.hp1 HG00639.hp1 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.7-1191_7-1190delGT | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167682668 | |||||
| chr1:167682668
|
AGTGT | A | 43 | a0001c0001t0001g0003a0001c0001t0001g0048a0001c0001t0001g0050others(40): Show | 44 | HG00408.hp2 HG00544.hp2 HG00673.hp2 others(41): Show |
intron_variant | MODIFIER | c.7-1193_7-1190delGT others(2): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167682668 | |||||
| chr1:167682668
|
AGTGTGT | A | 16 | a0001c0001t0001g0260a0001c0001t0001g0268a0001c0001t0001g0270others(13): Show | 16 | HG02027.hp1 HG02148.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.7-1195_7-1190delGT others(4): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167682668 | |||||
| chr1:167682668
|
AGTGTGTG others(3): Show |
A | 3 | a0001c0001t0001g0013a0001c0001t0003g0133a0001c0001t0011g0100 | 3 | HG00735.hp2 HG02074.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.7-1199_7-1190delGT others(8): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167682668 | |||||
| chr1:167682668
|
AGTGTGTG others(5): Show |
A | 7 | a0001c0001t0011g0043a0001c0001t0011g0067a0001c0001t0011g0274others(4): Show | 7 | HG01074.hp2 HG01175.hp2 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.7-1201_7-1190delGT others(10): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167682668 | |||||
| chr1:167682720
|
T | C | 8 | a0001c0001t0001g0003a0001c0001t0001g0279a0001c0001t0001g0281others(5): Show | 9 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.7-1180T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167682720 | ||||||
| chr1:167682727
|
G | A | 4 | a0001c0001t0001g0105a0001c0001t0002g0166a0001c0001t0004g0056others(1): Show | 4 | HG00438.hp1 HG02027.hp2 HG02056.hp1 others(1): Show |
intron_variant | MODIFIER | c.7-1173G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167682727 | ||||||
| chr1:167682750
|
G | T | 101 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0025others(98): Show | 101 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.7-1150G>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167682750 | ||||||
| chr1:167682783
|
G | GA | 14 | a0001c0001t0001g0003a0001c0001t0001g0268a0001c0001t0001g0279others(11): Show | 15 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.7-1117_7-1116insA | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167682783 | ||||||
| chr1:167682885
|
C | A | 14 | a0001c0001t0001g0003a0001c0001t0001g0268a0001c0001t0001g0279others(11): Show | 15 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.7-1015C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167682885 | ||||||
| chr1:167682904
|
A | C | 6 | a0001c0001t0001g0268a0001c0001t0015g0052a0001c0001t0015g0239others(3): Show | 6 | HG02451.hp2 HG02723.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.7-996A>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167682904 | ||||||
| chr1:167682932
|
G | A | 20 | a0001c0001t0001g0241a0001c0001t0001g0328a0001c0001t0003g0004others(17): Show | 20 | HG01081.hp2 HG02257.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.7-968G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167682932 | ||||||
| chr1:167682969
|
T | C | 1 | a0001c0001t0001g0263 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.7-931T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167682969 | ||||||
| chr1:167683035
|
C | A | 124 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0025others(121): Show | 124 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.7-865C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167683035 | ||||||
| chr1:167683103
|
G | A | 3 | a0003c0004t0025g0034a0003c0004t0025g0240a0005c0007t0017g0243 | 3 | HG02280.hp1 HG02976.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.7-797G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167683103 | ||||||
| chr1:167683107
|
G | T | 3 | a0001c0001t0001g0221a0001c0001t0001g0302a0001c0001t0005g0069 | 3 | HG02145.hp2 HG02647.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.7-793G>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167683107 | ||||||
| chr1:167683281
|
G | A | 8 | a0001c0001t0005g0111a0001c0001t0016g0112a0001c0001t0016g0253others(5): Show | 8 | HG02258.hp2 HG02572.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.7-619G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167683281 | ||||||
| chr1:167683409
|
T | C | 8 | a0001c0001t0001g0003a0001c0001t0001g0279a0001c0001t0001g0281others(5): Show | 9 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.7-491T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167683409 | ||||||
| chr1:167683419
|
C | A | 1 | a0001c0001t0001g0270 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.7-481C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167683419 | ||||||
| chr1:167683423
|
C | T | 151 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0013others(148): Show | 152 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.7-477C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167683423 | ||||||
| chr1:167683550
|
A | C | 2 | a0001c0001t0003g0283a0001c0001t0003g0284 | 2 | NA18939.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.7-350A>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167683550 | ||||||
| chr1:167683575
|
G | A | 1 | a0001c0001t0001g0261 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.7-325G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167683575 | ||||||
| chr1:167683578
|
G | A | 4 | a0001c0001t0005g0237a0001c0001t0023g0227a0001c0001t0023g0259others(1): Show | 4 | HG01070.hp1 HG02109.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.7-322G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167683578 | ||||||
| chr1:167683703
|
G | A | 11 | a0001c0001t0001g0003a0001c0001t0001g0221a0001c0001t0001g0279others(8): Show | 12 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.7-197G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167683703 | ||||||
| chr1:167683758
|
C | A | 9 | a0001c0001t0011g0042a0001c0001t0011g0043a0001c0001t0011g0067others(6): Show | 9 | HG00438.hp2 HG01074.hp2 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.7-142C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167683758 | ||||||
| chr1:167683765
|
G | A | 37 | a0001c0001t0001g0241a0001c0001t0001g0328a0001c0001t0003g0004others(34): Show | 37 | HG01070.hp1 HG01081.hp2 HG01109.hp2 others(34): Show |
intron_variant | MODIFIER | c.7-135G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167683765 | ||||||
| chr1:167683864
|
T | C | 1 | a0001c0001t0015g0239 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.7-36T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167683864 | ||||||
| chr1:167683892
|
T | C | 1 | a0001c0001t0002g0209 | 1 | HG00140.hp2 | splice_region_variant&intron_variant | LOW | c.7-8T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167683892 | ||||||
| chr1:167684039
|
G | C | 1 | a0001c0001t0001g0154 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.108+38G>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 2/6 | chr1 | 167684039 | ||||||
| chr1:167684404
|
G | A | 1 | a0001c0001t0003g0286 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.108+403G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 2/6 | chr1 | 167684404 | ||||||
| chr1:167684422
|
G | T | 7 | a0001c0001t0001g0221a0001c0001t0001g0302a0001c0001t0005g0069others(4): Show | 7 | HG01070.hp1 HG02109.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.108+421G>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 2/6 | chr1 | 167684422 | ||||||
| chr1:167684490
|
G | A | 1 | a0001c0001t0001g0082 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.108+489G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 2/6 | chr1 | 167684490 | ||||||
| chr1:167684596
|
C | G | 1 | a0001c0001t0013g0204 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.108+595C>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 2/6 | chr1 | 167684596 | ||||||
| chr1:167684612
|
C | T | 6 | a0001c0001t0001g0268a0001c0001t0015g0052a0001c0001t0015g0239others(3): Show | 6 | HG02451.hp2 HG02723.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.108+611C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 2/6 | chr1 | 167684612 | ||||||
| chr1:167684730
|
C | T | 1 | a0001c0001t0002g0121 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.109-691C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 2/6 | chr1 | 167684730 | ||||||
| chr1:167684751
|
G | A | 17 | a0001c0001t0001g0003a0001c0001t0001g0221a0001c0001t0001g0279others(14): Show | 18 | HG01070.hp1 HG01109.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.109-670G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 2/6 | chr1 | 167684751 | ||||||
| chr1:167684806
|
G | A | 1 | a0001c0001t0001g0136 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.109-615G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 2/6 | chr1 | 167684806 | ||||||
| chr1:167684871
|
T | A | 6 | a0001c0001t0001g0268a0001c0001t0015g0052a0001c0001t0015g0239others(3): Show | 6 | HG02451.hp2 HG02723.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.109-550T>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 2/6 | chr1 | 167684871 | ||||||
| chr1:167685000
|
G | A | 1 | a0001c0001t0004g0126 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.109-421G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 2/6 | chr1 | 167685000 | ||||||
| chr1:167685102
|
C | A | 1 | a0001c0001t0001g0101 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.109-319C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 2/6 | chr1 | 167685102 | ||||||
| chr1:167685120
|
T | C | 8 | a0001c0001t0001g0003a0001c0001t0001g0279a0001c0001t0001g0281others(5): Show | 9 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.109-301T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 2/6 | chr1 | 167685120 | ||||||
