Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 6709 |
| ensemblid | ENSG00000197694.19 |
| hgncid | 11273 |
| symbol | SPTAN1 |
| name | spectrin alpha, non-erythrocytic 1 |
| refseq_nuc | NM_001130438.3 |
| refseq_prot | NP_001123910.1 |
| ensembl_nuc | ENST00000372739.7 |
| ensembl_prot | ENSP00000361824.4 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 128552587 |
| end | 128633662 |
| strand | + |
| ver | v1.2 |
| region | chr9:128552587-128633662 |
| region5000 | chr9:128547587-128638662 |
| regionname0 | SPTAN1_chr9_128552587_128633662 |
| regionname5000 | SPTAN1_chr9_128547587_128638662 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 2477 | 294 | 83 | 38 | 133 | 12 | 26 | 104 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | MDPSG others(2472): Show |
chr9 | 128547587 | 128638662 |
| a0002 | 0/0 | 2477 | 11 | 0 | 0 | 9 | 0 | 2 | 8 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | MDPSG others(2472): Show |
chr9 | 128547587 | 128638662 |
| a0003 | 0/0 | 2477 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | MDPSG others(2472): Show |
chr9 | 128547587 | 128638662 |
| a0004 | 0/0 | 2477 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | MDPSG others(2472): Show |
chr9 | 128547587 | 128638662 |
| a0005 | 0/0 | 2477 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | MDPSG others(2472): Show |
chr9 | 128547587 | 128638662 |
| a0006 | 0/0 | 2477 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | MDPSG others(2472): Show |
chr9 | 128547587 | 128638662 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 7431 | 119 | 25 | 17 | 52 | 10 | 14 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | ATGGA others(7426): Show |
chr9 | 128547587 | 128638662 | ||
| a0001c0002 | 0/0 | 7431 | 104 | 19 | 11 | 61 | 2 | 11 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | ATGGA others(7426): Show |
chr9 | 128547587 | 128638662 | ||
| a0001c0003 | 0/0 | 7431 | 13 | 0 | 0 | 13 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | ATGGA others(7426): Show |
chr9 | 128547587 | 128638662 | ||
| a0001c0005 | 1/0 | 7431 | 9 | 8 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | ATGGA others(7426): Show |
chr9 | 128547587 | 128638662 | ||
| a0001c0006 | 0/0 | 7431 | 8 | 6 | 2 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | ATGGA others(7426): Show |
chr9 | 128547587 | 128638662 | ||
| a0001c0007 | 0/0 | 7431 | 7 | 7 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | ATGGA others(7426): Show |
chr9 | 128547587 | 128638662 | ||
| a0001c0008 | 0/0 | 7431 | 6 | 4 | 2 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | ATGGA others(7426): Show |
chr9 | 128547587 | 128638662 | ||
| a0001c0009 | 0/0 | 7431 | 3 | 3 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | ATGGA others(7426): Show |
chr9 | 128547587 | 128638662 | ||
| a0001c0010 | 0/0 | 7431 | 3 | 3 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | ATGGA others(7426): Show |
chr9 | 128547587 | 128638662 | ||
| a0001c0012 | 0/0 | 7431 | 3 | 0 | 3 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | ATGGA others(7426): Show |
chr9 | 128547587 | 128638662 | ||
| a0001c0013 | 0/0 | 7431 | 3 | 0 | 0 | 3 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | ATGGA others(7426): Show |
chr9 | 128547587 | 128638662 | ||
| a0001c0014 | 0/0 | 7431 | 2 | 2 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | ATGGA others(7426): Show |
chr9 | 128547587 | 128638662 | ||
| a0001c0016 | 0/0 | 7431 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | ATGGA others(7426): Show |
chr9 | 128547587 | 128638662 | ||
| a0001c0017 | 0/0 | 7431 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | ATGGA others(7426): Show |
chr9 | 128547587 | 128638662 | ||
| a0001c0018 | 0/0 | 7431 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | ATGGA others(7426): Show |
chr9 | 128547587 | 128638662 | ||
| a0001c0019 | 0/0 | 7431 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | ATGGA others(7426): Show |
chr9 | 128547587 | 128638662 | ||
| a0001c0021 | 0/0 | 7431 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | ATGGA others(7426): Show |
chr9 | 128547587 | 128638662 | ||
| a0001c0022 | 0/0 | 7431 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | ATGGA others(7426): Show |
chr9 | 128547587 | 128638662 | ||
| a0001c0023 | 0/0 | 7431 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | ATGGA others(7426): Show |
chr9 | 128547587 | 128638662 | ||
| a0001c0024 | 0/0 | 7431 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | ATGGA others(7426): Show |
chr9 | 128547587 | 128638662 | ||
| a0001c0025 | 0/0 | 7431 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | ATGGA others(7426): Show |
chr9 | 128547587 | 128638662 | ||
| a0001c0026 | 0/0 | 7431 | 1 | 0 | 0 | 0 | 0 | 1 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | ATGGA others(7426): Show |
chr9 | 128547587 | 128638662 | ||
| a0001c0027 | 0/0 | 7431 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | ATGGA others(7426): Show |
chr9 | 128547587 | 128638662 | ||
| a0001c0028 | 0/0 | 7431 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | ATGGA others(7426): Show |
chr9 | 128547587 | 128638662 | ||
| a0001c0029 | 0/0 | 7431 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | ATGGA others(7426): Show |
chr9 | 128547587 | 128638662 | ||
| a0001c0030 | 0/0 | 7431 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | ATGGA others(7426): Show |
chr9 | 128547587 | 128638662 | ||
| a0002c0004 | 0/0 | 7431 | 11 | 0 | 0 | 9 | 0 | 2 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | ATGGA others(7426): Show |
chr9 | 128547587 | 128638662 | ||
| a0003c0011 | 0/0 | 7431 | 3 | 0 | 0 | 3 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | ATGGA others(7426): Show |
chr9 | 128547587 | 128638662 | ||
| a0004c0015 | 0/0 | 7431 | 2 | 0 | 2 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | ATGGA others(7426): Show |
chr9 | 128547587 | 128638662 | ||
| a0005c0020 | 0/0 | 7431 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | ATGGA others(7426): Show |
chr9 | 128547587 | 128638662 | ||
| a0006c0031 | 0/0 | 7431 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | ATGGA others(7426): Show |
chr9 | 128547587 | 128638662 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 7875 | 117 | 25 | 17 | 50 | 10 | 14 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | GCCAC others(7870): Show |
chr9 | 128547587 | 128638662 |
| a0001c0001t0007 | 0/0 | 7875 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | GCCAC others(7870): Show |
chr9 | 128547587 | 128638662 |
| a0001c0001t0008 | 0/0 | 7875 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | GCCAC others(7870): Show |
chr9 | 128547587 | 128638662 |
| a0001c0002t0001 | 0/0 | 7875 | 103 | 19 | 11 | 61 | 2 | 10 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | GCCAC others(7870): Show |
chr9 | 128547587 | 128638662 |
| a0001c0002t0005 | 0/0 | 7875 | 1 | 0 | 0 | 0 | 0 | 1 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | GCCAC others(7870): Show |
chr9 | 128547587 | 128638662 |
| a0001c0003t0001 | 0/0 | 7875 | 13 | 0 | 0 | 13 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | GCCAC others(7870): Show |
chr9 | 128547587 | 128638662 |
| a0001c0005t0001 | 1/0 | 7875 | 9 | 8 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | GCCAC others(7870): Show |
chr9 | 128547587 | 128638662 |
| a0001c0006t0001 | 0/0 | 7875 | 8 | 6 | 2 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | GCCAC others(7870): Show |
chr9 | 128547587 | 128638662 |
| a0001c0007t0001 | 0/0 | 7875 | 7 | 7 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | GCCAC others(7870): Show |
chr9 | 128547587 | 128638662 |
| a0001c0008t0001 | 0/0 | 7875 | 6 | 4 | 2 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | GCCAC others(7870): Show |
chr9 | 128547587 | 128638662 |
| a0001c0009t0001 | 0/0 | 7875 | 3 | 3 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | GCCAC others(7870): Show |
chr9 | 128547587 | 128638662 |
| a0001c0010t0001 | 0/0 | 7875 | 3 | 3 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | GCCAC others(7870): Show |
chr9 | 128547587 | 128638662 |
| a0001c0012t0001 | 0/0 | 7875 | 3 | 0 | 3 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | GCCAC others(7870): Show |
chr9 | 128547587 | 128638662 |
| a0001c0013t0001 | 0/0 | 7875 | 3 | 0 | 0 | 3 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | GCCAC others(7870): Show |
chr9 | 128547587 | 128638662 |
| a0001c0014t0003 | 0/0 | 7875 | 2 | 2 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | GCCAC others(7870): Show |
chr9 | 128547587 | 128638662 |
| a0001c0016t0001 | 0/0 | 7875 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | GCCAC others(7870): Show |
chr9 | 128547587 | 128638662 |
| a0001c0017t0006 | 0/0 | 7875 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | GCCAC others(7870): Show |
chr9 | 128547587 | 128638662 |
| a0001c0018t0004 | 0/0 | 7875 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | GCCAC others(7870): Show |
chr9 | 128547587 | 128638662 |
| a0001c0019t0001 | 0/0 | 7875 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | GCCAC others(7870): Show |
chr9 | 128547587 | 128638662 |
| a0001c0021t0001 | 0/0 | 7875 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | GCCAC others(7870): Show |
chr9 | 128547587 | 128638662 |
| a0001c0022t0001 | 0/0 | 7875 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | GCCAC others(7870): Show |
chr9 | 128547587 | 128638662 |
| a0001c0023t0001 | 0/0 | 7875 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | GCCAC others(7870): Show |
chr9 | 128547587 | 128638662 |
| a0001c0024t0001 | 0/0 | 7875 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | GCCAC others(7870): Show |
chr9 | 128547587 | 128638662 |
| a0001c0025t0001 | 0/0 | 7875 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | GCCAC others(7870): Show |
chr9 | 128547587 | 128638662 |
| a0001c0026t0001 | 0/0 | 7875 | 1 | 0 | 0 | 0 | 0 | 1 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | GCCAC others(7870): Show |
chr9 | 128547587 | 128638662 |
| a0001c0027t0001 | 0/0 | 7875 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | GCCAC others(7870): Show |
chr9 | 128547587 | 128638662 |
| a0001c0028t0001 | 0/0 | 7875 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | GCCAC others(7870): Show |
chr9 | 128547587 | 128638662 |
| a0001c0029t0001 | 0/0 | 7875 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | GCCAC others(7870): Show |
chr9 | 128547587 | 128638662 |
| a0001c0030t0001 | 0/0 | 7875 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | GCCAC others(7870): Show |
chr9 | 128547587 | 128638662 |
| a0002c0004t0001 | 0/0 | 7875 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | GCCAC others(7870): Show |
chr9 | 128547587 | 128638662 |
| a0002c0004t0002 | 0/0 | 7875 | 10 | 0 | 0 | 8 | 0 | 2 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | GCCAC others(7870): Show |
chr9 | 128547587 | 128638662 |
| a0003c0011t0001 | 0/0 | 7875 | 3 | 0 | 0 | 3 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | GCCAC others(7870): Show |
chr9 | 128547587 | 128638662 |
| a0004c0015t0001 | 0/0 | 7875 | 2 | 0 | 2 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | GCCAC others(7870): Show |
chr9 | 128547587 | 128638662 |
| a0005c0020t0001 | 0/0 | 7875 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | GCCAC others(7870): Show |
chr9 | 128547587 | 128638662 |
| a0006c0031t0001 | 0/0 | 7875 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | GCCAC others(7870): Show |
chr9 | 128547587 | 128638662 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0050 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0007g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0008g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0005g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0003t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0003t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0003t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0003t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0003t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0003t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0003t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0003t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0003t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0003t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0003t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0003t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0003t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0005t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0005t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0005t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0005t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0005t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0005t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0005t0001g0023 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0005t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0005t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0006t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0006t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0006t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0006t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0006t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0006t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0006t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0006t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0007t0001g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0007t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0007t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0007t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0007t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0007t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0008t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0008t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0008t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0008t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0008t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0008t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0009t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0009t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0009t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0010t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0010t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0010t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0012t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0012t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0013t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0013t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0013t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0014t0003g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0014t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0016t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0017t0006g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0018t0004g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0019t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0021t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0022t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0023t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0024t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0025t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0026t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0027t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0028t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0029t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0030t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0002c0004t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0002c0004t0002g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0002c0004t0002g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0002c0004t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0002c0004t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0002c0004t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0002c0004t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0002c0004t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0002c0004t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0002c0004t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0002c0004t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0003c0011t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0003c0011t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0003c0011t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0004c0015t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0004c0015t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0005c0020t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0006c0031t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0094 | EUR | GBR | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0043 | EUR | GBR | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0093 | EUR | GBR | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0147 | EUR | GBR | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0288 | EUR | FIN | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG00280 | hp2 | a0001 | c0002 | t0001 | g0232 | EUR | FIN | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG00408 | hp1 | a0001 | c0003 | t0001 | g0137 | EAS | CHS | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | CHS | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | CHS | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG00423 | hp2 | a0001 | c0002 | t0001 | g0197 | EAS | CHS | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG00438 | hp1 | a0001 | c0002 | t0001 | g0202 | EAS | CHS | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | CHS | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | CHS | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG00558 | hp2 | a0001 | c0002 | t0001 | g0211 | EAS | CHS | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | CHS | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG00597 | hp2 | a0001 | c0002 | t0001 | g0256 | EAS | CHS | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG00609 | hp1 | a0001 | c0002 | t0001 | g0199 | EAS | CHS | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG00609 | hp2 | a0001 | c0027 | t0001 | g0117 | EAS | CHS | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG00621 | hp1 | a0001 | c0003 | t0001 | g0133 | EAS | CHS | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | CHS | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG00642 | hp1 | a0001 | c0002 | t0001 | g0186 | AMR | PUR | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG00735 | hp1 | a0001 | c0002 | t0001 | g0289 | AMR | PUR | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG00735 | hp2 | a0001 | c0012 | t0001 | g0124 | AMR | PUR | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG01069 | hp1 | a0001 | c0006 | t0001 | g0295 | AMR | PUR | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG01069 | hp2 | a0001 | c0030 | t0001 | g0285 | AMR | PUR | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG01099 | hp2 | a0001 | c0008 | t0001 | g0167 | AMR | PUR | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG01109 | hp1 | a0001 | c0002 | t0001 | g0188 | AMR | PUR | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG01109 | hp2 | a0001 | c0017 | t0006 | g0014 | AMR | PUR | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG01167 | hp2 | a0001 | c0006 | t0001 | g0290 | AMR | PUR | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG01192 | hp1 | a0001 | c0002 | t0001 | g0235 | AMR | PUR | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | CLM | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG01256 | hp2 | a0004 | c0015 | t0001 | g0173 | AMR | CLM | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG01257 | hp1 | a0001 | c0002 | t0001 | g0227 | AMR | CLM | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG01257 | hp2 | a0001 | c0012 | t0001 | g0001 | AMR | CLM | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG01258 | hp1 | a0004 | c0015 | t0001 | g0185 | AMR | CLM | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG01258 | hp2 | a0001 | c0012 | t0001 | g0001 | AMR | CLM | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | CLM | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG01361 | hp2 | a0001 | c0002 | t0001 | g0265 | AMR | CLM | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG01433 | hp1 | a0001 | c0002 | t0001 | g0233 | AMR | CLM | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | CLM | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | CLM | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG01496 | hp2 | a0001 | c0008 | t0001 | g0171 | AMR | CLM | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0131 | EUR | IBS | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0286 | EUR | IBS | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0128 | EUR | IBS | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0127 | EUR | IBS | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG01884 | hp1 | a0001 | c0007 | t0001 | g0010 | AFR | ACB | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG01884 | hp2 | a0001 | c0002 | t0001 | g0267 | AFR | ACB | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | ACB | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG01891 | hp2 | a0001 | c0009 | t0001 | g0028 | AFR | ACB | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG01934 | hp1 | a0001 | c0002 | t0001 | g0248 | AMR | PEL | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | PEL | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | PEL | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG01978 | hp2 | a0001 | c0029 | t0001 | g0086 | AMR | PEL | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0246 | AMR | PEL | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PEL | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | KHV | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | KHV | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02040 | hp1 | a0001 | c0024 | t0001 | g0196 | EAS | KHV | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02040 | hp2 | a0002 | c0004 | t0002 | g0280 | EAS | KHV | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0257 | AFR | ACB | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02055 | hp2 | a0001 | c0005 | t0001 | g0017 | AFR | ACB | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02071 | hp1 | a0001 | c0002 | t0001 | g0198 | EAS | KHV | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | KHV | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02074 | hp1 | a0001 | c0002 | t0001 | g0244 | EAS | KHV | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | KHV | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02080 | hp1 | a0001 | c0002 | t0001 | g0255 | EAS | KHV | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02080 | hp2 | a0001 | c0002 | t0001 | g0253 | EAS | KHV | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02083 | hp1 | a0001 | c0003 | t0001 | g0134 | EAS | KHV | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02083 | hp2 | a0001 | c0002 | t0001 | g0178 | EAS | KHV | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | KHV | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02135 | hp2 | a0001 | c0002 | t0001 | g0189 | EAS | KHV | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | ACB | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02145 | hp2 | a0001 | c0006 | t0001 | g0292 | AFR | ACB | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | CDX | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02155 | hp2 | a0001 | c0002 | t0001 | g0222 | EAS | CDX | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02258 | hp1 | a0001 | c0008 | t0001 | g0169 | AFR | ACB | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | ACB | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02280 | hp1 | a0001 | c0008 | t0001 | g0168 | AFR | ACB | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02280 | hp2 | a0001 | c0007 | t0001 | g0011 | AFR | ACB | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02300 | hp1 | a0001 | c0002 | t0001 | g0252 | AMR | PEL | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PEL | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02451 | hp1 | a0001 | c0006 | t0001 | g0296 | AFR | ACB | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02451 | hp2 | a0001 | c0002 | t0001 | g0216 | AFR | ACB | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02572 | hp1 | a0001 | c0023 | t0001 | g0303 | AFR | GWD | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | GWD | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02615 | hp1 | a0001 | c0010 | t0001 | g0299 | AFR | GWD | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02615 | hp2 | a0001 | c0007 | t0001 | g0002 | AFR | GWD | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | GWD | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02647 | hp2 | a0001 | c0002 | t0001 | g0258 | AFR | GWD | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02683 | hp1 | a0001 | c0002 | t0001 | g0264 | SAS | PJL | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0080 | SAS | PJL | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02698 | hp1 | a0001 | c0002 | t0001 | g0250 | SAS | PJL | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02717 | hp1 | a0001 | c0021 | t0001 | g0304 | AFR | GWD | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02717 | hp2 | a0001 | c0007 | t0001 | g0002 | AFR | GWD | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02723 | hp1 | a0001 | c0005 | t0001 | g0016 | AFR | GWD | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02723 | hp2 | a0001 | c0002 | t0001 | g0183 | AFR | GWD | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0049 | SAS | PJL | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02809 | hp1 | a0001 | c0010 | t0001 | g0300 | AFR | GWD | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | GWD | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02818 | hp2 | a0001 | c0002 | t0001 | g0263 | AFR | GWD | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | GWD | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02886 | hp2 | a0001 | c0005 | t0001 | g0018 | AFR | GWD | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02895 | hp1 | a0001 | c0002 | t0001 | g0269 | AFR | GWD | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02897 | hp1 | a0001 | c0002 | t0001 | g0306 | AFR | GWD | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | GWD | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02922 | hp1 | a0001 | c0007 | t0001 | g0047 | AFR | ESN | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02922 | hp2 | a0001 | c0016 | t0001 | g0026 | AFR | ESN | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0284 | AFR | ESN | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02965 | hp2 | a0001 | c0008 | t0001 | g0170 | AFR | ESN | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0298 | AFR | ESN | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02970 | hp2 | a0001 | c0006 | t0001 | g0294 | AFR | ESN | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG03041 | hp1 | a0001 | c0002 | t0001 | g0268 | AFR | GWD | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG03098 | hp1 | a0001 | c0007 | t0001 | g0009 | AFR | MSL | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | MSL | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | ESN | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG03130 | hp2 | a0001 | c0002 | t0001 | g0305 | AFR | ESN | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG03139 | hp1 | a0001 | c0006 | t0001 | g0291 | AFR | ESN | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG03139 | hp2 | a0005 | c0020 | t0001 | g0008 | AFR | ESN | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | ESN | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG03195 | hp2 | a0001 | c0002 | t0001 | g0261 | AFR | ESN | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG03209 | hp1 | a0001 | c0014 | t0003 | g0021 | AFR | MSL | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG03209 | hp2 | a0001 | c0007 | t0001 | g0272 | AFR | MSL | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG03225 | hp1 | a0001 | c0002 | t0001 | g0013 | AFR | MSL | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | MSL | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | MSL | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG03453 | hp2 | a0001 | c0006 | t0001 | g0297 | AFR | MSL | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG03490 | hp2 | a0001 | c0002 | t0005 | g0181 | SAS | PJL | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0287 | SAS | PJL | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG03516 | hp1 | a0001 | c0005 | t0001 | g0015 | AFR | ESN | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG03516 | hp2 | a0001 | c0009 | t0001 | g0006 | AFR | ESN | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG03540 | hp1 | a0001 | c0010 | t0001 | g0301 | AFR | GWD | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | GWD | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG03579 | hp1 | a0001 | c0002 | t0001 | g0262 | AFR | MSL | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG03579 | hp2 | a0001 | c0009 | t0001 | g0027 | AFR | MSL | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG03654 | hp1 | a0001 | c0002 | t0001 | g0228 | SAS | PJL | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG03669 | hp2 | a0002 | c0004 | t0002 | g0274 | SAS | PJL | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG03688 | hp1 | a0002 | c0004 | t0002 | g0273 | SAS | STU | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0146 | SAS | STU | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG03704 | hp1 | a0001 | c0002 | t0001 | g0251 | SAS | PJL | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | BEB | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG03831 | hp2 | a0001 | c0002 | t0001 | g0226 | SAS | BEB | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | BEB | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG03834 | hp2 | a0001 | c0002 | t0001 | g0221 | SAS | BEB | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG04184 | hp1 | a0001 | c0002 | t0001 | g0270 | SAS | BEB | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG04184 | hp2 | a0001 | c0026 | t0001 | g0209 | SAS | BEB | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0162 | SAS | STU | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG04204 | hp2 | a0001 | c0002 | t0001 | g0242 | SAS | STU | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG04228 | hp1 | a0001 | c0002 | t0001 | g0205 | SAS | STU | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG04228 | hp2 | a0001 | c0002 | t0001 | g0201 | SAS | STU | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18522 | hp1 | a0001 | c0002 | t0001 | g0192 | AFR | YRI | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | YRI | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18906 | hp1 | a0001 | c0002 | t0001 | g0012 | AFR | YRI | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18906 | hp2 | a0001 | c0008 | t0001 | g0172 | AFR | YRI | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18939 | hp2 | a0001 | c0002 | t0001 | g0224 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18941 | hp1 | a0001 | c0002 | t0001 | g0238 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18944 | hp1 | a0001 | c0001 | t0008 | g0098 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18944 | hp2 | a0001 | c0002 | t0001 | g0254 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18947 | hp1 | a0001 | c0002 | t0001 | g0230 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18948 | hp1 | a0001 | c0002 | t0001 | g0309 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18948 | hp2 | a0001 | c0003 | t0001 | g0118 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18949 | hp1 | a0002 | c0004 | t0002 | g0281 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18949 | hp2 | a0001 | c0002 | t0001 | g0208 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18950 | hp1 | a0001 | c0002 | t0001 | g0190 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18951 | hp2 | a0001 | c0002 | t0001 | g0176 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18952 | hp2 | a0001 | c0002 | t0001 | g0243 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18953 | hp2 | a0001 | c0002 | t0001 | g0240 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18954 | hp1 | a0001 | c0002 | t0001 | g0231 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18957 | hp1 | a0001 | c0003 | t0001 | g0140 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18957 | hp2 | a0001 | c0002 | t0001 | g0179 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18960 | hp1 | a0001 | c0001 | t0007 | g0065 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18960 | hp2 | a0001 | c0002 | t0001 | g0310 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18961 | hp1 | a0001 | c0003 | t0001 | g0030 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18961 | hp2 | a0001 | c0002 | t0001 | g0215 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18964 | hp2 | a0001 | c0002 | t0001 | g0234 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18967 | hp2 | a0001 | c0002 | t0001 | g0194 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18968 | hp1 | a0002 | c0004 | t0002 | g0276 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18968 | hp2 | a0001 | c0002 | t0001 | g0214 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18969 | hp2 | a0001 | c0002 | t0001 | g0307 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18972 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18974 | hp2 | a0001 | c0002 | t0001 | g0200 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18975 | hp2 | a0002 | c0004 | t0002 | g0283 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18977 | hp1 | a0001 | c0003 | t0001 | g0095 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18977 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18979 | hp1 | a0001 | c0002 | t0001 | g0206 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18980 | hp1 | a0003 | c0011 | t0001 | g0067 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18980 | hp2 | a0001 | c0002 | t0001 | g0210 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18982 | hp2 | a0001 | c0002 | t0001 | g0213 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18984 | hp2 | a0001 | c0002 | t0001 | g0239 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18985 | hp1 | a0001 | c0002 | t0001 | g0220 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18985 | hp2 | a0001 | c0013 | t0001 | g0165 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18986 | hp1 | a0001 | c0013 | t0001 | g0161 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18986 | hp2 | a0001 | c0002 | t0001 | g0184 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18988 | hp1 | a0001 | c0002 | t0001 | g0195 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18989 | hp1 | a0001 | c0013 | t0001 | g0163 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18989 | hp2 | a0001 | c0002 | t0001 | g0191 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18990 | hp1 | a0001 | c0002 | t0001 | g0236 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18994 | hp1 | a0001 | c0003 | t0001 | g0148 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18994 | hp2 | a0001 | c0002 | t0001 | g0219 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18998 | hp1 | a0002 | c0004 | t0002 | g0279 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18998 | hp2 | a0003 | c0011 | t0001 | g0063 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18999 | hp1 | a0002 | c0004 | t0002 | g0282 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18999 | hp2 | a0006 | c0031 | t0001 | g0225 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA19000 | hp1 | a0001 | c0002 | t0001 | g0271 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA19001 | hp2 | a0001 | c0002 | t0001 | g0175 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA19004 | hp2 | a0001 | c0002 | t0001 | g0207 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA19007 | hp1 | a0001 | c0002 | t0001 | g0223 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA19009 | hp1 | a0003 | c0011 | t0001 | g0066 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA19009 | hp2 | a0001 | c0002 | t0001 | g0187 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA19010 | hp2 | a0001 | c0002 | t0001 | g0177 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA19012 | hp2 | a0001 | c0002 | t0001 | g0229 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA19030 | hp1 | a0001 | c0002 | t0001 | g0033 | AFR | LWK | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA19030 | hp2 | a0001 | c0005 | t0001 | g0024 | AFR | LWK | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | LWK | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA19043 | hp2 | a0001 | c0025 | t0001 | g0182 | AFR | LWK | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA19056 | hp1 | a0001 | c0002 | t0001 | g0247 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA19057 | hp2 | a0002 | c0004 | t0002 | g0275 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA19063 | hp1 | a0001 | c0003 | t0001 | g0122 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA19063 | hp2 | a0001 | c0002 | t0001 | g0308 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA19065 | hp2 | a0001 | c0002 | t0001 | g0237 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA19066 | hp2 | a0001 | c0003 | t0001 | g0116 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA19070 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA19074 | hp1 | a0001 | c0003 | t0001 | g0031 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA19074 | hp2 | a0001 | c0002 | t0001 | g0241 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA19081 | hp1 | a0002 | c0004 | t0002 | g0277 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA19081 | hp2 | a0001 | c0019 | t0001 | g0218 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA19083 | hp2 | a0001 | c0002 | t0001 | g0174 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA19084 | hp1 | a0001 | c0002 | t0001 | g0203 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA19086 | hp1 | a0002 | c0004 | t0001 | g0278 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA19088 | hp1 | a0001 | c0003 | t0001 | g0123 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA19088 | hp2 | a0001 | c0002 | t0001 | g0212 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA19089 | hp1 | a0001 | c0002 | t0001 | g0180 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA19089 | hp2 | a0001 | c0003 | t0001 | g0129 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA19090 | hp1 | a0001 | c0002 | t0001 | g0249 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA19090 | hp2 | a0001 | c0028 | t0001 | g0160 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | YRI | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA19240 | hp2 | a0001 | c0002 | t0001 | g0032 | AFR | YRI | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA20752 | hp1 | a0001 | c0002 | t0001 | g0245 | EUR | TSI | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0113 | EUR | TSI | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG01123 | hp1 | a0001 | c0002 | t0001 | g0204 | AMR | CLM | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | CLM | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02109 | hp1 | a0001 | c0005 | t0001 | g0019 | AFR | ACB | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02109 | hp2 | a0001 | c0002 | t0001 | g0259 | AFR | ACB | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02486 | hp1 | a0001 | c0005 | t0001 | g0022 | AFR | ACB | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02486 | hp2 | a0001 | c0022 | t0001 | g0260 | AFR | ACB | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02559 | hp1 | a0001 | c0014 | t0003 | g0020 | AFR | ACB | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02559 | hp2 | a0001 | c0006 | t0001 | g0293 | AFR | ACB | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | MSL | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG03471 | hp2 | a0001 | c0005 | t0001 | g0025 | AFR | MSL | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG06807 | hp1 | a0001 | c0002 | t0001 | g0217 | AFR | USA | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | USA | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18955 | hp1 | a0001 | c0002 | t0001 | g0266 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | LWK | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA21309 | hp2 | a0001 | c0018 | t0004 | g0193 | AFR | LWK | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0050 | REF | REF | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| homoSapiens | grch38p0 | a0001 | c0005 | t0001 | g0023 | REF | REF | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:128577394 | C | T | 1 | a0006 | 1 | NA18999.hp2 | missense_variant | MODERATE | c.973C>T | p.His325Tyr | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 8/57 | 1086/7875 | 973/7434 | 325/2477 | chr9 | 128577394 | |||
