Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| 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 | 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 | MATAT others(468): Show |
chr9 | 92026147 | 92120413 |
| a0002 | 0/0 | 473 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | MATAT others(468): Show |
chr9 | 92026147 | 92120413 |
| a0003 | 0/0 | 473 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | MATAT others(468): Show |
chr9 | 92026147 | 92120413 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1419 | 352 | 81 | 60 | 167 | 12 | 30 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | ATGGC others(1414): Show |
chr9 | 92026147 | 92120413 | ||
| a0001c0002 | 0/0 | 1419 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | ATGGC others(1414): Show |
chr9 | 92026147 | 92120413 | ||
| a0001c0004 | 0/0 | 1419 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | ATGGC others(1414): Show |
chr9 | 92026147 | 92120413 | ||
| a0001c0005 | 0/0 | 1419 | 1 | 0 | 0 | 0 | 0 | 1 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | ATGGC others(1414): Show |
chr9 | 92026147 | 92120413 | ||
| a0001c0006 | 0/0 | 1419 | 1 | 0 | 0 | 0 | 0 | 1 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | ATGGC others(1414): Show |
chr9 | 92026147 | 92120413 | ||
| a0002c0003 | 0/0 | 1419 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | ATGGC others(1414): Show |
chr9 | 92026147 | 92120413 | ||
| a0003c0007 | 0/0 | 1419 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | ATGGC others(1414): Show |
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 | GGGAC others(2778): Show |
chr9 | 92026147 | 92120413 |
| a0001c0001t0002 | 0/0 | 2783 | 34 | 22 | 4 | 8 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | GGGAC others(2778): Show |
chr9 | 92026147 | 92120413 |
| a0001c0001t0003 | 0/0 | 2783 | 7 | 1 | 2 | 0 | 3 | 1 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | GGGAC others(2778): Show |
chr9 | 92026147 | 92120413 |
| a0001c0001t0004 | 0/0 | 2783 | 3 | 3 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | GGGAC others(2778): Show |
chr9 | 92026147 | 92120413 |
| a0001c0001t0005 | 0/0 | 2783 | 2 | 2 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | GGGAC others(2778): Show |
chr9 | 92026147 | 92120413 |
| a0001c0001t0006 | 0/0 | 2783 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | GGGAC others(2778): Show |
chr9 | 92026147 | 92120413 |
| a0001c0001t0007 | 0/0 | 2783 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | GGGAC others(2778): Show |
chr9 | 92026147 | 92120413 |
| a0001c0001t0008 | 0/0 | 2783 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | GGGAC others(2778): Show |
chr9 | 92026147 | 92120413 |
| a0001c0001t0009 | 0/0 | 2783 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | GGGAC others(2778): Show |
chr9 | 92026147 | 92120413 |
| a0001c0001t0010 | 0/0 | 2783 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | GGGAC others(2778): Show |
chr9 | 92026147 | 92120413 |
| a0001c0001t0011 | 0/0 | 2783 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | GGGAC others(2778): Show |
chr9 | 92026147 | 92120413 |
| a0001c0001t0012 | 0/0 | 2783 | 1 | 0 | 0 | 0 | 0 | 1 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | GGGAC others(2778): Show |
chr9 | 92026147 | 92120413 |
| a0001c0001t0013 | 0/0 | 2783 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | GGGAC others(2778): Show |
chr9 | 92026147 | 92120413 |
| a0001c0001t0014 | 0/0 | 2783 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | GGGAC others(2778): Show |
chr9 | 92026147 | 92120413 |
| a0001c0002t0002 | 0/0 | 2783 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | GGGAC others(2778): Show |
chr9 | 92026147 | 92120413 |
| a0001c0004t0001 | 0/0 | 2783 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | GGGAC others(2778): Show |
chr9 | 92026147 | 92120413 |
| a0001c0005t0001 | 0/0 | 2783 | 1 | 0 | 0 | 0 | 0 | 1 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | GGGAC others(2778): Show |
chr9 | 92026147 | 92120413 |
| a0001c0006t0001 | 0/0 | 2783 | 1 | 0 | 0 | 0 | 0 | 1 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | GGGAC others(2778): Show |
chr9 | 92026147 | 92120413 |
| a0002c0003t0003 | 0/0 | 2783 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | GGGAC others(2778): Show |
chr9 | 92026147 | 92120413 |
| a0003c0007t0001 | 0/0 | 2783 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | GGGAC others(2778): Show |
chr9 | 92026147 | 92120413 |
| actghapid | grch38/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 | 1 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 2 | 0 | 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 | 2 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | 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 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 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 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 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 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 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 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 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 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 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 | 0 | 1 | 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 | 1 | 0 | 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 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 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 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 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 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | 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 | 0 | 0 | 1 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 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 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0217 | 1/0 | 1 | 0 | 0 | 0 | 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 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 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 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 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 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 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 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 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 | 0 | 1 | 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 | 1 | 0 | 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 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0003g0020 | 0/0 | 2 | 0 | 0 | 0 | 2 | 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 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0003g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0003g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0003g0267 | 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 |
| a0001c0001t0004g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0005g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0005g0068 | 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 |
| a0001c0001t0011g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0012g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0013g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0001t0014g0262 | 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 |
| a0001c0004t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| a0001c0005t0001g0186 | 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 |
| a0003c0007t0001g0287 | 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 | g0188 | EUR | FIN | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0222 | EUR | FIN | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0077 | 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 | g0101 | EAS | CHS | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | CHS | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | CHS | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0226 | 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 | g0104 | EAS | CHS | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | CHS | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | CHS | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | CHS | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | CHS | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | CHS | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | CHS | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | CHS | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | PUR | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | CHS | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0163 | 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 | g0210 | AMR | PUR | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | PUR | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0283 | AMR | PUR | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0221 | 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 | g0161 | AMR | PUR | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0176 | 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 | g0263 | AMR | PUR | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0259 | AMR | PUR | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0096 | 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 | g0223 | AMR | PUR | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0012 | 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 | g0012 | AMR | PUR | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG01192 | hp1 | a0001 | c0004 | t0001 | g0187 | AMR | PUR | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | PUR | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0209 | 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 | g0160 | 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 | g0198 | 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 | g0094 | 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 | g0278 | AMR | CLM | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0166 | 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 | g0212 | EUR | IBS | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0020 | 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 | g0020 | 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 | g0272 | 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 | g0097 | AMR | PEL | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG01943 | hp1 | a0001 | c0001 | t0003 | g0264 | AMR | PEL | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | PEL | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0205 | 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 | g0277 | AMR | PEL | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | PEL | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0093 | 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 | g0167 | AMR | PEL | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | PEL | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02015 | hp2 | a0003 | c0007 | t0001 | g0287 | 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 | g0137 | 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 | g0289 | AFR | ACB | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | KHV | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0113 | 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 | g0244 | EAS | KHV | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | KHV | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | KHV | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | KHV | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | KHV | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | KHV | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0131 | 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 | g0230 | EAS | CDX | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | CDX | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0127 | 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 | g0111 | AFR | ACB | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02257 | hp2 | a0001 | c0001 | t0004 | g0120 | AFR | ACB | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0276 | AFR | ACB | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0258 | 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 | g0084 | 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 | g0200 | EAS | KHV | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | KHV | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0280 | 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 | g0255 | 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 | g0145 | AFR | GWD | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02615 | hp2 | a0001 | c0001 | t0004 | g0119 | AFR | GWD | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0267 | AFR | GWD | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0275 | AFR | GWD | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0279 | AFR | GWD | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0067 | 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 | g0124 | SAS | PJL | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0193 | SAS | PJL | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0260 | 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 | g0189 | AFR | GWD | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | GWD | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0290 | AFR | GWD | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02895 | hp1 | a0001 | c0001 | t0005 | g0066 | 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 | g0118 | 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 | g0068 | 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 | g0257 | AFR | ESN | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0273 | AFR | ESN | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | ESN | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0274 | AFR | ESN | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02976 | hp1 | a0001 | c0001 | t0014 | g0262 | 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 | g0152 | 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 | g0112 | 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 | g0144 | 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 | g0181 | 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 | g0010 | 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 | g0269 | AFR | MSL | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0284 | SAS | PJL | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0170 | 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 | g0009 | 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 | g0261 | AFR | MSL | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG03579 | hp2 | a0001 | c0001 | t0011 | g0254 | AFR | MSL | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0228 | SAS | PJL | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0019 | 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 | g0211 | 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 | g0194 | 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 | g0206 | SAS | PJL | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | BEB | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0197 | SAS | BEB | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0110 | 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 | g0252 | SAS | STU | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG04199 | hp1 | a0001 | c0001 | t0003 | g0265 | 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 | g0191 | 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 | g0213 | SAS | STU | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG04228 | hp2 | a0001 | c0005 | t0001 | g0186 | 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 | g0142 | AFR | YRI | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | CHB | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | CHB | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0073 | 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 | g0017 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0138 | 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 | g0098 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0201 | 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 | g0246 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0136 | 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 | g0251 | 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 | g0129 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0229 | 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 | g0183 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0249 | 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 | g0074 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0128 | 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 | g0225 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0018 | 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 | g0076 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0155 | 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 | g0015 | 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 | g0013 | 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 | g0158 | 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 | g0015 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0178 | 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 | g0123 | 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 | g0089 | 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 | g0092 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0173 | 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 | g0018 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0107 | 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 | g0190 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0169 | 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 | g0172 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0105 | 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 | g0199 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0153 | 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 | g0139 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | LWK | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | LWK | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0071 | 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 | g0236 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0224 | 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 | g0103 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0109 | 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 | g0235 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0147 | 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 | g0266 | EUR | TSI | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0165 | SAS | GIH | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0150 | 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 | g0143 | 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 | g0065 | AFR | ACB | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0281 | AFR | ACB | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0271 | AFR | ACB | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG03471 | hp1 | a0001 | c0001 | t0013 | g0268 | AFR | MSL | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0216 | 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 | g0179 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0241 | 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 | g0288 | AFR | LWK | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | LWK | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0295 | REF | REF | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0217 | REF | REF | SPTLC1_chr9_92026147_92120413 | SPTLC1 | chr9 | 92026147 | 92120413 |
| view | 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 |
| view | 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 |
| view | 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 | a0001c0001t0002 a0001c0001t0009 a0001c0001t0010 others(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 | a0001c0001t0003 a0001c0001t0013 a0001c0001t0014 others(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 | a0001c0001t0006 a0001c0001t0007 |
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 |
| view | 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 | a0001c0001t0011g0254 | 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 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0031 others(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 | a0001c0001t0001g0112 | 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 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(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 | a0001c0001t0001g0269 | 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 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0032 others(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 | a0001c0001t0001g0012 a0001c0001t0001g0154 a0001c0001t0001g0179 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(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 | a0001c0001t0001g0247 | 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 | a0001c0001t0001g0009 a0001c0001t0001g0063 a0001c0001t0001g0064 others(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 | 206 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(203): Show |
221 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(218): Show |
intron_variant | MODIFIER | c.1328+1100A>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 14/14 | chr9 | 92033710 | |||||||
| chr9:92033723 | T | G | 37 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0065 others(34): Show |
39 | HG00280.hp1 HG00733.hp1 HG01074.hp1 others(36): 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 | a0001c0001t0001g0269 | 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 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0031 others(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 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0274 |
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 | a0001c0001t0001g0010 a0001c0001t0001g0147 a0001c0001t0001g0148 others(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 | a0001c0001t0001g0010 a0001c0001t0001g0146 a0001c0001t0001g0147 others(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 | a0001c0001t0003g0020 a0001c0001t0003g0263 a0001c0001t0003g0264 others(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 | a0001c0001t0001g0175 | 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 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0031 others(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 | a0001c0001t0001g0010 a0001c0001t0001g0141 a0001c0001t0001g0142 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0063 a0001c0001t0001g0064 others(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 | 37 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0065 others(34): Show |
39 | HG00280.hp1 HG00733.hp1 HG01074.hp1 others(36): 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 | a0001c0001t0003g0263 | 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 | a0001c0001t0001g0099 a0001c0001t0001g0108 a0001c0001t0001g0114 |
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 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0001g0290 |
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 | a0001c0001t0001g0220 | 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 | a0001c0001t0001g0227 a0001c0001t0001g0232 |
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 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0005g0066 others(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 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0016 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0063 a0001c0001t0001g0064 |
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 | a0001c0001t0003g0020 a0001c0001t0003g0263 a0001c0001t0003g0264 others(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 | a0001c0001t0001g0112 | 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 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(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 | a0001c0001t0001g0269 | 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 | a0001c0001t0001g0010 a0001c0001t0001g0141 a0001c0001t0001g0142 others(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 | a0001c0001t0001g0279 a0001c0001t0001g0280 |
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 | a0001c0001t0001g0079 | 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 | a0001c0001t0001g0249 | 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 | a0001c0001t0001g0258 | 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 | a0001c0001t0003g0020 a0001c0001t0003g0263 a0001c0001t0003g0264 others(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 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0031 others(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 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0031 others(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 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0005g0066 others(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 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0272 others(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 | a0001c0001t0001g0269 | 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 | a0001c0001t0001g0318 a0001c0001t0008g0319 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0158 a0001c0001t0001g0159 others(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 | a0001c0001t0003g0020 a0001c0001t0003g0263 a0001c0001t0003g0264 others(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 | a0001c0001t0001g0140 | 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 | a0001c0001t0001g0080 | 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 | 206 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(203): Show |
221 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(218): 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 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0031 others(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 | a0001c0001t0001g0019 a0001c0001t0001g0255 |
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 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0275 others(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 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(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 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0031 others(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 | a0001c0001t0001g0160 | 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 | a0001c0001t0001g0100 | 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 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0031 others(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 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0274 |