| chr1:167685128
|
G | A | 1 | a0001c0009t0005g0062 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.109-293G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 2/6 | chr1 | 167685128 | ||||||
| chr1:167685344
|
T | C | 17 | a0001c0001t0001g0003a0001c0001t0001g0221a0001c0001t0001g0279others(14): Show | 18 | HG01070.hp1 HG01109.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.109-77T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 2/6 | chr1 | 167685344 | ||||||
| chr1:167685361
|
C | T | 21 | a0001c0001t0001g0021a0001c0001t0001g0027a0001c0001t0001g0028others(18): Show | 21 | HG00099.hp1 HG00609.hp1 HG00621.hp1 others(18): Show |
intron_variant | MODIFIER | c.109-60C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 2/6 | chr1 | 167685361 | ||||||
| chr1:167685407
|
C | T | 3 | a0001c0001t0005g0332a0001c0001t0008g0329a0001c0001t0008g0331 | 3 | HG01891.hp1 HG02622.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.109-14C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 2/6 | chr1 | 167685407 | ||||||
| chr1:167685900
|
G | A | 1 | a0001c0001t0001g0101 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.198+390G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 3/6 | chr1 | 167685900 | ||||||
| chr1:167685912
|
T | C | 1 | a0001c0001t0001g0265 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.198+402T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 3/6 | chr1 | 167685912 | ||||||
| chr1:167685989
|
T | C | 1 | a0001c0001t0016g0253 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.198+479T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 3/6 | chr1 | 167685989 | ||||||
| chr1:167686005
|
C | T | 20 | a0001c0001t0001g0241a0001c0001t0001g0328a0001c0001t0003g0004others(17): Show | 20 | HG01081.hp2 HG02257.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.198+495C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 3/6 | chr1 | 167686005 | ||||||
| chr1:167686020
|
G | A | 2 | a0001c0001t0003g0041a0001c0001t0003g0053 | 2 | HG02293.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.198+510G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 3/6 | chr1 | 167686020 | ||||||
| chr1:167686326
|
C | T | 3 | a0001c0001t0018g0330a0001c0001t0018g0339a0001c0001t0018g0340 | 3 | HG01884.hp2 HG03130.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.198+816C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 3/6 | chr1 | 167686326 | ||||||
| chr1:167686352
|
G | A | 1 | a0001c0001t0001g0268 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.198+842G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 3/6 | chr1 | 167686352 | ||||||
| chr1:167686774
|
C | T | 8 | a0001c0001t0001g0003a0001c0001t0001g0279a0001c0001t0001g0281others(5): Show | 9 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.198+1264C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 3/6 | chr1 | 167686774 | ||||||
| chr1:167686864
|
G | A | 8 | a0001c0001t0001g0268a0001c0001t0015g0052a0001c0001t0015g0239others(5): Show | 8 | HG01109.hp2 HG02451.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.198+1354G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 3/6 | chr1 | 167686864 | ||||||
| chr1:167687003
|
G | C | 1 | a0001c0001t0004g0118 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.198+1493G>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 3/6 | chr1 | 167687003 | ||||||
| chr1:167687120
|
G | A | 86 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0025others(83): Show | 86 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.198+1610G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 3/6 | chr1 | 167687120 | ||||||
| chr1:167687139
|
G | A | 1 | a0001c0001t0001g0013 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.198+1629G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 3/6 | chr1 | 167687139 | ||||||
| chr1:167687153
|
A | G | 15 | a0001c0001t0001g0221a0001c0001t0001g0268a0001c0001t0001g0302others(12): Show | 15 | HG01070.hp1 HG01109.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.198+1643A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 3/6 | chr1 | 167687153 | ||||||
| chr1:167687221
|
G | A | 1 | a0001c0001t0001g0050 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.198+1711G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 3/6 | chr1 | 167687221 | ||||||
| chr1:167687378
|
G | GC | 55 | a0001c0001t0001g0221a0001c0001t0001g0241a0001c0001t0001g0268others(52): Show | 55 | HG00438.hp2 HG01070.hp1 HG01074.hp2 others(52): Show |
intron_variant | MODIFIER | c.198+1869dupC | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 167687378 | |||||
| chr1:167687392
|
A | G | 3 | a0001c0001t0001g0013a0001c0001t0001g0050a0001c0001t0002g0205 | 3 | HG02074.hp2 NA18949.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.198+1882A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 3/6 | chr1 | 167687392 | ||||||
| chr1:167687395
|
C | A | 1 | a0001c0001t0001g0038 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.198+1885C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 3/6 | chr1 | 167687395 | ||||||
| chr1:167687477
|
C | A | 11 | a0001c0001t0005g0111a0001c0001t0016g0112a0001c0001t0016g0253others(8): Show | 11 | HG01884.hp2 HG02258.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.198+1967C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 3/6 | chr1 | 167687477 | ||||||
| chr1:167687501
|
T | C | 1 | a0001c0001t0002g0162 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.198+1991T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 3/6 | chr1 | 167687501 | ||||||
| chr1:167687511
|
A | G | 1 | a0001c0001t0012g0277 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.198+2001A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 3/6 | chr1 | 167687511 | ||||||
| chr1:167687522
|
C | CA | 33 | a0001c0001t0001g0014a0001c0001t0001g0131a0001c0001t0001g0221others(30): Show | 33 | HG01081.hp2 HG01884.hp2 HG01978.hp1 others(30): Show |
intron_variant | MODIFIER | c.198+2028dupA | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 167687522 | |||||
| chr1:167687534
|
A | G | 6 | a0001c0001t0001g0268a0001c0001t0015g0052a0001c0001t0015g0239others(3): Show | 6 | HG02451.hp2 HG02723.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.198+2024A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 3/6 | chr1 | 167687534 | ||||||
| chr1:167687539
|
G | A | 3 | a0001c0001t0017g0338a0001c0001t0017g0341a0001c0001t0021g0005 | 3 | HG03209.hp2 HG03471.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.198+2029G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 3/6 | chr1 | 167687539 | ||||||
| chr1:167687700
|
C | T | 1 | a0001c0001t0003g0004 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.198+2190C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 3/6 | chr1 | 167687700 | ||||||
| chr1:167687964
|
T | C | 3 | a0001c0001t0003g0084a0001c0001t0003g0130a0001c0001t0003g0140 | 3 | NA18968.hp1 NA18969.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.199-2085T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 3/6 | chr1 | 167687964 | ||||||
| chr1:167687995
|
C | CTA | 8 | a0001c0001t0001g0268a0001c0001t0015g0052a0001c0001t0015g0239others(5): Show | 8 | HG01109.hp2 HG02451.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.199-2045_199-2044d others(4): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 167687995 | |||||
| chr1:167688126
|
C | T | 4 | a0001c0001t0012g0315a0001c0001t0027g0078a0001c0001t0027g0089others(1): Show | 4 | HG00544.hp1 NA18947.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.199-1923C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 3/6 | chr1 | 167688126 | ||||||
| chr1:167688262
|
G | C | 20 | a0001c0001t0001g0241a0001c0001t0001g0328a0001c0001t0003g0004others(17): Show | 20 | HG01081.hp2 HG02257.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.199-1787G>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 3/6 | chr1 | 167688262 | ||||||
| chr1:167688627
|
A | T | 1 | a0001c0001t0018g0340 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.199-1422A>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 3/6 | chr1 | 167688627 | ||||||
| chr1:167688738
|
A | C | 19 | a0001c0001t0001g0241a0001c0001t0001g0328a0001c0001t0008g0219others(16): Show | 19 | HG01081.hp2 HG02257.hp1 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.199-1311A>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 3/6 | chr1 | 167688738 | ||||||
| chr1:167688969
|
A | G | 55 | a0001c0001t0001g0221a0001c0001t0001g0241a0001c0001t0001g0268others(52): Show | 55 | HG00438.hp2 HG01070.hp1 HG01074.hp2 others(52): Show |
intron_variant | MODIFIER | c.199-1080A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 3/6 | chr1 | 167688969 | ||||||
| chr1:167689002
|
G | A | 1 | a0001c0001t0003g0224 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.199-1047G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 3/6 | chr1 | 167689002 | ||||||
| chr1:167689078
|
A | G | 55 | a0001c0001t0001g0221a0001c0001t0001g0241a0001c0001t0001g0268others(52): Show | 55 | HG00438.hp2 HG01070.hp1 HG01074.hp2 others(52): Show |
intron_variant | MODIFIER | c.199-971A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 3/6 | chr1 | 167689078 | ||||||
| chr1:167689086
|
A | G | 1 | a0001c0001t0007g0036 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.199-963A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 3/6 | chr1 | 167689086 | ||||||
| chr1:167689095
|
G | A | 1 | a0001c0001t0003g0004 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.199-954G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 3/6 | chr1 | 167689095 | ||||||
| chr1:167689225
|
