Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 6687 |
| ensemblid | ENSG00000197912.16 |
| hgncid | 11237 |
| symbol | SPG7 |
| name | SPG7 matrix AAA peptidase subunit, paraplegin |
| refseq_nuc | NM_003119.4 |
| refseq_prot | NP_003110.1 |
| ensembl_nuc | ENST00000645818.2 |
| ensembl_prot | ENSP00000495795.2 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 89508403 |
| end | 89557766 |
| strand | + |
| ver | v1.2 |
| region | chr16:89508403-89557766 |
| region5000 | chr16:89503403-89562766 |
| regionname0 | SPG7_chr16_89508403_89557766 |
| regionname5000 | SPG7_chr16_89503403_89562766 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 795 | 307 | 80 | 69 | 113 | 12 | 32 | 77 | SPG7_chr16_89503403_89562766 | SPG7 | MAVLL others(790): Show |
chr16 | 89503403 | 89562766 |
| a0002 | 0/1 | 795 | 34 | 1 | 4 | 15 | 3 | 10 | 12 | SPG7_chr16_89503403_89562766 | SPG7 | MAVLL others(790): Show |
chr16 | 89503403 | 89562766 |
| a0003 | 0/0 | 795 | 8 | 8 | 0 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | MAVLL others(790): Show |
chr16 | 89503403 | 89562766 |
| a0004 | 0/0 | 795 | 2 | 1 | 0 | 1 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | MAVLL others(790): Show |
chr16 | 89503403 | 89562766 |
| a0005 | 0/0 | 795 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | MAVLL others(790): Show |
chr16 | 89503403 | 89562766 |
| a0006 | 0/0 | 795 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | MAVLL others(790): Show |
chr16 | 89503403 | 89562766 |
| a0007 | 0/0 | 795 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | MAVLL others(790): Show |
chr16 | 89503403 | 89562766 |
| a0008 | 0/0 | 795 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | MAVLL others(790): Show |
chr16 | 89503403 | 89562766 |
| a0009 | 0/0 | 795 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | MAVLL others(790): Show |
chr16 | 89503403 | 89562766 |
| a0010 | 0/0 | 795 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | MAVLL others(790): Show |
chr16 | 89503403 | 89562766 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 2385 | 292 | 73 | 67 | 109 | 10 | 32 | SPG7_chr16_89503403_89562766 | SPG7 | ATGGC others(2380): Show |
chr16 | 89503403 | 89562766 | ||
| a0001c0004 | 0/0 | 2385 | 4 | 1 | 0 | 2 | 1 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | ATGGC others(2380): Show |
chr16 | 89503403 | 89562766 | ||
| a0001c0005 | 0/0 | 2385 | 4 | 4 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | ATGGC others(2380): Show |
chr16 | 89503403 | 89562766 | ||
| a0001c0006 | 0/0 | 2385 | 2 | 0 | 1 | 0 | 1 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | ATGGC others(2380): Show |
chr16 | 89503403 | 89562766 | ||
| a0001c0011 | 0/0 | 2385 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | ATGGC others(2380): Show |
chr16 | 89503403 | 89562766 | ||
| a0001c0012 | 0/0 | 2385 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | ATGGC others(2380): Show |
chr16 | 89503403 | 89562766 | ||
| a0001c0013 | 0/0 | 2385 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | ATGGC others(2380): Show |
chr16 | 89503403 | 89562766 | ||
| a0001c0016 | 0/0 | 2385 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | ATGGC others(2380): Show |
chr16 | 89503403 | 89562766 | ||
| a0001c0019 | 0/0 | 2385 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | ATGGC others(2380): Show |
chr16 | 89503403 | 89562766 | ||
| a0002c0002 | 0/1 | 2385 | 33 | 1 | 4 | 15 | 3 | 9 | SPG7_chr16_89503403_89562766 | SPG7 | ATGGC others(2380): Show |
chr16 | 89503403 | 89562766 | ||
| a0002c0015 | 0/0 | 2385 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | ATGGC others(2380): Show |
chr16 | 89503403 | 89562766 | ||
| a0003c0003 | 0/0 | 2385 | 8 | 8 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | ATGGC others(2380): Show |
chr16 | 89503403 | 89562766 | ||
| a0004c0008 | 0/0 | 2385 | 2 | 1 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | ATGGC others(2380): Show |
chr16 | 89503403 | 89562766 | ||
| a0005c0007 | 0/0 | 2385 | 2 | 2 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | ATGGC others(2380): Show |
chr16 | 89503403 | 89562766 | ||
| a0006c0014 | 0/0 | 2385 | 1 | 0 | 0 | 0 | 1 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | ATGGC others(2380): Show |
chr16 | 89503403 | 89562766 | ||
| a0007c0017 | 0/0 | 2385 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | ATGGC others(2380): Show |
chr16 | 89503403 | 89562766 | ||
| a0008c0009 | 0/0 | 2385 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | ATGGC others(2380): Show |
chr16 | 89503403 | 89562766 | ||
| a0009c0018 | 0/0 | 2385 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | ATGGC others(2380): Show |
chr16 | 89503403 | 89562766 | ||
| a0010c0010 | 0/0 | 2385 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | ATGGC others(2380): Show |
chr16 | 89503403 | 89562766 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 3076 | 271 | 57 | 66 | 108 | 10 | 29 | SPG7_chr16_89503403_89562766 | SPG7 | GGCTT others(3071): Show |
chr16 | 89503403 | 89562766 |
| a0001c0001t0002 | 0/0 | 3080 | 11 | 7 | 1 | 1 | 0 | 2 | SPG7_chr16_89503403_89562766 | SPG7 | GGCTT others(3075): Show |
chr16 | 89503403 | 89562766 |
| a0001c0001t0003 | 0/0 | 3080 | 4 | 4 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | GGCTT others(3075): Show |
chr16 | 89503403 | 89562766 |
| a0001c0001t0004 | 0/0 | 3076 | 4 | 4 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | GGCTT others(3071): Show |
chr16 | 89503403 | 89562766 |
| a0001c0001t0007 | 0/0 | 3080 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | GGCTT others(3075): Show |
chr16 | 89503403 | 89562766 |
| a0001c0001t0008 | 0/0 | 3076 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | GGCTT others(3071): Show |
chr16 | 89503403 | 89562766 |
| a0001c0004t0001 | 0/0 | 3076 | 4 | 1 | 0 | 2 | 1 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | GGCTT others(3071): Show |
chr16 | 89503403 | 89562766 |
| a0001c0005t0005 | 0/0 | 3080 | 2 | 2 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | GGCTT others(3075): Show |
chr16 | 89503403 | 89562766 |
| a0001c0005t0009 | 0/0 | 3080 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | GGCTT others(3075): Show |
chr16 | 89503403 | 89562766 |
| a0001c0005t0010 | 0/0 | 3080 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | GGCTT others(3075): Show |
chr16 | 89503403 | 89562766 |
| a0001c0006t0001 | 0/0 | 3076 | 2 | 0 | 1 | 0 | 1 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | GGCTT others(3071): Show |
chr16 | 89503403 | 89562766 |
| a0001c0011t0001 | 0/0 | 3076 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | GGCTT others(3071): Show |
chr16 | 89503403 | 89562766 |
| a0001c0012t0001 | 0/0 | 3076 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | GGCTT others(3071): Show |
chr16 | 89503403 | 89562766 |
| a0001c0013t0003 | 0/0 | 3080 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | GGCTT others(3075): Show |
chr16 | 89503403 | 89562766 |
| a0001c0016t0001 | 0/0 | 3076 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | GGCTT others(3071): Show |
chr16 | 89503403 | 89562766 |
| a0001c0019t0003 | 0/0 | 3080 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | GGCTT others(3075): Show |
chr16 | 89503403 | 89562766 |
| a0002c0002t0002 | 0/1 | 3080 | 32 | 1 | 4 | 14 | 3 | 9 | SPG7_chr16_89503403_89562766 | SPG7 | GGCTT others(3075): Show |
chr16 | 89503403 | 89562766 |
| a0002c0002t0006 | 0/0 | 3080 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | GGCTT others(3075): Show |
chr16 | 89503403 | 89562766 |
| a0002c0015t0002 | 0/0 | 3080 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | GGCTT others(3075): Show |
chr16 | 89503403 | 89562766 |
| a0003c0003t0002 | 0/0 | 3080 | 8 | 8 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | GGCTT others(3075): Show |
chr16 | 89503403 | 89562766 |
| a0004c0008t0002 | 0/0 | 3080 | 2 | 1 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | GGCTT others(3075): Show |
chr16 | 89503403 | 89562766 |
| a0005c0007t0001 | 0/0 | 3076 | 2 | 2 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | GGCTT others(3071): Show |
chr16 | 89503403 | 89562766 |
| a0006c0014t0001 | 0/0 | 3076 | 1 | 0 | 0 | 0 | 1 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | GGCTT others(3071): Show |
chr16 | 89503403 | 89562766 |
| a0007c0017t0001 | 0/0 | 3076 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | GGCTT others(3071): Show |
chr16 | 89503403 | 89562766 |
| a0008c0009t0001 | 0/0 | 3076 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | GGCTT others(3071): Show |
chr16 | 89503403 | 89562766 |
| a0009c0018t0001 | 0/0 | 3076 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | GGCTT others(3071): Show |
chr16 | 89503403 | 89562766 |
| a0010c0010t0001 | 0/0 | 3076 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | GGCTT others(3071): Show |
chr16 | 89503403 | 89562766 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0336 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0002g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0002g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0002g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0003g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0003g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0003g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0003g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0004g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0004g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0004g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0004g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0007g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0008g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0004t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0004t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0004t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0004t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0005t0005g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0005t0005g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0005t0009g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0005t0010g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0006t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0006t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0011t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0012t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0013t0003g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0016t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0019t0003g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0002c0002t0002g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0002c0002t0002g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0002c0002t0002g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0002c0002t0002g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0002c0002t0002g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0002c0002t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0002c0002t0002g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0002c0002t0002g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0002c0002t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0002c0002t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0002c0002t0002g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0002c0002t0002g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0002c0002t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0002c0002t0002g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0002c0002t0002g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0002c0002t0002g0027 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0002c0002t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0002c0002t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0002c0002t0002g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0002c0002t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0002c0002t0002g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0002c0002t0002g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0002c0002t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0002c0002t0002g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0002c0002t0002g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0002c0002t0002g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0002c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0002c0002t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0002c0002t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0002c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0002c0002t0002g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0002c0002t0002g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0002c0002t0006g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0002c0015t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0003c0003t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0003c0003t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0003c0003t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0003c0003t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0003c0003t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0003c0003t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0003c0003t0002g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0003c0003t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0004c0008t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0004c0008t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0005c0007t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0005c0007t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0006c0014t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0007c0017t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0008c0009t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0009c0018t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0010c0010t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0006 | c0014 | t0001 | g0262 | EUR | GBR | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0135 | EUR | GBR | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0213 | EUR | GBR | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0263 | EUR | GBR | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG00280 | hp1 | a0001 | c0004 | t0001 | g0300 | EUR | FIN | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0153 | EUR | FIN | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG00323 | hp1 | a0002 | c0002 | t0002 | g0017 | EUR | FIN | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0269 | EUR | FIN | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | CHS | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | CHS | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | CHS | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | CHS | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | CHS | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | CHS | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | CHS | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | CHS | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG00621 | hp1 | a0002 | c0002 | t0002 | g0018 | EAS | CHS | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | CHS | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | CHS | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG00673 | hp2 | a0002 | c0002 | t0002 | g0042 | EAS | CHS | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | PUR | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG00741 | hp2 | a0002 | c0002 | t0002 | g0035 | AMR | PUR | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01074 | hp1 | a0001 | c0006 | t0001 | g0058 | AMR | PUR | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0222 | AMR | PUR | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0290 | AMR | PUR | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01106 | hp1 | a0007 | c0017 | t0001 | g0152 | AMR | PUR | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0293 | AMR | PUR | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0314 | AMR | PUR | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0316 | AMR | PUR | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0327 | AMR | PUR | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0212 | AMR | PUR | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0242 | AMR | PUR | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01255 | hp1 | a0002 | c0002 | t0002 | g0014 | AMR | CLM | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0264 | AMR | CLM | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | CLM | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | CLM | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0265 | AMR | CLM | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0289 | AMR | CLM | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0304 | AMR | CLM | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | CLM | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | CLM | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | CLM | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | CLM | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | CLM | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | CLM | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0267 | EUR | IBS | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01515 | hp2 | a0002 | c0002 | t0002 | g0025 | EUR | IBS | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0132 | EUR | IBS | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01516 | hp2 | a0001 | c0006 | t0001 | g0104 | EUR | IBS | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0131 | EUR | IBS | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01517 | hp2 | a0002 | c0002 | t0002 | g0036 | EUR | IBS | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01884 | hp1 | a0004 | c0008 | t0002 | g0105 | AFR | ACB | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01884 | hp2 | a0005 | c0007 | t0001 | g0297 | AFR | ACB | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01891 | hp1 | a0003 | c0003 | t0002 | g0211 | AFR | ACB | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01891 | hp2 | a0001 | c0013 | t0003 | g0341 | AFR | ACB | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PEL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01928 | hp2 | a0001 | c0016 | t0001 | g0288 | AMR | PEL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0266 | AMR | PEL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | PEL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0311 | AMR | PEL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PEL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0276 | AMR | PEL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0261 | AMR | PEL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0319 | AMR | PEL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01978 | hp2 | a0002 | c0002 | t0002 | g0038 | AMR | PEL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0301 | AMR | PEL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | KHV | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | KHV | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | KHV | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | KHV | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | KHV | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | KHV | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0348 | AFR | ACB | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0339 | AFR | ACB | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | KHV | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0342 | EAS | KHV | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | KHV | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | KHV | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02080 | hp1 | a0001 | c0012 | t0001 | g0063 | EAS | KHV | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0352 | EAS | KHV | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | KHV | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | KHV | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | KHV | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | KHV | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | KHV | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02132 | hp2 | a0002 | c0002 | t0002 | g0012 | EAS | KHV | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02145 | hp1 | a0005 | c0007 | t0001 | g0298 | AFR | ACB | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | ACB | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PEL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0312 | AMR | PEL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | CDX | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | CDX | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | CDX | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | CDX | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0349 | AFR | ACB | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0313 | AFR | ACB | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0275 | AFR | ACB | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02258 | hp2 | a0001 | c0005 | t0010 | g0238 | AFR | ACB | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0272 | AMR | PEL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PEL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0344 | AFR | ACB | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | ACB | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02300 | hp1 | a0002 | c0002 | t0002 | g0024 | AMR | PEL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PEL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0251 | AFR | ACB | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02451 | hp2 | a0003 | c0003 | t0002 | g0236 | AFR | ACB | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | KHV | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | KHV | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0233 | AFR | GWD | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02572 | hp2 | a0002 | c0002 | t0002 | g0009 | AFR | GWD | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0026 | SAS | PJL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0280 | SAS | PJL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0324 | AFR | GWD | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02615 | hp2 | a0003 | c0003 | t0002 | g0057 | AFR | GWD | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | GWD | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0325 | AFR | GWD | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | GWD | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0334 | AFR | GWD | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0194 | SAS | PJL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0299 | SAS | PJL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02717 | hp1 | a0003 | c0003 | t0002 | g0234 | AFR | GWD | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | GWD | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0253 | AFR | GWD | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02723 | hp2 | a0001 | c0001 | t0004 | g0201 | AFR | GWD | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02735 | hp1 | a0002 | c0002 | t0002 | g0016 | SAS | PJL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0230 | AFR | GWD | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0224 | AFR | GWD | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0328 | AFR | GWD | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0323 | AFR | GWD | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | GWD | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0228 | AFR | GWD | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0330 | AFR | GWD | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02896 | hp2 | a0001 | c0001 | t0004 | g0205 | AFR | GWD | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0331 | AFR | GWD | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0303 | AFR | GWD | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0260 | AFR | ESN | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0295 | AFR | ESN | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | ESN | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02965 | hp2 | a0001 | c0019 | t0003 | g0220 | AFR | ESN | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02970 | hp1 | a0003 | c0003 | t0002 | g0237 | AFR | ESN | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02970 | hp2 | a0003 | c0003 | t0002 | g0056 | AFR | ESN | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | ESN | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0239 | AFR | ESN | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0279 | SAS | PJL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG03017 | hp2 | a0001 | c0001 | t0007 | g0010 | SAS | PJL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0249 | AFR | GWD | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG03041 | hp2 | a0003 | c0003 | t0002 | g0235 | AFR | GWD | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0326 | AFR | MSL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0329 | AFR | MSL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0255 | AFR | ESN | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG03130 | hp2 | a0001 | c0001 | t0004 | g0203 | AFR | ESN | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0346 | AFR | ESN | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0232 | AFR | ESN | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0332 | AFR | ESN | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0333 | AFR | ESN | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG03209 | hp1 | a0001 | c0001 | t0008 | g0306 | AFR | MSL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | MSL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0345 | AFR | MSL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | MSL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0268 | SAS | PJL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | MSL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0247 | AFR | MSL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG03486 | hp1 | a0001 | c0001 | t0003 | g0296 | AFR | MSL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0204 | AFR | MSL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0199 | SAS | PJL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG03491 | hp2 | a0002 | c0002 | t0002 | g0011 | SAS | PJL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0069 | SAS | PJL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG03492 | hp2 | a0002 | c0002 | t0002 | g0034 | SAS | PJL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | ESN | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | ESN | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0337 | AFR | GWD | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG03579 | hp1 | a0001 | c0005 | t0009 | g0340 | AFR | MSL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0338 | AFR | MSL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0107 | SAS | STU | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG03688 | hp2 | a0002 | c0002 | t0002 | g0030 | SAS | STU | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG03704 | hp1 | a0002 | c0002 | t0002 | g0021 | SAS | PJL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0198 | SAS | PJL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0133 | SAS | PJL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0271 | SAS | BEB | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0175 | SAS | BEB | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG03834 | hp1 | a0002 | c0015 | t0002 | g0041 | SAS | BEB | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0193 | SAS | BEB | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0287 | SAS | BEB | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG03927 | hp2 | a0002 | c0002 | t0002 | g0037 | SAS | BEB | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | BEB | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0155 | SAS | BEB | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0315 | SAS | STU | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0046 | SAS | STU | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG04184 | hp1 | a0002 | c0002 | t0002 | g0033 | SAS | BEB | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG04184 | hp2 | a0002 | c0002 | t0002 | g0171 | SAS | BEB | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0254 | SAS | STU | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0150 | SAS | STU | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0139 | SAS | STU | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0031 | SAS | STU | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG04228 | hp1 | a0002 | c0002 | t0002 | g0020 | SAS | STU | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0138 | SAS | STU | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | YRI | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0350 | AFR | YRI | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | CHB | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | CHB | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18747 | hp1 | a0008 | c0009 | t0001 | g0120 | EAS | CHB | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | CHB | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18940 | hp1 | a0002 | c0002 | t0002 | g0028 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18942 | hp1 | a0002 | c0002 | t0002 | g0039 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18945 | hp2 | a0002 | c0002 | t0002 | g0022 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18953 | hp1 | a0001 | c0004 | t0001 | g0308 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18960 | hp1 | a0002 | c0002 | t0006 | g0001 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18960 | hp2 | a0002 | c0002 | t0002 | g0072 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18972 | hp1 | a0002 | c0002 | t0002 | g0351 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18975 | hp1 | a0001 | c0004 | t0001 | g0008 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18983 | hp1 | a0002 | c0002 | t0002 | g0029 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18984 | hp2 | a0002 | c0002 | t0002 | g0032 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18989 | hp1 | a0001 | c0011 | t0001 | g0181 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18991 | hp1 | a0004 | c0008 | t0002 | g0318 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18994 | hp2 | a0009 | c0018 | t0001 | g0246 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18995 | hp1 | a0002 | c0002 | t0002 | g0015 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0343 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA19010 | hp2 | a0010 | c0010 | t0001 | g0240 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0270 | AFR | LWK | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA19030 | hp2 | a0001 | c0005 | t0005 | g0305 | AFR | LWK | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0335 | AFR | LWK | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA19043 | hp2 | a0001 | c0001 | t0003 | g0347 | AFR | LWK | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA19077 | hp2 | a0002 | c0002 | t0002 | g0040 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA19085 | hp1 | a0002 | c0002 | t0002 | g0019 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA19088 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA20129 | hp1 | a0001 | c0004 | t0001 | g0179 | AFR | ASW | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | ASW | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0013 | EUR | TSI | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0283 | EUR | TSI | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | CLM | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0307 | AMR | CLM | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | ACB | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | ACB | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | ACB | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | ACB | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02559 | hp1 | a0001 | c0005 | t0005 | g0302 | AFR | ACB | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | ACB | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | MSL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | MSL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0294 | AFR | USA | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG06807 | hp2 | a0003 | c0003 | t0002 | g0055 | AFR | USA | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA20300 | hp1 | a0001 | c0001 | t0004 | g0202 | AFR | USA | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0309 | AFR | USA | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0320 | AFR | LWK | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | LWK | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0002 | g0027 | REF | REF | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0336 | REF | REF | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:89513008 | C | T | 1 | a0009 | 1 | NA18994.hp2 | missense_variant | MODERATE | c.347C>T | p.Ser116Leu | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/17 | 362/3076 | 347/2388 | 116/795 | chr16 | 89513008 | |||
| chr16:89526366 | T | C | 1 | a0008 | 1 | NA18747.hp1 | missense_variant | MODERATE | c.656T>C | p.Ile219Thr | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/17 | 671/3076 | 656/2388 | 219/795 | chr16 | 89526366 | |||
| chr16:89530702 | G | A | 1 | a0005 | 2 | HG01884.hp2 HG02145.hp1 |
missense_variant | MODERATE | c.881G>A | p.Arg294His | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 7/17 | 896/3076 | 881/2388 | 294/795 | chr16 | 89530702 | |||
| chr16:89530785 | C | T | 1 | a0007 | 1 | HG01106.hp1 | missense_variant | MODERATE | c.964C>T | p.Arg322Cys | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 7/17 | 979/3076 | 964/2388 | 322/795 | chr16 | 89530785 | |||
| chr16:89532480 | G | C | 1 | a0010 | 1 | NA19010.hp2 | missense_variant | MODERATE | c.1168G>C | p.Val390Leu | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/17 | 1183/3076 | 1168/2388 | 390/795 | chr16 | 89532480 | |||
| chr16:89546715 | A | G | 1 | a0002 | 33 | HG00323.hp1 HG00621.hp1 HG00673.hp2 others(30): Show |
missense_variant | MODERATE | c.1507A>G | p.Thr503Ala | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 11/17 | 1522/3076 | 1507/2388 | 503/795 | chr16 | 89546715 | |||
| chr16:89546737 | C | T | 1 | a0006 | 1 | HG00099.hp1 | missense_variant | MODERATE | c.1529C>T | p.Ala510Val | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 11/17 | 1544/3076 | 1529/2388 | 510/795 | chr16 | 89546737 | |||
| chr16:89553920 | G | A | 2 | a0002 a0004 |
35 | HG00323.hp1 HG00621.hp1 HG00673.hp2 others(32): Show |
missense_variant | MODERATE | c.2063G>A | p.Arg688Gln | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 15/17 | 2078/3076 | 2063/2388 | 688/795 | chr16 | 89553920 | |||
| chr16:89556893 | A | G | 1 | a0003 | 8 | HG01891.hp1 HG02451.hp2 HG02615.hp2 others(5): Show |
missense_variant | MODERATE | c.2188A>G | p.Asn730Asp | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 17/17 | 2203/3076 | 2188/2388 | 730/795 | chr16 | 89556893 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:89508426 | G | T | 1 | a0001c0019 | 1 | HG02965.hp2 | synonymous_variant | LOW | c.9G>T | p.Val3Val | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 1/17 | 24/3076 | 9/2388 | 3/795 | chr16 | 89508426 | |||
| chr16:89508537 | G | A | 1 | a0001c0006 | 2 | HG01074.hp1 HG01516.hp2 |
synonymous_variant | LOW | c.120G>A | p.Gly40Gly | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 1/17 | 135/3076 | 120/2388 | 40/795 | chr16 | 89508537 | |||
| chr16:89531909 | A | G | 1 | a0001c0016 | 1 | HG01928.hp2 | synonymous_variant | LOW | c.993A>G | p.Pro331Pro | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 8/17 | 1008/3076 | 993/2388 | 331/795 | chr16 | 89531909 | |||
| chr16:89550570 | G | A | 1 | a0001c0011 | 1 | NA18989.hp1 | synonymous_variant | LOW | c.1740G>A | p.Leu580Leu | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 13/17 | 1755/3076 | 1740/2388 | 580/795 | chr16 | 89550570 | |||
| chr16:89550600 | C | T | 2 | a0001c0013 a0001c0019 |
2 | HG01891.hp2 HG02965.hp2 |
synonymous_variant | LOW | c.1770C>T | p.Ala590Ala | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 13/17 | 1785/3076 | 1770/2388 | 590/795 | chr16 | 89550600 | |||
| chr16:89553011 | G | A | 1 | a0001c0012 | 1 | HG02080.hp1 | synonymous_variant | LOW | c.1812G>A | p.Leu604Leu | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 14/17 | 1827/3076 | 1812/2388 | 604/795 | chr16 | 89553011 | |||
| chr16:89553894 | G | A | 2 | a0001c0013 a0001c0019 |
2 | HG01891.hp2 HG02965.hp2 |
synonymous_variant | LOW | c.2037G>A | p.Ala679Ala | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 15/17 | 2052/3076 | 2037/2388 | 679/795 | chr16 | 89553894 | |||
| chr16:89556985 | G | A | 1 | a0001c0004 | 4 | HG00280.hp1 NA18953.hp1 NA18975.hp1 others(1): Show |
synonymous_variant | LOW | c.2280G>A | p.Pro760Pro | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 17/17 | 2295/3076 | 2280/2388 | 760/795 | chr16 | 89556985 | |||
| chr16:89556997 | C | T | 1 | a0002c0015 | 1 | HG03834.hp1 | synonymous_variant | LOW | c.2292C>T | p.Ile764Ile | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 17/17 | 2307/3076 | 2292/2388 | 764/795 | chr16 | 89556997 | |||
| chr16:89557000 | C | T | 1 | a0001c0005 | 4 | HG02258.hp2 HG02559.hp1 HG03579.hp1 others(1): Show |
synonymous_variant | LOW | c.2295C>T | p.Asp765Asp | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 17/17 | 2310/3076 | 2295/2388 | 765/795 | chr16 | 89557000 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:89557104 | T | A | 1 | a0002c0002t0006 | 1 | NA18960.hp1 | 3_prime_UTR_variant | MODIFIER | c.*11T>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 17/17 | 11 | chr16 | 89557104 | ||||||
| chr16:89557126 | C | T | 6 | a0001c0001t0003 a0001c0005t0005 a0001c0005t0009 others(3): Show |
10 | HG01891.hp2 HG02055.hp1 HG02258.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*33C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 17/17 | 33 | chr16 | 89557126 | ||||||
| chr16:89557199 | A | G | 3 | a0001c0005t0005 a0001c0005t0009 a0001c0005t0010 |
4 | HG02258.hp2 HG02559.hp1 HG03579.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*106A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 17/17 | 106 | chr16 | 89557199 | ||||||
| chr16:89557211 | A | G | 3 | a0001c0005t0005 a0001c0005t0009 a0001c0005t0010 |
4 | HG02258.hp2 HG02559.hp1 HG03579.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*118A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 17/17 | 118 | chr16 | 89557211 | ||||||
| chr16:89557215 | T | C | 3 | a0001c0005t0005 a0001c0005t0009 a0001c0005t0010 |
4 | HG02258.hp2 HG02559.hp1 HG03579.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*122T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 17/17 | 122 | chr16 | 89557215 | ||||||
| chr16:89557233 | G | T | 3 | a0001c0005t0005 a0001c0005t0009 a0001c0005t0010 |
4 | HG02258.hp2 HG02559.hp1 HG03579.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*140G>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 17/17 | 140 | chr16 | 89557233 | ||||||
| chr16:89557288 | C | T | 3 | a0001c0005t0005 a0001c0005t0009 a0001c0005t0010 |
4 | HG02258.hp2 HG02559.hp1 HG03579.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*195C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 17/17 | 195 | chr16 | 89557288 | ||||||
| chr16:89557290 | T | C | 1 | a0002c0002t0006 | 1 | NA18960.hp1 | 3_prime_UTR_variant | MODIFIER | c.*197T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 17/17 | 197 | chr16 | 89557290 | ||||||
| chr16:89557455 | C | T | 2 | a0001c0005t0009 a0001c0005t0010 |
2 | HG02258.hp2 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*362C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 17/17 | 362 | chr16 | 89557455 | ||||||
| chr16:89557491 | G | A | 1 | a0001c0005t0009 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*398G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 17/17 | 398 | chr16 | 89557491 | ||||||
| chr16:89557525 | G | A | 1 | a0001c0001t0007 | 1 | HG03017.hp2 | 3_prime_UTR_variant | MODIFIER | c.*432G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 17/17 | 432 | chr16 | 89557525 | ||||||
| chr16:89557528 | A | G | 1 | a0001c0001t0008 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*435A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 17/17 | 435 | chr16 | 89557528 | ||||||
| chr16:89557534 | T | C | 1 | a0001c0001t0004 | 4 | HG02723.hp2 HG02896.hp2 HG03130.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*441T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 17/17 | 441 | chr16 | 89557534 | ||||||
| chr16:89557582 | C | CCACA | 13 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0007 others(10): Show |
65 | HG00323.hp1 HG00621.hp1 HG00673.hp2 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*491_*492insCACA | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 17/17 | 492 | INFO_REALIGN_3_PRIME | chr16 | 89557582 | |||||
| chr16:89557642 | A | C | 2 | a0001c0005t0009 a0001c0005t0010 |