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 | a0001c0001t0001g0269 | 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 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0031 others(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 | a0001c0001t0001g0077 | 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 | a0001c0001t0001g0228 a0001c0001t0001g0281 a0001c0001t0001g0282 others(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 | a0001c0001t0001g0234 | 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 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0272 others(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 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0269 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0001g0122 others(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 | a0001c0001t0003g0020 a0001c0001t0003g0263 a0001c0001t0003g0264 others(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 | a0001c0001t0001g0010 a0001c0001t0001g0067 a0001c0001t0001g0069 others(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 | a0001c0001t0001g0240 | 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 | 39 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0065 others(36): Show |
41 | HG00280.hp1 HG00733.hp1 HG01074.hp1 others(38): 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 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(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 | a0001c0001t0003g0020 a0001c0001t0003g0263 a0001c0001t0003g0264 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0121 others(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 | a0001c0001t0011g0254 | 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 | a0001c0001t0003g0020 a0001c0001t0003g0263 a0001c0001t0003g0264 others(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 | a0001c0001t0001g0134 | 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 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0001g0122 others(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 | a0001c0001t0001g0309 a0001c0001t0001g0310 a0001c0001t0001g0311 others(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 | a0001c0001t0001g0214 | 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 | a0001c0001t0001g0243 a0001c0001t0001g0244 |
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 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0073 |
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 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0073 |
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 | a0001c0001t0001g0151 | 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 | a0001c0001t0001g0260 | 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 | a0001c0001t0001g0193 | 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 | a0001c0001t0001g0019 a0001c0001t0001g0255 |
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 | a0001c0001t0002g0033 a0001c0001t0002g0253 |
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 | a0001c0001t0002g0033 a0001c0001t0002g0253 |
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 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0005g0066 others(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 | a0001c0001t0002g0007 a0001c0001t0002g0032 a0001c0001t0002g0033 others(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 | a0001c0001t0001g0010 a0001c0001t0001g0141 a0001c0001t0001g0142 others(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 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0001g0290 |
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 | 205 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(202): Show |
220 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(217): 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 | a0001c0001t0001g0010 a0001c0001t0001g0067 a0001c0001t0001g0069 others(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 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0274 |
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 | a0001c0001t0001g0271 | 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 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0005g0066 others(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 | 206 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(203): Show |
221 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(218): 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 | a0001c0001t0003g0264 | 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 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0195 others(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 | a0001c0001t0004g0118 a0001c0001t0004g0119 a0001c0001t0004g0120 |
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 | a0001c0001t0001g0145 | 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 | a0001c0001t0014g0262 | 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 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0031 others(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 | a0001c0001t0003g0020 a0001c0001t0003g0263 a0001c0001t0003g0264 others(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 | a0001c0001t0003g0020 a0001c0001t0003g0263 a0001c0001t0003g0264 others(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 | a0001c0001t0001g0279 a0001c0001t0001g0280 |
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 | a0001c0001t0001g0318 a0001c0001t0008g0319 |
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 | a0001c0001t0001g0005 a0001c0001t0001g0019 a0001c0001t0001g0121 others(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 | a0001c0001t0011g0254 | 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 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0031 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0063 others(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 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0005g0066 others(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 | a0001c0001t0004g0118 a0001c0001t0004g0119 a0001c0001t0004g0120 |
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 | a0001c0001t0001g0009 a0001c0001t0001g0063 a0001c0001t0001g0064 |
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 | a0001c0001t0001g0218 | 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 | 95 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(92): Show |
111 | HG00323.hp2 HG00438.hp1 HG00544.hp2 others(108): Show |
intron_variant | MODIFIER | c.1136+474dupT | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 12/14 | chr9 | 92045524 | |||||||
| chr9:92045524 | T | TAA | 40 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0030 others(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 | a0001c0001t0001g0010 a0001c0001t0001g0111 a0001c0001t0001g0112 others(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 | a0001c0001t0001g0141 a0001c0001t0001g0148 a0001c0001t0002g0031 others(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 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0273 others(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 | a0001c0001t0003g0020 a0001c0001t0003g0263 a0001c0001t0003g0264 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0063 a0001c0001t0001g0064 |
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 | a0001c0001t0004g0118 a0001c0001t0004g0119 a0001c0001t0004g0120 |
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 | a0001c0001t0001g0269 | 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 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0001g0290 |
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 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0005g0066 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0095 |
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 | a0001c0001t0001g0010 a0001c0001t0001g0141 a0001c0001t0001g0142 others(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 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0204 |
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 | a0001c0001t0001g0010 a0001c0001t0001g0141 a0001c0001t0001g0142 others(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 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0269 others(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 | a0001c0001t0001g0165 | 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 | a0001c0001t0011g0254 | 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 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0274 |
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 | a0001c0001t0003g0020 a0001c0001t0003g0263 a0001c0001t0003g0264 others(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 | 29 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0065 others(26): Show |
31 | HG00280.hp1 HG01074.hp1 HG01123.hp1 others(28): 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 | a0001c0001t0003g0020 a0001c0001t0003g0263 a0001c0001t0003g0264 others(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 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0001g0290 |
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 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(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 | a0001c0001t0014g0262 | 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 | a0001c0001t0006g0307 a0001c0001t0007g0308 |
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 | a0001c0001t0001g0010 a0001c0001t0001g0141 a0001c0001t0001g0142 others(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 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0258 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0122 a0001c0001t0001g0123 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0002g0050 a0001c0001t0002g0051 |
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 | a0001c0001t0001g0241 | 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 | a0001c0001t0001g0010 a0001c0001t0001g0141 a0001c0001t0001g0142 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0084 others(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 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0274 |
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 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0031 others(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 | a0001c0001t0001g0079 | 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 | a0001c0001t0001g0189 | 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 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0005g0066 others(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 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0005g0066 others(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 | a0001c0001t0002g0031 a0001c0001t0002g0054 a0001c0001t0002g0055 others(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 | a0001c0001t0001g0012 a0001c0001t0001g0160 a0001c0001t0001g0162 others(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 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0031 others(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 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0001g0290 |
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 | a0001c0001t0001g0221 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0031 others(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 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0031 others(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 | a0001c0001t0001g0121 | 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 | a0001c0001t0001g0309 a0001c0001t0001g0310 a0001c0001t0001g0311 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0001g0122 others(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 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0031 others(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 | a0001c0001t0001g0121 | 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 | a0001c0001t0002g0002 a0001c0001t0002g0038 a0001c0002t0002g0039 |
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 | a0001c0001t0013g0268 | 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 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0001g0290 |
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 | a0001c0001t0001g0167 | 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 | a0001c0001t0014g0262 | 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 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0183 others(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 | a0001c0001t0001g0011 a0001c0001t0001g0171 a0001c0001t0001g0172 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(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 | a0001c0001t0001g0121 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0023 a0001c0001t0001g0063 others(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 | a0001c0001t0001g0108 a0001c0001t0001g0114 a0001c0001t0001g0324 others(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 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0065 others(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 |
23 | a0001c0001t0001g0019 a0001c0001t0001g0255 a0001c0001t0001g0256 others(20): Show |
24 | HG00733.hp1 HG01123.hp1 HG01169.hp1 others(21): 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 | a0001c0001t0001g0010 a0001c0001t0001g0141 a0001c0001t0001g0142 others(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 | a0001c0001t0001g0124 a0001c0001t0001g0127 a0001c0001t0001g0128 others(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 | a0001c0001t0001g0123 a0001c0001t0001g0126 a0001c0001t0001g0129 others(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 | a0001c0001t0001g0122 a0001c0001t0001g0125 a0001c0001t0001g0138 |
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 | a0001c0001t0001g0137 a0001c0001t0001g0285 |