C | T | 2 | a0001c0001t0006g0225a0001c0001t0006g0226 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.199-824C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 3/6 | chr1 | 167689225 | ||||||
| chr1:167689226
|
G | A | 1 | a0001c0001t0008g0310 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.199-823G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 3/6 | chr1 | 167689226 | ||||||
| chr1:167689368
|
G | A | 1 | a0001c0001t0001g0050 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.199-681G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 3/6 | chr1 | 167689368 | ||||||
| chr1:167689413
|
C | T | 1 | a0001c0001t0003g0004 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.199-636C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 3/6 | chr1 | 167689413 | ||||||
| chr1:167689475
|
T | C | 7 | a0001c0001t0001g0268a0001c0001t0003g0004a0001c0001t0015g0052others(4): Show | 7 | HG02451.hp2 HG02723.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.199-574T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 3/6 | chr1 | 167689475 | ||||||
| chr1:167689492
|
A | AAG | 9 | a0001c0001t0011g0042a0001c0001t0011g0043a0001c0001t0011g0067others(6): Show | 9 | HG00438.hp2 HG01074.hp2 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.199-556_199-555ins others(2): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 167689492 | |||||
| chr1:167689493
|
A | G | 35 | a0001c0001t0001g0021a0001c0001t0001g0027a0001c0001t0001g0028others(32): Show | 35 | HG00099.hp1 HG00609.hp1 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.199-556A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 3/6 | chr1 | 167689493 | ||||||
| chr1:167689494
|
A | AG | 26 | a0001c0001t0001g0241a0001c0001t0001g0328a0001c0001t0005g0111others(23): Show | 26 | HG01081.hp2 HG01884.hp2 HG02257.hp1 others(23): Show |
intron_variant | MODIFIER | c.199-555_199-554ins others(1): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 3/6 | chr1 | 167689494 | ||||||
| chr1:167689494
|
A | G | 1 | a0001c0001t0021g0005 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.199-555A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 3/6 | chr1 | 167689494 | ||||||
| chr1:167689567
|
C | T | 1 | a0001c0001t0003g0004 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.199-482C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 3/6 | chr1 | 167689567 | ||||||
| chr1:167690227
|
A | G | 1 | a0001c0001t0003g0004 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.270+107A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167690227 | ||||||
| chr1:167690466
|
G | T | 1 | a0001c0001t0003g0004 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.270+346G>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167690466 | ||||||
| chr1:167690499
|
C | A | 1 | a0001c0001t0002g0195 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.270+379C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167690499 | ||||||
| chr1:167690502
|
T | C | 7 | a0001c0001t0001g0268a0001c0001t0003g0004a0001c0001t0015g0052others(4): Show | 7 | HG02451.hp2 HG02723.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.270+382T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167690502 | ||||||
| chr1:167690525
|
T | C | 9 | a0001c0001t0011g0042a0001c0001t0011g0043a0001c0001t0011g0067others(6): Show | 9 | HG00438.hp2 HG01074.hp2 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.270+405T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167690525 | ||||||
| chr1:167690557
|
C | T | 1 | a0001c0001t0001g0266 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.270+437C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167690557 | ||||||
| chr1:167690573
|
C | A | 5 | a0001c0001t0001g0241a0001c0001t0008g0219a0001c0001t0008g0262others(2): Show | 5 | HG02280.hp2 HG02717.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.270+453C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167690573 | ||||||
| chr1:167690626
|
G | T | 2 | a0001c0003t0026g0218a0001c0003t0026g0303 | 2 | HG01109.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.270+506G>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167690626 | ||||||
| chr1:167690680
|
C | T | 4 | a0001c0001t0005g0237a0001c0001t0023g0227a0001c0001t0023g0259others(1): Show | 4 | HG01070.hp1 HG02109.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.270+560C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167690680 | ||||||
| chr1:167690705
|
G | A | 1 | a0001c0001t0003g0245 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.270+585G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167690705 | ||||||
| chr1:167690736
|
T | TC | 7 | a0001c0001t0001g0268a0001c0001t0003g0004a0001c0001t0015g0052others(4): Show | 7 | HG02451.hp2 HG02723.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.270+616_270+617ins others(1): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167690736 | ||||||
| chr1:167690749
|
C | T | 6 | a0001c0001t0001g0268a0001c0001t0015g0052a0001c0001t0015g0239others(3): Show | 6 | HG02451.hp2 HG02723.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.270+629C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167690749 | ||||||
| chr1:167690812
|
C | G | 8 | a0001c0001t0001g0001a0001c0001t0001g0115a0001c0001t0001g0138others(5): Show | 9 | HG00741.hp2 HG01123.hp2 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.270+692C>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167690812 | ||||||
| chr1:167690850
|
A | G | 7 | a0001c0001t0001g0268a0001c0001t0003g0004a0001c0001t0015g0052others(4): Show | 7 | HG02451.hp2 HG02723.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.270+730A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167690850 | ||||||
| chr1:167690881
|
C | T | 1 | a0001c0001t0001g0260 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.270+761C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167690881 | ||||||
| chr1:167690886
|
A | G | 2 | a0001c0003t0026g0218a0001c0003t0026g0303 | 2 | HG01109.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.270+766A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167690886 | ||||||
| chr1:167690915
|
G | A | 6 | a0001c0001t0001g0268a0001c0001t0015g0052a0001c0001t0015g0239others(3): Show | 6 | HG02451.hp2 HG02723.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.270+795G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167690915 | ||||||
| chr1:167691046
|
T | C | 7 | a0001c0001t0001g0268a0001c0001t0003g0004a0001c0001t0015g0052others(4): Show | 7 | HG02451.hp2 HG02723.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.270+926T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167691046 | ||||||
| chr1:167691262
|
T | C | 9 | a0001c0001t0001g0221a0001c0001t0001g0302a0001c0001t0005g0069others(6): Show | 9 | HG01070.hp1 HG01109.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.270+1142T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167691262 | ||||||
| chr1:167691375
|
C | T | 1 | a0001c0001t0016g0112 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.270+1255C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167691375 | ||||||
| chr1:167691423
|
G | A | 1 | a0001c0001t0001g0113 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.270+1303G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167691423 | ||||||
| chr1:167691490
|
G | A | 1 | a0001c0001t0011g0042 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.270+1370G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167691490 | ||||||
| chr1:167691497
|
T | C | 50 | a0001c0001t0001g0221a0001c0001t0001g0268a0001c0001t0001g0302others(47): Show | 50 | HG00438.hp2 HG01070.hp1 HG01074.hp2 others(47): Show |
intron_variant | MODIFIER | c.270+1377T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167691497 | ||||||
| chr1:167691533
|
G | A | 2 | a0001c0001t0004g0125a0001c0001t0004g0127 | 2 | HG00323.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.270+1413G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167691533 | ||||||
| chr1:167691583
|
G | A | 7 | a0001c0001t0001g0268a0001c0001t0003g0004a0001c0001t0015g0052others(4): Show | 7 | HG02451.hp2 HG02723.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.270+1463G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167691583 | ||||||
| chr1:167691634
|
G | A | 10 | a0001c0001t0011g0042a0001c0001t0011g0043a0001c0001t0011g0067others(7): Show | 10 | HG00438.hp2 HG01074.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.270+1514G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167691634 | ||||||
| chr1:167691654
|
C | G | 7 | a0001c0001t0001g0268a0001c0001t0003g0004a0001c0001t0015g0052others(4): Show | 7 | HG02451.hp2 HG02723.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.270+1534C>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167691654 | ||||||
| chr1:167691698
|
C | T | 7 | a0001c0001t0001g0268a0001c0001t0003g0004a0001c0001t0015g0052others(4): Show | 7 | HG02451.hp2 HG02723.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.270+1578C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167691698 | ||||||
| chr1:167691884
|
G | A | 6 | a0001c0001t0001g0268a0001c0001t0015g0052a0001c0001t0015g0239others(3): Show | 6 | HG02451.hp2 HG02723.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.270+1764G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167691884 | ||||||
| chr1:167691899
|
G | C | 7 | a0001c0001t0001g0268a0001c0001t0003g0004a0001c0001t0015g0052others(4): Show | 7 | HG02451.hp2 HG02723.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.270+1779G>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167691899 | ||||||
| chr1:167691921
|
T | C | 1 | a0001c0001t0003g0026 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.270+1801T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167691921 | ||||||
| chr1:167691922
|
C | T | 1 | a0001c0001t0003g0026 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.270+1802C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167691922 | ||||||
