| geneid | 10558 |
|---|---|
| ensemblid | ENSG00000090054.16 |
| hgncid | 11277 |
| symbol | SPTLC1 |
| name | serine palmitoyltransferase long chain base subunit 1 |
| refseq_nuc | NM_006415.4 |
| refseq_prot | NP_006406.1 |
| ensembl_nuc | ENST00000262554.7 |
| ensembl_prot | ENSP00000262554.2 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 92031147 |
| end | 92115413 |
| strand | - |
| ver | v1.2 |
| region | chr9:92031147-92115413 |
| region5000 | chr9:92026147-92120413 |
| regionname0 | SPTLC1_chr9_92031147_92115413 |
| regionname5000 | SPTLC1_chr9_92026147_92120413 |
| 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 | 473 | 356 | 81 | 62 | 167 | 12 | 32 | 126 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | copy fasta | chr9 | 92026147 | 92120413 |
| a0002 | 0/0 | 473 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | copy fasta | chr9 | 92026147 | 92120413 |
| a0003 | 0/0 | 473 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | copy fasta | chr9 | 92026147 | 92120413 |
| 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 | 1422 | 352 | 81 | 60 | 167 | 12 | 30 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | copy fasta | chr9 | 92026147 | 92120413 |
| c0002 | 0/0 | 1422 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | copy fasta | chr9 | 92026147 | 92120413 |
| c0003 | 0/0 | 1422 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | copy fasta | chr9 | 92026147 | 92120413 |
| c0004 | 0/0 | 1422 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | copy fasta | chr9 | 92026147 | 92120413 |
| c0005 | 0/0 | 1422 | 1 | 0 | 0 | 0 | 0 | 1 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | copy fasta | chr9 | 92026147 | 92120413 |
| c0006 | 0/0 | 1422 | 1 | 0 | 0 | 0 | 0 | 1 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | copy fasta | chr9 | 92026147 | 92120413 |
| c0007 | 0/0 | 1422 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | copy fasta | chr9 | 92026147 | 92120413 |
| 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 | 1/1 | 1362 | 301 | 48 | 52 | 160 | 9 | 30 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | copy fasta | chr9 | 92026147 | 92120413 |
| t0002 | 0/0 | 1362 | 35 | 22 | 5 | 8 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | copy fasta | chr9 | 92026147 | 92120413 |
| t0003 | 0/0 | 1362 | 8 | 2 | 2 | 0 | 3 | 1 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | copy fasta | chr9 | 92026147 | 92120413 |
| t0004 | 0/0 | 1362 | 3 | 3 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | copy fasta | chr9 | 92026147 | 92120413 |
| t0005 | 0/0 | 1362 | 2 | 2 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | copy fasta | chr9 | 92026147 | 92120413 |
| t0006 | 0/0 | 1362 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | copy fasta | chr9 | 92026147 | 92120413 |
| t0007 | 0/0 | 1362 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | copy fasta | chr9 | 92026147 | 92120413 |
| t0008 | 0/0 | 1362 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | copy fasta | chr9 | 92026147 | 92120413 |
| t0009 | 0/0 | 1362 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | copy fasta | chr9 | 92026147 | 92120413 |
| t0010 | 0/0 | 1362 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | copy fasta | chr9 | 92026147 | 92120413 |
| t0011 | 0/0 | 1362 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | copy fasta | chr9 | 92026147 | 92120413 |
| t0012 | 0/0 | 1362 | 1 | 0 | 0 | 0 | 0 | 1 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | copy fasta | chr9 | 92026147 | 92120413 |
| t0013 | 0/0 | 1362 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | copy fasta | chr9 | 92026147 | 92120413 |
| t0014 | 0/0 | 1362 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | copy fasta | chr9 | 92026147 | 92120413 |
| 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 | 5 | 0 | 1 | 4 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0002 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0003 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0007 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0018 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0019 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0020 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0022 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0216 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0294 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0295 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0326 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| 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 | 1422 | 352 | 81 | 60 | 167 | 12 | 30 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | copy fasta | chr9 | 92026147 | 92120413 |
| a0001c0002 | 0/0 | 1422 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | copy fasta | chr9 | 92026147 | 92120413 |
| a0001c0004 | 0/0 | 1422 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | copy fasta | chr9 | 92026147 | 92120413 |
| a0001c0005 | 0/0 | 1422 | 1 | 0 | 0 | 0 | 0 | 1 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | copy fasta | chr9 | 92026147 | 92120413 |
| a0001c0006 | 0/0 | 1422 | 1 | 0 | 0 | 0 | 0 | 1 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | copy fasta | chr9 | 92026147 | 92120413 |
| a0002c0003 | 0/0 | 1422 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | copy fasta | chr9 | 92026147 | 92120413 |
| a0003c0007 | 0/0 | 1422 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | copy fasta | chr9 | 92026147 | 92120413 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2783 | 297 | 48 | 51 | 159 | 9 | 28 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | copy fasta | chr9 | 92026147 | 92120413 |
| a0001c0001t0002 | 0/0 | 2783 | 34 | 22 | 4 | 8 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | copy fasta | chr9 | 92026147 | 92120413 |
| a0001c0001t0003 | 0/0 | 2783 | 7 | 1 | 2 | 0 | 3 | 1 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | copy fasta | chr9 | 92026147 | 92120413 |
| a0001c0001t0004 | 0/0 | 2783 | 3 | 3 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | copy fasta | chr9 | 92026147 | 92120413 |
| a0001c0001t0005 | 0/0 | 2783 | 2 | 2 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | copy fasta | chr9 | 92026147 | 92120413 |
| a0001c0001t0006 | 0/0 | 2783 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | copy fasta | chr9 | 92026147 | 92120413 |
| a0001c0001t0007 | 0/0 | 2783 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | copy fasta | chr9 | 92026147 | 92120413 |
| a0001c0001t0008 | 0/0 | 2783 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | copy fasta | chr9 | 92026147 | 92120413 |
| a0001c0001t0009 | 0/0 | 2783 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | copy fasta | chr9 | 92026147 | 92120413 |
| a0001c0001t0010 | 0/0 | 2783 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | copy fasta | chr9 | 92026147 | 92120413 |
| a0001c0001t0011 | 0/0 | 2783 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | copy fasta | chr9 | 92026147 | 92120413 |
| a0001c0001t0012 | 0/0 | 2783 | 1 | 0 | 0 | 0 | 0 | 1 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | copy fasta | chr9 | 92026147 | 92120413 |
| a0001c0001t0013 | 0/0 | 2783 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | copy fasta | chr9 | 92026147 | 92120413 |
| a0001c0001t0014 | 0/0 | 2783 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | copy fasta | chr9 | 92026147 | 92120413 |
| a0001c0002t0002 | 0/0 | 2783 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | copy fasta | chr9 | 92026147 | 92120413 |
| a0001c0004t0001 | 0/0 | 2783 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | copy fasta | chr9 | 92026147 | 92120413 |
| a0001c0005t0001 | 0/0 | 2783 | 1 | 0 | 0 | 0 | 0 | 1 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | copy fasta | chr9 | 92026147 | 92120413 |
| a0001c0006t0001 | 0/0 | 2783 | 1 | 0 | 0 | 0 | 0 | 1 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | copy fasta | chr9 | 92026147 | 92120413 |
| a0002c0003t0003 | 0/0 | 2783 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | copy fasta | chr9 | 92026147 | 92120413 |
| a0003c0007t0001 | 0/0 | 2783 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | copy fasta | chr9 | 92026147 | 92120413 |
| 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 | 5 | 0 | 1 | 4 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0003 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0020 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0216 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0295 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0002g0002 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0002g0007 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0003g0019 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0003g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0003g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0003g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0003g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0003g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0004g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0004g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0004g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0005g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0005g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0006g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0007g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0008g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0009g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0010g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0011g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0012g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0013g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0014g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0002t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0004t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0005t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0006t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0002c0003t0003g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0003c0007t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0294 | EUR | FIN | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0187 | EUR | FIN | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0221 | EUR | FIN | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0076 | EUR | FIN | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | CHS | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | CHS | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | CHS | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | CHS | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | CHS | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | CHS | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | CHS | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | CHS | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | CHS | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | CHS | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | CHS | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | CHS | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0219 | AMR | PUR | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | CHS | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | CHS | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG00733 | hp1 | a0001 | c0001 | t0007 | g0308 | AMR | PUR | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG00733 | hp2 | a0001 | c0001 | t0010 | g0045 | AMR | PUR | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0231 | AMR | PUR | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0226 | AMR | PUR | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0281 | AMR | PUR | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | PUR | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0325 | AMR | PUR | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG01074 | hp2 | a0001 | c0001 | t0003 | g0262 | AMR | PUR | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0258 | AMR | PUR | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | PUR | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0282 | AMR | PUR | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0036 | AMR | PUR | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | PUR | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0297 | AMR | PUR | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG01192 | hp1 | a0001 | c0004 | t0001 | g0186 | AMR | PUR | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | PUR | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0041 | AMR | CLM | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | CLM | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG01257 | hp1 | a0001 | c0001 | t0006 | g0307 | AMR | CLM | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | CLM | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0323 | AMR | CLM | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0038 | AMR | CLM | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG01358 | hp1 | a0001 | c0002 | t0002 | g0039 | AMR | CLM | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | CLM | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0324 | AMR | CLM | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0277 | AMR | CLM | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0165 | EUR | IBS | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0022 | EUR | IBS | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0211 | EUR | IBS | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0019 | EUR | IBS | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0326 | EUR | IBS | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG01517 | hp2 | a0001 | c0001 | t0003 | g0019 | EUR | IBS | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0056 | AFR | ACB | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG01884 | hp2 | a0002 | c0003 | t0003 | g0062 | AFR | ACB | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0061 | AFR | ACB | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0271 | AFR | ACB | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | PEL | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG01943 | hp1 | a0001 | c0001 | t0003 | g0263 | AMR | PEL | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | PEL | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | PEL | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0322 | AMR | PEL | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0276 | AMR | PEL | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PEL | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PEL | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0327 | AMR | PEL | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | PEL | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | PEL | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | KHV | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02015 | hp2 | a0003 | c0007 | t0001 | g0286 | EAS | KHV | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | KHV | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | KHV | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02055 | hp1 | a0001 | c0001 | t0008 | g0319 | AFR | ACB | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0288 | AFR | ACB | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | KHV | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | KHV | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | KHV | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | KHV | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | KHV | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | KHV | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | KHV | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | KHV | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | KHV | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | KHV | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | KHV | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | KHV | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | KHV | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0037 | AFR | ACB | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0314 | AFR | ACB | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | CDX | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | CDX | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | CDX | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CDX | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | ACB | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02257 | hp2 | a0001 | c0001 | t0004 | g0119 | AFR | ACB | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0275 | AFR | ACB | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | ACB | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0321 | AMR | PEL | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PEL | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | KHV | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | KHV | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0279 | AFR | GWD | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02572 | hp2 | a0001 | c0001 | t0009 | g0042 | AFR | GWD | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0254 | SAS | PJL | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0317 | SAS | PJL | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02615 | hp2 | a0001 | c0001 | t0004 | g0118 | AFR | GWD | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0266 | AFR | GWD | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0274 | AFR | GWD | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0278 | AFR | GWD | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | GWD | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0312 | AFR | GWD | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0060 | AFR | GWD | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0192 | SAS | PJL | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0259 | AFR | GWD | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0053 | AFR | GWD | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | GWD | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | GWD | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | GWD | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0289 | AFR | GWD | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02895 | hp1 | a0001 | c0001 | t0005 | g0065 | AFR | GWD | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | GWD | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02896 | hp1 | a0001 | c0001 | t0004 | g0117 | AFR | GWD | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0313 | AFR | GWD | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02897 | hp1 | a0001 | c0001 | t0005 | g0067 | AFR | GWD | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0309 | AFR | GWD | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0031 | AFR | ESN | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | ESN | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | ESN | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0272 | AFR | ESN | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0255 | AFR | ESN | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0273 | AFR | ESN | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02976 | hp1 | a0001 | c0001 | t0014 | g0261 | AFR | ESN | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0058 | AFR | ESN | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0030 | SAS | PJL | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0329 | SAS | PJL | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | GWD | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0059 | AFR | GWD | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | MSL | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0054 | AFR | MSL | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0057 | AFR | ESN | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | ESN | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0040 | AFR | ESN | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0034 | AFR | ESN | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0318 | AFR | MSL | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | MSL | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0301 | SAS | PJL | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0180 | SAS | PJL | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0043 | AFR | MSL | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | MSL | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0268 | AFR | MSL | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0283 | SAS | PJL | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0169 | SAS | PJL | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0046 | AFR | ESN | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0055 | AFR | ESN | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0310 | AFR | GWD | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0260 | AFR | MSL | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG03579 | hp2 | a0001 | c0001 | t0011 | g0253 | AFR | MSL | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0227 | SAS | PJL | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0315 | SAS | PJL | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0210 | SAS | PJL | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0316 | SAS | STU | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0193 | SAS | STU | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0293 | SAS | PJL | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0205 | SAS | PJL | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0018 | SAS | BEB | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0196 | SAS | BEB | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | BEB | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG03927 | hp2 | a0001 | c0006 | t0001 | g0300 | SAS | BEB | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0298 | SAS | STU | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG04115 | hp2 | a0001 | c0001 | t0012 | g0251 | SAS | STU | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG04199 | hp1 | a0001 | c0001 | t0003 | g0264 | SAS | STU | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0299 | SAS | STU | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0190 | SAS | STU | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0296 | SAS | STU | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0212 | SAS | STU | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG04228 | hp2 | a0001 | c0005 | t0001 | g0185 | SAS | STU | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0035 | AFR | YRI | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | YRI | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | CHB | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | CHB | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA19001 | hp2 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | LWK | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | LWK | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | ASW | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0032 | AFR | ASW | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0022 | EUR | TSI | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0265 | EUR | TSI | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0164 | SAS | GIH | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0149 | SAS | GIH | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0320 | AMR | CLM | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | ACB | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0311 | AFR | ACB | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0052 | AFR | ACB | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0290 | AFR | ACB | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0280 | AFR | ACB | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0270 | AFR | ACB | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG03471 | hp1 | a0001 | c0001 | t0013 | g0267 | AFR | MSL | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | USA | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | USA | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0240 | AFR | USA | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0044 | AFR | USA | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0287 | AFR | LWK | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | LWK | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0295 | REF | REF | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0216 | REF | REF | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:92038349
|
C | T | 1 | a0002 | 1 | HG01884.hp2 | missense_variant | MODERATE | c.1153G>A | p.Val385Met | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 13/15 | 1196/2783 | 1153/1422 | 385/473 | chr9 | 92038349 | ||
| chr9:92108750
|
T | C | 1 | a0003 | 1 | HG02015.hp2 | missense_variant | MODERATE | c.250A>G | p.Ile84Val | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/15 | 293/2783 | 250/1422 | 84/473 | chr9 | 92108750 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:92032549
|
A | G | 1 | a0001c0004 | 1 | HG01192.hp1 | synonymous_variant | LOW | c.1338T>C | p.Val446Val | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 15/15 | 1381/2783 | 1338/1422 | 446/473 | chr9 | 92032549 | ||
| chr9:92047197
|
G | A | 1 | a0001c0005 | 1 | HG04228.hp2 | synonymous_variant | LOW | c.1056C>T | p.Ala352Ala | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 11/15 | 1099/2783 | 1056/1422 | 352/473 | chr9 | 92047197 | ||
| chr9:92047628
|
A | G | 1 | a0001c0002 | 1 | HG01358.hp1 | synonymous_variant | LOW | c.969T>C | p.Phe323Phe | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 10/15 | 1012/2783 | 969/1422 | 323/473 | chr9 | 92047628 | ||
| chr9:92080056
|
G | A | 1 | a0001c0006 | 1 | HG03927.hp2 | synonymous_variant | LOW | c.387C>T | p.Gly129Gly | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/15 | 430/2783 | 387/1422 | 129/473 | chr9 | 92080056 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:92031163
|
A | C | 4 | a0001c0001t0002a0001c0001t0009a0001c0001t0010others(1): Show | 37 | HG00733.hp2 HG01109.hp1 HG01255.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*1302T>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 15/15 | 1302 | chr9 | 92031163 | |||||
| chr9:92031295
|
A | G | 1 | a0001c0001t0005 | 2 | HG02895.hp1 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1170T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 15/15 | 1170 | chr9 | 92031295 | |||||
| chr9:92031311
|
A | G | 1 | a0001c0001t0014 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1154T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 15/15 | 1154 | chr9 | 92031311 | |||||
| chr9:92031413
|
T | C | 1 | a0001c0001t0010 | 1 | HG00733.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1052A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 15/15 | 1052 | chr9 | 92031413 | |||||
| chr9:92031590
|
T | A | 1 | a0001c0001t0011 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*875A>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 15/15 | 875 | chr9 | 92031590 | |||||
| chr9:92031637
|
A | C | 1 | a0001c0001t0013 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*828T>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 15/15 | 828 | chr9 | 92031637 | |||||
| chr9:92031778
|
T | C | 1 | a0001c0001t0011 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*687A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 15/15 | 687 | chr9 | 92031778 | |||||
| chr9:92031795
|
C | T | 1 | a0001c0001t0009 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*670G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 15/15 | 670 | chr9 | 92031795 | |||||
| chr9:92031975
|
T | C | 1 | a0001c0001t0004 | 3 | HG02257.hp2 HG02615.hp2 HG02896.hp1 |
3_prime_UTR_variant | MODIFIER | c.*490A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 15/15 | 490 | chr9 | 92031975 | |||||
| chr9:92031977
|
C | A | 1 | a0001c0001t0007 | 1 | HG00733.hp1 | 3_prime_UTR_variant | MODIFIER | c.*488G>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 15/15 | 488 | chr9 | 92031977 | |||||
| chr9:92031982
|
T | C | 1 | a0001c0001t0012 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*483A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 15/15 | 483 | chr9 | 92031982 | |||||
| chr9:92032020
|
T | C | 4 | a0001c0001t0003a0001c0001t0013a0001c0001t0014others(1): Show | 10 | HG01074.hp2 HG01516.hp2 HG01517.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*445A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 15/15 | 445 | chr9 | 92032020 | |||||
| chr9:92032145
|
C | T | 1 | a0001c0001t0008 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*320G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 15/15 | 320 | chr9 | 92032145 | |||||
| chr9:92032287
|
A | T | 2 | a0001c0001t0006a0001c0001t0007 | 2 | HG00733.hp1 HG01257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*178T>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 15/15 | 178 | chr9 | 92032287 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:92032604
|
G | A | 1 | a0001c0001t0011g0253 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1329-46C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 14/14 | chr9 | 92032604 | ||||||
| chr9:92032640
|
G | A | 35 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0031others(32): Show | 38 | HG00733.hp2 HG01109.hp1 HG01255.hp1 others(35): Show |
intron_variant | MODIFIER | c.1329-82C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 14/14 | chr9 | 92032640 | ||||||
| chr9:92032681
|
C | T | 1 | a0001c0001t0001g0111 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1329-123G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 14/14 | chr9 | 92032681 | ||||||
| chr9:92032748
|
T | C | 22 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0123others(19): Show | 22 | HG02015.hp2 HG02040.hp2 HG02132.hp1 others(19): Show |
intron_variant | MODIFIER | c.1329-190A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 14/14 | chr9 | 92032748 | ||||||
| chr9:92032808
|
G | A | 1 | a0001c0001t0001g0268 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1329-250C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 14/14 | chr9 | 92032808 | ||||||
| chr9:92032832
|
C | T | 26 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0032others(23): Show | 29 | HG00733.hp2 HG01109.hp1 HG01255.hp1 others(26): Show |
intron_variant | MODIFIER | c.1329-274G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 14/14 | chr9 | 92032832 | ||||||
| chr9:92032857
|
C | A | 1 | a0002c0003t0003g0062 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1329-299G>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 14/14 | chr9 | 92032857 | ||||||
| chr9:92032875
|
C | CA | 18 | a0001c0001t0001g0011a0001c0001t0001g0153a0001c0001t0001g0178others(15): Show | 19 | HG00738.hp2 HG01109.hp2 HG01167.hp2 others(16): Show |
intron_variant | MODIFIER | c.1329-318dupT | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 14/14 | chr9 | 92032875 | ||||||
| chr9:92032875
|
CA | C | 127 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(124): Show | 140 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(137): Show |
intron_variant | MODIFIER | c.1329-318delT | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 14/14 | chr9 | 92032875 | ||||||
| chr9:92032875
|
CAA | C | 22 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(19): Show | 22 | HG00642.hp2 HG01884.hp2 HG02040.hp2 others(19): Show |
intron_variant | MODIFIER | c.1329-319_1329-318d others(4): Show |
SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 14/14 | chr9 | 92032875 | ||||||
| chr9:92032891
|
C | A | 1 | a0001c0001t0001g0282 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1329-333G>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 14/14 | chr9 | 92032891 | ||||||
| chr9:92033139
|
T | A | 1 | a0002c0003t0003g0062 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1329-581A>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 14/14 | chr9 | 92033139 | ||||||
| chr9:92033337
|
A | T | 1 | a0001c0001t0001g0246 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1329-779T>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 14/14 | chr9 | 92033337 | ||||||
| chr9:92033541
|
C | T | 6 | a0001c0001t0001g0020a0001c0001t0001g0063a0001c0001t0001g0064others(3): Show | 7 | HG01081.hp2 HG02257.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1329-983G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 14/14 | chr9 | 92033541 | ||||||
| chr9:92033710
|
T | C | 207 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(204): Show | 222 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(219): Show |
intron_variant | MODIFIER | c.1328+1100A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 14/14 | chr9 | 92033710 | ||||||
| chr9:92033723
|
T | G | 38 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0290others(35): Show | 40 | HG00280.hp1 HG00733.hp1 HG01074.hp1 others(37): Show |
intron_variant | MODIFIER | c.1328+1087A>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 14/14 | chr9 | 92033723 | ||||||
| chr9:92033756
|
A | G | 1 | a0001c0001t0001g0268 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1328+1054T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 14/14 | chr9 | 92033756 | ||||||
| chr9:92033848
|
A | G | 44 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0031others(41): Show | 48 | HG00733.hp2 HG01074.hp2 HG01109.hp1 others(45): Show |
intron_variant | MODIFIER | c.1328+962T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 14/14 | chr9 | 92033848 | ||||||
| chr9:92033920
|
G | C | 3 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0273 | 3 | HG01891.hp2 HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1328+890C>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 14/14 | chr9 | 92033920 | ||||||
| chr9:92033923
|
G | A | 4 | a0001c0001t0001g0009a0001c0001t0001g0146a0001c0001t0001g0147others(1): Show | 5 | HG01243.hp1 HG03453.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1328+887C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 14/14 | chr9 | 92033923 | ||||||
| chr9:92033926
|