| chr9:128580928 | G | A | 1 | a0002 | 11 | HG02040.hp2 HG03669.hp2 HG03688.hp1 others(8): Show |
missense_variant | MODERATE | c.1330G>A | p.Val444Ile | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 11/57 | 1443/7875 | 1330/7434 | 444/2477 | chr9 | 128580928 | |||
| chr9:128608922 | G | A | 1 | a0003 | 3 | NA18980.hp1 NA18998.hp2 NA19009.hp1 |
missense_variant | MODERATE | c.4540G>A | p.Ala1514Thr | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 35/57 | 4653/7875 | 4540/7434 | 1514/2477 | chr9 | 128608922 | |||
| chr9:128618060 | C | T | 1 | a0005 | 1 | HG03139.hp2 | missense_variant | MODERATE | c.5552C>T | p.Ala1851Val | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 43/57 | 5665/7875 | 5552/7434 | 1851/2477 | chr9 | 128618060 | |||
| chr9:128632128 | G | A | 1 | a0004 | 2 | HG01256.hp2 HG01258.hp1 |
missense_variant&splice_region_variant | MODERATE | c.6764G>A | p.Arg2255His | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 53/57 | 6877/7875 | 6764/7434 | 2255/2477 | chr9 | 128632128 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:128583939 | A | C | 26 | a0001c0001 a0001c0002 a0001c0003 others(23): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
synonymous_variant | LOW | c.2163A>C | p.Ala721Ala | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 16/57 | 2276/7875 | 2163/7434 | 721/2477 | chr9 | 128583939 | |||
| chr9:128584431 | C | A | 2 | a0001c0006 a0001c0010 |
11 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(8): Show |
synonymous_variant | LOW | c.2343C>A | p.Ala781Ala | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 17/57 | 2456/7875 | 2343/7434 | 781/2477 | chr9 | 128584431 | |||
| chr9:128588817 | G | A | 1 | a0001c0018 | 1 | NA21309.hp2 | synonymous_variant | LOW | c.2880G>A | p.Val960Val | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/57 | 2993/7875 | 2880/7434 | 960/2477 | chr9 | 128588817 | |||
| chr9:128591521 | G | A | 1 | a0001c0019 | 1 | NA19081.hp2 | synonymous_variant | LOW | c.3051G>A | p.Pro1017Pro | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 22/57 | 3164/7875 | 3051/7434 | 1017/2477 | chr9 | 128591521 | |||
| chr9:128594259 | G | A | 1 | a0001c0006 | 8 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(5): Show |
synonymous_variant | LOW | c.3300G>A | p.Ala1100Ala | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/57 | 3413/7875 | 3300/7434 | 1100/2477 | chr9 | 128594259 | |||
| chr9:128598471 | C | T | 10 | a0001c0001 a0001c0003 a0001c0008 others(7): Show |
150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
synonymous_variant | LOW | c.3486C>T | p.Leu1162Leu | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 25/57 | 3599/7875 | 3486/7434 | 1162/2477 | chr9 | 128598471 | |||
| chr9:128600082 | T | C | 2 | a0001c0007 a0005c0020 |
8 | HG01884.hp1 HG02280.hp2 HG02615.hp2 others(5): Show |
splice_region_variant&synonymous_variant | LOW | c.3546T>C | p.Asp1182Asp | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/57 | 3659/7875 | 3546/7434 | 1182/2477 | chr9 | 128600082 | |||
| chr9:128605076 | A | G | 1 | a0001c0026 | 1 | HG04184.hp2 | synonymous_variant | LOW | c.3762A>G | p.Gln1254Gln | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 30/57 | 3875/7875 | 3762/7434 | 1254/2477 | chr9 | 128605076 | |||
| chr9:128608195 | C | T | 1 | a0001c0009 | 3 | HG01891.hp2 HG03516.hp2 HG03579.hp2 |
synonymous_variant | LOW | c.4410C>T | p.Thr1470Thr | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 34/57 | 4523/7875 | 4410/7434 | 1470/2477 | chr9 | 128608195 | |||
| chr9:128608924 | C | T | 1 | a0001c0025 | 1 | NA19043.hp2 | synonymous_variant | LOW | c.4542C>T | p.Ala1514Ala | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 35/57 | 4655/7875 | 4542/7434 | 1514/2477 | chr9 | 128608924 | |||
| chr9:128612222 | G | A | 1 | a0001c0016 | 1 | HG02922.hp2 | synonymous_variant | LOW | c.5019G>A | p.Lys1673Lys | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 39/57 | 5132/7875 | 5019/7434 | 1673/2477 | chr9 | 128612222 | |||
| chr9:128613422 | A | G | 29 | a0001c0001 a0001c0002 a0001c0003 others(26): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
synonymous_variant | LOW | c.5085A>G | p.Leu1695Leu | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 40/57 | 5198/7875 | 5085/7434 | 1695/2477 | chr9 | 128613422 | |||
| chr9:128613443 | G | A | 1 | a0001c0021 | 1 | HG02717.hp1 | synonymous_variant | LOW | c.5106G>A | p.Leu1702Leu | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 40/57 | 5219/7875 | 5106/7434 | 1702/2477 | chr9 | 128613443 | |||
| chr9:128615784 | A | G | 1 | a0001c0030 | 1 | HG01069.hp2 | synonymous_variant | LOW | c.5301A>G | p.Glu1767Glu | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 41/57 | 5414/7875 | 5301/7434 | 1767/2477 | chr9 | 128615784 | |||
| chr9:128617688 | C | T | 9 | a0001c0001 a0001c0003 a0001c0012 others(6): Show |
144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
synonymous_variant | LOW | c.5406C>T | p.Thr1802Thr | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 42/57 | 5519/7875 | 5406/7434 | 1802/2477 | chr9 | 128617688 | |||
| chr9:128617719 | C | A | 2 | a0001c0003 a0001c0024 |
14 | HG00408.hp1 HG00621.hp1 HG02040.hp1 others(11): Show |
synonymous_variant | LOW | c.5437C>A | p.Arg1813Arg | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 42/57 | 5550/7875 | 5437/7434 | 1813/2477 | chr9 | 128617719 | |||
| chr9:128618031 | C | T | 1 | a0001c0013 | 3 | NA18985.hp2 NA18986.hp1 NA18989.hp1 |
synonymous_variant | LOW | c.5523C>T | p.Ile1841Ile | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 43/57 | 5636/7875 | 5523/7434 | 1841/2477 | chr9 | 128618031 | |||
| chr9:128618052 | G | A | 1 | a0001c0028 | 1 | NA19090.hp2 | synonymous_variant | LOW | c.5544G>A | p.Gln1848Gln | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 43/57 | 5657/7875 | 5544/7434 | 1848/2477 | chr9 | 128618052 | |||
| chr9:128621199 | C | T | 1 | a0001c0012 | 3 | HG00735.hp2 HG01257.hp2 HG01258.hp2 |
synonymous_variant | LOW | c.5775C>T | p.Thr1925Thr | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 45/57 | 5888/7875 | 5775/7434 | 1925/2477 | chr9 | 128621199 | |||
| chr9:128621214 | C | T | 1 | a0001c0023 | 1 | HG02572.hp1 | synonymous_variant | LOW | c.5790C>T | p.Arg1930Arg | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 45/57 | 5903/7875 | 5790/7434 | 1930/2477 | chr9 | 128621214 | |||
| chr9:128624420 | G | A | 2 | a0001c0009 a0001c0016 |
4 | HG01891.hp2 HG02922.hp2 HG03516.hp2 others(1): Show |
synonymous_variant | LOW | c.5925G>A | p.Ala1975Ala | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 46/57 | 6038/7875 | 5925/7434 | 1975/2477 | chr9 | 128624420 | |||
| chr9:128626660 | C | A | 1 | a0001c0009 | 3 | HG01891.hp2 HG03516.hp2 HG03579.hp2 |
synonymous_variant | LOW | c.6549C>A | p.Thr2183Thr | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 49/57 | 6662/7875 | 6549/7434 | 2183/2477 | chr9 | 128626660 | |||
| chr9:128627463 | C | T | 1 | a0001c0022 | 1 | HG02486.hp2 | synonymous_variant | LOW | c.6654C>T | p.His2218His | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 50/57 | 6767/7875 | 6654/7434 | 2218/2477 | chr9 | 128627463 | |||
| chr9:128627469 | C | T | 1 | a0001c0010 | 3 | HG02615.hp1 HG02809.hp1 HG03540.hp1 |
synonymous_variant | LOW | c.6660C>T | p.Asn2220Asn | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 50/57 | 6773/7875 | 6660/7434 | 2220/2477 | chr9 | 128627469 | |||
| chr9:128632626 | C | T | 1 | a0001c0029 | 1 | HG01978.hp2 | synonymous_variant | LOW | c.7068C>T | p.Cys2356Cys | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 55/57 | 7181/7875 | 7068/7434 | 2356/2477 | chr9 | 128632626 | |||
| chr9:128633289 | C | T | 1 | a0001c0008 | 6 | HG01099.hp2 HG01496.hp2 HG02258.hp1 others(3): Show |
synonymous_variant | LOW | c.7389C>T | p.Thr2463Thr | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 57/57 | 7502/7875 | 7389/7434 | 2463/2477 | chr9 | 128633289 | |||
| chr9:128633292 | G | A | 1 | a0001c0017 | 1 | HG01109.hp2 | synonymous_variant | LOW | c.7392G>A | p.Ala2464Ala | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 57/57 | 7505/7875 | 7392/7434 | 2464/2477 | chr9 | 128633292 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:128633393 | C | T | 1 | a0001c0001t0008 | 1 | NA18944.hp1 | 3_prime_UTR_variant | MODIFIER | c.*59C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 57/57 | 59 | chr9 | 128633393 | ||||||
| chr9:128633445 | G | T | 1 | a0002c0004t0002 | 10 | HG02040.hp2 HG03669.hp2 HG03688.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*111G>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 57/57 | 111 | chr9 | 128633445 | ||||||
| chr9:128633482 | C | T | 1 | a0001c0014t0003 | 2 | HG02559.hp1 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*148C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 57/57 | 148 | chr9 | 128633482 | ||||||
| chr9:128633483 | G | A | 1 | a0001c0018t0004 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*149G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 57/57 | 149 | chr9 | 128633483 | ||||||
| chr9:128633489 | G | A | 2 | a0001c0002t0005 a0001c0017t0006 |
2 | HG01109.hp2 HG03490.hp2 |
3_prime_UTR_variant | MODIFIER | c.*155G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 57/57 | 155 | chr9 | 128633489 | ||||||
| chr9:128633633 | A | G | 1 | a0001c0001t0007 | 1 | NA18960.hp1 | 3_prime_UTR_variant | MODIFIER | c.*299A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 57/57 | 299 | chr9 | 128633633 | ||||||
| chr9:128633658 | C | G | 1 | a0001c0017t0006 | 1 | HG01109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*324C>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 57/57 | 324 | chr9 | 128633658 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:128552743 | C | G | 4 | a0001c0002t0001g0307 a0001c0002t0001g0308 a0001c0002t0001g0309 others(1): Show |
4 | NA18948.hp1 NA18960.hp2 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.-4+47C>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128552743 | |||||||
| chr9:128552752 | C | G | 4 | a0001c0002t0001g0305 a0001c0002t0001g0306 a0001c0021t0001g0304 others(1): Show |
4 | HG02572.hp1 HG02717.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-4+56C>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128552752 | |||||||
| chr9:128552759 | G | C | 3 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0005 |
3 | NA18972.hp2 NA18977.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.-4+63G>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128552759 | |||||||
| chr9:128552821 | C | A | 1 | a0001c0009t0001g0006 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-4+125C>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128552821 | |||||||
| chr9:128552976 | C | T | 1 | a0001c0001t0001g0302 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-4+280C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128552976 | |||||||
| chr9:128553103 | G | A | 1 | a0001c0001t0001g0007 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-4+407G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128553103 | |||||||
| chr9:128553239 | C | T | 12 | a0001c0001t0001g0298 a0001c0006t0001g0290 a0001c0006t0001g0291 others(9): Show |
12 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.-4+543C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128553239 | |||||||
| chr9:128553291 | G | A | 6 | a0001c0002t0001g0012 a0001c0002t0001g0013 a0001c0007t0001g0009 others(3): Show |
6 | HG01884.hp1 HG02280.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.-4+595G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128553291 | |||||||
| chr9:128553320 | C | G | 1 | a0001c0002t0001g0289 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-4+624C>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128553320 | |||||||
| chr9:128553401 | ATAACT | A | 293 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(290): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.-4+709_-4+713delCT others(3): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128553401 | ||||||
| chr9:128553658 | A | G | 12 | a0001c0001t0001g0298 a0001c0006t0001g0290 a0001c0006t0001g0291 others(9): Show |
12 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.-4+962A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128553658 | |||||||
| chr9:128553787 | C | G | 3 | a0001c0001t0001g0286 a0001c0001t0001g0287 a0001c0001t0001g0288 |
3 | HG00280.hp1 HG01515.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.-4+1091C>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128553787 | |||||||
| chr9:128553805 | C | T | 1 | a0001c0030t0001g0285 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-4+1109C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128553805 | |||||||
| chr9:128553847 | G | A | 1 | a0001c0017t0006g0014 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-4+1151G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128553847 | |||||||
| chr9:128553878 | G | A | 1 | a0001c0001t0001g0029 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-4+1182G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128553878 | |||||||
| chr9:128553962 | A | G | 4 | a0001c0001t0001g0298 a0001c0010t0001g0299 a0001c0010t0001g0300 others(1): Show |
4 | HG02615.hp1 HG02809.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.-4+1266A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128553962 | |||||||
| chr9:128554002 | G | A | 6 | a0001c0002t0001g0012 a0001c0002t0001g0013 a0001c0007t0001g0009 others(3): Show |
6 | HG01884.hp1 HG02280.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.-4+1306G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128554002 | |||||||
| chr9:128554004 | C | A | 1 | a0001c0003t0001g0030 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-4+1308C>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128554004 | |||||||
| chr9:128554107 | A | G | 1 | a0001c0001t0001g0284 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-4+1411A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128554107 | |||||||
| chr9:128554338 | A | G | 11 | a0002c0004t0001g0278 a0002c0004t0002g0273 a0002c0004t0002g0274 others(8): Show |
11 | HG02040.hp2 HG03669.hp2 HG03688.hp1 others(8): Show |
intron_variant | MODIFIER | c.-4+1642A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128554338 | |||||||
| chr9:128554453 | C | A | 4 | a0001c0001t0001g0298 a0001c0010t0001g0299 a0001c0010t0001g0300 others(1): Show |
4 | HG02615.hp1 HG02809.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.-4+1757C>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128554453 | |||||||
| chr9:128554586 | A | C | 1 | a0001c0007t0001g0002 | 2 | HG02615.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-4+1890A>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128554586 | |||||||
| chr9:128554597 | C | G | 1 | a0001c0007t0001g0272 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-4+1901C>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128554597 | |||||||
| chr9:128554668 | G | A | 1 | a0001c0003t0001g0031 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-4+1972G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128554668 | |||||||
| chr9:128554768 | C | T | 2 | a0001c0002t0001g0012 a0001c0002t0001g0013 |
2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-4+2072C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128554768 | |||||||
| chr9:128555054 | T | C | 1 | a0005c0020t0001g0008 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-4+2358T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128555054 | |||||||
| chr9:128555076 | G | A | 5 | a0001c0005t0001g0015 a0001c0005t0001g0016 a0001c0005t0001g0017 others(2): Show |
5 | HG02055.hp2 HG02109.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.-4+2380G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128555076 | |||||||
| chr9:128555122 | C | G | 116 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0005 others(113): Show |
116 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.-4+2426C>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128555122 | |||||||
| chr9:128555583 | A | G | 7 | a0001c0007t0001g0272 a0001c0008t0001g0167 a0001c0008t0001g0168 others(4): Show |
7 | HG01099.hp2 HG01496.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.-4+2887A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128555583 | |||||||
| chr9:128555620 | CT | C | 114 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0005 others(111): Show |
114 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.-4+2947delT | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128555620 | ||||||
| chr9:128555620 | CTT | C | 7 | a0001c0002t0001g0174 a0001c0002t0001g0175 a0001c0002t0001g0176 others(4): Show |
7 | HG01256.hp2 HG02083.hp2 NA18951.hp2 others(4): Show |
intron_variant | MODIFIER | c.-4+2946_-4+2947del others(2): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128555620 | ||||||
| chr9:128555621 | T | TTCC | 10 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0159 others(7): Show |
10 | HG02135.hp1 HG02300.hp2 HG04204.hp1 others(7): Show |
intron_variant | MODIFIER | c.-4+2926_-4+2927ins others(3): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128555621 | ||||||
| chr9:128555622 | T | TC | 37 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(34): Show |
37 | HG00099.hp2 HG01099.hp2 HG01167.hp1 others(34): Show |
intron_variant | MODIFIER | c.-4+2926_-4+2927ins others(1): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128555622 | |||||||
| chr9:128555622 | T | TCC | 120 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0048 others(117): Show |
122 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(119): Show |
intron_variant | MODIFIER | c.-4+2926_-4+2927ins others(2): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128555622 | |||||||
| chr9:128555623 | T | C | 51 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(48): Show |
51 | HG00099.hp2 HG01069.hp1 HG01099.hp2 others(48): Show |
intron_variant | MODIFIER | c.-4+2927T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128555623 | |||||||
| chr9:128555624 | T | C | 123 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0005 others(120): Show |
123 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.-4+2928T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128555624 | |||||||
| chr9:128555625 | T | C | 116 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0005 others(113): Show |
116 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.-4+2929T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128555625 | |||||||
| chr9:128555626 | T | C | 7 | a0001c0002t0001g0174 a0001c0002t0001g0175 a0001c0002t0001g0176 others(4): Show |
7 | HG01256.hp2 HG02083.hp2 NA18951.hp2 others(4): Show |
intron_variant | MODIFIER | c.-4+2930T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128555626 | |||||||
| chr9:128555792 | G | A | 295 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(292): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.-4+3096G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128555792 | |||||||
| chr9:128556039 | G | C | 2 | a0001c0014t0003g0020 a0001c0014t0003g0021 |
2 | HG02559.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-4+3343G>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128556039 | |||||||
| chr9:128556057 | T | C | 1 | a0001c0001t0001g0048 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.-4+3361T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128556057 | |||||||
| chr9:128556286 | G | A | 1 | a0001c0001t0001g0049 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-4+3590G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128556286 | |||||||
| chr9:128556288 | C | T | 8 | a0002c0004t0001g0278 a0002c0004t0002g0276 a0002c0004t0002g0277 others(5): Show |
8 | HG02040.hp2 NA18949.hp1 NA18968.hp1 others(5): Show |
intron_variant | MODIFIER | c.-4+3592C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128556288 | |||||||
| chr9:128556299 | C | CA | 4 | a0001c0001t0001g0034 a0001c0001t0001g0052 a0001c0001t0001g0053 others(1): Show |
4 | HG02074.hp2 NA18984.hp1 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.-4+3604dupA | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128556299 | ||||||
| chr9:128556300 | AC | A | 3 | a0001c0001t0001g0051 a0001c0002t0001g0179 a0001c0002t0001g0180 |
3 | NA18957.hp2 NA18982.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.-4+3605delC | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128556300 | |||||||
| chr9:128556301 | C | A | 288 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(285): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.-4+3605C>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128556301 | |||||||
| chr9:128556341 | A | G | 1 | a0001c0001t0001g0049 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-4+3645A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128556341 | |||||||
| chr9:128556570 | A | T | 1 | a0001c0001t0001g0156 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.-4+3874A>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128556570 | |||||||
| chr9:128556894 | A | G | 4 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(1): Show |
4 | NA18969.hp1 NA18974.hp1 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.-4+4198A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128556894 | |||||||
| chr9:128556923 | G | A | 4 | a0001c0001t0001g0298 a0001c0010t0001g0299 a0001c0010t0001g0300 others(1): Show |
4 | HG02615.hp1 HG02809.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.-4+4227G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128556923 | |||||||
| chr9:128557133 | A | T | 1 | a0001c0001t0001g0151 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-4+4437A>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128557133 | |||||||
| chr9:128557268 | G | A | 291 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(288): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.-4+4572G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128557268 | |||||||
| chr9:128557318 | A | G | 9 | a0002c0004t0001g0278 a0002c0004t0002g0275 a0002c0004t0002g0276 others(6): Show |
9 | HG02040.hp2 NA18949.hp1 NA18968.hp1 others(6): Show |
intron_variant | MODIFIER | c.-4+4622A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128557318 | |||||||
| chr9:128557366 | A | G | 9 | a0002c0004t0001g0278 a0002c0004t0002g0275 a0002c0004t0002g0276 others(6): Show |
9 | HG02040.hp2 NA18949.hp1 NA18968.hp1 others(6): Show |
intron_variant | MODIFIER | c.-4+4670A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128557366 | |||||||
| chr9:128557588 | C | CCCCCAAA others(23): Show |
1 | a0001c0001t0001g0166 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-4+4901_-4+4930dup others(30): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128557588 | ||||||
| chr9:128557660 | G | A | 291 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(288): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.-4+4964G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128557660 | |||||||
| chr9:128557711 | A | G | 3 | a0001c0002t0001g0267 a0001c0002t0001g0268 a0001c0002t0001g0269 |
3 | HG01884.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-4+5015A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128557711 | |||||||
| chr9:128557798 | TC | T | 3 | a0001c0010t0001g0299 a0001c0010t0001g0300 a0001c0010t0001g0301 |
3 | HG02615.hp1 HG02809.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-4+5103delC | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128557798 | |||||||
| chr9:128557799 | C | CT | 8 | a0001c0002t0001g0032 a0001c0002t0001g0033 a0001c0002t0001g0174 others(5): Show |
8 | HG02109.hp1 HG03669.hp2 NA19000.hp1 others(5): Show |
intron_variant | MODIFIER | c.-4+5125dupT | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128557799 | ||||||
| chr9:128557799 | C | T | 1 | a0001c0001t0001g0298 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-4+5103C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128557799 | |||||||
| chr9:128557799 | CT | C | 87 | a0001c0001t0001g0057 a0001c0001t0001g0059 a0001c0001t0001g0070 others(84): Show |
87 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.-4+5125delT | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128557799 | ||||||
| chr9:128557799 | CTT | C | 138 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(135): Show |
139 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(136): Show |
intron_variant | MODIFIER | c.-4+5124_-4+5125del others(2): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128557799 | ||||||
| chr9:128557961 | G | A | 1 | a0001c0001t0001g0055 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-4+5265G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128557961 | |||||||
| chr9:128558005 | G | A | 1 | a0001c0001t0001g0055 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-4+5309G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128558005 | |||||||
| chr9:128558093 | G | A | 1 | a0001c0001t0001g0056 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-4+5397G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128558093 | |||||||
| chr9:128558094 | C | T | 2 | a0001c0001t0001g0149 a0001c0001t0001g0150 |
2 | HG01891.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-4+5398C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128558094 | |||||||
| chr9:128558100 | G | A | 2 | a0001c0002t0001g0032 a0001c0002t0001g0033 |
2 | NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-4+5404G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128558100 | |||||||
| chr9:128558174 | T | C | 1 | a0001c0007t0001g0272 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-4+5478T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128558174 | |||||||
| chr9:128558260 | C | G | 121 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0005 others(118): Show |
122 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.-4+5564C>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128558260 | |||||||
| chr9:128558326 | C | T | 1 | a0001c0016t0001g0026 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-4+5630C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128558326 | |||||||
| chr9:128558530 | G | C | 1 | a0001c0001t0001g0057 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-4+5834G>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128558530 | |||||||
| chr9:128558632 | T | C | 3 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0060 |
3 | HG02145.hp1 HG02886.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-4+5936T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128558632 | |||||||
| chr9:128558639 | T | C | 114 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0005 others(111): Show |
114 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.-4+5943T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128558639 | |||||||
| chr9:128558761 | C | T | 293 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(290): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.-4+6065C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128558761 | |||||||
| chr9:128558792 | C | T | 293 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(290): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.-4+6096C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128558792 | |||||||
| chr9:128558888 | C | T | 1 | a0001c0002t0001g0266 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-4+6192C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128558888 | |||||||
| chr9:128558933 | A | C | 1 | a0001c0005t0001g0025 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-4+6237A>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128558933 | |||||||
| chr9:128558997 | T | C | 29 | a0001c0001t0001g0035 a0001c0001t0001g0052 a0001c0001t0001g0061 others(26): Show |
29 | HG00408.hp2 HG00438.hp2 HG00621.hp2 others(26): Show |
intron_variant | MODIFIER | c.-4+6301T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128558997 | |||||||
| chr9:128559022 | G | A | 293 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(290): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.-4+6326G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128559022 | |||||||
| chr9:128559141 | C | A | 1 | a0001c0002t0001g0266 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-4+6445C>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128559141 | |||||||
| chr9:128559221 | G | A | 1 | a0001c0001t0001g0061 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-4+6525G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128559221 | |||||||
| chr9:128559500 | G | A | 2 | a0001c0001t0001g0079 a0001c0002t0005g0181 |
2 | HG01433.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.-4+6804G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128559500 | |||||||
| chr9:128559626 | C | T | 1 | a0001c0002t0001g0265 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-4+6930C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128559626 | |||||||
| chr9:128559735 | A | AT | 22 | a0001c0001t0001g0035 a0001c0001t0001g0055 a0001c0001t0001g0057 others(19): Show |
22 | HG00140.hp2 HG00621.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.-3-6989dupT | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128559735 | ||||||
| chr9:128559798 | G | A | 31 | a0001c0001t0001g0007 a0001c0001t0001g0036 a0001c0001t0001g0037 others(28): Show |
31 | HG00140.hp1 HG00280.hp1 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.-3-6940G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128559798 | |||||||
| chr9:128559838 | G | A | 1 | a0001c0001t0001g0094 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-3-6900G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128559838 | |||||||
| chr9:128559884 | G | A | 1 | a0001c0025t0001g0182 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-3-6854G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128559884 | |||||||
| chr9:128560029 | C | G | 2 | a0001c0001t0001g0046 a0001c0001t0001g0145 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-3-6709C>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128560029 | |||||||
| chr9:128560084 | C | CTT | 14 | a0001c0001t0001g0039 a0001c0001t0001g0080 a0001c0003t0001g0095 others(11): Show |
15 | HG02040.hp2 HG02615.hp2 HG02683.hp2 others(12): Show |
intron_variant | MODIFIER | c.-3-6640_-3-6639dup others(2): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128560084 | ||||||
| chr9:128560084 | C | CTTT | 163 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(160): Show |
164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.-3-6641_-3-6639dup others(3): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128560084 | ||||||
| chr9:128560084 | C | CTTTT | 103 | a0001c0001t0001g0045 a0001c0001t0001g0166 a0001c0001t0001g0284 others(100): Show |
103 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.-3-6642_-3-6639dup others(4): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128560084 | ||||||
| chr9:128560084 | C | CTTTTT | 12 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0005 others(9): Show |
12 | HG02055.hp1 HG02109.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.-3-6643_-3-6639dup others(5): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128560084 | ||||||
| chr9:128560107 | A | T | 2 | a0001c0001t0001g0071 a0001c0001t0001g0078 |
2 | NA18947.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.-3-6631A>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128560107 | |||||||
| chr9:128560145 | G | A | 5 | a0001c0002t0001g0032 a0001c0002t0001g0033 a0001c0002t0001g0186 others(2): Show |
5 | HG00642.hp1 HG01256.hp2 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.-3-6593G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128560145 | |||||||
| chr9:128560169 | A | G | 293 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(290): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.-3-6569A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128560169 | |||||||
| chr9:128560228 | C | T | 1 | a0001c0001t0001g0144 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-3-6510C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128560228 | |||||||
| chr9:128560233 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-3-6505G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128560233 | |||||||
| chr9:128560368 | G | A | 1 | a0001c0007t0001g0272 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-3-6370G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128560368 | |||||||
| chr9:128560373 | C | T | 6 | a0001c0008t0001g0167 a0001c0008t0001g0168 a0001c0008t0001g0169 others(3): Show |
6 | HG01099.hp2 HG01496.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.-3-6365C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128560373 | |||||||
| chr9:128560382 | C | CT | 16 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0093 others(13): Show |
16 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(13): Show |
intron_variant | MODIFIER | c.-3-6340dupT | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128560382 | ||||||
| chr9:128560466 | C | T | 1 | a0001c0002t0005g0181 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-3-6272C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128560466 | |||||||
| chr9:128560474 | A | G | 293 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(290): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.-3-6264A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128560474 | |||||||
| chr9:128560495 | C | T | 113 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0005 others(110): Show |
113 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.-3-6243C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128560495 | |||||||
| chr9:128560632 | C | CG | 293 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(290): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.-3-6105dupG | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128560632 | ||||||
| chr9:128560675 | T | A | 1 | a0001c0002t0001g0187 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-3-6063T>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128560675 | |||||||
| chr9:128560999 | G | C | 113 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0005 others(110): Show |
113 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.-3-5739G>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128560999 | |||||||
| chr9:128561015 | C | CA | 114 | a0001c0001t0001g0080 a0001c0001t0001g0286 a0001c0002t0001g0003 others(111): Show |
114 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.-3-5703dupA | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128561015 | ||||||
| chr9:128561015 | C | CAA | 139 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(136): Show |
141 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.-3-5704_-3-5703dup others(2): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128561015 | ||||||
| chr9:128561015 | CA | C | 7 | a0001c0001t0001g0298 a0001c0005t0001g0017 a0001c0005t0001g0018 others(4): Show |
7 | HG02055.hp2 HG02109.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.-3-5703delA | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128561015 | ||||||
| chr9:128561033 | A | AAG | 6 | a0001c0008t0001g0167 a0001c0008t0001g0168 a0001c0008t0001g0169 others(3): Show |
6 | HG01099.hp2 HG01496.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.-3-5704_-3-5703ins others(2): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128561033 | ||||||
| chr9:128561096 | A | G | 9 | a0002c0004t0001g0278 a0002c0004t0002g0275 a0002c0004t0002g0276 others(6): Show |
9 | HG02040.hp2 NA18949.hp1 NA18968.hp1 others(6): Show |
intron_variant | MODIFIER | c.-3-5642A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128561096 | |||||||
| chr9:128561110 | C | T | 1 | a0001c0003t0001g0140 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.-3-5628C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128561110 | |||||||
| chr9:128561144 | C | T | 9 | a0002c0004t0001g0278 a0002c0004t0002g0275 a0002c0004t0002g0276 others(6): Show |
9 | HG02040.hp2 NA18949.hp1 NA18968.hp1 others(6): Show |
intron_variant | MODIFIER | c.-3-5594C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128561144 | |||||||
| chr9:128561145 | G | A | 1 | a0001c0014t0003g0021 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-3-5593G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128561145 | |||||||
| chr9:128561278 | C | G | 2 | a0001c0001t0001g0039 a0001c0001t0001g0057 |