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 | a0001c0001t0011g0254 | 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 | a0001c0001t0001g0278 | 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 | a0001c0001t0003g0020 a0001c0001t0003g0263 a0001c0001t0003g0264 others(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 | a0001c0001t0001g0110 | 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 | a0001c0001t0002g0253 | 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 | a0001c0001t0011g0254 | 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 | a0001c0001t0001g0269 | 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 | a0001c0001t0003g0020 a0001c0001t0003g0263 a0001c0001t0003g0264 others(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 | a0001c0001t0001g0315 a0001c0001t0001g0316 a0001c0001t0001g0317 |
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 | a0001c0004t0001g0187 | 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 | a0001c0001t0001g0215 | 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 | a0001c0001t0001g0074 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0274 |
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 | a0001c0001t0001g0269 | 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 | a0001c0001t0001g0275 a0001c0001t0001g0276 |
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 | a0001c0001t0003g0020 a0001c0001t0003g0263 a0001c0001t0003g0264 others(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 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0274 |
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 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0065 others(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 | a0001c0001t0001g0077 a0001c0001t0001g0272 a0001c0001t0001g0273 others(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 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0031 others(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 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0005g0066 others(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 | a0001c0001t0001g0291 a0001c0001t0001g0302 a0001c0001t0001g0303 others(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 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0258 others(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 | 37 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0065 others(34): Show |
39 | HG00280.hp1 HG00733.hp1 HG01074.hp1 others(36): 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 | a0001c0001t0001g0270 | 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 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0001g0122 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0010 a0001c0001t0001g0141 a0001c0001t0001g0142 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0003g0020 a0001c0001t0003g0263 a0001c0001t0003g0264 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0010 a0001c0001t0001g0141 a0001c0001t0001g0142 others(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 | a0001c0001t0001g0010 a0001c0001t0001g0141 a0001c0001t0001g0142 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0170 | 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 | a0001c0001t0001g0132 | 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 | a0001c0001t0011g0254 | 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 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0258 others(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 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0258 others(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 | a0001c0001t0002g0002 a0001c0001t0002g0038 a0001c0001t0010g0045 others(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 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0001g0122 others(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 | a0001c0001t0003g0020 a0001c0001t0003g0263 a0001c0001t0003g0264 others(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 | a0001c0001t0001g0010 a0001c0001t0001g0141 a0001c0001t0001g0142 others(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 | a0003c0007t0001g0287 | 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 | a0001c0001t0001g0210 | 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 | a0001c0001t0003g0020 a0001c0001t0003g0263 a0001c0001t0003g0264 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0063 a0001c0001t0001g0064 others(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 | a0001c0001t0001g0121 | 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 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0031 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0003g0020 a0001c0001t0003g0263 a0001c0001t0003g0264 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0213 | 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 | a0001c0001t0001g0010 a0001c0001t0001g0141 a0001c0001t0001g0142 others(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 | a0001c0001t0001g0194 a0001c0001t0001g0196 a0001c0001t0001g0213 others(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 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(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 | a0001c0001t0003g0020 a0001c0001t0003g0263 a0001c0001t0003g0264 others(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 | a0001c0001t0001g0291 a0001c0001t0001g0302 a0001c0001t0001g0303 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0063 a0001c0001t0001g0064 others(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 | a0001c0004t0001g0187 | 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 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0031 others(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 | a0001c0001t0001g0010 a0001c0001t0001g0141 a0001c0001t0001g0142 others(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 | a0001c0001t0001g0011 a0001c0001t0001g0171 a0001c0001t0001g0172 others(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 | a0001c0001t0001g0086 a0001c0001t0001g0089 |
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 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0274 |
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 | a0001c0001t0001g0212 | 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 | 1 | a0001c0001t0001g0294 | 1 | HG00280.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 | a0001c0001t0003g0020 a0001c0001t0003g0263 a0001c0001t0003g0264 others(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 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0258 others(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 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0258 others(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 | a0001c0001t0001g0194 | 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 | a0001c0001t0001g0009 a0001c0001t0001g0063 a0001c0001t0001g0064 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0063 a0001c0001t0001g0064 |
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 | a0001c0001t0003g0020 a0001c0001t0003g0263 a0001c0001t0003g0264 others(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 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0001g0122 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0063 a0001c0001t0001g0064 others(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 | a0001c0001t0001g0269 | 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 | 206 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(203): Show |
221 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(218): 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 | a0001c0001t0003g0020 a0001c0001t0003g0263 a0001c0001t0003g0264 others(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 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0031 others(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 | a0001c0001t0001g0194 | 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 | 205 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(202): Show |
220 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(217): 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 | a0001c0001t0001g0138 | 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 | a0001c0001t0001g0085 | 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 | 37 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0065 others(34): Show |
39 | HG00280.hp1 HG00733.hp1 HG01074.hp1 others(36): 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 | a0001c0001t0006g0307 a0001c0001t0007g0308 |
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 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0001g0290 |
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 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0001g0122 others(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 | a0001c0001t0003g0020 a0001c0001t0003g0263 a0001c0001t0003g0264 others(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 | a0001c0001t0001g0117 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0232 | 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 | a0001c0001t0001g0236 | 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 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0001g0290 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0195 others(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 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0001g0122 others(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 | a0001c0001t0003g0020 a0001c0001t0003g0263 a0001c0001t0003g0264 others(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 | a0001c0001t0001g0121 | 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 | a0001c0001t0001g0318 a0001c0001t0008g0319 |
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 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0031 others(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 | a0001c0001t0001g0131 | 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 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0031 others(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 | a0001c0001t0003g0020 a0001c0001t0003g0263 a0001c0001t0003g0264 others(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 | a0001c0001t0001g0269 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0318 a0001c0001t0008g0319 |
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 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0031 others(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 | a0001c0001t0001g0189 | 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 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(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 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0031 others(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 | a0001c0001t0001g0284 | 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 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0024 others(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 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0001g0122 others(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 | a0003c0007t0001g0287 | 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 | a0001c0001t0001g0269 | 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 | a0001c0001t0001g0160 | 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 | a0001c0001t0002g0040 a0001c0001t0002g0041 a0001c0001t0002g0053 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0221 | 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 | 52 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0064 others(49): Show |
55 | HG00280.hp1 HG00733.hp1 HG01074.hp1 others(52): Show |
intron_variant | MODIFIER | c.561-1605dupT | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 6/14 | chr9 | 92060912 | |||||||
| chr9:92060912 | CAA | C | 35 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0031 others(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 | a0001c0001t0001g0111 | 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 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0258 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0063 a0001c0001t0001g0064 |
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 | a0001c0001t0001g0010 a0001c0001t0001g0141 a0001c0001t0001g0142 others(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 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0031 others(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 | a0001c0001t0001g0011 a0001c0001t0001g0171 a0001c0001t0001g0172 others(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 | a0001c0001t0001g0011 a0001c0001t0001g0171 a0001c0001t0001g0172 others(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 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0031 others(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 | a0001c0001t0001g0010 a0001c0001t0001g0146 a0001c0001t0001g0147 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0004g0120 | 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 | a0001c0001t0003g0020 a0001c0001t0003g0263 a0001c0001t0003g0264 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0063 a0001c0001t0001g0064 others(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 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0031 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0269 | 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 | a0001c0001t0003g0267 | 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 | a0001c0001t0002g0002 a0001c0001t0002g0038 a0001c0002t0002g0039 |
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 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(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 | 31 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0065 others(28): Show |