A | G | 8 | a0001c0001t0001g0009a0001c0001t0001g0145a0001c0001t0001g0146others(5): Show | 9 | HG01099.hp1 HG01243.hp1 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.1328+884T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 14/14 | chr9 | 92033926 | ||||||
| chr9:92033996
|
T | C | 9 | a0001c0001t0003g0019a0001c0001t0003g0262a0001c0001t0003g0263others(6): Show | 10 | HG01074.hp2 HG01516.hp2 HG01517.hp2 others(7): Show |
intron_variant | MODIFIER | c.1328+814A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 14/14 | chr9 | 92033996 | ||||||
| chr9:92034011
|
C | T | 1 | a0001c0001t0001g0025 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1328+799G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 14/14 | chr9 | 92034011 | ||||||
| chr9:92034107
|
G | A | 1 | a0001c0001t0001g0174 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1328+703C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 14/14 | chr9 | 92034107 | ||||||
| chr9:92034109
|
T | C | 44 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0031others(41): Show | 48 | HG00733.hp2 HG01074.hp2 HG01109.hp1 others(45): Show |
intron_variant | MODIFIER | c.1328+701A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 14/14 | chr9 | 92034109 | ||||||
| chr9:92034134
|
A | G | 13 | a0001c0001t0001g0009a0001c0001t0001g0140a0001c0001t0001g0141others(10): Show | 14 | HG01099.hp1 HG01243.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1328+676T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 14/14 | chr9 | 92034134 | ||||||
| chr9:92034195
|
A | G | 6 | a0001c0001t0001g0020a0001c0001t0001g0063a0001c0001t0001g0064others(3): Show | 7 | HG01081.hp2 HG02257.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1328+615T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 14/14 | chr9 | 92034195 | ||||||
| chr9:92034209
|
C | T | 38 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0290others(35): Show | 40 | HG00280.hp1 HG00733.hp1 HG01074.hp1 others(37): Show |
intron_variant | MODIFIER | c.1328+601G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 14/14 | chr9 | 92034209 | ||||||
| chr9:92034332
|
C | T | 1 | a0001c0001t0003g0262 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1328+478G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 14/14 | chr9 | 92034332 | ||||||
| chr9:92034456
|
C | T | 3 | a0001c0001t0001g0098a0001c0001t0001g0107a0001c0001t0001g0113 | 3 | HG02129.hp1 NA18967.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.1328+354G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 14/14 | chr9 | 92034456 | ||||||
| chr9:92034619
|
C | T | 1 | a0001c0001t0001g0298 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1328+191G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 14/14 | chr9 | 92034619 | ||||||
| chr9:92034621
|
T | G | 3 | a0001c0001t0001g0274a0001c0001t0001g0275a0001c0001t0001g0289 | 3 | HG02258.hp1 HG02622.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1328+189A>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 14/14 | chr9 | 92034621 | ||||||
| chr9:92034665
|
C | A | 1 | a0001c0001t0001g0219 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1328+145G>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 14/14 | chr9 | 92034665 | ||||||
| chr9:92034758
|
T | C | 2 | a0001c0001t0001g0226a0001c0001t0001g0231 | 2 | HG00735.hp2 HG00738.hp1 |
intron_variant | MODIFIER | c.1328+52A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 14/14 | chr9 | 92034758 | ||||||
| chr9:92034890
|
G | A | 4 | a0001c0001t0001g0066a0001c0001t0001g0068a0001c0001t0005g0065others(1): Show | 4 | HG02630.hp2 HG02809.hp2 HG02895.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.1255-7C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 13/14 | chr9 | 92034890 | ||||||
| chr9:92034967
|
C | T | 35 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(32): Show | 40 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.1255-84G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 13/14 | chr9 | 92034967 | ||||||
| chr9:92035127
|
C | G | 3 | a0001c0001t0001g0020a0001c0001t0001g0063a0001c0001t0001g0064 | 4 | HG01081.hp2 HG02895.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1255-244G>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 13/14 | chr9 | 92035127 | ||||||
| chr9:92035220
|
T | C | 9 | a0001c0001t0003g0019a0001c0001t0003g0262a0001c0001t0003g0263others(6): Show | 10 | HG01074.hp2 HG01516.hp2 HG01517.hp2 others(7): Show |
intron_variant | MODIFIER | c.1255-337A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 13/14 | chr9 | 92035220 | ||||||
| chr9:92035318
|
G | A | 1 | a0001c0001t0001g0111 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1255-435C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 13/14 | chr9 | 92035318 | ||||||
| chr9:92035536
|
GTTTC | G | 5 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0071others(2): Show | 5 | HG02056.hp2 HG02074.hp2 NA18939.hp2 others(2): Show |
intron_variant | MODIFIER | c.1255-657_1255-654d others(6): Show |
SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 13/14 | chr9 | 92035536 | ||||||
| chr9:92035665
|
T | C | 1 | a0001c0001t0001g0268 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1255-782A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 13/14 | chr9 | 92035665 | ||||||
| chr9:92035771
|
G | A | 13 | a0001c0001t0001g0009a0001c0001t0001g0140a0001c0001t0001g0141others(10): Show | 14 | HG01099.hp1 HG01243.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1255-888C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 13/14 | chr9 | 92035771 | ||||||
| chr9:92035790
|
A | C | 2 | a0001c0001t0001g0278a0001c0001t0001g0279 | 2 | HG02572.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.1255-907T>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 13/14 | chr9 | 92035790 | ||||||
| chr9:92035882
|
T | C | 1 | a0001c0001t0001g0078 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1255-999A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 13/14 | chr9 | 92035882 | ||||||
| chr9:92035888
|
G | A | 1 | a0001c0001t0001g0248 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1255-1005C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 13/14 | chr9 | 92035888 | ||||||
| chr9:92036301
|
T | C | 1 | a0001c0001t0001g0257 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1255-1418A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 13/14 | chr9 | 92036301 | ||||||
| chr9:92036501
|
A | G | 5 | a0001c0001t0003g0019a0001c0001t0003g0262a0001c0001t0003g0263others(2): Show | 6 | HG01074.hp2 HG01516.hp2 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.1255-1618T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 13/14 | chr9 | 92036501 | ||||||
| chr9:92036571
|
T | C | 44 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0031others(41): Show | 48 | HG00733.hp2 HG01074.hp2 HG01109.hp1 others(45): Show |
intron_variant | MODIFIER | c.1254+1677A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 13/14 | chr9 | 92036571 | ||||||
| chr9:92036748
|
C | T | 44 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0031others(41): Show | 48 | HG00733.hp2 HG01074.hp2 HG01109.hp1 others(45): Show |
intron_variant | MODIFIER | c.1254+1500G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 13/14 | chr9 | 92036748 | ||||||
| chr9:92036824
|
G | A | 4 | a0001c0001t0001g0066a0001c0001t0001g0068a0001c0001t0005g0065others(1): Show | 4 | HG02630.hp2 HG02809.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1254+1424C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 13/14 | chr9 | 92036824 | ||||||
| chr9:92037100
|
G | A | 1 | a0001c0001t0002g0034 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1254+1148C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 13/14 | chr9 | 92037100 | ||||||
| chr9:92037165
|
C | T | 10 | a0001c0001t0001g0066a0001c0001t0001g0068a0001c0001t0001g0271others(7): Show | 10 | HG01891.hp2 HG02258.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.1254+1083G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 13/14 | chr9 | 92037165 | ||||||
| chr9:92037308
|
C | G | 1 | a0001c0001t0001g0268 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1254+940G>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 13/14 | chr9 | 92037308 | ||||||
| chr9:92037317
|
T | C | 2 | a0001c0001t0001g0318a0001c0001t0008g0319 | 2 | HG02055.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1254+931A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 13/14 | chr9 | 92037317 | ||||||
| chr9:92037333
|
A | C | 7 | a0001c0001t0001g0001a0001c0001t0001g0157a0001c0001t0001g0158others(4): Show | 11 | HG01070.hp2 HG01934.hp1 NA18945.hp1 others(8): Show |
intron_variant | MODIFIER | c.1254+915T>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 13/14 | chr9 | 92037333 | ||||||
| chr9:92037380
|
G | A | 8 | a0001c0001t0003g0019a0001c0001t0003g0262a0001c0001t0003g0263others(5): Show | 9 | HG01074.hp2 HG01516.hp2 HG01517.hp2 others(6): Show |
intron_variant | MODIFIER | c.1254+868C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 13/14 | chr9 | 92037380 | ||||||
| chr9:92037536
|
C | T | 1 | a0001c0001t0001g0139 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1254+712G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 13/14 | chr9 | 92037536 | ||||||
| chr9:92037611
|
A | C | 1 | a0001c0001t0001g0079 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1254+637T>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 13/14 | chr9 | 92037611 | ||||||
| chr9:92037864
|
T | G | 207 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(204): Show | 222 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(219): Show |
intron_variant | MODIFIER | c.1254+384A>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 13/14 | chr9 | 92037864 | ||||||
| chr9:92037964
|
G | A | 1 | a0001c0001t0001g0030 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1254+284C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 13/14 | chr9 | 92037964 | ||||||
| chr9:92038025
|
C | T | 44 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0031others(41): Show | 48 | HG00733.hp2 HG01074.hp2 HG01109.hp1 others(45): Show |
intron_variant | MODIFIER | c.1254+223G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 13/14 | chr9 | 92038025 | ||||||
| chr9:92038238
|
G | A | 2 | a0001c0001t0001g0018a0001c0001t0001g0254 | 3 | HG02602.hp1 HG03654.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.1254+10C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 13/14 | chr9 | 92038238 | ||||||
| chr9:92038378
|
A | AAC | 7 | a0001c0001t0001g0066a0001c0001t0001g0068a0001c0001t0001g0274others(4): Show | 7 | HG02258.hp1 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1137-15_1137-14dup others(2): Show |
SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 12/14 | chr9 | 92038378 | ||||||
| chr9:92038408
|
G | C | 22 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0123others(19): Show | 22 | HG02015.hp2 HG02040.hp2 HG02132.hp1 others(19): Show |
intron_variant | MODIFIER | c.1137-43C>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 12/14 | chr9 | 92038408 | ||||||
| chr9:92038573
|
A | G | 44 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0031others(41): Show | 48 | HG00733.hp2 HG01074.hp2 HG01109.hp1 others(45): Show |
intron_variant | MODIFIER | c.1137-208T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 12/14 | chr9 | 92038573 | ||||||
| chr9:92038745
|
AGCTCCAG others(4): Show |
A | 1 | a0001c0001t0001g0301 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1137-391_1137-381d others(13): Show |
SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 12/14 | chr9 | 92038745 | ||||||
| chr9:92038849
|
T | A | 1 | a0001c0001t0001g0159 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1137-484A>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 12/14 | chr9 | 92038849 | ||||||
| chr9:92038967
|
TAAAACAA others(5): Show |
T | 1 | a0001c0001t0001g0099 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1137-614_1137-603d others(14): Show |
SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 12/14 | chr9 | 92038967 | ||||||
| chr9:92039004
|
G | A | 44 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0031others(41): Show | 48 | HG00733.hp2 HG01074.hp2 HG01109.hp1 others(45): Show |
intron_variant | MODIFIER | c.1137-639C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 12/14 | chr9 | 92039004 | ||||||
| chr9:92039133
|
CA | C | 3 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0273 | 3 | HG01891.hp2 HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1137-769delT | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 12/14 | chr9 | 92039133 | ||||||
| chr9:92039226
|
T | C | 1 | a0001c0001t0001g0296 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1137-861A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 12/14 | chr9 | 92039226 | ||||||
| chr9:92039241
|
T | C | 1 | a0001c0001t0001g0268 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1137-876A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 12/14 | chr9 | 92039241 | ||||||
| chr9:92039416
|
C | CTAT | 34 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0031others(31): Show | 37 | HG00733.hp2 HG01109.hp1 HG01255.hp1 others(34): Show |
intron_variant | MODIFIER | c.1137-1054_1137-105 others(7): Show |
SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 12/14 | chr9 | 92039416 | ||||||
| chr9:92039488
|
G | A | 1 | a0001c0001t0001g0076 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1137-1123C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 12/14 | chr9 | 92039488 | ||||||
| chr9:92039656
|
G | A | 6 | a0001c0001t0001g0227a0001c0001t0001g0280a0001c0001t0001g0281others(3): Show | 6 | HG00738.hp2 HG01106.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.1137-1291C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 12/14 | chr9 | 92039656 | ||||||
| chr9:92039656
|
G | T | 1 | a0001c0001t0001g0233 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1137-1291C>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 12/14 | chr9 | 92039656 | ||||||
| chr9:92039873
|
TCTCAA | T | 10 | a0001c0001t0001g0066a0001c0001t0001g0068a0001c0001t0001g0271others(7): Show | 10 | HG01891.hp2 HG02258.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.1137-1513_1137-150 others(9): Show |
SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 12/14 | chr9 | 92039873 | ||||||
| chr9:92040061
|
T | G | 11 | a0001c0001t0001g0066a0001c0001t0001g0068a0001c0001t0001g0268others(8): Show | 11 | HG01891.hp2 HG02258.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.1137-1696A>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 12/14 | chr9 | 92040061 | ||||||
| chr9:92040107
|
C | T | 67 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(64): Show | 73 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.1137-1742G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 12/14 | chr9 | 92040107 | ||||||
| chr9:92040126
|
T | C | 25 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0001g0121others(22): Show | 26 | HG00642.hp2 HG02015.hp2 HG02040.hp2 others(23): Show |
intron_variant | MODIFIER | c.1137-1761A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 12/14 | chr9 | 92040126 | ||||||
| chr9:92040195
|
C | A | 5 | a0001c0001t0003g0019a0001c0001t0003g0262a0001c0001t0003g0263others(2): Show | 6 | HG01074.hp2 HG01516.hp2 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.1137-1830G>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 12/14 | chr9 | 92040195 | ||||||
| chr9:92040241
|
A | G | 68 | a0001c0001t0001g0009a0001c0001t0001g0066a0001c0001t0001g0068others(65): Show | 73 | HG00733.hp2 HG01074.hp2 HG01099.hp1 others(70): Show |
intron_variant | MODIFIER | c.1137-1876T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 12/14 | chr9 | 92040241 | ||||||
| chr9:92040305
|
G | A | 1 | a0001c0001t0001g0239 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1137-1940C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 12/14 | chr9 | 92040305 | ||||||
| chr9:92040364
|
C | T | 40 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0290others(37): Show | 42 | HG00280.hp1 HG00733.hp1 HG01074.hp1 others(39): Show |
intron_variant | MODIFIER | c.1137-1999G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 12/14 | chr9 | 92040364 | ||||||
| chr9:92040484
|
C | T | 22 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0123others(19): Show | 22 | HG02015.hp2 HG02040.hp2 HG02132.hp1 others(19): Show |
intron_variant | MODIFIER | c.1137-2119G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 12/14 | chr9 | 92040484 | ||||||
| chr9:92040722
|
T | C | 9 | a0001c0001t0003g0019a0001c0001t0003g0262a0001c0001t0003g0263others(6): Show | 10 | HG01074.hp2 HG01516.hp2 HG01517.hp2 others(7): Show |
intron_variant | MODIFIER | c.1137-2357A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 12/14 | chr9 | 92040722 | ||||||
| chr9:92040762
|
GA | G | 37 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0120others(34): Show | 42 | HG00642.hp2 HG01070.hp2 HG01934.hp1 others(39): Show |
intron_variant | MODIFIER | c.1137-2398delT | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 12/14 | chr9 | 92040762 | ||||||
| chr9:92040769
|
A | G | 1 | a0001c0001t0011g0253 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1137-2404T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 12/14 | chr9 | 92040769 | ||||||
| chr9:92040780
|
A | G | 1 | a0002c0003t0003g0062 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1137-2415T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 12/14 | chr9 | 92040780 | ||||||
| chr9:92040879
|
C | T | 9 | a0001c0001t0003g0019a0001c0001t0003g0262a0001c0001t0003g0263others(6): Show | 10 | HG01074.hp2 HG01516.hp2 HG01517.hp2 others(7): Show |
intron_variant | MODIFIER | c.1137-2514G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 12/14 | chr9 | 92040879 | ||||||
| chr9:92040894
|
C | T | 1 | a0001c0001t0001g0133 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1137-2529G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 12/14 | chr9 | 92040894 | ||||||
| chr9:92041040
|
C | T | 25 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0001g0121others(22): Show | 26 | HG00642.hp2 HG02015.hp2 HG02040.hp2 others(23): Show |
intron_variant | MODIFIER | c.1137-2675G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 12/14 | chr9 | 92041040 | ||||||
| chr9:92041089
|
G | A | 6 | a0001c0001t0001g0309a0001c0001t0001g0310a0001c0001t0001g0311others(3): Show | 6 | HG02109.hp2 HG02145.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1137-2724C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 12/14 | chr9 | 92041089 | ||||||
| chr9:92041094
|
C | T | 1 | a0001c0001t0001g0299 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1137-2729G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 12/14 | chr9 | 92041094 | ||||||
| chr9:92041609
|
G | A | 1 | a0001c0001t0001g0213 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1137-3244C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 12/14 | chr9 | 92041609 | ||||||
| chr9:92041710
|
T | C | 2 | a0001c0001t0001g0242a0001c0001t0001g0243 | 2 | HG00438.hp1 HG02071.hp2 |
intron_variant | MODIFIER | c.1137-3345A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 12/14 | chr9 | 92041710 | ||||||
| chr9:92041742
|
A | T | 3 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0072 | 3 | HG02074.hp2 NA18939.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.1137-3377T>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 12/14 | chr9 | 92041742 | ||||||
| chr9:92041749
|
A | T | 3 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0072 | 3 | HG02074.hp2 NA18939.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.1137-3384T>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 12/14 | chr9 | 92041749 | ||||||
| chr9:92041780
|
G | A | 1 | a0001c0001t0001g0150 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1137-3415C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 12/14 | chr9 | 92041780 | ||||||
| chr9:92041885
|
A | G | 1 | a0001c0001t0001g0259 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1137-3520T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 12/14 | chr9 | 92041885 | ||||||
| chr9:92041921
|
G | A | 1 | a0001c0001t0001g0192 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1137-3556C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 12/14 | chr9 | 92041921 | ||||||
| chr9:92042122
|
CA | C | 2 | a0001c0001t0001g0018a0001c0001t0001g0254 | 3 | HG02602.hp1 HG03654.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.1137-3758delT | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 12/14 | chr9 | 92042122 | ||||||
| chr9:92042166
|
T | A | 2 | a0001c0001t0002g0033a0001c0001t0002g0252 | 2 | NA18988.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.1137-3801A>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 12/14 | chr9 | 92042166 | ||||||
| chr9:92042167
|
A | T | 2 | a0001c0001t0002g0033a0001c0001t0002g0252 | 2 | NA18988.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.1137-3802T>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 12/14 | chr9 | 92042167 | ||||||
| chr9:92042192
|
G | A | 4 | a0001c0001t0001g0066a0001c0001t0001g0068a0001c0001t0005g0065others(1): Show | 4 | HG02630.hp2 HG02809.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1136+3807C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 12/14 | chr9 | 92042192 | ||||||
| chr9:92042204
|
T | C | 1 | a0002c0003t0003g0062 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1136+3795A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 12/14 | chr9 | 92042204 | ||||||
| chr9:92042362
|
A | G | 1 | a0002c0003t0003g0062 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1136+3637T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 12/14 | chr9 | 92042362 | ||||||
| chr9:92042437
|
T | C | 19 | a0001c0001t0002g0007a0001c0001t0002g0032a0001c0001t0002g0033others(16): Show | 20 | HG01109.hp1 HG01255.hp1 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1136+3562A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 12/14 | chr9 | 92042437 | ||||||
| chr9:92042636
|
TG | T | 13 | a0001c0001t0001g0009a0001c0001t0001g0140a0001c0001t0001g0141others(10): Show | 14 | HG01099.hp1 HG01243.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1136+3362delC | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 12/14 | chr9 | 92042636 | ||||||
| chr9:92042689
|
G | C | 3 | a0001c0001t0001g0274a0001c0001t0001g0275a0001c0001t0001g0289 | 3 | HG02258.hp1 HG02622.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1136+3310C>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 12/14 | chr9 | 92042689 | ||||||
| chr9:92043024
|
C | T | 206 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(203): Show | 221 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(218): Show |
intron_variant | MODIFIER | c.1136+2975G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 12/14 | chr9 | 92043024 | ||||||
| chr9:92043304
|
A | G | 68 | a0001c0001t0001g0009a0001c0001t0001g0066a0001c0001t0001g0068others(65): Show | 73 | HG00733.hp2 HG01074.hp2 HG01099.hp1 others(70): Show |
intron_variant | MODIFIER | c.1136+2695T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 12/14 | chr9 | 92043304 | ||||||
| chr9:92043411
|
T | C | 3 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0273 | 3 | HG01891.hp2 HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1136+2588A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 12/14 | chr9 | 92043411 | ||||||
| chr9:92043673
|
G | A | 1 | a0001c0001t0001g0270 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1136+2326C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 12/14 | chr9 | 92043673 | ||||||
| chr9:92043692
|
A | G | 1 | a0001c0001t0001g0028 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1136+2307T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 12/14 | chr9 | 92043692 | ||||||
| chr9:92043729
|
C | A | 4 | a0001c0001t0001g0066a0001c0001t0001g0068a0001c0001t0005g0065others(1): Show | 4 | HG02630.hp2 HG02809.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1136+2270G>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 12/14 | chr9 | 92043729 | ||||||
| chr9:92044049
|
T | C | 207 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(204): Show | 222 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(219): Show |
intron_variant | MODIFIER | c.1136+1950A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 12/14 | chr9 | 92044049 | ||||||
| chr9:92044188
|
G | A | 1 | a0001c0001t0003g0263 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1136+1811C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 12/14 | chr9 | 92044188 | ||||||
| chr9:92044224
|
G | C | 11 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0194others(8): Show | 13 | HG00597.hp1 HG00673.hp1 HG02074.hp1 others(10): Show |
intron_variant | MODIFIER | c.1136+1775C>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 12/14 | chr9 | 92044224 | ||||||
| chr9:92044303
|
G | A | 3 | a0001c0001t0004g0117a0001c0001t0004g0118a0001c0001t0004g0119 | 3 | HG02257.hp2 HG02615.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.1136+1696C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 12/14 | chr9 | 92044303 | ||||||
| chr9:92044342
|
G | A | 1 | a0001c0001t0001g0144 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1136+1657C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 12/14 | chr9 | 92044342 | ||||||
| chr9:92044365
|
A | G | 1 | a0001c0001t0014g0261 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1136+1634T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 12/14 | chr9 | 92044365 | ||||||
| chr9:92044479
|
G | A | 35 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0031others(32): Show | 38 | HG00733.hp2 HG01109.hp1 HG01255.hp1 others(35): Show |
intron_variant | MODIFIER | c.1136+1520C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 12/14 | chr9 | 92044479 | ||||||
| chr9:92044546
|
C | T | 1 | a0001c0001t0002g0043 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1136+1453G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 12/14 | chr9 | 92044546 | ||||||
| chr9:92044747
|
G | A | 9 | a0001c0001t0003g0019a0001c0001t0003g0262a0001c0001t0003g0263others(6): Show | 10 | HG01074.hp2 HG01516.hp2 HG01517.hp2 others(7): Show |
intron_variant | MODIFIER | c.1136+1252C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 12/14 | chr9 | 92044747 | ||||||
| chr9:92045216
|
G | A | 8 | a0001c0001t0003g0019a0001c0001t0003g0262a0001c0001t0003g0263others(5): Show | 9 | HG01074.hp2 HG01516.hp2 HG01517.hp2 others(6): Show |
intron_variant | MODIFIER | c.1136+783C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 12/14 | chr9 | 92045216 | ||||||
| chr9:92045285
|
C | T | 2 | a0001c0001t0001g0278a0001c0001t0001g0279 | 2 | HG02572.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.1136+714G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 12/14 | chr9 | 92045285 | ||||||
| chr9:92045343
|
C | A | 2 | a0001c0001t0001g0318a0001c0001t0008g0319 | 2 | HG02055.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1136+656G>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 12/14 | chr9 | 92045343 | ||||||
| chr9:92045347
|
A | AT | 29 | a0001c0001t0001g0005a0001c0001t0001g0018a0001c0001t0001g0120others(26): Show | 32 | HG00408.hp1 HG00438.hp2 HG00642.hp2 others(29): Show |
intron_variant | MODIFIER | c.1136+651dupA | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 12/14 | chr9 | 92045347 | ||||||
| chr9:92045347
|
A | G | 1 | a0001c0001t0011g0253 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1136+652T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 12/14 | chr9 | 92045347 | ||||||
| chr9:92045469
|
T | C | 35 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0031others(32): Show | 38 | HG00733.hp2 HG01109.hp1 HG01255.hp1 others(35): Show |
intron_variant | MODIFIER | c.1136+530A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 12/14 | chr9 | 92045469 | ||||||
| chr9:92045495
|
TA | T | 17 | a0001c0001t0001g0009a0001c0001t0001g0020a0001c0001t0001g0063others(14): Show | 19 | HG00438.hp1 HG01081.hp2 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.1136+503delT | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 12/14 | chr9 | 92045495 | ||||||
| chr9:92045496
|
A | T | 4 | a0001c0001t0001g0066a0001c0001t0001g0068a0001c0001t0005g0065others(1): Show | 4 | HG02630.hp2 HG02809.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1136+503T>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 12/14 | chr9 | 92045496 | ||||||
| chr9:92045498
|
A | T | 3 | a0001c0001t0004g0117a0001c0001t0004g0118a0001c0001t0004g0119 | 3 | HG02257.hp2 HG02615.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.1136+501T>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 12/14 | chr9 | 92045498 | ||||||
| chr9:92045499
|
A | T | 3 | a0001c0001t0001g0020a0001c0001t0001g0063a0001c0001t0001g0064 | 4 | HG01081.hp2 HG02895.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1136+500T>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 12/14 | chr9 | 92045499 | ||||||
| chr9:92045509
|
G | A | 1 | a0001c0001t0001g0217 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1136+490C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 12/14 | chr9 | 92045509 | ||||||
| chr9:92045524
|
T | TA | 96 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(93): Show | 112 | HG00323.hp2 HG00438.hp1 HG00544.hp2 others(109): Show |
intron_variant | MODIFIER | c.1136+474dupT | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 12/14 | chr9 | 92045524 | ||||||
| chr9:92045524
|
T | TAA | 40 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0030others(37): Show | 41 | HG00408.hp2 HG00609.hp2 HG00733.hp1 others(38): Show |
intron_variant | MODIFIER | c.1136+473_1136+474d others(4): Show |
SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 12/14 | chr9 | 92045524 | ||||||
| chr9:92045524
|
T | TAAA | 28 | a0001c0001t0001g0009a0001c0001t0001g0110a0001c0001t0001g0111others(25): Show | 29 | HG00642.hp2 HG01081.hp1 HG01099.hp1 others(26): Show |
intron_variant | MODIFIER | c.1136+472_1136+474d others(5): Show |
SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 12/14 | chr9 | 92045524 | ||||||
| chr9:92045524
|
T | TAAAA | 6 | a0001c0001t0001g0140a0001c0001t0001g0147a0001c0001t0002g0031others(3): Show | 6 | HG01243.hp1 HG01884.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1136+471_1136+474d others(6): Show |
SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 12/14 | chr9 | 92045524 | ||||||
| chr9:92045524
|
TAAAA | T | 6 | a0001c0001t0001g0066a0001c0001t0001g0068a0001c0001t0001g0272others(3): Show | 6 | HG02630.hp2 HG02809.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1136+471_1136+474d others(6): Show |
SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 12/14 | chr9 | 92045524 | ||||||
| chr9:92045524
|
TAAAAAAA | T | 6 | a0001c0001t0003g0019a0001c0001t0003g0262a0001c0001t0003g0263others(3): Show | 7 | HG01074.hp2 HG01516.hp2 HG01517.hp2 others(4): Show |
intron_variant | MODIFIER | c.1136+468_1136+474d others(9): Show |
SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 12/14 | chr9 | 92045524 | ||||||
| chr9:92045524
|
TAAAAAAA others(5): Show |
T | 3 | a0001c0001t0001g0020a0001c0001t0001g0063a0001c0001t0001g0064 | 4 | HG01081.hp2 HG02895.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1136+463_1136+474d others(14): Show |
SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 12/14 | chr9 | 92045524 | ||||||
| chr9:92045524
|
TAAAAAAA others(6): Show |
T | 3 | a0001c0001t0004g0117a0001c0001t0004g0118a0001c0001t0004g0119 | 3 | HG02257.hp2 HG02615.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.1136+462_1136+474d others(15): Show |
SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 12/14 | chr9 | 92045524 | ||||||
| chr9:92045543
|
A | ACCAAAAA others(5): Show |
1 | a0001c0001t0001g0268 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1136+455_1136+456i others(14): Show |
SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 12/14 | chr9 | 92045543 | ||||||
| chr9:92045552
|
A | C | 3 | a0001c0001t0001g0274a0001c0001t0001g0275a0001c0001t0001g0289 | 3 | HG02258.hp1 HG02622.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1136+447T>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 12/14 | chr9 | 92045552 | ||||||
| chr9:92045753
|
C | G | 4 | a0001c0001t0001g0066a0001c0001t0001g0068a0001c0001t0005g0065others(1): Show | 4 | HG02630.hp2 HG02809.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1136+246G>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 12/14 | chr9 | 92045753 | ||||||
| chr9:92045841
|
G | A | 2 | a0001c0001t0001g0008a0001c0001t0001g0094 | 3 | NA18965.hp2 NA18987.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.1136+158C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 12/14 | chr9 | 92045841 | ||||||
| chr9:92045881
|
T | C | 13 | a0001c0001t0001g0009a0001c0001t0001g0140a0001c0001t0001g0141others(10): Show | 14 | HG01099.hp1 HG01243.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1136+118A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 12/14 | chr9 | 92045881 | ||||||
| chr9:92045892
|
C | G | 3 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0203 | 3 | NA19006.hp1 NA19012.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.1136+107G>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 12/14 | chr9 | 92045892 | ||||||
| chr9:92045933
|
C | T | 13 | a0001c0001t0001g0009a0001c0001t0001g0140a0001c0001t0001g0141others(10): Show | 14 | HG01099.hp1 HG01243.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1136+66G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 12/14 | chr9 | 92045933 | ||||||
| chr9:92045987
|
T | C | 11 | a0001c0001t0001g0066a0001c0001t0001g0068a0001c0001t0001g0268others(8): Show | 11 | HG01891.hp2 HG02258.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.1136+12A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 12/14 | chr9 | 92045987 | ||||||
| chr9:92046095
|
T | C | 1 | a0001c0001t0001g0164 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1082-42A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 11/14 | chr9 | 92046095 | ||||||
| chr9:92046228
|
C | T | 1 | a0001c0001t0011g0253 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1082-175G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 11/14 | chr9 | 92046228 | ||||||
| chr9:92046229
|