2 | HG02572.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.-3-5460C>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128561278 | |||||||
| chr9:128561278 | C | T | 1 | a0002c0004t0002g0274 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-3-5460C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128561278 | |||||||
| chr9:128561313 | A | G | 4 | a0001c0001t0001g0298 a0001c0010t0001g0299 a0001c0010t0001g0300 others(1): Show |
4 | HG02615.hp1 HG02809.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.-3-5425A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128561313 | |||||||
| chr9:128561391 | C | T | 2 | a0001c0001t0001g0068 a0001c0001t0001g0159 |
2 | NA18941.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.-3-5347C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128561391 | |||||||
| chr9:128561430 | G | A | 1 | a0001c0001t0001g0048 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.-3-5308G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128561430 | |||||||
| chr9:128561466 | A | G | 1 | a0001c0002t0001g0306 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.-3-5272A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128561466 | |||||||
| chr9:128561587 | G | T | 286 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(283): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.-3-5151G>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128561587 | |||||||
| chr9:128561611 | C | T | 1 | a0001c0001t0001g0044 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-3-5127C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128561611 | |||||||
| chr9:128561620 | A | G | 299 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(296): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.-3-5118A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128561620 | |||||||
| chr9:128561662 | C | CA | 18 | a0001c0001t0001g0091 a0001c0001t0001g0136 a0001c0001t0001g0286 others(15): Show |
18 | HG00280.hp1 HG01515.hp2 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.-3-5050dupA | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128561662 | ||||||
| chr9:128561662 | C | CAA | 7 | a0001c0001t0001g0057 a0001c0001t0001g0135 a0001c0007t0001g0002 others(4): Show |
8 | HG02572.hp2 HG02615.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.-3-5051_-3-5050dup others(2): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128561662 | ||||||
| chr9:128561662 | C | CAAA | 8 | a0001c0001t0001g0038 a0001c0001t0001g0090 a0001c0001t0001g0156 others(5): Show |
8 | HG01934.hp1 HG03139.hp2 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.-3-5052_-3-5050dup others(3): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128561662 | ||||||
| chr9:128561662 | C | CAAAA | 63 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0175 others(60): Show |
63 | HG00280.hp2 HG00558.hp2 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.-3-5053_-3-5050dup others(4): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128561662 | ||||||
| chr9:128561662 | C | CAAAAA | 32 | a0001c0002t0001g0005 a0001c0002t0001g0174 a0001c0002t0001g0179 others(29): Show |
32 | HG00423.hp2 HG00438.hp1 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.-3-5054_-3-5050dup others(5): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128561662 | ||||||
| chr9:128561662 | C | CAAAAAA | 12 | a0001c0001t0001g0146 a0001c0002t0001g0191 a0001c0002t0001g0192 others(9): Show |
12 | HG02055.hp1 HG02486.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.-3-5055_-3-5050dup others(6): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128561662 | ||||||
| chr9:128561662 | C | CAAAAAAA | 7 | a0001c0001t0001g0159 a0001c0002t0001g0258 a0001c0002t0001g0259 others(4): Show |
7 | HG01099.hp2 HG02109.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.-3-5056_-3-5050dup others(7): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128561662 | ||||||
| chr9:128561662 | C | CAAAAAAA others(4): Show |
1 | a0001c0001t0001g0080 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-3-5060_-3-5050dup others(11): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128561662 | ||||||
| chr9:128561662 | C | CAAAAAAA others(5): Show |
4 | a0001c0001t0001g0046 a0001c0001t0001g0145 a0001c0003t0001g0134 others(1): Show |
4 | HG02083.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-3-5061_-3-5050dup others(12): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128561662 | ||||||
| chr9:128561662 | C | CAAAAAAA others(6): Show |
21 | a0001c0001t0001g0007 a0001c0001t0001g0035 a0001c0001t0001g0037 others(18): Show |
21 | HG00140.hp1 HG00621.hp1 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.-3-5062_-3-5050dup others(13): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128561662 | ||||||
| chr9:128561662 | C | CAAAAAAA others(7): Show |
35 | a0001c0001t0001g0029 a0001c0001t0001g0034 a0001c0001t0001g0036 others(32): Show |
35 | HG00408.hp2 HG00621.hp2 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.-3-5063_-3-5050dup others(14): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128561662 | ||||||
| chr9:128561662 | C | CAAAAAAA others(8): Show |
23 | a0001c0001t0001g0049 a0001c0001t0001g0053 a0001c0001t0001g0056 others(20): Show |
24 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(21): Show |
intron_variant | MODIFIER | c.-3-5064_-3-5050dup others(15): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128561662 | ||||||
| chr9:128561662 | C | CAAAAAAA others(9): Show |
8 | a0001c0001t0001g0055 a0001c0001t0001g0082 a0001c0001t0001g0114 others(5): Show |
8 | HG01123.hp2 HG02738.hp1 HG03834.hp1 others(5): Show |
intron_variant | MODIFIER | c.-3-5065_-3-5050dup others(16): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128561662 | ||||||
| chr9:128561662 | C | CAAAAAAA others(10): Show |
6 | a0001c0001t0001g0081 a0001c0001t0001g0113 a0001c0001t0001g0149 others(3): Show |
6 | HG01496.hp1 HG01891.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.-3-5066_-3-5050dup others(17): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128561662 | ||||||
| chr9:128561662 | C | CAAAAAAA others(11): Show |
4 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0112 others(1): Show |
4 | HG02135.hp1 HG03654.hp2 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.-3-5067_-3-5050dup others(18): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128561662 | ||||||
| chr9:128561662 | C | CAAAAAAA others(12): Show |
5 | a0001c0001t0001g0039 a0001c0001t0001g0041 a0001c0001t0001g0071 others(2): Show |
5 | HG02809.hp2 HG02818.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3-5068_-3-5050dup others(19): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128561662 | ||||||
| chr9:128561662 | C | CAAAAAAA others(13): Show |
9 | a0001c0001t0001g0040 a0001c0001t0001g0101 a0001c0001t0001g0102 others(6): Show |
9 | HG01981.hp2 HG02258.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.-3-5069_-3-5050dup others(20): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128561662 | ||||||
| chr9:128561662 | C | CAAAAAAA others(14): Show |
2 | a0001c0001t0001g0072 a0001c0001t0001g0142 |
2 | NA18955.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.-3-5070_-3-5050dup others(21): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128561662 | ||||||
| chr9:128561662 | C | CAAAAAAA others(15): Show |
5 | a0001c0001t0001g0048 a0001c0001t0001g0099 a0001c0001t0001g0100 others(2): Show |
5 | HG00558.hp1 HG00597.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.-3-5071_-3-5050dup others(22): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128561662 | ||||||
| chr9:128561662 | C | CAAAAAAA others(16): Show |
1 | a0001c0001t0001g0096 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-3-5072_-3-5050dup others(23): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128561662 | ||||||
| chr9:128561662 | C | CAAAAAAA others(18): Show |
1 | a0001c0001t0001g0162 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-3-5074_-3-5050dup others(25): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128561662 | ||||||
| chr9:128561662 | C | CAAAAAAA others(24): Show |
1 | a0001c0001t0001g0097 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-3-5050_-3-5049ins others(31): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128561662 | ||||||
| chr9:128561662 | CAA | C | 6 | a0001c0001t0001g0045 a0001c0001t0001g0139 a0001c0001t0001g0302 others(3): Show |
6 | HG02071.hp2 HG02559.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.-3-5051_-3-5050del others(2): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128561662 | ||||||
| chr9:128561686 | A | G | 1 | a0001c0007t0001g0010 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-3-5052A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128561686 | |||||||
| chr9:128561689 | G | A | 1 | a0001c0001t0001g0080 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-3-5049G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128561689 | |||||||
| chr9:128561789 | A | G | 1 | a0001c0007t0001g0272 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-3-4949A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128561789 | |||||||
| chr9:128561961 | T | C | 6 | a0001c0008t0001g0167 a0001c0008t0001g0168 a0001c0008t0001g0169 others(3): Show |
6 | HG01099.hp2 HG01496.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.-3-4777T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128561961 | |||||||
| chr9:128561995 | C | T | 9 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0068 others(6): Show |
9 | HG00408.hp2 NA18941.hp2 NA18942.hp2 others(6): Show |
intron_variant | MODIFIER | c.-3-4743C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128561995 | |||||||
| chr9:128562028 | A | G | 293 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(290): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.-3-4710A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128562028 | |||||||
| chr9:128562132 | T | A | 148 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(145): Show |
149 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(146): Show |
intron_variant | MODIFIER | c.-3-4606T>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128562132 | |||||||
| chr9:128562163 | C | T | 12 | a0001c0001t0001g0298 a0001c0006t0001g0290 a0001c0006t0001g0291 others(9): Show |
12 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.-3-4575C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128562163 | |||||||
| chr9:128562215 | G | C | 1 | a0001c0002t0001g0306 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.-3-4523G>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128562215 | |||||||
| chr9:128562283 | A | G | 6 | a0001c0008t0001g0167 a0001c0008t0001g0168 a0001c0008t0001g0169 others(3): Show |
6 | HG01099.hp2 HG01496.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.-3-4455A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128562283 | |||||||
| chr9:128562541 | C | T | 171 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(168): Show |
172 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): Show |
intron_variant | MODIFIER | c.-3-4197C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128562541 | |||||||
| chr9:128562708 | A | ATAT | 291 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(288): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.-3-4027_-3-4025dup others(3): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128562708 | ||||||
| chr9:128562774 | C | T | 293 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(290): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.-3-3964C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128562774 | |||||||
| chr9:128562780 | C | A | 2 | a0001c0001t0001g0157 a0001c0001t0001g0158 |
2 | NA19012.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.-3-3958C>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128562780 | |||||||
| chr9:128562788 | C | A | 2 | a0001c0002t0001g0032 a0001c0002t0001g0033 |
2 | NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-3-3950C>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128562788 | |||||||
| chr9:128562789 | G | C | 6 | a0001c0008t0001g0167 a0001c0008t0001g0168 a0001c0008t0001g0169 others(3): Show |
6 | HG01099.hp2 HG01496.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.-3-3949G>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128562789 | |||||||
| chr9:128562822 | G | T | 2 | a0001c0002t0001g0032 a0001c0002t0001g0033 |
2 | NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-3-3916G>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128562822 | |||||||
| chr9:128562887 | C | T | 293 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(290): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.-3-3851C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128562887 | |||||||
| chr9:128562943 | C | T | 12 | a0001c0001t0001g0298 a0001c0006t0001g0290 a0001c0006t0001g0291 others(9): Show |
12 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.-3-3795C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128562943 | |||||||
| chr9:128562969 | AAAATATA others(17): Show |
A | 20 | a0001c0002t0001g0183 a0001c0002t0001g0257 a0001c0002t0001g0258 others(17): Show |
20 | HG02040.hp2 HG02055.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.-3-3767_-3-3744del others(24): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128562969 | ||||||
| chr9:128562969 | AAAATATA others(19): Show |
A | 113 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0005 others(110): Show |
114 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.-3-3767_-3-3742del others(26): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128562969 | ||||||
| chr9:128562970 | AAATATAT others(15): Show |
A | 5 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0003t0001g0133 others(2): Show |
5 | HG00408.hp1 HG00609.hp2 HG00621.hp1 others(2): Show |
intron_variant | MODIFIER | c.-3-3767_-3-3746del others(22): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128562970 | |||||||
| chr9:128562971 | A | T | 137 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(134): Show |
138 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(135): Show |
intron_variant | MODIFIER | c.-3-3767A>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128562971 | |||||||
| chr9:128562971 | AATATATA others(12): Show |
A | 1 | a0001c0001t0001g0159 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.-3-3766_-3-3748del others(19): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128562971 | |||||||
| chr9:128562974 | ATATATAT others(11): Show |
A | 1 | a0001c0001t0001g0114 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.-3-3755_-3-3738del others(18): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128562974 | ||||||
| chr9:128562983 | CATGTATG others(3): Show |
C | 2 | a0001c0001t0001g0128 a0001c0001t0001g0131 |
2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.-3-3752_-3-3743del others(10): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128562983 | ||||||
| chr9:128562983 | CATGTATG others(5): Show |
C | 1 | a0001c0001t0001g0043 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-3-3752_-3-3741del others(12): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128562983 | ||||||
| chr9:128562983 | CATGTATG others(7): Show |
C | 13 | a0001c0001t0001g0036 a0001c0001t0001g0051 a0001c0001t0001g0083 others(10): Show |
13 | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(10): Show |
intron_variant | MODIFIER | c.-3-3752_-3-3739del others(14): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128562983 | ||||||
| chr9:128562983 | CATGTATG others(9): Show |
C | 17 | a0001c0001t0001g0037 a0001c0001t0001g0048 a0001c0001t0001g0055 others(14): Show |
17 | HG00140.hp2 HG00642.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.-3-3752_-3-3737del others(16): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128562983 | ||||||
| chr9:128562983 | CATGTATG others(11): Show |
C | 71 | a0001c0001t0001g0007 a0001c0001t0001g0034 a0001c0001t0001g0035 others(68): Show |
71 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(68): Show |
intron_variant | MODIFIER | c.-3-3752_-3-3735del others(18): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128562983 | ||||||
| chr9:128562983 | CATGTATG others(13): Show |
C | 31 | a0001c0001t0001g0029 a0001c0001t0001g0044 a0001c0001t0001g0046 others(28): Show |
32 | HG00735.hp2 HG01257.hp2 HG01258.hp2 others(29): Show |
intron_variant | MODIFIER | c.-3-3752_-3-3733del others(20): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128562983 | ||||||
| chr9:128562983 | CATGTATG others(15): Show |
C | 6 | a0001c0008t0001g0167 a0001c0008t0001g0168 a0001c0008t0001g0169 others(3): Show |
6 | HG01099.hp2 HG01496.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.-3-3752_-3-3731del others(22): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128562983 | ||||||
| chr9:128562983 | CATGTATG others(19): Show |
C | 12 | a0001c0001t0001g0298 a0001c0006t0001g0290 a0001c0006t0001g0291 others(9): Show |
12 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.-3-3752_-3-3727del others(26): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128562983 | ||||||
| chr9:128562990 | G | GTATATAT others(3): Show |
1 | a0001c0014t0003g0021 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-3-3747_-3-3746ins others(10): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128562990 | ||||||
| chr9:128562990 | G | GTATATAT others(9): Show |
1 | a0001c0014t0003g0020 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-3-3747_-3-3746ins others(16): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128562990 | ||||||
| chr9:128562990 | GTGTATAT others(3): Show |
G | 1 | a0001c0016t0001g0026 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-3-3746_-3-3737del others(10): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128562990 | ||||||
| chr9:128562992 | G | A | 6 | a0001c0001t0001g0159 a0001c0009t0001g0006 a0001c0009t0001g0027 others(3): Show |
6 | HG01891.hp2 HG02559.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.-3-3746G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128562992 | |||||||
| chr9:128562992 | G | GTATGTAT others(11): Show |
3 | a0001c0005t0001g0015 a0001c0005t0001g0016 a0001c0005t0001g0018 |
3 | HG02723.hp1 HG02886.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-3-3743_-3-3742ins others(18): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128562992 | ||||||
| chr9:128562992 | G | GTATGTAT others(13): Show |
1 | a0001c0005t0001g0017 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-3-3743_-3-3742ins others(20): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128562992 | ||||||
| chr9:128562992 | G | GTATGTAT others(17): Show |
1 | a0001c0005t0001g0019 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-3-3743_-3-3742ins others(24): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128562992 | ||||||
| chr9:128563002 | A | G | 1 | a0001c0017t0006g0014 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-3-3736A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128563002 | |||||||
| chr9:128563003 | T | C | 1 | a0001c0001t0001g0159 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.-3-3735T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128563003 | |||||||
| chr9:128563004 | A | G | 1 | a0001c0002t0001g0180 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-3-3734A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128563004 | |||||||
| chr9:128563005 | T | C | 5 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0003t0001g0133 others(2): Show |
5 | HG00408.hp1 HG00609.hp2 HG00621.hp1 others(2): Show |
intron_variant | MODIFIER | c.-3-3733T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128563005 | |||||||
| chr9:128563007 | T | C | 20 | a0001c0002t0001g0183 a0001c0002t0001g0257 a0001c0002t0001g0258 others(17): Show |
20 | HG02040.hp2 HG02055.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.-3-3731T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128563007 | |||||||
| chr9:128563009 | T | C | 113 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0005 others(110): Show |
114 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.-3-3729T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128563009 | |||||||
| chr9:128563024 | A | G | 5 | a0001c0005t0001g0015 a0001c0005t0001g0016 a0001c0005t0001g0017 others(2): Show |
5 | HG02055.hp2 HG02109.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.-3-3714A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128563024 | |||||||
| chr9:128563028 | G | A | 1 | a0001c0016t0001g0026 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-3-3710G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128563028 | |||||||
| chr9:128563239 | A | T | 1 | a0001c0001t0001g0093 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-3-3499A>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128563239 | |||||||
| chr9:128563240 | A | T | 1 | a0001c0001t0001g0093 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-3-3498A>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128563240 | |||||||
| chr9:128563241 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-3-3497C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128563241 | |||||||
| chr9:128563244 | C | G | 1 | a0001c0001t0001g0093 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-3-3494C>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128563244 | |||||||
| chr9:128563245 | A | C | 1 | a0001c0001t0001g0093 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-3-3493A>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128563245 | |||||||
| chr9:128563247 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-3-3491C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128563247 | |||||||
| chr9:128563249 | G | C | 1 | a0001c0001t0001g0093 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-3-3489G>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128563249 | |||||||
| chr9:128563251 | A | G | 1 | a0001c0001t0001g0093 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-3-3487A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128563251 | |||||||
| chr9:128563254 | A | G | 1 | a0001c0001t0001g0093 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-3-3484A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128563254 | |||||||
| chr9:128563256 | A | C | 1 | a0001c0001t0001g0093 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-3-3482A>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128563256 | |||||||
| chr9:128563257 | A | T | 1 | a0001c0001t0001g0093 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-3-3481A>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128563257 | |||||||
| chr9:128563258 | A | C | 1 | a0001c0001t0001g0093 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-3-3480A>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128563258 | |||||||
| chr9:128563260 | A | G | 4 | a0001c0007t0001g0002 a0001c0007t0001g0009 a0001c0007t0001g0010 others(1): Show |
5 | HG01884.hp1 HG02280.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3-3478A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128563260 | |||||||
| chr9:128563262 | A | T | 1 | a0001c0001t0001g0093 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-3-3476A>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128563262 | |||||||
| chr9:128563264 | A | T | 1 | a0001c0001t0001g0093 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-3-3474A>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128563264 | |||||||
| chr9:128563265 | A | C | 1 | a0001c0001t0001g0093 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-3-3473A>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128563265 | |||||||
| chr9:128563271 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-3-3467C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128563271 | |||||||
| chr9:128563275 | G | C | 1 | a0001c0001t0001g0093 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-3-3463G>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128563275 | |||||||
| chr9:128563277 | G | T | 1 | a0001c0001t0001g0093 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-3-3461G>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128563277 | |||||||
| chr9:128563279 | G | T | 1 | a0001c0001t0001g0093 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-3-3459G>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128563279 | |||||||
| chr9:128563280 | C | A | 1 | a0001c0001t0001g0093 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-3-3458C>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128563280 | |||||||
| chr9:128563282 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-3-3456G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128563282 | |||||||
| chr9:128563289 | G | T | 1 | a0001c0001t0001g0093 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-3-3449G>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128563289 | |||||||
| chr9:128563291 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-3-3447C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128563291 | |||||||
| chr9:128563293 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-3-3445G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128563293 | |||||||
| chr9:128563301 | A | T | 1 | a0001c0001t0001g0093 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-3-3437A>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128563301 | |||||||
| chr9:128563321 | C | T | 293 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(290): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.-3-3417C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128563321 | |||||||
| chr9:128563426 | C | A | 1 | a0001c0002t0001g0191 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-3-3312C>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128563426 | |||||||
| chr9:128563524 | T | C | 4 | a0001c0001t0001g0298 a0001c0010t0001g0299 a0001c0010t0001g0300 others(1): Show |
4 | HG02615.hp1 HG02809.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.-3-3214T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128563524 | |||||||
| chr9:128563587 | C | T | 1 | a0001c0001t0001g0132 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-3-3151C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128563587 | |||||||
| chr9:128563673 | C | T | 8 | a0001c0006t0001g0290 a0001c0006t0001g0291 a0001c0006t0001g0292 others(5): Show |
8 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.-3-3065C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128563673 | |||||||
| chr9:128563715 | C | CT | 13 | a0001c0002t0001g0210 a0001c0002t0001g0257 a0001c0005t0001g0025 others(10): Show |
13 | HG01891.hp2 HG02055.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.-3-3005dupT | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128563715 | ||||||
| chr9:128563715 | CT | C | 22 | a0001c0001t0001g0061 a0001c0001t0001g0145 a0001c0001t0001g0298 others(19): Show |
22 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.-3-3005delT | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128563715 | ||||||
| chr9:128563782 | T | C | 1 | a0001c0002t0001g0211 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-3-2956T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128563782 | |||||||
| chr9:128563957 | G | A | 299 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(296): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.-3-2781G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128563957 | |||||||
| chr9:128563994 | C | T | 14 | a0001c0001t0001g0298 a0001c0002t0001g0032 a0001c0002t0001g0033 others(11): Show |
14 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.-3-2744C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128563994 | |||||||
| chr9:128564159 | G | A | 2 | a0001c0001t0001g0149 a0001c0001t0001g0150 |
2 | HG01891.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-3-2579G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128564159 | |||||||
| chr9:128564163 | G | T | 114 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0005 others(111): Show |
114 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.-3-2575G>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128564163 | |||||||
| chr9:128564173 | C | T | 8 | a0001c0002t0001g0012 a0001c0002t0001g0013 a0001c0007t0001g0002 others(5): Show |
9 | HG01884.hp1 HG02280.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.-3-2565C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128564173 | |||||||
| chr9:128564247 | C | T | 1 | a0001c0007t0001g0272 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-3-2491C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128564247 | |||||||
| chr9:128564351 | A | G | 293 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(290): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.-3-2387A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128564351 | |||||||
| chr9:128564420 | GA | G | 9 | a0002c0004t0001g0278 a0002c0004t0002g0275 a0002c0004t0002g0276 others(6): Show |
9 | HG02040.hp2 NA18949.hp1 NA18968.hp1 others(6): Show |
intron_variant | MODIFIER | c.-3-2304delA | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128564420 | ||||||
| chr9:128564436 | T | C | 262 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(259): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.-3-2302T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128564436 | |||||||
| chr9:128564516 | G | A | 14 | a0001c0001t0001g0298 a0001c0002t0001g0032 a0001c0002t0001g0033 others(11): Show |
14 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.-3-2222G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128564516 | |||||||
| chr9:128564572 | C | T | 3 | a0001c0009t0001g0006 a0001c0009t0001g0027 a0001c0009t0001g0028 |
3 | HG01891.hp2 HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-3-2166C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128564572 | |||||||
| chr9:128564580 | C | CAAAT | 292 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(289): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.-3-2142_-3-2139dup others(4): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128564580 | ||||||
| chr9:128564930 | G | A | 4 | a0001c0002t0001g0195 a0001c0002t0001g0212 a0001c0002t0001g0213 others(1): Show |
4 | NA18968.hp2 NA18982.hp2 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.-3-1808G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128564930 | |||||||
| chr9:128564940 | T | G | 4 | a0001c0002t0001g0012 a0001c0002t0001g0013 a0001c0007t0001g0047 others(1): Show |
4 | HG02922.hp1 HG03139.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-3-1798T>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128564940 | |||||||
| chr9:128564968 | T | C | 1 | a0002c0004t0002g0277 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.-3-1770T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128564968 | |||||||
| chr9:128565189 | G | A | 2 | a0001c0002t0001g0032 a0001c0002t0001g0033 |
2 | NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-3-1549G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128565189 | |||||||
| chr9:128565286 | C | T | 1 | a0001c0001t0001g0043 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-3-1452C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128565286 | |||||||
| chr9:128565322 | A | G | 3 | a0001c0001t0001g0040 a0001c0014t0003g0020 a0001c0014t0003g0021 |
3 | HG02559.hp1 HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-3-1416A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128565322 | |||||||
| chr9:128565455 | T | C | 1 | a0001c0001t0001g0119 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-3-1283T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128565455 | |||||||
| chr9:128565703 | C | A | 112 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0005 others(109): Show |
112 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.-3-1035C>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128565703 | |||||||
| chr9:128565764 | A | G | 292 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(289): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.-3-974A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128565764 | |||||||
| chr9:128565810 | C | T | 2 | a0001c0002t0001g0032 a0001c0002t0001g0033 |
2 | NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-3-928C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128565810 | |||||||
| chr9:128566118 | G | A | 3 | a0001c0002t0001g0267 a0001c0002t0001g0268 a0001c0002t0001g0269 |
3 | HG01884.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-3-620G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128566118 | |||||||
| chr9:128566243 | A | C | 292 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(289): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.-3-495A>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128566243 | |||||||
| chr9:128566346 | G | A | 1 | a0001c0025t0001g0182 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-3-392G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128566346 | |||||||
| chr9:128566561 | C | T | 9 | a0002c0004t0001g0278 a0002c0004t0002g0275 a0002c0004t0002g0276 others(6): Show |
9 | HG02040.hp2 NA18949.hp1 NA18968.hp1 others(6): Show |
intron_variant | MODIFIER | c.-3-177C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128566561 | |||||||
| chr9:128566657 | T | C | 1 | a0001c0001t0001g0114 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.-3-81T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128566657 | |||||||
| chr9:128567123 | C | T | 2 | a0001c0002t0001g0032 a0001c0002t0001g0033 |
2 | NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.237+146C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 2/56 | chr9 | 128567123 | |||||||
| chr9:128567193 | G | A | 3 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0060 |
3 | HG02145.hp1 HG02886.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.237+216G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 2/56 | chr9 | 128567193 | |||||||
| chr9:128567312 | G | A | 293 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(290): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.237+335G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 2/56 | chr9 | 128567312 | |||||||
| chr9:128567401 | C | T | 8 | a0001c0006t0001g0290 a0001c0006t0001g0291 a0001c0006t0001g0292 others(5): Show |
8 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.237+424C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 2/56 | chr9 | 128567401 | |||||||
| chr9:128567411 | C | A | 2 | a0001c0002t0001g0032 a0001c0002t0001g0033 |
2 | NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.237+434C>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 2/56 | chr9 | 128567411 | |||||||
| chr9:128567432 | C | T | 1 | a0001c0026t0001g0209 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.237+455C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 2/56 | chr9 | 128567432 | |||||||
| chr9:128567804 | A | G | 149 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(146): Show |
150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
intron_variant | MODIFIER | c.237+827A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 2/56 | chr9 | 128567804 | |||||||
| chr9:128568065 | ACT | A | 4 | a0001c0007t0001g0002 a0001c0007t0001g0009 a0001c0007t0001g0010 others(1): Show |
5 | HG01884.hp1 HG02280.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.238-706_238-705del others(2): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 2/56 | chr9 | 128568065 | |||||||
| chr9:128568068 | T | A | 4 | a0001c0007t0001g0002 a0001c0007t0001g0009 a0001c0007t0001g0010 others(1): Show |
5 | HG01884.hp1 HG02280.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.238-704T>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 2/56 | chr9 | 128568068 | |||||||
| chr9:128568074 | A | G | 7 | a0001c0003t0001g0030 a0001c0003t0001g0095 a0001c0003t0001g0116 others(4): Show |
7 | HG01109.hp2 NA18948.hp2 NA18961.hp1 others(4): Show |
intron_variant | MODIFIER | c.238-698A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 2/56 | chr9 | 128568074 | |||||||
| chr9:128568202 | C | G | 1 | a0001c0026t0001g0209 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.238-570C>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 2/56 | chr9 | 128568202 | |||||||
| chr9:128568240 | C | G | 151 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(148): Show |
152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): Show |
intron_variant | MODIFIER | c.238-532C>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 2/56 | chr9 | 128568240 | |||||||
| chr9:128568286 | G | A | 8 | a0001c0006t0001g0290 a0001c0006t0001g0291 a0001c0006t0001g0292 others(5): Show |
8 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.238-486G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 2/56 | chr9 | 128568286 | |||||||
| chr9:128568355 | G | A | 111 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0005 others(108): Show |
111 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.238-417G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 2/56 | chr9 | 128568355 | |||||||
| chr9:128568407 | A | C | 8 | a0001c0002t0001g0012 a0001c0002t0001g0013 a0001c0007t0001g0002 others(5): Show |
9 | HG01884.hp1 HG02280.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.238-365A>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 2/56 | chr9 | 128568407 | |||||||
| chr9:128568420 | G | C | 9 | a0002c0004t0001g0278 a0002c0004t0002g0275 a0002c0004t0002g0276 others(6): Show |
9 | HG02040.hp2 NA18949.hp1 NA18968.hp1 others(6): Show |
intron_variant | MODIFIER | c.238-352G>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 2/56 | chr9 | 128568420 | |||||||
| chr9:128568706 | A | G | 8 | a0002c0004t0001g0278 a0002c0004t0002g0275 a0002c0004t0002g0276 others(5): Show |
8 | HG02040.hp2 NA18949.hp1 NA18968.hp1 others(5): Show |
intron_variant | MODIFIER | c.238-66A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 2/56 | chr9 | 128568706 | |||||||
| chr9:128568710 | C | G | 8 | a0002c0004t0001g0278 a0002c0004t0002g0275 a0002c0004t0002g0276 others(5): Show |
8 | HG02040.hp2 NA18949.hp1 NA18968.hp1 others(5): Show |
intron_variant | MODIFIER | c.238-62C>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 2/56 | chr9 | 128568710 | |||||||
| chr9:128569041 | C | T | 143 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(140): Show |
144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
intron_variant | MODIFIER | c.363+144C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128569041 | |||||||
| chr9:128569087 | T | C | 3 | a0001c0003t0001g0133 a0001c0003t0001g0137 a0001c0027t0001g0117 |
3 | HG00408.hp1 HG00609.hp2 HG00621.hp1 |
intron_variant | MODIFIER | c.363+190T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128569087 | |||||||
| chr9:128569171 | A | G | 112 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0005 others(109): Show |