| chr1:167692085
|
CACA | C | 7 | a0001c0001t0001g0268a0001c0001t0003g0004a0001c0001t0015g0052others(4): Show | 7 | HG02451.hp2 HG02723.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.270+1971_270+1973d others(5): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 167692085 | |||||
| chr1:167692223
|
C | T | 1 | a0001c0009t0005g0062 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.271-1876C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167692223 | ||||||
| chr1:167692226
|
C | T | 12 | a0001c0001t0001g0221a0001c0001t0001g0268a0001c0001t0001g0302others(9): Show | 12 | HG00280.hp2 HG01070.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.271-1873C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167692226 | ||||||
| chr1:167692522
|
TA | T | 3 | a0001c0001t0003g0004a0001c0001t0034g0183a0001c0001t0047g0065 | 3 | HG00280.hp2 HG01070.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.271-1576delA | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167692522 | ||||||
| chr1:167692523
|
A | T | 4 | a0001c0001t0001g0221a0001c0001t0001g0268a0001c0001t0001g0302others(1): Show | 4 | HG02145.hp2 HG02451.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-1576A>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167692523 | ||||||
| chr1:167692525
|
T | A | 3 | a0001c0001t0001g0221a0001c0001t0001g0302a0001c0001t0005g0069 | 3 | HG02145.hp2 HG02647.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.271-1574T>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167692525 | ||||||
| chr1:167692533
|
T | A | 12 | a0001c0001t0001g0221a0001c0001t0001g0268a0001c0001t0001g0302others(9): Show | 12 | HG00280.hp2 HG01070.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.271-1566T>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167692533 | ||||||
| chr1:167692615
|
C | A | 6 | a0001c0001t0001g0221a0001c0001t0001g0302a0001c0001t0003g0004others(3): Show | 6 | HG00280.hp2 HG01070.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.271-1484C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167692615 | ||||||
| chr1:167692678
|
A | T | 2 | a0001c0001t0001g0010a0001c0001t0001g0016 | 2 | HG01081.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.271-1421A>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167692678 | ||||||
| chr1:167692680
|
A | G | 12 | a0001c0001t0001g0221a0001c0001t0001g0268a0001c0001t0001g0302others(9): Show | 12 | HG00280.hp2 HG01070.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.271-1419A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167692680 | ||||||
| chr1:167692723
|
C | T | 12 | a0001c0001t0001g0221a0001c0001t0001g0268a0001c0001t0001g0302others(9): Show | 12 | HG00280.hp2 HG01070.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.271-1376C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167692723 | ||||||
| chr1:167692769
|
A | C | 12 | a0001c0001t0001g0221a0001c0001t0001g0268a0001c0001t0001g0302others(9): Show | 12 | HG00280.hp2 HG01070.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.271-1330A>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167692769 | ||||||
| chr1:167692807
|
G | A | 63 | a0001c0001t0001g0260a0001c0001t0001g0320a0001c0001t0003g0006others(60): Show | 63 | HG00099.hp2 HG00423.hp2 HG00735.hp2 others(60): Show |
intron_variant | MODIFIER | c.271-1292G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167692807 | ||||||
| chr1:167692890
|
G | A | 10 | a0001c0001t0011g0042a0001c0001t0011g0043a0001c0001t0011g0067others(7): Show | 10 | HG00438.hp2 HG01074.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.271-1209G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167692890 | ||||||
| chr1:167692956
|
CCAGATA | C | 10 | a0001c0001t0011g0042a0001c0001t0011g0043a0001c0001t0011g0067others(7): Show | 10 | HG00438.hp2 HG01074.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.271-1142_271-1137d others(8): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167692956 | ||||||
| chr1:167693001
|
A | G | 11 | a0001c0001t0001g0221a0001c0001t0001g0302a0001c0001t0003g0004others(8): Show | 11 | HG00280.hp2 HG01070.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.271-1098A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167693001 | ||||||
| chr1:167693049
|
A | G | 20 | a0001c0001t0001g0003a0001c0001t0001g0241a0001c0001t0001g0268others(17): Show | 21 | HG01081.hp2 HG02257.hp1 HG02280.hp2 others(18): Show |
intron_variant | MODIFIER | c.271-1050A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167693049 | ||||||
| chr1:167693151
|
C | T | 8 | a0001c0001t0003g0004a0001c0001t0015g0052a0001c0001t0015g0239others(5): Show | 8 | HG00280.hp2 HG01070.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.271-948C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167693151 | ||||||
| chr1:167693203
|
C | A | 1 | a0001c0001t0001g0001 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.271-896C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167693203 | ||||||
| chr1:167693288
|
G | A | 1 | a0001c0008t0021g0185 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.271-811G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167693288 | ||||||
| chr1:167693298
|
G | A | 5 | a0001c0001t0003g0019a0001c0001t0003g0026a0001c0001t0010g0071others(2): Show | 5 | NA18956.hp1 NA18970.hp1 NA18972.hp1 others(2): Show |
intron_variant | MODIFIER | c.271-801G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167693298 | ||||||
| chr1:167693394
|
G | A | 3 | a0001c0001t0001g0221a0001c0001t0001g0302a0001c0001t0005g0069 | 3 | HG02145.hp2 HG02647.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.271-705G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167693394 | ||||||
| chr1:167693426
|
C | G | 1 | a0001c0010t0001g0012 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.271-673C>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167693426 | ||||||
| chr1:167693491
|
G | A | 1 | a0001c0001t0005g0332 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.271-608G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167693491 | ||||||
| chr1:167693593
|
A | G | 1 | a0001c0001t0001g0070 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.271-506A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167693593 | ||||||
| chr1:167693610
|
T | C | 72 | a0001c0001t0001g0003a0001c0001t0001g0221a0001c0001t0001g0241others(69): Show | 73 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.271-489T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167693610 | ||||||
| chr1:167693657
|
C | T | 10 | a0001c0001t0011g0042a0001c0001t0011g0043a0001c0001t0011g0067others(7): Show | 10 | HG00438.hp2 HG01074.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.271-442C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167693657 | ||||||
| chr1:167693814
|
A | G | 1 | a0001c0003t0026g0218 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.271-285A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167693814 | ||||||
| chr1:167693872
|
TTTTGGAA others(46): Show |
T | 1 | a0006c0012t0011g0234 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.271-225_271-173del others(53): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 167693872 | |||||
| chr1:167693910
|
A | G | 3 | a0001c0001t0003g0004a0001c0001t0034g0183a0001c0001t0047g0065 | 3 | HG00280.hp2 HG01070.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.271-189A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167693910 | ||||||
| chr1:167694355
|
G | A | 3 | a0001c0001t0001g0221a0001c0001t0001g0302a0001c0001t0005g0069 | 3 | HG02145.hp2 HG02647.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.474+53G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 5/6 | chr1 | 167694355 | ||||||
| chr1:167694392
|
A | C | 9 | a0001c0001t0003g0004a0001c0001t0016g0112a0001c0001t0016g0253others(6): Show | 9 | HG00280.hp2 HG01070.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.474+90A>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 5/6 | chr1 | 167694392 | ||||||
| chr1:167694441
|
G | T | 11 | a0001c0001t0011g0042a0001c0001t0011g0043a0001c0001t0011g0067others(8): Show | 11 | HG00408.hp1 HG00438.hp2 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.474+139G>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 5/6 | chr1 | 167694441 | ||||||
| chr1:167694533
|
A | G | 1 | a0001c0001t0014g0314 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.474+231A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 5/6 | chr1 | 167694533 | ||||||
| chr1:167694579
|
T | C | 1 | a0001c0001t0051g0117 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.474+277T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 5/6 | chr1 | 167694579 | ||||||
| chr1:167694645
|
G | T | 9 | a0001c0001t0005g0020a0001c0001t0005g0030a0001c0001t0005g0061others(6): Show | 9 | HG01109.hp2 HG01884.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.474+343G>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 5/6 | chr1 | 167694645 | ||||||
| chr1:167694760
|
C | A | 11 | a0001c0001t0011g0042a0001c0001t0011g0043a0001c0001t0011g0067others(8): Show | 11 | HG00408.hp1 HG00438.hp2 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.474+458C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 5/6 | chr1 | 167694760 | ||||||
| chr1:167694810
|
C | T | 11 | a0001c0001t0011g0042a0001c0001t0011g0043a0001c0001t0011g0067others(8): Show | 11 | HG00408.hp1 HG00438.hp2 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.474+508C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 5/6 | chr1 | 167694810 | ||||||
| chr1:167694877
|
T | C | 1 | a0001c0001t0001g0260 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.474+575T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 5/6 | chr1 | 167694877 | ||||||
| chr1:167694891
|