2 | HG02258.hp2 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*549A>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 17/17 | 549 | chr16 | 89557642 | ||||||
| chr16:89557680 | G | A | 3 | a0001c0005t0005 a0001c0005t0009 a0001c0005t0010 |
4 | HG02258.hp2 HG02559.hp1 HG03579.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*587G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 17/17 | 587 | chr16 | 89557680 | ||||||
| chr16:89557685 | C | T | 3 | a0001c0005t0005 a0001c0005t0009 a0001c0005t0010 |
4 | HG02258.hp2 HG02559.hp1 HG03579.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*592C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 17/17 | 592 | chr16 | 89557685 | ||||||
| chr16:89557749 | G | C | 3 | a0001c0005t0005 a0001c0005t0009 a0001c0005t0010 |
4 | HG02258.hp2 HG02559.hp1 HG03579.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*656G>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 17/17 | 656 | chr16 | 89557749 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:89508712 | C | T | 1 | a0001c0001t0001g0352 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.183+112C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 1/16 | chr16 | 89508712 | |||||||
| chr16:89508726 | G | A | 1 | a0001c0001t0001g0007 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.183+126G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 1/16 | chr16 | 89508726 | |||||||
| chr16:89509081 | C | T | 1 | a0002c0002t0002g0351 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.183+481C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 1/16 | chr16 | 89509081 | |||||||
| chr16:89509117 | C | G | 1 | a0001c0001t0001g0350 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.183+517C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 1/16 | chr16 | 89509117 | |||||||
| chr16:89509137 | C | A | 1 | a0001c0004t0001g0008 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.183+537C>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 1/16 | chr16 | 89509137 | |||||||
| chr16:89509200 | T | A | 36 | a0001c0001t0001g0013 a0001c0001t0002g0023 a0001c0001t0002g0026 others(33): Show |
36 | HG00323.hp1 HG00621.hp1 HG00673.hp2 others(33): Show |
intron_variant | MODIFIER | c.183+600T>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 1/16 | chr16 | 89509200 | |||||||
| chr16:89509220 | C | T | 5 | a0001c0001t0001g0346 a0001c0001t0001g0349 a0001c0001t0003g0345 others(2): Show |
5 | HG02055.hp1 HG02257.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.183+620C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 1/16 | chr16 | 89509220 | |||||||
| chr16:89509331 | A | G | 1 | a0001c0001t0001g0344 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.183+731A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 1/16 | chr16 | 89509331 | |||||||
| chr16:89509363 | G | A | 184 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0043 others(181): Show |
185 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.183+763G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 1/16 | chr16 | 89509363 | |||||||
| chr16:89509426 | T | A | 1 | a0001c0001t0001g0219 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.183+826T>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 1/16 | chr16 | 89509426 | |||||||
| chr16:89509483 | T | G | 1 | a0001c0001t0001g0043 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.183+883T>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 1/16 | chr16 | 89509483 | |||||||
| chr16:89509608 | A | T | 36 | a0001c0001t0001g0013 a0001c0001t0002g0023 a0001c0001t0002g0026 others(33): Show |
36 | HG00323.hp1 HG00621.hp1 HG00673.hp2 others(33): Show |
intron_variant | MODIFIER | c.184-882A>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 1/16 | chr16 | 89509608 | |||||||
| chr16:89509678 | T | G | 186 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0043 others(183): Show |
187 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.184-812T>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 1/16 | chr16 | 89509678 | |||||||
| chr16:89509786 | C | CT | 7 | a0001c0001t0001g0218 a0001c0001t0001g0342 a0001c0001t0001g0343 others(4): Show |
7 | HG00673.hp2 HG01891.hp2 HG02071.hp2 others(4): Show |
intron_variant | MODIFIER | c.184-682dupT | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 89509786 | ||||||
| chr16:89509786 | CT | C | 169 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0043 others(166): Show |
170 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(167): Show |
intron_variant | MODIFIER | c.184-682delT | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 89509786 | ||||||
| chr16:89509786 | CTT | C | 11 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0046 others(8): Show |
11 | HG00639.hp1 HG01069.hp1 HG01069.hp2 others(8): Show |
intron_variant | MODIFIER | c.184-683_184-682del others(2): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 89509786 | ||||||
| chr16:89509815 | A | G | 1 | a0001c0001t0001g0339 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.184-675A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 1/16 | chr16 | 89509815 | |||||||
| chr16:89509827 | C | T | 1 | a0001c0001t0002g0338 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.184-663C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 1/16 | chr16 | 89509827 | |||||||
| chr16:89509978 | A | G | 1 | a0001c0001t0001g0206 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.184-512A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 1/16 | chr16 | 89509978 | |||||||
| chr16:89510001 | G | A | 1 | a0001c0001t0001g0227 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.184-489G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 1/16 | chr16 | 89510001 | |||||||
| chr16:89510039 | A | G | 1 | a0001c0001t0001g0043 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.184-451A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 1/16 | chr16 | 89510039 | |||||||
| chr16:89510057 | C | G | 6 | a0001c0001t0001g0043 a0001c0001t0002g0204 a0001c0001t0004g0201 others(3): Show |
6 | HG01167.hp2 HG02723.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.184-433C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 1/16 | chr16 | 89510057 | |||||||
| chr16:89510099 | T | C | 237 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0013 others(234): Show |
238 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(235): Show |
intron_variant | MODIFIER | c.184-391T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 1/16 | chr16 | 89510099 | |||||||
| chr16:89510132 | G | A | 1 | a0001c0001t0001g0239 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.184-358G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 1/16 | chr16 | 89510132 | |||||||
| chr16:89510255 | G | A | 183 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0043 others(180): Show |
184 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.184-235G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 1/16 | chr16 | 89510255 | |||||||
| chr16:89510358 | T | C | 186 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0043 others(183): Show |
187 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.184-132T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 1/16 | chr16 | 89510358 | |||||||
| chr16:89510471 | GT | G | 178 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0043 others(175): Show |
179 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(176): Show |
splice_region_variant&intron_variant | LOW | c.184-4delT | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 89510471 | ||||||
| chr16:89510638 | C | T | 186 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0043 others(183): Show |
187 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.286+46C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 2/16 | chr16 | 89510638 | |||||||
| chr16:89510740 | C | A | 4 | a0001c0001t0001g0241 a0001c0001t0001g0242 a0001c0001t0001g0339 others(1): Show |
4 | HG01243.hp1 HG01891.hp2 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.286+148C>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 2/16 | chr16 | 89510740 | |||||||
| chr16:89510810 | G | A | 3 | a0003c0003t0002g0055 a0003c0003t0002g0056 a0003c0003t0002g0057 |
3 | HG02615.hp2 HG02970.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.286+218G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 2/16 | chr16 | 89510810 | |||||||
| chr16:89510903 | C | T | 1 | a0001c0001t0001g0217 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.286+311C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 2/16 | chr16 | 89510903 | |||||||
| chr16:89510949 | C | A | 1 | a0001c0006t0001g0058 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.286+357C>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 2/16 | chr16 | 89510949 | |||||||
| chr16:89510958 | A | G | 186 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0043 others(183): Show |
187 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.286+366A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 2/16 | chr16 | 89510958 | |||||||
| chr16:89511242 | T | G | 1 | a0001c0001t0001g0243 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.286+650T>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 2/16 | chr16 | 89511242 | |||||||
| chr16:89511282 | C | A | 1 | a0001c0001t0001g0207 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.286+690C>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 2/16 | chr16 | 89511282 | |||||||
| chr16:89511342 | T | G | 1 | a0001c0001t0002g0222 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.286+750T>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 2/16 | chr16 | 89511342 | |||||||
| chr16:89511363 | T | G | 1 | a0001c0019t0003g0220 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.286+771T>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 2/16 | chr16 | 89511363 | |||||||
| chr16:89511395 | C | G | 1 | a0001c0001t0001g0053 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.286+803C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 2/16 | chr16 | 89511395 | |||||||
| chr16:89511411 | T | A | 10 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(7): Show |
10 | HG01934.hp2 HG02080.hp1 HG02080.hp2 others(7): Show |
intron_variant | MODIFIER | c.286+819T>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 2/16 | chr16 | 89511411 | |||||||
| chr16:89511649 | C | T | 162 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0043 others(159): Show |
163 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.286+1057C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 2/16 | chr16 | 89511649 | |||||||
| chr16:89511700 | G | C | 1 | a0001c0001t0001g0206 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.286+1108G>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 2/16 | chr16 | 89511700 | |||||||
| chr16:89511733 | T | C | 184 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0043 others(181): Show |
185 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.286+1141T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 2/16 | chr16 | 89511733 | |||||||
| chr16:89511912 | G | GTTTAA | 184 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0043 others(181): Show |
185 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.287-1032_287-1031i others(7): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr16 | 89511912 | ||||||
| chr16:89511915 | T | G | 3 | a0002c0002t0002g0001 a0002c0002t0002g0351 a0002c0002t0006g0001 |
3 | NA18960.hp1 NA18972.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.287-1033T>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 2/16 | chr16 | 89511915 | |||||||
| chr16:89511916 | A | T | 3 | a0002c0002t0002g0001 a0002c0002t0002g0351 a0002c0002t0006g0001 |
3 | NA18960.hp1 NA18972.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.287-1032A>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 2/16 | chr16 | 89511916 | |||||||
| chr16:89511946 | C | G | 13 | a0001c0001t0001g0229 a0001c0001t0001g0231 a0001c0001t0002g0222 others(10): Show |
13 | HG01081.hp1 HG02109.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.287-1002C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 2/16 | chr16 | 89511946 | |||||||
| chr16:89511981 | C | T | 2 | a0002c0002t0002g0039 a0002c0002t0002g0040 |
2 | NA18942.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.287-967C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 2/16 | chr16 | 89511981 | |||||||
| chr16:89512090 | T | A | 2 | a0001c0001t0001g0093 a0001c0001t0001g0094 |
2 | HG02074.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.287-858T>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 2/16 | chr16 | 89512090 | |||||||
| chr16:89512160 | C | T | 1 | a0001c0001t0001g0221 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.287-788C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 2/16 | chr16 | 89512160 | |||||||
| chr16:89512348 | C | G | 182 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0043 others(179): Show |
183 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.287-600C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 2/16 | chr16 | 89512348 | |||||||
| chr16:89512554 | A | T | 2 | a0001c0005t0009g0340 a0001c0005t0010g0238 |
2 | HG02258.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.287-394A>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 2/16 | chr16 | 89512554 | |||||||
| chr16:89512562 | C | T | 1 | a0001c0001t0001g0052 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.287-386C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 2/16 | chr16 | 89512562 | |||||||
| chr16:89512668 | A | G | 42 | a0001c0001t0001g0013 a0001c0001t0001g0229 a0001c0001t0001g0231 others(39): Show |
42 | HG00323.hp1 HG00621.hp1 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.287-280A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 2/16 | chr16 | 89512668 | |||||||
| chr16:89512715 | G | A | 184 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0043 others(181): Show |
185 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.287-233G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 2/16 | chr16 | 89512715 | |||||||
| chr16:89512807 | A | G | 1 | a0001c0001t0001g0193 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.287-141A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 2/16 | chr16 | 89512807 | |||||||
| chr16:89512874 | G | A | 1 | a0001c0001t0001g0095 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.287-74G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 2/16 | chr16 | 89512874 | |||||||
| chr16:89513142 | G | T | 2 | a0001c0001t0001g0221 a0001c0019t0003g0220 |
2 | HG02109.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.376+105G>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89513142 | |||||||
| chr16:89513177 | C | T | 2 | a0001c0001t0001g0221 a0001c0019t0003g0220 |
2 | HG02109.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.376+140C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89513177 | |||||||
| chr16:89513285 | A | G | 1 | a0001c0001t0001g0337 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.376+248A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89513285 | |||||||
| chr16:89513388 | C | T | 185 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0043 others(182): Show |
186 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.376+351C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89513388 | |||||||
| chr16:89513398 | C | A | 3 | a0003c0003t0002g0055 a0003c0003t0002g0056 a0003c0003t0002g0057 |
3 | HG02615.hp2 HG02970.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.376+361C>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89513398 | |||||||
| chr16:89513463 | T | C | 185 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0043 others(182): Show |
186 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.376+426T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89513463 | |||||||
| chr16:89513500 | G | A | 1 | a0001c0001t0001g0227 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.376+463G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89513500 | |||||||
| chr16:89513529 | A | T | 4 | a0003c0003t0002g0234 a0003c0003t0002g0235 a0003c0003t0002g0236 others(1): Show |
4 | HG02451.hp2 HG02717.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.376+492A>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89513529 | |||||||
| chr16:89513539 | A | T | 1 | a0001c0001t0001g0192 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.376+502A>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89513539 | |||||||
| chr16:89513719 | T | G | 1 | a0001c0001t0001g0096 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.376+682T>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89513719 | |||||||
| chr16:89513761 | GT | G | 349 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(346): Show |
354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.376+726delT | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr16 | 89513761 | ||||||
| chr16:89514071 | G | T | 16 | a0001c0001t0001g0226 a0001c0001t0001g0243 a0001c0001t0001g0323 others(13): Show |
16 | HG01192.hp1 HG02280.hp1 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.376+1034G>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89514071 | |||||||
| chr16:89514276 | A | T | 36 | a0001c0001t0001g0013 a0001c0001t0002g0023 a0001c0001t0002g0026 others(33): Show |
36 | HG00323.hp1 HG00621.hp1 HG00673.hp2 others(33): Show |
intron_variant | MODIFIER | c.376+1239A>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89514276 | |||||||
| chr16:89514308 | CT | C | 99 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(96): Show |
102 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.376+1303delT | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr16 | 89514308 | ||||||
| chr16:89514308 | CTT | C | 30 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0089 others(27): Show |
30 | HG00621.hp2 HG01081.hp1 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.376+1302_376+1303d others(4): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr16 | 89514308 | ||||||
| chr16:89514308 | CTTT | C | 57 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(54): Show |
57 | HG00408.hp2 HG00597.hp1 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.376+1301_376+1303d others(5): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr16 | 89514308 | ||||||
| chr16:89514308 | CTTTT | C | 116 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0043 others(113): Show |
117 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.376+1300_376+1303d others(6): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr16 | 89514308 | ||||||
| chr16:89514308 | CTTTTTTT others(10): Show |
C | 1 | a0001c0001t0001g0066 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.376+1287_376+1303d others(19): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr16 | 89514308 | ||||||
| chr16:89514347 | A | G | 1 | a0001c0001t0001g0322 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.376+1310A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89514347 | |||||||
| chr16:89514361 | C | T | 1 | a0001c0001t0001g0168 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.376+1324C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89514361 | |||||||
| chr16:89514445 | G | C | 187 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0043 others(184): Show |
188 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.376+1408G>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89514445 | |||||||
| chr16:89514448 | G | A | 185 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0043 others(182): Show |
186 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.376+1411G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89514448 | |||||||
| chr16:89514532 | G | A | 2 | a0001c0001t0001g0221 a0001c0019t0003g0220 |
2 | HG02109.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.376+1495G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89514532 | |||||||
| chr16:89514625 | C | G | 1 | a0001c0001t0001g0206 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.376+1588C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89514625 | |||||||
| chr16:89514628 | G | A | 185 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0043 others(182): Show |
186 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.376+1591G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89514628 | |||||||
| chr16:89514787 | C | T | 1 | a0001c0001t0001g0223 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.376+1750C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89514787 | |||||||
| chr16:89514808 | A | G | 185 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0043 others(182): Show |