112 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.363+274A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128569171 | |||||||
| chr9:128569327 | C | CTGAG | 13 | a0001c0002t0001g0012 a0001c0002t0001g0013 a0002c0004t0001g0278 others(10): Show |
13 | HG02040.hp2 HG03225.hp1 HG03669.hp2 others(10): Show |
intron_variant | MODIFIER | c.363+430_363+431ins others(4): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128569327 | |||||||
| chr9:128569580 | T | A | 1 | a0001c0002t0001g0215 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.363+683T>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128569580 | |||||||
| chr9:128569745 | C | T | 1 | a0001c0001t0001g0154 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.363+848C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128569745 | |||||||
| chr9:128569768 | A | C | 2 | a0001c0002t0001g0032 a0001c0002t0001g0033 |
2 | NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.363+871A>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128569768 | |||||||
| chr9:128569986 | T | C | 1 | a0001c0025t0001g0182 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.363+1089T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128569986 | |||||||
| chr9:128570064 | A | T | 1 | a0001c0001t0001g0080 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.363+1167A>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128570064 | |||||||
| chr9:128570269 | A | C | 2 | a0001c0002t0001g0012 a0001c0002t0001g0013 |
2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.363+1372A>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128570269 | |||||||
| chr9:128570282 | C | A | 112 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0005 others(109): Show |
112 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.363+1385C>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128570282 | |||||||
| chr9:128570304 | T | TTATA | 3 | a0001c0002t0001g0012 a0001c0005t0001g0016 a0001c0017t0006g0014 |
3 | HG01109.hp2 HG02723.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.363+1431_363+1434d others(6): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | INFO_REALIGN_3_PRIME | chr9 | 128570304 | ||||||
| chr9:128570322 | ATATATAT others(10): Show |
A | 1 | a0001c0001t0001g0051 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.363+1427_363+1443d others(19): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | INFO_REALIGN_3_PRIME | chr9 | 128570322 | ||||||
| chr9:128570324 | ATATATAT others(4): Show |
A | 1 | a0001c0001t0001g0108 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.363+1429_363+1439d others(13): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | INFO_REALIGN_3_PRIME | chr9 | 128570324 | ||||||
| chr9:128570326 | ATATATTT others(2): Show |
A | 19 | a0001c0002t0001g0184 a0001c0002t0001g0204 a0001c0002t0001g0206 others(16): Show |
19 | HG01123.hp1 HG01934.hp1 HG01981.hp1 others(16): Show |
intron_variant | MODIFIER | c.363+1431_363+1439d others(11): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | INFO_REALIGN_3_PRIME | chr9 | 128570326 | ||||||
| chr9:128570326 | ATATATTT others(3): Show |
A | 2 | a0001c0002t0001g0227 a0001c0002t0001g0258 |
2 | HG01257.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.363+1431_363+1440d others(12): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | INFO_REALIGN_3_PRIME | chr9 | 128570326 | ||||||
| chr9:128570326 | ATATATTT others(4): Show |
A | 12 | a0001c0001t0001g0042 a0001c0001t0001g0048 a0001c0001t0001g0052 others(9): Show |
12 | HG01167.hp1 HG01256.hp1 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.363+1431_363+1441d others(13): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | INFO_REALIGN_3_PRIME | chr9 | 128570326 | ||||||
| chr9:128570326 | ATATATTT others(5): Show |
A | 3 | a0001c0001t0001g0036 a0001c0001t0001g0131 a0001c0001t0001g0158 |
3 | HG01515.hp1 NA18964.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.363+1431_363+1442d others(14): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | INFO_REALIGN_3_PRIME | chr9 | 128570326 | ||||||
| chr9:128570328 | ATATTTTT others(2): Show |
A | 51 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0032 others(48): Show |
51 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.363+1433_363+1441d others(11): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | INFO_REALIGN_3_PRIME | chr9 | 128570328 | ||||||
| chr9:128570328 | ATATTTTT others(3): Show |
A | 29 | a0001c0001t0001g0039 a0001c0001t0001g0049 a0001c0001t0001g0057 others(26): Show |
29 | HG00408.hp1 HG00609.hp2 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.363+1433_363+1442d others(12): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | INFO_REALIGN_3_PRIME | chr9 | 128570328 | ||||||
| chr9:128570328 | ATATTTTT others(4): Show |
A | 52 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0043 others(49): Show |
52 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(49): Show |
intron_variant | MODIFIER | c.363+1433_363+1443d others(13): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | INFO_REALIGN_3_PRIME | chr9 | 128570328 | ||||||
| chr9:128570328 | ATATTTTT others(5): Show |
A | 4 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(1): Show |
4 | NA18954.hp2 NA18979.hp2 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.363+1433_363+1444d others(14): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | INFO_REALIGN_3_PRIME | chr9 | 128570328 | ||||||
| chr9:128570330 | A | ATATATAT others(15): Show |
1 | a0002c0004t0002g0279 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.363+1434_363+1435i others(24): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | INFO_REALIGN_3_PRIME | chr9 | 128570330 | ||||||
| chr9:128570330 | A | ATATATAT others(17): Show |
1 | a0002c0004t0002g0277 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.363+1434_363+1435i others(26): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | INFO_REALIGN_3_PRIME | chr9 | 128570330 | ||||||
| chr9:128570330 | A | ATATATAT others(14): Show |
1 | a0002c0004t0002g0275 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.363+1434_363+1435i others(23): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | INFO_REALIGN_3_PRIME | chr9 | 128570330 | ||||||
| chr9:128570330 | A | ATATATAT others(17): Show |
1 | a0002c0004t0002g0283 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.363+1434_363+1435i others(26): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | INFO_REALIGN_3_PRIME | chr9 | 128570330 | ||||||
| chr9:128570330 | A | ATATATAT others(10): Show |
1 | a0002c0004t0002g0280 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.363+1434_363+1435i others(19): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | INFO_REALIGN_3_PRIME | chr9 | 128570330 | ||||||
| chr9:128570330 | A | ATATATAT others(15): Show |
1 | a0002c0004t0001g0278 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.363+1434_363+1435i others(24): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | INFO_REALIGN_3_PRIME | chr9 | 128570330 | ||||||
| chr9:128570330 | A | ATATATAT others(9): Show |
1 | a0002c0004t0002g0276 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.363+1434_363+1435i others(18): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | INFO_REALIGN_3_PRIME | chr9 | 128570330 | ||||||
| chr9:128570330 | A | ATATATAT others(9): Show |
1 | a0002c0004t0002g0281 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.363+1434_363+1435i others(18): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | INFO_REALIGN_3_PRIME | chr9 | 128570330 | ||||||
| chr9:128570330 | A | ATATATAT others(13): Show |
1 | a0002c0004t0002g0273 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.363+1434_363+1435i others(22): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | INFO_REALIGN_3_PRIME | chr9 | 128570330 | ||||||
| chr9:128570330 | A | ATATATAT others(10): Show |
1 | a0002c0004t0002g0274 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.363+1434_363+1435i others(19): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | INFO_REALIGN_3_PRIME | chr9 | 128570330 | ||||||
| chr9:128570330 | A | ATTTTTTT others(4): Show |
1 | a0002c0004t0002g0282 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.363+1447_363+1457d others(13): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | INFO_REALIGN_3_PRIME | chr9 | 128570330 | ||||||
| chr9:128570330 | A | T | 3 | a0001c0005t0001g0022 a0001c0005t0001g0024 a0001c0014t0003g0020 |
3 | HG02486.hp1 HG02559.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.363+1433A>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128570330 | |||||||
| chr9:128570330 | ATTTTTTT | A | 20 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(17): Show |
20 | HG00099.hp1 HG00597.hp2 HG01167.hp2 others(17): Show |
intron_variant | MODIFIER | c.363+1451_363+1457d others(9): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | INFO_REALIGN_3_PRIME | chr9 | 128570330 | ||||||
| chr9:128570330 | ATTTTTTT others(1): Show |
A | 6 | a0001c0002t0001g0186 a0001c0002t0001g0222 a0001c0002t0001g0265 others(3): Show |
6 | HG00642.hp1 HG01256.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.363+1450_363+1457d others(10): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | INFO_REALIGN_3_PRIME | chr9 | 128570330 | ||||||
| chr9:128570330 | ATTTTTTT others(2): Show |
A | 25 | a0001c0001t0001g0029 a0001c0001t0001g0062 a0001c0001t0001g0076 others(22): Show |
26 | HG00558.hp2 HG00735.hp2 HG01099.hp1 others(23): Show |
intron_variant | MODIFIER | c.363+1449_363+1457d others(11): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | INFO_REALIGN_3_PRIME | chr9 | 128570330 | ||||||
| chr9:128570330 | ATTTTTTT others(3): Show |
A | 7 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0101 others(4): Show |
7 | HG02258.hp2 HG02809.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.363+1448_363+1457d others(12): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | INFO_REALIGN_3_PRIME | chr9 | 128570330 | ||||||
| chr9:128570330 | ATTTTTTT others(4): Show |
A | 26 | a0001c0001t0001g0007 a0001c0001t0001g0037 a0001c0001t0001g0038 others(23): Show |
26 | HG00140.hp1 HG00280.hp1 HG00621.hp2 others(23): Show |
intron_variant | MODIFIER | c.363+1447_363+1457d others(13): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | INFO_REALIGN_3_PRIME | chr9 | 128570330 | ||||||
| chr9:128570331 | T | TA | 3 | a0001c0005t0001g0015 a0001c0005t0001g0017 a0001c0005t0001g0018 |
3 | HG02055.hp2 HG02886.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.363+1434_363+1435i others(3): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128570331 | |||||||
| chr9:128570332 | T | A | 4 | a0001c0002t0001g0012 a0001c0005t0001g0016 a0001c0005t0001g0025 others(1): Show |
4 | HG02615.hp2 HG02723.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.363+1435T>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128570332 | |||||||
| chr9:128570334 | T | A | 2 | a0001c0005t0001g0025 a0001c0007t0001g0002 |
2 | HG02615.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.363+1437T>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128570334 | |||||||
| chr9:128570336 | T | A | 2 | a0001c0007t0001g0002 a0001c0007t0001g0047 |
2 | HG02615.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.363+1439T>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128570336 | |||||||
| chr9:128570337 | T | A | 2 | a0001c0002t0001g0177 a0001c0002t0001g0243 |
2 | NA18952.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.363+1440T>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128570337 | |||||||
| chr9:128570338 | T | A | 3 | a0001c0002t0001g0187 a0001c0002t0001g0203 a0001c0007t0001g0002 |
4 | HG02615.hp2 HG02717.hp2 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.363+1441T>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128570338 | |||||||
| chr9:128570339 | T | A | 13 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(10): Show |
13 | HG00099.hp1 HG00597.hp2 HG01167.hp2 others(10): Show |
intron_variant | MODIFIER | c.363+1442T>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128570339 | |||||||
| chr9:128570340 | T | A | 2 | a0001c0002t0001g0265 a0001c0007t0001g0002 |
3 | HG01361.hp2 HG02615.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.363+1443T>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128570340 | |||||||
| chr9:128570341 | T | A | 11 | a0001c0001t0001g0062 a0001c0001t0001g0071 a0001c0001t0001g0073 others(8): Show |
11 | HG01433.hp2 HG02683.hp2 NA18939.hp1 others(8): Show |
intron_variant | MODIFIER | c.363+1444T>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128570341 | |||||||
| chr9:128570342 | T | A | 2 | a0001c0001t0007g0065 a0001c0007t0001g0002 |
3 | HG02615.hp2 HG02717.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.363+1445T>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128570342 | |||||||
| chr9:128570343 | T | A | 3 | a0001c0001t0001g0007 a0001c0001t0001g0085 a0001c0001t0001g0155 |
3 | NA18953.hp1 NA19057.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.363+1446T>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128570343 | |||||||
| chr9:128570348 | T | G | 1 | a0001c0002t0001g0224 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.363+1451T>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128570348 | |||||||
| chr9:128570432 | G | A | 3 | a0001c0010t0001g0299 a0001c0010t0001g0300 a0001c0010t0001g0301 |
3 | HG02615.hp1 HG02809.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.363+1535G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128570432 | |||||||
| chr9:128570499 | G | A | 112 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0005 others(109): Show |
112 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.363+1602G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128570499 | |||||||
| chr9:128570645 | C | CTTAT | 5 | a0001c0002t0001g0032 a0001c0002t0001g0033 a0003c0011t0001g0063 others(2): Show |
5 | NA18980.hp1 NA18998.hp2 NA19009.hp1 others(2): Show |
intron_variant | MODIFIER | c.363+1771_363+1774d others(6): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | INFO_REALIGN_3_PRIME | chr9 | 128570645 | ||||||
| chr9:128570725 | C | T | 112 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0005 others(109): Show |
112 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.363+1828C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128570725 | |||||||
| chr9:128570989 | A | G | 1 | a0001c0001t0001g0096 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.363+2092A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128570989 | |||||||
| chr9:128571003 | C | G | 2 | a0001c0002t0001g0012 a0001c0002t0001g0013 |
2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.363+2106C>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128571003 | |||||||
| chr9:128571044 | G | A | 11 | a0001c0006t0001g0290 a0001c0006t0001g0291 a0001c0006t0001g0292 others(8): Show |
11 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.363+2147G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128571044 | |||||||
| chr9:128571090 | C | T | 1 | a0001c0001t0001g0164 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.363+2193C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128571090 | |||||||
| chr9:128571140 | A | G | 1 | a0001c0007t0001g0047 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.363+2243A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128571140 | |||||||
| chr9:128571156 | G | T | 1 | a0001c0002t0001g0215 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.363+2259G>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128571156 | |||||||
| chr9:128571165 | C | A | 1 | a0001c0007t0001g0010 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.363+2268C>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128571165 | |||||||
| chr9:128571291 | G | GA | 147 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(144): Show |
148 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(145): Show |
intron_variant | MODIFIER | c.363+2405dupA | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | INFO_REALIGN_3_PRIME | chr9 | 128571291 | ||||||
| chr9:128571484 | C | T | 1 | a0001c0007t0001g0047 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.363+2587C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128571484 | |||||||
| chr9:128571719 | A | G | 6 | a0001c0007t0001g0002 a0001c0007t0001g0009 a0001c0007t0001g0010 others(3): Show |
7 | HG01884.hp1 HG02280.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.363+2822A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128571719 | |||||||
| chr9:128571844 | A | G | 6 | a0001c0007t0001g0002 a0001c0007t0001g0009 a0001c0007t0001g0010 others(3): Show |
7 | HG01884.hp1 HG02280.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.364-2831A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128571844 | |||||||
| chr9:128572086 | C | T | 2 | a0001c0002t0001g0012 a0001c0002t0001g0013 |
2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.364-2589C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128572086 | |||||||
| chr9:128572329 | GA | G | 113 | a0001c0001t0001g0159 a0001c0002t0001g0003 a0001c0002t0001g0004 others(110): Show |
113 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.364-2344delA | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | INFO_REALIGN_3_PRIME | chr9 | 128572329 | ||||||
| chr9:128572460 | C | A | 1 | a0001c0001t0001g0072 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.364-2215C>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128572460 | |||||||
| chr9:128572465 | C | T | 123 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0005 others(120): Show |
123 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.364-2210C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128572465 | |||||||
| chr9:128572477 | C | CT | 293 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(290): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.364-2195dupT | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | INFO_REALIGN_3_PRIME | chr9 | 128572477 | ||||||
| chr9:128572488 | G | A | 143 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(140): Show |
144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
intron_variant | MODIFIER | c.364-2187G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128572488 | |||||||
| chr9:128572563 | T | G | 280 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(277): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.364-2112T>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128572563 | |||||||
| chr9:128572611 | A | G | 280 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(277): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.364-2064A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128572611 | |||||||
| chr9:128572834 | G | GT | 11 | a0002c0004t0001g0278 a0002c0004t0002g0273 a0002c0004t0002g0274 others(8): Show |
11 | HG02040.hp2 HG03669.hp2 HG03688.hp1 others(8): Show |
intron_variant | MODIFIER | c.364-1840dupT | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | INFO_REALIGN_3_PRIME | chr9 | 128572834 | ||||||
| chr9:128572977 | C | T | 3 | a0001c0009t0001g0006 a0001c0009t0001g0027 a0001c0009t0001g0028 |
3 | HG01891.hp2 HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.364-1698C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128572977 | |||||||
| chr9:128573062 | A | G | 280 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(277): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.364-1613A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128573062 | |||||||
| chr9:128573385 | A | G | 1 | a0001c0001t0001g0064 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.364-1290A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128573385 | |||||||
| chr9:128573394 | A | G | 149 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(146): Show |
150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
intron_variant | MODIFIER | c.364-1281A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128573394 | |||||||
| chr9:128573473 | C | T | 11 | a0002c0004t0001g0278 a0002c0004t0002g0273 a0002c0004t0002g0274 others(8): Show |
11 | HG02040.hp2 HG03669.hp2 HG03688.hp1 others(8): Show |
intron_variant | MODIFIER | c.364-1202C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128573473 | |||||||
| chr9:128573648 | G | A | 36 | a0001c0001t0001g0034 a0001c0001t0001g0039 a0001c0001t0001g0040 others(33): Show |
37 | HG00099.hp1 HG00735.hp2 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.364-1027G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128573648 | |||||||
| chr9:128573676 | G | A | 1 | a0001c0001t0001g0035 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.364-999G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128573676 | |||||||
| chr9:128573719 | G | T | 2 | a0001c0002t0001g0012 a0001c0002t0001g0013 |
2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.364-956G>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128573719 | |||||||
| chr9:128573745 | C | T | 2 | a0001c0002t0001g0012 a0001c0002t0001g0013 |
2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.364-930C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128573745 | |||||||
| chr9:128573784 | C | T | 11 | a0001c0006t0001g0290 a0001c0006t0001g0291 a0001c0006t0001g0292 others(8): Show |
11 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.364-891C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128573784 | |||||||
| chr9:128573815 | A | C | 11 | a0002c0004t0001g0278 a0002c0004t0002g0273 a0002c0004t0002g0274 others(8): Show |
11 | HG02040.hp2 HG03669.hp2 HG03688.hp1 others(8): Show |
intron_variant | MODIFIER | c.364-860A>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128573815 | |||||||
| chr9:128573841 | A | C | 280 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(277): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.364-834A>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128573841 | |||||||
| chr9:128573846 | C | G | 151 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(148): Show |
152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): Show |
intron_variant | MODIFIER | c.364-829C>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128573846 | |||||||
| chr9:128573955 | A | G | 280 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(277): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.364-720A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128573955 | |||||||
| chr9:128573988 | C | T | 8 | a0001c0006t0001g0290 a0001c0006t0001g0291 a0001c0006t0001g0292 others(5): Show |
8 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.364-687C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128573988 | |||||||
| chr9:128574023 | A | G | 280 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(277): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.364-652A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128574023 | |||||||
| chr9:128574028 | C | G | 11 | a0001c0006t0001g0290 a0001c0006t0001g0291 a0001c0006t0001g0292 others(8): Show |
11 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.364-647C>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128574028 | |||||||
| chr9:128574043 | G | A | 112 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0005 others(109): Show |
112 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.364-632G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128574043 | |||||||
| chr9:128574320 | T | C | 2 | a0001c0001t0001g0141 a0001c0001t0001g0142 |
2 | NA18972.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.364-355T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128574320 | |||||||
| chr9:128574371 | G | T | 141 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(138): Show |
142 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(139): Show |
intron_variant | MODIFIER | c.364-304G>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128574371 | |||||||
| chr9:128574480 | A | G | 2 | a0001c0002t0001g0012 a0001c0002t0001g0013 |
2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.364-195A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128574480 | |||||||
| chr9:128574578 | G | A | 2 | a0001c0001t0001g0073 a0001c0001t0001g0075 |
2 | NA18939.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.364-97G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128574578 | |||||||
| chr9:128574578 | G | T | 2 | a0001c0002t0001g0012 a0001c0002t0001g0013 |
2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.364-97G>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128574578 | |||||||
| chr9:128574588 | G | T | 1 | a0001c0010t0001g0299 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.364-87G>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128574588 | |||||||
| chr9:128574972 | G | GCTCTCCA others(16): Show |
2 | a0001c0001t0001g0128 a0001c0001t0001g0131 |
2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.504+157_504+158ins others(23): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 4/56 | chr9 | 128574972 | |||||||
| chr9:128574974 | A | C | 2 | a0001c0001t0001g0128 a0001c0001t0001g0131 |
2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.504+159A>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 4/56 | chr9 | 128574974 | |||||||
| chr9:128574976 | G | A | 2 | a0001c0001t0001g0128 a0001c0001t0001g0131 |
2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.504+161G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 4/56 | chr9 | 128574976 | |||||||
| chr9:128574977 | T | G | 2 | a0001c0001t0001g0128 a0001c0001t0001g0131 |
2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.504+162T>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 4/56 | chr9 | 128574977 | |||||||
| chr9:128575023 | C | T | 282 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(279): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.505-176C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 4/56 | chr9 | 128575023 | |||||||
| chr9:128575110 | C | T | 142 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(139): Show |
143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.505-89C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 4/56 | chr9 | 128575110 | |||||||
| chr9:128575111 | G | A | 1 | a0001c0005t0001g0025 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.505-88G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 4/56 | chr9 | 128575111 | |||||||
| chr9:128575382 | A | C | 280 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(277): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.651+37A>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 5/56 | chr9 | 128575382 | |||||||
| chr9:128575398 | A | G | 11 | a0002c0004t0001g0278 a0002c0004t0002g0273 a0002c0004t0002g0274 others(8): Show |
11 | HG02040.hp2 HG03669.hp2 HG03688.hp1 others(8): Show |
intron_variant | MODIFIER | c.651+53A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 5/56 | chr9 | 128575398 | |||||||
| chr9:128575458 | G | A | 8 | a0001c0002t0001g0032 a0001c0002t0001g0033 a0001c0007t0001g0002 others(5): Show |
9 | HG01884.hp1 HG02280.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.651+113G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 5/56 | chr9 | 128575458 | |||||||
| chr9:128575480 | T | C | 1 | a0001c0001t0001g0082 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.651+135T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 5/56 | chr9 | 128575480 | |||||||
| chr9:128575564 | A | G | 149 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(146): Show |
150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
intron_variant | MODIFIER | c.651+219A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 5/56 | chr9 | 128575564 | |||||||
| chr9:128575592 | G | C | 1 | a0001c0002t0001g0270 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.651+247G>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 5/56 | chr9 | 128575592 | |||||||
| chr9:128575667 | G | A | 2 | a0001c0002t0001g0032 a0001c0002t0001g0033 |
2 | NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.651+322G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 5/56 | chr9 | 128575667 | |||||||
| chr9:128575680 | G | A | 1 | a0001c0002t0001g0197 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.651+335G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 5/56 | chr9 | 128575680 | |||||||
| chr9:128576179 | A | G | 1 | a0001c0002t0001g0246 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.652-644A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 5/56 | chr9 | 128576179 | |||||||
| chr9:128576321 | A | G | 282 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(279): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.652-502A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 5/56 | chr9 | 128576321 | |||||||
| chr9:128576425 | C | T | 6 | a0001c0007t0001g0002 a0001c0007t0001g0009 a0001c0007t0001g0010 others(3): Show |
7 | HG01884.hp1 HG02280.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.652-398C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 5/56 | chr9 | 128576425 | |||||||
| chr9:128576450 | T | C | 12 | a0001c0001t0001g0138 a0001c0006t0001g0290 a0001c0006t0001g0291 others(9): Show |
12 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.652-373T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 5/56 | chr9 | 128576450 | |||||||
| chr9:128576606 | A | G | 2 | a0001c0002t0001g0012 a0001c0002t0001g0013 |
2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.652-217A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 5/56 | chr9 | 128576606 | |||||||
| chr9:128576719 | A | G | 11 | a0002c0004t0001g0278 a0002c0004t0002g0273 a0002c0004t0002g0274 others(8): Show |
11 | HG02040.hp2 HG03669.hp2 HG03688.hp1 others(8): Show |
intron_variant | MODIFIER | c.652-104A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 5/56 | chr9 | 128576719 | |||||||
| chr9:128577112 | G | T | 2 | a0001c0002t0001g0012 a0001c0002t0001g0013 |
2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.786-17G>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 6/56 | chr9 | 128577112 | |||||||
| chr9:128577541 | T | C | 1 | a0005c0020t0001g0008 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1085+35T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 8/56 | chr9 | 128577541 | |||||||
| chr9:128577576 | T | TCTTC | 3 | a0001c0010t0001g0299 a0001c0010t0001g0300 a0001c0010t0001g0301 |
3 | HG02615.hp1 HG02809.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1085+70_1085+71ins others(4): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 8/56 | chr9 | 128577576 | |||||||
| chr9:128577784 | A | C | 1 | a0002c0004t0002g0273 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1085+278A>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 8/56 | chr9 | 128577784 | |||||||
| chr9:128577886 | T | TG | 158 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(155): Show |
160 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(157): Show |
intron_variant | MODIFIER | c.1086-220dupG | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 8/56 | INFO_REALIGN_3_PRIME | chr9 | 128577886 | ||||||
| chr9:128578027 | A | G | 293 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(290): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.1086-83A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 8/56 | chr9 | 128578027 | |||||||
| chr9:128578256 | C | T | 8 | a0001c0006t0001g0290 a0001c0006t0001g0291 a0001c0006t0001g0292 others(5): Show |
8 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.1221+11C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 9/56 | chr9 | 128578256 | |||||||
| chr9:128578360 | T | A | 1 | a0001c0005t0001g0024 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1221+115T>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 9/56 | chr9 | 128578360 | |||||||
| chr9:128578360 | T | C | 293 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(290): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.1221+115T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 9/56 | chr9 | 128578360 | |||||||
| chr9:128578404 | G | T | 2 | a0001c0002t0001g0012 a0001c0002t0001g0013 |
2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1221+159G>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 9/56 | chr9 | 128578404 | |||||||
| chr9:128578450 | G | A | 2 | a0001c0001t0001g0062 a0001c0001t0007g0065 |
2 | NA18960.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1221+205G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 9/56 | chr9 | 128578450 | |||||||
| chr9:128578483 | C | T | 1 | a0001c0002t0001g0245 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1221+238C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 9/56 | chr9 | 128578483 | |||||||
| chr9:128578490 | G | A | 2 | a0001c0002t0001g0012 a0001c0002t0001g0013 |
2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1221+245G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 9/56 | chr9 | 128578490 | |||||||
| chr9:128578531 | T | A | 158 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(155): Show |
160 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(157): Show |
intron_variant | MODIFIER | c.1221+286T>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 9/56 | chr9 | 128578531 | |||||||
| chr9:128578566 | T | C | 293 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(290): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.1221+321T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 9/56 | chr9 | 128578566 | |||||||
| chr9:128578595 | C | T | 7 | a0001c0007t0001g0002 a0001c0007t0001g0009 a0001c0007t0001g0010 others(4): Show |
8 | HG01884.hp1 HG02280.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1221+350C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 9/56 | chr9 | 128578595 | |||||||
| chr9:128578596 | T | C | 293 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(290): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.1221+351T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 9/56 | chr9 | 128578596 | |||||||
| chr9:128578672 | T | C | 111 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0005 others(108): Show |
111 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.1221+427T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 9/56 | chr9 | 128578672 | |||||||
| chr9:128578679 | G | A | 282 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(279): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.1221+434G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 9/56 | chr9 | 128578679 | |||||||
| chr9:128578810 | C | T | 2 | a0001c0002t0001g0012 a0001c0002t0001g0013 |
2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1221+565C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 9/56 | chr9 | 128578810 | |||||||
| chr9:128578835 | GA | G | 146 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(143): Show |
147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): Show |
intron_variant | MODIFIER | c.1221+609delA | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 9/56 | INFO_REALIGN_3_PRIME | chr9 | 128578835 | ||||||
| chr9:128578835 | GAA | G | 115 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0002t0001g0003 others(112): Show |
115 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.1221+608_1221+609d others(4): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 9/56 | INFO_REALIGN_3_PRIME | chr9 | 128578835 | ||||||
| chr9:128578835 | GAAA | G | 8 | a0001c0002t0001g0190 a0001c0007t0001g0002 a0001c0007t0001g0009 others(5): Show |
9 | HG01884.hp1 HG02280.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1221+607_1221+609d others(5): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 9/56 | INFO_REALIGN_3_PRIME | chr9 | 128578835 | ||||||
| chr9:128578864 | A | G | 2 | a0001c0014t0003g0020 a0001c0014t0003g0021 |
2 | HG02559.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1221+619A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 9/56 | chr9 | 128578864 | |||||||
| chr9:128579076 | A | G | 8 | a0001c0006t0001g0290 a0001c0006t0001g0291 a0001c0006t0001g0292 others(5): Show |
8 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.1222-561A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 9/56 | chr9 | 128579076 | |||||||
| chr9:128579103 | G | C | 2 | a0001c0002t0001g0032 a0001c0002t0001g0033 |
2 | NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1222-534G>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 9/56 | chr9 | 128579103 | |||||||
| chr9:128579182 | T | C | 11 | a0001c0006t0001g0290 a0001c0006t0001g0291 a0001c0006t0001g0292 others(8): Show |
11 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1222-455T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 9/56 | chr9 | 128579182 | |||||||
| chr9:128579363 | T | C | 293 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(290): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.1222-274T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 9/56 | chr9 | 128579363 | |||||||
| chr9:128579364 | G | A | 7 | a0001c0007t0001g0002 a0001c0007t0001g0009 a0001c0007t0001g0010 others(4): Show |
8 | HG01884.hp1 HG02280.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1222-273G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 9/56 | chr9 | 128579364 | |||||||
| chr9:128579390 | G | A | 111 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0005 others(108): Show |
111 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.1222-247G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 9/56 | chr9 | 128579390 | |||||||
| chr9:128579411 | C | G | 8 | a0001c0006t0001g0290 a0001c0006t0001g0291 a0001c0006t0001g0292 others(5): Show |
8 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.1222-226C>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 9/56 | chr9 | 128579411 | |||||||
| chr9:128579445 | A | G | 1 | a0001c0001t0001g0080 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1222-192A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 9/56 | chr9 | 128579445 | |||||||
| chr9:128579542 | A | G | 3 | a0001c0010t0001g0299 a0001c0010t0001g0300 a0001c0010t0001g0301 |
3 | HG02615.hp1 HG02809.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1222-95A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 9/56 | chr9 | 128579542 | |||||||
| chr9:128579803 | A | G | 1 | a0001c0002t0001g0188 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1323+65A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 10/56 | chr9 | 128579803 | |||||||
| chr9:128580039 | A | G | 2 | a0001c0002t0001g0012 a0001c0002t0001g0013 |
2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1323+301A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 10/56 | chr9 | 128580039 | |||||||
| chr9:128580197 | C | T | 3 | a0001c0010t0001g0299 a0001c0010t0001g0300 a0001c0010t0001g0301 |
3 | HG02615.hp1 HG02809.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1323+459C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 10/56 | chr9 | 128580197 | |||||||