G | A | 1 | a0001c0001t0005g0326 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.474+589G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 5/6 | chr1 | 167694891 | ||||||
| chr1:167694912
|
G | C | 1 | a0001c0001t0001g0268 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.474+610G>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 5/6 | chr1 | 167694912 | ||||||
| chr1:167695075
|
C | CA | 11 | a0001c0001t0011g0042a0001c0001t0011g0043a0001c0001t0011g0067others(8): Show | 11 | HG00408.hp1 HG00438.hp2 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.474+783dupA | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 167695075 | |||||
| chr1:167695271
|
A | G | 10 | a0001c0001t0011g0042a0001c0001t0011g0043a0001c0001t0011g0067others(7): Show | 10 | HG00438.hp2 HG01074.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.474+969A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 5/6 | chr1 | 167695271 | ||||||
| chr1:167695471
|
G | C | 1 | a0001c0001t0001g0110 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.474+1169G>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 5/6 | chr1 | 167695471 | ||||||
| chr1:167695538
|
A | AT | 11 | a0001c0001t0002g0203a0001c0001t0005g0020a0001c0001t0005g0030others(8): Show | 11 | HG01884.hp1 HG02055.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.474+1254dupT | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 167695538 | |||||
| chr1:167695538
|
A | ATTTTTT | 9 | a0001c0001t0011g0042a0001c0001t0011g0043a0001c0001t0011g0067others(6): Show | 9 | HG00438.hp2 HG01074.hp2 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.474+1249_474+1254d others(8): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 167695538 | |||||
| chr1:167695538
|
AT | A | 182 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(179): Show | 184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.474+1254delT | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 167695538 | |||||
| chr1:167695538
|
ATT | A | 9 | a0001c0001t0001g0221a0001c0001t0001g0302a0001c0001t0004g0126others(6): Show | 9 | HG00323.hp2 HG01433.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.474+1253_474+1254d others(4): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 167695538 | |||||
| chr1:167695674
|
A | G | 43 | a0001c0001t0001g0221a0001c0001t0001g0302a0001c0001t0004g0126others(40): Show | 43 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(40): Show |
intron_variant | MODIFIER | c.474+1372A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 5/6 | chr1 | 167695674 | ||||||
| chr1:167695827
|
T | C | 52 | a0001c0001t0001g0221a0001c0001t0001g0268a0001c0001t0001g0302others(49): Show | 52 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(49): Show |
intron_variant | MODIFIER | c.475-1272T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 5/6 | chr1 | 167695827 | ||||||
| chr1:167696035
|
G | A | 10 | a0001c0001t0005g0020a0001c0001t0005g0030a0001c0001t0005g0061others(7): Show | 10 | HG01109.hp2 HG01884.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.475-1064G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 5/6 | chr1 | 167696035 | ||||||
| chr1:167696090
|
A | G | 69 | a0001c0001t0001g0221a0001c0001t0001g0241a0001c0001t0001g0268others(66): Show | 69 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(66): Show |
intron_variant | MODIFIER | c.475-1009A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 5/6 | chr1 | 167696090 | ||||||
| chr1:167696142
|
C | T | 10 | a0001c0001t0005g0020a0001c0001t0005g0030a0001c0001t0005g0061others(7): Show | 10 | HG01109.hp2 HG01884.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.475-957C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 5/6 | chr1 | 167696142 | ||||||
| chr1:167696162
|
C | T | 10 | a0001c0001t0011g0042a0001c0001t0011g0043a0001c0001t0011g0067others(7): Show | 10 | HG00438.hp2 HG01074.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.475-937C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 5/6 | chr1 | 167696162 | ||||||
| chr1:167696169
|
G | A | 6 | a0001c0001t0001g0152a0001c0001t0001g0272a0001c0001t0002g0163others(3): Show | 6 | HG01255.hp1 HG01257.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.475-930G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 5/6 | chr1 | 167696169 | ||||||
| chr1:167696338
|
CTT | C | 3 | a0001c0001t0018g0330a0001c0001t0018g0339a0001c0001t0018g0340 | 3 | HG01884.hp2 HG03130.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.475-760_475-759del others(2): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 5/6 | chr1 | 167696338 | ||||||
| chr1:167696455
|
C | CT | 21 | a0001c0001t0001g0241a0001c0001t0008g0219a0001c0001t0008g0262others(18): Show | 21 | HG01884.hp2 HG01891.hp1 HG02258.hp2 others(18): Show |
intron_variant | MODIFIER | c.475-630dupT | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 167696455 | |||||
| chr1:167696489
|
C | T | 21 | a0001c0001t0005g0020a0001c0001t0005g0030a0001c0001t0005g0061others(18): Show | 21 | HG00408.hp1 HG00438.hp2 HG01074.hp2 others(18): Show |
intron_variant | MODIFIER | c.475-610C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 5/6 | chr1 | 167696489 | ||||||
| chr1:167696747
|
C | T | 3 | a0001c0001t0001g0221a0001c0001t0001g0302a0001c0001t0005g0069 | 3 | HG02145.hp2 HG02647.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.475-352C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 5/6 | chr1 | 167696747 | ||||||
| chr1:167696759
|
T | C | 1 | a0001c0009t0005g0062 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.475-340T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 5/6 | chr1 | 167696759 | ||||||
| chr1:167696797
|
C | T | 10 | a0001c0001t0005g0020a0001c0001t0005g0030a0001c0001t0005g0061others(7): Show | 10 | HG01109.hp2 HG01884.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.475-302C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 5/6 | chr1 | 167696797 | ||||||
| chr1:167696798
|
G | A | 15 | a0001c0001t0001g0221a0001c0001t0001g0268a0001c0001t0001g0302others(12): Show | 15 | HG01884.hp2 HG02145.hp2 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.475-301G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 5/6 | chr1 | 167696798 | ||||||
| chr1:167696935
|
T | C | 21 | a0001c0001t0005g0020a0001c0001t0005g0030a0001c0001t0005g0061others(18): Show | 21 | HG00408.hp1 HG00438.hp2 HG01074.hp2 others(18): Show |
intron_variant | MODIFIER | c.475-164T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 5/6 | chr1 | 167696935 | ||||||
| chr1:167696981
|
C | T | 20 | a0001c0001t0005g0020a0001c0001t0005g0030a0001c0001t0005g0061others(17): Show | 20 | HG00438.hp2 HG01074.hp2 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.475-118C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 5/6 | chr1 | 167696981 | ||||||
| chr1:167697079
|
T | C | 10 | a0001c0001t0011g0042a0001c0001t0011g0043a0001c0001t0011g0067others(7): Show | 10 | HG00438.hp2 HG01074.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.475-20T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 5/6 | chr1 | 167697079 | ||||||
| chr1:167697875
|
CA | C | 3 | a0001c0001t0001g0002a0001c0001t0001g0031a0001c0001t0001g0059 | 4 | HG03491.hp1 HG03492.hp2 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.1218+34delA | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167697875 | ||||||
| chr1:167697917
|
C | T | 4 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0129others(1): Show | 4 | HG00642.hp1 HG01081.hp1 HG01099.hp1 others(1): Show |
intron_variant | MODIFIER | c.1218+75C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167697917 | ||||||
| chr1:167697925
|
C | T | 1 | a0001c0001t0001g0106 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1218+83C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167697925 | ||||||
| chr1:167697954
|
A | G | 19 | a0001c0001t0001g0241a0001c0001t0001g0328a0001c0001t0008g0219others(16): Show | 19 | HG01081.hp2 HG01884.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.1218+112A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167697954 | ||||||
| chr1:167697969
|
T | C | 4 | a0001c0001t0001g0328a0001c0001t0022g0242a0001c0001t0022g0342others(1): Show | 4 | HG01081.hp2 HG02486.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1218+127T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167697969 | ||||||
| chr1:167697985
|
C | G | 1 | a0001c0001t0011g0042 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1218+143C>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167697985 | ||||||
| chr1:167698113
|
C | T | 18 | a0001c0001t0011g0042a0001c0001t0011g0043a0001c0001t0011g0067others(15): Show | 18 | HG00408.hp1 HG00438.hp2 HG01074.hp2 others(15): Show |
intron_variant | MODIFIER | c.1218+271C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167698113 | ||||||
| chr1:167698121
|
G | A | 9 | a0001c0001t0001g0131a0001c0001t0001g0278a0001c0001t0001g0298others(6): Show | 9 | HG00673.hp2 HG02015.hp1 HG02293.hp1 others(6): Show |
intron_variant | MODIFIER | c.1218+279G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167698121 | ||||||
| chr1:167698142
|
C | A | 1 | a0001c0001t0051g0117 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1218+300C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167698142 | ||||||
| chr1:167698156
|
T | C | 11 | a0001c0001t0001g0003a0001c0001t0001g0279a0001c0001t0001g0281others(8): Show | 12 | HG02055.hp2 HG02109.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1218+314T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167698156 | ||||||
| chr1:167698167
|
T | G | 10 | a0001c0001t0011g0042a0001c0001t0011g0043a0001c0001t0011g0067others(7): Show | 10 | HG00438.hp2 HG01074.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.1218+325T>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167698167 | ||||||