G | T | 3 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0273 | 3 | HG01891.hp2 HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1082-176C>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 11/14 | chr9 | 92046229 | ||||||
| chr9:92046375
|
T | A | 1 | a0001c0001t0001g0299 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1082-322A>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 11/14 | chr9 | 92046375 | ||||||
| chr9:92046404
|
T | C | 9 | a0001c0001t0003g0019a0001c0001t0003g0262a0001c0001t0003g0263others(6): Show | 10 | HG01074.hp2 HG01516.hp2 HG01517.hp2 others(7): Show |
intron_variant | MODIFIER | c.1082-351A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 11/14 | chr9 | 92046404 | ||||||
| chr9:92046495
|
G | A | 1 | a0001c0001t0001g0320 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1082-442C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 11/14 | chr9 | 92046495 | ||||||
| chr9:92046497
|
G | C | 30 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0290others(27): Show | 32 | HG00280.hp1 HG01074.hp1 HG01123.hp1 others(29): Show |
intron_variant | MODIFIER | c.1082-444C>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 11/14 | chr9 | 92046497 | ||||||
| chr9:92046575
|
T | A | 9 | a0001c0001t0003g0019a0001c0001t0003g0262a0001c0001t0003g0263others(6): Show | 10 | HG01074.hp2 HG01516.hp2 HG01517.hp2 others(7): Show |
intron_variant | MODIFIER | c.1082-522A>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 11/14 | chr9 | 92046575 | ||||||
| chr9:92046677
|
C | CT | 3 | a0001c0001t0001g0274a0001c0001t0001g0275a0001c0001t0001g0289 | 3 | HG02258.hp1 HG02622.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1081+494dupA | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 11/14 | chr9 | 92046677 | ||||||
| chr9:92046913
|
G | C | 99 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0018others(96): Show | 108 | HG00408.hp1 HG00438.hp2 HG00642.hp2 others(105): Show |
intron_variant | MODIFIER | c.1081+259C>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 11/14 | chr9 | 92046913 | ||||||
| chr9:92047273
|
G | A | 1 | a0001c0001t0014g0261 | 1 | HG02976.hp1 | splice_region_variant&intron_variant | LOW | c.985-5C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 10/14 | chr9 | 92047273 | ||||||
| chr9:92047294
|
T | C | 1 | a0002c0003t0003g0062 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.985-26A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 10/14 | chr9 | 92047294 | ||||||
| chr9:92047342
|
T | C | 2 | a0001c0001t0006g0307a0001c0001t0007g0308 | 2 | HG00733.hp1 HG01257.hp1 |
intron_variant | MODIFIER | c.985-74A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 10/14 | chr9 | 92047342 | ||||||
| chr9:92047804
|
C | A | 13 | a0001c0001t0001g0009a0001c0001t0001g0140a0001c0001t0001g0141others(10): Show | 14 | HG01099.hp1 HG01243.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.889-96G>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 9/14 | chr9 | 92047804 | ||||||
| chr9:92047956
|
TCACAG | T | 7 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(4): Show | 7 | HG01081.hp1 HG02258.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.889-253_889-249del others(5): Show |
SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 9/14 | chr9 | 92047956 | ||||||
| chr9:92047972
|
T | C | 26 | a0001c0001t0001g0005a0001c0001t0001g0121a0001c0001t0001g0122others(23): Show | 28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.889-264A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 9/14 | chr9 | 92047972 | ||||||
| chr9:92047982
|
G | A | 70 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(67): Show | 76 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.889-274C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 9/14 | chr9 | 92047982 | ||||||
| chr9:92048038
|
C | T | 2 | a0001c0001t0002g0050a0001c0001t0002g0051 | 2 | NA18950.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.889-330G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 9/14 | chr9 | 92048038 | ||||||
| chr9:92048058
|
T | C | 1 | a0001c0001t0001g0240 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.889-350A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 9/14 | chr9 | 92048058 | ||||||
| chr9:92048250
|
G | A | 13 | a0001c0001t0001g0009a0001c0001t0001g0140a0001c0001t0001g0141others(10): Show | 14 | HG01099.hp1 HG01243.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.889-542C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 9/14 | chr9 | 92048250 | ||||||
| chr9:92048368
|
G | C | 11 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0083others(8): Show | 14 | HG00741.hp1 HG01070.hp1 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.889-660C>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 9/14 | chr9 | 92048368 | ||||||
| chr9:92048386
|
T | C | 3 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0273 | 3 | HG01891.hp2 HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.889-678A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 9/14 | chr9 | 92048386 | ||||||
| chr9:92048390
|
C | G | 35 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0031others(32): Show | 38 | HG00733.hp2 HG01109.hp1 HG01255.hp1 others(35): Show |
intron_variant | MODIFIER | c.889-682G>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 9/14 | chr9 | 92048390 | ||||||
| chr9:92048508
|
C | A | 1 | a0001c0001t0001g0078 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.889-800G>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 9/14 | chr9 | 92048508 | ||||||
| chr9:92048603
|
C | A | 1 | a0001c0001t0001g0188 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.889-895G>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 9/14 | chr9 | 92048603 | ||||||
| chr9:92048650
|
C | T | 4 | a0001c0001t0001g0066a0001c0001t0001g0068a0001c0001t0005g0065others(1): Show | 4 | HG02630.hp2 HG02809.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.889-942G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 9/14 | chr9 | 92048650 | ||||||
| chr9:92048656
|
A | G | 4 | a0001c0001t0001g0066a0001c0001t0001g0068a0001c0001t0005g0065others(1): Show | 4 | HG02630.hp2 HG02809.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.889-948T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 9/14 | chr9 | 92048656 | ||||||
| chr9:92049017
|
G | A | 8 | a0001c0001t0002g0031a0001c0001t0002g0054a0001c0001t0002g0055others(5): Show | 8 | HG01884.hp1 HG01891.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.888+943C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 9/14 | chr9 | 92049017 | ||||||
| chr9:92049081
|
G | C | 6 | a0001c0001t0001g0011a0001c0001t0001g0159a0001c0001t0001g0161others(3): Show | 7 | HG01069.hp1 HG01071.hp2 HG01167.hp2 others(4): Show |
intron_variant | MODIFIER | c.888+879C>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 9/14 | chr9 | 92049081 | ||||||
| chr9:92049085
|
C | T | 35 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0031others(32): Show | 38 | HG00733.hp2 HG01109.hp1 HG01255.hp1 others(35): Show |
intron_variant | MODIFIER | c.888+875G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 9/14 | chr9 | 92049085 | ||||||
| chr9:92049156
|
C | T | 3 | a0001c0001t0001g0274a0001c0001t0001g0275a0001c0001t0001g0289 | 3 | HG02258.hp1 HG02622.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.888+804G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 9/14 | chr9 | 92049156 | ||||||
| chr9:92049188
|
C | T | 1 | a0001c0001t0001g0220 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.888+772G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 9/14 | chr9 | 92049188 | ||||||
| chr9:92049197
|
G | A | 60 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(57): Show | 66 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.888+763C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 9/14 | chr9 | 92049197 | ||||||
| chr9:92049231
|
A | G | 35 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0031others(32): Show | 38 | HG00733.hp2 HG01109.hp1 HG01255.hp1 others(35): Show |
intron_variant | MODIFIER | c.888+729T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 9/14 | chr9 | 92049231 | ||||||
| chr9:92049263
|
G | A | 35 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0031others(32): Show | 38 | HG00733.hp2 HG01109.hp1 HG01255.hp1 others(35): Show |
intron_variant | MODIFIER | c.888+697C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 9/14 | chr9 | 92049263 | ||||||
| chr9:92049474
|
G | T | 1 | a0001c0001t0001g0120 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.888+486C>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 9/14 | chr9 | 92049474 | ||||||
| chr9:92049478
|
T | C | 6 | a0001c0001t0001g0309a0001c0001t0001g0310a0001c0001t0001g0311others(3): Show | 6 | HG02109.hp2 HG02145.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.888+482A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 9/14 | chr9 | 92049478 | ||||||
| chr9:92049508
|
C | A | 60 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(57): Show | 66 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.888+452G>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 9/14 | chr9 | 92049508 | ||||||
| chr9:92049518
|
C | T | 25 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0001g0121others(22): Show | 26 | HG00642.hp2 HG02015.hp2 HG02040.hp2 others(23): Show |
intron_variant | MODIFIER | c.888+442G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 9/14 | chr9 | 92049518 | ||||||
| chr9:92049779
|
G | A | 35 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0031others(32): Show | 38 | HG00733.hp2 HG01109.hp1 HG01255.hp1 others(35): Show |
intron_variant | MODIFIER | c.888+181C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 9/14 | chr9 | 92049779 | ||||||
| chr9:92049786
|
T | C | 1 | a0001c0001t0002g0046 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.888+174A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 9/14 | chr9 | 92049786 | ||||||
| chr9:92049858
|
G | A | 1 | a0002c0003t0003g0062 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.888+102C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 9/14 | chr9 | 92049858 | ||||||
| chr9:92050073
|
T | C | 1 | a0001c0001t0001g0120 | 1 | HG00642.hp2 | splice_region_variant&intron_variant | LOW | c.781-6A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 8/14 | chr9 | 92050073 | ||||||
| chr9:92050217
|
T | C | 3 | a0001c0001t0002g0002a0001c0001t0002g0038a0001c0002t0002g0039 | 5 | HG01346.hp2 HG01358.hp1 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.781-150A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 8/14 | chr9 | 92050217 | ||||||
| chr9:92050248
|
G | A | 1 | a0001c0001t0013g0267 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.781-181C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 8/14 | chr9 | 92050248 | ||||||
| chr9:92050287
|
T | C | 3 | a0001c0001t0001g0274a0001c0001t0001g0275a0001c0001t0001g0289 | 3 | HG02258.hp1 HG02622.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.781-220A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 8/14 | chr9 | 92050287 | ||||||
| chr9:92050307
|
T | C | 1 | a0001c0001t0001g0166 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.781-240A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 8/14 | chr9 | 92050307 | ||||||
| chr9:92050397
|
G | A | 1 | a0001c0001t0014g0261 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.781-330C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 8/14 | chr9 | 92050397 | ||||||
| chr9:92050595
|
A | G | 16 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0182others(13): Show | 18 | HG00438.hp1 HG00558.hp2 HG00621.hp1 others(15): Show |
intron_variant | MODIFIER | c.781-528T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 8/14 | chr9 | 92050595 | ||||||
| chr9:92050678
|
C | G | 1 | a0001c0001t0001g0317 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.781-611G>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 8/14 | chr9 | 92050678 | ||||||
| chr9:92050806
|
T | C | 6 | a0001c0001t0001g0010a0001c0001t0001g0170a0001c0001t0001g0171others(3): Show | 7 | NA18952.hp2 NA18955.hp1 NA18956.hp1 others(4): Show |
intron_variant | MODIFIER | c.781-739A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 8/14 | chr9 | 92050806 | ||||||
| chr9:92050811
|
A | AT | 41 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(38): Show | 50 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.781-745dupA | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 8/14 | chr9 | 92050811 | ||||||
| chr9:92050811
|
A | ATTTTTTT others(7): Show |
1 | a0001c0001t0001g0120 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.781-745_781-744ins others(14): Show |
SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 8/14 | chr9 | 92050811 | ||||||
| chr9:92050811
|
A | ATTTTTTT others(1): Show |
47 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(44): Show | 53 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.781-752_781-745dup others(8): Show |
SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 8/14 | chr9 | 92050811 | ||||||
| chr9:92050811
|
A | ATTTTTTT others(2): Show |
26 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0063others(23): Show | 28 | HG00741.hp1 HG01071.hp1 HG01074.hp2 others(25): Show |
intron_variant | MODIFIER | c.781-753_781-745dup others(9): Show |
SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 8/14 | chr9 | 92050811 | ||||||
| chr9:92050811
|
A | ATTTTTTT others(3): Show |
18 | a0001c0001t0001g0107a0001c0001t0001g0113a0001c0001t0001g0324others(15): Show | 19 | HG00733.hp2 HG01496.hp1 HG02135.hp1 others(16): Show |
intron_variant | MODIFIER | c.781-754_781-745dup others(10): Show |
SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 8/14 | chr9 | 92050811 | ||||||
| chr9:92050811
|
A | ATTTTTTT others(4): Show |
45 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0256others(42): Show | 49 | HG00280.hp1 HG01074.hp1 HG01081.hp1 others(46): Show |
intron_variant | MODIFIER | c.781-755_781-745dup others(11): Show |
SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 8/14 | chr9 | 92050811 | ||||||
| chr9:92050811
|
A | ATTTTTTT others(5): Show |
24 | a0001c0001t0001g0018a0001c0001t0001g0254a0001c0001t0001g0255others(21): Show | 25 | HG00733.hp1 HG01123.hp1 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.781-756_781-745dup others(12): Show |
SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 8/14 | chr9 | 92050811 | ||||||
| chr9:92050811
|
A | ATTTTTTT others(6): Show |
17 | a0001c0001t0001g0009a0001c0001t0001g0140a0001c0001t0001g0141others(14): Show | 18 | HG01099.hp1 HG01243.hp1 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.781-757_781-745dup others(13): Show |
SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 8/14 | chr9 | 92050811 | ||||||
| chr9:92050811
|
A | ATTTTTTT others(7): Show |
11 | a0001c0001t0001g0123a0001c0001t0001g0126a0001c0001t0001g0127others(8): Show | 11 | HG01891.hp1 HG02132.hp1 HG02132.hp2 others(8): Show |
intron_variant | MODIFIER | c.781-758_781-745dup others(14): Show |
SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 8/14 | chr9 | 92050811 | ||||||
| chr9:92050811
|
A | ATTTTTTT others(8): Show |
9 | a0001c0001t0001g0122a0001c0001t0001g0125a0001c0001t0001g0128others(6): Show | 9 | HG02015.hp2 NA18947.hp2 NA18950.hp2 others(6): Show |
intron_variant | MODIFIER | c.781-759_781-745dup others(15): Show |
SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 8/14 | chr9 | 92050811 | ||||||
| chr9:92050811
|
A | ATTTTTTT others(9): Show |
3 | a0001c0001t0001g0121a0001c0001t0001g0124a0001c0001t0001g0137 | 3 | NA18943.hp1 NA18973.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.781-760_781-745dup others(16): Show |
SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 8/14 | chr9 | 92050811 | ||||||
| chr9:92050811
|
A | ATTTTTTT others(10): Show |
2 | a0001c0001t0001g0136a0001c0001t0001g0284 | 2 | HG02040.hp2 NA18953.hp2 |
intron_variant | MODIFIER | c.781-761_781-745dup others(17): Show |
SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 8/14 | chr9 | 92050811 | ||||||
| chr9:92050811
|
A | ATTTTTTT others(11): Show |
1 | a0001c0001t0011g0253 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.781-762_781-745dup others(18): Show |
SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 8/14 | chr9 | 92050811 | ||||||
| chr9:92050862
|
G | C | 1 | a0001c0001t0001g0277 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.781-795C>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 8/14 | chr9 | 92050862 | ||||||
| chr9:92050929
|
C | A | 1 | a0001c0001t0001g0325 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.781-862G>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 8/14 | chr9 | 92050929 | ||||||
| chr9:92050930
|
C | T | 8 | a0001c0001t0003g0019a0001c0001t0003g0262a0001c0001t0003g0263others(5): Show | 9 | HG01074.hp2 HG01516.hp2 HG01517.hp2 others(6): Show |
intron_variant | MODIFIER | c.781-863G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 8/14 | chr9 | 92050930 | ||||||
| chr9:92050931
|
G | A | 1 | a0001c0001t0001g0109 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.781-864C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 8/14 | chr9 | 92050931 | ||||||
| chr9:92051038
|
T | C | 1 | a0001c0001t0002g0252 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.781-971A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 8/14 | chr9 | 92051038 | ||||||
| chr9:92051077
|
C | T | 1 | a0001c0001t0011g0253 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.781-1010G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 8/14 | chr9 | 92051077 | ||||||
| chr9:92051247
|
T | C | 1 | a0001c0001t0001g0268 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.781-1180A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 8/14 | chr9 | 92051247 | ||||||
| chr9:92051249
|
G | C | 1 | a0001c0001t0001g0028 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.781-1182C>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 8/14 | chr9 | 92051249 | ||||||
| chr9:92051405
|
A | T | 1 | a0001c0001t0002g0052 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.781-1338T>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 8/14 | chr9 | 92051405 | ||||||
| chr9:92051421
|
C | T | 1 | a0001c0001t0002g0032 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.781-1354G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 8/14 | chr9 | 92051421 | ||||||
| chr9:92051504
|
A | G | 9 | a0001c0001t0003g0019a0001c0001t0003g0262a0001c0001t0003g0263others(6): Show | 10 | HG01074.hp2 HG01516.hp2 HG01517.hp2 others(7): Show |
intron_variant | MODIFIER | c.781-1437T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 8/14 | chr9 | 92051504 | ||||||
| chr9:92051546
|
C | T | 3 | a0001c0001t0001g0315a0001c0001t0001g0316a0001c0001t0001g0317 | 3 | HG02602.hp2 HG03669.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.781-1479G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 8/14 | chr9 | 92051546 | ||||||
| chr9:92051559
|
G | A | 1 | a0001c0004t0001g0186 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.781-1492C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 8/14 | chr9 | 92051559 | ||||||
| chr9:92051579
|
T | C | 1 | a0001c0001t0001g0214 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.781-1512A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 8/14 | chr9 | 92051579 | ||||||
| chr9:92051696
|
G | C | 1 | a0001c0001t0001g0073 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.781-1629C>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 8/14 | chr9 | 92051696 | ||||||
| chr9:92051937
|
T | C | 70 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(67): Show | 76 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.781-1870A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 8/14 | chr9 | 92051937 | ||||||
| chr9:92051958
|
T | C | 3 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0273 | 3 | HG01891.hp2 HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.781-1891A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 8/14 | chr9 | 92051958 | ||||||
| chr9:92052043
|
G | A | 1 | a0001c0001t0001g0268 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.781-1976C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 8/14 | chr9 | 92052043 | ||||||
| chr9:92052252
|
T | C | 2 | a0001c0001t0001g0274a0001c0001t0001g0275 | 2 | HG02258.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.781-2185A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 8/14 | chr9 | 92052252 | ||||||
| chr9:92052481
|
A | G | 1 | a0002c0003t0003g0062 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.781-2414T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 8/14 | chr9 | 92052481 | ||||||
| chr9:92052486
|
T | C | 9 | a0001c0001t0003g0019a0001c0001t0003g0262a0001c0001t0003g0263others(6): Show | 10 | HG01074.hp2 HG01516.hp2 HG01517.hp2 others(7): Show |
intron_variant | MODIFIER | c.781-2419A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 8/14 | chr9 | 92052486 | ||||||
| chr9:92052521
|
G | GATT | 3 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0273 | 3 | HG01891.hp2 HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.781-2457_781-2455d others(5): Show |
SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 8/14 | chr9 | 92052521 | ||||||
| chr9:92052534
|
A | T | 59 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0120others(56): Show | 61 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(58): Show |
intron_variant | MODIFIER | c.781-2467T>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 8/14 | chr9 | 92052534 | ||||||
| chr9:92052537
|
T | A | 7 | a0001c0001t0001g0076a0001c0001t0001g0271a0001c0001t0001g0272others(4): Show | 7 | HG00323.hp2 HG01891.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.781-2470A>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 8/14 | chr9 | 92052537 | ||||||
| chr9:92052623
|
A | G | 44 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0031others(41): Show | 48 | HG00733.hp2 HG01074.hp2 HG01109.hp1 others(45): Show |
intron_variant | MODIFIER | c.781-2556T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 8/14 | chr9 | 92052623 | ||||||
| chr9:92052675
|
G | A | 4 | a0001c0001t0001g0066a0001c0001t0001g0068a0001c0001t0005g0065others(1): Show | 4 | HG02630.hp2 HG02809.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.781-2608C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 8/14 | chr9 | 92052675 | ||||||
| chr9:92052966
|
A | G | 6 | a0001c0001t0001g0291a0001c0001t0001g0302a0001c0001t0001g0303others(3): Show | 6 | HG02040.hp1 HG02135.hp2 NA18949.hp1 others(3): Show |
intron_variant | MODIFIER | c.780+2439T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 8/14 | chr9 | 92052966 | ||||||
| chr9:92053035
|
T | C | 7 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(4): Show | 7 | HG01081.hp1 HG02258.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.780+2370A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 8/14 | chr9 | 92053035 | ||||||
| chr9:92053071
|
C | G | 38 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0290others(35): Show | 40 | HG00280.hp1 HG00733.hp1 HG01074.hp1 others(37): Show |
intron_variant | MODIFIER | c.780+2334G>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 8/14 | chr9 | 92053071 | ||||||
| chr9:92053084
|
T | G | 1 | a0001c0001t0001g0269 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.780+2321A>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 8/14 | chr9 | 92053084 | ||||||
| chr9:92053130
|
CAAA | C | 25 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0001g0121others(22): Show | 26 | HG00642.hp2 HG02015.hp2 HG02040.hp2 others(23): Show |
intron_variant | MODIFIER | c.780+2272_780+2274d others(5): Show |
SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 8/14 | chr9 | 92053130 | ||||||
| chr9:92053130
|
CAAAA | C | 71 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(68): Show | 77 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.780+2271_780+2274d others(6): Show |
SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 8/14 | chr9 | 92053130 | ||||||
| chr9:92053134
|
A | C | 57 | a0001c0001t0001g0009a0001c0001t0001g0140a0001c0001t0001g0141others(54): Show | 62 | HG00733.hp2 HG01074.hp2 HG01099.hp1 others(59): Show |
intron_variant | MODIFIER | c.780+2271T>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 8/14 | chr9 | 92053134 | ||||||
| chr9:92053312
|
A | G | 115 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(112): Show | 125 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.780+2093T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 8/14 | chr9 | 92053312 | ||||||
| chr9:92053380
|
T | C | 8 | a0001c0001t0003g0019a0001c0001t0003g0262a0001c0001t0003g0263others(5): Show | 9 | HG01074.hp2 HG01516.hp2 HG01517.hp2 others(6): Show |
intron_variant | MODIFIER | c.780+2025A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 8/14 | chr9 | 92053380 | ||||||
| chr9:92053486
|
C | T | 60 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(57): Show | 66 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.780+1919G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 8/14 | chr9 | 92053486 | ||||||
| chr9:92053491
|
G | A | 13 | a0001c0001t0001g0009a0001c0001t0001g0140a0001c0001t0001g0141others(10): Show | 14 | HG01099.hp1 HG01243.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.780+1914C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 8/14 | chr9 | 92053491 | ||||||
| chr9:92053611
|
G | A | 13 | a0001c0001t0001g0009a0001c0001t0001g0140a0001c0001t0001g0141others(10): Show | 14 | HG01099.hp1 HG01243.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.780+1794C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 8/14 | chr9 | 92053611 | ||||||
| chr9:92053875
|
C | G | 67 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(64): Show | 73 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.780+1530G>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 8/14 | chr9 | 92053875 | ||||||
| chr9:92053889
|
T | G | 1 | a0001c0001t0001g0169 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.780+1516A>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 8/14 | chr9 | 92053889 | ||||||
| chr9:92053977
|
T | C | 1 | a0001c0001t0001g0131 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.780+1428A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 8/14 | chr9 | 92053977 | ||||||
| chr9:92054257
|
G | C | 1 | a0001c0001t0011g0253 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.780+1148C>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 8/14 | chr9 | 92054257 | ||||||
| chr9:92054258
|
G | C | 1 | a0001c0001t0002g0057 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.780+1147C>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 8/14 | chr9 | 92054258 | ||||||
| chr9:92054389
|
G | A | 7 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(4): Show | 7 | HG01081.hp1 HG02258.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.780+1016C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 8/14 | chr9 | 92054389 | ||||||
| chr9:92054390
|
C | T | 7 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(4): Show | 7 | HG01081.hp1 HG02258.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.780+1015G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 8/14 | chr9 | 92054390 | ||||||
| chr9:92054393
|
T | C | 1 | a0001c0001t0010g0045 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.780+1012A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 8/14 | chr9 | 92054393 | ||||||
| chr9:92054506
|
G | A | 4 | a0001c0001t0002g0002a0001c0001t0002g0038a0001c0001t0010g0045others(1): Show | 6 | HG00733.hp2 HG01346.hp2 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.780+899C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 8/14 | chr9 | 92054506 | ||||||
| chr9:92054590
|
C | T | 25 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0001g0121others(22): Show | 26 | HG00642.hp2 HG02015.hp2 HG02040.hp2 others(23): Show |
intron_variant | MODIFIER | c.780+815G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 8/14 | chr9 | 92054590 | ||||||
| chr9:92054637
|
C | T | 5 | a0001c0001t0003g0019a0001c0001t0003g0262a0001c0001t0003g0263others(2): Show | 6 | HG01074.hp2 HG01516.hp2 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.780+768G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 8/14 | chr9 | 92054637 | ||||||
| chr9:92054648
|
C | T | 13 | a0001c0001t0001g0009a0001c0001t0001g0140a0001c0001t0001g0141others(10): Show | 14 | HG01099.hp1 HG01243.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.780+757G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 8/14 | chr9 | 92054648 | ||||||
| chr9:92054781
|
C | T | 1 | a0003c0007t0001g0286 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.780+624G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 8/14 | chr9 | 92054781 | ||||||
| chr9:92054782
|
G | A | 1 | a0001c0001t0001g0209 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.780+623C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 8/14 | chr9 | 92054782 | ||||||
| chr9:92054805
|
C | T | 9 | a0001c0001t0003g0019a0001c0001t0003g0262a0001c0001t0003g0263others(6): Show | 10 | HG01074.hp2 HG01516.hp2 HG01517.hp2 others(7): Show |
intron_variant | MODIFIER | c.780+600G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 8/14 | chr9 | 92054805 | ||||||
| chr9:92054806
|
G | A | 6 | a0001c0001t0001g0020a0001c0001t0001g0063a0001c0001t0001g0064others(3): Show | 7 | HG01081.hp2 HG02257.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.780+599C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 8/14 | chr9 | 92054806 | ||||||
| chr9:92054839
|
G | A | 1 | a0001c0001t0001g0120 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.780+566C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 8/14 | chr9 | 92054839 | ||||||
| chr9:92054845
|
G | A | 35 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0031others(32): Show | 38 | HG00733.hp2 HG01109.hp1 HG01255.hp1 others(35): Show |
intron_variant | MODIFIER | c.780+560C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 8/14 | chr9 | 92054845 | ||||||
| chr9:92054849
|
T | A | 60 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(57): Show | 66 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.780+556A>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 8/14 | chr9 | 92054849 | ||||||
| chr9:92054916
|
AG | A | 8 | a0001c0001t0003g0019a0001c0001t0003g0262a0001c0001t0003g0263others(5): Show | 9 | HG01074.hp2 HG01516.hp2 HG01517.hp2 others(6): Show |
intron_variant | MODIFIER | c.780+488delC | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 8/14 | chr9 | 92054916 | ||||||
| chr9:92054917
|
G | A | 158 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(155): Show | 170 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(167): Show |
intron_variant | MODIFIER | c.780+488C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 8/14 | chr9 | 92054917 | ||||||
| chr9:92055259
|
C | G | 1 | a0001c0001t0001g0212 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.780+146G>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 8/14 | chr9 | 92055259 | ||||||
| chr9:92055313
|
G | A | 13 | a0001c0001t0001g0009a0001c0001t0001g0140a0001c0001t0001g0141others(10): Show | 14 | HG01099.hp1 HG01243.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.780+92C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 8/14 | chr9 | 92055313 | ||||||
| chr9:92055600
|
AT | A | 6 | a0001c0001t0001g0193a0001c0001t0001g0195a0001c0001t0001g0212others(3): Show | 6 | HG00642.hp1 HG01069.hp2 HG01109.hp2 others(3): Show |
intron_variant | MODIFIER | c.691-107delA | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 7/14 | chr9 | 92055600 | ||||||
| chr9:92055677
|
C | T | 5 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0142others(2): Show | 5 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.691-183G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 7/14 | chr9 | 92055677 | ||||||
| chr9:92055806
|
A | G | 9 | a0001c0001t0003g0019a0001c0001t0003g0262a0001c0001t0003g0263others(6): Show | 10 | HG01074.hp2 HG01516.hp2 HG01517.hp2 others(7): Show |
intron_variant | MODIFIER | c.691-312T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 7/14 | chr9 | 92055806 | ||||||
| chr9:92055935
|
T | C | 1 | a0001c0001t0008g0319 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.691-441A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 7/14 | chr9 | 92055935 | ||||||
| chr9:92056022
|
C | A | 5 | a0001c0001t0001g0291a0001c0001t0001g0302a0001c0001t0001g0303others(2): Show | 5 | HG02135.hp2 NA18949.hp1 NA18972.hp1 others(2): Show |
intron_variant | MODIFIER | c.691-528G>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 7/14 | chr9 | 92056022 | ||||||
| chr9:92056027
|
G | T | 1 | a0001c0001t0001g0302 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.691-533C>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 7/14 | chr9 | 92056027 | ||||||
| chr9:92056086
|
T | G | 6 | a0001c0001t0001g0020a0001c0001t0001g0063a0001c0001t0001g0064others(3): Show | 7 | HG01081.hp2 HG02257.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.691-592A>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 7/14 | chr9 | 92056086 | ||||||
| chr9:92056101
|
C | T | 1 | a0001c0004t0001g0186 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.691-607G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 7/14 | chr9 | 92056101 | ||||||
| chr9:92056270
|
C | T | 1 | a0001c0006t0001g0300 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.691-776G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 7/14 | chr9 | 92056270 | ||||||
| chr9:92056304
|
G | T | 34 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0031others(31): Show | 37 | HG00733.hp2 HG01109.hp1 HG01255.hp1 others(34): Show |
intron_variant | MODIFIER | c.691-810C>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 7/14 | chr9 | 92056304 | ||||||
| chr9:92056349
|
C | T | 13 | a0001c0001t0001g0009a0001c0001t0001g0140a0001c0001t0001g0141others(10): Show | 14 | HG01099.hp1 HG01243.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.691-855G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 7/14 | chr9 | 92056349 | ||||||
| chr9:92056378
|
G | A | 6 | a0001c0001t0001g0010a0001c0001t0001g0170a0001c0001t0001g0171others(3): Show | 7 | NA18952.hp2 NA18955.hp1 NA18956.hp1 others(4): Show |
intron_variant | MODIFIER | c.691-884C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 7/14 | chr9 | 92056378 | ||||||
| chr9:92056477