| chr9:128580393 | C | G | 293 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(290): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.1324-529C>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 10/56 | chr9 | 128580393 | |||||||
| chr9:128580436 | T | C | 11 | a0001c0006t0001g0290 a0001c0006t0001g0291 a0001c0006t0001g0292 others(8): Show |
11 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1324-486T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 10/56 | chr9 | 128580436 | |||||||
| chr9:128580573 | T | G | 280 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(277): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.1324-349T>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 10/56 | chr9 | 128580573 | |||||||
| chr9:128580579 | G | A | 3 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0060 |
3 | HG02145.hp1 HG02886.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1324-343G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 10/56 | chr9 | 128580579 | |||||||
| chr9:128580862 | C | T | 2 | a0001c0002t0001g0012 a0001c0002t0001g0013 |
2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1324-60C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 10/56 | chr9 | 128580862 | |||||||
| chr9:128581474 | C | CA | 251 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(248): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.1462-294dupA | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 11/56 | INFO_REALIGN_3_PRIME | chr9 | 128581474 | ||||||
| chr9:128581474 | C | CAA | 8 | a0001c0001t0001g0040 a0001c0001t0001g0114 a0001c0002t0001g0179 others(5): Show |
8 | HG01981.hp1 HG02135.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1462-295_1462-294d others(4): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 11/56 | INFO_REALIGN_3_PRIME | chr9 | 128581474 | ||||||
| chr9:128581474 | CA | C | 8 | a0001c0006t0001g0290 a0001c0006t0001g0291 a0001c0006t0001g0292 others(5): Show |
8 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.1462-294delA | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 11/56 | INFO_REALIGN_3_PRIME | chr9 | 128581474 | ||||||
| chr9:128581485 | A | C | 3 | a0001c0010t0001g0299 a0001c0010t0001g0300 a0001c0010t0001g0301 |
3 | HG02615.hp1 HG02809.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1462-297A>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 11/56 | chr9 | 128581485 | |||||||
| chr9:128581487 | AAC | A | 5 | a0001c0007t0001g0002 a0001c0007t0001g0009 a0001c0007t0001g0010 others(2): Show |
6 | HG01884.hp1 HG02280.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1462-293_1462-292d others(4): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 11/56 | INFO_REALIGN_3_PRIME | chr9 | 128581487 | ||||||
| chr9:128581493 | C | A | 1 | a0001c0016t0001g0026 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1462-289C>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 11/56 | chr9 | 128581493 | |||||||
| chr9:128581718 | T | C | 1 | a0001c0007t0001g0272 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1462-64T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 11/56 | chr9 | 128581718 | |||||||
| chr9:128581755 | T | A | 8 | a0001c0006t0001g0290 a0001c0006t0001g0291 a0001c0006t0001g0292 others(5): Show |
8 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.1462-27T>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 11/56 | chr9 | 128581755 | |||||||
| chr9:128581769 | T | G | 1 | a0001c0001t0001g0048 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1462-13T>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 11/56 | chr9 | 128581769 | |||||||
| chr9:128581927 | C | A | 2 | a0001c0002t0001g0012 a0001c0002t0001g0013 |
2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1572+35C>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 12/56 | chr9 | 128581927 | |||||||
| chr9:128582035 | A | G | 1 | a0001c0007t0001g0002 | 2 | HG02615.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1572+143A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 12/56 | chr9 | 128582035 | |||||||
| chr9:128582048 | G | A | 11 | a0002c0004t0001g0278 a0002c0004t0002g0273 a0002c0004t0002g0274 others(8): Show |
11 | HG02040.hp2 HG03669.hp2 HG03688.hp1 others(8): Show |
intron_variant | MODIFIER | c.1572+156G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 12/56 | chr9 | 128582048 | |||||||
| chr9:128582100 | A | T | 3 | a0001c0002t0001g0267 a0001c0002t0001g0268 a0001c0002t0001g0269 |
3 | HG01884.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1572+208A>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 12/56 | chr9 | 128582100 | |||||||
| chr9:128582229 | G | A | 2 | a0001c0014t0003g0020 a0001c0014t0003g0021 |
2 | HG02559.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1573-250G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 12/56 | chr9 | 128582229 | |||||||
| chr9:128582299 | G | A | 307 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(304): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.1573-180G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 12/56 | chr9 | 128582299 | |||||||
| chr9:128582328 | GA | G | 280 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(277): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.1573-145delA | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 12/56 | INFO_REALIGN_3_PRIME | chr9 | 128582328 | ||||||
| chr9:128582357 | A | G | 1 | a0001c0001t0001g0114 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1573-122A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 12/56 | chr9 | 128582357 | |||||||
| chr9:128582590 | T | C | 1 | a0001c0002t0001g0247 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1650+34T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 13/56 | chr9 | 128582590 | |||||||
| chr9:128582596 | A | G | 2 | a0001c0002t0001g0012 a0001c0002t0001g0013 |
2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1650+40A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 13/56 | chr9 | 128582596 | |||||||
| chr9:128582883 | G | A | 11 | a0002c0004t0001g0278 a0002c0004t0002g0273 a0002c0004t0002g0274 others(8): Show |
11 | HG02040.hp2 HG03669.hp2 HG03688.hp1 others(8): Show |
intron_variant | MODIFIER | c.1806+34G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 14/56 | chr9 | 128582883 | |||||||
| chr9:128583309 | A | G | 4 | a0001c0007t0001g0002 a0001c0007t0001g0009 a0001c0007t0001g0010 others(1): Show |
5 | HG01884.hp1 HG02280.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.2011+28A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 15/56 | chr9 | 128583309 | |||||||
| chr9:128583311 | G | A | 3 | a0001c0010t0001g0299 a0001c0010t0001g0300 a0001c0010t0001g0301 |
3 | HG02615.hp1 HG02809.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2011+30G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 15/56 | chr9 | 128583311 | |||||||
| chr9:128583312 | C | A | 1 | a0001c0001t0001g0061 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.2011+31C>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 15/56 | chr9 | 128583312 | |||||||
| chr9:128583375 | A | G | 6 | a0001c0007t0001g0002 a0001c0007t0001g0009 a0001c0007t0001g0010 others(3): Show |
7 | HG01884.hp1 HG02280.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.2011+94A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 15/56 | chr9 | 128583375 | |||||||
| chr9:128583518 | C | G | 2 | a0001c0001t0001g0149 a0001c0001t0001g0150 |
2 | HG01891.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.2011+237C>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 15/56 | chr9 | 128583518 | |||||||
| chr9:128583520 | T | C | 6 | a0001c0003t0001g0030 a0001c0003t0001g0095 a0001c0003t0001g0116 others(3): Show |
6 | NA18948.hp2 NA18961.hp1 NA18977.hp1 others(3): Show |
intron_variant | MODIFIER | c.2011+239T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 15/56 | chr9 | 128583520 | |||||||
| chr9:128583642 | T | C | 6 | a0001c0008t0001g0167 a0001c0008t0001g0168 a0001c0008t0001g0169 others(3): Show |
6 | HG01099.hp2 HG01496.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.2012-146T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 15/56 | chr9 | 128583642 | |||||||
| chr9:128584193 | G | A | 4 | a0001c0009t0001g0006 a0001c0009t0001g0027 a0001c0009t0001g0028 others(1): Show |
4 | HG01891.hp2 HG02922.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.2194-89G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 16/56 | chr9 | 128584193 | |||||||
| chr9:128584200 | A | G | 293 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(290): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.2194-82A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 16/56 | chr9 | 128584200 | |||||||
| chr9:128584216 | A | G | 1 | a0001c0001t0001g0130 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2194-66A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 16/56 | chr9 | 128584216 | |||||||
| chr9:128584269 | T | G | 4 | a0001c0009t0001g0006 a0001c0009t0001g0027 a0001c0009t0001g0028 others(1): Show |
4 | HG01891.hp2 HG02922.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.2194-13T>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 16/56 | chr9 | 128584269 | |||||||
| chr9:128584879 | G | A | 3 | a0001c0003t0001g0133 a0001c0003t0001g0137 a0001c0027t0001g0117 |
3 | HG00408.hp1 HG00609.hp2 HG00621.hp1 |
intron_variant | MODIFIER | c.2560+36G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 18/56 | chr9 | 128584879 | |||||||
| chr9:128584886 | G | A | 291 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(288): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.2560+43G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 18/56 | chr9 | 128584886 | |||||||
| chr9:128584890 | C | T | 142 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(139): Show |
143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.2560+47C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 18/56 | chr9 | 128584890 | |||||||
| chr9:128585015 | C | CT | 133 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0005 others(130): Show |
134 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.2560+189dupT | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 18/56 | INFO_REALIGN_3_PRIME | chr9 | 128585015 | ||||||
| chr9:128585015 | C | T | 1 | a0001c0005t0001g0025 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2560+172C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 18/56 | chr9 | 128585015 | |||||||
| chr9:128585015 | CT | C | 7 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0060 others(4): Show |
7 | HG02145.hp1 HG02886.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.2560+189delT | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 18/56 | INFO_REALIGN_3_PRIME | chr9 | 128585015 | ||||||
| chr9:128585173 | C | G | 1 | a0001c0001t0001g0043 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2560+330C>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 18/56 | chr9 | 128585173 | |||||||
| chr9:128585286 | C | T | 11 | a0002c0004t0001g0278 a0002c0004t0002g0273 a0002c0004t0002g0274 others(8): Show |
11 | HG02040.hp2 HG03669.hp2 HG03688.hp1 others(8): Show |
intron_variant | MODIFIER | c.2560+443C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 18/56 | chr9 | 128585286 | |||||||
| chr9:128585404 | C | T | 1 | a0001c0010t0001g0301 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2561-344C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 18/56 | chr9 | 128585404 | |||||||
| chr9:128585407 | A | G | 11 | a0002c0004t0001g0278 a0002c0004t0002g0273 a0002c0004t0002g0274 others(8): Show |
11 | HG02040.hp2 HG03669.hp2 HG03688.hp1 others(8): Show |
intron_variant | MODIFIER | c.2561-341A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 18/56 | chr9 | 128585407 | |||||||
| chr9:128585408 | G | A | 278 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(275): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.2561-340G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 18/56 | chr9 | 128585408 | |||||||
| chr9:128585492 | A | G | 1 | a0001c0001t0001g0114 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.2561-256A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 18/56 | chr9 | 128585492 | |||||||
| chr9:128585568 | G | C | 2 | a0001c0002t0001g0012 a0001c0002t0001g0013 |
2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2561-180G>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 18/56 | chr9 | 128585568 | |||||||
| chr9:128585697 | G | C | 1 | a0001c0005t0001g0024 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2561-51G>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 18/56 | chr9 | 128585697 | |||||||
| chr9:128586033 | TAGG | T | 8 | a0001c0006t0001g0290 a0001c0006t0001g0291 a0001c0006t0001g0292 others(5): Show |
8 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.2778+71_2778+73del others(3): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 19/56 | INFO_REALIGN_3_PRIME | chr9 | 128586033 | ||||||
| chr9:128586050 | C | T | 1 | a0001c0002t0001g0211 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2778+85C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 19/56 | chr9 | 128586050 | |||||||
| chr9:128586112 | G | GT | 20 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0005 others(17): Show |
20 | HG02055.hp2 HG02074.hp1 HG02486.hp2 others(17): Show |
intron_variant | MODIFIER | c.2778+172dupT | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 19/56 | INFO_REALIGN_3_PRIME | chr9 | 128586112 | ||||||
| chr9:128586112 | GT | G | 175 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0035 others(172): Show |
175 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(172): Show |
intron_variant | MODIFIER | c.2778+172delT | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 19/56 | INFO_REALIGN_3_PRIME | chr9 | 128586112 | ||||||
| chr9:128586112 | GTT | G | 21 | a0001c0001t0001g0034 a0001c0002t0001g0184 a0001c0002t0001g0227 others(18): Show |
22 | HG00735.hp2 HG01069.hp1 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.2778+171_2778+172d others(4): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 19/56 | INFO_REALIGN_3_PRIME | chr9 | 128586112 | ||||||
| chr9:128586112 | GTTTTTTT others(3): Show |
G | 4 | a0001c0009t0001g0006 a0001c0009t0001g0027 a0001c0009t0001g0028 others(1): Show |
4 | HG01891.hp2 HG02922.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.2778+163_2778+172d others(12): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 19/56 | INFO_REALIGN_3_PRIME | chr9 | 128586112 | ||||||
| chr9:128586161 | C | G | 148 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(145): Show |
149 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(146): Show |
intron_variant | MODIFIER | c.2778+196C>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 19/56 | chr9 | 128586161 | |||||||
| chr9:128586222 | G | A | 142 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(139): Show |
143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.2778+257G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 19/56 | chr9 | 128586222 | |||||||
| chr9:128586330 | G | A | 8 | a0001c0006t0001g0290 a0001c0006t0001g0291 a0001c0006t0001g0292 others(5): Show |
8 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.2778+365G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 19/56 | chr9 | 128586330 | |||||||
| chr9:128586432 | C | G | 2 | a0001c0002t0001g0012 a0001c0002t0001g0013 |
2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2778+467C>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 19/56 | chr9 | 128586432 | |||||||
| chr9:128586504 | C | T | 143 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(140): Show |
144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
intron_variant | MODIFIER | c.2778+539C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 19/56 | chr9 | 128586504 | |||||||
| chr9:128586506 | A | G | 1 | a0001c0002t0001g0239 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.2778+541A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 19/56 | chr9 | 128586506 | |||||||
| chr9:128586617 | C | T | 1 | a0001c0002t0001g0305 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2778+652C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 19/56 | chr9 | 128586617 | |||||||
| chr9:128586644 | C | G | 1 | a0001c0001t0001g0100 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2778+679C>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 19/56 | chr9 | 128586644 | |||||||
| chr9:128586716 | T | C | 3 | a0001c0002t0001g0258 a0001c0002t0001g0259 a0001c0002t0001g0261 |
3 | HG02109.hp2 HG02647.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.2778+751T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 19/56 | chr9 | 128586716 | |||||||
| chr9:128586772 | A | G | 1 | a0001c0007t0001g0047 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2778+807A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 19/56 | chr9 | 128586772 | |||||||
| chr9:128586783 | C | G | 278 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(275): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.2778+818C>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 19/56 | chr9 | 128586783 | |||||||
| chr9:128586822 | C | CT | 260 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(257): Show |
261 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(258): Show |
intron_variant | MODIFIER | c.2779-773dupT | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 19/56 | INFO_REALIGN_3_PRIME | chr9 | 128586822 | ||||||
| chr9:128586886 | C | T | 2 | a0001c0001t0001g0128 a0001c0001t0001g0131 |
2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.2779-720C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 19/56 | chr9 | 128586886 | |||||||
| chr9:128587100 | C | T | 1 | a0002c0004t0002g0281 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.2779-506C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 19/56 | chr9 | 128587100 | |||||||
| chr9:128587111 | G | A | 1 | a0001c0002t0001g0228 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2779-495G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 19/56 | chr9 | 128587111 | |||||||
| chr9:128587155 | G | A | 1 | a0001c0002t0001g0174 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.2779-451G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 19/56 | chr9 | 128587155 | |||||||
| chr9:128587166 | G | A | 278 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(275): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.2779-440G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 19/56 | chr9 | 128587166 | |||||||
| chr9:128587272 | A | G | 1 | a0001c0010t0001g0299 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2779-334A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 19/56 | chr9 | 128587272 | |||||||
| chr9:128587434 | A | G | 293 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(290): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.2779-172A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 19/56 | chr9 | 128587434 | |||||||
| chr9:128587463 | T | C | 10 | a0001c0002t0001g0183 a0001c0002t0001g0188 a0001c0002t0001g0257 others(7): Show |
10 | HG01109.hp1 HG02055.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.2779-143T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 19/56 | chr9 | 128587463 | |||||||
| chr9:128587494 | G | A | 278 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(275): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.2779-112G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 19/56 | chr9 | 128587494 | |||||||
| chr9:128587515 | G | C | 1 | a0001c0002t0001g0255 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.2779-91G>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 19/56 | chr9 | 128587515 | |||||||
| chr9:128587833 | A | G | 260 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(257): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.2871+135A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 20/56 | chr9 | 128587833 | |||||||
| chr9:128587838 | G | GATTT | 5 | a0001c0002t0001g0012 a0001c0002t0001g0013 a0001c0009t0001g0006 others(2): Show |
5 | HG01891.hp2 HG03225.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.2871+162_2871+165d others(6): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 20/56 | INFO_REALIGN_3_PRIME | chr9 | 128587838 | ||||||
| chr9:128587926 | A | C | 279 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(276): Show |
281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.2871+228A>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 20/56 | chr9 | 128587926 | |||||||
| chr9:128588013 | A | AT | 124 | a0001c0001t0001g0110 a0001c0001t0001g0145 a0001c0002t0001g0003 others(121): Show |
125 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.2871+331dupT | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 20/56 | INFO_REALIGN_3_PRIME | chr9 | 128588013 | ||||||
| chr9:128588013 | A | ATT | 162 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(159): Show |
163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
intron_variant | MODIFIER | c.2871+330_2871+331d others(4): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 20/56 | INFO_REALIGN_3_PRIME | chr9 | 128588013 | ||||||
| chr9:128588038 | G | A | 4 | a0001c0002t0001g0183 a0001c0002t0001g0257 a0001c0002t0001g0262 others(1): Show |
4 | HG02055.hp1 HG02723.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.2871+340G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 20/56 | chr9 | 128588038 | |||||||
| chr9:128588087 | TC | T | 3 | a0001c0007t0001g0009 a0001c0007t0001g0010 a0001c0007t0001g0011 |
3 | HG01884.hp1 HG02280.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2871+392delC | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 20/56 | INFO_REALIGN_3_PRIME | chr9 | 128588087 | ||||||
| chr9:128588310 | A | AT | 22 | a0001c0002t0001g0032 a0001c0002t0001g0033 a0001c0007t0001g0002 others(19): Show |
23 | HG01884.hp1 HG02040.hp2 HG02280.hp2 others(20): Show |
intron_variant | MODIFIER | c.2872-481dupT | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 20/56 | INFO_REALIGN_3_PRIME | chr9 | 128588310 | ||||||
| chr9:128588310 | A | ATT | 16 | a0001c0001t0001g0046 a0001c0001t0001g0128 a0001c0001t0001g0130 others(13): Show |
16 | HG01099.hp2 HG01361.hp1 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.2872-482_2872-481d others(4): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 20/56 | INFO_REALIGN_3_PRIME | chr9 | 128588310 | ||||||
| chr9:128588310 | A | ATTT | 248 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(245): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.2872-483_2872-481d others(5): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 20/56 | INFO_REALIGN_3_PRIME | chr9 | 128588310 | ||||||
| chr9:128588310 | A | ATTTT | 6 | a0001c0001t0001g0105 a0001c0001t0001g0298 a0001c0002t0001g0206 others(3): Show |
6 | HG01981.hp1 HG02572.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.2872-484_2872-481d others(6): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 20/56 | INFO_REALIGN_3_PRIME | chr9 | 128588310 | ||||||
| chr9:128588329 | G | T | 1 | a0001c0001t0001g0093 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2872-480G>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 20/56 | chr9 | 128588329 | |||||||
| chr9:128588330 | A | T | 1 | a0001c0001t0001g0093 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2872-479A>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 20/56 | chr9 | 128588330 | |||||||
| chr9:128588437 | G | A | 1 | a0001c0001t0001g0040 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2872-372G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 20/56 | chr9 | 128588437 | |||||||
| chr9:128588468 | C | T | 2 | a0001c0014t0003g0020 a0001c0014t0003g0021 |
2 | HG02559.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2872-341C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 20/56 | chr9 | 128588468 | |||||||
| chr9:128588600 | C | T | 1 | a0001c0007t0001g0272 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2872-209C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 20/56 | chr9 | 128588600 | |||||||
| chr9:128588763 | G | A | 1 | a0001c0001t0001g0091 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2872-46G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 20/56 | chr9 | 128588763 | |||||||
| chr9:128588767 | G | A | 7 | a0001c0002t0001g0012 a0001c0002t0001g0013 a0001c0007t0001g0002 others(4): Show |
8 | HG01884.hp1 HG02615.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.2872-42G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 20/56 | chr9 | 128588767 | |||||||
| chr9:128588966 | G | C | 2 | a0001c0002t0001g0012 a0001c0002t0001g0013 |
2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.3006+23G>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | chr9 | 128588966 | |||||||
| chr9:128589012 | T | C | 2 | a0004c0015t0001g0173 a0004c0015t0001g0185 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.3006+69T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | chr9 | 128589012 | |||||||
| chr9:128589043 | G | C | 1 | a0001c0001t0001g0120 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3006+100G>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | chr9 | 128589043 | |||||||
| chr9:128589260 | C | T | 1 | a0001c0002t0005g0181 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.3006+317C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | chr9 | 128589260 | |||||||
| chr9:128589290 | C | CT | 112 | a0001c0001t0001g0007 a0001c0001t0001g0049 a0001c0001t0001g0055 others(109): Show |
112 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.3006+363dupT | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | INFO_REALIGN_3_PRIME | chr9 | 128589290 | ||||||
| chr9:128589294 | T | TC | 13 | a0001c0002t0001g0189 a0001c0002t0001g0190 a0001c0002t0001g0199 others(10): Show |
13 | HG00609.hp1 HG02080.hp1 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.3006+351_3006+352i others(3): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | chr9 | 128589294 | |||||||
| chr9:128589319 | C | A | 11 | a0002c0004t0001g0278 a0002c0004t0002g0273 a0002c0004t0002g0274 others(8): Show |
11 | HG02040.hp2 HG03669.hp2 HG03688.hp1 others(8): Show |
intron_variant | MODIFIER | c.3006+376C>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | chr9 | 128589319 | |||||||
| chr9:128589319 | C | T | 5 | a0001c0007t0001g0002 a0001c0007t0001g0009 a0001c0007t0001g0010 others(2): Show |
6 | HG01884.hp1 HG02280.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.3006+376C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | chr9 | 128589319 | |||||||
| chr9:128589337 | A | G | 275 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(272): Show |
276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.3006+394A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | chr9 | 128589337 | |||||||
| chr9:128589362 | C | A | 3 | a0001c0001t0001g0128 a0001c0001t0001g0130 a0001c0001t0001g0131 |
3 | HG01361.hp1 HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.3006+419C>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | chr9 | 128589362 | |||||||
| chr9:128589526 | T | C | 1 | a0001c0001t0001g0097 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.3006+583T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | chr9 | 128589526 | |||||||
| chr9:128589566 | G | A | 1 | a0001c0002t0001g0226 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.3006+623G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | chr9 | 128589566 | |||||||
| chr9:128589571 | C | T | 2 | a0001c0001t0001g0062 a0001c0001t0007g0065 |
2 | NA18960.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.3006+628C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | chr9 | 128589571 | |||||||
| chr9:128589572 | G | C | 1 | a0001c0002t0001g0305 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3006+629G>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | chr9 | 128589572 | |||||||
| chr9:128589575 | CT | C | 25 | a0001c0001t0001g0096 a0001c0001t0001g0150 a0001c0001t0001g0156 others(22): Show |
26 | HG01884.hp1 HG02040.hp2 HG02280.hp2 others(23): Show |
intron_variant | MODIFIER | c.3006+650delT | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | INFO_REALIGN_3_PRIME | chr9 | 128589575 | ||||||
| chr9:128589575 | CTT | C | 266 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(263): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.3006+649_3006+650d others(4): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | INFO_REALIGN_3_PRIME | chr9 | 128589575 | ||||||
| chr9:128589604 | C | A | 2 | a0001c0001t0001g0046 a0001c0001t0001g0145 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.3006+661C>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | chr9 | 128589604 | |||||||
| chr9:128589649 | C | T | 7 | a0001c0007t0001g0002 a0001c0007t0001g0009 a0001c0007t0001g0010 others(4): Show |
8 | HG01884.hp1 HG02280.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.3006+706C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | chr9 | 128589649 | |||||||
| chr9:128589686 | C | G | 2 | a0001c0002t0001g0012 a0001c0002t0001g0013 |
2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.3006+743C>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | chr9 | 128589686 | |||||||
| chr9:128589709 | G | A | 1 | a0001c0002t0001g0247 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.3006+766G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | chr9 | 128589709 | |||||||
| chr9:128589732 | C | T | 1 | a0001c0001t0001g0099 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.3006+789C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | chr9 | 128589732 | |||||||
| chr9:128589810 | C | T | 1 | a0001c0007t0001g0272 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3006+867C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | chr9 | 128589810 | |||||||
| chr9:128589822 | G | A | 1 | a0001c0018t0004g0193 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3006+879G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | chr9 | 128589822 | |||||||
| chr9:128589844 | A | G | 291 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(288): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.3006+901A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | chr9 | 128589844 | |||||||
| chr9:128589874 | C | T | 2 | a0001c0014t0003g0020 a0001c0014t0003g0021 |
2 | HG02559.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.3006+931C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | chr9 | 128589874 | |||||||
| chr9:128590182 | A | G | 11 | a0002c0004t0001g0278 a0002c0004t0002g0273 a0002c0004t0002g0274 others(8): Show |
11 | HG02040.hp2 HG03669.hp2 HG03688.hp1 others(8): Show |
intron_variant | MODIFIER | c.3006+1239A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | chr9 | 128590182 | |||||||
| chr9:128590240 | C | T | 3 | a0001c0001t0001g0128 a0001c0001t0001g0130 a0001c0001t0001g0131 |
3 | HG01361.hp1 HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.3007-1237C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | chr9 | 128590240 | |||||||
| chr9:128590288 | G | T | 2 | a0001c0014t0003g0020 a0001c0014t0003g0021 |
2 | HG02559.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.3007-1189G>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | chr9 | 128590288 | |||||||
| chr9:128590390 | G | A | 1 | a0001c0001t0001g0088 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.3007-1087G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | chr9 | 128590390 | |||||||
| chr9:128590436 | G | T | 3 | a0001c0010t0001g0299 a0001c0010t0001g0300 a0001c0010t0001g0301 |
3 | HG02615.hp1 HG02809.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.3007-1041G>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | chr9 | 128590436 | |||||||
| chr9:128590547 | T | TA | 124 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(121): Show |
125 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(122): Show |
intron_variant | MODIFIER | c.3007-924dupA | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | INFO_REALIGN_3_PRIME | chr9 | 128590547 | ||||||
| chr9:128590547 | T | TAA | 23 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(20): Show |
23 | HG01891.hp1 HG01981.hp2 HG02135.hp1 others(20): Show |
intron_variant | MODIFIER | c.3007-925_3007-924d others(4): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | INFO_REALIGN_3_PRIME | chr9 | 128590547 | ||||||
| chr9:128590552 | AAG | A | 7 | a0001c0006t0001g0290 a0001c0006t0001g0291 a0001c0006t0001g0293 others(4): Show |
7 | HG01069.hp1 HG01167.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.3007-923_3007-922d others(4): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | INFO_REALIGN_3_PRIME | chr9 | 128590552 | ||||||
| chr9:128590553 | AG | A | 15 | a0001c0002t0001g0203 a0001c0002t0001g0258 a0001c0002t0001g0269 others(12): Show |
15 | HG01884.hp1 HG02145.hp2 HG02647.hp2 others(12): Show |
intron_variant | MODIFIER | c.3007-923delG | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | chr9 | 128590553 | |||||||
| chr9:128590554 | G | A | 268 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(265): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.3007-923G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | chr9 | 128590554 | |||||||
| chr9:128590589 | C | T | 143 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(140): Show |
144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
intron_variant | MODIFIER | c.3007-888C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | chr9 | 128590589 | |||||||
| chr9:128590661 | C | T | 8 | a0001c0006t0001g0290 a0001c0006t0001g0291 a0001c0006t0001g0292 others(5): Show |
8 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.3007-816C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | chr9 | 128590661 | |||||||
| chr9:128590687 | TAAAATAC others(3): Show |
T | 3 | a0001c0010t0001g0299 a0001c0010t0001g0300 a0001c0010t0001g0301 |
3 | HG02615.hp1 HG02809.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.3007-784_3007-775d others(12): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | INFO_REALIGN_3_PRIME | chr9 | 128590687 | ||||||
| chr9:128590756 | C | T | 143 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(140): Show |
144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
intron_variant | MODIFIER | c.3007-721C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | chr9 | 128590756 | |||||||
| chr9:128590766 | A | G | 293 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(290): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.3007-711A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | chr9 | 128590766 | |||||||
| chr9:128590807 | T | C | 290 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(287): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.3007-670T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | chr9 | 128590807 | |||||||
| chr9:128590841 | C | T | 1 | a0001c0002t0001g0289 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.3007-636C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | chr9 | 128590841 | |||||||
| chr9:128590864 | T | C | 1 | a0001c0003t0001g0031 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.3007-613T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | chr9 | 128590864 | |||||||
| chr9:128590882 | A | C | 2 | a0001c0002t0001g0012 a0001c0002t0001g0013 |
2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.3007-595A>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | chr9 | 128590882 | |||||||
| chr9:128590903 | G | A | 1 | a0005c0020t0001g0008 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.3007-574G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | chr9 | 128590903 | |||||||
| chr9:128590974 | C | T | 262 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(259): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.3007-503C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | chr9 | 128590974 | |||||||
| chr9:128591007 | G | A | 7 | a0001c0007t0001g0002 a0001c0007t0001g0009 a0001c0007t0001g0010 others(4): Show |
8 | HG01884.hp1 HG02280.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.3007-470G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | chr9 | 128591007 | |||||||
| chr9:128591067 | CT | C | 278 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(275): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.3007-400delT | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | INFO_REALIGN_3_PRIME | chr9 | 128591067 | ||||||
| chr9:128591102 | C | T | 272 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(269): Show |
274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.3007-375C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | chr9 | 128591102 | |||||||
| chr9:128591126 | A | G | 1 | a0001c0017t0006g0014 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.3007-351A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | chr9 | 128591126 | |||||||
| chr9:128591265 | A | G | 280 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(277): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.3007-212A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | chr9 | 128591265 | |||||||
| chr9:128591288 | C | G | 280 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(277): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.3007-189C>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | chr9 | 128591288 | |||||||
| chr9:128591313 | G | A | 1 | a0001c0005t0001g0025 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3007-164G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | chr9 | 128591313 | |||||||
| chr9:128591365 | C | T | 1 | a0001c0001t0001g0056 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.3007-112C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | chr9 | 128591365 | |||||||
| chr9:128591438 | G | A | 2 | a0001c0001t0001g0062 a0001c0001t0007g0065 |
2 | NA18960.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.3007-39G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | chr9 | 128591438 | |||||||
| chr9:128591703 | G | A | 2 | a0001c0009t0001g0006 a0001c0009t0001g0027 |
2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.3155+78G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 22/56 | chr9 | 128591703 | |||||||
| chr9:128591710 | G | A | 271 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(268): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.3155+85G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 22/56 | chr9 | 128591710 | |||||||
| chr9:128591778 | G | C | 8 | a0001c0006t0001g0290 a0001c0006t0001g0291 a0001c0006t0001g0292 others(5): Show |
8 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.3155+153G>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 22/56 | chr9 | 128591778 | |||||||
| chr9:128591930 | C | T | 3 | a0001c0010t0001g0299 a0001c0010t0001g0300 a0001c0010t0001g0301 |
3 | HG02615.hp1 HG02809.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.3155+305C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 22/56 | chr9 | 128591930 | |||||||