| chr1:167698226
|
G | T | 1 | a0001c0008t0021g0185 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1218+384G>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167698226 | ||||||
| chr1:167698271
|
C | G | 54 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0027others(51): Show | 55 | HG00099.hp1 HG00323.hp1 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.1218+429C>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167698271 | ||||||
| chr1:167698303
|
G | A | 13 | a0001c0001t0001g0221a0001c0001t0001g0302a0001c0001t0005g0069others(10): Show | 13 | HG00438.hp2 HG01074.hp2 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.1218+461G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167698303 | ||||||
| chr1:167698383
|
C | T | 78 | a0001c0001t0001g0003a0001c0001t0001g0221a0001c0001t0001g0241others(75): Show | 79 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.1218+541C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167698383 | ||||||
| chr1:167698502
|
C | T | 12 | a0001c0001t0001g0294a0001c0001t0004g0095a0001c0001t0011g0042others(9): Show | 12 | HG00438.hp2 HG01074.hp2 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.1218+660C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167698502 | ||||||
| chr1:167698557
|
T | C | 2 | a0001c0001t0042g0215a0001c0001t0051g0117 | 2 | HG00408.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.1218+715T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167698557 | ||||||
| chr1:167698608
|
CCTAT | C | 3 | a0001c0001t0018g0330a0001c0001t0018g0339a0001c0001t0018g0340 | 3 | HG01884.hp2 HG03130.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1218+771_1218+774d others(6): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 167698608 | |||||
| chr1:167698666
|
T | C | 2 | a0001c0001t0042g0215a0001c0001t0051g0117 | 2 | HG00408.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.1218+824T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167698666 | ||||||
| chr1:167698690
|
C | A | 11 | a0001c0001t0001g0046a0001c0001t0001g0050a0001c0001t0001g0307others(8): Show | 11 | HG01496.hp1 HG02083.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.1218+848C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167698690 | ||||||
| chr1:167698772
|
G | T | 76 | a0001c0001t0001g0003a0001c0001t0001g0221a0001c0001t0001g0241others(73): Show | 77 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.1218+930G>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167698772 | ||||||
| chr1:167698807
|
G | GT | 10 | a0001c0001t0016g0112a0001c0001t0016g0253a0001c0001t0016g0327others(7): Show | 10 | HG00280.hp2 HG01070.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1218+970dupT | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 167698807 | |||||
| chr1:167698807
|
G | GTT | 10 | a0001c0001t0011g0042a0001c0001t0011g0043a0001c0001t0011g0067others(7): Show | 10 | HG00438.hp2 HG01074.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.1218+969_1218+970d others(4): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 167698807 | |||||
| chr1:167698813
|
G | T | 294 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(291): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.1218+971G>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167698813 | ||||||
| chr1:167698853
|
G | T | 305 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(302): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.1218+1011G>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167698853 | ||||||
| chr1:167698862
|
G | C | 305 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(302): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.1218+1020G>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167698862 | ||||||
| chr1:167698997
|
A | C | 2 | a0001c0001t0034g0183a0001c0001t0047g0065 | 2 | HG00280.hp2 HG01070.hp1 |
intron_variant | MODIFIER | c.1218+1155A>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167698997 | ||||||
| chr1:167699000
|
G | A | 12 | a0001c0001t0011g0042a0001c0001t0011g0043a0001c0001t0011g0067others(9): Show | 12 | HG00280.hp2 HG00438.hp2 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.1218+1158G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167699000 | ||||||
| chr1:167699094
|
G | C | 2 | a0001c0001t0003g0283a0001c0001t0003g0284 | 2 | NA18939.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.1218+1252G>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167699094 | ||||||
| chr1:167699126
|
C | CT | 25 | a0001c0001t0001g0003a0001c0001t0001g0241a0001c0001t0001g0279others(22): Show | 26 | HG01081.hp2 HG01891.hp1 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.1218+1292dupT | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 167699126 | |||||
| chr1:167699182
|
G | T | 10 | a0001c0001t0011g0042a0001c0001t0011g0043a0001c0001t0011g0067others(7): Show | 10 | HG00438.hp2 HG01074.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.1218+1340G>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167699182 | ||||||
| chr1:167699185
|
T | C | 1 | a0001c0001t0003g0230 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1218+1343T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167699185 | ||||||
| chr1:167699517
|
C | T | 2 | a0001c0001t0034g0183a0001c0001t0047g0065 | 2 | HG00280.hp2 HG01070.hp1 |
intron_variant | MODIFIER | c.1218+1675C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167699517 | ||||||
| chr1:167699545
|
T | C | 1 | a0001c0001t0003g0267 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1218+1703T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167699545 | ||||||
| chr1:167699639
|
T | C | 3 | a0001c0001t0018g0330a0001c0001t0018g0339a0001c0001t0018g0340 | 3 | HG01884.hp2 HG03130.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1218+1797T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167699639 | ||||||
| chr1:167699711
|
C | T | 10 | a0001c0001t0001g0268a0001c0001t0005g0020a0001c0001t0005g0030others(7): Show | 10 | HG01109.hp2 HG01884.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.1218+1869C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167699711 | ||||||
| chr1:167699792
|
C | T | 1 | a0001c0001t0046g0058 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1218+1950C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167699792 | ||||||
| chr1:167699907
|
G | A | 1 | a0001c0001t0009g0213 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1218+2065G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167699907 | ||||||
| chr1:167700020
|
T | A | 16 | a0001c0001t0001g0241a0001c0001t0008g0219a0001c0001t0008g0262others(13): Show | 16 | HG01081.hp2 HG01891.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.1218+2178T>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167700020 | ||||||
| chr1:167700077
|
T | A | 1 | a0001c0001t0001g0221 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1218+2235T>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167700077 | ||||||
| chr1:167700139
|
A | G | 1 | a0001c0001t0047g0065 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1218+2297A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167700139 | ||||||
| chr1:167700250
|
C | T | 308 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(305): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.1218+2408C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167700250 | ||||||
| chr1:167700419
|
C | T | 2 | a0001c0001t0013g0200a0001c0001t0013g0204 | 2 | NA18983.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.1218+2577C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167700419 | ||||||
| chr1:167700420
|
G | T | 2 | a0003c0004t0025g0034a0003c0004t0025g0240 | 2 | HG02280.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1218+2578G>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167700420 | ||||||
| chr1:167700608
|
G | A | 2 | a0003c0004t0025g0034a0003c0004t0025g0240 | 2 | HG02280.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1218+2766G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167700608 | ||||||
| chr1:167700650
|
C | CA | 13 | a0001c0001t0001g0023a0001c0001t0001g0046a0001c0001t0001g0216others(10): Show | 13 | HG00741.hp1 HG01884.hp1 HG01934.hp1 others(10): Show |
intron_variant | MODIFIER | c.1218+2823dupA | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 167700650 | |||||
| chr1:167700698
|
A | G | 1 | a0001c0001t0001g0266 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1218+2856A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167700698 | ||||||
| chr1:167700859
|
G | A | 1 | a0001c0001t0001g0323 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1218+3017G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167700859 | ||||||
| chr1:167700914
|
C | A | 3 | a0001c0001t0003g0135a0001c0001t0007g0142a0001c0001t0048g0102 | 3 | HG03927.hp1 NA18959.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.1218+3072C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167700914 | ||||||
| chr1:167701165
|
C | T | 1 | a0001c0001t0001g0268 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1218+3323C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167701165 | ||||||
| chr1:167701192
|
C | T | 1 | a0001c0001t0003g0224 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1218+3350C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167701192 | ||||||
| chr1:167701202
|
C | T | 81 | a0001c0001t0001g0221a0001c0001t0001g0302a0001c0001t0003g0004others(78): Show | 81 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.1218+3360C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167701202 | ||||||
| chr1:167701230
|
C | T | 55 | a0001c0001t0003g0004a0001c0001t0003g0006a0001c0001t0003g0007others(52): Show | 55 | HG00099.hp2 HG00423.hp2 HG00735.hp2 others(52): Show |