|
C | T | 2 | a0001c0001t0001g0085a0001c0001t0001g0088 | 2 | NA18959.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.691-983G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 7/14 | chr9 | 92056477 | ||||||
| chr9:92056497
|
A | G | 3 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0273 | 3 | HG01891.hp2 HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.691-1003T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 7/14 | chr9 | 92056497 | ||||||
| chr9:92056504
|
C | T | 1 | a0001c0001t0001g0211 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.691-1010G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 7/14 | chr9 | 92056504 | ||||||
| chr9:92056610
|
A | G | 2 | a0001c0001t0001g0294a0001c0001t0001g0295 | 2 | HG00280.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.691-1116T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 7/14 | chr9 | 92056610 | ||||||
| chr9:92056777
|
C | A | 8 | a0001c0001t0003g0019a0001c0001t0003g0262a0001c0001t0003g0263others(5): Show | 9 | HG01074.hp2 HG01516.hp2 HG01517.hp2 others(6): Show |
intron_variant | MODIFIER | c.691-1283G>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 7/14 | chr9 | 92056777 | ||||||
| chr9:92056805
|
T | C | 7 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(4): Show | 7 | HG01081.hp1 HG02258.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.691-1311A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 7/14 | chr9 | 92056805 | ||||||
| chr9:92056808
|
T | C | 1 | a0002c0003t0003g0062 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.691-1314A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 7/14 | chr9 | 92056808 | ||||||
| chr9:92056809
|
TGAG | T | 7 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(4): Show | 7 | HG01081.hp1 HG02258.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.691-1318_691-1316d others(5): Show |
SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 7/14 | chr9 | 92056809 | ||||||
| chr9:92057229
|
T | G | 1 | a0001c0001t0001g0193 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.691-1735A>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 7/14 | chr9 | 92057229 | ||||||
| chr9:92057263
|
T | C | 6 | a0001c0001t0001g0020a0001c0001t0001g0063a0001c0001t0001g0064others(3): Show | 7 | HG01081.hp2 HG02257.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.691-1769A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 7/14 | chr9 | 92057263 | ||||||
| chr9:92057280
|
TG | T | 3 | a0001c0001t0001g0020a0001c0001t0001g0063a0001c0001t0001g0064 | 4 | HG01081.hp2 HG02895.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.691-1787delC | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 7/14 | chr9 | 92057280 | ||||||
| chr9:92057692
|
G | A | 8 | a0001c0001t0003g0019a0001c0001t0003g0262a0001c0001t0003g0263others(5): Show | 9 | HG01074.hp2 HG01516.hp2 HG01517.hp2 others(6): Show |
intron_variant | MODIFIER | c.690+1487C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 7/14 | chr9 | 92057692 | ||||||
| chr9:92057848
|
A | T | 25 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0001g0121others(22): Show | 26 | HG00642.hp2 HG02015.hp2 HG02040.hp2 others(23): Show |
intron_variant | MODIFIER | c.690+1331T>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 7/14 | chr9 | 92057848 | ||||||
| chr9:92057912
|
A | G | 1 | a0001c0001t0002g0034 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.690+1267T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 7/14 | chr9 | 92057912 | ||||||
| chr9:92058070
|
A | C | 6 | a0001c0001t0001g0020a0001c0001t0001g0063a0001c0001t0001g0064others(3): Show | 7 | HG01081.hp2 HG02257.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.690+1109T>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 7/14 | chr9 | 92058070 | ||||||
| chr9:92058110
|
T | C | 1 | a0001c0001t0001g0268 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.690+1069A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 7/14 | chr9 | 92058110 | ||||||
| chr9:92058164
|
T | C | 207 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(204): Show | 222 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(219): Show |
intron_variant | MODIFIER | c.690+1015A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 7/14 | chr9 | 92058164 | ||||||
| chr9:92058419
|
G | C | 9 | a0001c0001t0003g0019a0001c0001t0003g0262a0001c0001t0003g0263others(6): Show | 10 | HG01074.hp2 HG01516.hp2 HG01517.hp2 others(7): Show |
intron_variant | MODIFIER | c.690+760C>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 7/14 | chr9 | 92058419 | ||||||
| chr9:92058427
|
GA | G | 35 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0031others(32): Show | 38 | HG00733.hp2 HG01109.hp1 HG01255.hp1 others(35): Show |
intron_variant | MODIFIER | c.690+751delT | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 7/14 | chr9 | 92058427 | ||||||
| chr9:92058518
|
A | C | 1 | a0001c0001t0001g0193 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.690+661T>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 7/14 | chr9 | 92058518 | ||||||
| chr9:92058611
|
C | T | 206 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(203): Show | 221 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(218): Show |
intron_variant | MODIFIER | c.690+568G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 7/14 | chr9 | 92058611 | ||||||
| chr9:92058911
|
A | G | 1 | a0001c0001t0001g0137 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.690+268T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 7/14 | chr9 | 92058911 | ||||||
| chr9:92058950
|
A | G | 1 | a0001c0001t0001g0311 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.690+229T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 7/14 | chr9 | 92058950 | ||||||
| chr9:92058955
|
C | A | 1 | a0001c0001t0001g0084 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.690+224G>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 7/14 | chr9 | 92058955 | ||||||
| chr9:92058975
|
T | C | 38 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0290others(35): Show | 40 | HG00280.hp1 HG00733.hp1 HG01074.hp1 others(37): Show |
intron_variant | MODIFIER | c.690+204A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 7/14 | chr9 | 92058975 | ||||||
| chr9:92059035
|
C | T | 2 | a0001c0001t0006g0307a0001c0001t0007g0308 | 2 | HG00733.hp1 HG01257.hp1 |
intron_variant | MODIFIER | c.690+144G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 7/14 | chr9 | 92059035 | ||||||
| chr9:92059037
|
A | AAGT | 3 | a0001c0001t0001g0274a0001c0001t0001g0275a0001c0001t0001g0289 | 3 | HG02258.hp1 HG02622.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.690+139_690+141dup others(3): Show |
SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 7/14 | chr9 | 92059037 | ||||||
| chr9:92059116
|
T | G | 26 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0001g0121others(23): Show | 27 | HG00642.hp2 HG02015.hp2 HG02040.hp2 others(24): Show |
intron_variant | MODIFIER | c.690+63A>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 7/14 | chr9 | 92059116 | ||||||
| chr9:92059384
|
G | C | 9 | a0001c0001t0003g0019a0001c0001t0003g0262a0001c0001t0003g0263others(6): Show | 10 | HG01074.hp2 HG01516.hp2 HG01517.hp2 others(7): Show |
intron_variant | MODIFIER | c.561-76C>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92059384 | ||||||
| chr9:92059400
|
C | G | 1 | a0001c0001t0001g0116 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.561-92G>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92059400 | ||||||
| chr9:92059579
|
A | G | 67 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(64): Show | 73 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.561-271T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92059579 | ||||||
| chr9:92059598
|
C | T | 1 | a0001c0001t0001g0231 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.561-290G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92059598 | ||||||
| chr9:92059705
|
C | T | 1 | a0001c0001t0001g0235 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.561-397G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92059705 | ||||||
| chr9:92059745
|
A | G | 3 | a0001c0001t0001g0274a0001c0001t0001g0275a0001c0001t0001g0289 | 3 | HG02258.hp1 HG02622.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.561-437T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92059745 | ||||||
| chr9:92059800
|
T | C | 1 | a0002c0003t0003g0062 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.561-492A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92059800 | ||||||
| chr9:92059864
|
A | C | 127 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(124): Show | 138 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(135): Show |
intron_variant | MODIFIER | c.561-556T>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92059864 | ||||||
| chr9:92059919
|
A | G | 11 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0194others(8): Show | 13 | HG00597.hp1 HG00673.hp1 HG02074.hp1 others(10): Show |
intron_variant | MODIFIER | c.561-611T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92059919 | ||||||
| chr9:92059978
|
G | A | 25 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0001g0121others(22): Show | 26 | HG00642.hp2 HG02015.hp2 HG02040.hp2 others(23): Show |
intron_variant | MODIFIER | c.561-670C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92059978 | ||||||
| chr9:92059996
|
C | T | 9 | a0001c0001t0003g0019a0001c0001t0003g0262a0001c0001t0003g0263others(6): Show | 10 | HG01074.hp2 HG01516.hp2 HG01517.hp2 others(7): Show |
intron_variant | MODIFIER | c.561-688G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92059996 | ||||||
| chr9:92060009
|
G | A | 1 | a0001c0001t0001g0120 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.561-701C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92060009 | ||||||
| chr9:92060029
|
C | A | 2 | a0001c0001t0001g0318a0001c0001t0008g0319 | 2 | HG02055.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.561-721G>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92060029 | ||||||
| chr9:92060127
|
C | T | 34 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0031others(31): Show | 37 | HG00733.hp2 HG01109.hp1 HG01255.hp1 others(34): Show |
intron_variant | MODIFIER | c.561-819G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92060127 | ||||||
| chr9:92060131
|
T | G | 1 | a0001c0001t0001g0130 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.561-823A>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92060131 | ||||||
| chr9:92060136
|
C | G | 34 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0031others(31): Show | 37 | HG00733.hp2 HG01109.hp1 HG01255.hp1 others(34): Show |
intron_variant | MODIFIER | c.561-828G>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92060136 | ||||||
| chr9:92060165
|
T | C | 8 | a0001c0001t0003g0019a0001c0001t0003g0262a0001c0001t0003g0263others(5): Show | 9 | HG01074.hp2 HG01516.hp2 HG01517.hp2 others(6): Show |
intron_variant | MODIFIER | c.561-857A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92060165 | ||||||
| chr9:92060184
|
C | T | 1 | a0001c0001t0001g0268 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.561-876G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92060184 | ||||||
| chr9:92060258
|
G | A | 114 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(111): Show | 124 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(121): Show |
intron_variant | MODIFIER | c.561-950C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92060258 | ||||||
| chr9:92060279
|
G | C | 1 | a0002c0003t0003g0062 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.561-971C>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92060279 | ||||||
| chr9:92060402
|
G | A | 2 | a0001c0001t0001g0318a0001c0001t0008g0319 | 2 | HG02055.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.561-1094C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92060402 | ||||||
| chr9:92060501
|
A | G | 44 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0031others(41): Show | 48 | HG00733.hp2 HG01074.hp2 HG01109.hp1 others(45): Show |
intron_variant | MODIFIER | c.561-1193T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92060501 | ||||||
| chr9:92060506
|
T | C | 1 | a0001c0001t0001g0188 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.561-1198A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92060506 | ||||||
| chr9:92060607
|
T | C | 22 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0123others(19): Show | 22 | HG02015.hp2 HG02040.hp2 HG02132.hp1 others(19): Show |
intron_variant | MODIFIER | c.561-1299A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92060607 | ||||||
| chr9:92060633
|
G | A | 34 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0031others(31): Show | 37 | HG00733.hp2 HG01109.hp1 HG01255.hp1 others(34): Show |
intron_variant | MODIFIER | c.561-1325C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92060633 | ||||||
| chr9:92060722
|
T | C | 1 | a0001c0001t0001g0283 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.561-1414A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92060722 | ||||||
| chr9:92060743
|
TA | T | 29 | a0001c0001t0001g0006a0001c0001t0001g0023a0001c0001t0001g0024others(26): Show | 30 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(27): Show |
intron_variant | MODIFIER | c.561-1436delT | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92060743 | ||||||
| chr9:92060790
|
G | T | 25 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0001g0121others(22): Show | 26 | HG00642.hp2 HG02015.hp2 HG02040.hp2 others(23): Show |
intron_variant | MODIFIER | c.561-1482C>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92060790 | ||||||
| chr9:92060805
|
C | A | 1 | a0003c0007t0001g0286 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.561-1497G>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92060805 | ||||||
| chr9:92060806
|
G | A | 1 | a0001c0001t0001g0268 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.561-1498C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92060806 | ||||||
| chr9:92060825
|
A | G | 1 | a0001c0001t0001g0159 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.561-1517T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92060825 | ||||||
| chr9:92060837
|
C | T | 3 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0053 | 3 | HG01255.hp1 HG02723.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.561-1529G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92060837 | ||||||
| chr9:92060845
|
G | A | 70 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(67): Show | 76 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.561-1537C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92060845 | ||||||
| chr9:92060870
|
G | A | 1 | a0001c0001t0001g0220 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.561-1562C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92060870 | ||||||
| chr9:92060900
|
G | A | 1 | a0002c0003t0003g0062 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.561-1592C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92060900 | ||||||
| chr9:92060912
|
C | CA | 53 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0064others(50): Show | 56 | HG00280.hp1 HG00733.hp1 HG01074.hp1 others(53): Show |
intron_variant | MODIFIER | c.561-1605dupT | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92060912 | ||||||
| chr9:92060912
|
CAA | C | 35 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0031others(32): Show | 38 | HG00733.hp2 HG01109.hp1 HG01255.hp1 others(35): Show |
intron_variant | MODIFIER | c.561-1606_561-1605d others(4): Show |
SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92060912 | ||||||
| chr9:92060997
|
C | T | 1 | a0001c0001t0001g0110 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.561-1689G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92060997 | ||||||
| chr9:92061041
|
T | C | 7 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(4): Show | 7 | HG01081.hp1 HG02258.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.561-1733A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92061041 | ||||||
| chr9:92061167
|
T | A | 3 | a0001c0001t0001g0020a0001c0001t0001g0063a0001c0001t0001g0064 | 4 | HG01081.hp2 HG02895.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.561-1859A>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92061167 | ||||||
| chr9:92061193
|
C | T | 13 | a0001c0001t0001g0009a0001c0001t0001g0140a0001c0001t0001g0141others(10): Show | 14 | HG01099.hp1 HG01243.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.561-1885G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92061193 | ||||||
| chr9:92061567
|
G | A | 35 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0031others(32): Show | 38 | HG00733.hp2 HG01109.hp1 HG01255.hp1 others(35): Show |
intron_variant | MODIFIER | c.561-2259C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92061567 | ||||||
| chr9:92061686
|
T | A | 1 | a0002c0003t0003g0062 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.561-2378A>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92061686 | ||||||
| chr9:92061985
|
C | CA | 6 | a0001c0001t0001g0010a0001c0001t0001g0170a0001c0001t0001g0171others(3): Show | 7 | NA18952.hp2 NA18955.hp1 NA18956.hp1 others(4): Show |
intron_variant | MODIFIER | c.561-2678_561-2677i others(3): Show |
SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92061985 | ||||||
| chr9:92061986
|
T | G | 6 | a0001c0001t0001g0010a0001c0001t0001g0170a0001c0001t0001g0171others(3): Show | 7 | NA18952.hp2 NA18955.hp1 NA18956.hp1 others(4): Show |
intron_variant | MODIFIER | c.561-2678A>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92061986 | ||||||
| chr9:92062185
|
C | T | 35 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0031others(32): Show | 38 | HG00733.hp2 HG01109.hp1 HG01255.hp1 others(35): Show |
intron_variant | MODIFIER | c.561-2877G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92062185 | ||||||
| chr9:92062287
|
C | T | 8 | a0001c0001t0001g0009a0001c0001t0001g0145a0001c0001t0001g0146others(5): Show | 9 | HG01099.hp1 HG01243.hp1 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.561-2979G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92062287 | ||||||
| chr9:92062468
|
C | T | 157 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(154): Show | 170 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(167): Show |
intron_variant | MODIFIER | c.561-3160G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92062468 | ||||||
| chr9:92062477
|
C | T | 1 | a0001c0001t0004g0119 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.561-3169G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92062477 | ||||||
| chr9:92062479
|
A | C | 8 | a0001c0001t0003g0019a0001c0001t0003g0262a0001c0001t0003g0263others(5): Show | 9 | HG01074.hp2 HG01516.hp2 HG01517.hp2 others(6): Show |
intron_variant | MODIFIER | c.561-3171T>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92062479 | ||||||
| chr9:92062887
|
G | A | 1 | a0001c0001t0001g0318 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.561-3579C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92062887 | ||||||
| chr9:92063018
|
T | C | 6 | a0001c0001t0001g0020a0001c0001t0001g0063a0001c0001t0001g0064others(3): Show | 7 | HG01081.hp2 HG02257.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.561-3710A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92063018 | ||||||
| chr9:92063218
|
A | C | 35 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0031others(32): Show | 38 | HG00733.hp2 HG01109.hp1 HG01255.hp1 others(35): Show |
intron_variant | MODIFIER | c.561-3910T>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92063218 | ||||||
| chr9:92063383
|
C | A | 57 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(54): Show | 63 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.561-4075G>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92063383 | ||||||
| chr9:92063565
|
T | C | 1 | a0001c0001t0001g0268 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.561-4257A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92063565 | ||||||
| chr9:92063641
|
A | C | 1 | a0001c0001t0003g0266 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.560+4325T>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92063641 | ||||||
| chr9:92063754
|
A | C | 3 | a0001c0001t0002g0002a0001c0001t0002g0038a0001c0002t0002g0039 | 5 | HG01346.hp2 HG01358.hp1 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.560+4212T>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92063754 | ||||||
| chr9:92063807
|
C | A | 22 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0123others(19): Show | 22 | HG02015.hp2 HG02040.hp2 HG02132.hp1 others(19): Show |
intron_variant | MODIFIER | c.560+4159G>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92063807 | ||||||
| chr9:92063814
|
T | C | 32 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0290others(29): Show | 34 | HG00280.hp1 HG00733.hp1 HG01074.hp1 others(31): Show |
intron_variant | MODIFIER | c.560+4152A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92063814 | ||||||
| chr9:92063875
|
A | T | 26 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0032others(23): Show | 29 | HG00733.hp2 HG01109.hp1 HG01255.hp1 others(26): Show |
intron_variant | MODIFIER | c.560+4091T>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92063875 | ||||||
| chr9:92063926
|
G | A | 22 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0123others(19): Show | 22 | HG02015.hp2 HG02040.hp2 HG02132.hp1 others(19): Show |
intron_variant | MODIFIER | c.560+4040C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92063926 | ||||||
| chr9:92064043
|
AAAAT | A | 4 | a0001c0001t0001g0066a0001c0001t0001g0068a0001c0001t0005g0065others(1): Show | 4 | HG02630.hp2 HG02809.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.560+3919_560+3922d others(6): Show |
SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92064043 | ||||||
| chr9:92064183
|
C | T | 157 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(154): Show | 170 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(167): Show |
intron_variant | MODIFIER | c.560+3783G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92064183 | ||||||
| chr9:92064212
|
G | A | 2 | a0001c0001t0001g0318a0001c0001t0008g0319 | 2 | HG02055.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.560+3754C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92064212 | ||||||
| chr9:92064264
|
T | C | 1 | a0001c0001t0001g0226 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.560+3702A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92064264 | ||||||
| chr9:92064331
|
C | T | 1 | a0001c0001t0002g0046 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.560+3635G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92064331 | ||||||
| chr9:92064652
|
C | T | 40 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0290others(37): Show | 42 | HG00280.hp1 HG00733.hp1 HG01074.hp1 others(39): Show |
intron_variant | MODIFIER | c.560+3314G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92064652 | ||||||
| chr9:92064749
|
T | C | 26 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0001g0121others(23): Show | 27 | HG00642.hp2 HG02015.hp2 HG02040.hp2 others(24): Show |
intron_variant | MODIFIER | c.560+3217A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92064749 | ||||||
| chr9:92064829
|
C | T | 7 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(4): Show | 7 | HG01081.hp1 HG02258.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.560+3137G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92064829 | ||||||
| chr9:92064830
|
G | A | 1 | a0002c0003t0003g0062 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.560+3136C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92064830 | ||||||
| chr9:92064912
|
A | C | 1 | a0001c0001t0004g0119 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.560+3054T>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92064912 | ||||||
| chr9:92064956
|
A | G | 1 | a0001c0001t0001g0112 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.560+3010T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92064956 | ||||||
| chr9:92065083
|
A | G | 3 | a0001c0001t0001g0274a0001c0001t0001g0275a0001c0001t0001g0289 | 3 | HG02258.hp1 HG02622.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.560+2883T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92065083 | ||||||
| chr9:92065182
|
T | C | 13 | a0001c0001t0001g0009a0001c0001t0001g0140a0001c0001t0001g0141others(10): Show | 14 | HG01099.hp1 HG01243.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.560+2784A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92065182 | ||||||
| chr9:92065364
|
A | T | 2 | a0001c0001t0004g0117a0001c0001t0004g0118 | 2 | HG02615.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.560+2602T>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92065364 | ||||||
| chr9:92065602
|
A | G | 1 | a0001c0001t0001g0190 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.560+2364T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92065602 | ||||||
| chr9:92065709
|
C | T | 1 | a0002c0003t0003g0062 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.560+2257G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92065709 | ||||||
| chr9:92065789
|
CACATTAG | C | 3 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0259 | 3 | HG02723.hp1 HG02965.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.560+2170_560+2176d others(9): Show |
SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92065789 | ||||||
| chr9:92066056
|
C | T | 13 | a0001c0001t0001g0009a0001c0001t0001g0140a0001c0001t0001g0141others(10): Show | 14 | HG01099.hp1 HG01243.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.560+1910G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92066056 | ||||||
| chr9:92066182
|
G | A | 1 | a0001c0001t0001g0131 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.560+1784C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92066182 | ||||||
| chr9:92066225
|
G | A | 13 | a0001c0001t0001g0009a0001c0001t0001g0140a0001c0001t0001g0141others(10): Show | 14 | HG01099.hp1 HG01243.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.560+1741C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92066225 | ||||||
| chr9:92066238
|
T | C | 1 | a0003c0007t0001g0286 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.560+1728A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92066238 | ||||||
| chr9:92066258
|
G | A | 4 | a0001c0001t0002g0035a0001c0001t0002g0036a0001c0001t0002g0037others(1): Show | 4 | HG01109.hp1 HG02145.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.560+1708C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92066258 | ||||||
| chr9:92066271
|
G | A | 2 | a0001c0001t0002g0033a0001c0001t0002g0252 | 2 | NA18988.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.560+1695C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92066271 | ||||||
| chr9:92066336
|
C | G | 1 | a0001c0001t0001g0280 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.560+1630G>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92066336 | ||||||
| chr9:92066381
|
C | T | 1 | a0001c0001t0001g0235 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.560+1585G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92066381 | ||||||
| chr9:92066468
|
G | A | 1 | a0001c0001t0001g0283 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.560+1498C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92066468 | ||||||
| chr9:92066525
|
G | C | 1 | a0001c0001t0001g0268 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.560+1441C>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92066525 | ||||||
| chr9:92066690
|
AT | A | 5 | a0001c0001t0001g0010a0001c0001t0001g0171a0001c0001t0001g0173others(2): Show | 6 | NA18952.hp2 NA18955.hp1 NA18956.hp1 others(3): Show |
intron_variant | MODIFIER | c.560+1275delA | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92066690 | ||||||
| chr9:92066745
|
A | G | 205 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(202): Show | 220 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(217): Show |
intron_variant | MODIFIER | c.560+1221T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92066745 | ||||||
| chr9:92066874
|
A | G | 159 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(156): Show | 172 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(169): Show |
intron_variant | MODIFIER | c.560+1092T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92066874 | ||||||
| chr9:92067026
|
G | A | 67 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(64): Show | 73 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.560+940C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92067026 | ||||||
| chr9:92067115
|
C | T | 1 | a0001c0001t0001g0222 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.560+851G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92067115 | ||||||
| chr9:92067180
|
T | A | 1 | a0002c0003t0003g0062 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.560+786A>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92067180 | ||||||
| chr9:92067192
|
A | G | 44 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0031others(41): Show | 48 | HG00733.hp2 HG01074.hp2 HG01109.hp1 others(45): Show |
intron_variant | MODIFIER | c.560+774T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92067192 | ||||||
| chr9:92067255
|
C | T | 67 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(64): Show | 73 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.560+711G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92067255 | ||||||
| chr9:92067304
|
C | CA | 13 | a0001c0001t0001g0027a0001c0001t0001g0084a0001c0001t0001g0155others(10): Show | 13 | HG00438.hp1 HG00438.hp2 HG02056.hp1 others(10): Show |
intron_variant | MODIFIER | c.560+661dupT | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92067304 | ||||||
| chr9:92067305
|
A | AC | 38 | a0001c0001t0001g0128a0001c0001t0001g0271a0001c0001t0001g0272others(35): Show | 41 | HG00733.hp2 HG01109.hp1 HG01255.hp1 others(38): Show |
intron_variant | MODIFIER | c.560+660_560+661ins others(1): Show |
SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92067305 | ||||||
| chr9:92067306
|
A | C | 32 | a0001c0001t0001g0010a0001c0001t0001g0018a0001c0001t0001g0109others(29): Show | 34 | HG00642.hp2 HG02015.hp2 HG02040.hp2 others(31): Show |
intron_variant | MODIFIER | c.560+660T>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92067306 | ||||||
| chr9:92067307
|
A | C | 2 | a0001c0001t0001g0128a0001c0001t0001g0284 | 2 | NA18950.hp2 NA18953.hp2 |
intron_variant | MODIFIER | c.560+659T>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92067307 | ||||||
| chr9:92067308
|
A | C | 23 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0001g0121others(20): Show | 24 | HG00642.hp2 HG02015.hp2 HG02040.hp2 others(21): Show |
intron_variant | MODIFIER | c.560+658T>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92067308 | ||||||
| chr9:92067314
|
A | C | 2 | a0001c0001t0001g0232a0001c0001t0001g0233 | 2 | HG02083.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.560+652T>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92067314 | ||||||
| chr9:92067318
|
AC | A | 7 | a0001c0001t0001g0066a0001c0001t0001g0068a0001c0001t0001g0274others(4): Show | 7 | HG02258.hp1 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.560+647delG | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92067318 | ||||||
| chr9:92067319
|
C | A | 60 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(57): Show | 66 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.560+647G>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92067319 | ||||||
| chr9:92067321
|
G | C | 67 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(64): Show | 73 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.560+645C>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92067321 | ||||||
| chr9:92067372
|
G | A | 67 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(64): Show | 73 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.560+594C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92067372 | ||||||
| chr9:92067431
|
G | A | 4 | a0001c0001t0001g0066a0001c0001t0001g0068a0001c0001t0005g0065others(1): Show | 4 | HG02630.hp2 HG02809.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.560+535C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92067431 | ||||||
| chr9:92067431
|
G | T | 1 | a0002c0003t0003g0062 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.560+535C>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92067431 | ||||||
| chr9:92067525
|
G | C | 2 | a0001c0001t0001g0271a0001c0001t0001g0272 | 2 | HG01891.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.560+441C>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92067525 | ||||||
| chr9:92067623
|
G | A | 60 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(57): Show | 66 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.560+343C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92067623 | ||||||
| chr9:92067848
|
T | C | 1 | a0002c0003t0003g0062 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.560+118A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92067848 | ||||||
| chr9:92067950
|
C | G | 44 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0031others(41): Show | 48 | HG00733.hp2 HG01074.hp2 HG01109.hp1 others(45): Show |
intron_variant | MODIFIER | c.560+16G>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92067950 | ||||||
| chr9:92068364
|
A | G | 3 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0273 | 3 | HG01891.hp2 HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.428-266T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92068364 | ||||||
| chr9:92068525
|
A | G | 2 | a0001c0001t0001g0017a0001c0001t0001g0244 | 3 | NA18975.hp1 NA18992.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.428-427T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92068525 | ||||||
| chr9:92068580
|
T | C | 26 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0032others(23): Show | 29 | HG00733.hp2 HG01109.hp1 HG01255.hp1 others(26): Show |
intron_variant | MODIFIER | c.428-482A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92068580 | ||||||
| chr9:92068594
|
A | G | 25 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0001g0121others(22): Show | 26 | HG00642.hp2 HG02015.hp2 HG02040.hp2 others(23): Show |