| chr9:128592182 | T | G | 2 | a0001c0014t0003g0020 a0001c0014t0003g0021 |
2 | HG02559.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.3155+557T>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 22/56 | chr9 | 128592182 | |||||||
| chr9:128592266 | T | C | 11 | a0002c0004t0001g0278 a0002c0004t0002g0273 a0002c0004t0002g0274 others(8): Show |
11 | HG02040.hp2 HG03669.hp2 HG03688.hp1 others(8): Show |
intron_variant | MODIFIER | c.3155+641T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 22/56 | chr9 | 128592266 | |||||||
| chr9:128592277 | CT | C | 262 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(259): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.3155+667delT | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 22/56 | INFO_REALIGN_3_PRIME | chr9 | 128592277 | ||||||
| chr9:128592350 | C | G | 2 | a0001c0002t0001g0256 a0001c0002t0001g0266 |
2 | HG00597.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.3156-633C>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 22/56 | chr9 | 128592350 | |||||||
| chr9:128592461 | G | C | 9 | a0001c0001t0001g0138 a0001c0006t0001g0290 a0001c0006t0001g0291 others(6): Show |
9 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.3156-522G>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 22/56 | chr9 | 128592461 | |||||||
| chr9:128592602 | T | C | 2 | a0001c0002t0001g0012 a0001c0002t0001g0013 |
2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.3156-381T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 22/56 | chr9 | 128592602 | |||||||
| chr9:128592603 | C | T | 1 | a0001c0017t0006g0014 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.3156-380C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 22/56 | chr9 | 128592603 | |||||||
| chr9:128592632 | C | T | 6 | a0001c0008t0001g0167 a0001c0008t0001g0168 a0001c0008t0001g0169 others(3): Show |
6 | HG01099.hp2 HG01496.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.3156-351C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 22/56 | chr9 | 128592632 | |||||||
| chr9:128592762 | C | T | 7 | a0001c0007t0001g0002 a0001c0007t0001g0009 a0001c0007t0001g0010 others(4): Show |
8 | HG01884.hp1 HG02280.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.3156-221C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 22/56 | chr9 | 128592762 | |||||||
| chr9:128593108 | C | T | 1 | a0001c0001t0001g0162 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.3215+66C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 23/56 | chr9 | 128593108 | |||||||
| chr9:128593171 | T | A | 2 | a0002c0004t0002g0276 a0002c0004t0002g0281 |
2 | NA18949.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.3215+129T>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 23/56 | chr9 | 128593171 | |||||||
| chr9:128593485 | T | C | 2 | a0001c0001t0001g0108 a0001c0001t0001g0110 |
2 | NA18942.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.3215+443T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 23/56 | chr9 | 128593485 | |||||||
| chr9:128593533 | A | T | 3 | a0001c0007t0001g0009 a0001c0007t0001g0010 a0001c0007t0001g0011 |
3 | HG01884.hp1 HG02280.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.3215+491A>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 23/56 | chr9 | 128593533 | |||||||
| chr9:128593657 | T | C | 1 | a0001c0014t0003g0020 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.3216-518T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 23/56 | chr9 | 128593657 | |||||||
| chr9:128593747 | T | G | 1 | a0001c0002t0001g0194 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.3216-428T>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 23/56 | chr9 | 128593747 | |||||||
| chr9:128593748 | C | A | 1 | a0001c0002t0001g0194 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.3216-427C>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 23/56 | chr9 | 128593748 | |||||||
| chr9:128594429 | A | AT | 15 | a0001c0002t0001g0189 a0001c0002t0001g0192 a0001c0002t0001g0214 others(12): Show |
15 | HG01099.hp2 HG01496.hp2 HG02080.hp2 others(12): Show |
intron_variant | MODIFIER | c.3414+77dupT | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | INFO_REALIGN_3_PRIME | chr9 | 128594429 | ||||||
| chr9:128594429 | A | ATT | 12 | a0001c0001t0001g0035 a0001c0001t0001g0089 a0001c0001t0001g0101 others(9): Show |
12 | HG02040.hp2 HG02258.hp2 HG03669.hp2 others(9): Show |
intron_variant | MODIFIER | c.3414+76_3414+77dup others(2): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | INFO_REALIGN_3_PRIME | chr9 | 128594429 | ||||||
| chr9:128594429 | A | ATTT | 134 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(131): Show |
135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.3414+75_3414+77dup others(3): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | INFO_REALIGN_3_PRIME | chr9 | 128594429 | ||||||
| chr9:128594429 | A | ATTTT | 7 | a0001c0001t0001g0055 a0001c0001t0001g0073 a0001c0001t0001g0143 others(4): Show |
7 | HG01123.hp2 HG03688.hp2 HG06807.hp2 others(4): Show |
intron_variant | MODIFIER | c.3414+74_3414+77dup others(4): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | INFO_REALIGN_3_PRIME | chr9 | 128594429 | ||||||
| chr9:128594686 | G | C | 11 | a0002c0004t0001g0278 a0002c0004t0002g0273 a0002c0004t0002g0274 others(8): Show |
11 | HG02040.hp2 HG03669.hp2 HG03688.hp1 others(8): Show |
intron_variant | MODIFIER | c.3414+313G>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128594686 | |||||||
| chr9:128594708 | A | G | 1 | a0001c0001t0001g0080 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.3414+335A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128594708 | |||||||
| chr9:128594723 | C | T | 1 | a0001c0007t0001g0010 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3414+350C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128594723 | |||||||
| chr9:128594804 | C | CT | 7 | a0001c0001t0001g0072 a0001c0001t0001g0120 a0001c0001t0001g0135 others(4): Show |
7 | HG01243.hp1 HG02109.hp1 HG03490.hp1 others(4): Show |
intron_variant | MODIFIER | c.3414+450dupT | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | INFO_REALIGN_3_PRIME | chr9 | 128594804 | ||||||
| chr9:128594804 | CT | C | 24 | a0001c0001t0001g0035 a0001c0001t0001g0048 a0001c0001t0001g0076 others(21): Show |
25 | HG00280.hp1 HG01256.hp1 HG02040.hp2 others(22): Show |
intron_variant | MODIFIER | c.3414+450delT | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | INFO_REALIGN_3_PRIME | chr9 | 128594804 | ||||||
| chr9:128594804 | CTT | C | 113 | a0001c0001t0001g0143 a0001c0002t0001g0003 a0001c0002t0001g0004 others(110): Show |
113 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.3414+449_3414+450d others(4): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | INFO_REALIGN_3_PRIME | chr9 | 128594804 | ||||||
| chr9:128594804 | CTTT | C | 16 | a0001c0002t0001g0175 a0001c0002t0001g0200 a0001c0002t0001g0241 others(13): Show |
16 | HG01069.hp1 HG01167.hp2 HG02080.hp1 others(13): Show |
intron_variant | MODIFIER | c.3414+448_3414+450d others(5): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | INFO_REALIGN_3_PRIME | chr9 | 128594804 | ||||||
| chr9:128594826 | A | AT | 6 | a0001c0008t0001g0167 a0001c0008t0001g0168 a0001c0008t0001g0169 others(3): Show |
6 | HG01099.hp2 HG01496.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.3414+466dupT | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | INFO_REALIGN_3_PRIME | chr9 | 128594826 | ||||||
| chr9:128594826 | AT | A | 11 | a0002c0004t0001g0278 a0002c0004t0002g0273 a0002c0004t0002g0274 others(8): Show |
11 | HG02040.hp2 HG03669.hp2 HG03688.hp1 others(8): Show |
intron_variant | MODIFIER | c.3414+466delT | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | INFO_REALIGN_3_PRIME | chr9 | 128594826 | ||||||
| chr9:128594918 | C | T | 7 | a0001c0007t0001g0002 a0001c0007t0001g0009 a0001c0007t0001g0010 others(4): Show |
8 | HG01884.hp1 HG02280.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.3414+545C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128594918 | |||||||
| chr9:128595065 | C | T | 1 | a0001c0001t0001g0100 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.3414+692C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128595065 | |||||||
| chr9:128595069 | C | T | 1 | a0001c0002t0001g0240 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.3414+696C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128595069 | |||||||
| chr9:128595098 | C | T | 2 | a0001c0002t0001g0177 a0001c0002t0001g0243 |
2 | NA18952.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.3414+725C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128595098 | |||||||
| chr9:128595105 | C | T | 3 | a0001c0010t0001g0299 a0001c0010t0001g0300 a0001c0010t0001g0301 |
3 | HG02615.hp1 HG02809.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.3414+732C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128595105 | |||||||
| chr9:128595110 | TCA | T | 116 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0005 others(113): Show |
116 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.3414+738_3414+739d others(4): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128595110 | |||||||
| chr9:128595301 | G | T | 2 | a0001c0001t0001g0068 a0001c0001t0001g0159 |
2 | NA18941.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.3414+928G>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128595301 | |||||||
| chr9:128595362 | A | C | 7 | a0001c0007t0001g0002 a0001c0007t0001g0009 a0001c0007t0001g0010 others(4): Show |
8 | HG01884.hp1 HG02280.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.3414+989A>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128595362 | |||||||
| chr9:128595511 | T | C | 6 | a0001c0007t0001g0002 a0001c0007t0001g0009 a0001c0007t0001g0010 others(3): Show |
7 | HG01884.hp1 HG02280.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.3414+1138T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128595511 | |||||||
| chr9:128595576 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.3414+1203G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128595576 | |||||||
| chr9:128595689 | C | T | 7 | a0001c0007t0001g0002 a0001c0007t0001g0009 a0001c0007t0001g0010 others(4): Show |
8 | HG01884.hp1 HG02280.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.3414+1316C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128595689 | |||||||
| chr9:128595720 | C | T | 11 | a0002c0004t0001g0278 a0002c0004t0002g0273 a0002c0004t0002g0274 others(8): Show |
11 | HG02040.hp2 HG03669.hp2 HG03688.hp1 others(8): Show |
intron_variant | MODIFIER | c.3414+1347C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128595720 | |||||||
| chr9:128595929 | C | T | 11 | a0002c0004t0001g0278 a0002c0004t0002g0273 a0002c0004t0002g0274 others(8): Show |
11 | HG02040.hp2 HG03669.hp2 HG03688.hp1 others(8): Show |
intron_variant | MODIFIER | c.3414+1556C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128595929 | |||||||
| chr9:128596085 | C | G | 8 | a0001c0006t0001g0290 a0001c0006t0001g0291 a0001c0006t0001g0292 others(5): Show |
8 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.3414+1712C>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128596085 | |||||||
| chr9:128596133 | C | T | 1 | a0001c0001t0001g0048 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.3414+1760C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128596133 | |||||||
| chr9:128596140 | G | A | 2 | a0001c0002t0001g0012 a0001c0002t0001g0013 |
2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.3414+1767G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128596140 | |||||||
| chr9:128596209 | A | C | 4 | a0001c0009t0001g0006 a0001c0009t0001g0027 a0001c0009t0001g0028 others(1): Show |
4 | HG01891.hp2 HG02922.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.3414+1836A>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128596209 | |||||||
| chr9:128596299 | CAG | C | 3 | a0001c0010t0001g0299 a0001c0010t0001g0300 a0001c0010t0001g0301 |
3 | HG02615.hp1 HG02809.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.3414+1929_3414+193 others(6): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | INFO_REALIGN_3_PRIME | chr9 | 128596299 | ||||||
| chr9:128596307 | C | T | 130 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0005 others(127): Show |
131 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.3414+1934C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128596307 | |||||||
| chr9:128596341 | A | G | 1 | a0001c0001t0001g0284 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3414+1968A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128596341 | |||||||
| chr9:128596402 | G | A | 131 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0005 others(128): Show |
132 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.3415-1998G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128596402 | |||||||
| chr9:128596433 | C | T | 1 | a0001c0002t0005g0181 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.3415-1967C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128596433 | |||||||
| chr9:128596497 | T | C | 2 | a0001c0002t0001g0012 a0001c0002t0001g0013 |
2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.3415-1903T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128596497 | |||||||
| chr9:128596523 | G | A | 116 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0005 others(113): Show |
116 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.3415-1877G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128596523 | |||||||
| chr9:128596528 | G | A | 11 | a0002c0004t0001g0278 a0002c0004t0002g0273 a0002c0004t0002g0274 others(8): Show |
11 | HG02040.hp2 HG03669.hp2 HG03688.hp1 others(8): Show |
intron_variant | MODIFIER | c.3415-1872G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128596528 | |||||||
| chr9:128596542 | C | T | 1 | a0001c0001t0001g0085 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.3415-1858C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128596542 | |||||||
| chr9:128596566 | A | G | 293 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(290): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.3415-1834A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128596566 | |||||||
| chr9:128596607 | C | A | 2 | a0001c0002t0001g0012 a0001c0002t0001g0013 |
2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.3415-1793C>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128596607 | |||||||
| chr9:128596609 | C | CAAATATA others(9): Show |
2 | a0001c0002t0001g0012 a0001c0002t0001g0013 |
2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.3415-1791_3415-179 others(20): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128596609 | |||||||
| chr9:128596610 | T | G | 2 | a0001c0002t0001g0012 a0001c0002t0001g0013 |
2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.3415-1790T>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128596610 | |||||||
| chr9:128596612 | A | T | 2 | a0001c0002t0001g0012 a0001c0002t0001g0013 |
2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.3415-1788A>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128596612 | |||||||
| chr9:128596613 | A | T | 2 | a0001c0002t0001g0012 a0001c0002t0001g0013 |
2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.3415-1787A>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128596613 | |||||||
| chr9:128596615 | A | T | 2 | a0001c0002t0001g0012 a0001c0002t0001g0013 |
2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.3415-1785A>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128596615 | |||||||
| chr9:128596616 | G | C | 2 | a0001c0002t0001g0012 a0001c0002t0001g0013 |
2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.3415-1784G>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128596616 | |||||||
| chr9:128596617 | G | C | 2 | a0001c0002t0001g0012 a0001c0002t0001g0013 |
2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.3415-1783G>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128596617 | |||||||
| chr9:128596718 | G | T | 3 | a0001c0009t0001g0006 a0001c0009t0001g0027 a0001c0009t0001g0028 |
3 | HG01891.hp2 HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.3415-1682G>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128596718 | |||||||
| chr9:128596755 | A | G | 6 | a0001c0008t0001g0167 a0001c0008t0001g0168 a0001c0008t0001g0169 others(3): Show |
6 | HG01099.hp2 HG01496.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.3415-1645A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128596755 | |||||||
| chr9:128596781 | C | T | 2 | a0001c0002t0001g0012 a0001c0002t0001g0013 |
2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.3415-1619C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128596781 | |||||||
| chr9:128596816 | G | A | 11 | a0002c0004t0001g0278 a0002c0004t0002g0273 a0002c0004t0002g0274 others(8): Show |
11 | HG02040.hp2 HG03669.hp2 HG03688.hp1 others(8): Show |
intron_variant | MODIFIER | c.3415-1584G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128596816 | |||||||
| chr9:128596851 | C | G | 4 | a0001c0002t0001g0192 a0001c0002t0001g0216 a0001c0002t0001g0217 others(1): Show |
4 | HG02451.hp2 HG06807.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.3415-1549C>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128596851 | |||||||
| chr9:128596946 | G | T | 1 | a0002c0004t0002g0282 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.3415-1454G>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128596946 | |||||||
| chr9:128596976 | A | G | 2 | a0001c0002t0001g0012 a0001c0002t0001g0013 |
2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.3415-1424A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128596976 | |||||||
| chr9:128596978 | G | A | 3 | a0001c0010t0001g0299 a0001c0010t0001g0300 a0001c0010t0001g0301 |
3 | HG02615.hp1 HG02809.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.3415-1422G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128596978 | |||||||
| chr9:128597019 | G | A | 1 | a0001c0007t0001g0272 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3415-1381G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128597019 | |||||||
| chr9:128597110 | T | C | 149 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(146): Show |
150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
intron_variant | MODIFIER | c.3415-1290T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128597110 | |||||||
| chr9:128597191 | G | A | 1 | a0001c0001t0001g0151 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.3415-1209G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128597191 | |||||||
| chr9:128597441 | T | C | 7 | a0001c0007t0001g0002 a0001c0007t0001g0009 a0001c0007t0001g0010 others(4): Show |
8 | HG01884.hp1 HG02280.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.3415-959T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128597441 | |||||||
| chr9:128597454 | G | A | 2 | a0001c0001t0001g0135 a0001c0001t0001g0136 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.3415-946G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128597454 | |||||||
| chr9:128597500 | G | C | 1 | a0001c0002t0001g0201 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.3415-900G>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128597500 | |||||||
| chr9:128597641 | G | GTTTTGTT others(4): Show |
1 | a0001c0007t0001g0272 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3415-744_3415-734d others(13): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | INFO_REALIGN_3_PRIME | chr9 | 128597641 | ||||||
| chr9:128597737 | C | T | 113 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0005 others(110): Show |
113 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.3415-663C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128597737 | |||||||
| chr9:128597763 | G | C | 1 | a0001c0005t0001g0025 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3415-637G>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128597763 | |||||||
| chr9:128597775 | C | T | 1 | a0001c0001t0001g0138 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.3415-625C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128597775 | |||||||
| chr9:128597806 | G | A | 9 | a0001c0003t0001g0030 a0001c0003t0001g0095 a0001c0003t0001g0116 others(6): Show |
9 | HG00408.hp1 HG00609.hp2 HG00621.hp1 others(6): Show |
intron_variant | MODIFIER | c.3415-594G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128597806 | |||||||
| chr9:128597947 | C | A | 1 | a0001c0002t0001g0253 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.3415-453C>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128597947 | |||||||
| chr9:128597957 | T | A | 8 | a0001c0006t0001g0290 a0001c0006t0001g0291 a0001c0006t0001g0292 others(5): Show |
8 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.3415-443T>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128597957 | |||||||
| chr9:128598074 | G | A | 3 | a0001c0001t0001g0038 a0001c0001t0001g0090 a0001c0001t0001g0156 |
3 | NA18967.hp1 NA18979.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.3415-326G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128598074 | |||||||
| chr9:128598092 | G | A | 1 | a0001c0001t0001g0109 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3415-308G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128598092 | |||||||
| chr9:128598095 | T | C | 1 | a0001c0030t0001g0285 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.3415-305T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128598095 | |||||||
| chr9:128598168 | G | A | 1 | a0002c0004t0002g0273 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.3415-232G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128598168 | |||||||
| chr9:128598245 | C | T | 2 | a0001c0001t0001g0287 a0001c0001t0001g0288 |
2 | HG00280.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.3415-155C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128598245 | |||||||
| chr9:128598275 | T | C | 4 | a0001c0002t0001g0235 a0001c0007t0001g0047 a0001c0017t0006g0014 others(1): Show |
4 | HG01109.hp2 HG01192.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.3415-125T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128598275 | |||||||
| chr9:128598530 | G | T | 2 | a0001c0002t0001g0012 a0001c0002t0001g0013 |
2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.3519+26G>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 25/56 | chr9 | 128598530 | |||||||
| chr9:128598749 | T | A | 1 | a0001c0001t0001g0119 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.3520-214T>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 25/56 | chr9 | 128598749 | |||||||
| chr9:128598754 | A | G | 8 | a0001c0006t0001g0290 a0001c0006t0001g0291 a0001c0006t0001g0292 others(5): Show |
8 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.3520-209A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 25/56 | chr9 | 128598754 | |||||||
| chr9:128598870 | A | G | 8 | a0001c0006t0001g0290 a0001c0006t0001g0291 a0001c0006t0001g0292 others(5): Show |
8 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.3520-93A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 25/56 | chr9 | 128598870 | |||||||
| chr9:128598949 | C | G | 1 | a0001c0025t0001g0182 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3520-14C>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 25/56 | chr9 | 128598949 | |||||||
| chr9:128599355 | G | A | 8 | a0001c0006t0001g0290 a0001c0006t0001g0291 a0001c0006t0001g0292 others(5): Show |
8 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.3543+369G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 26/56 | chr9 | 128599355 | |||||||
| chr9:128599391 | T | C | 2 | a0001c0001t0001g0046 a0001c0001t0001g0145 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.3543+405T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 26/56 | chr9 | 128599391 | |||||||
| chr9:128599426 | T | C | 291 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(288): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.3543+440T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 26/56 | chr9 | 128599426 | |||||||
| chr9:128599443 | G | A | 2 | a0002c0004t0002g0276 a0002c0004t0002g0281 |
2 | NA18949.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.3543+457G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 26/56 | chr9 | 128599443 | |||||||
| chr9:128599479 | T | A | 1 | a0001c0002t0001g0222 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.3543+493T>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 26/56 | chr9 | 128599479 | |||||||
| chr9:128599482 | G | GGT | 10 | a0002c0004t0001g0278 a0002c0004t0002g0273 a0002c0004t0002g0274 others(7): Show |
10 | HG02040.hp2 HG03669.hp2 HG03688.hp1 others(7): Show |
intron_variant | MODIFIER | c.3543+496_3543+497i others(4): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 26/56 | chr9 | 128599482 | |||||||
| chr9:128599482 | G | GT | 141 | a0001c0001t0001g0035 a0001c0001t0001g0071 a0001c0001t0001g0072 others(138): Show |
142 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.3543+509dupT | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 26/56 | INFO_REALIGN_3_PRIME | chr9 | 128599482 | ||||||
| chr9:128599482 | G | GTT | 8 | a0001c0002t0001g0187 a0001c0002t0001g0191 a0001c0002t0001g0220 others(5): Show |
8 | HG02615.hp1 HG02809.hp1 HG03540.hp1 others(5): Show |
intron_variant | MODIFIER | c.3543+508_3543+509d others(4): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 26/56 | INFO_REALIGN_3_PRIME | chr9 | 128599482 | ||||||
| chr9:128599583 | G | C | 2 | a0001c0002t0001g0012 a0001c0002t0001g0013 |
2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.3544-497G>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 26/56 | chr9 | 128599583 | |||||||
| chr9:128599604 | G | A | 1 | a0001c0001t0001g0162 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.3544-476G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 26/56 | chr9 | 128599604 | |||||||
| chr9:128599633 | C | T | 1 | a0001c0007t0001g0047 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3544-447C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 26/56 | chr9 | 128599633 | |||||||
| chr9:128599685 | T | TA | 133 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0035 others(130): Show |
134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.3544-374dupA | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 26/56 | INFO_REALIGN_3_PRIME | chr9 | 128599685 | ||||||
| chr9:128599685 | T | TAA | 13 | a0001c0001t0001g0034 a0001c0001t0001g0053 a0001c0001t0001g0054 others(10): Show |
13 | HG01099.hp2 HG01496.hp2 HG02027.hp1 others(10): Show |
intron_variant | MODIFIER | c.3544-375_3544-374d others(4): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 26/56 | INFO_REALIGN_3_PRIME | chr9 | 128599685 | ||||||
| chr9:128599685 | TA | T | 118 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0005 others(115): Show |
118 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.3544-374delA | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 26/56 | INFO_REALIGN_3_PRIME | chr9 | 128599685 | ||||||
| chr9:128599685 | TAA | T | 17 | a0001c0002t0001g0195 a0001c0002t0001g0201 a0001c0002t0001g0213 others(14): Show |
17 | HG01069.hp1 HG01256.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.3544-375_3544-374d others(4): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 26/56 | INFO_REALIGN_3_PRIME | chr9 | 128599685 | ||||||
| chr9:128599685 | TAAAA | T | 10 | a0002c0004t0001g0278 a0002c0004t0002g0273 a0002c0004t0002g0274 others(7): Show |
10 | HG02040.hp2 HG03669.hp2 HG03688.hp1 others(7): Show |
intron_variant | MODIFIER | c.3544-377_3544-374d others(6): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 26/56 | INFO_REALIGN_3_PRIME | chr9 | 128599685 | ||||||
| chr9:128599686 | A | T | 3 | a0001c0009t0001g0006 a0001c0009t0001g0027 a0001c0009t0001g0028 |
3 | HG01891.hp2 HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.3544-394A>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 26/56 | chr9 | 128599686 | |||||||
| chr9:128599710 | T | C | 1 | a0001c0006t0001g0293 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.3544-370T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 26/56 | chr9 | 128599710 | |||||||
| chr9:128599788 | T | G | 1 | a0001c0003t0001g0031 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.3544-292T>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 26/56 | chr9 | 128599788 | |||||||
| chr9:128600279 | G | C | 3 | a0001c0010t0001g0299 a0001c0010t0001g0300 a0001c0010t0001g0301 |
3 | HG02615.hp1 HG02809.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.3579+164G>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | chr9 | 128600279 | |||||||
| chr9:128600312 | G | A | 11 | a0002c0004t0001g0278 a0002c0004t0002g0273 a0002c0004t0002g0274 others(8): Show |
11 | HG02040.hp2 HG03669.hp2 HG03688.hp1 others(8): Show |
intron_variant | MODIFIER | c.3579+197G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | chr9 | 128600312 | |||||||
| chr9:128600340 | C | T | 8 | a0001c0006t0001g0290 a0001c0006t0001g0291 a0001c0006t0001g0292 others(5): Show |
8 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.3579+225C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | chr9 | 128600340 | |||||||
| chr9:128600373 | G | A | 3 | a0001c0010t0001g0299 a0001c0010t0001g0300 a0001c0010t0001g0301 |
3 | HG02615.hp1 HG02809.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.3579+258G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | chr9 | 128600373 | |||||||
| chr9:128600702 | ACCCAGGC others(314): Show |
A | 1 | a0001c0001t0001g0044 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.3579+611_3579+931d others(2): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | INFO_REALIGN_3_PRIME | chr9 | 128600702 | ||||||
| chr9:128600809 | T | C | 6 | a0001c0007t0001g0002 a0001c0007t0001g0009 a0001c0007t0001g0010 others(3): Show |
7 | HG01884.hp1 HG02280.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.3579+694T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | chr9 | 128600809 | |||||||
| chr9:128600833 | T | G | 113 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0002t0001g0003 others(110): Show |
113 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.3579+718T>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | chr9 | 128600833 | |||||||
| chr9:128600854 | G | A | 1 | a0002c0004t0002g0281 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.3579+739G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | chr9 | 128600854 | |||||||
| chr9:128600974 | C | CT | 11 | a0001c0002t0001g0033 a0001c0005t0001g0017 a0001c0005t0001g0019 others(8): Show |
11 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.3579+886dupT | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | INFO_REALIGN_3_PRIME | chr9 | 128600974 | ||||||
| chr9:128600974 | C | CTT | 9 | a0001c0006t0001g0292 a0001c0006t0001g0295 a0001c0007t0001g0002 others(6): Show |
10 | HG01069.hp1 HG02145.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.3579+885_3579+886d others(4): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | INFO_REALIGN_3_PRIME | chr9 | 128600974 | ||||||
| chr9:128600974 | C | CTTTTTTT others(2): Show |
21 | a0001c0001t0001g0042 a0001c0001t0001g0045 a0001c0001t0001g0051 others(18): Show |
21 | HG00099.hp1 HG00408.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.3579+878_3579+886d others(11): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | INFO_REALIGN_3_PRIME | chr9 | 128600974 | ||||||
| chr9:128600974 | C | CTTTTTTT others(3): Show |
47 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0035 others(44): Show |
47 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(44): Show |
intron_variant | MODIFIER | c.3579+877_3579+886d others(12): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | INFO_REALIGN_3_PRIME | chr9 | 128600974 | ||||||
| chr9:128600974 | C | CTTTTTTT others(4): Show |
77 | a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0041 others(74): Show |
77 | HG00280.hp2 HG00609.hp1 HG00609.hp2 others(74): Show |
intron_variant | MODIFIER | c.3579+876_3579+886d others(13): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | INFO_REALIGN_3_PRIME | chr9 | 128600974 | ||||||
| chr9:128600974 | C | CTTTTTTT others(5): Show |
43 | a0001c0001t0001g0043 a0001c0001t0001g0058 a0001c0001t0001g0071 others(40): Show |
43 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.3579+875_3579+886d others(14): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | INFO_REALIGN_3_PRIME | chr9 | 128600974 | ||||||
| chr9:128600974 | C | CTTTTTTT others(6): Show |
34 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0082 others(31): Show |
34 | HG00423.hp1 HG00423.hp2 HG01361.hp2 others(31): Show |
intron_variant | MODIFIER | c.3579+874_3579+886d others(15): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | INFO_REALIGN_3_PRIME | chr9 | 128600974 | ||||||
| chr9:128600974 | C | CTTTTTTT others(7): Show |
15 | a0001c0001t0001g0149 a0001c0001t0001g0156 a0001c0001t0001g0284 others(12): Show |
15 | HG01109.hp1 HG01891.hp1 HG02071.hp1 others(12): Show |
intron_variant | MODIFIER | c.3579+873_3579+886d others(16): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | INFO_REALIGN_3_PRIME | chr9 | 128600974 | ||||||
| chr9:128600974 | C | CTTTTTTT others(8): Show |
8 | a0001c0001t0001g0119 a0001c0002t0001g0003 a0001c0002t0001g0005 others(5): Show |
8 | HG00558.hp2 HG01243.hp2 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.3579+872_3579+886d others(17): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | INFO_REALIGN_3_PRIME | chr9 | 128600974 | ||||||
| chr9:128600974 | C | CTTTTTTT others(10): Show |
2 | a0001c0002t0001g0194 a0001c0002t0001g0241 |
2 | NA18967.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.3579+870_3579+886d others(19): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | INFO_REALIGN_3_PRIME | chr9 | 128600974 | ||||||
| chr9:128600974 | CTTT | C | 9 | a0002c0004t0002g0273 a0002c0004t0002g0274 a0002c0004t0002g0275 others(6): Show |
9 | HG02040.hp2 HG03669.hp2 HG03688.hp1 others(6): Show |
intron_variant | MODIFIER | c.3579+884_3579+886d others(5): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | INFO_REALIGN_3_PRIME | chr9 | 128600974 | ||||||
| chr9:128600974 | CTTTTTTT others(5): Show |
C | 6 | a0001c0008t0001g0167 a0001c0008t0001g0168 a0001c0008t0001g0169 others(3): Show |
6 | HG01099.hp2 HG01496.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.3579+875_3579+886d others(14): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | INFO_REALIGN_3_PRIME | chr9 | 128600974 | ||||||
| chr9:128601015 | G | A | 2 | a0001c0002t0001g0012 a0001c0002t0001g0013 |
2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.3579+900G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | chr9 | 128601015 | |||||||
| chr9:128601404 | A | T | 2 | a0001c0002t0001g0012 a0001c0002t0001g0013 |
2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.3579+1289A>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | chr9 | 128601404 | |||||||
| chr9:128601454 | T | G | 7 | a0001c0007t0001g0002 a0001c0007t0001g0009 a0001c0007t0001g0010 others(4): Show |
8 | HG01884.hp1 HG02280.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.3579+1339T>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | chr9 | 128601454 | |||||||
| chr9:128601459 | GCTCACAC others(7): Show |
G | 1 | a0001c0001t0001g0082 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.3579+1346_3579+135 others(18): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | INFO_REALIGN_3_PRIME | chr9 | 128601459 | ||||||
| chr9:128601460 | C | T | 6 | a0001c0008t0001g0167 a0001c0008t0001g0168 a0001c0008t0001g0169 others(3): Show |
6 | HG01099.hp2 HG01496.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.3579+1345C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | chr9 | 128601460 | |||||||
| chr9:128601558 | CAAATAA | C | 113 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0002t0001g0003 others(110): Show |
113 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.3579+1454_3579+145 others(10): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | INFO_REALIGN_3_PRIME | chr9 | 128601558 | ||||||
| chr9:128601640 | C | T | 3 | a0001c0009t0001g0006 a0001c0009t0001g0027 a0001c0009t0001g0028 |
3 | HG01891.hp2 HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.3579+1525C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | chr9 | 128601640 | |||||||
| chr9:128601645 | A | G | 8 | a0001c0006t0001g0290 a0001c0006t0001g0291 a0001c0006t0001g0292 others(5): Show |
8 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.3579+1530A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | chr9 | 128601645 | |||||||
| chr9:128601704 | T | C | 3 | a0001c0010t0001g0299 a0001c0010t0001g0300 a0001c0010t0001g0301 |
3 | HG02615.hp1 HG02809.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.3579+1589T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | chr9 | 128601704 | |||||||
| chr9:128601729 | C | T | 1 | a0001c0002t0001g0243 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.3579+1614C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | chr9 | 128601729 | |||||||
| chr9:128601732 | T | C | 293 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(290): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.3579+1617T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | chr9 | 128601732 | |||||||
| chr9:128601960 | C | A | 11 | a0002c0004t0001g0278 a0002c0004t0002g0273 a0002c0004t0002g0274 others(8): Show |
11 | HG02040.hp2 HG03669.hp2 HG03688.hp1 others(8): Show |
intron_variant | MODIFIER | c.3580-1583C>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | chr9 | 128601960 | |||||||
| chr9:128601973 | G | T | 307 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(304): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.3580-1570G>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | chr9 | 128601973 | |||||||
| chr9:128602053 | T | A | 1 | a0001c0005t0001g0025 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3580-1490T>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | chr9 | 128602053 | |||||||
| chr9:128602190 | T | G | 2 | a0001c0007t0001g0047 a0005c0020t0001g0008 |
2 | HG02922.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.3580-1353T>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | chr9 | 128602190 | |||||||
| chr9:128602191 | T | G | 11 | a0002c0004t0001g0278 a0002c0004t0002g0273 a0002c0004t0002g0274 others(8): Show |
11 | HG02040.hp2 HG03669.hp2 HG03688.hp1 others(8): Show |
intron_variant | MODIFIER | c.3580-1352T>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | chr9 | 128602191 | |||||||
| chr9:128602213 | T | G | 2 | a0001c0001t0001g0102 a0001c0001t0001g0115 |
2 | HG03834.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.3580-1330T>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | chr9 | 128602213 | |||||||
| chr9:128602221 | G | GTT | 8 | a0001c0006t0001g0290 a0001c0006t0001g0291 a0001c0006t0001g0292 others(5): Show |