intron_variant | MODIFIER | c.1218+3388C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167701230 | ||||||
| chr1:167701252
|
G | GTTTC | 48 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0035others(45): Show | 48 | HG00609.hp2 HG00639.hp1 HG00673.hp1 others(45): Show |
intron_variant | MODIFIER | c.1219-3348_1219-334 others(8): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 167701252 | |||||
| chr1:167701252
|
G | GTTTCTTT others(1): Show |
63 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0028others(60): Show | 64 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(61): Show |
intron_variant | MODIFIER | c.1219-3352_1219-334 others(12): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 167701252 | |||||
| chr1:167701252
|
G | GTTTCTTT others(5): Show |
24 | a0001c0001t0001g0029a0001c0001t0001g0051a0001c0001t0001g0054others(21): Show | 24 | HG00642.hp2 HG01070.hp1 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.1219-3356_1219-334 others(16): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 167701252 | |||||
| chr1:167701252
|
G | GTTTCTTT others(9): Show |
21 | a0001c0001t0001g0103a0001c0001t0001g0114a0001c0001t0001g0160others(18): Show | 21 | HG00639.hp2 HG02083.hp1 HG02148.hp1 others(18): Show |
intron_variant | MODIFIER | c.1219-3360_1219-334 others(20): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 167701252 | |||||
| chr1:167701252
|
G | GTTTCTTT others(13): Show |
16 | a0001c0001t0001g0186a0001c0001t0001g0254a0001c0001t0002g0145others(13): Show | 16 | HG00280.hp2 HG01516.hp1 HG01516.hp2 others(13): Show |
intron_variant | MODIFIER | c.1219-3364_1219-334 others(24): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 167701252 | |||||
| chr1:167701252
|
G | GTTTCTTT others(17): Show |
3 | a0001c0001t0003g0018a0001c0001t0003g0039a0001c0001t0003g0060 | 3 | HG02004.hp2 HG02698.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.1219-3368_1219-334 others(28): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 167701252 | |||||
| chr1:167701252
|
G | GTTTCTTT others(21): Show |
6 | a0001c0001t0003g0011a0001c0001t0003g0041a0001c0001t0003g0214others(3): Show | 6 | HG00741.hp1 HG01981.hp2 HG02293.hp2 others(3): Show |
intron_variant | MODIFIER | c.1219-3372_1219-334 others(32): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 167701252 | |||||
| chr1:167701252
|
G | GTTTCTTT others(25): Show |
1 | a0001c0001t0006g0257 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1219-3376_1219-334 others(36): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 167701252 | |||||
| chr1:167701252
|
G | GTTTCTTT others(29): Show |
2 | a0001c0001t0019g0099a0001c0001t0033g0180 | 2 | HG01255.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.1219-3380_1219-334 others(40): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 167701252 | |||||
| chr1:167701252
|
G | GTTTCTTT others(41): Show |
1 | a0001c0001t0003g0230 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1219-3392_1219-334 others(52): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 167701252 | |||||
| chr1:167701252
|
G | GTTTCTTT others(57): Show |
1 | a0001c0001t0003g0255 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1219-3408_1219-334 others(68): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 167701252 | |||||
| chr1:167701252
|
G | GTTTGTTT others(5): Show |
1 | a0001c0001t0014g0314 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1219-3409_1219-340 others(16): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 167701252 | |||||
| chr1:167701252
|
G | GTTTGTTT others(9): Show |
2 | a0001c0001t0011g0067a0001c0001t0011g0100 | 2 | HG01243.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.1219-3409_1219-340 others(20): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 167701252 | |||||
| chr1:167701252
|
G | GTTTGTTT others(13): Show |
2 | a0001c0001t0014g0177a0001c0001t0014g0202 | 2 | NA18979.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.1219-3409_1219-340 others(24): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 167701252 | |||||
| chr1:167701252
|
G | GTTTGTTT others(21): Show |
1 | a0001c0001t0011g0274 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1219-3409_1219-340 others(32): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 167701252 | |||||
| chr1:167701252
|
GTTTC | G | 26 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0038others(23): Show | 26 | HG00323.hp1 HG00558.hp2 HG00621.hp2 others(23): Show |
intron_variant | MODIFIER | c.1219-3348_1219-334 others(8): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 167701252 | |||||
| chr1:167701252
|
GTTTCTTT others(1): Show |
G | 15 | a0001c0001t0001g0003a0001c0001t0001g0222a0001c0001t0001g0229others(12): Show | 16 | HG01109.hp2 HG02109.hp2 HG02165.hp2 others(13): Show |
intron_variant | MODIFIER | c.1219-3352_1219-334 others(12): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 167701252 | |||||
| chr1:167701252
|
GTTTCTTT others(5): Show |
G | 5 | a0001c0001t0001g0033a0001c0001t0001g0268a0001c0001t0005g0237others(2): Show | 5 | HG02109.hp1 HG02451.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1219-3356_1219-334 others(16): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 167701252 | |||||
| chr1:167701252
|
GTTTCTTT others(9): Show |
G | 3 | a0001c0001t0001g0241a0001c0001t0001g0261a0001c0008t0021g0185 | 3 | HG02280.hp2 HG02976.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1219-3360_1219-334 others(20): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 167701252 | |||||
| chr1:167701252
|
GTTTCTTT others(13): Show |
G | 5 | a0001c0001t0016g0112a0001c0001t0016g0253a0001c0001t0016g0327others(2): Show | 5 | HG02258.hp2 HG02922.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1219-3364_1219-334 others(24): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 167701252 | |||||
| chr1:167701252
|
GTTTCTTT others(29): Show |
G | 1 | a0001c0001t0005g0332 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1219-3380_1219-334 others(40): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 167701252 | |||||
| chr1:167701256
|
C | G | 2 | a0001c0001t0011g0042a0001c0001t0011g0043 | 2 | HG00438.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.1219-3408C>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167701256 | ||||||
| chr1:167701277
|
T | TTTCTTTC others(60): Show |
1 | a0001c0001t0019g0093 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1219-3345_1219-334 others(71): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 167701277 | |||||
| chr1:167701312
|
C | CTTTCTTT others(5): Show |
1 | a0001c0001t0013g0148 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1219-3345_1219-334 others(16): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 167701312 | |||||
| chr1:167701316
|
CTTTT | C | 4 | a0001c0001t0003g0019a0001c0001t0003g0026a0001c0001t0003g0345others(1): Show | 4 | HG01515.hp1 HG03239.hp2 NA18972.hp1 others(1): Show |
intron_variant | MODIFIER | c.1219-3343_1219-334 others(8): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 167701316 | |||||
| chr1:167701317
|
T | TTTCTTTC | 4 | a0001c0001t0001g0216a0001c0001t0008g0329a0001c0001t0020g0301others(1): Show | 4 | HG01243.hp1 HG02622.hp1 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.1219-3345_1219-334 others(11): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 167701317 | |||||
| chr1:167701317
|
T | TTTCTTTC others(4): Show |
4 | a0001c0001t0002g0165a0001c0001t0002g0168a0001c0001t0002g0196others(1): Show | 4 | HG02004.hp1 HG02056.hp1 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.1219-3345_1219-334 others(15): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 167701317 | |||||
| chr1:167701317
|
T | TTTCTTTC others(8): Show |
2 | a0001c0001t0002g0209a0001c0001t0049g0211 | 2 | HG00140.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.1219-3345_1219-334 others(19): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 167701317 | |||||
| chr1:167701317
|
T | TTTCTTTC others(32): Show |
1 | a0001c0001t0048g0102 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1219-3345_1219-334 others(43): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 167701317 | |||||
| chr1:167701318
|
T | TTCTTTCT others(3): Show |
1 | a0001c0001t0001g0055 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1219-3345_1219-334 others(14): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 167701318 | |||||
| chr1:167701319
|
T | TCTTTC | 3 | a0001c0001t0001g0025a0001c0001t0005g0020a0001c0001t0037g0325 | 3 | HG02055.hp1 HG02083.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.1219-3345_1219-334 others(9): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167701319 | ||||||
| chr1:167701320
|
T | C | 76 | a0001c0001t0001g0221a0001c0001t0001g0302a0001c0001t0003g0004others(73): Show | 76 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.1219-3344T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167701320 | ||||||
| chr1:167701321
|
T | C | 2 | a0001c0001t0048g0102a0001c0001t0049g0211 | 2 | NA18961.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.1219-3343T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167701321 | ||||||
| chr1:167701332
|
G | A | 5 | a0001c0001t0015g0052a0001c0001t0015g0239a0001c0001t0015g0304others(2): Show | 5 | HG02723.hp1 HG02723.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1219-3332G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167701332 | ||||||
| chr1:167701721
|
C | T | 2 | a0001c0001t0001g0268a0001c0001t0001g0328 | 2 | HG02451.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1219-2943C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167701721 | ||||||
| chr1:167701808
|
G | A | 1 | a0001c0001t0006g0223 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1219-2856G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167701808 | ||||||
| chr1:167701921
|