186 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.376+1771A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89514808 | |||||||
| chr16:89514828 | T | C | 187 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0043 others(184): Show |
188 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.376+1791T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89514828 | |||||||
| chr16:89514891 | A | G | 3 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0001t0001g0187 |
3 | NA18941.hp1 NA18964.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.376+1854A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89514891 | |||||||
| chr16:89514922 | G | A | 1 | a0001c0001t0001g0169 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.376+1885G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89514922 | |||||||
| chr16:89514935 | C | CT | 10 | a0001c0001t0001g0250 a0001c0001t0001g0301 a0001c0001t0001g0334 others(7): Show |
10 | HG00280.hp1 HG01978.hp2 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.376+1917dupT | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr16 | 89514935 | ||||||
| chr16:89514935 | CT | C | 13 | a0001c0001t0001g0085 a0001c0001t0001g0165 a0001c0001t0001g0186 others(10): Show |
13 | HG01081.hp1 HG01433.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.376+1917delT | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr16 | 89514935 | ||||||
| chr16:89514935 | CTT | C | 183 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0043 others(180): Show |
184 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.376+1916_376+1917d others(4): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr16 | 89514935 | ||||||
| chr16:89514968 | G | A | 1 | a0001c0001t0002g0224 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.376+1931G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89514968 | |||||||
| chr16:89515017 | A | G | 2 | a0001c0005t0009g0340 a0001c0005t0010g0238 |
2 | HG02258.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.376+1980A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89515017 | |||||||
| chr16:89515048 | T | C | 1 | a0001c0001t0001g0050 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.376+2011T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89515048 | |||||||
| chr16:89515181 | G | C | 200 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0043 others(197): Show |
201 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.376+2144G>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89515181 | |||||||
| chr16:89515242 | C | CT | 185 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0043 others(182): Show |
186 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.376+2217dupT | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr16 | 89515242 | ||||||
| chr16:89515291 | C | T | 6 | a0001c0001t0001g0229 a0001c0001t0001g0231 a0001c0001t0002g0222 others(3): Show |
6 | HG01081.hp1 HG02109.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.376+2254C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89515291 | |||||||
| chr16:89515304 | T | C | 1 | a0001c0001t0001g0059 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.376+2267T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89515304 | |||||||
| chr16:89515378 | C | G | 1 | a0001c0001t0001g0223 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.376+2341C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89515378 | |||||||
| chr16:89515503 | G | A | 1 | a0001c0001t0001g0097 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.376+2466G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89515503 | |||||||
| chr16:89515516 | T | C | 187 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0043 others(184): Show |
188 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.376+2479T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89515516 | |||||||
| chr16:89515610 | C | T | 1 | a0001c0001t0001g0164 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.376+2573C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89515610 | |||||||
| chr16:89515660 | A | C | 1 | a0001c0001t0001g0299 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.376+2623A>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89515660 | |||||||
| chr16:89515709 | A | T | 1 | a0001c0019t0003g0220 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.376+2672A>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89515709 | |||||||
| chr16:89515712 | A | T | 19 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 others(16): Show |
19 | HG01081.hp1 HG02109.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.376+2675A>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89515712 | |||||||
| chr16:89515715 | A | G | 1 | a0001c0005t0005g0302 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.376+2678A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89515715 | |||||||
| chr16:89515715 | A | T | 242 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0013 others(239): Show |
243 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(240): Show |
intron_variant | MODIFIER | c.376+2678A>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89515715 | |||||||
| chr16:89515721 | T | G | 1 | a0001c0001t0001g0098 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.376+2684T>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89515721 | |||||||
| chr16:89515724 | T | G | 182 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0043 others(179): Show |
183 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.376+2687T>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89515724 | |||||||
| chr16:89515724 | T | TG | 5 | a0001c0001t0001g0346 a0001c0001t0001g0349 a0001c0001t0003g0345 others(2): Show |
5 | HG02055.hp1 HG02257.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.376+2687_376+2688i others(3): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89515724 | |||||||
| chr16:89515748 | G | T | 2 | a0001c0001t0001g0295 a0001c0001t0003g0296 |
2 | HG02922.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.376+2711G>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89515748 | |||||||
| chr16:89516060 | T | C | 1 | a0001c0001t0001g0221 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.376+3023T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89516060 | |||||||
| chr16:89516276 | C | T | 185 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0043 others(182): Show |
186 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.376+3239C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89516276 | |||||||
| chr16:89516398 | A | G | 1 | a0001c0001t0001g0301 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.376+3361A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89516398 | |||||||
| chr16:89516421 | C | T | 1 | a0001c0001t0001g0199 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.376+3384C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89516421 | |||||||
| chr16:89516445 | G | A | 13 | a0001c0001t0001g0229 a0001c0001t0001g0231 a0001c0001t0002g0222 others(10): Show |
13 | HG01081.hp1 HG02109.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.376+3408G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89516445 | |||||||
| chr16:89516504 | T | C | 1 | a0001c0001t0001g0229 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.376+3467T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89516504 | |||||||
| chr16:89516520 | C | T | 33 | a0001c0001t0001g0097 a0001c0001t0001g0139 a0001c0001t0001g0140 others(30): Show |
33 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(30): Show |
intron_variant | MODIFIER | c.376+3483C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89516520 | |||||||
| chr16:89516523 | C | G | 1 | a0001c0001t0001g0294 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.376+3486C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89516523 | |||||||
| chr16:89516534 | G | C | 36 | a0001c0001t0001g0013 a0001c0001t0002g0023 a0001c0001t0002g0026 others(33): Show |
36 | HG00323.hp1 HG00621.hp1 HG00673.hp2 others(33): Show |
intron_variant | MODIFIER | c.376+3497G>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89516534 | |||||||
| chr16:89516659 | G | A | 185 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0043 others(182): Show |
186 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.376+3622G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89516659 | |||||||
| chr16:89516679 | T | C | 4 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(1): Show |
4 | HG02717.hp2 HG02965.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.376+3642T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89516679 | |||||||
| chr16:89516781 | C | T | 185 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0043 others(182): Show |
186 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.376+3744C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89516781 | |||||||
| chr16:89516782 | G | A | 1 | a0001c0001t0002g0222 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.376+3745G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89516782 | |||||||
| chr16:89516796 | C | T | 1 | a0001c0001t0001g0241 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.376+3759C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89516796 | |||||||
| chr16:89517038 | G | A | 1 | a0001c0001t0001g0085 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.376+4001G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89517038 | |||||||
| chr16:89517170 | G | A | 185 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0043 others(182): Show |
186 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.376+4133G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89517170 | |||||||
| chr16:89517202 | C | T | 185 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0043 others(182): Show |
186 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.376+4165C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89517202 | |||||||
| chr16:89517220 | T | TG | 187 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0043 others(184): Show |
188 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.376+4184dupG | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr16 | 89517220 | ||||||
| chr16:89517239 | A | ATTCCTGG others(32): Show |
1 | a0001c0001t0001g0206 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.376+4211_376+4249d others(41): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr16 | 89517239 | ||||||
| chr16:89517248 | AGGAATGG others(32): Show |
A | 11 | a0001c0001t0001g0139 a0001c0001t0001g0158 a0001c0001t0001g0159 others(8): Show |
11 | HG00597.hp2 HG04204.hp1 NA18946.hp2 others(8): Show |
intron_variant | MODIFIER | c.376+4250_376+4288d others(41): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr16 | 89517248 | ||||||
| chr16:89517287 | G | A | 176 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0043 others(173): Show |
177 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.376+4250G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89517287 | |||||||
| chr16:89517333 | G | C | 1 | a0002c0002t0002g0012 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.376+4296G>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89517333 | |||||||
| chr16:89517401 | C | T | 184 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0043 others(181): Show |
185 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.376+4364C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89517401 | |||||||
| chr16:89517614 | G | T | 186 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0043 others(183): Show |
187 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.376+4577G>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89517614 | |||||||
| chr16:89517616 | C | CT | 10 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0168 others(7): Show |
10 | HG00438.hp2 HG01192.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.376+4599dupT | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr16 | 89517616 | ||||||
| chr16:89517616 | CT | C | 47 | a0001c0001t0001g0013 a0001c0001t0001g0043 a0001c0001t0001g0068 others(44): Show |
47 | HG00323.hp1 HG00621.hp1 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.376+4599delT | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr16 | 89517616 | ||||||
| chr16:89517616 | CTT | C | 10 | a0001c0001t0001g0229 a0001c0001t0001g0231 a0001c0001t0002g0026 others(7): Show |
10 | HG01081.hp1 HG02109.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.376+4598_376+4599d others(4): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr16 | 89517616 | ||||||
| chr16:89517777 | G | T | 36 | a0001c0001t0001g0013 a0001c0001t0002g0023 a0001c0001t0002g0026 others(33): Show |
36 | HG00323.hp1 HG00621.hp1 HG00673.hp2 others(33): Show |
intron_variant | MODIFIER | c.376+4740G>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89517777 | |||||||
| chr16:89517956 | C | A | 5 | a0001c0001t0001g0229 a0001c0001t0001g0251 a0001c0001t0001g0252 others(2): Show |
5 | HG02451.hp1 HG02723.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.376+4919C>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89517956 | |||||||
| chr16:89517994 | G | A | 1 | a0001c0001t0001g0221 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.376+4957G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89517994 | |||||||
| chr16:89518249 | A | C | 2 | a0001c0001t0001g0221 a0001c0019t0003g0220 |
2 | HG02109.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.376+5212A>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89518249 | |||||||
| chr16:89518748 | C | T | 1 | a0001c0001t0001g0138 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.377-5258C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89518748 | |||||||
| chr16:89518769 | G | A | 2 | a0001c0001t0001g0013 a0002c0015t0002g0041 |
2 | HG03834.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.377-5237G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89518769 | |||||||
| chr16:89518886 | C | T | 4 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(1): Show |
4 | HG02523.hp2 NA18945.hp1 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.377-5120C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89518886 | |||||||
| chr16:89518992 | A | T | 184 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0043 others(181): Show |
185 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.377-5014A>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89518992 | |||||||
| chr16:89519053 | T | G | 2 | a0001c0001t0001g0323 a0001c0001t0001g0334 |
2 | HG02647.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.377-4953T>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89519053 | |||||||
| chr16:89519076 | C | T | 187 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0043 others(184): Show |
188 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.377-4930C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89519076 | |||||||
| chr16:89519087 | G | A | 1 | a0001c0001t0001g0254 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.377-4919G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89519087 | |||||||
| chr16:89519219 | A | G | 186 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0043 others(183): Show |
187 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.377-4787A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89519219 | |||||||
| chr16:89519290 | G | T | 5 | a0001c0001t0002g0224 a0003c0003t0002g0234 a0003c0003t0002g0235 others(2): Show |
5 | HG02451.hp2 HG02717.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.377-4716G>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89519290 | |||||||
| chr16:89519380 | T | A | 1 | a0001c0001t0001g0229 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.377-4626T>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89519380 | |||||||
| chr16:89519381 | T | G | 1 | a0001c0001t0001g0255 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.377-4625T>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89519381 | |||||||
| chr16:89519406 | A | G | 187 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0043 others(184): Show |
188 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.377-4600A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89519406 | |||||||
| chr16:89519467 | G | A | 1 | a0001c0001t0007g0010 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.377-4539G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89519467 | |||||||
| chr16:89519594 | CT | C | 185 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0043 others(182): Show |
186 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.377-4410delT | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr16 | 89519594 | ||||||
| chr16:89519602 | A | G | 186 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0043 others(183): Show |
187 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.377-4404A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89519602 | |||||||
| chr16:89519609 | C | T | 1 | a0001c0005t0005g0302 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.377-4397C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89519609 | |||||||
| chr16:89519629 | G | A | 1 | a0001c0001t0002g0233 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.377-4377G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89519629 | |||||||
| chr16:89519711 | T | G | 1 | a0001c0001t0001g0256 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.377-4295T>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89519711 | |||||||
| chr16:89520052 | G | A | 1 | a0001c0019t0003g0220 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.377-3954G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89520052 | |||||||
| chr16:89520072 | G | A | 1 | a0001c0001t0001g0304 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.377-3934G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89520072 | |||||||
| chr16:89520080 | G | A | 36 | a0001c0001t0001g0013 a0001c0001t0002g0023 a0001c0001t0002g0026 others(33): Show |
36 | HG00323.hp1 HG00621.hp1 HG00673.hp2 others(33): Show |
intron_variant | MODIFIER | c.377-3926G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89520080 | |||||||
| chr16:89520148 | G | A | 1 | a0001c0005t0005g0305 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.377-3858G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89520148 | |||||||
| chr16:89520180 | A | G | 1 | a0001c0001t0001g0293 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.377-3826A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89520180 | |||||||
| chr16:89520184 | A | T | 36 | a0001c0001t0001g0013 a0001c0001t0002g0023 a0001c0001t0002g0026 others(33): Show |
36 | HG00323.hp1 HG00621.hp1 HG00673.hp2 others(33): Show |
intron_variant | MODIFIER | c.377-3822A>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89520184 | |||||||
| chr16:89520251 | A | C | 224 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0013 others(221): Show |
225 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(222): Show |
intron_variant | MODIFIER | c.377-3755A>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89520251 | |||||||
| chr16:89520483 | G | A | 2 | a0001c0001t0001g0221 a0001c0001t0001g0223 |
2 | HG02109.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.377-3523G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89520483 | |||||||
| chr16:89520542 | G | A | 1 | a0001c0001t0001g0069 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.377-3464G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89520542 | |||||||
| chr16:89520587 | G | A | 36 | a0001c0001t0001g0013 a0001c0001t0002g0023 a0001c0001t0002g0026 others(33): Show |
36 | HG00323.hp1 HG00621.hp1 HG00673.hp2 others(33): Show |
intron_variant | MODIFIER | c.377-3419G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89520587 | |||||||
| chr16:89520622 | C | T | 184 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0043 others(181): Show |
185 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.377-3384C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89520622 | |||||||
| chr16:89520672 | C | T | 1 | a0001c0001t0001g0290 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.377-3334C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89520672 | |||||||
| chr16:89520710 | GT | G | 186 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0043 others(183): Show |
187 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.377-3286delT | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr16 | 89520710 | ||||||
| chr16:89520720 | T | C | 3 | a0001c0001t0001g0177 a0001c0001t0001g0323 a0001c0001t0001g0334 |