intron_variant | MODIFIER | c.428-496T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92068594 | ||||||
| chr9:92068692
|
T | C | 156 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(153): Show | 169 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(166): Show |
intron_variant | MODIFIER | c.428-594A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92068692 | ||||||
| chr9:92068817
|
T | C | 1 | a0001c0001t0014g0261 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.428-719A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92068817 | ||||||
| chr9:92068824
|
G | A | 3 | a0001c0001t0001g0315a0001c0001t0001g0316a0001c0001t0001g0317 | 3 | HG02602.hp2 HG03669.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.428-726C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92068824 | ||||||
| chr9:92068889
|
A | C | 1 | a0001c0001t0001g0287 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.428-791T>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92068889 | ||||||
| chr9:92068957
|
A | C | 8 | a0001c0001t0003g0019a0001c0001t0003g0262a0001c0001t0003g0263others(5): Show | 9 | HG01074.hp2 HG01516.hp2 HG01517.hp2 others(6): Show |
intron_variant | MODIFIER | c.428-859T>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92068957 | ||||||
| chr9:92069058
|
G | C | 1 | a0001c0001t0001g0268 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.428-960C>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92069058 | ||||||
| chr9:92069229
|
T | C | 206 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(203): Show | 221 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(218): Show |
intron_variant | MODIFIER | c.428-1131A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92069229 | ||||||
| chr9:92069432
|
G | A | 1 | a0002c0003t0003g0062 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.428-1334C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92069432 | ||||||
| chr9:92069449
|
C | A | 1 | a0002c0003t0003g0062 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.428-1351G>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92069449 | ||||||
| chr9:92069531
|
G | A | 1 | a0001c0001t0001g0268 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.428-1433C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92069531 | ||||||
| chr9:92069573
|
A | G | 35 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0031others(32): Show | 38 | HG00733.hp2 HG01109.hp1 HG01255.hp1 others(35): Show |
intron_variant | MODIFIER | c.428-1475T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92069573 | ||||||
| chr9:92069701
|
A | T | 3 | a0001c0001t0001g0020a0001c0001t0001g0063a0001c0001t0001g0064 | 4 | HG01081.hp2 HG02895.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.428-1603T>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92069701 | ||||||
| chr9:92069743
|
T | C | 3 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0273 | 3 | HG01891.hp2 HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.428-1645A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92069743 | ||||||
| chr9:92069761
|
G | A | 114 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(111): Show | 124 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(121): Show |
intron_variant | MODIFIER | c.428-1663C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92069761 | ||||||
| chr9:92070263
|
T | C | 7 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(4): Show | 7 | HG01081.hp1 HG02258.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.428-2165A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92070263 | ||||||
| chr9:92070282
|
G | C | 35 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0031others(32): Show | 38 | HG00733.hp2 HG01109.hp1 HG01255.hp1 others(35): Show |
intron_variant | MODIFIER | c.428-2184C>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92070282 | ||||||
| chr9:92070673
|
C | T | 3 | a0001c0001t0001g0274a0001c0001t0001g0275a0001c0001t0001g0289 | 3 | HG02258.hp1 HG02622.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.428-2575G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92070673 | ||||||
| chr9:92070727
|
G | A | 1 | a0001c0001t0001g0079 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.428-2629C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92070727 | ||||||
| chr9:92070905
|
A | C | 2 | a0001c0001t0001g0318a0001c0001t0008g0319 | 2 | HG02055.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.428-2807T>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92070905 | ||||||
| chr9:92070921
|
T | C | 1 | a0001c0001t0002g0036 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.428-2823A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92070921 | ||||||
| chr9:92070981
|
G | A | 3 | a0001c0001t0004g0117a0001c0001t0004g0118a0001c0001t0004g0119 | 3 | HG02257.hp2 HG02615.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.428-2883C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92070981 | ||||||
| chr9:92071075
|
C | G | 3 | a0001c0001t0004g0117a0001c0001t0004g0118a0001c0001t0004g0119 | 3 | HG02257.hp2 HG02615.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.428-2977G>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92071075 | ||||||
| chr9:92071114
|
G | C | 1 | a0001c0001t0001g0268 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.428-3016C>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92071114 | ||||||
| chr9:92071227
|
T | TA | 62 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0027others(59): Show | 65 | HG00280.hp1 HG00280.hp2 HG00733.hp1 others(62): Show |
intron_variant | MODIFIER | c.428-3130dupT | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92071227 | ||||||
| chr9:92071227
|
TA | T | 10 | a0001c0001t0001g0029a0001c0001t0001g0086a0001c0001t0001g0184others(7): Show | 10 | HG01167.hp1 HG01884.hp2 HG01943.hp2 others(7): Show |
intron_variant | MODIFIER | c.428-3130delT | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92071227 | ||||||
| chr9:92071362
|
C | T | 1 | a0001c0001t0003g0262 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.428-3264G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92071362 | ||||||
| chr9:92071373
|
T | C | 37 | a0001c0001t0001g0268a0001c0001t0002g0002a0001c0001t0002g0007others(34): Show | 40 | HG00733.hp2 HG01109.hp1 HG01255.hp1 others(37): Show |
intron_variant | MODIFIER | c.428-3275A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92071373 | ||||||
| chr9:92071440
|
T | C | 4 | a0001c0001t0001g0066a0001c0001t0001g0068a0001c0001t0005g0065others(1): Show | 4 | HG02630.hp2 HG02809.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.428-3342A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92071440 | ||||||
| chr9:92071556
|
G | A | 1 | a0001c0001t0001g0275 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.428-3458C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92071556 | ||||||
| chr9:92071647
|
G | C | 1 | a0002c0003t0003g0062 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.428-3549C>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92071647 | ||||||
| chr9:92071688
|
G | T | 1 | a0001c0001t0002g0032 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.428-3590C>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92071688 | ||||||
| chr9:92071853
|
C | T | 34 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0031others(31): Show | 37 | HG00733.hp2 HG01109.hp1 HG01255.hp1 others(34): Show |
intron_variant | MODIFIER | c.428-3755G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92071853 | ||||||
| chr9:92071858
|
C | T | 1 | a0001c0001t0003g0266 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.428-3760G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92071858 | ||||||
| chr9:92071908
|
T | C | 6 | a0001c0001t0001g0017a0001c0001t0001g0182a0001c0001t0001g0236others(3): Show | 7 | HG00621.hp1 NA18946.hp2 NA18952.hp1 others(4): Show |
intron_variant | MODIFIER | c.428-3810A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92071908 | ||||||
| chr9:92071921
|
C | A | 2 | a0001c0001t0005g0065a0001c0001t0005g0067 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.428-3823G>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92071921 | ||||||
| chr9:92072056
|
C | T | 1 | a0001c0001t0001g0023 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.428-3958G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92072056 | ||||||
| chr9:92072057
|
G | A | 24 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(21): Show | 24 | HG00642.hp2 HG02015.hp2 HG02040.hp2 others(21): Show |
intron_variant | MODIFIER | c.428-3959C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92072057 | ||||||
| chr9:92072059
|
G | A | 35 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0031others(32): Show | 38 | HG00733.hp2 HG01109.hp1 HG01255.hp1 others(35): Show |
intron_variant | MODIFIER | c.428-3961C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92072059 | ||||||
| chr9:92072126
|
A | G | 4 | a0001c0001t0001g0195a0001c0001t0001g0212a0001c0001t0001g0220others(1): Show | 4 | HG01069.hp2 HG01109.hp2 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.428-4028T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92072126 | ||||||
| chr9:92072190
|
C | T | 1 | a0001c0001t0001g0136 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.428-4092G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92072190 | ||||||
| chr9:92072290
|
C | T | 1 | a0001c0001t0001g0081 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.428-4192G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92072290 | ||||||
| chr9:92072482
|
T | C | 1 | a0001c0001t0013g0267 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.428-4384A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92072482 | ||||||
| chr9:92072526
|
T | C | 2 | a0001c0001t0003g0266a0001c0001t0013g0267 | 2 | HG02622.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.428-4428A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92072526 | ||||||
| chr9:92072654
|
T | C | 5 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0142others(2): Show | 5 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.428-4556A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92072654 | ||||||
| chr9:92072769
|
G | C | 3 | a0001c0001t0003g0019a0001c0001t0003g0263a0001c0001t0003g0264 | 4 | HG01516.hp2 HG01517.hp2 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.428-4671C>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92072769 | ||||||
| chr9:92072769
|
G | T | 201 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(198): Show | 215 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(212): Show |
intron_variant | MODIFIER | c.428-4671C>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92072769 | ||||||
| chr9:92072959
|
A | C | 194 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(191): Show | 208 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(205): Show |
intron_variant | MODIFIER | c.428-4861T>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92072959 | ||||||
| chr9:92073028
|
C | T | 200 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(197): Show | 213 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(210): Show |
intron_variant | MODIFIER | c.428-4930G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92073028 | ||||||
| chr9:92073128
|
G | A | 23 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(20): Show | 23 | HG00642.hp2 HG02015.hp2 HG02040.hp2 others(20): Show |
intron_variant | MODIFIER | c.428-5030C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92073128 | ||||||
| chr9:92073140
|
G | A | 35 | a0001c0001t0001g0268a0001c0001t0002g0002a0001c0001t0002g0007others(32): Show | 38 | HG00733.hp2 HG01109.hp1 HG01255.hp1 others(35): Show |
intron_variant | MODIFIER | c.428-5042C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92073140 | ||||||
| chr9:92073228
|
C | A | 1 | a0001c0001t0011g0253 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.428-5130G>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92073228 | ||||||
| chr9:92073326
|
A | G | 1 | a0001c0001t0001g0111 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.428-5228T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92073326 | ||||||
| chr9:92073384
|
C | T | 2 | a0001c0001t0001g0201a0001c0001t0001g0202 | 2 | NA19006.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.428-5286G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92073384 | ||||||
| chr9:92073635
|
A | AT | 67 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(64): Show | 73 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.428-5538dupA | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92073635 | ||||||
| chr9:92073644
|
C | T | 3 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0288 | 3 | HG00735.hp1 HG01243.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.428-5546G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92073644 | ||||||
| chr9:92073742
|
A | G | 1 | a0001c0001t0001g0123 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.428-5644T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92073742 | ||||||
| chr9:92073894
|
T | C | 1 | a0001c0001t0001g0268 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.428-5796A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92073894 | ||||||
| chr9:92073941
|
C | T | 60 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(57): Show | 66 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.428-5843G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92073941 | ||||||
| chr9:92074008
|
A | T | 5 | a0001c0001t0003g0019a0001c0001t0003g0262a0001c0001t0003g0263others(2): Show | 6 | HG01074.hp2 HG01516.hp2 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.428-5910T>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92074008 | ||||||
| chr9:92074030
|
T | C | 36 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0031others(33): Show | 39 | HG00733.hp2 HG01109.hp1 HG01255.hp1 others(36): Show |
intron_variant | MODIFIER | c.428-5932A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92074030 | ||||||
| chr9:92074056
|
C | A | 1 | a0001c0001t0001g0270 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.428-5958G>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92074056 | ||||||
| chr9:92074098
|
G | A | 1 | a0001c0001t0001g0231 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.427+5918C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92074098 | ||||||
| chr9:92074107
|
G | A | 60 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(57): Show | 66 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.427+5909C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92074107 | ||||||
| chr9:92074142
|
G | A | 1 | a0001c0001t0001g0144 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.427+5874C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92074142 | ||||||
| chr9:92074170
|
C | T | 2 | a0001c0001t0001g0018a0001c0001t0001g0254 | 3 | HG02602.hp1 HG03654.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.427+5846G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92074170 | ||||||
| chr9:92074185
|
C | T | 1 | a0002c0003t0003g0062 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.427+5831G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92074185 | ||||||
| chr9:92074239
|
T | C | 35 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0031others(32): Show | 38 | HG00733.hp2 HG01109.hp1 HG01255.hp1 others(35): Show |
intron_variant | MODIFIER | c.427+5777A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92074239 | ||||||
| chr9:92074340
|
T | C | 1 | a0001c0001t0001g0020 | 2 | HG01081.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.427+5676A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92074340 | ||||||
| chr9:92074468
|
C | T | 1 | a0001c0001t0001g0290 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.427+5548G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92074468 | ||||||
| chr9:92074503
|
C | A | 1 | a0001c0001t0014g0261 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.427+5513G>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92074503 | ||||||
| chr9:92074532
|
C | T | 1 | a0001c0001t0014g0261 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.427+5484G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92074532 | ||||||
| chr9:92074568
|
T | G | 1 | a0001c0001t0011g0253 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.427+5448A>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92074568 | ||||||
| chr9:92074663
|
C | A | 1 | a0001c0001t0001g0141 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.427+5353G>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92074663 | ||||||
| chr9:92074679
|
C | T | 3 | a0001c0001t0001g0274a0001c0001t0001g0275a0001c0001t0001g0289 | 3 | HG02258.hp1 HG02622.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.427+5337G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92074679 | ||||||
| chr9:92074783
|
A | G | 25 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0001g0121others(22): Show | 26 | HG00642.hp2 HG02015.hp2 HG02040.hp2 others(23): Show |
intron_variant | MODIFIER | c.427+5233T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92074783 | ||||||
| chr9:92074809
|
T | TA | 35 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0031others(32): Show | 38 | HG00733.hp2 HG01109.hp1 HG01255.hp1 others(35): Show |
intron_variant | MODIFIER | c.427+5206dupT | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92074809 | ||||||
| chr9:92074816
|
C | T | 1 | a0001c0001t0001g0076 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.427+5200G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92074816 | ||||||
| chr9:92074850
|
C | T | 8 | a0001c0001t0001g0211a0001c0001t0001g0221a0001c0001t0001g0227others(5): Show | 8 | HG00323.hp1 HG00738.hp2 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.427+5166G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92074850 | ||||||
| chr9:92074906
|
C | T | 3 | a0001c0001t0001g0020a0001c0001t0001g0063a0001c0001t0001g0064 | 4 | HG01081.hp2 HG02895.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.427+5110G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92074906 | ||||||
| chr9:92075242
|
C | T | 5 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(2): Show | 5 | HG00741.hp2 HG01884.hp2 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.427+4774G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92075242 | ||||||
| chr9:92075308
|
T | C | 1 | a0002c0003t0003g0062 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.427+4708A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92075308 | ||||||
| chr9:92075441
|
A | G | 8 | a0001c0001t0003g0019a0001c0001t0003g0262a0001c0001t0003g0263others(5): Show | 9 | HG01074.hp2 HG01516.hp2 HG01517.hp2 others(6): Show |
intron_variant | MODIFIER | c.427+4575T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92075441 | ||||||
| chr9:92075476
|
G | A | 1 | a0001c0001t0001g0109 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.427+4540C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92075476 | ||||||
| chr9:92075526
|
G | A | 1 | a0001c0001t0001g0268 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.427+4490C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92075526 | ||||||
| chr9:92075550
|
C | A | 64 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(61): Show | 70 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.427+4466G>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92075550 | ||||||
| chr9:92075661
|
C | G | 2 | a0001c0001t0001g0074a0001c0001t0001g0082 | 2 | HG02015.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.427+4355G>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92075661 | ||||||
| chr9:92075750
|
C | T | 3 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0245 | 3 | HG00621.hp1 NA18946.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.427+4266G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92075750 | ||||||
| chr9:92075795
|
T | G | 1 | a0001c0001t0002g0037 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.427+4221A>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92075795 | ||||||
| chr9:92075804
|
C | T | 1 | a0001c0001t0001g0270 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.427+4212G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92075804 | ||||||
| chr9:92075848
|
C | T | 38 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(35): Show | 46 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(43): Show |
intron_variant | MODIFIER | c.427+4168G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92075848 | ||||||
| chr9:92075874
|
C | G | 1 | a0001c0001t0011g0253 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.427+4142G>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92075874 | ||||||
| chr9:92076007
|
G | A | 1 | a0001c0001t0001g0131 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.427+4009C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92076007 | ||||||
| chr9:92076031
|
T | G | 40 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0290others(37): Show | 42 | HG00280.hp1 HG00733.hp1 HG01074.hp1 others(39): Show |
intron_variant | MODIFIER | c.427+3985A>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92076031 | ||||||
| chr9:92076183
|
G | C | 1 | a0001c0001t0011g0253 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.427+3833C>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92076183 | ||||||
| chr9:92076321
|
C | G | 1 | a0001c0001t0001g0187 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.427+3695G>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92076321 | ||||||
| chr9:92076823
|
T | C | 146 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(143): Show | 158 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(155): Show |
intron_variant | MODIFIER | c.427+3193A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92076823 | ||||||
| chr9:92076847
|
C | T | 67 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(64): Show | 73 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.427+3169G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92076847 | ||||||
| chr9:92076900
|
A | T | 2 | a0001c0001t0001g0074a0001c0001t0001g0082 | 2 | HG02015.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.427+3116T>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92076900 | ||||||
| chr9:92076945
|
G | A | 6 | a0001c0001t0001g0020a0001c0001t0001g0063a0001c0001t0001g0064others(3): Show | 7 | HG01081.hp2 HG02257.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.427+3071C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92076945 | ||||||
| chr9:92076992
|
C | T | 1 | a0001c0001t0001g0268 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.427+3024G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92076992 | ||||||
| chr9:92077060
|
A | G | 153 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(150): Show | 165 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(162): Show |
intron_variant | MODIFIER | c.427+2956T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92077060 | ||||||
| chr9:92077062
|
C | T | 1 | a0001c0001t0001g0085 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.427+2954G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92077062 | ||||||
| chr9:92077091
|
C | A | 67 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(64): Show | 73 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.427+2925G>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92077091 | ||||||
| chr9:92077119
|
C | G | 1 | a0001c0001t0011g0253 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.427+2897G>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92077119 | ||||||
| chr9:92077169
|
C | T | 25 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0001g0121others(22): Show | 26 | HG00642.hp2 HG02015.hp2 HG02040.hp2 others(23): Show |
intron_variant | MODIFIER | c.427+2847G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92077169 | ||||||
| chr9:92077170
|
G | A | 7 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(4): Show | 7 | HG01081.hp1 HG02258.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.427+2846C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92077170 | ||||||
| chr9:92077224
|
C | T | 34 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0031others(31): Show | 37 | HG00733.hp2 HG01109.hp1 HG01255.hp1 others(34): Show |
intron_variant | MODIFIER | c.427+2792G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92077224 | ||||||
| chr9:92077225
|
T | C | 1 | a0001c0001t0001g0220 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.427+2791A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92077225 | ||||||
| chr9:92077353
|
G | A | 40 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0290others(37): Show | 42 | HG00280.hp1 HG00733.hp1 HG01074.hp1 others(39): Show |
intron_variant | MODIFIER | c.427+2663C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92077353 | ||||||
| chr9:92077367
|
T | C | 206 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(203): Show | 221 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(218): Show |
intron_variant | MODIFIER | c.427+2649A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92077367 | ||||||
| chr9:92077401
|
C | T | 4 | a0001c0001t0001g0066a0001c0001t0001g0068a0001c0001t0005g0065others(1): Show | 4 | HG02630.hp2 HG02809.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.427+2615G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92077401 | ||||||
| chr9:92077402
|
G | A | 40 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0290others(37): Show | 42 | HG00280.hp1 HG00733.hp1 HG01074.hp1 others(39): Show |
intron_variant | MODIFIER | c.427+2614C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92077402 | ||||||
| chr9:92077565
|
T | C | 2 | a0001c0001t0001g0018a0001c0001t0001g0254 | 3 | HG02602.hp1 HG03654.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.427+2451A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92077565 | ||||||
| chr9:92077625
|
G | A | 2 | a0001c0001t0001g0132a0001c0001t0001g0285 | 2 | NA19000.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.427+2391C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92077625 | ||||||
| chr9:92077626
|
G | A | 1 | a0001c0001t0001g0268 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.427+2390C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92077626 | ||||||
| chr9:92077689
|
C | T | 2 | a0001c0001t0001g0310a0001c0001t0001g0314 | 2 | HG02145.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.427+2327G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92077689 | ||||||
| chr9:92077825
|
G | A | 3 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0288 | 3 | HG00735.hp1 HG01243.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.427+2191C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92077825 | ||||||
| chr9:92077829
|
A | T | 3 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0288 | 3 | HG00735.hp1 HG01243.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.427+2187T>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92077829 | ||||||
| chr9:92077924
|
T | C | 153 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(150): Show | 165 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(162): Show |
intron_variant | MODIFIER | c.427+2092A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92077924 | ||||||
| chr9:92078039
|
C | T | 35 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0031others(32): Show | 38 | HG00733.hp2 HG01109.hp1 HG01255.hp1 others(35): Show |
intron_variant | MODIFIER | c.427+1977G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92078039 | ||||||
| chr9:92078105
|
A | G | 3 | a0001c0001t0001g0274a0001c0001t0001g0275a0001c0001t0001g0289 | 3 | HG02258.hp1 HG02622.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.427+1911T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92078105 | ||||||
| chr9:92078557
|
C | G | 1 | a0001c0001t0001g0142 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.427+1459G>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92078557 | ||||||
| chr9:92078577
|
G | A | 3 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0273 | 3 | HG01891.hp2 HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.427+1439C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92078577 | ||||||
| chr9:92078649
|
C | T | 25 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0001g0121others(22): Show | 26 | HG00642.hp2 HG02015.hp2 HG02040.hp2 others(23): Show |
intron_variant | MODIFIER | c.427+1367G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92078649 | ||||||
| chr9:92078652
|
A | G | 36 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0031others(33): Show | 39 | HG00733.hp2 HG01109.hp1 HG01255.hp1 others(36): Show |
intron_variant | MODIFIER | c.427+1364T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92078652 | ||||||
| chr9:92078697
|
T | C | 206 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(203): Show | 221 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(218): Show |
intron_variant | MODIFIER | c.427+1319A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92078697 | ||||||
| chr9:92078730
|
C | T | 4 | a0001c0001t0001g0066a0001c0001t0001g0068a0001c0001t0005g0065others(1): Show | 4 | HG02630.hp2 HG02809.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.427+1286G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92078730 | ||||||
| chr9:92078898
|
T | C | 3 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192 | 3 | HG00741.hp2 HG02683.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.427+1118A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92078898 | ||||||
| chr9:92078976
|
G | A | 40 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0290others(37): Show | 42 | HG00280.hp1 HG00733.hp1 HG01074.hp1 others(39): Show |
intron_variant | MODIFIER | c.427+1040C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92078976 | ||||||
| chr9:92078985
|
T | C | 1 | a0001c0001t0010g0045 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.427+1031A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92078985 | ||||||
| chr9:92079410
|
G | T | 5 | a0001c0001t0001g0320a0001c0001t0001g0321a0001c0001t0001g0322others(2): Show | 5 | HG01123.hp1 HG01346.hp1 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.427+606C>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92079410 | ||||||
| chr9:92079418
|
A | G | 1 | a0001c0001t0002g0046 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.427+598T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92079418 | ||||||
| chr9:92079445
|
G | A | 1 | a0001c0001t0001g0268 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.427+571C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92079445 | ||||||
| chr9:92079570
|
G | A | 1 | a0001c0001t0001g0011 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.427+446C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92079570 | ||||||
| chr9:92079655
|
G | A | 8 | a0001c0001t0003g0019a0001c0001t0003g0262a0001c0001t0003g0263others(5): Show | 9 | HG01074.hp2 HG01516.hp2 HG01517.hp2 others(6): Show |
intron_variant | MODIFIER | c.427+361C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92079655 | ||||||
| chr9:92079674
|
A | T | 1 | a0001c0001t0001g0150 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.427+342T>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92079674 | ||||||
| chr9:92079687
|
C | T | 19 | a0001c0001t0002g0007a0001c0001t0002g0032a0001c0001t0002g0033others(16): Show | 20 | HG01109.hp1 HG01255.hp1 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.427+329G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92079687 | ||||||
| chr9:92079698
|
G | A | 103 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(100): Show | 112 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(109): Show |
intron_variant | MODIFIER | c.427+318C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92079698 | ||||||
| chr9:92079710
|
C | T | 2 | a0001c0001t0001g0318a0001c0001t0008g0319 | 2 | HG02055.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.427+306G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92079710 | ||||||
| chr9:92079766
|
C | T | 8 | a0001c0001t0003g0019a0001c0001t0003g0262a0001c0001t0003g0263others(5): Show | 9 | HG01074.hp2 HG01516.hp2 HG01517.hp2 others(6): Show |
intron_variant | MODIFIER | c.427+250G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92079766 | ||||||
| chr9:92080217
|
C | G | 1 | a0001c0001t0001g0289 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.355-129G>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 4/14 | chr9 | 92080217 | ||||||
| chr9:92080229
|
C | A | 67 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(64): Show | 73 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.355-141G>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 4/14 | chr9 | 92080229 | ||||||
| chr9:92080299
|
A | G | 1 | a0001c0001t0011g0253 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.355-211T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 4/14 | chr9 | 92080299 | ||||||
| chr9:92080410
|
G | T | 1 | a0001c0001t0001g0136 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.355-322C>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 4/14 | chr9 | 92080410 | ||||||
| chr9:92080433
|
T | C | 67 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(64): Show | 73 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.355-345A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 4/14 | chr9 | 92080433 | ||||||
| chr9:92080697
|
C | T | 3 | a0001c0001t0001g0274a0001c0001t0001g0275a0001c0001t0001g0289 | 3 | HG02258.hp1 HG02622.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.354+173G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 4/14 | chr9 | 92080697 | ||||||
| chr9:92080700
|
T | C | 1 | a0001c0001t0001g0268 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.354+170A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 4/14 | chr9 | 92080700 | ||||||
| chr9:92080825
|
A | C | 1 | a0001c0001t0001g0268 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.354+45T>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 4/14 | chr9 | 92080825 | ||||||
| chr9:92081198
|
A | G | 8 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0071others(5): Show | 8 | HG02015.hp1 HG02056.hp2 HG02074.hp2 others(5): Show |