C | G | 10 | a0001c0001t0011g0042a0001c0001t0011g0043a0001c0001t0011g0067others(7): Show | 10 | HG00438.hp2 HG01074.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.1219-2743C>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167701921 | ||||||
| chr1:167702146
|
C | T | 1 | a0001c0001t0041g0311 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1219-2518C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167702146 | ||||||
| chr1:167702205
|
G | A | 95 | a0001c0001t0001g0221a0001c0001t0001g0302a0001c0001t0003g0004others(92): Show | 95 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.1219-2459G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167702205 | ||||||
| chr1:167702219
|
G | A | 55 | a0001c0001t0003g0004a0001c0001t0003g0006a0001c0001t0003g0007others(52): Show | 55 | HG00099.hp2 HG00423.hp2 HG00735.hp2 others(52): Show |
intron_variant | MODIFIER | c.1219-2445G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167702219 | ||||||
| chr1:167702226
|
G | A | 1 | a0001c0001t0041g0311 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1219-2438G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167702226 | ||||||
| chr1:167702236
|
A | G | 8 | a0001c0001t0016g0112a0001c0001t0016g0253a0001c0001t0016g0327others(5): Show | 8 | HG02258.hp2 HG02922.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.1219-2428A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167702236 | ||||||
| chr1:167702272
|
C | T | 2 | a0001c0001t0042g0215a0001c0001t0051g0117 | 2 | HG00408.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.1219-2392C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167702272 | ||||||
| chr1:167702505
|
G | A | 1 | a0001c0001t0001g0025 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1219-2159G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167702505 | ||||||
| chr1:167702595
|
A | G | 1 | a0001c0001t0041g0311 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1219-2069A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167702595 | ||||||
| chr1:167702632
|
A | G | 1 | a0001c0001t0001g0082 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1219-2032A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167702632 | ||||||
| chr1:167702693
|
C | T | 1 | a0001c0001t0003g0133 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1219-1971C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167702693 | ||||||
| chr1:167702694
|
G | A | 14 | a0001c0001t0001g0221a0001c0001t0001g0302a0001c0001t0006g0098others(11): Show | 14 | HG01255.hp2 HG01433.hp2 HG01928.hp2 others(11): Show |
intron_variant | MODIFIER | c.1219-1970G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167702694 | ||||||
| chr1:167702781
|
A | C | 14 | a0001c0001t0001g0221a0001c0001t0001g0302a0001c0001t0006g0098others(11): Show | 14 | HG01255.hp2 HG01433.hp2 HG01928.hp2 others(11): Show |
intron_variant | MODIFIER | c.1219-1883A>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167702781 | ||||||
| chr1:167702786
|
AATAAATA others(1): Show |
A | 17 | a0001c0001t0001g0221a0001c0001t0001g0302a0001c0001t0006g0098others(14): Show | 17 | HG01255.hp2 HG01433.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.1219-1854_1219-184 others(12): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 167702786 | |||||
| chr1:167702826
|
T | C | 2 | a0001c0001t0004g0088a0001c0001t0004g0120 | 2 | HG00673.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.1219-1838T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167702826 | ||||||
| chr1:167702997
|
C | T | 1 | a0001c0001t0001g0051 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1219-1667C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167702997 | ||||||
| chr1:167703013
|
G | A | 1 | a0001c0001t0001g0299 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1219-1651G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167703013 | ||||||
| chr1:167703015
|
T | A | 1 | a0001c0001t0001g0299 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1219-1649T>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167703015 | ||||||
| chr1:167703115
|
G | A | 4 | a0001c0001t0021g0005a0001c0008t0021g0185a0003c0004t0025g0034others(1): Show | 4 | HG02280.hp1 HG02976.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1219-1549G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167703115 | ||||||
| chr1:167703262
|
C | T | 1 | a0001c0001t0007g0192 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1219-1402C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167703262 | ||||||
| chr1:167703547
|
C | T | 2 | a0001c0001t0021g0005a0001c0008t0021g0185 | 2 | HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1219-1117C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167703547 | ||||||
| chr1:167703572
|
C | T | 81 | a0001c0001t0001g0221a0001c0001t0001g0302a0001c0001t0003g0004others(78): Show | 81 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.1219-1092C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167703572 | ||||||
| chr1:167703604
|
A | G | 2 | a0001c0001t0002g0193a0001c0001t0002g0194 | 2 | NA18951.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.1219-1060A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167703604 | ||||||
| chr1:167703615
|
G | A | 2 | a0001c0001t0003g0041a0001c0001t0003g0053 | 2 | HG02293.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1219-1049G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167703615 | ||||||
| chr1:167703650
|
G | A | 1 | a0001c0001t0001g0265 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1219-1014G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167703650 | ||||||
| chr1:167703732
|
A | G | 57 | a0001c0001t0003g0004a0001c0001t0003g0006a0001c0001t0003g0007others(54): Show | 57 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(54): Show |
intron_variant | MODIFIER | c.1219-932A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167703732 | ||||||
| chr1:167703956
|
C | T | 1 | a0001c0001t0001g0287 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1219-708C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167703956 | ||||||
| chr1:167704027
|
A | G | 2 | a0001c0001t0001g0268a0001c0001t0001g0328 | 2 | HG02451.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1219-637A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167704027 | ||||||
| chr1:167704045
|
C | T | 6 | a0001c0001t0021g0005a0001c0001t0042g0215a0001c0001t0051g0117others(3): Show | 6 | HG00408.hp1 HG02280.hp1 HG02602.hp2 others(3): Show |
intron_variant | MODIFIER | c.1219-619C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167704045 | ||||||
| chr1:167704046
|
A | G | 2 | a0001c0001t0001g0038a0001c0001t0001g0222 | 2 | HG03688.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.1219-618A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167704046 | ||||||
| chr1:167704075
|
C | A | 3 | a0001c0001t0018g0330a0001c0001t0018g0339a0001c0001t0018g0340 | 3 | HG01884.hp2 HG03130.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1219-589C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167704075 | ||||||
| chr1:167704079
|
G | A | 1 | a0001c0001t0051g0117 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1219-585G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167704079 | ||||||
| chr1:167704205
|
C | T | 1 | a0001c0001t0001g0263 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1219-459C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167704205 | ||||||
| chr1:167704232
|
G | A | 8 | a0001c0001t0009g0128a0001c0001t0009g0213a0001c0001t0009g0290others(5): Show | 8 | HG02257.hp1 HG02451.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1219-432G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167704232 | ||||||
| chr1:167704309
|
A | AG | 79 | a0001c0001t0003g0004a0001c0001t0003g0006a0001c0001t0003g0007others(76): Show | 79 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.1219-352dupG | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 167704309 | |||||
| chr1:167704318
|
A | G | 79 | a0001c0001t0003g0004a0001c0001t0003g0006a0001c0001t0003g0007others(76): Show | 79 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.1219-346A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167704318 | ||||||
| chr1:167704426
|
T | C | 8 | a0001c0001t0015g0052a0001c0001t0015g0239a0001c0001t0015g0304others(5): Show | 8 | HG01884.hp2 HG02723.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1219-238T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167704426 | ||||||
| chr1:167704458
|
A | C | 79 | a0001c0001t0003g0004a0001c0001t0003g0006a0001c0001t0003g0007others(76): Show | 79 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.1219-206A>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167704458 | ||||||
| chr1:167704491
|
A | G | 1 | a0001c0001t0002g0045 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1219-173A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167704491 | ||||||
| chr1:167704501
|
T | TA | 79 | a0001c0001t0003g0004a0001c0001t0003g0006a0001c0001t0003g0007others(76): Show | 79 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.1219-155dupA | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 167704501 | |||||
| chr1:167704616
|
G | T | 11 | a0001c0001t0008g0219a0001c0001t0008g0262a0001c0001t0008g0300others(8): Show | 11 | HG01081.hp2 HG01891.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1219-48G>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167704616 | ||||||
| chr1:167704627
|
C | T | 1 | a0001c0001t0003g0053 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1219-37C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167704627 | ||||||
| chr1:167704644
|
C | A | 1 | a0001c0001t0001g0275 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1219-20C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167704644 |