3 | HG02647.hp2 HG02886.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.377-3286T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89520720 | |||||||
| chr16:89520723 | C | A | 1 | a0001c0001t0001g0257 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.377-3283C>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89520723 | |||||||
| chr16:89520879 | T | A | 185 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0043 others(182): Show |
186 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.377-3127T>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89520879 | |||||||
| chr16:89521030 | C | G | 184 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0043 others(181): Show |
185 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.377-2976C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89521030 | |||||||
| chr16:89521147 | T | G | 1 | a0001c0001t0001g0103 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.377-2859T>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89521147 | |||||||
| chr16:89521151 | T | C | 1 | a0001c0001t0001g0103 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.377-2855T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89521151 | |||||||
| chr16:89521171 | C | T | 187 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0043 others(184): Show |
188 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.377-2835C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89521171 | |||||||
| chr16:89521368 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.377-2638C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89521368 | |||||||
| chr16:89521463 | A | C | 187 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0043 others(184): Show |
188 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.377-2543A>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89521463 | |||||||
| chr16:89521586 | T | G | 1 | a0001c0006t0001g0104 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.377-2420T>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89521586 | |||||||
| chr16:89521600 | G | A | 2 | a0001c0001t0001g0247 a0001c0001t0001g0248 |
2 | HG03453.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.377-2406G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89521600 | |||||||
| chr16:89521612 | G | A | 1 | a0001c0001t0001g0043 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.377-2394G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89521612 | |||||||
| chr16:89521767 | C | A | 1 | a0001c0001t0001g0244 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.377-2239C>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89521767 | |||||||
| chr16:89521920 | A | G | 2 | a0002c0002t0002g0025 a0002c0002t0002g0036 |
2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.377-2086A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89521920 | |||||||
| chr16:89521972 | G | A | 6 | a0001c0001t0001g0323 a0001c0001t0001g0324 a0001c0001t0001g0325 others(3): Show |
6 | HG01192.hp1 HG02615.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.377-2034G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89521972 | |||||||
| chr16:89522080 | A | G | 185 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0043 others(182): Show |
186 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.377-1926A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89522080 | |||||||
| chr16:89522158 | G | A | 1 | a0002c0002t0002g0014 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.377-1848G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89522158 | |||||||
| chr16:89522164 | G | T | 8 | a0001c0001t0001g0323 a0001c0001t0001g0324 a0001c0001t0001g0325 others(5): Show |
8 | HG01192.hp1 HG02615.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.377-1842G>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89522164 | |||||||
| chr16:89522327 | C | T | 5 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(2): Show |
5 | HG00639.hp1 HG02145.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.377-1679C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89522327 | |||||||
| chr16:89522337 | C | T | 1 | a0001c0001t0001g0156 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.377-1669C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89522337 | |||||||
| chr16:89522349 | C | G | 1 | a0001c0019t0003g0220 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.377-1657C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89522349 | |||||||
| chr16:89522365 | C | T | 1 | a0001c0001t0001g0349 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.377-1641C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89522365 | |||||||
| chr16:89522367 | C | T | 1 | a0001c0001t0001g0322 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.377-1639C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89522367 | |||||||
| chr16:89522410 | G | T | 16 | a0001c0001t0001g0226 a0001c0001t0001g0243 a0001c0001t0001g0323 others(13): Show |
16 | HG01192.hp1 HG02280.hp1 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.377-1596G>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89522410 | |||||||
| chr16:89522439 | G | A | 1 | a0001c0001t0001g0304 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.377-1567G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89522439 | |||||||
| chr16:89522443 | C | T | 2 | a0001c0001t0001g0092 a0001c0001t0001g0210 |
2 | NA18989.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.377-1563C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89522443 | |||||||
| chr16:89522444 | G | T | 1 | a0001c0001t0001g0135 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.377-1562G>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89522444 | |||||||
| chr16:89522488 | A | G | 223 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0013 others(220): Show |
224 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(221): Show |
intron_variant | MODIFIER | c.377-1518A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89522488 | |||||||
| chr16:89522495 | G | C | 1 | a0001c0001t0001g0221 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.377-1511G>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89522495 | |||||||
| chr16:89522499 | T | C | 4 | a0003c0003t0002g0234 a0003c0003t0002g0235 a0003c0003t0002g0236 others(1): Show |
4 | HG02451.hp2 HG02717.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.377-1507T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89522499 | |||||||
| chr16:89522574 | C | T | 13 | a0001c0001t0001g0229 a0001c0001t0001g0231 a0001c0001t0002g0222 others(10): Show |
13 | HG01081.hp1 HG02109.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.377-1432C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89522574 | |||||||
| chr16:89522612 | G | A | 1 | a0001c0001t0001g0200 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.377-1394G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89522612 | |||||||
| chr16:89522699 | C | G | 2 | a0001c0001t0001g0241 a0001c0001t0001g0242 |
2 | HG01243.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.377-1307C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89522699 | |||||||
| chr16:89522717 | G | A | 187 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0043 others(184): Show |
188 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.377-1289G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89522717 | |||||||
| chr16:89522869 | C | T | 1 | a0001c0001t0001g0289 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.377-1137C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89522869 | |||||||
| chr16:89522902 | C | T | 5 | a0001c0001t0002g0224 a0003c0003t0002g0234 a0003c0003t0002g0235 others(2): Show |
5 | HG02451.hp2 HG02717.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.377-1104C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89522902 | |||||||
| chr16:89523000 | G | A | 221 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0013 others(218): Show |
222 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.377-1006G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89523000 | |||||||
| chr16:89523033 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.377-973C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89523033 | |||||||
| chr16:89523037 | C | A | 1 | a0001c0001t0001g0223 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.377-969C>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89523037 | |||||||
| chr16:89523287 | G | A | 1 | a0001c0001t0001g0043 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.377-719G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89523287 | |||||||
| chr16:89523345 | A | C | 5 | a0001c0001t0002g0224 a0003c0003t0002g0234 a0003c0003t0002g0235 others(2): Show |
5 | HG02451.hp2 HG02717.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.377-661A>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89523345 | |||||||
| chr16:89523355 | G | A | 2 | a0001c0001t0001g0258 a0001c0001t0001g0259 |
2 | HG02155.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.377-651G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89523355 | |||||||
| chr16:89523571 | G | A | 1 | a0001c0001t0001g0059 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.377-435G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89523571 | |||||||
| chr16:89523625 | A | T | 1 | a0001c0001t0001g0193 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.377-381A>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89523625 | |||||||
| chr16:89523652 | G | A | 185 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0043 others(182): Show |
186 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.377-354G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89523652 | |||||||
| chr16:89523708 | G | A | 1 | a0001c0001t0001g0098 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.377-298G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89523708 | |||||||
| chr16:89523730 | A | G | 1 | a0001c0001t0002g0224 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.377-276A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89523730 | |||||||
| chr16:89523760 | T | TATCTC | 192 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0043 others(189): Show |
193 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.377-245_377-244ins others(5): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr16 | 89523760 | ||||||
| chr16:89523804 | A | G | 1 | a0001c0001t0001g0221 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.377-202A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89523804 | |||||||
| chr16:89523835 | G | A | 185 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0043 others(182): Show |
186 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.377-171G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89523835 | |||||||
| chr16:89523857 | G | A | 1 | a0004c0008t0002g0105 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.377-149G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89523857 | |||||||
| chr16:89523949 | C | T | 1 | a0002c0002t0002g0351 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.377-57C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89523949 | |||||||
| chr16:89524249 | TGAGTGAG others(51): Show |
T | 1 | a0001c0001t0001g0293 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.618+11_618+68delGT others(56): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr16 | 89524249 | ||||||
| chr16:89524259 | T | C | 193 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0043 others(190): Show |
194 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.618+12T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 4/16 | chr16 | 89524259 | |||||||
| chr16:89524338 | G | T | 1 | a0001c0001t0001g0084 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.618+91G>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 4/16 | chr16 | 89524338 | |||||||
| chr16:89524350 | G | A | 1 | a0002c0002t0002g0351 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.618+103G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 4/16 | chr16 | 89524350 | |||||||
| chr16:89524417 | C | T | 36 | a0001c0001t0001g0013 a0001c0001t0002g0023 a0001c0001t0002g0026 others(33): Show |
36 | HG00323.hp1 HG00621.hp1 HG00673.hp2 others(33): Show |
intron_variant | MODIFIER | c.618+170C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 4/16 | chr16 | 89524417 | |||||||
| chr16:89524686 | C | T | 1 | a0001c0001t0002g0224 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.618+439C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 4/16 | chr16 | 89524686 | |||||||
| chr16:89524724 | C | T | 1 | a0001c0004t0001g0300 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.618+477C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 4/16 | chr16 | 89524724 | |||||||
| chr16:89524768 | A | G | 2 | a0001c0001t0001g0241 a0001c0001t0001g0242 |
2 | HG01243.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.618+521A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 4/16 | chr16 | 89524768 | |||||||
| chr16:89524841 | C | T | 5 | a0001c0001t0001g0329 a0001c0001t0001g0332 a0001c0001t0001g0333 others(2): Show |
5 | HG02280.hp1 HG03098.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.618+594C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 4/16 | chr16 | 89524841 | |||||||
| chr16:89524865 | G | A | 1 | a0001c0001t0002g0260 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.618+618G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 4/16 | chr16 | 89524865 | |||||||
| chr16:89524881 | G | A | 1 | a0001c0001t0001g0052 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.618+634G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 4/16 | chr16 | 89524881 | |||||||
| chr16:89524953 | C | CT | 94 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0044 others(91): Show |
95 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.618+723dupT | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr16 | 89524953 | ||||||
| chr16:89524953 | C | CTT | 10 | a0001c0001t0001g0095 a0001c0001t0001g0134 a0001c0001t0001g0162 others(7): Show |
10 | HG00642.hp1 HG00735.hp1 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.618+722_618+723dup others(2): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr16 | 89524953 | ||||||
| chr16:89525037 | G | A | 2 | a0002c0002t0002g0039 a0002c0002t0002g0040 |
2 | NA18942.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.618+790G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 4/16 | chr16 | 89525037 | |||||||
| chr16:89525106 | C | A | 2 | a0001c0001t0001g0221 a0001c0019t0003g0220 |
2 | HG02109.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.618+859C>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 4/16 | chr16 | 89525106 | |||||||
| chr16:89525107 | G | A | 5 | a0001c0001t0002g0224 a0003c0003t0002g0234 a0003c0003t0002g0235 others(2): Show |
5 | HG02451.hp2 HG02717.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.618+860G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 4/16 | chr16 | 89525107 | |||||||
| chr16:89525127 | T | G | 1 | a0001c0001t0001g0221 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.618+880T>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 4/16 | chr16 | 89525127 | |||||||
| chr16:89525624 | T | A | 1 | a0001c0001t0001g0301 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.619-705T>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 4/16 | chr16 | 89525624 | |||||||
| chr16:89525645 | G | A | 36 | a0001c0001t0001g0013 a0001c0001t0002g0023 a0001c0001t0002g0026 others(33): Show |
36 | HG00323.hp1 HG00621.hp1 HG00673.hp2 others(33): Show |
intron_variant | MODIFIER | c.619-684G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 4/16 | chr16 | 89525645 | |||||||
| chr16:89525669 | G | A | 184 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0043 others(181): Show |
185 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.619-660G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 4/16 | chr16 | 89525669 | |||||||
| chr16:89525701 | T | C | 1 | a0001c0001t0001g0140 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.619-628T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 4/16 | chr16 | 89525701 | |||||||
| chr16:89525840 | G | A | 1 | a0001c0001t0001g0054 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.619-489G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 4/16 | chr16 | 89525840 | |||||||
| chr16:89525930 | A | C | 36 | a0001c0001t0001g0013 a0001c0001t0002g0023 a0001c0001t0002g0026 others(33): Show |
36 | HG00323.hp1 HG00621.hp1 HG00673.hp2 others(33): Show |
intron_variant | MODIFIER | c.619-399A>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 4/16 | chr16 | 89525930 | |||||||
| chr16:89526003 | G | A | 1 | a0001c0001t0001g0189 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.619-326G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 4/16 | chr16 | 89526003 | |||||||
| chr16:89526014 | AACAAATT others(9): Show |
A | 1 | a0001c0001t0001g0084 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.619-314_619-299del others(16): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 4/16 | chr16 | 89526014 | |||||||
| chr16:89526096 | C | T | 6 | a0001c0001t0001g0223 a0001c0001t0002g0224 a0003c0003t0002g0234 others(3): Show |
6 | HG02451.hp2 HG02717.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.619-233C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 4/16 | chr16 | 89526096 | |||||||
| chr16:89526101 | C | T | 2 | a0001c0001t0001g0241 a0001c0001t0001g0242 |
2 | HG01243.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.619-228C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 4/16 | chr16 | 89526101 | |||||||
| chr16:89526118 | A | G | 1 | a0001c0016t0001g0288 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.619-211A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 4/16 | chr16 | 89526118 | |||||||
| chr16:89526214 | C | T | 51 | a0001c0001t0001g0002 a0001c0001t0001g0044 a0001c0001t0001g0045 others(48): Show |
52 | HG00099.hp2 HG00597.hp2 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.619-115C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 4/16 | chr16 | 89526214 | |||||||
| chr16:89526279 | C | T | 8 | a0001c0001t0001g0229 a0001c0001t0001g0231 a0001c0001t0002g0222 others(5): Show |
8 | HG01081.hp1 HG02109.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.619-50C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 4/16 | chr16 | 89526279 | |||||||
| chr16:89526282 | G | A | 36 | a0001c0001t0001g0013 a0001c0001t0002g0023 a0001c0001t0002g0026 others(33): Show |
36 | HG00323.hp1 HG00621.hp1 HG00673.hp2 others(33): Show |
intron_variant | MODIFIER | c.619-47G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 4/16 | chr16 | 89526282 | |||||||
| chr16:89526636 | T | G | 6 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(3): Show |
6 | NA18950.hp2 NA18961.hp1 NA18964.hp1 others(3): Show |
intron_variant | MODIFIER | c.758+168T>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89526636 | |||||||
| chr16:89526679 | C | T | 1 | a0001c0019t0003g0220 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.758+211C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89526679 | |||||||
| chr16:89526762 | C | T | 4 | a0002c0002t0002g0011 a0002c0002t0002g0034 a0002c0002t0002g0035 others(1): Show |
4 | HG00741.hp2 HG01978.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.758+294C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89526762 | |||||||
| chr16:89526784 | A | G | 1 | a0001c0019t0003g0220 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.758+316A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89526784 | |||||||
| chr16:89526790 | C | T | 44 | a0001c0001t0001g0013 a0001c0001t0001g0229 a0001c0001t0001g0231 others(41): Show |
44 | HG00323.hp1 HG00621.hp1 HG00673.hp2 others(41): Show |
intron_variant | MODIFIER | c.758+322C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89526790 | |||||||
| chr16:89526809 | G | A | 8 | a0001c0001t0001g0229 a0001c0001t0001g0231 a0001c0001t0002g0222 others(5): Show |
8 | HG01081.hp1 HG02109.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.758+341G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89526809 | |||||||
| chr16:89526817 | G | GCGAAGTC others(21): Show |
177 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0013 others(174): Show |
178 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(175): Show |
intron_variant | MODIFIER | c.758+433_758+460dup others(28): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr16 | 89526817 | ||||||
| chr16:89526817 | G | GCGAAGTC others(49): Show |
3 | a0001c0001t0001g0060 a0001c0001t0001g0221 a0001c0019t0003g0220 |