33 | HG00280.hp1 HG00733.hp1 HG01074.hp1 others(30): 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 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0032 others(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 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(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 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0005g0066 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0318 a0001c0001t0008g0319 |
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 | a0001c0001t0001g0227 | 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 | 39 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0065 others(36): Show |
41 | HG00280.hp1 HG00733.hp1 HG01074.hp1 others(38): 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 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0001g0122 others(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 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0258 others(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 | a0001c0001t0004g0120 | 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 | a0001c0001t0001g0113 | 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 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0001g0290 |
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 | a0001c0001t0001g0010 a0001c0001t0001g0141 a0001c0001t0001g0142 others(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 | a0001c0001t0004g0118 a0001c0001t0004g0119 |
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 | a0001c0001t0001g0191 | 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 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0260 |
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 | a0001c0001t0001g0010 a0001c0001t0001g0141 a0001c0001t0001g0142 others(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 | a0001c0001t0001g0132 | 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 | a0001c0001t0001g0010 a0001c0001t0001g0141 a0001c0001t0001g0142 others(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 | a0003c0007t0001g0287 | 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 | a0001c0001t0002g0035 a0001c0001t0002g0036 a0001c0001t0002g0037 others(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 | a0001c0001t0002g0033 a0001c0001t0002g0253 |
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 | a0001c0001t0001g0281 | 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 | a0001c0001t0001g0236 | 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 | a0001c0001t0001g0284 | 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 | a0001c0001t0001g0269 | 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 | a0001c0001t0001g0011 a0001c0001t0001g0172 a0001c0001t0001g0174 others(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 | 204 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(201): Show |
219 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(216): 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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0223 | 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 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0031 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0027 a0001c0001t0001g0085 a0001c0001t0001g0156 others(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 | a0001c0001t0001g0129 a0001c0001t0001g0272 a0001c0001t0001g0273 others(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 | a0001c0001t0001g0011 a0001c0001t0001g0019 a0001c0001t0001g0110 others(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 | a0001c0001t0001g0129 a0001c0001t0001g0285 |
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 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0001g0122 others(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 | a0001c0001t0001g0233 a0001c0001t0001g0234 |
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 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0275 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0005g0066 others(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 | a0001c0001t0001g0272 a0001c0001t0001g0273 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0031 others(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 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0274 |
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 | a0001c0001t0001g0018 a0001c0001t0001g0245 |
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 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0032 others(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 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0001g0122 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0014g0262 | 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 | a0001c0001t0001g0315 a0001c0001t0001g0316 a0001c0001t0001g0317 |
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 | a0001c0001t0001g0288 | 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 | a0001c0001t0003g0020 a0001c0001t0003g0263 a0001c0001t0003g0264 others(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 | a0001c0001t0001g0269 | 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 | 205 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(202): Show |
220 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(217): 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 | a0001c0001t0001g0269 | 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 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0031 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0063 a0001c0001t0001g0064 |
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 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0274 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0258 others(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 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0031 others(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 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0001g0290 |
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 | a0001c0001t0001g0080 | 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 | a0001c0001t0001g0318 a0001c0001t0008g0319 |
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 | a0001c0001t0004g0118 a0001c0001t0004g0119 a0001c0001t0004g0120 |
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 | a0001c0001t0004g0118 a0001c0001t0004g0119 a0001c0001t0004g0120 |
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 | a0001c0001t0001g0269 | 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 | 61 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0027 others(58): Show |
64 | HG00280.hp1 HG00280.hp2 HG00733.hp1 others(61): Show |
intron_variant | MODIFIER | c.428-3130dupT | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92071227 | |||||||
| chr9:92071227 | TA | T | 10 | a0001c0001t0001g0029 a0001c0001t0001g0087 a0001c0001t0001g0185 others(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 | a0001c0001t0003g0263 | 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 | a0001c0001t0001g0269 a0001c0001t0002g0002 a0001c0001t0002g0007 others(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 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0005g0066 others(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 | a0001c0001t0001g0276 | 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 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0031 others(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 | a0001c0001t0003g0267 | 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 | a0001c0001t0001g0018 a0001c0001t0001g0183 a0001c0001t0001g0237 others(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 | a0001c0001t0005g0066 a0001c0001t0005g0068 |
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 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(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 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0031 others(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 | a0001c0001t0001g0196 a0001c0001t0001g0213 a0001c0001t0001g0221 others(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 | a0001c0001t0001g0137 | 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 | a0001c0001t0001g0082 | 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 | a0001c0001t0013g0268 | 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 | a0001c0001t0003g0267 a0001c0001t0013g0268 |
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 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(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 | a0001c0001t0003g0020 a0001c0001t0003g0264 a0001c0001t0003g0265 |
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 | 200 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(197): Show |
214 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(211): Show |
intron_variant | MODIFIER | c.428-4671C>A | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92072769 | |||||||
| chr9:92072959 | A | C | 193 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(190): Show |
207 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(204): Show |
intron_variant | MODIFIER | c.428-4861T>G | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92072959 | |||||||
| chr9:92073028 | C | T | 199 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(196): Show |
212 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(209): 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 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(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 | a0001c0001t0001g0269 a0001c0001t0002g0002 a0001c0001t0002g0007 others(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 | a0001c0001t0011g0254 | 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 | a0001c0001t0001g0112 | 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 | a0001c0001t0001g0202 a0001c0001t0001g0203 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0289 |
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 | a0001c0001t0001g0124 | 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 | a0001c0001t0001g0269 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0003g0020 a0001c0001t0003g0263 a0001c0001t0003g0264 others(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 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0031 others(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 | a0001c0001t0001g0271 | 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 | a0001c0001t0001g0232 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0145 | 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 | a0001c0001t0001g0019 a0001c0001t0001g0255 |
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 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0031 others(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 | a0001c0001t0001g0009 | 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 | a0001c0001t0001g0065 | 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 | a0001c0001t0014g0262 | 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 | a0001c0001t0014g0262 | 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 | a0001c0001t0011g0254 | 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 | a0001c0001t0001g0142 | 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 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0001g0290 |
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 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0001g0122 others(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 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0031 others(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 | a0001c0001t0001g0077 | 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 | a0001c0001t0001g0212 a0001c0001t0001g0222 a0001c0001t0001g0228 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0063 a0001c0001t0001g0064 |
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 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0193 others(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 | a0001c0001t0003g0020 a0001c0001t0003g0263 a0001c0001t0003g0264 others(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 | a0001c0001t0001g0110 | 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 | a0001c0001t0001g0269 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0075 a0001c0001t0001g0083 |
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 | a0001c0001t0001g0237 a0001c0001t0001g0238 a0001c0001t0001g0246 |
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 | a0001c0001t0001g0271 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(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 | a0001c0001t0011g0254 | 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 | a0001c0001t0001g0132 | 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 | 39 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0065 others(36): Show |
41 | HG00280.hp1 HG00733.hp1 HG01074.hp1 others(38): 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 | a0001c0001t0011g0254 | 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 | a0001c0001t0001g0188 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0075 a0001c0001t0001g0083 |
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 | a0001c0001t0001g0009 a0001c0001t0001g0063 a0001c0001t0001g0064 others(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 | a0001c0001t0001g0269 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0086 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0011g0254 | 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 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0001g0122 others(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 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0258 others(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 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0031 others(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 | a0001c0001t0001g0221 | 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 | 39 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0065 others(36): Show |