8 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.3580-1310_3580-130 others(6): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | INFO_REALIGN_3_PRIME | chr9 | 128602221 | ||||||
| chr9:128602225 | T | G | 2 | a0001c0002t0001g0032 a0001c0002t0001g0033 |
2 | NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3580-1318T>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | chr9 | 128602225 | |||||||
| chr9:128602287 | G | T | 36 | a0001c0001t0001g0034 a0001c0001t0001g0039 a0001c0001t0001g0040 others(33): Show |
37 | HG00099.hp1 HG00735.hp2 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.3580-1256G>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | chr9 | 128602287 | |||||||
| chr9:128602312 | G | C | 1 | a0001c0001t0001g0101 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3580-1231G>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | chr9 | 128602312 | |||||||
| chr9:128602313 | T | G | 1 | a0001c0002t0001g0200 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.3580-1230T>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | chr9 | 128602313 | |||||||
| chr9:128602317 | A | G | 2 | a0001c0001t0001g0073 a0001c0001t0001g0075 |
2 | NA18939.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.3580-1226A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | chr9 | 128602317 | |||||||
| chr9:128602463 | C | T | 1 | a0001c0007t0001g0272 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3580-1080C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | chr9 | 128602463 | |||||||
| chr9:128602542 | G | A | 6 | a0001c0008t0001g0167 a0001c0008t0001g0168 a0001c0008t0001g0169 others(3): Show |
6 | HG01099.hp2 HG01496.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.3580-1001G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | chr9 | 128602542 | |||||||
| chr9:128602697 | G | A | 6 | a0001c0001t0001g0036 a0001c0001t0001g0038 a0001c0001t0001g0088 others(3): Show |
6 | NA18954.hp2 NA18964.hp1 NA18967.hp1 others(3): Show |
intron_variant | MODIFIER | c.3580-846G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | chr9 | 128602697 | |||||||
| chr9:128602742 | T | G | 113 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0002t0001g0003 others(110): Show |
113 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.3580-801T>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | chr9 | 128602742 | |||||||
| chr9:128602886 | T | G | 1 | a0001c0001t0001g0162 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.3580-657T>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | chr9 | 128602886 | |||||||
| chr9:128602897 | A | G | 1 | a0001c0002t0001g0215 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.3580-646A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | chr9 | 128602897 | |||||||
| chr9:128602964 | C | CTACGTTG others(8): Show |
10 | a0001c0002t0001g0195 a0002c0004t0001g0278 a0002c0004t0002g0273 others(7): Show |
10 | HG02040.hp2 HG03669.hp2 HG03688.hp1 others(7): Show |
intron_variant | MODIFIER | c.3580-535_3580-521d others(17): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | INFO_REALIGN_3_PRIME | chr9 | 128602964 | ||||||
| chr9:128602964 | CTACGTTG others(8): Show |
C | 4 | a0001c0002t0001g0253 a0001c0010t0001g0299 a0001c0010t0001g0300 others(1): Show |
4 | HG02080.hp2 HG02615.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.3580-535_3580-521d others(17): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | INFO_REALIGN_3_PRIME | chr9 | 128602964 | ||||||
| chr9:128603110 | A | G | 11 | a0002c0004t0001g0278 a0002c0004t0002g0273 a0002c0004t0002g0274 others(8): Show |
11 | HG02040.hp2 HG03669.hp2 HG03688.hp1 others(8): Show |
intron_variant | MODIFIER | c.3580-433A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | chr9 | 128603110 | |||||||
| chr9:128603230 | A | T | 1 | a0001c0001t0001g0045 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.3580-313A>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | chr9 | 128603230 | |||||||
| chr9:128603264 | C | G | 6 | a0001c0008t0001g0167 a0001c0008t0001g0168 a0001c0008t0001g0169 others(3): Show |
6 | HG01099.hp2 HG01496.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.3580-279C>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | chr9 | 128603264 | |||||||
| chr9:128603297 | C | G | 262 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(259): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.3580-246C>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | chr9 | 128603297 | |||||||
| chr9:128603754 | C | T | 1 | a0001c0007t0001g0010 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3627+164C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 28/56 | chr9 | 128603754 | |||||||
| chr9:128603791 | G | A | 141 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(138): Show |
142 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(139): Show |
intron_variant | MODIFIER | c.3627+201G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 28/56 | chr9 | 128603791 | |||||||
| chr9:128603819 | C | T | 1 | a0001c0002t0001g0233 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.3627+229C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 28/56 | chr9 | 128603819 | |||||||
| chr9:128603902 | C | T | 6 | a0001c0008t0001g0167 a0001c0008t0001g0168 a0001c0008t0001g0169 others(3): Show |
6 | HG01099.hp2 HG01496.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.3627+312C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 28/56 | chr9 | 128603902 | |||||||
| chr9:128603977 | G | A | 1 | a0001c0005t0001g0024 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3628-349G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 28/56 | chr9 | 128603977 | |||||||
| chr9:128604127 | T | C | 1 | a0001c0007t0001g0272 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3628-199T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 28/56 | chr9 | 128604127 | |||||||
| chr9:128604148 | A | G | 1 | a0001c0001t0001g0036 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.3628-178A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 28/56 | chr9 | 128604148 | |||||||
| chr9:128604651 | G | C | 3 | a0001c0001t0001g0038 a0001c0001t0001g0090 a0001c0001t0001g0156 |
3 | NA18967.hp1 NA18979.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.3719+234G>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 29/56 | chr9 | 128604651 | |||||||
| chr9:128604820 | A | T | 1 | a0001c0001t0001g0051 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.3720-214A>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 29/56 | chr9 | 128604820 | |||||||
| chr9:128604828 | G | A | 1 | a0001c0016t0001g0026 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.3720-206G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 29/56 | chr9 | 128604828 | |||||||
| chr9:128604907 | G | A | 1 | a0001c0001t0001g0121 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.3720-127G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 29/56 | chr9 | 128604907 | |||||||
| chr9:128605029 | T | G | 3 | a0001c0002t0001g0186 a0004c0015t0001g0173 a0004c0015t0001g0185 |
3 | HG00642.hp1 HG01256.hp2 HG01258.hp1 |
splice_region_variant&intron_variant | LOW | c.3720-5T>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 29/56 | chr9 | 128605029 | |||||||
| chr9:128605480 | A | G | 1 | a0001c0006t0001g0291 | 1 | HG03139.hp1 | splice_region_variant&intron_variant | LOW | c.4046+3A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 31/56 | chr9 | 128605480 | |||||||
| chr9:128605579 | C | T | 11 | a0002c0004t0001g0278 a0002c0004t0002g0273 a0002c0004t0002g0274 others(8): Show |
11 | HG02040.hp2 HG03669.hp2 HG03688.hp1 others(8): Show |
intron_variant | MODIFIER | c.4046+102C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 31/56 | chr9 | 128605579 | |||||||
| chr9:128605632 | T | A | 3 | a0001c0010t0001g0299 a0001c0010t0001g0300 a0001c0010t0001g0301 |
3 | HG02615.hp1 HG02809.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.4046+155T>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 31/56 | chr9 | 128605632 | |||||||
| chr9:128605673 | A | G | 11 | a0002c0004t0001g0278 a0002c0004t0002g0273 a0002c0004t0002g0274 others(8): Show |
11 | HG02040.hp2 HG03669.hp2 HG03688.hp1 others(8): Show |
intron_variant | MODIFIER | c.4046+196A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 31/56 | chr9 | 128605673 | |||||||
| chr9:128605718 | A | G | 299 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(296): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.4046+241A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 31/56 | chr9 | 128605718 | |||||||
| chr9:128605763 | G | A | 11 | a0002c0004t0001g0278 a0002c0004t0002g0273 a0002c0004t0002g0274 others(8): Show |
11 | HG02040.hp2 HG03669.hp2 HG03688.hp1 others(8): Show |
intron_variant | MODIFIER | c.4046+286G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 31/56 | chr9 | 128605763 | |||||||
| chr9:128605764 | G | A | 1 | a0001c0002t0001g0219 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.4046+287G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 31/56 | chr9 | 128605764 | |||||||
| chr9:128605851 | G | T | 6 | a0001c0008t0001g0167 a0001c0008t0001g0168 a0001c0008t0001g0169 others(3): Show |
6 | HG01099.hp2 HG01496.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.4046+374G>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 31/56 | chr9 | 128605851 | |||||||
| chr9:128605975 | A | G | 1 | a0001c0023t0001g0303 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.4046+498A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 31/56 | chr9 | 128605975 | |||||||
| chr9:128605992 | CA | C | 146 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(143): Show |
147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): Show |
intron_variant | MODIFIER | c.4046+530delA | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 31/56 | INFO_REALIGN_3_PRIME | chr9 | 128605992 | ||||||
| chr9:128606082 | G | T | 1 | a0001c0023t0001g0303 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.4046+605G>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 31/56 | chr9 | 128606082 | |||||||
| chr9:128606374 | C | CAAA | 8 | a0001c0006t0001g0290 a0001c0006t0001g0291 a0001c0006t0001g0292 others(5): Show |
8 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.4046+913_4046+915d others(5): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 31/56 | INFO_REALIGN_3_PRIME | chr9 | 128606374 | ||||||
| chr9:128606374 | C | CAAAAAAA | 179 | a0001c0001t0001g0029 a0001c0001t0001g0034 a0001c0001t0001g0035 others(176): Show |
180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.4046+909_4046+915d others(9): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 31/56 | INFO_REALIGN_3_PRIME | chr9 | 128606374 | ||||||
| chr9:128606374 | C | CAAAAAAA others(1): Show |
83 | a0001c0001t0001g0007 a0001c0001t0001g0036 a0001c0001t0001g0037 others(80): Show |
83 | HG00423.hp1 HG00621.hp1 HG00621.hp2 others(80): Show |
intron_variant | MODIFIER | c.4046+908_4046+915d others(10): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 31/56 | INFO_REALIGN_3_PRIME | chr9 | 128606374 | ||||||
| chr9:128606374 | C | CAAAAAAA others(2): Show |
9 | a0001c0001t0001g0057 a0001c0001t0001g0101 a0001c0001t0001g0106 others(6): Show |
9 | HG02258.hp2 HG02572.hp2 HG03471.hp1 others(6): Show |
intron_variant | MODIFIER | c.4046+907_4046+915d others(11): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 31/56 | INFO_REALIGN_3_PRIME | chr9 | 128606374 | ||||||
| chr9:128606374 | CAAAAAAA | C | 6 | a0001c0007t0001g0002 a0001c0007t0001g0009 a0001c0007t0001g0010 others(3): Show |
7 | HG01884.hp1 HG02280.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.4046+909_4046+915d others(9): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 31/56 | INFO_REALIGN_3_PRIME | chr9 | 128606374 | ||||||
| chr9:128606429 | C | T | 1 | a0001c0006t0001g0293 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.4046+952C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 31/56 | chr9 | 128606429 | |||||||
| chr9:128606484 | TA | T | 13 | a0001c0002t0001g0174 a0001c0002t0001g0179 a0001c0002t0001g0237 others(10): Show |
14 | HG01884.hp1 HG02280.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.4046+1008delA | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 31/56 | chr9 | 128606484 | |||||||
| chr9:128606485 | A | T | 12 | a0001c0002t0001g0032 a0001c0009t0001g0006 a0001c0009t0001g0027 others(9): Show |
12 | HG01891.hp2 HG02040.hp2 HG03516.hp2 others(9): Show |
intron_variant | MODIFIER | c.4046+1008A>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 31/56 | chr9 | 128606485 | |||||||
| chr9:128606486 | TA | T | 247 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(244): Show |
248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.4046+1010delA | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 31/56 | chr9 | 128606486 | |||||||
| chr9:128606487 | A | T | 38 | a0001c0001t0001g0099 a0001c0001t0001g0108 a0001c0001t0001g0150 others(35): Show |
39 | HG00597.hp1 HG01192.hp2 HG01884.hp1 others(36): Show |
intron_variant | MODIFIER | c.4046+1010A>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 31/56 | chr9 | 128606487 | |||||||
| chr9:128606488 | T | TA | 8 | a0001c0006t0001g0290 a0001c0006t0001g0291 a0001c0006t0001g0292 others(5): Show |
8 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.4046+1011_4046+101 others(5): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 31/56 | chr9 | 128606488 | |||||||
| chr9:128606495 | T | G | 3 | a0001c0001t0001g0099 a0001c0001t0001g0150 a0001c0001t0001g0151 |
3 | HG00597.hp1 HG01192.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.4046+1018T>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 31/56 | chr9 | 128606495 | |||||||
| chr9:128606496 | T | G | 16 | a0001c0001t0001g0042 a0001c0001t0001g0089 a0001c0001t0001g0094 others(13): Show |
17 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(14): Show |
intron_variant | MODIFIER | c.4046+1019T>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 31/56 | chr9 | 128606496 | |||||||
| chr9:128606497 | T | G | 154 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(151): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.4046+1020T>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 31/56 | chr9 | 128606497 | |||||||
| chr9:128606498 | G | T | 14 | a0001c0001t0001g0102 a0001c0001t0001g0104 a0001c0001t0001g0106 others(11): Show |
14 | HG02040.hp2 HG02647.hp1 HG03471.hp1 others(11): Show |
intron_variant | MODIFIER | c.4046+1021G>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 31/56 | chr9 | 128606498 | |||||||
| chr9:128606499 | G | T | 1 | a0002c0004t0002g0276 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.4046+1022G>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 31/56 | chr9 | 128606499 | |||||||
| chr9:128606506 | A | G | 8 | a0001c0006t0001g0290 a0001c0006t0001g0291 a0001c0006t0001g0292 others(5): Show |
8 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.4046+1029A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 31/56 | chr9 | 128606506 | |||||||
| chr9:128606508 | G | A | 181 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(178): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.4046+1031G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 31/56 | chr9 | 128606508 | |||||||
| chr9:128606593 | C | T | 6 | a0001c0007t0001g0002 a0001c0007t0001g0009 a0001c0007t0001g0010 others(3): Show |
7 | HG01884.hp1 HG02280.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.4047-1011C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 31/56 | chr9 | 128606593 | |||||||
| chr9:128606640 | A | C | 143 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(140): Show |
144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
intron_variant | MODIFIER | c.4047-964A>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 31/56 | chr9 | 128606640 | |||||||
| chr9:128606692 | G | A | 11 | a0002c0004t0001g0278 a0002c0004t0002g0273 a0002c0004t0002g0274 others(8): Show |
11 | HG02040.hp2 HG03669.hp2 HG03688.hp1 others(8): Show |
intron_variant | MODIFIER | c.4047-912G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 31/56 | chr9 | 128606692 | |||||||
| chr9:128606737 | C | T | 1 | a0001c0001t0001g0048 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.4047-867C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 31/56 | chr9 | 128606737 | |||||||
| chr9:128606766 | G | A | 1 | a0001c0002t0001g0222 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.4047-838G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 31/56 | chr9 | 128606766 | |||||||
| chr9:128606893 | C | T | 1 | a0001c0002t0001g0258 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.4047-711C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 31/56 | chr9 | 128606893 | |||||||
| chr9:128606975 | C | T | 1 | a0001c0007t0001g0010 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.4047-629C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 31/56 | chr9 | 128606975 | |||||||
| chr9:128607026 | A | G | 2 | a0001c0002t0001g0032 a0001c0002t0001g0033 |
2 | NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.4047-578A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 31/56 | chr9 | 128607026 | |||||||
| chr9:128607118 | T | C | 293 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(290): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.4047-486T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 31/56 | chr9 | 128607118 | |||||||
| chr9:128607179 | T | C | 11 | a0002c0004t0001g0278 a0002c0004t0002g0273 a0002c0004t0002g0274 others(8): Show |
11 | HG02040.hp2 HG03669.hp2 HG03688.hp1 others(8): Show |
intron_variant | MODIFIER | c.4047-425T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 31/56 | chr9 | 128607179 | |||||||
| chr9:128607215 | A | G | 305 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(302): Show |
307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.4047-389A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 31/56 | chr9 | 128607215 | |||||||
| chr9:128607241 | C | T | 2 | a0001c0001t0001g0007 a0001c0001t0001g0085 |
2 | NA18953.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.4047-363C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 31/56 | chr9 | 128607241 | |||||||
| chr9:128607335 | G | A | 1 | a0001c0002t0001g0187 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.4047-269G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 31/56 | chr9 | 128607335 | |||||||
| chr9:128607363 | C | T | 2 | a0001c0001t0001g0128 a0001c0001t0001g0131 |
2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.4047-241C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 31/56 | chr9 | 128607363 | |||||||
| chr9:128607382 | T | C | 1 | a0002c0004t0002g0276 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.4047-222T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 31/56 | chr9 | 128607382 | |||||||
| chr9:128607551 | G | A | 11 | a0002c0004t0001g0278 a0002c0004t0002g0273 a0002c0004t0002g0274 others(8): Show |
11 | HG02040.hp2 HG03669.hp2 HG03688.hp1 others(8): Show |
intron_variant | MODIFIER | c.4047-53G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 31/56 | chr9 | 128607551 | |||||||
| chr9:128607723 | G | C | 1 | a0001c0001t0001g0302 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.4146+20G>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 32/56 | chr9 | 128607723 | |||||||
| chr9:128608116 | C | T | 1 | a0001c0002t0001g0215 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.4345-14C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 33/56 | chr9 | 128608116 | |||||||
| chr9:128608453 | G | GA | 11 | a0002c0004t0001g0278 a0002c0004t0002g0273 a0002c0004t0002g0274 others(8): Show |
11 | HG02040.hp2 HG03669.hp2 HG03688.hp1 others(8): Show |
intron_variant | MODIFIER | c.4491+177_4491+178i others(3): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 34/56 | chr9 | 128608453 | |||||||
| chr9:128608477 | T | C | 266 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(263): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.4491+201T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 34/56 | chr9 | 128608477 | |||||||
| chr9:128608565 | G | A | 8 | a0001c0006t0001g0290 a0001c0006t0001g0291 a0001c0006t0001g0292 others(5): Show |
8 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.4491+289G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 34/56 | chr9 | 128608565 | |||||||
| chr9:128608691 | A | G | 1 | a0001c0007t0001g0047 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.4492-183A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 34/56 | chr9 | 128608691 | |||||||
| chr9:128608795 | A | G | 2 | a0001c0001t0001g0073 a0001c0001t0001g0075 |
2 | NA18939.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.4492-79A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 34/56 | chr9 | 128608795 | |||||||
| chr9:128608847 | T | A | 1 | a0001c0002t0001g0265 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.4492-27T>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 34/56 | chr9 | 128608847 | |||||||
| chr9:128609393 | G | T | 19 | a0001c0001t0001g0043 a0001c0001t0001g0048 a0001c0001t0001g0096 others(16): Show |
19 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(16): Show |
intron_variant | MODIFIER | c.4758+109G>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 36/56 | chr9 | 128609393 | |||||||
| chr9:128609549 | G | T | 1 | a0001c0001t0001g0088 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.4759-102G>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 36/56 | chr9 | 128609549 | |||||||
| chr9:128609983 | C | T | 2 | a0001c0002t0001g0032 a0001c0002t0001g0033 |
2 | NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.4773+318C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 37/56 | chr9 | 128609983 | |||||||
| chr9:128609988 | G | A | 8 | a0001c0006t0001g0290 a0001c0006t0001g0291 a0001c0006t0001g0292 others(5): Show |
8 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.4773+323G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 37/56 | chr9 | 128609988 | |||||||
| chr9:128610177 | A | G | 2 | a0001c0002t0001g0032 a0001c0002t0001g0033 |
2 | NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.4773+512A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 37/56 | chr9 | 128610177 | |||||||
| chr9:128610332 | G | A | 2 | a0001c0002t0001g0012 a0001c0002t0001g0013 |
2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.4773+667G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 37/56 | chr9 | 128610332 | |||||||
| chr9:128611326 | T | C | 299 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(296): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.4774-388T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 37/56 | chr9 | 128611326 | |||||||
| chr9:128611427 | G | A | 1 | a0002c0004t0001g0278 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.4774-287G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 37/56 | chr9 | 128611427 | |||||||
| chr9:128611491 | A | G | 8 | a0001c0006t0001g0290 a0001c0006t0001g0291 a0001c0006t0001g0292 others(5): Show |
8 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.4774-223A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 37/56 | chr9 | 128611491 | |||||||
| chr9:128611886 | C | G | 291 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(288): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.4905+41C>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 38/56 | chr9 | 128611886 | |||||||
| chr9:128612458 | A | G | 1 | a0001c0001t0001g0070 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.5043+212A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 39/56 | chr9 | 128612458 | |||||||
| chr9:128612629 | A | C | 1 | a0001c0002t0001g0013 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.5043+383A>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 39/56 | chr9 | 128612629 | |||||||
| chr9:128612724 | G | A | 2 | a0001c0001t0001g0081 a0001c0001t0001g0146 |
2 | HG01496.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.5043+478G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 39/56 | chr9 | 128612724 | |||||||
| chr9:128612796 | C | T | 11 | a0002c0004t0001g0278 a0002c0004t0002g0273 a0002c0004t0002g0274 others(8): Show |
11 | HG02040.hp2 HG03669.hp2 HG03688.hp1 others(8): Show |
intron_variant | MODIFIER | c.5043+550C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 39/56 | chr9 | 128612796 | |||||||
| chr9:128612924 | C | CA | 12 | a0001c0002t0001g0235 a0002c0004t0001g0278 a0002c0004t0002g0273 others(9): Show |
12 | HG01192.hp1 HG02040.hp2 HG03669.hp2 others(9): Show |
intron_variant | MODIFIER | c.5044-445dupA | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 39/56 | INFO_REALIGN_3_PRIME | chr9 | 128612924 | ||||||
| chr9:128612937 | T | A | 2 | a0001c0002t0001g0032 a0001c0002t0001g0033 |
2 | NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.5044-444T>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 39/56 | chr9 | 128612937 | |||||||
| chr9:128613054 | G | C | 11 | a0002c0004t0001g0278 a0002c0004t0002g0273 a0002c0004t0002g0274 others(8): Show |
11 | HG02040.hp2 HG03669.hp2 HG03688.hp1 others(8): Show |
intron_variant | MODIFIER | c.5044-327G>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 39/56 | chr9 | 128613054 | |||||||
| chr9:128613105 | G | T | 2 | a0001c0001t0001g0287 a0001c0001t0001g0288 |
2 | HG00280.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.5044-276G>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 39/56 | chr9 | 128613105 | |||||||
| chr9:128613526 | A | G | 11 | a0002c0004t0001g0278 a0002c0004t0002g0273 a0002c0004t0002g0274 others(8): Show |
11 | HG02040.hp2 HG03669.hp2 HG03688.hp1 others(8): Show |
intron_variant | MODIFIER | c.5148+41A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 40/56 | chr9 | 128613526 | |||||||
| chr9:128613554 | A | G | 1 | a0001c0002t0001g0238 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.5148+69A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 40/56 | chr9 | 128613554 | |||||||
| chr9:128613731 | C | T | 11 | a0002c0004t0001g0278 a0002c0004t0002g0273 a0002c0004t0002g0274 others(8): Show |
11 | HG02040.hp2 HG03669.hp2 HG03688.hp1 others(8): Show |
intron_variant | MODIFIER | c.5148+246C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 40/56 | chr9 | 128613731 | |||||||
| chr9:128613802 | G | A | 1 | a0001c0001t0001g0091 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.5148+317G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 40/56 | chr9 | 128613802 | |||||||
| chr9:128613812 | C | T | 1 | a0005c0020t0001g0008 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.5148+327C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 40/56 | chr9 | 128613812 | |||||||
| chr9:128614077 | G | A | 2 | a0001c0002t0001g0012 a0001c0002t0001g0013 |
2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.5148+592G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 40/56 | chr9 | 128614077 | |||||||
| chr9:128614257 | C | T | 1 | a0001c0002t0001g0264 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.5148+772C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 40/56 | chr9 | 128614257 | |||||||
| chr9:128614265 | G | C | 11 | a0002c0004t0001g0278 a0002c0004t0002g0273 a0002c0004t0002g0274 others(8): Show |
11 | HG02040.hp2 HG03669.hp2 HG03688.hp1 others(8): Show |
intron_variant | MODIFIER | c.5148+780G>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 40/56 | chr9 | 128614265 | |||||||
| chr9:128614453 | G | A | 3 | a0001c0009t0001g0006 a0001c0009t0001g0027 a0001c0009t0001g0028 |
3 | HG01891.hp2 HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.5148+968G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 40/56 | chr9 | 128614453 | |||||||
| chr9:128614588 | TCAAAAAA others(4): Show |
T | 2 | a0001c0001t0001g0042 a0001c0001t0001g0151 |
2 | HG01167.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.5149-1030_5149-102 others(15): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 40/56 | INFO_REALIGN_3_PRIME | chr9 | 128614588 | ||||||
| chr9:128614609 | A | C | 4 | a0001c0007t0001g0002 a0001c0007t0001g0009 a0001c0007t0001g0010 others(1): Show |
5 | HG01884.hp1 HG02280.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.5149-1023A>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 40/56 | chr9 | 128614609 | |||||||
| chr9:128614610 | A | C | 15 | a0001c0002t0001g0247 a0001c0006t0001g0290 a0001c0006t0001g0291 others(12): Show |
16 | HG01069.hp1 HG01167.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.5149-1022A>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 40/56 | chr9 | 128614610 | |||||||
| chr9:128614637 | G | A | 11 | a0002c0004t0001g0278 a0002c0004t0002g0273 a0002c0004t0002g0274 others(8): Show |
11 | HG02040.hp2 HG03669.hp2 HG03688.hp1 others(8): Show |
intron_variant | MODIFIER | c.5149-995G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 40/56 | chr9 | 128614637 | |||||||
| chr9:128614832 | C | G | 1 | a0001c0001t0001g0109 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.5149-800C>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 40/56 | chr9 | 128614832 | |||||||
| chr9:128614901 | C | T | 142 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0005 others(139): Show |
143 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.5149-731C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 40/56 | chr9 | 128614901 | |||||||
| chr9:128614957 | A | G | 3 | a0001c0010t0001g0299 a0001c0010t0001g0300 a0001c0010t0001g0301 |
3 | HG02615.hp1 HG02809.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.5149-675A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 40/56 | chr9 | 128614957 | |||||||
| chr9:128615047 | C | G | 1 | a0001c0005t0001g0025 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.5149-585C>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 40/56 | chr9 | 128615047 | |||||||
| chr9:128615155 | G | A | 2 | a0001c0007t0001g0047 a0005c0020t0001g0008 |
2 | HG02922.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.5149-477G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 40/56 | chr9 | 128615155 | |||||||
| chr9:128615445 | G | A | 3 | a0001c0010t0001g0299 a0001c0010t0001g0300 a0001c0010t0001g0301 |
3 | HG02615.hp1 HG02809.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.5149-187G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 40/56 | chr9 | 128615445 | |||||||
| chr9:128615578 | A | G | 1 | a0001c0002t0001g0183 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.5149-54A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 40/56 | chr9 | 128615578 | |||||||
| chr9:128615998 | C | T | 1 | a0001c0017t0006g0014 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.5357+158C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 41/56 | chr9 | 128615998 | |||||||
| chr9:128615999 | G | A | 1 | a0001c0021t0001g0304 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.5357+159G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 41/56 | chr9 | 128615999 | |||||||
| chr9:128616188 | A | G | 3 | a0001c0002t0001g0267 a0001c0002t0001g0268 a0001c0002t0001g0269 |
3 | HG01884.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.5357+348A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 41/56 | chr9 | 128616188 | |||||||
| chr9:128616193 | T | C | 1 | a0001c0007t0001g0047 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.5357+353T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 41/56 | chr9 | 128616193 | |||||||
| chr9:128616403 | G | T | 1 | a0001c0001t0001g0121 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.5357+563G>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 41/56 | chr9 | 128616403 | |||||||
| chr9:128616425 | G | A | 307 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(304): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.5357+585G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 41/56 | chr9 | 128616425 | |||||||
| chr9:128616611 | A | G | 1 | a0001c0007t0001g0047 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.5357+771A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 41/56 | chr9 | 128616611 | |||||||
| chr9:128616640 | G | A | 12 | a0001c0002t0001g0189 a0001c0002t0001g0190 a0001c0002t0001g0206 others(9): Show |
12 | HG02080.hp1 HG02135.hp2 HG02683.hp1 others(9): Show |
intron_variant | MODIFIER | c.5357+800G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 41/56 | chr9 | 128616640 | |||||||
| chr9:128616651 | C | T | 2 | a0001c0002t0001g0012 a0001c0002t0001g0013 |
2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.5357+811C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 41/56 | chr9 | 128616651 | |||||||
| chr9:128616681 | C | T | 3 | a0001c0007t0001g0009 a0001c0007t0001g0010 a0001c0007t0001g0011 |
3 | HG01884.hp1 HG02280.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.5357+841C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 41/56 | chr9 | 128616681 | |||||||
| chr9:128616732 | A | G | 6 | a0001c0008t0001g0167 a0001c0008t0001g0168 a0001c0008t0001g0169 others(3): Show |
6 | HG01099.hp2 HG01496.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.5357+892A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 41/56 | chr9 | 128616732 | |||||||
| chr9:128616777 | T | G | 1 | a0001c0007t0001g0011 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.5358-863T>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 41/56 | chr9 | 128616777 | |||||||
| chr9:128616802 | C | T | 2 | a0001c0002t0001g0012 a0001c0002t0001g0013 |
2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.5358-838C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 41/56 | chr9 | 128616802 | |||||||
| chr9:128616868 | A | G | 139 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0005 others(136): Show |
140 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(137): Show |
intron_variant | MODIFIER | c.5358-772A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 41/56 | chr9 | 128616868 | |||||||
| chr9:128616972 | T | C | 1 | a0001c0001t0001g0071 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.5358-668T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 41/56 | chr9 | 128616972 | |||||||
| chr9:128617162 | C | T | 7 | a0001c0002t0001g0183 a0001c0002t0001g0258 a0001c0002t0001g0259 others(4): Show |
7 | HG02109.hp2 HG02486.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.5358-478C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 41/56 | chr9 | 128617162 | |||||||
| chr9:128617265 | T | A | 1 | a0001c0016t0001g0026 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.5358-375T>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 41/56 | chr9 | 128617265 | |||||||
| chr9:128617426 | C | T | 9 | a0001c0005t0001g0024 a0001c0006t0001g0291 a0001c0006t0001g0293 others(6): Show |
9 | HG01109.hp2 HG02451.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.5358-214C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 41/56 | chr9 | 128617426 | |||||||
| chr9:128617445 | A | G | 6 | a0001c0002t0001g0012 a0001c0002t0001g0013 a0001c0006t0001g0297 others(3): Show |
6 | HG01884.hp1 HG02280.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.5358-195A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 41/56 | chr9 | 128617445 | |||||||
| chr9:128617793 | AG | A | 3 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0298 |
3 | HG02809.hp2 HG02970.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.5478+35delG | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 42/56 | INFO_REALIGN_3_PRIME | chr9 | 128617793 | ||||||
| chr9:128617843 | A | G | 3 | a0001c0010t0001g0299 a0001c0010t0001g0300 a0001c0010t0001g0301 |
3 | HG02615.hp1 HG02809.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.5478+83A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 42/56 | chr9 | 128617843 | |||||||
| chr9:128617870 | C | G | 180 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(177): Show |
181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.5478+110C>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 42/56 | chr9 | 128617870 | |||||||
| chr9:128617946 | A | C | 131 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0005 others(128): Show |
132 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.5479-41A>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 42/56 | chr9 | 128617946 | |||||||
| chr9:128617950 | G | A | 2 | a0001c0002t0001g0012 a0001c0002t0001g0013 |
2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.5479-37G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 42/56 | chr9 | 128617950 | |||||||
| chr9:128618307 | T | A | 1 | a0005c0020t0001g0008 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.5600+199T>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 43/56 | chr9 | 128618307 | |||||||
| chr9:128618552 | C | T | 1 | a0001c0002t0001g0265 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.5601-319C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 43/56 | chr9 | 128618552 | |||||||
| chr9:128618625 | A | G | 1 | a0001c0001t0001g0139 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.5601-246A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 43/56 | chr9 | 128618625 | |||||||
| chr9:128618673 | C | T | 1 | a0001c0001t0001g0162 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.5601-198C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 43/56 | chr9 | 128618673 | |||||||
| chr9:128618684 | C | T | 2 | a0001c0002t0001g0012 a0001c0002t0001g0013 |
2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.5601-187C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 43/56 | chr9 | 128618684 | |||||||
| chr9:128618704 | C | T | 1 | a0001c0002t0001g0188 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.5601-167C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 43/56 | chr9 | 128618704 | |||||||
| chr9:128618715 | T | C | 292 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(289): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.5601-156T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 43/56 | chr9 | 128618715 | |||||||
| chr9:128618765 | G | T | 1 | a0001c0001t0001g0076 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.5601-106G>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 43/56 | chr9 | 128618765 | |||||||
| chr9:128619038 | C | T | 1 | a0001c0001t0001g0147 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.5733+35C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 44/56 | chr9 | 128619038 | |||||||
| chr9:128619196 | T | C | 1 | a0001c0002t0001g0306 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.5733+193T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 44/56 | chr9 | 128619196 | |||||||
| chr9:128619258 | T | C | 3 | a0001c0001t0001g0052 a0001c0001t0001g0064 a0001c0001t0001g0069 |
3 | HG00438.hp2 HG02074.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.5733+255T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 44/56 | chr9 | 128619258 | |||||||