3 | HG02109.hp2 HG02300.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.758+405_758+460dup others(56): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr16 | 89526817 | ||||||
| chr16:89526901 | CCGAAGTC others(21): Show |
C | 3 | a0001c0001t0001g0247 a0001c0001t0001g0248 a0001c0001t0001g0249 |
3 | HG03041.hp1 HG03453.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.758+505_758+532del others(28): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr16 | 89526901 | ||||||
| chr16:89526929 | G | C | 235 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0013 others(232): Show |
236 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(233): Show |
intron_variant | MODIFIER | c.758+461G>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89526929 | |||||||
| chr16:89526945 | C | T | 1 | a0001c0001t0001g0320 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.758+477C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89526945 | |||||||
| chr16:89526957 | G | C | 1 | a0001c0001t0001g0106 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.758+489G>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89526957 | |||||||
| chr16:89526974 | G | A | 1 | a0001c0001t0001g0332 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.758+506G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89526974 | |||||||
| chr16:89527084 | C | G | 1 | a0001c0001t0001g0319 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.758+616C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89527084 | |||||||
| chr16:89527183 | C | T | 7 | a0001c0001t0001g0223 a0001c0001t0001g0320 a0001c0001t0002g0224 others(4): Show |
7 | HG02451.hp2 HG02717.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.758+715C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89527183 | |||||||
| chr16:89527293 | T | C | 1 | a0001c0001t0001g0223 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.758+825T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89527293 | |||||||
| chr16:89527294 | G | C | 348 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(345): Show |
353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.758+826G>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89527294 | |||||||
| chr16:89527388 | G | A | 1 | a0001c0001t0001g0320 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.758+920G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89527388 | |||||||
| chr16:89527433 | C | T | 2 | a0001c0001t0001g0221 a0001c0019t0003g0220 |
2 | HG02109.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.758+965C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89527433 | |||||||
| chr16:89527568 | C | T | 18 | a0001c0001t0001g0219 a0001c0001t0001g0256 a0001c0001t0001g0257 others(15): Show |
18 | HG00408.hp1 HG00438.hp1 HG00673.hp1 others(15): Show |
intron_variant | MODIFIER | c.758+1100C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89527568 | |||||||
| chr16:89527663 | C | A | 3 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0001t0001g0187 |
3 | NA18941.hp1 NA18964.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.758+1195C>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89527663 | |||||||
| chr16:89527666 | G | A | 1 | a0001c0001t0001g0053 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.758+1198G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89527666 | |||||||
| chr16:89527688 | G | A | 3 | a0001c0001t0001g0044 a0001c0001t0001g0124 a0001c0001t0001g0125 |
3 | HG01106.hp2 HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.758+1220G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89527688 | |||||||
| chr16:89527718 | C | T | 1 | a0001c0001t0001g0279 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.758+1250C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89527718 | |||||||
| chr16:89528068 | G | C | 1 | a0001c0001t0001g0261 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.759-1409G>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89528068 | |||||||
| chr16:89528161 | C | A | 2 | a0001c0001t0001g0344 a0001c0001t0001g0350 |
2 | HG02280.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.759-1316C>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89528161 | |||||||
| chr16:89528162 | G | A | 1 | a0001c0001t0001g0177 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.759-1315G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89528162 | |||||||
| chr16:89528218 | G | A | 183 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0043 others(180): Show |
184 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.759-1259G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89528218 | |||||||
| chr16:89528293 | G | T | 8 | a0001c0001t0001g0229 a0001c0001t0001g0231 a0001c0001t0002g0222 others(5): Show |
8 | HG01081.hp1 HG02109.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.759-1184G>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89528293 | |||||||
| chr16:89528316 | C | T | 8 | a0001c0001t0001g0229 a0001c0001t0001g0231 a0001c0001t0002g0222 others(5): Show |
8 | HG01081.hp1 HG02109.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.759-1161C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89528316 | |||||||
| chr16:89528317 | G | A | 1 | a0001c0001t0001g0223 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.759-1160G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89528317 | |||||||
| chr16:89528323 | C | T | 182 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0043 others(179): Show |
183 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.759-1154C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89528323 | |||||||
| chr16:89528331 | A | G | 7 | a0001c0001t0001g0223 a0001c0001t0001g0320 a0001c0001t0002g0224 others(4): Show |
7 | HG02451.hp2 HG02717.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.759-1146A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89528331 | |||||||
| chr16:89528395 | C | CA | 6 | a0001c0001t0001g0107 a0001c0001t0001g0138 a0001c0001t0001g0208 others(3): Show |
6 | HG02602.hp2 HG03471.hp1 HG03688.hp1 others(3): Show |
intron_variant | MODIFIER | c.759-1066dupA | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr16 | 89528395 | ||||||
| chr16:89528409 | A | G | 1 | a0001c0001t0001g0221 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.759-1068A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89528409 | |||||||
| chr16:89528411 | A | AT | 32 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0068 others(29): Show |
32 | HG00621.hp2 HG00642.hp2 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.759-1066_759-1065i others(3): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89528411 | |||||||
| chr16:89528483 | G | T | 1 | a0001c0001t0001g0080 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.759-994G>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89528483 | |||||||
| chr16:89528531 | A | G | 7 | a0001c0001t0001g0223 a0001c0001t0001g0320 a0001c0001t0002g0224 others(4): Show |
7 | HG02451.hp2 HG02717.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.759-946A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89528531 | |||||||
| chr16:89528603 | C | CA | 47 | a0001c0001t0001g0044 a0001c0001t0001g0049 a0001c0001t0001g0054 others(44): Show |
47 | HG00438.hp2 HG00597.hp1 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.759-874_759-873ins others(1): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89528603 | |||||||
| chr16:89528603 | C | CT | 67 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0225 others(64): Show |
68 | HG00280.hp1 HG00323.hp1 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.759-854dupT | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr16 | 89528603 | ||||||
| chr16:89528603 | C | CTT | 13 | a0001c0001t0001g0231 a0001c0001t0002g0023 a0001c0001t0002g0232 others(10): Show |
13 | HG00741.hp2 HG01978.hp2 HG02071.hp1 others(10): Show |
intron_variant | MODIFIER | c.759-855_759-854dup others(2): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr16 | 89528603 | ||||||
| chr16:89528603 | CTT | C | 7 | a0001c0001t0001g0223 a0001c0001t0002g0224 a0001c0019t0003g0220 others(4): Show |
7 | HG02451.hp2 HG02717.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.759-855_759-854del others(2): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr16 | 89528603 | ||||||
| chr16:89528604 | T | A | 134 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0043 others(131): Show |
135 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.759-873T>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89528604 | |||||||
| chr16:89528606 | T | A | 6 | a0001c0001t0001g0223 a0001c0001t0002g0224 a0003c0003t0002g0234 others(3): Show |
6 | HG02451.hp2 HG02717.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.759-871T>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89528606 | |||||||
| chr16:89528628 | T | A | 191 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0043 others(188): Show |
192 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.759-849T>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89528628 | |||||||
| chr16:89528651 | G | T | 1 | a0001c0019t0003g0220 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.759-826G>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89528651 | |||||||
| chr16:89528673 | C | G | 1 | a0001c0001t0002g0204 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.759-804C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89528673 | |||||||
| chr16:89528678 | C | T | 6 | a0001c0001t0001g0223 a0001c0001t0002g0224 a0003c0003t0002g0234 others(3): Show |
6 | HG02451.hp2 HG02717.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.759-799C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89528678 | |||||||
| chr16:89528808 | C | G | 3 | a0001c0001t0001g0044 a0001c0001t0001g0124 a0001c0001t0001g0125 |
3 | HG01106.hp2 HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.759-669C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89528808 | |||||||
| chr16:89528853 | T | C | 192 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0043 others(189): Show |
193 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.759-624T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89528853 | |||||||
| chr16:89528932 | C | G | 1 | a0001c0001t0001g0274 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.759-545C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89528932 | |||||||
| chr16:89528967 | A | G | 1 | a0001c0001t0001g0194 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.759-510A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89528967 | |||||||
| chr16:89529101 | C | G | 6 | a0001c0001t0001g0223 a0001c0001t0002g0224 a0003c0003t0002g0234 others(3): Show |
6 | HG02451.hp2 HG02717.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.759-376C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89529101 | |||||||
| chr16:89529101 | C | T | 184 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0043 others(181): Show |
185 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.759-376C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89529101 | |||||||
| chr16:89529108 | G | A | 185 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0043 others(182): Show |
186 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.759-369G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89529108 | |||||||
| chr16:89529144 | G | A | 6 | a0001c0001t0001g0223 a0001c0001t0002g0224 a0003c0003t0002g0234 others(3): Show |
6 | HG02451.hp2 HG02717.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.759-333G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89529144 | |||||||
| chr16:89529296 | G | A | 1 | a0006c0014t0001g0262 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.759-181G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89529296 | |||||||
| chr16:89529312 | C | T | 1 | a0001c0004t0001g0008 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.759-165C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89529312 | |||||||
| chr16:89529315 | G | A | 184 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0043 others(181): Show |
185 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.759-162G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89529315 | |||||||
| chr16:89529322 | C | A | 1 | a0002c0015t0002g0041 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.759-155C>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89529322 | |||||||
| chr16:89529351 | C | T | 8 | a0001c0001t0001g0229 a0001c0001t0001g0231 a0001c0001t0002g0222 others(5): Show |
8 | HG01081.hp1 HG02109.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.759-126C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89529351 | |||||||
| chr16:89529375 | G | A | 1 | a0002c0002t0002g0012 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.759-102G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89529375 | |||||||
| chr16:89529698 | C | T | 184 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0043 others(181): Show |
185 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.861+119C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 6/16 | chr16 | 89529698 | |||||||
| chr16:89529748 | C | A | 2 | a0001c0001t0001g0255 a0001c0001t0008g0306 |
2 | HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.861+169C>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 6/16 | chr16 | 89529748 | |||||||
| chr16:89529775 | C | T | 1 | a0001c0001t0001g0316 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.861+196C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 6/16 | chr16 | 89529775 | |||||||
| chr16:89529784 | C | A | 1 | a0003c0003t0002g0234 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.861+205C>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 6/16 | chr16 | 89529784 | |||||||
| chr16:89529892 | T | C | 6 | a0001c0001t0001g0223 a0001c0001t0002g0224 a0003c0003t0002g0234 others(3): Show |
6 | HG02451.hp2 HG02717.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.861+313T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 6/16 | chr16 | 89529892 | |||||||
| chr16:89529894 | C | G | 1 | a0001c0001t0001g0087 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.861+315C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 6/16 | chr16 | 89529894 | |||||||
| chr16:89529900 | T | C | 6 | a0001c0001t0001g0223 a0001c0001t0002g0224 a0003c0003t0002g0234 others(3): Show |
6 | HG02451.hp2 HG02717.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.861+321T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 6/16 | chr16 | 89529900 | |||||||
| chr16:89529951 | T | A | 6 | a0001c0001t0001g0223 a0001c0001t0002g0224 a0003c0003t0002g0234 others(3): Show |
6 | HG02451.hp2 HG02717.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.861+372T>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 6/16 | chr16 | 89529951 | |||||||
| chr16:89529958 | G | A | 2 | a0001c0001t0001g0061 a0001c0001t0001g0062 |
2 | HG02129.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.861+379G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 6/16 | chr16 | 89529958 | |||||||
| chr16:89529964 | C | A | 8 | a0001c0001t0001g0229 a0001c0001t0001g0231 a0001c0001t0002g0222 others(5): Show |
8 | HG01081.hp1 HG02109.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.861+385C>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 6/16 | chr16 | 89529964 | |||||||
| chr16:89529965 | G | A | 1 | a0001c0001t0002g0260 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.861+386G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 6/16 | chr16 | 89529965 | |||||||
| chr16:89530072 | C | T | 6 | a0001c0001t0001g0223 a0001c0001t0002g0224 a0003c0003t0002g0234 others(3): Show |
6 | HG02451.hp2 HG02717.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.861+493C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 6/16 | chr16 | 89530072 | |||||||
| chr16:89530147 | T | G | 1 | a0001c0001t0001g0263 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.862-536T>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 6/16 | chr16 | 89530147 | |||||||
| chr16:89530147 | TTG | T | 46 | a0001c0001t0001g0013 a0001c0001t0001g0221 a0001c0001t0001g0229 others(43): Show |
46 | HG00323.hp1 HG00621.hp1 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.862-519_862-518del others(2): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr16 | 89530147 | ||||||
| chr16:89530149 | G | T | 189 | a0001c0001t0001g0002 a0001c0001t0001g0043 a0001c0001t0001g0044 others(186): Show |
190 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.862-534G>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 6/16 | chr16 | 89530149 | |||||||
| chr16:89530151 | G | T | 38 | a0001c0001t0001g0013 a0001c0001t0001g0221 a0001c0001t0002g0023 others(35): Show |
38 | HG00323.hp1 HG00621.hp1 HG00673.hp2 others(35): Show |
intron_variant | MODIFIER | c.862-532G>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 6/16 | chr16 | 89530151 | |||||||
| chr16:89530245 | A | G | 6 | a0001c0001t0001g0223 a0001c0001t0002g0224 a0003c0003t0002g0234 others(3): Show |
6 | HG02451.hp2 HG02717.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.862-438A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 6/16 | chr16 | 89530245 | |||||||
| chr16:89530306 | A | G | 236 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0013 others(233): Show |
237 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(234): Show |
intron_variant | MODIFIER | c.862-377A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 6/16 | chr16 | 89530306 | |||||||
| chr16:89530342 | C | T | 1 | a0001c0001t0007g0010 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.862-341C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 6/16 | chr16 | 89530342 | |||||||
| chr16:89530360 | G | A | 3 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0012t0001g0063 |
3 | HG02080.hp1 HG02129.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.862-323G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 6/16 | chr16 | 89530360 | |||||||
| chr16:89530382 | G | A | 1 | a0001c0001t0001g0243 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.862-301G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 6/16 | chr16 | 89530382 | |||||||
| chr16:89530600 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.862-83C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 6/16 | chr16 | 89530600 | |||||||
| chr16:89530606 | C | T | 1 | a0001c0001t0001g0311 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.862-77C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 6/16 | chr16 | 89530606 | |||||||
| chr16:89530649 | G | T | 184 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0043 others(181): Show |
185 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.862-34G>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 6/16 | chr16 | 89530649 | |||||||
| chr16:89530813 | A | G | 193 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0043 others(190): Show |
194 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(191): Show |
splice_region_variant&intron_variant | LOW | c.987+5A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 7/16 | chr16 | 89530813 | |||||||
| chr16:89530827 | G | A | 1 | a0001c0001t0001g0103 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.987+19G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 7/16 | chr16 | 89530827 | |||||||
| chr16:89530865 | C | T | 1 | a0001c0019t0003g0220 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.987+57C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 7/16 | chr16 | 89530865 | |||||||
| chr16:89530938 | C | T | 1 | a0002c0002t0002g0032 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.987+130C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 7/16 | chr16 | 89530938 | |||||||
| chr16:89530959 | T | C | 5 | a0001c0001t0002g0204 a0001c0001t0004g0201 a0001c0001t0004g0202 others(2): Show |
5 | HG02723.hp2 HG02896.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.987+151T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 7/16 | chr16 | 89530959 | |||||||
| chr16:89531024 | A | G | 2 | a0001c0001t0001g0221 a0001c0019t0003g0220 |
2 | HG02109.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.987+216A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 7/16 | chr16 | 89531024 | |||||||
| chr16:89531098 | C | A | 8 | a0001c0001t0001g0229 a0001c0001t0001g0231 a0001c0001t0002g0222 others(5): Show |
8 | HG01081.hp1 HG02109.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.987+290C>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 7/16 | chr16 | 89531098 | |||||||
| chr16:89531120 | T | C | 4 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0264 others(1): Show |