41 | HG00280.hp1 HG00733.hp1 HG01074.hp1 others(38): Show |
intron_variant | MODIFIER | c.427+2663C>T | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 5/14 | chr9 | 92077353 | |||||||
| chr9:92077367 | T | C | 205 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(202): Show |
220 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(217): 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 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0005g0066 others(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 | 39 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0065 others(36): Show |
41 | HG00280.hp1 HG00733.hp1 HG01074.hp1 others(38): 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 | a0001c0001t0001g0019 a0001c0001t0001g0255 |
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 | a0001c0001t0001g0133 a0001c0001t0001g0286 |
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 | a0001c0001t0001g0269 | 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 | a0001c0001t0001g0310 a0001c0001t0001g0314 |
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 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0289 |
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 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0289 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0031 others(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 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0001g0290 |
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 | a0001c0001t0001g0143 | 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 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0274 |
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 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0001g0122 others(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 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0031 others(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 | 205 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(202): Show |
220 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(217): 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 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0005g0066 others(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 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0193 |
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 | 39 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0065 others(36): Show |
41 | HG00280.hp1 HG00733.hp1 HG01074.hp1 others(38): 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 | a0001c0001t0001g0320 a0001c0001t0001g0321 a0001c0001t0001g0322 others(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 | a0001c0001t0001g0269 | 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 | a0001c0001t0001g0012 | 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 | a0001c0001t0003g0020 a0001c0001t0003g0263 a0001c0001t0003g0264 others(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 | a0001c0001t0001g0151 | 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 | a0001c0001t0002g0007 a0001c0001t0002g0032 a0001c0001t0002g0033 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0318 a0001c0001t0008g0319 |
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 | a0001c0001t0003g0020 a0001c0001t0003g0263 a0001c0001t0003g0264 others(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 | a0001c0001t0001g0290 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0011g0254 | 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 | a0001c0001t0001g0137 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0001g0290 |
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 | a0001c0001t0001g0269 | 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 | a0001c0001t0001g0269 | 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 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(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 | a0001c0001t0001g0309 a0001c0001t0001g0313 |
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 | a0001c0001t0001g0230 | 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 | a0001c0001t0001g0269 | 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 | a0001c0001t0014g0262 | 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 | a0001c0001t0001g0309 a0001c0001t0001g0310 a0001c0001t0001g0311 others(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 | a0001c0001t0002g0002 a0001c0001t0002g0038 a0001c0002t0002g0039 |
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 | a0001c0001t0001g0269 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0063 a0001c0001t0001g0064 others(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 | a0001c0004t0001g0187 | 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 | a0001c0001t0001g0288 | 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 | a0001c0001t0011g0254 | 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 | a0001c0001t0001g0194 | 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 | a0001c0001t0001g0222 | 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 | a0001c0001t0001g0017 a0001c0001t0001g0073 a0001c0001t0001g0096 others(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 | a0001c0001t0001g0112 | 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 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0031 others(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 | a0001c0001t0001g0236 | 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 | a0001c0001t0001g0269 a0001c0001t0002g0032 |
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 | a0001c0001t0003g0267 | 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 | a0001c0001t0001g0121 | 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 | 205 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(202): Show |
220 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(217): 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 | a0001c0001t0001g0288 | 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 | a0001c0001t0001g0288 | 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 | a0001c0001t0011g0254 | 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 | a0001c0001t0001g0235 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0121 | 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 | a0001c0001t0001g0009 a0001c0001t0001g0063 a0001c0001t0001g0064 others(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 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0182 |
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 | a0001c0001t0001g0112 | 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 | a0001c0001t0001g0279 a0001c0001t0001g0280 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0001g0290 |
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 | a0001c0001t0001g0085 | 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 | a0001c0005t0001g0186 | 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 | a0001c0001t0001g0009 a0001c0001t0001g0063 a0001c0001t0001g0064 others(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 | a0001c0001t0011g0254 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0245 |
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 | a0001c0001t0001g0235 | 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 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0258 others(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 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0258 others(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 | a0001c0001t0001g0190 | 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 | a0001c0001t0004g0120 | 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 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0274 |
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 | a0001c0001t0001g0227 a0001c0001t0001g0232 |
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 | a0001c0001t0002g0035 a0001c0001t0002g0036 a0001c0001t0002g0037 others(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 | a0001c0001t0001g0205 | 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 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0031 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0004g0118 a0001c0001t0004g0119 |
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 | 37 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0065 others(34): Show |
39 | HG00280.hp1 HG00733.hp1 HG01074.hp1 others(36): 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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0002g0031 a0001c0001t0002g0054 a0001c0001t0002g0055 others(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 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0182 |
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 | a0001c0001t0001g0205 a0001c0001t0001g0256 a0001c0001t0001g0257 others(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 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0031 others(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 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0032 others(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 | a0001c0001t0003g0020 a0001c0001t0003g0263 a0001c0001t0003g0264 others(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 | a0001c0001t0001g0318 a0001c0001t0008g0319 |
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 | a0001c0001t0011g0254 | 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 | a0001c0001t0001g0121 | 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 | a0001c0001t0006g0307 a0001c0001t0007g0308 |
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 | a0001c0001t0001g0009 a0001c0001t0001g0063 a0001c0001t0001g0064 others(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 | a0001c0001t0001g0269 | 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 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0001g0122 others(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 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(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 | a0001c0001t0001g0103 | 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 | a0001c0001t0001g0189 | 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 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0031 others(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 | a0001c0001t0003g0020 a0001c0001t0003g0263 a0001c0001t0003g0264 others(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 | a0001c0001t0003g0263 a0001c0001t0003g0266 |
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 | a0001c0001t0001g0104 a0001c0001t0001g0105 |
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 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0001g0122 others(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 | a0001c0001t0001g0157 | 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 | a0001c0001t0001g0124 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0063 a0001c0001t0001g0064 others(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 | a0001c0001t0001g0181 | 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 | a0001c0001t0001g0271 | 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 | a0001c0001t0001g0291 a0001c0001t0001g0306 |
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 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0031 others(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 | a0001c0001t0003g0266 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | 206 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(203): Show |
221 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(218): 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 | a0001c0001t0001g0107 | 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 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0001g0122 others(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 | a0001c0001t0003g0020 a0001c0001t0003g0263 a0001c0001t0003g0264 others(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 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0001g0290 |
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 | a0001c0001t0001g0228 | 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 | a0001c0001t0001g0318 a0001c0001t0008g0319 |
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 | a0001c0001t0001g0019 a0001c0001t0001g0255 |
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 | a0001c0001t0001g0134 | 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 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(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 | a0001c0001t0003g0267 a0001c0001t0013g0268 |
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 | a0001c0001t0001g0269 | 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 | a0001c0001t0001g0009 a0001c0001t0001g0063 a0001c0001t0001g0064 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0063 a0001c0001t0001g0064 others(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 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0001g0290 others(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 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0204 |
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 | a0001c0001t0001g0135 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0184 |