| chr9:128619384 | C | T | 2 | a0001c0002t0001g0032 a0001c0002t0001g0033 |
2 | NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.5733+381C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 44/56 | chr9 | 128619384 | |||||||
| chr9:128619458 | C | A | 8 | a0001c0006t0001g0290 a0001c0006t0001g0291 a0001c0006t0001g0292 others(5): Show |
8 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.5733+455C>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 44/56 | chr9 | 128619458 | |||||||
| chr9:128619583 | C | G | 148 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(145): Show |
149 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(146): Show |
intron_variant | MODIFIER | c.5733+580C>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 44/56 | chr9 | 128619583 | |||||||
| chr9:128619649 | G | C | 142 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(139): Show |
143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.5733+646G>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 44/56 | chr9 | 128619649 | |||||||
| chr9:128619663 | C | G | 102 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0002t0001g0003 others(99): Show |
102 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.5733+660C>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 44/56 | chr9 | 128619663 | |||||||
| chr9:128619678 | G | T | 19 | a0001c0006t0001g0290 a0001c0006t0001g0291 a0001c0006t0001g0292 others(16): Show |
19 | HG01069.hp1 HG01167.hp2 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.5733+675G>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 44/56 | chr9 | 128619678 | |||||||
| chr9:128619735 | A | G | 11 | a0002c0004t0001g0278 a0002c0004t0002g0273 a0002c0004t0002g0274 others(8): Show |
11 | HG02040.hp2 HG03669.hp2 HG03688.hp1 others(8): Show |
intron_variant | MODIFIER | c.5733+732A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 44/56 | chr9 | 128619735 | |||||||
| chr9:128619902 | G | A | 8 | a0001c0006t0001g0290 a0001c0006t0001g0291 a0001c0006t0001g0292 others(5): Show |
8 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.5733+899G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 44/56 | chr9 | 128619902 | |||||||
| chr9:128620188 | A | G | 2 | a0001c0002t0001g0012 a0001c0002t0001g0013 |
2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.5734-970A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 44/56 | chr9 | 128620188 | |||||||
| chr9:128620259 | C | T | 4 | a0001c0007t0001g0002 a0001c0007t0001g0009 a0001c0007t0001g0010 others(1): Show |
5 | HG01884.hp1 HG02280.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.5734-899C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 44/56 | chr9 | 128620259 | |||||||
| chr9:128620365 | T | G | 1 | a0001c0005t0001g0024 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.5734-793T>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 44/56 | chr9 | 128620365 | |||||||
| chr9:128620442 | T | C | 11 | a0002c0004t0001g0278 a0002c0004t0002g0273 a0002c0004t0002g0274 others(8): Show |
11 | HG02040.hp2 HG03669.hp2 HG03688.hp1 others(8): Show |
intron_variant | MODIFIER | c.5734-716T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 44/56 | chr9 | 128620442 | |||||||
| chr9:128620507 | A | G | 3 | a0001c0010t0001g0299 a0001c0010t0001g0300 a0001c0010t0001g0301 |
3 | HG02615.hp1 HG02809.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.5734-651A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 44/56 | chr9 | 128620507 | |||||||
| chr9:128620724 | GA | G | 114 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0002t0001g0003 others(111): Show |
114 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.5734-424delA | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 44/56 | INFO_REALIGN_3_PRIME | chr9 | 128620724 | ||||||
| chr9:128620724 | GAA | G | 11 | a0002c0004t0001g0278 a0002c0004t0002g0273 a0002c0004t0002g0274 others(8): Show |
11 | HG02040.hp2 HG03669.hp2 HG03688.hp1 others(8): Show |
intron_variant | MODIFIER | c.5734-425_5734-424d others(4): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 44/56 | INFO_REALIGN_3_PRIME | chr9 | 128620724 | ||||||
| chr9:128620893 | G | T | 3 | a0001c0001t0001g0102 a0001c0001t0001g0104 a0001c0001t0001g0106 |
3 | HG02647.hp1 HG03471.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.5734-265G>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 44/56 | chr9 | 128620893 | |||||||
| chr9:128621025 | T | C | 2 | a0001c0002t0001g0032 a0001c0002t0001g0033 |
2 | NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.5734-133T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 44/56 | chr9 | 128621025 | |||||||
| chr9:128621278 | G | C | 1 | a0001c0006t0001g0296 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.5832+22G>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 45/56 | chr9 | 128621278 | |||||||
| chr9:128621587 | A | G | 2 | a0001c0002t0001g0012 a0001c0002t0001g0013 |
2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.5832+331A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 45/56 | chr9 | 128621587 | |||||||
| chr9:128621587 | A | T | 1 | a0001c0001t0001g0073 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.5832+331A>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 45/56 | chr9 | 128621587 | |||||||
| chr9:128621619 | A | G | 10 | a0001c0002t0001g0184 a0001c0002t0001g0204 a0001c0002t0001g0210 others(7): Show |
10 | HG01123.hp1 HG01257.hp1 HG01934.hp1 others(7): Show |
intron_variant | MODIFIER | c.5832+363A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 45/56 | chr9 | 128621619 | |||||||
| chr9:128621748 | C | T | 6 | a0001c0007t0001g0002 a0001c0007t0001g0009 a0001c0007t0001g0010 others(3): Show |
7 | HG01884.hp1 HG02280.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.5832+492C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 45/56 | chr9 | 128621748 | |||||||
| chr9:128622090 | A | G | 1 | a0001c0001t0001g0082 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.5832+834A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 45/56 | chr9 | 128622090 | |||||||
| chr9:128622283 | G | A | 6 | a0001c0007t0001g0002 a0001c0007t0001g0009 a0001c0007t0001g0010 others(3): Show |
7 | HG01884.hp1 HG02280.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.5832+1027G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 45/56 | chr9 | 128622283 | |||||||
| chr9:128622293 | C | CT | 122 | a0001c0001t0001g0007 a0001c0001t0001g0038 a0001c0001t0001g0042 others(119): Show |
122 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.5832+1060dupT | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 45/56 | INFO_REALIGN_3_PRIME | chr9 | 128622293 | ||||||
| chr9:128622293 | C | CTT | 27 | a0001c0001t0001g0150 a0001c0002t0001g0004 a0001c0002t0001g0187 others(24): Show |
27 | HG01109.hp1 HG01257.hp1 HG01433.hp1 others(24): Show |
intron_variant | MODIFIER | c.5832+1059_5832+106 others(6): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 45/56 | INFO_REALIGN_3_PRIME | chr9 | 128622293 | ||||||
| chr9:128622323 | G | T | 1 | a0001c0002t0001g0234 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.5832+1067G>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 45/56 | chr9 | 128622323 | |||||||
| chr9:128622521 | A | G | 11 | a0002c0004t0001g0278 a0002c0004t0002g0273 a0002c0004t0002g0274 others(8): Show |
11 | HG02040.hp2 HG03669.hp2 HG03688.hp1 others(8): Show |
intron_variant | MODIFIER | c.5832+1265A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 45/56 | chr9 | 128622521 | |||||||
| chr9:128622580 | T | C | 8 | a0001c0006t0001g0290 a0001c0006t0001g0291 a0001c0006t0001g0292 others(5): Show |
8 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.5832+1324T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 45/56 | chr9 | 128622580 | |||||||
| chr9:128622601 | C | T | 1 | a0001c0022t0001g0260 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.5832+1345C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 45/56 | chr9 | 128622601 | |||||||
| chr9:128622668 | C | T | 1 | a0001c0001t0001g0073 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.5832+1412C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 45/56 | chr9 | 128622668 | |||||||
| chr9:128622669 | T | C | 1 | a0001c0001t0001g0073 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.5832+1413T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 45/56 | chr9 | 128622669 | |||||||
| chr9:128622737 | G | GTTTA | 17 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0005 others(14): Show |
17 | HG02040.hp2 HG02109.hp2 HG02615.hp1 others(14): Show |
intron_variant | MODIFIER | c.5832+1509_5832+151 others(8): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 45/56 | INFO_REALIGN_3_PRIME | chr9 | 128622737 | ||||||
| chr9:128622737 | G | GTTTATTT others(1): Show |
10 | a0001c0002t0001g0238 a0001c0006t0001g0290 a0001c0006t0001g0291 others(7): Show |
10 | HG01069.hp1 HG01109.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.5832+1505_5832+151 others(12): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 45/56 | INFO_REALIGN_3_PRIME | chr9 | 128622737 | ||||||
| chr9:128622944 | G | T | 1 | a0001c0001t0001g0144 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.5833-1384G>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 45/56 | chr9 | 128622944 | |||||||
| chr9:128623095 | G | A | 1 | a0001c0003t0001g0031 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.5833-1233G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 45/56 | chr9 | 128623095 | |||||||
| chr9:128623177 | T | TG | 8 | a0001c0006t0001g0290 a0001c0006t0001g0291 a0001c0006t0001g0292 others(5): Show |
8 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.5833-1151_5833-115 others(5): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 45/56 | chr9 | 128623177 | |||||||
| chr9:128623178 | C | A | 8 | a0001c0006t0001g0290 a0001c0006t0001g0291 a0001c0006t0001g0292 others(5): Show |
8 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.5833-1150C>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 45/56 | chr9 | 128623178 | |||||||
| chr9:128623179 | C | A | 8 | a0001c0006t0001g0290 a0001c0006t0001g0291 a0001c0006t0001g0292 others(5): Show |
8 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.5833-1149C>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 45/56 | chr9 | 128623179 | |||||||
| chr9:128623239 | C | CT | 10 | a0001c0001t0001g0036 a0001c0001t0001g0038 a0001c0001t0001g0088 others(7): Show |
10 | HG02922.hp2 NA18954.hp2 NA18964.hp1 others(7): Show |
intron_variant | MODIFIER | c.5833-1077dupT | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 45/56 | INFO_REALIGN_3_PRIME | chr9 | 128623239 | ||||||
| chr9:128623276 | T | G | 1 | a0001c0001t0001g0298 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.5833-1052T>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 45/56 | chr9 | 128623276 | |||||||
| chr9:128623424 | T | C | 12 | a0001c0001t0001g0052 a0001c0001t0001g0061 a0001c0001t0001g0064 others(9): Show |
12 | HG00408.hp2 HG00438.hp2 HG02074.hp2 others(9): Show |
intron_variant | MODIFIER | c.5833-904T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 45/56 | chr9 | 128623424 | |||||||
| chr9:128623507 | G | A | 11 | a0001c0006t0001g0290 a0001c0006t0001g0291 a0001c0006t0001g0292 others(8): Show |
11 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.5833-821G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 45/56 | chr9 | 128623507 | |||||||
| chr9:128623622 | A | AT | 53 | a0001c0001t0001g0007 a0001c0001t0001g0034 a0001c0001t0001g0046 others(50): Show |
53 | HG00408.hp1 HG00609.hp2 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.5833-684dupT | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 45/56 | INFO_REALIGN_3_PRIME | chr9 | 128623622 | ||||||
| chr9:128623622 | A | ATT | 14 | a0001c0001t0001g0056 a0001c0001t0001g0059 a0001c0001t0001g0144 others(11): Show |
14 | HG01099.hp2 HG01496.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.5833-685_5833-684d others(4): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 45/56 | INFO_REALIGN_3_PRIME | chr9 | 128623622 | ||||||
| chr9:128623622 | AT | A | 106 | a0001c0001t0001g0051 a0001c0001t0001g0149 a0001c0001t0001g0150 others(103): Show |
106 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.5833-684delT | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 45/56 | INFO_REALIGN_3_PRIME | chr9 | 128623622 | ||||||
| chr9:128623622 | ATT | A | 5 | a0001c0002t0001g0192 a0001c0002t0001g0216 a0001c0002t0001g0217 others(2): Show |
6 | HG00735.hp1 HG02451.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.5833-685_5833-684d others(4): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 45/56 | INFO_REALIGN_3_PRIME | chr9 | 128623622 | ||||||
| chr9:128623622 | ATTTTTTT others(1): Show |
A | 10 | a0002c0004t0001g0278 a0002c0004t0002g0273 a0002c0004t0002g0274 others(7): Show |
10 | HG02040.hp2 HG03669.hp2 HG03688.hp1 others(7): Show |
intron_variant | MODIFIER | c.5833-691_5833-684d others(10): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 45/56 | INFO_REALIGN_3_PRIME | chr9 | 128623622 | ||||||
| chr9:128623670 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.5833-658C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 45/56 | chr9 | 128623670 | |||||||
| chr9:128623735 | G | T | 1 | a0001c0001t0001g0036 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.5833-593G>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 45/56 | chr9 | 128623735 | |||||||
| chr9:128623737 | G | A | 1 | a0001c0001t0001g0154 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.5833-591G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 45/56 | chr9 | 128623737 | |||||||
| chr9:128623843 | T | A | 1 | a0001c0016t0001g0026 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.5833-485T>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 45/56 | chr9 | 128623843 | |||||||
| chr9:128623856 | T | C | 144 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0002t0001g0003 others(141): Show |
145 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.5833-472T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 45/56 | chr9 | 128623856 | |||||||
| chr9:128623959 | AT | A | 144 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0002t0001g0003 others(141): Show |
145 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.5833-367delT | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 45/56 | INFO_REALIGN_3_PRIME | chr9 | 128623959 | ||||||
| chr9:128623975 | C | T | 11 | a0002c0004t0001g0278 a0002c0004t0002g0273 a0002c0004t0002g0274 others(8): Show |
11 | HG02040.hp2 HG03669.hp2 HG03688.hp1 others(8): Show |
intron_variant | MODIFIER | c.5833-353C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 45/56 | chr9 | 128623975 | |||||||
| chr9:128624065 | G | A | 1 | a0001c0017t0006g0014 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.5833-263G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 45/56 | chr9 | 128624065 | |||||||
| chr9:128624086 | C | CA | 61 | a0001c0001t0001g0007 a0001c0001t0001g0034 a0001c0001t0001g0039 others(58): Show |
62 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(59): Show |
intron_variant | MODIFIER | c.5833-216dupA | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 45/56 | INFO_REALIGN_3_PRIME | chr9 | 128624086 | ||||||
| chr9:128624086 | C | CAA | 11 | a0001c0001t0001g0045 a0001c0001t0001g0053 a0001c0001t0001g0057 others(8): Show |
11 | HG01192.hp2 HG01981.hp2 HG02027.hp1 others(8): Show |
intron_variant | MODIFIER | c.5833-217_5833-216d others(4): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 45/56 | INFO_REALIGN_3_PRIME | chr9 | 128624086 | ||||||
| chr9:128624086 | CA | C | 15 | a0001c0001t0001g0061 a0001c0001t0001g0136 a0001c0003t0001g0031 others(12): Show |
15 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.5833-216delA | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 45/56 | INFO_REALIGN_3_PRIME | chr9 | 128624086 | ||||||
| chr9:128624086 | CAA | C | 8 | a0002c0004t0002g0273 a0002c0004t0002g0275 a0002c0004t0002g0276 others(5): Show |
8 | HG02040.hp2 HG03688.hp1 NA18968.hp1 others(5): Show |
intron_variant | MODIFIER | c.5833-217_5833-216d others(4): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 45/56 | INFO_REALIGN_3_PRIME | chr9 | 128624086 | ||||||
| chr9:128624086 | CAAAAAAA others(3): Show |
C | 1 | a0001c0002t0001g0267 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.5833-225_5833-216d others(12): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 45/56 | INFO_REALIGN_3_PRIME | chr9 | 128624086 | ||||||
| chr9:128624086 | CAAAAAAA others(4): Show |
C | 112 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0002t0001g0003 others(109): Show |
112 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.5833-226_5833-216d others(13): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 45/56 | INFO_REALIGN_3_PRIME | chr9 | 128624086 | ||||||
| chr9:128624086 | CAAAAAAA others(5): Show |
C | 5 | a0001c0002t0001g0241 a0001c0007t0001g0002 a0001c0007t0001g0009 others(2): Show |
6 | HG01884.hp1 HG02280.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.5833-227_5833-216d others(14): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 45/56 | INFO_REALIGN_3_PRIME | chr9 | 128624086 | ||||||
| chr9:128624166 | G | A | 1 | a0001c0007t0001g0272 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.5833-162G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 45/56 | chr9 | 128624166 | |||||||
| chr9:128624569 | G | C | 1 | a0001c0001t0001g0105 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.5992+82G>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 46/56 | chr9 | 128624569 | |||||||
| chr9:128624739 | CATA | C | 4 | a0001c0002t0001g0307 a0001c0002t0001g0308 a0001c0002t0001g0309 others(1): Show |
4 | NA18948.hp1 NA18960.hp2 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.5992+255_5992+257d others(5): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 46/56 | INFO_REALIGN_3_PRIME | chr9 | 128624739 | ||||||
| chr9:128624820 | C | G | 1 | a0001c0017t0006g0014 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.5993-283C>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 46/56 | chr9 | 128624820 | |||||||
| chr9:128625012 | C | CA | 11 | a0002c0004t0001g0278 a0002c0004t0002g0273 a0002c0004t0002g0274 others(8): Show |
11 | HG02040.hp2 HG03669.hp2 HG03688.hp1 others(8): Show |
intron_variant | MODIFIER | c.5993-85dupA | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 46/56 | INFO_REALIGN_3_PRIME | chr9 | 128625012 | ||||||
| chr9:128625599 | C | T | 11 | a0002c0004t0001g0278 a0002c0004t0002g0273 a0002c0004t0002g0274 others(8): Show |
11 | HG02040.hp2 HG03669.hp2 HG03688.hp1 others(8): Show |
intron_variant | MODIFIER | c.6070-170C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 47/56 | chr9 | 128625599 | |||||||
| chr9:128625628 | T | A | 1 | a0001c0001t0001g0115 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.6070-141T>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 47/56 | chr9 | 128625628 | |||||||
| chr9:128626045 | G | C | 1 | a0001c0007t0001g0272 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.6279+67G>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 48/56 | chr9 | 128626045 | |||||||
| chr9:128626292 | G | A | 1 | a0001c0021t0001g0304 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.6280-99G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 48/56 | chr9 | 128626292 | |||||||
| chr9:128626295 | T | C | 11 | a0002c0004t0001g0278 a0002c0004t0002g0273 a0002c0004t0002g0274 others(8): Show |
11 | HG02040.hp2 HG03669.hp2 HG03688.hp1 others(8): Show |
intron_variant | MODIFIER | c.6280-96T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 48/56 | chr9 | 128626295 | |||||||
| chr9:128626364 | C | T | 143 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(140): Show |
144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
intron_variant | MODIFIER | c.6280-27C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 48/56 | chr9 | 128626364 | |||||||
| chr9:128626781 | C | CAA | 305 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(302): Show |
307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.6576+94_6576+95ins others(2): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 49/56 | chr9 | 128626781 | |||||||
| chr9:128626817 | T | C | 4 | a0001c0009t0001g0006 a0001c0009t0001g0027 a0001c0009t0001g0028 others(1): Show |
4 | HG01891.hp2 HG02922.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.6576+130T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 49/56 | chr9 | 128626817 | |||||||
| chr9:128626817 | T | TC | 14 | a0001c0007t0001g0002 a0001c0007t0001g0009 a0001c0007t0001g0010 others(11): Show |
15 | HG01884.hp1 HG02280.hp2 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.6576+131dupC | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 49/56 | INFO_REALIGN_3_PRIME | chr9 | 128626817 | ||||||
| chr9:128626838 | A | G | 10 | a0002c0004t0001g0278 a0002c0004t0002g0273 a0002c0004t0002g0274 others(7): Show |
10 | HG03669.hp2 HG03688.hp1 NA18949.hp1 others(7): Show |
intron_variant | MODIFIER | c.6576+151A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 49/56 | chr9 | 128626838 | |||||||
| chr9:128626880 | C | A | 15 | a0001c0002t0001g0033 a0001c0009t0001g0006 a0001c0009t0001g0027 others(12): Show |
15 | HG01891.hp2 HG02040.hp2 HG03516.hp2 others(12): Show |
intron_variant | MODIFIER | c.6576+193C>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 49/56 | chr9 | 128626880 | |||||||
| chr9:128626897 | C | G | 2 | a0001c0001t0001g0073 a0001c0001t0001g0075 |
2 | NA18939.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.6576+210C>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 49/56 | chr9 | 128626897 | |||||||
| chr9:128626915 | G | C | 154 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(151): Show |
155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.6576+228G>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 49/56 | chr9 | 128626915 | |||||||
| chr9:128626936 | T | C | 112 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0002t0001g0003 others(109): Show |
112 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.6576+249T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 49/56 | chr9 | 128626936 | |||||||
| chr9:128626971 | C | T | 2 | a0001c0001t0001g0037 a0001c0002t0001g0204 |
2 | HG01123.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.6576+284C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 49/56 | chr9 | 128626971 | |||||||
| chr9:128627125 | TTC | T | 3 | a0001c0007t0001g0009 a0001c0007t0001g0010 a0001c0007t0001g0011 |
3 | HG01884.hp1 HG02280.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.6577-259_6577-258d others(4): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 49/56 | INFO_REALIGN_3_PRIME | chr9 | 128627125 | ||||||
| chr9:128627195 | C | T | 1 | a0001c0002t0001g0178 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.6577-191C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 49/56 | chr9 | 128627195 | |||||||
| chr9:128627202 | G | C | 1 | a0001c0002t0001g0263 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.6577-184G>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 49/56 | chr9 | 128627202 | |||||||
| chr9:128627241 | C | T | 2 | a0001c0007t0001g0047 a0005c0020t0001g0008 |
2 | HG02922.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.6577-145C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 49/56 | chr9 | 128627241 | |||||||
| chr9:128627265 | C | T | 121 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0002t0001g0003 others(118): Show |
121 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.6577-121C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 49/56 | chr9 | 128627265 | |||||||
| chr9:128627515 | G | A | 3 | a0001c0001t0001g0034 a0001c0001t0001g0053 a0001c0001t0001g0054 |
3 | NA18984.hp1 NA18990.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.6689+17G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 50/56 | chr9 | 128627515 | |||||||
| chr9:128627515 | G | C | 1 | a0001c0002t0001g0195 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.6689+17G>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 50/56 | chr9 | 128627515 | |||||||
| chr9:128627517 | C | G | 1 | a0001c0002t0001g0195 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.6689+19C>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 50/56 | chr9 | 128627517 | |||||||
| chr9:128627662 | G | A | 2 | a0001c0001t0001g0128 a0001c0001t0001g0131 |
2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.6689+164G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 50/56 | chr9 | 128627662 | |||||||
| chr9:128628060 | A | G | 6 | a0001c0008t0001g0167 a0001c0008t0001g0168 a0001c0008t0001g0169 others(3): Show |
6 | HG01099.hp2 HG01496.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.6707+118A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 51/56 | chr9 | 128628060 | |||||||
| chr9:128628081 | G | A | 4 | a0001c0007t0001g0002 a0001c0007t0001g0009 a0001c0007t0001g0010 others(1): Show |
5 | HG01884.hp1 HG02280.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.6707+139G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 51/56 | chr9 | 128628081 | |||||||
| chr9:128628096 | G | T | 1 | a0001c0026t0001g0209 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.6707+154G>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 51/56 | chr9 | 128628096 | |||||||
| chr9:128628162 | G | A | 8 | a0001c0006t0001g0290 a0001c0006t0001g0291 a0001c0006t0001g0292 others(5): Show |
8 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.6707+220G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 51/56 | chr9 | 128628162 | |||||||
| chr9:128628193 | C | A | 126 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0002t0001g0003 others(123): Show |
126 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.6707+251C>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 51/56 | chr9 | 128628193 | |||||||
| chr9:128628261 | G | A | 1 | a0001c0002t0001g0255 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.6707+319G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 51/56 | chr9 | 128628261 | |||||||
| chr9:128628326 | G | A | 1 | a0001c0001t0001g0056 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.6707+384G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 51/56 | chr9 | 128628326 | |||||||
| chr9:128628362 | T | C | 3 | a0001c0010t0001g0299 a0001c0010t0001g0300 a0001c0010t0001g0301 |
3 | HG02615.hp1 HG02809.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.6707+420T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 51/56 | chr9 | 128628362 | |||||||
| chr9:128628369 | G | A | 142 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(139): Show |
143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.6707+427G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 51/56 | chr9 | 128628369 | |||||||
| chr9:128628561 | G | A | 8 | a0001c0006t0001g0290 a0001c0006t0001g0291 a0001c0006t0001g0292 others(5): Show |
8 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.6707+619G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 51/56 | chr9 | 128628561 | |||||||
| chr9:128628563 | C | G | 1 | a0001c0001t0001g0061 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.6707+621C>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 51/56 | chr9 | 128628563 | |||||||
| chr9:128628751 | A | G | 1 | a0001c0002t0001g0235 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.6707+809A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 51/56 | chr9 | 128628751 | |||||||
| chr9:128628844 | C | G | 1 | a0001c0010t0001g0299 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.6707+902C>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 51/56 | chr9 | 128628844 | |||||||
| chr9:128628923 | C | T | 1 | a0001c0001t0001g0119 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.6707+981C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 51/56 | chr9 | 128628923 | |||||||
| chr9:128629016 | G | A | 1 | a0001c0007t0001g0047 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.6707+1074G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 51/56 | chr9 | 128629016 | |||||||
| chr9:128629096 | T | C | 1 | a0002c0004t0002g0282 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.6707+1154T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 51/56 | chr9 | 128629096 | |||||||
| chr9:128629139 | G | A | 1 | a0001c0002t0001g0306 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.6708-1182G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 51/56 | chr9 | 128629139 | |||||||
| chr9:128629284 | G | A | 8 | a0001c0006t0001g0290 a0001c0006t0001g0291 a0001c0006t0001g0292 others(5): Show |
8 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.6708-1037G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 51/56 | chr9 | 128629284 | |||||||
| chr9:128629322 | C | T | 4 | a0001c0006t0001g0290 a0001c0006t0001g0292 a0001c0006t0001g0294 others(1): Show |
4 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.6708-999C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 51/56 | chr9 | 128629322 | |||||||
| chr9:128629366 | C | T | 1 | a0002c0004t0002g0276 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.6708-955C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 51/56 | chr9 | 128629366 | |||||||
| chr9:128629506 | T | C | 298 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(295): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.6708-815T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 51/56 | chr9 | 128629506 | |||||||
| chr9:128629541 | C | T | 1 | a0001c0001t0001g0138 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.6708-780C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 51/56 | chr9 | 128629541 | |||||||
| chr9:128629558 | C | T | 1 | a0001c0022t0001g0260 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.6708-763C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 51/56 | chr9 | 128629558 | |||||||
| chr9:128629569 | G | A | 1 | a0001c0002t0001g0032 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.6708-752G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 51/56 | chr9 | 128629569 | |||||||
| chr9:128629579 | G | A | 3 | a0001c0007t0001g0009 a0001c0007t0001g0010 a0001c0007t0001g0011 |
3 | HG01884.hp1 HG02280.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.6708-742G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 51/56 | chr9 | 128629579 | |||||||
| chr9:128629617 | C | T | 1 | a0001c0002t0001g0184 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.6708-704C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 51/56 | chr9 | 128629617 | |||||||
| chr9:128629707 | C | T | 3 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0147 |
3 | HG00140.hp2 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.6708-614C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 51/56 | chr9 | 128629707 | |||||||
| chr9:128629795 | A | G | 3 | a0001c0001t0001g0045 a0001c0001t0001g0139 a0001c0001t0001g0302 |
3 | HG02071.hp2 NA18951.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.6708-526A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 51/56 | chr9 | 128629795 | |||||||
| chr9:128629804 | C | T | 1 | a0001c0002t0001g0230 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.6708-517C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 51/56 | chr9 | 128629804 | |||||||
| chr9:128629828 | G | A | 1 | a0001c0017t0006g0014 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.6708-493G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 51/56 | chr9 | 128629828 | |||||||
| chr9:128630077 | C | T | 11 | a0001c0006t0001g0290 a0001c0006t0001g0291 a0001c0006t0001g0292 others(8): Show |
11 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.6708-244C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 51/56 | chr9 | 128630077 | |||||||
| chr9:128630168 | C | T | 1 | a0001c0002t0001g0253 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.6708-153C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 51/56 | chr9 | 128630168 | |||||||
| chr9:128630243 | C | T | 7 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0082 others(4): Show |
7 | HG00099.hp2 HG00741.hp2 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.6708-78C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 51/56 | chr9 | 128630243 | |||||||
| chr9:128630274 | G | A | 267 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(264): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.6708-47G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 51/56 | chr9 | 128630274 | |||||||
| chr9:128630314 | C | T | 12 | a0001c0002t0001g0032 a0001c0002t0001g0033 a0001c0005t0001g0015 others(9): Show |
12 | HG01891.hp2 HG02055.hp2 HG02109.hp1 others(9): Show |
splice_region_variant&intron_variant | LOW | c.6708-7C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 51/56 | chr9 | 128630314 | |||||||
| chr9:128630568 | C | T | 1 | a0001c0025t0001g0182 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.6762+193C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 52/56 | chr9 | 128630568 | |||||||
| chr9:128630625 | G | GT | 307 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(304): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.6762+251dupT | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 52/56 | INFO_REALIGN_3_PRIME | chr9 | 128630625 | ||||||
| chr9:128630638 | C | T | 1 | a0001c0002t0001g0254 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.6762+263C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 52/56 | chr9 | 128630638 | |||||||
| chr9:128630648 | C | G | 1 | a0001c0016t0001g0026 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.6762+273C>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 52/56 | chr9 | 128630648 | |||||||
| chr9:128630663 | T | G | 293 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(290): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.6762+288T>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 52/56 | chr9 | 128630663 | |||||||
| chr9:128630693 | A | G | 1 | a0002c0004t0002g0282 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.6762+318A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 52/56 | chr9 | 128630693 | |||||||
| chr9:128630980 | A | G | 2 | a0001c0001t0001g0127 a0001c0001t0001g0132 |
2 | HG00741.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.6762+605A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 52/56 | chr9 | 128630980 | |||||||
| chr9:128631103 | C | T | 1 | a0001c0001t0001g0088 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.6762+728C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 52/56 | chr9 | 128631103 | |||||||
| chr9:128631224 | G | A | 2 | a0001c0002t0001g0012 a0001c0002t0001g0013 |
2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.6762+849G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 52/56 | chr9 | 128631224 | |||||||
| chr9:128631369 | G | A | 4 | a0001c0007t0001g0002 a0001c0007t0001g0009 a0001c0007t0001g0010 others(1): Show |
5 | HG01884.hp1 HG02280.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.6763-758G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 52/56 | chr9 | 128631369 | |||||||
| chr9:128631582 | T | C | 1 | a0001c0002t0001g0250 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.6763-545T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 52/56 | chr9 | 128631582 | |||||||
| chr9:128631655 | G | A | 2 | a0001c0002t0001g0012 a0001c0002t0001g0013 |
2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.6763-472G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 52/56 | chr9 | 128631655 | |||||||
| chr9:128631776 | C | T | 2 | a0001c0001t0001g0039 a0001c0001t0001g0057 |
2 | HG02572.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.6763-351C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 52/56 | chr9 | 128631776 | |||||||
| chr9:128631777 | G | A | 5 | a0001c0005t0001g0015 a0001c0005t0001g0016 a0001c0005t0001g0017 others(2): Show |
5 | HG02055.hp2 HG02109.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.6763-350G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 52/56 | chr9 | 128631777 | |||||||
| chr9:128631873 | T | C | 1 | a0001c0006t0001g0293 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.6763-254T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 52/56 | chr9 | 128631873 | |||||||
| chr9:128631880 | C | T | 1 | a0001c0002t0001g0202 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.6763-247C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 52/56 | chr9 | 128631880 | |||||||
| chr9:128631946 | A | G | 1 | a0001c0001t0007g0065 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.6763-181A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 52/56 | chr9 | 128631946 | |||||||
| chr9:128632016 | C | T | 1 | a0001c0001t0001g0072 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.6763-111C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 52/56 | chr9 | 128632016 | |||||||
| chr9:128632018 | A | G | 259 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0034 others(256): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.6763-109A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 52/56 | chr9 | 128632018 | |||||||
| chr9:128632083 | G | A | 2 | a0001c0001t0001g0007 a0001c0001t0001g0085 |
2 | NA18953.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.6763-44G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 52/56 | chr9 | 128632083 | |||||||
| chr9:128632095 | C | T | 1 | a0001c0001t0001g0075 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.6763-32C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 52/56 | chr9 | 128632095 | |||||||
| chr9:128632541 | C | G | 3 | a0001c0001t0001g0057 a0001c0001t0001g0092 a0001c0025t0001g0182 |
3 | HG02572.hp2 HG03130.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.7014-31C>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 54/56 | chr9 | 128632541 | |||||||
| chr9:128632556 | C | T | 1 | a0001c0003t0001g0122 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.7014-16C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 54/56 | chr9 | 128632556 | |||||||
| chr9:128632756 | C | G | 1 | a0001c0002t0001g0266 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.7160+38C>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 55/56 | chr9 | 128632756 | |||||||
| chr9:128632800 | G | A | 1 | a0001c0002t0001g0289 | 1 | HG00735.hp1 | splice_region_variant&intron_variant | LOW | c.7161-8G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 55/56 | chr9 | 128632800 | |||||||
| chr9:128632985 | T | C | 1 | a0001c0007t0001g0047 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.7308+30T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 56/56 | chr9 | 128632985 | |||||||
| chr9:128633005 | C | T | 1 | a0001c0016t0001g0026 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.7308+50C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 56/56 | chr9 | 128633005 |