intron_variant | MODIFIER | c.261-235T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92081198 | ||||||
| chr9:92081385
|
G | T | 2 | a0001c0001t0001g0309a0001c0001t0001g0313 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.261-422C>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92081385 | ||||||
| chr9:92081404
|
T | C | 1 | a0001c0001t0001g0229 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.261-441A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92081404 | ||||||
| chr9:92081408
|
T | C | 1 | a0001c0001t0001g0268 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.261-445A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92081408 | ||||||
| chr9:92081548
|
G | A | 1 | a0001c0001t0014g0261 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.261-585C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92081548 | ||||||
| chr9:92081675
|
T | G | 6 | a0001c0001t0001g0309a0001c0001t0001g0310a0001c0001t0001g0311others(3): Show | 6 | HG02109.hp2 HG02145.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.261-712A>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92081675 | ||||||
| chr9:92081741
|
C | T | 3 | a0001c0001t0002g0002a0001c0001t0002g0038a0001c0002t0002g0039 | 5 | HG01346.hp2 HG01358.hp1 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.261-778G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92081741 | ||||||
| chr9:92081820
|
T | A | 1 | a0001c0001t0001g0268 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.261-857A>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92081820 | ||||||
| chr9:92081868
|
T | C | 70 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(67): Show | 76 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.261-905A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92081868 | ||||||
| chr9:92081996
|
T | A | 6 | a0001c0001t0001g0020a0001c0001t0001g0063a0001c0001t0001g0064others(3): Show | 7 | HG01081.hp2 HG02257.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.261-1033A>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92081996 | ||||||
| chr9:92082056
|
T | C | 1 | a0001c0004t0001g0186 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.261-1093A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92082056 | ||||||
| chr9:92082109
|
T | C | 1 | a0001c0001t0001g0287 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.261-1146A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92082109 | ||||||
| chr9:92082130
|
G | C | 1 | a0002c0003t0003g0062 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.261-1167C>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92082130 | ||||||
| chr9:92082286
|
A | T | 1 | a0001c0001t0011g0253 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.261-1323T>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92082286 | ||||||
| chr9:92082303
|
A | C | 1 | a0001c0001t0001g0193 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.261-1340T>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92082303 | ||||||
| chr9:92082310
|
T | C | 1 | a0001c0001t0001g0221 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.261-1347A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92082310 | ||||||
| chr9:92082390
|
T | TC | 50 | a0001c0001t0001g0016a0001c0001t0001g0072a0001c0001t0001g0095others(47): Show | 51 | HG00544.hp1 HG00609.hp1 HG01071.hp2 others(48): Show |
intron_variant | MODIFIER | c.261-1428dupG | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92082390 | ||||||
| chr9:92082644
|
G | A | 1 | a0001c0001t0001g0111 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.261-1681C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92082644 | ||||||
| chr9:92082765
|
T | C | 1 | a0002c0003t0003g0062 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.261-1802A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92082765 | ||||||
| chr9:92082810
|
G | A | 35 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0031others(32): Show | 38 | HG00733.hp2 HG01109.hp1 HG01255.hp1 others(35): Show |
intron_variant | MODIFIER | c.261-1847C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92082810 | ||||||
| chr9:92082864
|
A | G | 1 | a0001c0001t0001g0235 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.261-1901T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92082864 | ||||||
| chr9:92082918
|
G | T | 2 | a0001c0001t0001g0268a0001c0001t0002g0032 | 2 | HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.261-1955C>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92082918 | ||||||
| chr9:92082924
|
C | T | 1 | a0001c0001t0002g0032 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.261-1961G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92082924 | ||||||
| chr9:92082931
|
T | A | 1 | a0001c0001t0010g0045 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.261-1968A>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92082931 | ||||||
| chr9:92082932
|
C | G | 1 | a0001c0001t0010g0045 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.261-1969G>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92082932 | ||||||
| chr9:92082933
|
T | A | 1 | a0001c0001t0010g0045 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.261-1970A>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92082933 | ||||||
| chr9:92082989
|
A | C | 1 | a0001c0001t0003g0266 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.261-2026T>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92082989 | ||||||
| chr9:92083043
|
G | C | 1 | a0001c0001t0001g0120 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.261-2080C>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92083043 | ||||||
| chr9:92083084
|
A | G | 206 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(203): Show | 221 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(218): Show |
intron_variant | MODIFIER | c.261-2121T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92083084 | ||||||
| chr9:92083140
|
G | C | 1 | a0001c0001t0001g0287 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.261-2177C>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92083140 | ||||||
| chr9:92083146
|
T | G | 1 | a0001c0001t0001g0287 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.261-2183A>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92083146 | ||||||
| chr9:92083240
|
T | C | 1 | a0001c0001t0011g0253 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.261-2277A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92083240 | ||||||
| chr9:92083317
|
T | G | 1 | a0001c0001t0001g0234 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.261-2354A>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92083317 | ||||||
| chr9:92083380
|
C | T | 67 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(64): Show | 73 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.261-2417G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92083380 | ||||||
| chr9:92083434
|
G | A | 1 | a0001c0001t0001g0120 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.261-2471C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92083434 | ||||||
| chr9:92083510
|
A | G | 14 | a0001c0001t0001g0020a0001c0001t0001g0063a0001c0001t0001g0064others(11): Show | 16 | HG01074.hp2 HG01081.hp2 HG01516.hp2 others(13): Show |
intron_variant | MODIFIER | c.261-2547T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92083510 | ||||||
| chr9:92083510
|
A | T | 3 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0181 | 3 | NA18959.hp1 NA18983.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.261-2547T>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92083510 | ||||||
| chr9:92083561
|
C | T | 1 | a0001c0001t0001g0111 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.261-2598G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92083561 | ||||||
| chr9:92083562
|
G | A | 2 | a0001c0001t0001g0278a0001c0001t0001g0279 | 2 | HG02572.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.261-2599C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92083562 | ||||||
| chr9:92083679
|
C | A | 67 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(64): Show | 73 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.261-2716G>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92083679 | ||||||
| chr9:92083717
|
G | A | 1 | a0001c0001t0001g0028 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.261-2754C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92083717 | ||||||
| chr9:92083721
|
T | C | 3 | a0001c0001t0001g0274a0001c0001t0001g0275a0001c0001t0001g0289 | 3 | HG02258.hp1 HG02622.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.261-2758A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92083721 | ||||||
| chr9:92083770
|
C | G | 1 | a0001c0001t0001g0084 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.261-2807G>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92083770 | ||||||
| chr9:92083879
|
A | G | 1 | a0001c0005t0001g0185 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.261-2916T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92083879 | ||||||
| chr9:92083939
|
C | T | 1 | a0002c0003t0003g0062 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.261-2976G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92083939 | ||||||
| chr9:92083956
|
T | C | 6 | a0001c0001t0001g0020a0001c0001t0001g0063a0001c0001t0001g0064others(3): Show | 7 | HG01081.hp2 HG02257.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.261-2993A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92083956 | ||||||
| chr9:92083997
|
G | A | 1 | a0001c0001t0011g0253 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.261-3034C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92083997 | ||||||
| chr9:92084107
|
G | C | 1 | a0001c0001t0002g0060 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.261-3144C>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92084107 | ||||||
| chr9:92084126
|
T | G | 1 | a0001c0001t0002g0051 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.261-3163A>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92084126 | ||||||
| chr9:92084194
|
C | A | 67 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(64): Show | 73 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.261-3231G>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92084194 | ||||||
| chr9:92084245
|
C | A | 1 | a0001c0001t0001g0030 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.261-3282G>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92084245 | ||||||
| chr9:92084296
|
G | C | 2 | a0001c0001t0001g0017a0001c0001t0001g0244 | 3 | NA18975.hp1 NA18992.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.261-3333C>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92084296 | ||||||
| chr9:92084327
|
A | C | 1 | a0001c0001t0001g0234 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.261-3364T>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92084327 | ||||||
| chr9:92084378
|
C | T | 7 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(4): Show | 7 | HG01081.hp1 HG02258.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.261-3415G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92084378 | ||||||
| chr9:92084380
|
G | A | 7 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(4): Show | 7 | HG01081.hp1 HG02258.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.261-3417C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92084380 | ||||||
| chr9:92084455
|
T | G | 1 | a0001c0001t0001g0189 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.261-3492A>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92084455 | ||||||
| chr9:92084519
|
T | C | 1 | a0001c0001t0004g0119 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.261-3556A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92084519 | ||||||
| chr9:92084524
|
T | C | 3 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0273 | 3 | HG01891.hp2 HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.261-3561A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92084524 | ||||||
| chr9:92084547
|
T | C | 2 | a0001c0001t0001g0226a0001c0001t0001g0231 | 2 | HG00735.hp2 HG00738.hp1 |
intron_variant | MODIFIER | c.261-3584A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92084547 | ||||||
| chr9:92084635
|
C | T | 1 | a0001c0006t0001g0300 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.261-3672G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92084635 | ||||||
| chr9:92084636
|
G | A | 4 | a0001c0001t0002g0035a0001c0001t0002g0036a0001c0001t0002g0037others(1): Show | 4 | HG01109.hp1 HG02145.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.261-3673C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92084636 | ||||||
| chr9:92084685
|
T | C | 1 | a0001c0001t0001g0204 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.261-3722A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92084685 | ||||||
| chr9:92084691
|
T | C | 35 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0031others(32): Show | 38 | HG00733.hp2 HG01109.hp1 HG01255.hp1 others(35): Show |
intron_variant | MODIFIER | c.261-3728A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92084691 | ||||||
| chr9:92084752
|
T | C | 67 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(64): Show | 73 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.261-3789A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92084752 | ||||||
| chr9:92084777
|
T | C | 106 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(103): Show | 115 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(112): Show |
intron_variant | MODIFIER | c.261-3814A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92084777 | ||||||
| chr9:92084815
|
G | T | 2 | a0001c0001t0004g0117a0001c0001t0004g0118 | 2 | HG02615.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.261-3852C>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92084815 | ||||||
| chr9:92084822
|
G | C | 38 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0290others(35): Show | 40 | HG00280.hp1 HG00733.hp1 HG01074.hp1 others(37): Show |
intron_variant | MODIFIER | c.261-3859C>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92084822 | ||||||
| chr9:92085042
|
G | T | 153 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(150): Show | 165 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(162): Show |
intron_variant | MODIFIER | c.261-4079C>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92085042 | ||||||
| chr9:92085078
|
A | G | 9 | a0001c0001t0002g0031a0001c0001t0002g0054a0001c0001t0002g0055others(6): Show | 9 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.261-4115T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92085078 | ||||||
| chr9:92085207
|
A | G | 3 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0181 | 3 | NA18959.hp1 NA18983.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.261-4244T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92085207 | ||||||
| chr9:92085258
|
C | T | 8 | a0001c0001t0001g0204a0001c0001t0001g0255a0001c0001t0001g0256others(5): Show | 8 | HG01081.hp1 HG01952.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.261-4295G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92085258 | ||||||
| chr9:92085439
|
G | A | 35 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0031others(32): Show | 38 | HG00733.hp2 HG01109.hp1 HG01255.hp1 others(35): Show |
intron_variant | MODIFIER | c.261-4476C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92085439 | ||||||
| chr9:92085548
|
G | A | 1 | a0001c0001t0002g0032 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.261-4585C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92085548 | ||||||
| chr9:92085570
|
C | T | 26 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0032others(23): Show | 29 | HG00733.hp2 HG01109.hp1 HG01255.hp1 others(26): Show |
intron_variant | MODIFIER | c.261-4607G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92085570 | ||||||
| chr9:92085587
|
T | C | 5 | a0001c0001t0003g0019a0001c0001t0003g0262a0001c0001t0003g0263others(2): Show | 6 | HG01074.hp2 HG01516.hp2 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.261-4624A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92085587 | ||||||
| chr9:92085685
|
G | A | 2 | a0001c0001t0001g0318a0001c0001t0008g0319 | 2 | HG02055.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.261-4722C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92085685 | ||||||
| chr9:92085695
|
G | A | 1 | a0001c0001t0011g0253 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.261-4732C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92085695 | ||||||
| chr9:92085799
|
T | C | 1 | a0002c0003t0003g0062 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.261-4836A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92085799 | ||||||
| chr9:92085814
|
G | A | 1 | a0001c0001t0001g0120 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.261-4851C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92085814 | ||||||
| chr9:92085965
|
C | G | 2 | a0001c0001t0006g0307a0001c0001t0007g0308 | 2 | HG00733.hp1 HG01257.hp1 |
intron_variant | MODIFIER | c.261-5002G>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92085965 | ||||||
| chr9:92085977
|
A | G | 6 | a0001c0001t0001g0020a0001c0001t0001g0063a0001c0001t0001g0064others(3): Show | 7 | HG01081.hp2 HG02257.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.261-5014T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92085977 | ||||||
| chr9:92086077
|
T | C | 1 | a0001c0001t0001g0268 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.261-5114A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92086077 | ||||||
| chr9:92086118
|
T | C | 25 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0001g0121others(22): Show | 26 | HG00642.hp2 HG02015.hp2 HG02040.hp2 others(23): Show |
intron_variant | MODIFIER | c.261-5155A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92086118 | ||||||
| chr9:92086144
|
G | A | 5 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0142others(2): Show | 5 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.261-5181C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92086144 | ||||||
| chr9:92086159
|
T | C | 1 | a0001c0001t0001g0102 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.261-5196A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92086159 | ||||||
| chr9:92086224
|
A | G | 1 | a0001c0001t0001g0188 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.261-5261T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92086224 | ||||||
| chr9:92086382
|
G | A | 35 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0031others(32): Show | 38 | HG00733.hp2 HG01109.hp1 HG01255.hp1 others(35): Show |
intron_variant | MODIFIER | c.261-5419C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92086382 | ||||||
| chr9:92086399
|
T | G | 1 | a0001c0001t0002g0046 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.261-5436A>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92086399 | ||||||
| chr9:92086434
|
C | G | 5 | a0001c0001t0003g0019a0001c0001t0003g0262a0001c0001t0003g0263others(2): Show | 6 | HG01074.hp2 HG01516.hp2 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.261-5471G>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92086434 | ||||||
| chr9:92086449
|
A | G | 2 | a0001c0001t0003g0262a0001c0001t0003g0265 | 2 | HG01074.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.261-5486T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92086449 | ||||||
| chr9:92086569
|
T | C | 2 | a0001c0001t0001g0103a0001c0001t0001g0104 | 2 | HG00558.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.261-5606A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92086569 | ||||||
| chr9:92086718
|
GT | G | 25 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0001g0121others(22): Show | 26 | HG00642.hp2 HG02015.hp2 HG02040.hp2 others(23): Show |
intron_variant | MODIFIER | c.261-5756delA | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92086718 | ||||||
| chr9:92086725
|
A | G | 1 | a0001c0001t0001g0156 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.261-5762T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92086725 | ||||||
| chr9:92086737
|
C | T | 1 | a0001c0001t0001g0123 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.261-5774G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92086737 | ||||||
| chr9:92086738
|
A | G | 61 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(58): Show | 67 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(64): Show |
intron_variant | MODIFIER | c.261-5775T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92086738 | ||||||
| chr9:92086844
|
A | G | 6 | a0001c0001t0001g0020a0001c0001t0001g0063a0001c0001t0001g0064others(3): Show | 7 | HG01081.hp2 HG02257.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.261-5881T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92086844 | ||||||
| chr9:92086863
|
G | A | 1 | a0001c0001t0001g0180 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.261-5900C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92086863 | ||||||
| chr9:92086985
|
C | A | 1 | a0001c0001t0001g0270 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.261-6022G>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92086985 | ||||||
| chr9:92087004
|
C | T | 2 | a0001c0001t0001g0291a0001c0001t0001g0306 | 2 | HG02135.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.261-6041G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92087004 | ||||||
| chr9:92087063
|
A | G | 36 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0031others(33): Show | 39 | HG00733.hp2 HG01109.hp1 HG01255.hp1 others(36): Show |
intron_variant | MODIFIER | c.261-6100T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92087063 | ||||||
| chr9:92087256
|
C | A | 1 | a0001c0001t0003g0265 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.261-6293G>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92087256 | ||||||
| chr9:92087316
|
T | G | 67 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(64): Show | 73 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.261-6353A>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92087316 | ||||||
| chr9:92087573
|
G | C | 207 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(204): Show | 222 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(219): Show |
intron_variant | MODIFIER | c.261-6610C>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92087573 | ||||||
| chr9:92087592
|
G | A | 1 | a0001c0001t0001g0106 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.261-6629C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92087592 | ||||||
| chr9:92087613
|
C | T | 25 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0001g0121others(22): Show | 26 | HG00642.hp2 HG02015.hp2 HG02040.hp2 others(23): Show |
intron_variant | MODIFIER | c.261-6650G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92087613 | ||||||
| chr9:92087618
|
G | A | 8 | a0001c0001t0003g0019a0001c0001t0003g0262a0001c0001t0003g0263others(5): Show | 9 | HG01074.hp2 HG01516.hp2 HG01517.hp2 others(6): Show |
intron_variant | MODIFIER | c.261-6655C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92087618 | ||||||
| chr9:92087694
|
G | A | 3 | a0001c0001t0001g0274a0001c0001t0001g0275a0001c0001t0001g0289 | 3 | HG02258.hp1 HG02622.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.261-6731C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92087694 | ||||||
| chr9:92087718
|
G | A | 1 | a0001c0001t0001g0227 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.261-6755C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92087718 | ||||||
| chr9:92087745
|
C | T | 1 | a0001c0001t0001g0293 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.261-6782G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92087745 | ||||||
| chr9:92087746
|
G | A | 2 | a0001c0001t0001g0318a0001c0001t0008g0319 | 2 | HG02055.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.261-6783C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92087746 | ||||||
| chr9:92087919
|
G | T | 2 | a0001c0001t0001g0018a0001c0001t0001g0254 | 3 | HG02602.hp1 HG03654.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.261-6956C>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92087919 | ||||||
| chr9:92087924
|
G | C | 1 | a0001c0001t0001g0133 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.261-6961C>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92087924 | ||||||
| chr9:92087951
|
C | T | 4 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(1): Show | 4 | HG01099.hp2 HG01192.hp2 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.261-6988G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92087951 | ||||||
| chr9:92087966
|
C | T | 2 | a0001c0001t0003g0266a0001c0001t0013g0267 | 2 | HG02622.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.261-7003G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92087966 | ||||||
| chr9:92087979
|
G | A | 1 | a0001c0001t0001g0268 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.261-7016C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92087979 | ||||||
| chr9:92088020
|
G | A | 6 | a0001c0001t0001g0020a0001c0001t0001g0063a0001c0001t0001g0064others(3): Show | 7 | HG01081.hp2 HG02257.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.261-7057C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92088020 | ||||||
| chr9:92088052
|
G | T | 1 | a0002c0003t0003g0062 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.261-7089C>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92088052 | ||||||
| chr9:92088058
|
G | T | 6 | a0001c0001t0001g0020a0001c0001t0001g0063a0001c0001t0001g0064others(3): Show | 7 | HG01081.hp2 HG02257.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.261-7095C>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92088058 | ||||||
| chr9:92088063
|
T | G | 38 | a0001c0001t0001g0274a0001c0001t0001g0275a0001c0001t0001g0289others(35): Show | 41 | HG00733.hp2 HG01109.hp1 HG01255.hp1 others(38): Show |
intron_variant | MODIFIER | c.261-7100A>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92088063 | ||||||
| chr9:92088103
|
C | T | 3 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0203 | 3 | NA19006.hp1 NA19012.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.261-7140G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92088103 | ||||||
| chr9:92088116
|
T | C | 1 | a0001c0001t0001g0134 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.261-7153A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92088116 | ||||||
| chr9:92088134
|
T | C | 153 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(150): Show | 165 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(162): Show |
intron_variant | MODIFIER | c.261-7171A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92088134 | ||||||
| chr9:92088185
|
C | A | 1 | a0002c0003t0003g0062 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.261-7222G>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92088185 | ||||||
| chr9:92088217
|
A | G | 3 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0183 | 3 | NA18967.hp2 NA18978.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.261-7254T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92088217 | ||||||
| chr9:92088218
|
C | A | 8 | a0001c0001t0003g0019a0001c0001t0003g0262a0001c0001t0003g0263others(5): Show | 9 | HG01074.hp2 HG01516.hp2 HG01517.hp2 others(6): Show |
intron_variant | MODIFIER | c.261-7255G>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92088218 | ||||||
| chr9:92088244
|
C | A | 1 | a0001c0001t0011g0253 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.261-7281G>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92088244 | ||||||
| chr9:92088249
|
C | G | 1 | a0001c0001t0001g0321 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.261-7286G>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92088249 | ||||||
| chr9:92088319
|
A | G | 1 | a0001c0001t0001g0278 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.261-7356T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92088319 | ||||||
| chr9:92088327
|
C | T | 6 | a0001c0001t0001g0020a0001c0001t0001g0063a0001c0001t0001g0064others(3): Show | 7 | HG01081.hp2 HG02257.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.261-7364G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92088327 | ||||||
| chr9:92088335
|
G | C | 3 | a0001c0001t0002g0047a0001c0001t0002g0050a0001c0001t0002g0051 | 3 | HG02135.hp1 NA18950.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.261-7372C>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92088335 | ||||||
| chr9:92088616
|
G | A | 1 | a0001c0001t0001g0228 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.261-7653C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92088616 | ||||||
| chr9:92088776
|
G | C | 38 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0290others(35): Show | 40 | HG00280.hp1 HG00733.hp1 HG01074.hp1 others(37): Show |
intron_variant | MODIFIER | c.261-7813C>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92088776 | ||||||
| chr9:92088821
|
C | T | 2 | a0001c0001t0001g0232a0001c0001t0001g0233 | 2 | HG02083.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.261-7858G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92088821 | ||||||
| chr9:92088830
|
A | C | 3 | a0001c0001t0004g0117a0001c0001t0004g0118a0001c0001t0004g0119 | 3 | HG02257.hp2 HG02615.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.261-7867T>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92088830 | ||||||
| chr9:92088922
|
T | A | 7 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(4): Show | 7 | HG01081.hp1 HG02258.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.261-7959A>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92088922 | ||||||
| chr9:92088933
|
G | A | 1 | a0001c0001t0001g0229 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.261-7970C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92088933 | ||||||
| chr9:92089174
|
G | A | 1 | a0001c0001t0001g0110 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.261-8211C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92089174 | ||||||
| chr9:92089265
|
A | T | 36 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0031others(33): Show | 39 | HG00733.hp2 HG01109.hp1 HG01255.hp1 others(36): Show |
intron_variant | MODIFIER | c.261-8302T>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92089265 | ||||||
| chr9:92089281
|
C | T | 8 | a0001c0001t0002g0031a0001c0001t0002g0054a0001c0001t0002g0055others(5): Show | 8 | HG01884.hp1 HG01891.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.261-8318G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92089281 | ||||||
| chr9:92089293
|
A | G | 2 | a0001c0001t0001g0291a0001c0001t0001g0306 | 2 | HG02135.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.261-8330T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92089293 | ||||||
| chr9:92089413
|
C | A | 1 | a0001c0001t0002g0048 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.261-8450G>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92089413 | ||||||
| chr9:92089605
|
C | T | 1 | a0002c0003t0003g0062 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.261-8642G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92089605 | ||||||
| chr9:92089723
|
G | A | 1 | a0001c0001t0001g0080 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.261-8760C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92089723 | ||||||
| chr9:92089771
|
G | A | 8 | a0001c0001t0003g0019a0001c0001t0003g0262a0001c0001t0003g0263others(5): Show | 9 | HG01074.hp2 HG01516.hp2 HG01517.hp2 others(6): Show |
intron_variant | MODIFIER | c.261-8808C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92089771 | ||||||
| chr9:92089816
|
T | C | 1 | a0001c0001t0001g0299 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.261-8853A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92089816 | ||||||
| chr9:92089850
|
T | C | 1 | a0001c0001t0002g0049 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.261-8887A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92089850 | ||||||
| chr9:92089873
|
T | C | 3 | a0001c0001t0004g0117a0001c0001t0004g0118a0001c0001t0004g0119 | 3 | HG02257.hp2 HG02615.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.261-8910A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92089873 | ||||||
| chr9:92089910
|
G | A | 35 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0031others(32): Show | 38 | HG00733.hp2 HG01109.hp1 HG01255.hp1 others(35): Show |
intron_variant | MODIFIER | c.261-8947C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92089910 | ||||||
| chr9:92090102
|
G | T | 1 | a0001c0001t0001g0097 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.261-9139C>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92090102 | ||||||
| chr9:92090167
|
G | C | 1 | a0001c0006t0001g0300 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.261-9204C>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92090167 | ||||||
| chr9:92090351
|
G | A | 50 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(47): Show | 58 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.261-9388C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92090351 | ||||||
| chr9:92090546
|
A | G | 34 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0031others(31): Show | 37 | HG00733.hp2 HG01109.hp1 HG01255.hp1 others(34): Show |
intron_variant | MODIFIER | c.261-9583T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92090546 | ||||||
| chr9:92090552
|
C | A | 1 | a0001c0001t0001g0145 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.261-9589G>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92090552 | ||||||
| chr9:92090618
|
CA | C | 67 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(64): Show | 73 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.261-9656delT | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92090618 | ||||||
| chr9:92090621
|
AC | A | 74 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0063others(71): Show | 80 | HG00642.hp2 HG00733.hp2 HG01074.hp2 others(77): Show |
intron_variant | MODIFIER | c.261-9659delG | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92090621 | ||||||
| chr9:92090622
|
C | A | 11 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(8): Show | 11 | HG01081.hp1 HG01884.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.261-9659G>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92090622 | ||||||
| chr9:92090726
|