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 | a0001c0001t0003g0020 a0001c0001t0003g0263 a0001c0001t0003g0264 others(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 | a0001c0001t0011g0254 | 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 | a0001c0001t0001g0279 | 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 | a0001c0001t0001g0009 a0001c0001t0001g0063 a0001c0001t0001g0064 others(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 | a0001c0001t0002g0047 a0001c0001t0002g0050 a0001c0001t0002g0051 |
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 | a0001c0001t0001g0229 | 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 | 37 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0065 others(34): Show |
39 | HG00280.hp1 HG00733.hp1 HG01074.hp1 others(36): 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 | a0001c0001t0001g0233 a0001c0001t0001g0234 |
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 | a0001c0001t0004g0118 a0001c0001t0004g0119 a0001c0001t0004g0120 |
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 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0258 others(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 | a0001c0001t0001g0230 | 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 | a0001c0001t0001g0111 | 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 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0031 others(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 | a0001c0001t0002g0031 a0001c0001t0002g0054 a0001c0001t0002g0055 others(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 | a0001c0001t0001g0291 a0001c0001t0001g0306 |
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 | a0001c0001t0001g0081 | 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 | a0001c0001t0003g0020 a0001c0001t0003g0263 a0001c0001t0003g0264 others(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 | a0001c0001t0004g0118 a0001c0001t0004g0119 a0001c0001t0004g0120 |
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 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0031 others(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 | a0001c0001t0001g0098 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(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 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0031 others(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 | a0001c0001t0001g0146 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0063 others(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 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0258 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0075 | 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 | a0001c0001t0004g0118 a0001c0001t0004g0119 a0001c0001t0004g0120 |
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 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0005g0066 others(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 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0005g0066 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0084 others(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 | a0001c0001t0003g0020 a0001c0001t0003g0263 a0001c0001t0003g0264 others(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 | a0001c0001t0001g0201 | 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 | a0001c0001t0001g0084 | 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 | a0001c0001t0001g0269 | 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 | a0001c0001t0011g0254 | 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 | a0001c0001t0002g0031 a0001c0001t0002g0054 a0001c0001t0002g0055 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0320 a0001c0001t0001g0321 others(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 | 37 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0065 others(34): Show |
39 | HG00280.hp1 HG00733.hp1 HG01074.hp1 others(36): 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 | a0001c0001t0002g0035 a0001c0001t0002g0036 a0001c0001t0002g0037 others(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 | a0001c0001t0001g0147 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0004g0118 a0001c0001t0004g0119 a0001c0001t0004g0120 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0258 others(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 | a0001c0001t0014g0262 | 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 | a0001c0001t0001g0318 a0001c0001t0008g0319 |
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 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0258 others(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 | a0001c0001t0001g0231 a0001c0001t0001g0249 |
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 | a0001c0001t0001g0231 a0001c0001t0001g0249 |
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 | 205 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(202): Show |
220 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(217): 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 | a0001c0001t0001g0153 a0001c0001t0001g0154 |
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 | a0001c0001t0001g0146 a0001c0001t0001g0247 a0001c0001t0001g0248 others(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 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0274 |
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 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0031 others(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 | a0001c0001t0011g0254 | 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 | a0001c0001t0001g0269 | 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 | a0001c0001t0003g0020 a0001c0001t0003g0263 a0001c0001t0003g0264 others(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 | a0001c0001t0001g0231 | 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 | a0001c0001t0003g0020 a0001c0001t0003g0263 a0001c0001t0003g0264 others(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 | a0001c0001t0001g0106 a0001c0001t0001g0107 |
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 | a0001c0001t0001g0019 a0001c0001t0001g0255 |
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 | 206 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(203): Show |
221 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(218): 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 | a0001c0001t0004g0118 a0001c0001t0004g0119 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0031 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0277 a0001c0001t0001g0278 |
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 | a0001c0001t0001g0200 | 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 | a0001c0001t0001g0029 a0001c0001t0002g0002 a0001c0001t0002g0007 others(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 | a0001c0001t0001g0275 | 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 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0031 others(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 | a0001c0001t0001g0010 a0001c0001t0001g0141 a0001c0001t0001g0142 others(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 | a0001c0001t0004g0118 a0001c0001t0004g0119 a0001c0001t0004g0120 |
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 | a0001c0001t0002g0035 a0001c0001t0002g0036 a0001c0001t0002g0037 others(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 | a0001c0001t0001g0075 a0001c0001t0001g0083 |
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 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(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 | a0001c0001t0001g0121 | 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 | a0001c0001t0001g0009 a0001c0001t0001g0063 a0001c0001t0001g0064 others(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 | a0001c0001t0001g0082 | 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 | a0001c0001t0001g0274 | 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 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0031 others(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 | a0001c0001t0001g0269 | 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 | a0001c0001t0003g0020 a0001c0001t0003g0263 a0001c0001t0003g0264 others(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 | a0001c0001t0001g0107 | 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 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(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 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0136 |
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 | a0001c0001t0003g0020 a0001c0001t0003g0263 a0001c0001t0003g0264 others(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 | a0001c0001t0001g0246 | 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 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0031 others(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 | a0001c0001t0004g0120 | 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 | a0001c0001t0001g0269 | 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 | a0001c0001t0011g0254 | 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 | a0001c0001t0001g0251 | 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 | a0001c0001t0001g0010 a0001c0001t0001g0141 a0001c0001t0001g0142 others(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 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0001g0122 others(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 | a0001c0001t0001g0291 a0001c0001t0001g0302 a0001c0001t0001g0303 others(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 | a0001c0001t0001g0065 | 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 | a0001c0001t0001g0256 a0001c0001t0001g0257 |
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 | a0001c0001t0011g0254 | 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 | 205 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(202): Show |
220 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(217): 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 | a0001c0001t0011g0254 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0063 a0001c0001t0001g0064 |
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 | a0001c0001t0001g0075 a0001c0001t0001g0083 |
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 | 29 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0065 others(26): Show |
31 | HG00280.hp1 HG01074.hp1 HG01123.hp1 others(28): 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 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0031 others(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 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0031 others(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 | a0001c0001t0001g0153 a0001c0001t0001g0154 |
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 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0031 others(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 | a0001c0001t0002g0050 a0001c0001t0002g0051 |
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 | a0001c0001t0014g0262 | 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 | a0001c0001t0003g0020 a0001c0001t0003g0263 a0001c0001t0003g0264 others(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 | a0001c0001t0001g0010 a0001c0001t0001g0067 a0001c0001t0001g0069 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0083 a0001c0001t0002g0031 a0001c0001t0002g0054 others(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 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0001g0122 others(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 | a0001c0001t0014g0262 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0063 a0001c0001t0001g0064 others(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 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0258 others(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 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0031 others(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 | a0001c0001t0001g0190 a0001c0001t0001g0199 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0258 others(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 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0001g0122 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(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 | a0001c0001t0002g0050 a0001c0001t0002g0051 |
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 | a0001c0001t0001g0111 | 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 | 113 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(110): Show |
122 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.260+7178delT | SPTLC1 | ENSG00000090054.16 | transcript | ENST00000262554.7 | protein_coding | 3/14 | chr9 | 92101561 | |||||||
| chr9:92101561 | CAA | C | 39 | a0001c0001t0001g0019 a0001c0001t0001g0063 a0001c0001t0001g0074 others(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 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0031 others(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 | a0001c0001t0001g0269 | 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 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0031 others(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 | a0001c0001t0001g0121 | 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 | a0001c0005t0001g0186 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0121 | 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 | a0001c0001t0003g0020 a0001c0001t0003g0263 a0001c0001t0003g0264 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0197 | 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 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0258 others(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 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0274 |