6 | HG01074.hp2 HG01255.hp2 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.987+312T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 7/16 | chr16 | 89531120 | |||||||
| chr16:89531151 | C | T | 1 | a0001c0005t0005g0305 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.987+343C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 7/16 | chr16 | 89531151 | |||||||
| chr16:89531156 | C | CT | 6 | a0001c0001t0001g0223 a0001c0001t0002g0224 a0003c0003t0002g0234 others(3): Show |
6 | HG02451.hp2 HG02717.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.987+350dupT | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr16 | 89531156 | ||||||
| chr16:89531184 | C | T | 6 | a0001c0001t0001g0223 a0001c0001t0002g0224 a0003c0003t0002g0234 others(3): Show |
6 | HG02451.hp2 HG02717.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.987+376C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 7/16 | chr16 | 89531184 | |||||||
| chr16:89531185 | G | A | 1 | a0001c0001t0001g0279 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.987+377G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 7/16 | chr16 | 89531185 | |||||||
| chr16:89531225 | CAT | C | 6 | a0001c0001t0001g0223 a0001c0001t0002g0224 a0003c0003t0002g0234 others(3): Show |
6 | HG02451.hp2 HG02717.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.987+418_987+419del others(2): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 7/16 | chr16 | 89531225 | |||||||
| chr16:89531332 | G | A | 2 | a0001c0001t0001g0164 a0001c0001t0001g0190 |
2 | NA18954.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.987+524G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 7/16 | chr16 | 89531332 | |||||||
| chr16:89531436 | C | A | 36 | a0001c0001t0001g0013 a0001c0001t0002g0023 a0001c0001t0002g0026 others(33): Show |
36 | HG00323.hp1 HG00621.hp1 HG00673.hp2 others(33): Show |
intron_variant | MODIFIER | c.988-468C>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 7/16 | chr16 | 89531436 | |||||||
| chr16:89531456 | C | T | 5 | a0001c0001t0001g0053 a0001c0001t0001g0131 a0001c0001t0001g0132 others(2): Show |
5 | HG00735.hp2 HG01070.hp2 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.988-448C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 7/16 | chr16 | 89531456 | |||||||
| chr16:89531460 | A | G | 1 | a0001c0001t0001g0323 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.988-444A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 7/16 | chr16 | 89531460 | |||||||
| chr16:89531468 | A | G | 185 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0043 others(182): Show |
186 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.988-436A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 7/16 | chr16 | 89531468 | |||||||
| chr16:89531663 | C | G | 1 | a0001c0001t0001g0121 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.988-241C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 7/16 | chr16 | 89531663 | |||||||
| chr16:89531669 | T | G | 1 | a0001c0005t0005g0302 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.988-235T>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 7/16 | chr16 | 89531669 | |||||||
| chr16:89531700 | G | GCGTGGTG others(6): Show |
1 | a0001c0001t0001g0214 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.988-203_988-191dup others(13): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr16 | 89531700 | ||||||
| chr16:89531772 | GTTTGAGG others(11): Show |
G | 4 | a0002c0002t0002g0016 a0002c0002t0002g0017 a0002c0002t0002g0021 others(1): Show |
4 | HG00323.hp1 HG02300.hp1 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.988-130_988-113del others(18): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr16 | 89531772 | ||||||
| chr16:89531779 | G | A | 1 | a0001c0001t0001g0352 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.988-125G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 7/16 | chr16 | 89531779 | |||||||
| chr16:89531789 | G | A | 1 | a0001c0005t0010g0238 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.988-115G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 7/16 | chr16 | 89531789 | |||||||
| chr16:89531794 | C | T | 1 | a0001c0005t0009g0340 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.988-110C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 7/16 | chr16 | 89531794 | |||||||
| chr16:89532283 | C | G | 1 | a0001c0001t0001g0255 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1151-180C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 8/16 | chr16 | 89532283 | |||||||
| chr16:89532329 | G | T | 4 | a0001c0001t0001g0059 a0001c0001t0001g0061 a0001c0001t0001g0062 others(1): Show |
4 | HG02080.hp1 HG02129.hp2 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.1151-134G>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 8/16 | chr16 | 89532329 | |||||||
| chr16:89532352 | A | G | 193 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0043 others(190): Show |
194 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.1151-111A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 8/16 | chr16 | 89532352 | |||||||
| chr16:89532724 | C | T | 1 | a0002c0002t0002g0014 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1324+88C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89532724 | |||||||
| chr16:89532772 | G | GA | 187 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0043 others(184): Show |
188 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.1324+148dupA | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89532772 | ||||||
| chr16:89532801 | A | T | 1 | a0008c0009t0001g0120 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1324+165A>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89532801 | |||||||
| chr16:89532821 | C | T | 4 | a0003c0003t0002g0234 a0003c0003t0002g0235 a0003c0003t0002g0236 others(1): Show |
4 | HG02451.hp2 HG02717.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1324+185C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89532821 | |||||||
| chr16:89532833 | C | T | 191 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0043 others(188): Show |
192 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.1324+197C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89532833 | |||||||
| chr16:89532858 | C | T | 3 | a0003c0003t0002g0055 a0003c0003t0002g0056 a0003c0003t0002g0057 |
3 | HG02615.hp2 HG02970.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1324+222C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89532858 | |||||||
| chr16:89532908 | A | G | 3 | a0001c0001t0001g0231 a0001c0001t0002g0230 a0001c0001t0002g0233 |
3 | HG02109.hp1 HG02572.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1324+272A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89532908 | |||||||
| chr16:89532938 | C | T | 2 | a0005c0007t0001g0297 a0005c0007t0001g0298 |
2 | HG01884.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.1324+302C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89532938 | |||||||
| chr16:89532944 | G | T | 185 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0043 others(182): Show |
186 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.1324+308G>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89532944 | |||||||
| chr16:89532947 | G | A | 185 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0043 others(182): Show |
186 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.1324+311G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89532947 | |||||||
| chr16:89532957 | C | A | 2 | a0005c0007t0001g0297 a0005c0007t0001g0298 |
2 | HG01884.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.1324+321C>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89532957 | |||||||
| chr16:89532994 | C | T | 2 | a0001c0001t0002g0023 a0001c0001t0002g0031 |
2 | HG02071.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1324+358C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89532994 | |||||||
| chr16:89533004 | A | G | 1 | a0001c0001t0001g0195 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1324+368A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89533004 | |||||||
| chr16:89533073 | C | CA | 165 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0043 others(162): Show |
166 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.1324+457dupA | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89533073 | ||||||
| chr16:89533073 | C | CAA | 19 | a0001c0001t0001g0064 a0001c0001t0001g0067 a0001c0001t0001g0070 others(16): Show |
19 | HG00438.hp2 HG01109.hp1 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.1324+456_1324+457d others(4): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89533073 | ||||||
| chr16:89533073 | CA | C | 82 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(79): Show |
86 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.1324+457delA | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89533073 | ||||||
| chr16:89533091 | A | AC | 3 | a0003c0003t0002g0055 a0003c0003t0002g0056 a0003c0003t0002g0057 |
3 | HG02615.hp2 HG02970.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1324+455_1324+456i others(3): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89533091 | |||||||
| chr16:89533094 | C | A | 4 | a0001c0001t0001g0094 a0001c0001t0001g0102 a0001c0001t0001g0108 others(1): Show |
4 | HG02015.hp1 HG02074.hp2 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.1324+458C>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89533094 | |||||||
| chr16:89533122 | A | G | 193 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0043 others(190): Show |
194 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.1324+486A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89533122 | |||||||
| chr16:89533172 | C | T | 1 | a0001c0001t0001g0138 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1324+536C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89533172 | |||||||
| chr16:89533182 | CTT | C | 7 | a0001c0001t0001g0223 a0001c0001t0001g0329 a0001c0001t0002g0224 others(4): Show |
7 | HG02451.hp2 HG02717.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1324+551_1324+552d others(4): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89533182 | ||||||
| chr16:89533192 | T | C | 194 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0043 others(191): Show |
195 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(192): Show |
intron_variant | MODIFIER | c.1324+556T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89533192 | |||||||
| chr16:89533208 | C | A | 1 | a0001c0001t0001g0221 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1324+572C>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89533208 | |||||||
| chr16:89533220 | C | T | 2 | a0001c0001t0001g0330 a0001c0001t0001g0331 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1324+584C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89533220 | |||||||
| chr16:89533221 | G | A | 3 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0186 |
3 | HG02717.hp2 HG03471.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1324+585G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89533221 | |||||||
| chr16:89533261 | G | A | 6 | a0001c0001t0001g0223 a0001c0001t0002g0224 a0003c0003t0002g0234 others(3): Show |
6 | HG02451.hp2 HG02717.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1324+625G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89533261 | |||||||
| chr16:89533267 | T | A | 2 | a0001c0001t0001g0330 a0001c0001t0001g0331 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1324+631T>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89533267 | |||||||
| chr16:89533302 | A | G | 1 | a0001c0001t0001g0078 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1324+666A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89533302 | |||||||
| chr16:89533436 | A | G | 4 | a0001c0001t0001g0231 a0001c0001t0002g0230 a0001c0001t0002g0233 others(1): Show |
4 | HG02109.hp1 HG02572.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1324+800A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89533436 | |||||||
| chr16:89533578 | G | C | 1 | a0001c0001t0004g0201 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1324+942G>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89533578 | |||||||
| chr16:89533629 | G | A | 9 | a0001c0001t0001g0221 a0001c0001t0001g0242 a0001c0001t0001g0251 others(6): Show |
9 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1324+993G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89533629 | |||||||
| chr16:89533666 | A | T | 4 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0253 others(1): Show |
4 | HG02451.hp1 HG02723.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1324+1030A>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89533666 | |||||||
| chr16:89533753 | T | C | 1 | a0001c0005t0009g0340 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1324+1117T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89533753 | |||||||
| chr16:89533769 | A | T | 187 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0013 others(184): Show |
188 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.1324+1133A>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89533769 | |||||||
| chr16:89533808 | T | G | 9 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 others(6): Show |
9 | HG00597.hp2 NA18946.hp2 NA18974.hp1 others(6): Show |
intron_variant | MODIFIER | c.1324+1172T>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89533808 | |||||||
| chr16:89533823 | T | A | 192 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0013 others(189): Show |
193 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.1324+1187T>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89533823 | |||||||
| chr16:89533837 | T | C | 333 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(330): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.1324+1201T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89533837 | |||||||
| chr16:89533926 | G | T | 1 | a0003c0003t0002g0211 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1324+1290G>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89533926 | |||||||
| chr16:89533946 | A | T | 1 | a0001c0001t0001g0119 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1324+1310A>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89533946 | |||||||
| chr16:89533953 | C | T | 1 | a0001c0005t0005g0302 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1324+1317C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89533953 | |||||||
| chr16:89533994 | C | T | 1 | a0002c0002t0002g0021 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1324+1358C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89533994 | |||||||
| chr16:89534035 | A | G | 1 | a0001c0004t0001g0179 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1324+1399A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89534035 | |||||||
| chr16:89534136 | G | A | 6 | a0001c0001t0001g0223 a0001c0001t0002g0224 a0003c0003t0002g0234 others(3): Show |
6 | HG02451.hp2 HG02717.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1324+1500G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89534136 | |||||||
| chr16:89534199 | G | C | 8 | a0001c0001t0001g0229 a0001c0001t0001g0231 a0001c0001t0002g0222 others(5): Show |
8 | HG01081.hp1 HG02109.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1324+1563G>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89534199 | |||||||
| chr16:89534231 | A | G | 1 | a0002c0002t0002g0351 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1324+1595A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89534231 | |||||||
| chr16:89534310 | C | T | 192 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0013 others(189): Show |
193 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.1324+1674C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89534310 | |||||||
| chr16:89534370 | G | A | 1 | a0001c0001t0001g0221 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1324+1734G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89534370 | |||||||
| chr16:89534394 | T | C | 193 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0013 others(190): Show |
194 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.1324+1758T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89534394 | |||||||
| chr16:89534569 | G | T | 1 | a0001c0001t0001g0253 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1324+1933G>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89534569 | |||||||
| chr16:89534821 | C | A | 1 | a0001c0001t0001g0279 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1324+2185C>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89534821 | |||||||
| chr16:89534826 | C | T | 35 | a0001c0001t0002g0023 a0001c0001t0002g0026 a0001c0001t0002g0031 others(32): Show |
35 | HG00323.hp1 HG00621.hp1 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.1324+2190C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89534826 | |||||||
| chr16:89535064 | C | G | 192 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0013 others(189): Show |
193 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.1324+2428C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89535064 | |||||||
| chr16:89535076 | A | G | 35 | a0001c0001t0002g0023 a0001c0001t0002g0026 a0001c0001t0002g0031 others(32): Show |
35 | HG00323.hp1 HG00621.hp1 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.1324+2440A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89535076 | |||||||
| chr16:89535084 | A | G | 35 | a0001c0001t0002g0023 a0001c0001t0002g0026 a0001c0001t0002g0031 others(32): Show |
35 | HG00323.hp1 HG00621.hp1 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.1324+2448A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89535084 | |||||||
| chr16:89535146 | T | C | 37 | a0001c0001t0001g0103 a0001c0001t0001g0279 a0001c0001t0002g0023 others(34): Show |
37 | HG00323.hp1 HG00621.hp1 HG00673.hp2 others(34): Show |
intron_variant | MODIFIER | c.1324+2510T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89535146 | |||||||
| chr16:89535176 | G | T | 1 | a0001c0001t0002g0230 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1324+2540G>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89535176 | |||||||
| chr16:89535280 | C | T | 1 | a0005c0007t0001g0298 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1324+2644C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89535280 | |||||||
| chr16:89535305 | G | A | 2 | a0001c0001t0001g0221 a0001c0013t0003g0341 |
2 | HG01891.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.1324+2669G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89535305 | |||||||
| chr16:89535357 | A | T | 42 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(39): Show |
45 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(42): Show |
intron_variant | MODIFIER | c.1324+2721A>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89535357 | |||||||
| chr16:89535427 | G | A | 1 | a0001c0001t0001g0321 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1324+2791G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89535427 | |||||||
| chr16:89535485 | C | T | 132 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(129): Show |
135 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.1324+2849C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89535485 | |||||||
| chr16:89535501 | C | T | 1 | a0001c0001t0001g0332 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1324+2865C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89535501 | |||||||
| chr16:89535548 | C | T | 1 | a0001c0001t0001g0052 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1324+2912C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89535548 | |||||||
| chr16:89535582 | G | A | 36 | a0001c0001t0001g0221 a0001c0001t0002g0023 a0001c0001t0002g0026 others(33): Show |
36 | HG00323.hp1 HG00621.hp1 HG00673.hp2 others(33): Show |
intron_variant | MODIFIER | c.1324+2946G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89535582 | |||||||
| chr16:89535598 | C | G | 134 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(131): Show |
138 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.1324+2962C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89535598 | |||||||
| chr16:89535620 | T | G | 35 | a0001c0001t0002g0023 a0001c0001t0002g0026 a0001c0001t0002g0031 others(32): Show |
35 | HG00323.hp1 HG00621.hp1 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.1324+2984T>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89535620 | |||||||
| chr16:89535659 | G | A | 1 | a0001c0001t0001g0320 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1324+3023G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89535659 | |||||||
| chr16:89535741 | C | T | 193 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0013 others(190): Show |