A | G | 66 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(63): Show | 72 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.261-9763T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92090726 | ||||||
| chr9:92090734
|
A | G | 1 | a0001c0001t0001g0074 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.261-9771T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92090734 | ||||||
| chr9:92091087
|
A | G | 3 | a0001c0001t0004g0117a0001c0001t0004g0118a0001c0001t0004g0119 | 3 | HG02257.hp2 HG02615.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.261-10124T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92091087 | ||||||
| chr9:92091090
|
ATCTCTAA others(10): Show |
A | 4 | a0001c0001t0001g0066a0001c0001t0001g0068a0001c0001t0005g0065others(1): Show | 4 | HG02630.hp2 HG02809.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.261-10144_261-1012 others(21): Show |
SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92091090 | ||||||
| chr9:92091227
|
A | C | 4 | a0001c0001t0001g0066a0001c0001t0001g0068a0001c0001t0005g0065others(1): Show | 4 | HG02630.hp2 HG02809.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.261-10264T>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92091227 | ||||||
| chr9:92091290
|
G | A | 1 | a0001c0006t0001g0300 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.261-10327C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92091290 | ||||||
| chr9:92091320
|
A | G | 17 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0083others(14): Show | 20 | HG00741.hp1 HG01070.hp1 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.261-10357T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92091320 | ||||||
| chr9:92091399
|
A | T | 8 | a0001c0001t0003g0019a0001c0001t0003g0262a0001c0001t0003g0263others(5): Show | 9 | HG01074.hp2 HG01516.hp2 HG01517.hp2 others(6): Show |
intron_variant | MODIFIER | c.261-10436T>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92091399 | ||||||
| chr9:92091481
|
A | G | 1 | a0001c0001t0001g0200 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.261-10518T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92091481 | ||||||
| chr9:92091553
|
A | G | 1 | a0001c0001t0001g0083 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.261-10590T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92091553 | ||||||
| chr9:92091757
|
T | C | 1 | a0001c0001t0001g0327 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.261-10794A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92091757 | ||||||
| chr9:92092021
|
A | T | 1 | a0001c0001t0001g0268 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.261-11058T>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92092021 | ||||||
| chr9:92092105
|
C | T | 1 | a0001c0001t0011g0253 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.261-11142G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92092105 | ||||||
| chr9:92092126
|
T | G | 8 | a0001c0001t0002g0031a0001c0001t0002g0054a0001c0001t0002g0055others(5): Show | 8 | HG01884.hp1 HG01891.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.261-11163A>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92092126 | ||||||
| chr9:92092212
|
G | A | 44 | a0001c0001t0001g0022a0001c0001t0001g0320a0001c0001t0001g0321others(41): Show | 48 | HG00733.hp2 HG01074.hp1 HG01109.hp1 others(45): Show |
intron_variant | MODIFIER | c.261-11249C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92092212 | ||||||
| chr9:92092234
|
A | G | 38 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0290others(35): Show | 40 | HG00280.hp1 HG00733.hp1 HG01074.hp1 others(37): Show |
intron_variant | MODIFIER | c.261-11271T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92092234 | ||||||
| chr9:92092264
|
A | G | 4 | a0001c0001t0002g0035a0001c0001t0002g0036a0001c0001t0002g0037others(1): Show | 4 | HG01109.hp1 HG02145.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.261-11301T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92092264 | ||||||
| chr9:92092297
|
C | T | 1 | a0001c0001t0001g0146 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.261-11334G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92092297 | ||||||
| chr9:92092344
|
G | A | 64 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(61): Show | 70 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.261-11381C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92092344 | ||||||
| chr9:92092489
|
G | C | 3 | a0001c0001t0004g0117a0001c0001t0004g0118a0001c0001t0004g0119 | 3 | HG02257.hp2 HG02615.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.261-11526C>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92092489 | ||||||
| chr9:92092513
|
G | A | 67 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(64): Show | 73 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.261-11550C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92092513 | ||||||
| chr9:92092589
|
G | A | 7 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(4): Show | 7 | HG01081.hp1 HG02258.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.261-11626C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92092589 | ||||||
| chr9:92092608
|
A | G | 1 | a0001c0001t0014g0261 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.261-11645T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92092608 | ||||||
| chr9:92092673
|
T | C | 2 | a0001c0001t0001g0318a0001c0001t0008g0319 | 2 | HG02055.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.261-11710A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92092673 | ||||||
| chr9:92092844
|
G | A | 7 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(4): Show | 7 | HG01081.hp1 HG02258.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.261-11881C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92092844 | ||||||
| chr9:92093121
|
A | T | 2 | a0001c0001t0001g0230a0001c0001t0001g0248 | 2 | NA18963.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.261-12158T>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92093121 | ||||||
| chr9:92093122
|
G | T | 2 | a0001c0001t0001g0230a0001c0001t0001g0248 | 2 | NA18963.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.261-12159C>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92093122 | ||||||
| chr9:92093271
|
A | C | 206 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(203): Show | 221 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(218): Show |
intron_variant | MODIFIER | c.261-12308T>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92093271 | ||||||
| chr9:92093272
|
C | A | 2 | a0001c0001t0001g0152a0001c0001t0001g0153 | 2 | NA19011.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.261-12309G>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92093272 | ||||||
| chr9:92093469
|
G | GCA | 4 | a0001c0001t0001g0145a0001c0001t0001g0246a0001c0001t0001g0247others(1): Show | 4 | HG01099.hp1 HG02257.hp2 NA18965.hp1 others(1): Show |
intron_variant | MODIFIER | c.261-12508_261-1250 others(6): Show |
SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92093469 | ||||||
| chr9:92093552
|
C | G | 3 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0273 | 3 | HG01891.hp2 HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.261-12589G>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92093552 | ||||||
| chr9:92093561
|
A | T | 35 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0031others(32): Show | 38 | HG00733.hp2 HG01109.hp1 HG01255.hp1 others(35): Show |
intron_variant | MODIFIER | c.261-12598T>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92093561 | ||||||
| chr9:92093654
|
T | A | 1 | a0001c0001t0011g0253 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.261-12691A>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92093654 | ||||||
| chr9:92093777
|
A | G | 1 | a0001c0001t0001g0268 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.261-12814T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92093777 | ||||||
| chr9:92094041
|
A | T | 7 | a0001c0001t0003g0019a0001c0001t0003g0262a0001c0001t0003g0263others(4): Show | 8 | HG01074.hp2 HG01516.hp2 HG01517.hp2 others(5): Show |
intron_variant | MODIFIER | c.261-13078T>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92094041 | ||||||
| chr9:92094058
|
G | A | 1 | a0001c0001t0001g0230 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.261-13095C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92094058 | ||||||
| chr9:92094099
|
G | A | 8 | a0001c0001t0003g0019a0001c0001t0003g0262a0001c0001t0003g0263others(5): Show | 9 | HG01074.hp2 HG01516.hp2 HG01517.hp2 others(6): Show |
intron_variant | MODIFIER | c.261-13136C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92094099 | ||||||
| chr9:92094124
|
G | A | 1 | a0002c0003t0003g0062 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.261-13161C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92094124 | ||||||
| chr9:92094143
|
G | A | 2 | a0001c0001t0001g0105a0001c0001t0001g0106 | 2 | HG00621.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.261-13180C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92094143 | ||||||
| chr9:92094191
|
G | GT | 2 | a0001c0001t0001g0018a0001c0001t0001g0254 | 3 | HG02602.hp1 HG03654.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.261-13229dupA | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92094191 | ||||||
| chr9:92094213
|
C | T | 207 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(204): Show | 222 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(219): Show |
intron_variant | MODIFIER | c.261-13250G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92094213 | ||||||
| chr9:92094227
|
G | A | 2 | a0001c0001t0004g0117a0001c0001t0004g0118 | 2 | HG02615.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.261-13264C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92094227 | ||||||
| chr9:92094235
|
G | C | 67 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(64): Show | 73 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.261-13272C>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92094235 | ||||||
| chr9:92094365
|
T | C | 34 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0031others(31): Show | 37 | HG00733.hp2 HG01109.hp1 HG01255.hp1 others(34): Show |
intron_variant | MODIFIER | c.261-13402A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92094365 | ||||||
| chr9:92094537
|
G | T | 64 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(61): Show | 70 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.261-13574C>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92094537 | ||||||
| chr9:92094555
|
G | A | 2 | a0001c0001t0001g0276a0001c0001t0001g0277 | 2 | HG01496.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.261-13592C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92094555 | ||||||
| chr9:92094751
|
C | A | 1 | a0001c0001t0002g0033 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.261-13788G>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92094751 | ||||||
| chr9:92094831
|
C | T | 1 | a0001c0001t0001g0292 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.261-13868G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92094831 | ||||||
| chr9:92095039
|
A | T | 1 | a0001c0001t0001g0199 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.260+13701T>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92095039 | ||||||
| chr9:92095087
|
C | A | 1 | a0001c0001t0001g0305 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.260+13653G>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92095087 | ||||||
| chr9:92095121
|
T | TA | 37 | a0001c0001t0001g0029a0001c0001t0002g0002a0001c0001t0002g0007others(34): Show | 40 | HG00733.hp2 HG01109.hp1 HG01255.hp1 others(37): Show |
intron_variant | MODIFIER | c.260+13618dupT | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92095121 | ||||||
| chr9:92095275
|
C | T | 1 | a0001c0001t0001g0274 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.260+13465G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92095275 | ||||||
| chr9:92095842
|
G | A | 35 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0031others(32): Show | 38 | HG00733.hp2 HG01109.hp1 HG01255.hp1 others(35): Show |
intron_variant | MODIFIER | c.260+12898C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92095842 | ||||||
| chr9:92095905
|
C | T | 13 | a0001c0001t0001g0009a0001c0001t0001g0140a0001c0001t0001g0141others(10): Show | 14 | HG01099.hp1 HG01243.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.260+12835G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92095905 | ||||||
| chr9:92095906
|
G | A | 3 | a0001c0001t0004g0117a0001c0001t0004g0118a0001c0001t0004g0119 | 3 | HG02257.hp2 HG02615.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.260+12834C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92095906 | ||||||
| chr9:92096065
|
C | T | 1 | a0002c0003t0003g0062 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.260+12675G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92096065 | ||||||
| chr9:92096265
|
A | G | 4 | a0001c0001t0002g0035a0001c0001t0002g0036a0001c0001t0002g0037others(1): Show | 4 | HG01109.hp1 HG02145.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.260+12475T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92096265 | ||||||
| chr9:92096394
|
T | G | 2 | a0001c0001t0001g0074a0001c0001t0001g0082 | 2 | HG02015.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.260+12346A>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92096394 | ||||||
| chr9:92096572
|
A | G | 22 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0123others(19): Show | 22 | HG02015.hp2 HG02040.hp2 HG02132.hp1 others(19): Show |
intron_variant | MODIFIER | c.260+12168T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92096572 | ||||||
| chr9:92096651
|
T | G | 1 | a0001c0001t0001g0301 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.260+12089A>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92096651 | ||||||
| chr9:92096894
|
A | G | 1 | a0001c0001t0001g0120 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.260+11846T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92096894 | ||||||
| chr9:92096899
|
GA | G | 6 | a0001c0001t0001g0020a0001c0001t0001g0063a0001c0001t0001g0064others(3): Show | 7 | HG01081.hp2 HG02257.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.260+11840delT | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92096899 | ||||||
| chr9:92096925
|
T | A | 1 | a0001c0001t0001g0081 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.260+11815A>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92096925 | ||||||
| chr9:92096933
|
G | A | 1 | a0001c0001t0001g0273 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.260+11807C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92096933 | ||||||
| chr9:92097019
|
T | C | 1 | a0001c0001t0002g0049 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.260+11721A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92097019 | ||||||
| chr9:92097070
|
G | A | 36 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0031others(33): Show | 39 | HG00733.hp2 HG01109.hp1 HG01255.hp1 others(36): Show |
intron_variant | MODIFIER | c.260+11670C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92097070 | ||||||
| chr9:92097288
|
A | G | 1 | a0001c0001t0001g0268 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.260+11452T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92097288 | ||||||
| chr9:92097344
|
G | A | 8 | a0001c0001t0003g0019a0001c0001t0003g0262a0001c0001t0003g0263others(5): Show | 9 | HG01074.hp2 HG01516.hp2 HG01517.hp2 others(6): Show |
intron_variant | MODIFIER | c.260+11396C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92097344 | ||||||
| chr9:92097375
|
T | C | 1 | a0001c0001t0001g0106 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.260+11365A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92097375 | ||||||
| chr9:92097414
|
C | T | 22 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0123others(19): Show | 22 | HG02015.hp2 HG02040.hp2 HG02132.hp1 others(19): Show |
intron_variant | MODIFIER | c.260+11326G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92097414 | ||||||
| chr9:92097566
|
C | T | 3 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0135 | 3 | NA18947.hp2 NA18973.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.260+11174G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92097566 | ||||||
| chr9:92097601
|
A | C | 5 | a0001c0001t0003g0019a0001c0001t0003g0262a0001c0001t0003g0263others(2): Show | 6 | HG01074.hp2 HG01516.hp2 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.260+11139T>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92097601 | ||||||
| chr9:92097710
|
G | A | 1 | a0001c0001t0001g0245 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.260+11030C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92097710 | ||||||
| chr9:92097713
|
G | A | 35 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0031others(32): Show | 38 | HG00733.hp2 HG01109.hp1 HG01255.hp1 others(35): Show |
intron_variant | MODIFIER | c.260+11027C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92097713 | ||||||
| chr9:92097813
|
T | A | 1 | a0001c0001t0004g0119 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.260+10927A>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92097813 | ||||||
| chr9:92097839
|
G | A | 1 | a0001c0001t0001g0268 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.260+10901C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92097839 | ||||||
| chr9:92097928
|
G | C | 1 | a0001c0001t0011g0253 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.260+10812C>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92097928 | ||||||
| chr9:92097949
|
G | A | 1 | a0001c0001t0001g0250 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.260+10791C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92097949 | ||||||
| chr9:92097954
|
C | T | 13 | a0001c0001t0001g0009a0001c0001t0001g0140a0001c0001t0001g0141others(10): Show | 14 | HG01099.hp1 HG01243.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.260+10786G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92097954 | ||||||
| chr9:92097956
|
C | A | 25 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0001g0121others(22): Show | 26 | HG00642.hp2 HG02015.hp2 HG02040.hp2 others(23): Show |
intron_variant | MODIFIER | c.260+10784G>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92097956 | ||||||
| chr9:92097999
|
T | C | 6 | a0001c0001t0001g0291a0001c0001t0001g0302a0001c0001t0001g0303others(3): Show | 6 | HG02040.hp1 HG02135.hp2 NA18949.hp1 others(3): Show |
intron_variant | MODIFIER | c.260+10741A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92097999 | ||||||
| chr9:92098063
|
G | A | 1 | a0001c0001t0001g0290 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.260+10677C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92098063 | ||||||
| chr9:92098193
|
C | T | 2 | a0001c0001t0001g0255a0001c0001t0001g0256 | 2 | HG02965.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.260+10547G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92098193 | ||||||
| chr9:92098203
|
C | A | 1 | a0001c0001t0011g0253 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.260+10537G>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92098203 | ||||||
| chr9:92098296
|
T | C | 206 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(203): Show | 221 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(218): Show |
intron_variant | MODIFIER | c.260+10444A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92098296 | ||||||
| chr9:92098338
|
A | G | 1 | a0002c0003t0003g0062 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.260+10402T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92098338 | ||||||
| chr9:92098342
|
C | T | 1 | a0001c0001t0011g0253 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.260+10398G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92098342 | ||||||
| chr9:92098343
|
T | G | 153 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(150): Show | 165 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(162): Show |
intron_variant | MODIFIER | c.260+10397A>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92098343 | ||||||
| chr9:92098348
|
A | G | 3 | a0001c0001t0001g0020a0001c0001t0001g0063a0001c0001t0001g0064 | 4 | HG01081.hp2 HG02895.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.260+10392T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92098348 | ||||||
| chr9:92098381
|
C | T | 2 | a0001c0001t0001g0074a0001c0001t0001g0082 | 2 | HG02015.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.260+10359G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92098381 | ||||||
| chr9:92098615
|
G | C | 30 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0290others(27): Show | 32 | HG00280.hp1 HG01074.hp1 HG01123.hp1 others(29): Show |
intron_variant | MODIFIER | c.260+10125C>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92098615 | ||||||
| chr9:92098697
|
G | T | 35 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0031others(32): Show | 38 | HG00733.hp2 HG01109.hp1 HG01255.hp1 others(35): Show |
intron_variant | MODIFIER | c.260+10043C>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92098697 | ||||||
| chr9:92098702
|
C | CA | 34 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0031others(31): Show | 37 | HG00733.hp2 HG01109.hp1 HG01255.hp1 others(34): Show |
intron_variant | MODIFIER | c.260+10037dupT | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92098702 | ||||||
| chr9:92098740
|
A | G | 2 | a0001c0001t0001g0152a0001c0001t0001g0153 | 2 | NA19011.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.260+10000T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92098740 | ||||||
| chr9:92098885
|
G | GGATA | 36 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0031others(33): Show | 39 | HG00733.hp2 HG01109.hp1 HG01255.hp1 others(36): Show |
intron_variant | MODIFIER | c.260+9854_260+9855i others(6): Show |
SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92098885 | ||||||
| chr9:92099166
|
A | G | 2 | a0001c0001t0002g0050a0001c0001t0002g0051 | 2 | NA18950.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.260+9574T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92099166 | ||||||
| chr9:92099402
|
T | C | 1 | a0001c0001t0014g0261 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.260+9338A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92099402 | ||||||
| chr9:92099419
|
C | T | 8 | a0001c0001t0003g0019a0001c0001t0003g0262a0001c0001t0003g0263others(5): Show | 9 | HG01074.hp2 HG01516.hp2 HG01517.hp2 others(6): Show |
intron_variant | MODIFIER | c.260+9321G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92099419 | ||||||
| chr9:92099480
|
CT | C | 29 | a0001c0001t0001g0009a0001c0001t0001g0066a0001c0001t0001g0068others(26): Show | 30 | HG01081.hp1 HG01243.hp1 HG02109.hp1 others(27): Show |
intron_variant | MODIFIER | c.260+9259delA | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92099480 | ||||||
| chr9:92099480
|
CTT | C | 130 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(127): Show | 141 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(138): Show |
intron_variant | MODIFIER | c.260+9258_260+9259d others(4): Show |
SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92099480 | ||||||
| chr9:92099480
|
CTTT | C | 6 | a0001c0001t0001g0082a0001c0001t0002g0031a0001c0001t0002g0054others(3): Show | 6 | HG02015.hp1 HG02922.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.260+9257_260+9259d others(5): Show |
SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92099480 | ||||||
| chr9:92099640
|
C | T | 26 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0001g0121others(23): Show | 27 | HG00642.hp2 HG02015.hp2 HG02040.hp2 others(24): Show |
intron_variant | MODIFIER | c.260+9100G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92099640 | ||||||
| chr9:92099664
|
T | C | 1 | a0001c0001t0002g0032 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.260+9076A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92099664 | ||||||
| chr9:92099767
|
C | G | 1 | a0001c0001t0014g0261 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.260+8973G>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92099767 | ||||||
| chr9:92100041
|
G | A | 66 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(63): Show | 73 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.260+8699C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92100041 | ||||||
| chr9:92100114
|
C | CA | 40 | a0001c0001t0001g0020a0001c0001t0001g0063a0001c0001t0001g0064others(37): Show | 44 | HG00733.hp2 HG01081.hp2 HG01109.hp1 others(41): Show |
intron_variant | MODIFIER | c.260+8625dupT | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92100114 | ||||||
| chr9:92100181
|
G | A | 7 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(4): Show | 7 | HG01081.hp1 HG02258.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.260+8559C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92100181 | ||||||
| chr9:92100626
|
T | C | 36 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0031others(33): Show | 39 | HG00733.hp2 HG01109.hp1 HG01255.hp1 others(36): Show |
intron_variant | MODIFIER | c.260+8114A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92100626 | ||||||
| chr9:92100727
|
C | T | 2 | a0001c0001t0001g0189a0001c0001t0001g0198 | 2 | NA18999.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.260+8013G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92100727 | ||||||
| chr9:92100782
|
A | G | 103 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(100): Show | 112 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(109): Show |
intron_variant | MODIFIER | c.260+7958T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92100782 | ||||||
| chr9:92100837
|
GA | G | 15 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(12): Show | 16 | HG01074.hp2 HG01081.hp1 HG01516.hp2 others(13): Show |
intron_variant | MODIFIER | c.260+7902delT | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92100837 | ||||||
| chr9:92101289
|
G | A | 25 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0001g0121others(22): Show | 26 | HG00642.hp2 HG02015.hp2 HG02040.hp2 others(23): Show |
intron_variant | MODIFIER | c.260+7451C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92101289 | ||||||
| chr9:92101315
|
C | A | 32 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(29): Show | 37 | HG00408.hp2 HG00558.hp1 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.260+7425G>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92101315 | ||||||
| chr9:92101494
|
G | A | 2 | a0001c0001t0002g0050a0001c0001t0002g0051 | 2 | NA18950.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.260+7246C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92101494 | ||||||
| chr9:92101556
|
C | T | 1 | a0001c0001t0001g0110 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.260+7184G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92101556 | ||||||
| chr9:92101561
|
CA | C | 114 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(111): Show | 123 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.260+7178delT | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92101561 | ||||||
| chr9:92101561
|
CAA | C | 39 | a0001c0001t0001g0018a0001c0001t0001g0063a0001c0001t0001g0073others(36): Show | 41 | HG00642.hp2 HG01074.hp2 HG01257.hp1 others(38): Show |
intron_variant | MODIFIER | c.260+7177_260+7178d others(4): Show |
SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92101561 | ||||||
| chr9:92101578
|
AAAAAGAG | A | 33 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0031others(30): Show | 36 | HG00733.hp2 HG01109.hp1 HG01255.hp1 others(33): Show |
intron_variant | MODIFIER | c.260+7155_260+7161d others(9): Show |
SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92101578 | ||||||
| chr9:92101581
|
A | G | 1 | a0001c0001t0001g0268 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.260+7159T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92101581 | ||||||
| chr9:92101588
|
A | G | 36 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0031others(33): Show | 39 | HG00733.hp2 HG01109.hp1 HG01255.hp1 others(36): Show |
intron_variant | MODIFIER | c.260+7152T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92101588 | ||||||
| chr9:92101614
|
A | G | 1 | a0001c0001t0001g0120 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.260+7126T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92101614 | ||||||
| chr9:92101687
|
A | G | 1 | a0002c0003t0003g0062 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.260+7053T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92101687 | ||||||
| chr9:92101949
|
C | T | 1 | a0001c0005t0001g0185 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.260+6791G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92101949 | ||||||
| chr9:92102040
|
A | G | 146 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(143): Show | 158 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(155): Show |
intron_variant | MODIFIER | c.260+6700T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92102040 | ||||||
| chr9:92102325
|
G | A | 1 | a0001c0001t0001g0120 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.260+6415C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92102325 | ||||||
| chr9:92102327
|
C | A | 5 | a0001c0001t0003g0019a0001c0001t0003g0262a0001c0001t0003g0263others(2): Show | 6 | HG01074.hp2 HG01516.hp2 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.260+6413G>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92102327 | ||||||
| chr9:92102472
|
A | C | 142 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(139): Show | 154 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(151): Show |
intron_variant | MODIFIER | c.260+6268T>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92102472 | ||||||
| chr9:92102516
|
A | T | 1 | a0001c0001t0001g0196 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.260+6224T>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92102516 | ||||||
| chr9:92102689
|
A | C | 7 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(4): Show | 7 | HG01081.hp1 HG02258.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.260+6051T>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92102689 | ||||||
| chr9:92102745
|
C | T | 3 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0273 | 3 | HG01891.hp2 HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.260+5995G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92102745 | ||||||
| chr9:92102930
|
A | AT | 13 | a0001c0001t0001g0009a0001c0001t0001g0140a0001c0001t0001g0141others(10): Show | 14 | HG01099.hp1 HG01243.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.260+5809dupA | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92102930 | ||||||
| chr9:92102974
|
T | C | 1 | a0001c0001t0001g0108 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.260+5766A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92102974 | ||||||
| chr9:92102983
|
G | A | 12 | a0001c0001t0001g0302a0001c0001t0001g0303a0001c0001t0001g0304others(9): Show | 13 | HG01074.hp2 HG01516.hp2 HG01517.hp2 others(10): Show |
intron_variant | MODIFIER | c.260+5757C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92102983 | ||||||
| chr9:92103111
|
T | G | 1 | a0001c0001t0002g0059 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.260+5629A>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92103111 | ||||||
| chr9:92103157
|
C | T | 1 | a0001c0001t0001g0195 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.260+5583G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92103157 | ||||||
| chr9:92103190
|
G | A | 1 | a0001c0001t0001g0188 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.260+5550C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92103190 | ||||||
| chr9:92103374
|
C | T | 36 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0031others(33): Show | 39 | HG00733.hp2 HG01109.hp1 HG01255.hp1 others(36): Show |
intron_variant | MODIFIER | c.260+5366G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92103374 | ||||||
| chr9:92103529
|
C | T | 1 | a0001c0001t0001g0194 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.260+5211G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92103529 | ||||||
| chr9:92103591
|
G | A | 35 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0031others(32): Show | 38 | HG00733.hp2 HG01109.hp1 HG01255.hp1 others(35): Show |
intron_variant | MODIFIER | c.260+5149C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92103591 | ||||||
| chr9:92103596
|
C | T | 1 | a0001c0001t0001g0329 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.260+5144G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92103596 | ||||||
| chr9:92103629
|
G | A | 7 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(4): Show | 7 | HG01081.hp1 HG02258.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.260+5111C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92103629 | ||||||
| chr9:92103645
|
T | C | 1 | a0001c0001t0002g0052 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.260+5095A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92103645 | ||||||
| chr9:92103704
|
G | A | 8 | a0001c0001t0003g0019a0001c0001t0003g0262a0001c0001t0003g0263others(5): Show | 9 | HG01074.hp2 HG01516.hp2 HG01517.hp2 others(6): Show |
intron_variant | MODIFIER | c.260+5036C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92103704 | ||||||
| chr9:92103758
|
A | G | 207 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(204): Show | 222 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(219): Show |
intron_variant | MODIFIER | c.260+4982T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92103758 | ||||||
| chr9:92103769
|
G | T | 2 | a0001c0001t0001g0318a0001c0001t0008g0319 | 2 | HG02055.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.260+4971C>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92103769 | ||||||
| chr9:92103865
|
C | T | 2 | a0001c0001t0001g0018a0001c0001t0001g0254 | 3 | HG02602.hp1 HG03654.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.260+4875G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92103865 | ||||||
| chr9:92103880
|
G | A | 34 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0031others(31): Show | 37 | HG00733.hp2 HG01109.hp1 HG01255.hp1 others(34): Show |