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 | a0001c0001t0001g0010 a0001c0001t0001g0141 a0001c0001t0001g0142 others(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 | a0001c0001t0001g0109 | 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 | a0001c0001t0001g0302 a0001c0001t0001g0303 a0001c0001t0001g0304 others(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 | a0001c0001t0001g0196 | 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 | a0001c0001t0001g0189 | 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 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0031 others(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 | a0001c0001t0001g0195 | 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 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0031 others(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 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0258 others(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 | a0001c0001t0003g0020 a0001c0001t0003g0263 a0001c0001t0003g0264 others(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 | 206 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(203): Show |
221 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(218): 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 | a0001c0001t0001g0318 a0001c0001t0008g0319 |
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 | a0001c0001t0001g0019 a0001c0001t0001g0255 |
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 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0031 others(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 | a0001c0001t0001g0232 | 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 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0258 others(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 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(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 | a0001c0001t0001g0247 a0001c0001t0001g0248 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0002g0031 a0001c0001t0002g0054 a0001c0001t0002g0055 others(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 | a0001c0001t0003g0020 a0001c0001t0003g0263 a0001c0001t0003g0264 others(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 | a0001c0001t0001g0291 a0001c0001t0001g0306 |
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 | a0001c0001t0001g0149 | 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 | a0001c0001t0001g0069 | 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 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | 52 | a0001c0001t0001g0010 a0001c0001t0001g0021 a0001c0001t0001g0022 others(49): Show |
55 | HG00280.hp1 HG00733.hp1 HG01074.hp1 others(52): 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 | a0001c0001t0001g0138 | 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 | a0001c0001t0001g0010 a0001c0001t0001g0147 a0001c0001t0001g0148 others(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 | 205 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(202): Show |
220 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(217): 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 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0031 others(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 | a0001c0001t0001g0110 | 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 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0031 others(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 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0001g0290 |
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 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0001g0290 |
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 | a0001c0001t0001g0009 a0001c0001t0001g0063 a0001c0001t0001g0064 others(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 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0031 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0063 a0001c0001t0001g0064 |
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 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(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 | a0001c0001t0004g0118 a0001c0001t0004g0119 a0001c0001t0004g0120 |
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 | a0001c0001t0001g0270 | 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 | a0001c0001t0001g0111 a0001c0001t0001g0146 a0001c0001t0001g0152 |
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 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0031 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0010 a0001c0001t0001g0141 a0001c0001t0001g0142 others(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 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0114 others(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 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0274 |
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 | a0001c0001t0001g0269 | 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 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0274 |
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 | a0001c0001t0001g0009 a0001c0001t0001g0063 a0001c0001t0001g0064 |
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 | a0001c0001t0001g0151 | 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 | a0001c0001t0002g0031 a0001c0001t0002g0054 a0001c0001t0002g0055 others(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 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0031 others(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 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0031 others(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 | a0001c0004t0001g0187 | 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 | 205 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(202): Show |
220 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(217): 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 | a0001c0001t0013g0268 | 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 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0001g0122 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0011g0254 | 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 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0001g0122 others(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 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0031 others(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 | 52 | a0001c0001t0001g0010 a0001c0001t0001g0021 a0001c0001t0001g0022 others(49): Show |
55 | HG00280.hp1 HG00733.hp1 HG01074.hp1 others(52): 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 | a0001c0001t0004g0118 a0001c0001t0004g0119 a0001c0001t0004g0120 |
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 | a0001c0001t0001g0269 | 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 | a0001c0001t0001g0152 | 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 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(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 | a0001c0001t0001g0194 | 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 | 204 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(201): Show |
219 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(216): 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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0146 | 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 | a0001c0001t0001g0269 | 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 | a0001c0001t0001g0272 | 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 | a0001c0001t0001g0269 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0063 a0001c0001t0001g0064 others(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 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0031 others(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 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0031 others(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 | a0001c0001t0012g0252 | 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 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(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 | a0001c0001t0002g0031 a0001c0001t0002g0054 a0001c0001t0002g0055 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0063 a0001c0001t0001g0064 |
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 | a0001c0005t0001g0186 | 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 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0274 |
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 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0193 |
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 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0031 others(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 | a0001c0001t0001g0190 | 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 | 37 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0065 others(34): Show |
39 | HG00280.hp1 HG00733.hp1 HG01074.hp1 others(36): 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 | a0001c0001t0001g0139 | 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 | a0001c0001t0001g0010 a0001c0001t0001g0141 a0001c0001t0001g0142 others(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 | a0001c0001t0004g0118 a0001c0001t0004g0119 a0001c0001t0004g0120 |
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 | a0001c0001t0001g0010 a0001c0001t0001g0141 a0001c0001t0001g0142 others(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 | 250 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(247): Show |
273 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(270): 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 | a0001c0001t0011g0254 | 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 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0031 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0063 a0001c0001t0001g0064 others(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 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0274 |
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 | a0001c0001t0002g0031 a0001c0001t0002g0054 a0001c0001t0002g0055 others(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 | a0001c0001t0001g0140 | 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 | a0001c0001t0001g0009 a0001c0001t0001g0063 a0001c0001t0001g0064 others(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 | 247 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(244): Show |
270 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(267): 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 | a0001c0001t0001g0010 a0001c0001t0001g0141 a0001c0001t0001g0142 others(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 | 205 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(202): Show |
220 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(217): 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 | a0001c0001t0001g0010 a0001c0001t0001g0141 a0001c0001t0001g0142 others(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 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(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 | a0001c0001t0001g0269 | 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 | a0001c0001t0001g0115 a0001c0001t0001g0116 |
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 | a0001c0001t0001g0270 | 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 | a0001c0001t0001g0009 a0001c0001t0001g0063 a0001c0001t0001g0064 others(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 | a0001c0001t0001g0271 | 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 | a0001c0001t0001g0117 | 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 | 28 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0065 others(25): Show |
30 | HG00280.hp1 HG01074.hp1 HG01123.hp1 others(27): 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 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0005g0066 others(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 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0274 |
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 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0001g0290 |
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 | a0001c0001t0001g0277 a0001c0001t0001g0278 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0315 a0001c0001t0001g0316 a0001c0001t0001g0317 |
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 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0005g0066 others(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 | 37 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0065 others(34): Show |
39 | HG00280.hp1 HG00733.hp1 HG01074.hp1 others(36): 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 | a0001c0001t0001g0279 a0001c0001t0001g0280 |
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 | a0001c0001t0001g0281 a0001c0001t0001g0282 a0001c0001t0001g0283 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0320 a0001c0001t0001g0321 others(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 | a0001c0001t0001g0285 a0001c0001t0001g0286 a0001c0001t0001g0288 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0063 a0001c0001t0001g0064 |
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 | a0001c0001t0001g0063 a0001c0001t0001g0064 |
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 | 38 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0291 others(35): Show |
40 | HG00280.hp1 HG00733.hp1 HG01074.hp1 others(37): 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 | a0001c0001t0001g0065 | 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 | a0001c0001t0001g0065 | 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 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0031 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0024 others(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 |