intron_variant | MODIFIER | c.260+4860C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92103880 | ||||||
| chr9:92103905
|
C | A | 1 | a0001c0001t0001g0231 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.260+4835G>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92103905 | ||||||
| chr9:92104028
|
C | A | 7 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(4): Show | 7 | HG01081.hp1 HG02258.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.260+4712G>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92104028 | ||||||
| chr9:92104072
|
A | T | 1 | a0002c0003t0003g0062 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.260+4668T>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92104072 | ||||||
| chr9:92104192
|
C | T | 5 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0142others(2): Show | 5 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.260+4548G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92104192 | ||||||
| chr9:92104240
|
G | A | 2 | a0001c0001t0001g0246a0001c0001t0001g0247 | 2 | NA18965.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.260+4500C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92104240 | ||||||
| chr9:92104454
|
G | A | 67 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(64): Show | 73 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.260+4286C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92104454 | ||||||
| chr9:92104500
|
C | G | 1 | a0001c0001t0002g0061 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.260+4240G>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92104500 | ||||||
| chr9:92104641
|
G | A | 8 | a0001c0001t0002g0031a0001c0001t0002g0054a0001c0001t0002g0055others(5): Show | 8 | HG01884.hp1 HG01891.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.260+4099C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92104641 | ||||||
| chr9:92104763
|
C | T | 1 | a0002c0003t0003g0062 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.260+3977G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92104763 | ||||||
| chr9:92104915
|
G | A | 8 | a0001c0001t0003g0019a0001c0001t0003g0262a0001c0001t0003g0263others(5): Show | 9 | HG01074.hp2 HG01516.hp2 HG01517.hp2 others(6): Show |
intron_variant | MODIFIER | c.260+3825C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92104915 | ||||||
| chr9:92104971
|
A | C | 2 | a0001c0001t0001g0291a0001c0001t0001g0306 | 2 | HG02135.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.260+3769T>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92104971 | ||||||
| chr9:92105013
|
G | A | 1 | a0001c0001t0001g0148 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.260+3727C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92105013 | ||||||
| chr9:92105074
|
T | G | 1 | a0001c0001t0001g0068 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.260+3666A>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92105074 | ||||||
| chr9:92105085
|
G | A | 22 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0123others(19): Show | 22 | HG02015.hp2 HG02040.hp2 HG02132.hp1 others(19): Show |
intron_variant | MODIFIER | c.260+3655C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92105085 | ||||||
| chr9:92105129
|
G | A | 60 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(57): Show | 66 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.260+3611C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92105129 | ||||||
| chr9:92105185
|
G | A | 53 | a0001c0001t0001g0009a0001c0001t0001g0021a0001c0001t0001g0022others(50): Show | 56 | HG00280.hp1 HG00733.hp1 HG01074.hp1 others(53): Show |
intron_variant | MODIFIER | c.260+3555C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92105185 | ||||||
| chr9:92105208
|
G | A | 1 | a0001c0001t0001g0137 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.260+3532C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92105208 | ||||||
| chr9:92105346
|
G | A | 6 | a0001c0001t0001g0009a0001c0001t0001g0146a0001c0001t0001g0147others(3): Show | 7 | HG01243.hp1 HG03453.hp2 HG03471.hp2 others(4): Show |
intron_variant | MODIFIER | c.260+3394C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92105346 | ||||||
| chr9:92105526
|
T | C | 206 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(203): Show | 221 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(218): Show |
intron_variant | MODIFIER | c.260+3214A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92105526 | ||||||
| chr9:92105733
|
C | T | 36 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0031others(33): Show | 39 | HG00733.hp2 HG01109.hp1 HG01255.hp1 others(36): Show |
intron_variant | MODIFIER | c.260+3007G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92105733 | ||||||
| chr9:92105736
|
G | A | 1 | a0001c0001t0001g0109 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.260+3004C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92105736 | ||||||
| chr9:92105753
|
T | G | 34 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0031others(31): Show | 37 | HG00733.hp2 HG01109.hp1 HG01255.hp1 others(34): Show |
intron_variant | MODIFIER | c.260+2987A>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92105753 | ||||||
| chr9:92105761
|
C | T | 3 | a0001c0001t0001g0274a0001c0001t0001g0275a0001c0001t0001g0289 | 3 | HG02258.hp1 HG02622.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.260+2979G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92105761 | ||||||
| chr9:92105802
|
G | A | 3 | a0001c0001t0001g0274a0001c0001t0001g0275a0001c0001t0001g0289 | 3 | HG02258.hp1 HG02622.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.260+2938C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92105802 | ||||||
| chr9:92105850
|
G | A | 6 | a0001c0001t0001g0020a0001c0001t0001g0063a0001c0001t0001g0064others(3): Show | 7 | HG01081.hp2 HG02257.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.260+2890C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92105850 | ||||||
| chr9:92105917
|
C | T | 1 | a0002c0003t0003g0062 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.260+2823G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92105917 | ||||||
| chr9:92105918
|
G | A | 35 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0031others(32): Show | 38 | HG00733.hp2 HG01109.hp1 HG01255.hp1 others(35): Show |
intron_variant | MODIFIER | c.260+2822C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92105918 | ||||||
| chr9:92105961
|
C | T | 1 | a0001c0001t0002g0034 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.260+2779G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92105961 | ||||||
| chr9:92106016
|
C | A | 103 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(100): Show | 112 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(109): Show |
intron_variant | MODIFIER | c.260+2724G>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92106016 | ||||||
| chr9:92106038
|
G | A | 3 | a0001c0001t0001g0020a0001c0001t0001g0063a0001c0001t0001g0064 | 4 | HG01081.hp2 HG02895.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.260+2702C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92106038 | ||||||
| chr9:92106067
|
G | A | 21 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(18): Show | 24 | HG00438.hp1 HG00558.hp2 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.260+2673C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92106067 | ||||||
| chr9:92106090
|
T | C | 3 | a0001c0001t0004g0117a0001c0001t0004g0118a0001c0001t0004g0119 | 3 | HG02257.hp2 HG02615.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.260+2650A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92106090 | ||||||
| chr9:92106098
|
G | C | 1 | a0001c0001t0001g0269 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.260+2642C>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92106098 | ||||||
| chr9:92106117
|
G | A | 3 | a0001c0001t0001g0110a0001c0001t0001g0145a0001c0001t0001g0151 | 3 | HG01099.hp1 HG02257.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.260+2623C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92106117 | ||||||
| chr9:92106147
|
G | C | 34 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0031others(31): Show | 37 | HG00733.hp2 HG01109.hp1 HG01255.hp1 others(34): Show |
intron_variant | MODIFIER | c.260+2593C>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92106147 | ||||||
| chr9:92106271
|
T | C | 103 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(100): Show | 112 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(109): Show |
intron_variant | MODIFIER | c.260+2469A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92106271 | ||||||
| chr9:92106368
|
A | G | 103 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(100): Show | 112 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(109): Show |
intron_variant | MODIFIER | c.260+2372T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92106368 | ||||||
| chr9:92106423
|
G | A | 1 | a0002c0003t0003g0062 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.260+2317C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92106423 | ||||||
| chr9:92106468
|
G | A | 13 | a0001c0001t0001g0009a0001c0001t0001g0140a0001c0001t0001g0141others(10): Show | 14 | HG01099.hp1 HG01243.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.260+2272C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92106468 | ||||||
| chr9:92106472
|
C | CA | 58 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(55): Show | 61 | HG00733.hp2 HG01081.hp1 HG01109.hp1 others(58): Show |
intron_variant | MODIFIER | c.260+2267dupT | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92106472 | ||||||
| chr9:92106613
|
C | T | 1 | a0002c0003t0003g0062 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.260+2127G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92106613 | ||||||
| chr9:92106614
|
G | A | 3 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0273 | 3 | HG01891.hp2 HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.260+2126C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92106614 | ||||||
| chr9:92106645
|
C | T | 1 | a0001c0001t0001g0268 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.260+2095G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92106645 | ||||||
| chr9:92106690
|
T | C | 3 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0273 | 3 | HG01891.hp2 HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.260+2050A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92106690 | ||||||
| chr9:92106710
|
T | G | 3 | a0001c0001t0001g0020a0001c0001t0001g0063a0001c0001t0001g0064 | 4 | HG01081.hp2 HG02895.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.260+2030A>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92106710 | ||||||
| chr9:92107086
|
T | C | 1 | a0001c0001t0001g0150 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.260+1654A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92107086 | ||||||
| chr9:92107122
|
G | T | 7 | a0001c0001t0002g0031a0001c0001t0002g0054a0001c0001t0002g0055others(4): Show | 7 | HG01884.hp1 HG02922.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.260+1618C>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92107122 | ||||||
| chr9:92107169
|
A | G | 36 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0031others(33): Show | 39 | HG00733.hp2 HG01109.hp1 HG01255.hp1 others(36): Show |
intron_variant | MODIFIER | c.260+1571T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92107169 | ||||||
| chr9:92107190
|
C | T | 35 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0031others(32): Show | 38 | HG00733.hp2 HG01109.hp1 HG01255.hp1 others(35): Show |
intron_variant | MODIFIER | c.260+1550G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92107190 | ||||||
| chr9:92107394
|
A | C | 1 | a0001c0004t0001g0186 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.260+1346T>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92107394 | ||||||
| chr9:92107405
|
T | C | 206 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(203): Show | 221 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(218): Show |
intron_variant | MODIFIER | c.260+1335A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92107405 | ||||||
| chr9:92107484
|
G | A | 1 | a0001c0001t0013g0267 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.260+1256C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92107484 | ||||||
| chr9:92107608
|
C | T | 1 | a0002c0003t0003g0062 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.260+1132G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92107608 | ||||||
| chr9:92107684
|
G | A | 25 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0001g0121others(22): Show | 26 | HG00642.hp2 HG02015.hp2 HG02040.hp2 others(23): Show |
intron_variant | MODIFIER | c.260+1056C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92107684 | ||||||
| chr9:92107865
|
C | A | 1 | a0001c0001t0002g0053 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.260+875G>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92107865 | ||||||
| chr9:92107870
|
C | A | 145 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(142): Show | 157 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(154): Show |
intron_variant | MODIFIER | c.260+870G>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92107870 | ||||||
| chr9:92107955
|
T | A | 1 | a0002c0003t0003g0062 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.260+785A>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92107955 | ||||||
| chr9:92108054
|
G | T | 1 | a0001c0001t0011g0253 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.260+686C>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92108054 | ||||||
| chr9:92108140
|
G | T | 26 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0001g0121others(23): Show | 27 | HG00642.hp2 HG02015.hp2 HG02040.hp2 others(24): Show |
intron_variant | MODIFIER | c.260+600C>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92108140 | ||||||
| chr9:92108544
|
A | C | 1 | a0002c0003t0003g0062 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.260+196T>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92108544 | ||||||
| chr9:92108583
|
T | C | 33 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0031others(30): Show | 36 | HG00733.hp2 HG01109.hp1 HG01255.hp1 others(33): Show |
intron_variant | MODIFIER | c.260+157A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92108583 | ||||||
| chr9:92108962
|
T | C | 1 | a0002c0003t0003g0062 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.166-128A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 2/14 | chr9 | 92108962 | ||||||
| chr9:92109199
|
C | T | 53 | a0001c0001t0001g0009a0001c0001t0001g0021a0001c0001t0001g0022others(50): Show | 56 | HG00280.hp1 HG00733.hp1 HG01074.hp1 others(53): Show |
intron_variant | MODIFIER | c.166-365G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 2/14 | chr9 | 92109199 | ||||||
| chr9:92109200
|
G | A | 3 | a0001c0001t0004g0117a0001c0001t0004g0118a0001c0001t0004g0119 | 3 | HG02257.hp2 HG02615.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.166-366C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 2/14 | chr9 | 92109200 | ||||||
| chr9:92109291
|
G | A | 1 | a0001c0001t0001g0268 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.166-457C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 2/14 | chr9 | 92109291 | ||||||
| chr9:92109296
|
T | C | 1 | a0001c0001t0001g0151 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.166-462A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 2/14 | chr9 | 92109296 | ||||||
| chr9:92109335
|
C | G | 4 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0071others(1): Show | 4 | HG02074.hp2 NA18939.hp2 NA19064.hp2 others(1): Show |
intron_variant | MODIFIER | c.166-501G>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 2/14 | chr9 | 92109335 | ||||||
| chr9:92109428
|
A | T | 1 | a0001c0001t0001g0193 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.166-594T>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 2/14 | chr9 | 92109428 | ||||||
| chr9:92109438
|
G | A | 205 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(202): Show | 220 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(217): Show |
intron_variant | MODIFIER | c.166-604C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 2/14 | chr9 | 92109438 | ||||||
| chr9:92109545
|
A | G | 1 | a0001c0001t0002g0032 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.166-711T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 2/14 | chr9 | 92109545 | ||||||
| chr9:92109648
|
A | T | 67 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(64): Show | 73 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.166-814T>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 2/14 | chr9 | 92109648 | ||||||
| chr9:92109651
|
C | G | 1 | a0001c0001t0001g0145 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.166-817G>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 2/14 | chr9 | 92109651 | ||||||
| chr9:92109705
|
G | A | 1 | a0001c0001t0001g0268 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.166-871C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 2/14 | chr9 | 92109705 | ||||||
| chr9:92109720
|
C | T | 1 | a0001c0001t0001g0271 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.166-886G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 2/14 | chr9 | 92109720 | ||||||
| chr9:92109738
|
C | T | 1 | a0001c0001t0001g0268 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.166-904G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 2/14 | chr9 | 92109738 | ||||||
| chr9:92109771
|
G | A | 60 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(57): Show | 66 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.166-937C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 2/14 | chr9 | 92109771 | ||||||
| chr9:92109790
|
T | C | 22 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0123others(19): Show | 22 | HG02015.hp2 HG02040.hp2 HG02132.hp1 others(19): Show |
intron_variant | MODIFIER | c.166-956A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 2/14 | chr9 | 92109790 | ||||||
| chr9:92109904
|
C | T | 6 | a0001c0001t0001g0020a0001c0001t0001g0063a0001c0001t0001g0064others(3): Show | 7 | HG01081.hp2 HG02257.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.166-1070G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 2/14 | chr9 | 92109904 | ||||||
| chr9:92109905
|
G | A | 34 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0031others(31): Show | 37 | HG00733.hp2 HG01109.hp1 HG01255.hp1 others(34): Show |
intron_variant | MODIFIER | c.166-1071C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 2/14 | chr9 | 92109905 | ||||||
| chr9:92109984
|
A | G | 34 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0031others(31): Show | 37 | HG00733.hp2 HG01109.hp1 HG01255.hp1 others(34): Show |
intron_variant | MODIFIER | c.166-1150T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 2/14 | chr9 | 92109984 | ||||||
| chr9:92110231
|
T | C | 1 | a0001c0001t0012g0251 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.166-1397A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 2/14 | chr9 | 92110231 | ||||||
| chr9:92110349
|
C | T | 5 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0142others(2): Show | 5 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.166-1515G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 2/14 | chr9 | 92110349 | ||||||
| chr9:92110367
|
A | G | 1 | a0002c0003t0003g0062 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.166-1533T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 2/14 | chr9 | 92110367 | ||||||
| chr9:92110401
|
C | T | 8 | a0001c0001t0002g0031a0001c0001t0002g0054a0001c0001t0002g0055others(5): Show | 8 | HG01884.hp1 HG01891.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.166-1567G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 2/14 | chr9 | 92110401 | ||||||
| chr9:92110548
|
T | C | 3 | a0001c0001t0001g0020a0001c0001t0001g0063a0001c0001t0001g0064 | 4 | HG01081.hp2 HG02895.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.166-1714A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 2/14 | chr9 | 92110548 | ||||||
| chr9:92110612
|
C | T | 1 | a0001c0001t0002g0054 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.166-1778G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 2/14 | chr9 | 92110612 | ||||||
| chr9:92110642
|
G | A | 1 | a0001c0005t0001g0185 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.166-1808C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 2/14 | chr9 | 92110642 | ||||||
| chr9:92110726
|
T | C | 3 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0273 | 3 | HG01891.hp2 HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.165+1729A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 2/14 | chr9 | 92110726 | ||||||
| chr9:92110766
|
A | C | 3 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192 | 3 | HG00741.hp2 HG02683.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.165+1689T>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 2/14 | chr9 | 92110766 | ||||||
| chr9:92110974
|
T | C | 36 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0031others(33): Show | 39 | HG00733.hp2 HG01109.hp1 HG01255.hp1 others(36): Show |
intron_variant | MODIFIER | c.165+1481A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 2/14 | chr9 | 92110974 | ||||||
| chr9:92111033
|
C | T | 1 | a0001c0001t0001g0189 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.165+1422G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 2/14 | chr9 | 92111033 | ||||||
| chr9:92111042
|
A | G | 38 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0290others(35): Show | 40 | HG00280.hp1 HG00733.hp1 HG01074.hp1 others(37): Show |
intron_variant | MODIFIER | c.165+1413T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 2/14 | chr9 | 92111042 | ||||||
| chr9:92111114
|
T | A | 1 | a0001c0001t0001g0138 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.165+1341A>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 2/14 | chr9 | 92111114 | ||||||
| chr9:92111144
|
T | C | 13 | a0001c0001t0001g0009a0001c0001t0001g0140a0001c0001t0001g0141others(10): Show | 14 | HG01099.hp1 HG01243.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.165+1311A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 2/14 | chr9 | 92111144 | ||||||
| chr9:92111262
|
C | T | 3 | a0001c0001t0004g0117a0001c0001t0004g0118a0001c0001t0004g0119 | 3 | HG02257.hp2 HG02615.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.165+1193G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 2/14 | chr9 | 92111262 | ||||||
| chr9:92111464
|
T | G | 13 | a0001c0001t0001g0009a0001c0001t0001g0140a0001c0001t0001g0141others(10): Show | 14 | HG01099.hp1 HG01243.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.165+991A>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 2/14 | chr9 | 92111464 | ||||||
| chr9:92111485
|
A | G | 251 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(248): Show | 274 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(271): Show |
intron_variant | MODIFIER | c.165+970T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 2/14 | chr9 | 92111485 | ||||||
| chr9:92111511
|
C | A | 1 | a0001c0001t0011g0253 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.165+944G>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 2/14 | chr9 | 92111511 | ||||||
| chr9:92111630
|
G | A | 35 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0031others(32): Show | 38 | HG00733.hp2 HG01109.hp1 HG01255.hp1 others(35): Show |
intron_variant | MODIFIER | c.165+825C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 2/14 | chr9 | 92111630 | ||||||
| chr9:92111689
|
A | G | 38 | a0001c0001t0001g0020a0001c0001t0001g0063a0001c0001t0001g0064others(35): Show | 42 | HG00733.hp2 HG01081.hp2 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.165+766T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 2/14 | chr9 | 92111689 | ||||||
| chr9:92111701
|
G | A | 3 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0273 | 3 | HG01891.hp2 HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.165+754C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 2/14 | chr9 | 92111701 | ||||||
| chr9:92111738
|
T | C | 8 | a0001c0001t0002g0031a0001c0001t0002g0054a0001c0001t0002g0055others(5): Show | 8 | HG01884.hp1 HG01891.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.165+717A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 2/14 | chr9 | 92111738 | ||||||
| chr9:92111893
|
T | G | 1 | a0001c0001t0001g0139 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.165+562A>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 2/14 | chr9 | 92111893 | ||||||
| chr9:92111940
|
C | A | 6 | a0001c0001t0001g0020a0001c0001t0001g0063a0001c0001t0001g0064others(3): Show | 7 | HG01081.hp2 HG02257.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.165+515G>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 2/14 | chr9 | 92111940 | ||||||
| chr9:92112028
|
A | C | 248 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(245): Show | 271 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(268): Show |
intron_variant | MODIFIER | c.165+427T>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 2/14 | chr9 | 92112028 | ||||||
| chr9:92112367
|
A | T | 13 | a0001c0001t0001g0009a0001c0001t0001g0140a0001c0001t0001g0141others(10): Show | 14 | HG01099.hp1 HG01243.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.165+88T>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 2/14 | chr9 | 92112367 | ||||||
| chr9:92112369
|
G | A | 206 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(203): Show | 221 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(218): Show |
intron_variant | MODIFIER | c.165+86C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 2/14 | chr9 | 92112369 | ||||||
| chr9:92112384
|
A | T | 13 | a0001c0001t0001g0009a0001c0001t0001g0140a0001c0001t0001g0141others(10): Show | 14 | HG01099.hp1 HG01243.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.165+71T>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 2/14 | chr9 | 92112384 | ||||||
| chr9:92112618
|
C | T | 23 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(20): Show | 23 | HG00642.hp2 HG02015.hp2 HG02040.hp2 others(20): Show |
intron_variant | MODIFIER | c.58-56G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 1/14 | chr9 | 92112618 | ||||||
| chr9:92112649
|
T | G | 1 | a0001c0001t0001g0268 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.58-87A>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 1/14 | chr9 | 92112649 | ||||||
| chr9:92112878
|
T | A | 2 | a0001c0001t0001g0114a0001c0001t0001g0115 | 2 | NA18984.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.58-316A>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 1/14 | chr9 | 92112878 | ||||||
| chr9:92113048
|
G | A | 1 | a0001c0001t0001g0269 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.58-486C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 1/14 | chr9 | 92113048 | ||||||
| chr9:92113055
|
C | T | 6 | a0001c0001t0001g0020a0001c0001t0001g0063a0001c0001t0001g0064others(3): Show | 7 | HG01081.hp2 HG02257.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.58-493G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 1/14 | chr9 | 92113055 | ||||||
| chr9:92113103
|
G | A | 1 | a0001c0001t0001g0270 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.58-541C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 1/14 | chr9 | 92113103 | ||||||
| chr9:92113105
|
C | T | 1 | a0001c0001t0001g0116 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.58-543G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 1/14 | chr9 | 92113105 | ||||||
| chr9:92113107
|
C | CAAAT | 29 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0290others(26): Show | 31 | HG00280.hp1 HG01074.hp1 HG01123.hp1 others(28): Show |
intron_variant | MODIFIER | c.58-549_58-546dupAT others(2): Show |
SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 1/14 | chr9 | 92113107 | ||||||
| chr9:92113193
|
C | T | 4 | a0001c0001t0001g0066a0001c0001t0001g0068a0001c0001t0005g0065others(1): Show | 4 | HG02630.hp2 HG02809.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.58-631G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 1/14 | chr9 | 92113193 | ||||||
| chr9:92113257
|
T | C | 3 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0273 | 3 | HG01891.hp2 HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.58-695A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 1/14 | chr9 | 92113257 | ||||||
| chr9:92113309
|
C | G | 1 | a0001c0001t0002g0031 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.58-747G>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 1/14 | chr9 | 92113309 | ||||||
| chr9:92113470
|
T | C | 3 | a0001c0001t0001g0274a0001c0001t0001g0275a0001c0001t0001g0289 | 3 | HG02258.hp1 HG02622.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.58-908A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 1/14 | chr9 | 92113470 | ||||||
| chr9:92113519
|
C | G | 1 | a0001c0001t0001g0320 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.58-957G>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 1/14 | chr9 | 92113519 | ||||||
| chr9:92113528
|
G | A | 2 | a0001c0001t0001g0276a0001c0001t0001g0277 | 2 | HG01496.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.58-966C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 1/14 | chr9 | 92113528 | ||||||
| chr9:92113652
|
G | A | 1 | a0001c0001t0001g0030 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.58-1090C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 1/14 | chr9 | 92113652 | ||||||
| chr9:92113698
|
A | G | 60 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(57): Show | 66 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.58-1136T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 1/14 | chr9 | 92113698 | ||||||
| chr9:92113726
|
G | A | 3 | a0001c0001t0001g0315a0001c0001t0001g0316a0001c0001t0001g0317 | 3 | HG02602.hp2 HG03669.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.58-1164C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 1/14 | chr9 | 92113726 | ||||||
| chr9:92114021
|
C | G | 4 | a0001c0001t0001g0066a0001c0001t0001g0068a0001c0001t0005g0065others(1): Show | 4 | HG02630.hp2 HG02809.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.57+1293G>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 1/14 | chr9 | 92114021 | ||||||
| chr9:92114246
|
C | T | 38 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0290others(35): Show | 40 | HG00280.hp1 HG00733.hp1 HG01074.hp1 others(37): Show |
intron_variant | MODIFIER | c.57+1068G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 1/14 | chr9 | 92114246 | ||||||
| chr9:92114383
|
C | A | 2 | a0001c0001t0001g0278a0001c0001t0001g0279 | 2 | HG02572.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.57+931G>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 1/14 | chr9 | 92114383 | ||||||
| chr9:92114581
|
C | A | 4 | a0001c0001t0001g0280a0001c0001t0001g0281a0001c0001t0001g0282others(1): Show | 4 | HG00738.hp2 HG01106.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.57+733G>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 1/14 | chr9 | 92114581 | ||||||
| chr9:92114599
|
G | A | 1 | a0001c0001t0002g0060 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.57+715C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 1/14 | chr9 | 92114599 | ||||||
| chr9:92114723
|
G | A | 9 | a0001c0001t0001g0022a0001c0001t0001g0320a0001c0001t0001g0321others(6): Show | 10 | HG01074.hp1 HG01123.hp1 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.57+591C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 1/14 | chr9 | 92114723 | ||||||
| chr9:92114735
|
C | CA | 7 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0001t0001g0287others(4): Show | 7 | HG01891.hp1 HG02015.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.57+578dupT | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 1/14 | chr9 | 92114735 | ||||||
| chr9:92114748
|
C | A | 3 | a0001c0001t0001g0020a0001c0001t0001g0063a0001c0001t0001g0064 | 4 | HG01081.hp2 HG02895.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.57+566G>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 1/14 | chr9 | 92114748 | ||||||
| chr9:92114750
|
A | T | 2 | a0001c0001t0001g0063a0001c0001t0001g0064 | 2 | HG02895.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.57+564T>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 1/14 | chr9 | 92114750 | ||||||
| chr9:92114750
|
AAAAT | A | 39 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0291others(36): Show | 41 | HG00280.hp1 HG00733.hp1 HG01074.hp1 others(38): Show |
intron_variant | MODIFIER | c.57+560_57+563delAT others(2): Show |
SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 1/14 | chr9 | 92114750 | ||||||
| chr9:92114752
|
A | C | 1 | a0001c0001t0001g0290 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.57+562T>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 1/14 | chr9 | 92114752 | ||||||
| chr9:92114754
|
T | A | 1 | a0001c0001t0001g0290 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.57+560A>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 1/14 | chr9 | 92114754 | ||||||
| chr9:92114791
|
A | G | 1 | a0002c0003t0003g0062 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.57+523T>C | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 1/14 | chr9 | 92114791 | ||||||
| chr9:92114814
|
CAGA | C | 33 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0031others(30): Show | 36 | HG00733.hp2 HG01109.hp1 HG01255.hp1 others(33): Show |
intron_variant | MODIFIER | c.57+497_57+499delTC others(1): Show |
SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 1/14 | chr9 | 92114814 | ||||||
| chr9:92114912
|
C | A | 1 | a0001c0001t0001g0328 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.57+402G>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 1/14 | chr9 | 92114912 | ||||||
| chr9:92115003
|
C | T | 9 | a0001c0001t0001g0006a0001c0001t0001g0023a0001c0001t0001g0024others(6): Show | 10 | HG00544.hp2 HG02165.hp2 HG03017.hp1 others(7): Show |
intron_variant | MODIFIER | c.57+311G>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 1/14 | chr9 | 92115003 | ||||||
| chr9:92115128
|
C | A | 1 | a0001c0001t0001g0329 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.57+186G>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 1/14 | chr9 | 92115128 |