194 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.1324+3105C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89535741 | |||||||
| chr16:89535745 | G | C | 156 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(153): Show |
160 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.1324+3109G>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89535745 | |||||||
| chr16:89535746 | A | G | 1 | a0001c0001t0001g0315 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1324+3110A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89535746 | |||||||
| chr16:89535755 | C | T | 5 | a0001c0001t0002g0224 a0003c0003t0002g0234 a0003c0003t0002g0235 others(2): Show |
5 | HG02451.hp2 HG02717.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1324+3119C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89535755 | |||||||
| chr16:89535815 | A | ATGTGGCC others(365): Show |
1 | a0001c0001t0001g0221 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1324+3209_1324+321 others(376): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89535815 | ||||||
| chr16:89535815 | A | ATGTGGCC others(272): Show |
2 | a0001c0013t0003g0341 a0001c0019t0003g0220 |
2 | HG01891.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1324+3292_1324+329 others(283): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89535815 | ||||||
| chr16:89535854 | TCTCTGGT others(394): Show |
T | 1 | a0001c0001t0003g0296 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1324+3241_1324+364 others(4): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89535854 | ||||||
| chr16:89535877 | C | G | 184 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0013 others(181): Show |
185 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.1324+3241C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89535877 | |||||||
| chr16:89535908 | C | G | 6 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(3): Show |
6 | HG00639.hp1 HG01069.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.1324+3272C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89535908 | |||||||
| chr16:89535916 | T | TCTCTGGT others(24): Show |
1 | a0001c0001t0001g0048 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1324+3292_1324+329 others(35): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89535916 | ||||||
| chr16:89535916 | T | TCTCTGGT others(272): Show |
4 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0003c0003t0002g0055 others(1): Show |
4 | HG01346.hp2 HG02486.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1324+3292_1324+329 others(283): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89535916 | ||||||
| chr16:89535929 | A | G | 191 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0013 others(188): Show |
192 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.1324+3293A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89535929 | |||||||
| chr16:89535939 | G | GTGTGGCC others(86): Show |
1 | a0001c0001t0001g0007 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1324+3310_1324+331 others(97): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89535939 | ||||||
| chr16:89535939 | G | GTGTGGCC others(55): Show |
5 | a0001c0001t0001g0047 a0001c0001t0001g0049 a0001c0001t0001g0050 others(2): Show |
5 | HG00639.hp1 HG01069.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.1324+3310_1324+331 others(66): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89535939 | ||||||
| chr16:89535939 | G | GTGTGGCC others(55): Show |
1 | a0001c0001t0001g0192 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1324+3333_1324+333 others(66): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89535939 | ||||||
| chr16:89535939 | G | GTGTGGCC others(86): Show |
159 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0043 others(156): Show |
160 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.1324+3333_1324+333 others(97): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89535939 | ||||||
| chr16:89535939 | G | GTGTGGCC others(117): Show |
2 | a0001c0001t0001g0106 a0008c0009t0001g0120 |
2 | NA18747.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.1324+3333_1324+333 others(128): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89535939 | ||||||
| chr16:89535939 | G | GTGTGGCC others(673): Show |
3 | a0001c0001t0001g0107 a0001c0001t0001g0197 a0001c0001t0001g0214 |
3 | HG00408.hp2 HG02129.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.1324+3333_1324+333 others(684): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89535939 | ||||||
| chr16:89535939 | G | GTGTGGCC others(86): Show |
6 | a0001c0001t0001g0228 a0001c0001t0001g0346 a0001c0001t0001g0349 others(3): Show |
6 | HG02055.hp1 HG02257.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1324+3316_1324+331 others(97): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89535939 | ||||||
| chr16:89535939 | GTGTGGCC others(24): Show |
G | 1 | a0001c0001t0002g0224 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1324+3396_1324+342 others(35): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89535939 | ||||||
| chr16:89535947 | T | TCTCTGGT others(24): Show |
2 | a0001c0001t0001g0188 a0001c0001t0001g0199 |
2 | HG03491.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.1324+3333_1324+333 others(35): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89535947 | ||||||
| chr16:89535947 | T | TCTCTGGT others(86): Show |
1 | a0001c0001t0001g0137 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1324+3333_1324+333 others(97): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89535947 | ||||||
| chr16:89535970 | C | G | 12 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 others(9): Show |
12 | HG01243.hp1 HG01346.hp2 HG01358.hp2 others(9): Show |
intron_variant | MODIFIER | c.1324+3334C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89535970 | |||||||
| chr16:89535978 | T | G | 4 | a0001c0001t0001g0046 a0001c0001t0001g0078 a0001c0001t0001g0085 others(1): Show |
4 | HG02647.hp1 HG03654.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.1324+3342T>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89535978 | |||||||
| chr16:89536001 | C | G | 7 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 others(4): Show |
7 | HG01243.hp1 HG01346.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1324+3365C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536001 | |||||||
| chr16:89536032 | C | CTGTGGCC others(415): Show |
1 | a0001c0001t0001g0078 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1324+3426_1324+342 others(426): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89536032 | ||||||
| chr16:89536032 | C | CTGTGGCC others(365): Show |
1 | a0001c0001t0001g0085 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1324+3426_1324+342 others(376): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89536032 | ||||||
| chr16:89536032 | C | CTGTGGCC others(209): Show |
1 | a0001c0001t0001g0145 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1324+3426_1324+342 others(220): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89536032 | ||||||
| chr16:89536032 | C | G | 4 | a0003c0003t0002g0234 a0003c0003t0002g0235 a0003c0003t0002g0236 others(1): Show |
4 | HG02451.hp2 HG02717.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1324+3396C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536032 | |||||||
| chr16:89536040 | T | G | 4 | a0003c0003t0002g0234 a0003c0003t0002g0235 a0003c0003t0002g0236 others(1): Show |
4 | HG02451.hp2 HG02717.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1324+3404T>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536040 | |||||||
| chr16:89536063 | G | C | 8 | a0001c0001t0001g0188 a0001c0001t0001g0231 a0001c0001t0002g0222 others(5): Show |
8 | HG01081.hp1 HG02109.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1324+3427G>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536063 | |||||||
| chr16:89536071 | G | T | 6 | a0001c0001t0001g0145 a0001c0001t0001g0188 a0001c0001t0001g0192 others(3): Show |
6 | HG01891.hp2 HG02109.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1324+3435G>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536071 | |||||||
| chr16:89536094 | G | C | 2 | a0001c0001t0001g0145 a0001c0001t0001g0188 |
2 | NA18961.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.1324+3458G>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536094 | |||||||
| chr16:89536102 | G | GCTCTGGT others(148): Show |
1 | a0001c0001t0001g0192 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1324+3496_1324+349 others(159): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89536102 | ||||||
| chr16:89536102 | G | GCTCTGGT others(117): Show |
1 | a0001c0001t0001g0107 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1324+3527_1324+352 others(128): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89536102 | ||||||
| chr16:89536102 | G | GCTCTGGT others(551): Show |
4 | a0001c0001t0002g0222 a0001c0001t0002g0232 a0001c0005t0009g0340 others(1): Show |
4 | HG01081.hp1 HG02258.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1324+3527_1324+352 others(562): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89536102 | ||||||
| chr16:89536102 | G | GCTCTGGT others(551): Show |
3 | a0001c0001t0001g0231 a0001c0001t0002g0230 a0001c0001t0002g0233 |
3 | HG02109.hp1 HG02572.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1324+3527_1324+352 others(562): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89536102 | ||||||
| chr16:89536102 | G | T | 8 | a0001c0001t0001g0106 a0001c0001t0001g0145 a0001c0001t0001g0188 others(5): Show |
8 | HG02451.hp2 HG02717.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.1324+3466G>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536102 | |||||||
| chr16:89536102 | GCTCTGGT others(24): Show |
G | 35 | a0001c0001t0002g0023 a0001c0001t0002g0026 a0001c0001t0002g0031 others(32): Show |
35 | HG00323.hp1 HG00621.hp1 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.1324+3497_1324+352 others(35): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89536102 | ||||||
| chr16:89536123 | C | A | 3 | a0001c0001t0001g0221 a0001c0013t0003g0341 a0001c0019t0003g0220 |
3 | HG01891.hp2 HG02109.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1324+3487C>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536123 | |||||||
| chr16:89536125 | G | C | 1 | a0001c0001t0001g0188 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1324+3489G>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536125 | |||||||
| chr16:89536133 | T | G | 2 | a0001c0001t0001g0145 a0001c0001t0001g0192 |
2 | HG03516.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.1324+3497T>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536133 | |||||||
| chr16:89536133 | T | TCTCTGGT others(117): Show |
1 | a0003c0003t0002g0057 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1324+3527_1324+352 others(128): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89536133 | ||||||
| chr16:89536133 | T | TCTCTGGT others(86): Show |
2 | a0001c0001t0001g0106 a0008c0009t0001g0120 |
2 | NA18747.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.1324+3527_1324+352 others(97): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89536133 | ||||||
| chr16:89536133 | T | TCTCTGGT others(117): Show |
83 | a0001c0001t0001g0007 a0001c0001t0001g0043 a0001c0001t0001g0046 others(80): Show |
83 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(80): Show |
intron_variant | MODIFIER | c.1324+3527_1324+352 others(128): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89536133 | ||||||
| chr16:89536136 | C | CTGGTGCT others(148): Show |
1 | a0001c0001t0001g0221 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1324+3524_1324+352 others(159): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89536136 | ||||||
| chr16:89536136 | C | CTGGTGCT others(148): Show |
2 | a0001c0013t0003g0341 a0001c0019t0003g0220 |
2 | HG01891.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1324+3527_1324+352 others(159): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89536136 | ||||||
| chr16:89536164 | G | T | 101 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0044 others(98): Show |
102 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.1324+3528G>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536164 | |||||||
| chr16:89536195 | T | G | 1 | a0001c0001t0001g0188 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1324+3559T>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536195 | |||||||
| chr16:89536195 | T | TCTCTGGT others(22): Show |
9 | a0001c0001t0001g0013 a0001c0001t0001g0047 a0001c0001t0001g0048 others(6): Show |
9 | HG00639.hp1 HG01069.hp2 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.1324+3564_1324+359 others(33): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89536195 | ||||||
| chr16:89536206 | G | C | 1 | a0001c0001t0003g0347 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1324+3570G>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536206 | |||||||
| chr16:89536211 | G | T | 35 | a0001c0001t0002g0023 a0001c0001t0002g0026 a0001c0001t0002g0031 others(32): Show |
35 | HG00323.hp1 HG00621.hp1 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.1324+3575G>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536211 | |||||||
| chr16:89536218 | G | C | 120 | a0001c0001t0001g0002 a0001c0001t0001g0044 a0001c0001t0001g0045 others(117): Show |
121 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.1324+3582G>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536218 | |||||||
| chr16:89536249 | G | C | 1 | a0001c0001t0002g0224 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1324+3613G>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536249 | |||||||
| chr16:89536255 | C | CCG | 13 | a0001c0001t0001g0013 a0001c0001t0001g0047 a0001c0001t0001g0048 others(10): Show |
13 | HG00639.hp1 HG01069.hp2 HG01256.hp1 others(10): Show |
intron_variant | MODIFIER | c.1324+3620_1324+362 others(6): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89536255 | ||||||
| chr16:89536255 | C | CCGCTCTG others(150): Show |
9 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0075 others(6): Show |
9 | HG00621.hp2 HG01243.hp2 HG02148.hp1 others(6): Show |
intron_variant | MODIFIER | c.1324+3620_1324+362 others(161): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89536255 | ||||||
| chr16:89536255 | C | CCGCTCTG others(148): Show |
1 | a0001c0001t0001g0138 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1324+3620_1324+362 others(159): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89536255 | ||||||
| chr16:89536255 | C | CCGCTCTG others(179): Show |
73 | a0001c0001t0001g0002 a0001c0001t0001g0044 a0001c0001t0001g0045 others(70): Show |
74 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.1324+3620_1324+362 others(190): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89536255 | ||||||
| chr16:89536255 | C | CCGCTCTG others(86): Show |
4 | a0003c0003t0002g0234 a0003c0003t0002g0235 a0003c0003t0002g0236 others(1): Show |
4 | HG02451.hp2 HG02717.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1324+3620_1324+362 others(97): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89536255 | ||||||
| chr16:89536255 | C | CCTCTCTG others(117): Show |
1 | a0001c0001t0002g0224 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1324+3623_1324+362 others(128): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89536255 | ||||||
| chr16:89536255 | C | CCTCTCTG others(88): Show |
2 | a0001c0001t0001g0076 a0001c0001t0001g0077 |
2 | HG01346.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1324+3623_1324+362 others(99): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89536255 | ||||||
| chr16:89536255 | C | CCTCTCTG others(86): Show |
1 | a0001c0001t0001g0188 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1324+3623_1324+362 others(97): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89536255 | ||||||
| chr16:89536286 | T | G | 104 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0044 others(101): Show |
105 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.1324+3650T>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536286 | |||||||
| chr16:89536286 | T | TCTCTGGT others(55): Show |
1 | a0001c0001t0001g0190 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1324+3710_1324+371 others(66): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89536286 | ||||||
| chr16:89536317 | G | GCTCTGGT others(55): Show |
86 | a0001c0001t0001g0007 a0001c0001t0001g0046 a0001c0001t0001g0053 others(83): Show |
86 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(83): Show |
intron_variant | MODIFIER | c.1324+3710_1324+371 others(66): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89536317 | ||||||
| chr16:89536317 | G | GCTCTGGT others(55): Show |
1 | a0001c0001t0001g0043 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1324+3710_1324+371 others(66): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89536317 | ||||||
| chr16:89536317 | G | GCTCTGGT others(24): Show |
11 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0075 others(8): Show |
11 | HG00621.hp2 HG01243.hp2 HG02148.hp1 others(8): Show |
intron_variant | MODIFIER | c.1324+3710_1324+371 others(35): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89536317 | ||||||
| chr16:89536317 | G | T | 92 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0044 others(89): Show |
93 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.1324+3681G>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536317 | |||||||
| chr16:89536372 | T | C | 3 | a0001c0001t0001g0128 a0001c0001t0001g0175 a0001c0001t0001g0198 |
3 | HG01099.hp2 HG03704.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.1324+3736T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536372 | |||||||
| chr16:89536381 | G | A | 1 | a0001c0001t0001g0197 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1324+3745G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536381 | |||||||
| chr16:89536451 | CGGTGAGG others(2): Show |
C | 37 | a0001c0001t0002g0023 a0001c0001t0002g0026 a0001c0001t0002g0031 others(34): Show |
37 | HG00323.hp1 HG00621.hp1 HG00673.hp2 others(34): Show |
intron_variant | MODIFIER | c.1324+3841_1324+384 others(13): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89536451 | ||||||
| chr16:89536451 | CGGTGAGG others(11): Show |
C | 1 | a0001c0001t0001g0293 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1324+3832_1324+384 others(22): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89536451 | ||||||
| chr16:89536468 | C | CCGGGTGA others(69): Show |
1 | a0001c0001t0001g0078 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1324+3832_1324+383 others(80): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536468 | |||||||
| chr16:89536469 | G | A | 1 | a0001c0001t0001g0078 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1324+3833G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536469 | |||||||
| chr16:89536469 | G | GGGTGAGG others(45): Show |
4 | a0001c0001t0001g0069 a0001c0001t0001g0081 a0001c0001t0001g0088 others(1): Show |
4 | HG01074.hp1 HG01243.hp2 HG02148.hp1 others(1): Show |
intron_variant | MODIFIER | c.1324+3841_1324+384 others(56): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89536469 | ||||||
| chr16:89536469 | G | GGGTGAGG others(78): Show |
180 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0013 others(177): Show |
181 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(178): Show |
intron_variant | MODIFIER | c.1324+3841_1324+384 others(89): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89536469 | ||||||
| chr16:89536469 | G | GGGTGAGG others(40): Show |
3 | a0001c0001t0001g0221 a0001c0013t0003g0341 a0001c0019t0003g0220 |
3 | HG01891.hp2 HG02109.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1324+3849_1324+385 others(51): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89536469 | ||||||
| chr16:89536469 | G | GGGTGAGG others(12): Show |
1 | a0001c0001t0001g0253 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1324+3842_1324+386 others(23): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89536469 | ||||||
| chr16:89536469 | G | GGGTGAGG others(45): Show |
1 | a0001c0001t0002g0260 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1324+3903_1324+395 others(56): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89536469 | ||||||
| chr16:89536469 | GGGTGAGG others(26): Show |
G | 4 | a0003c0003t0002g0234 a0003c0003t0002g0235 a0003c0003t0002g0236 others(1): Show |
4 | HG02451.hp2 HG02717.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1324+3861_1324+389 others(37): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89536469 | ||||||
| chr16:89536472 | T | TGAGGCCG others(12): Show |
3 | a0001c0001t0001g0097 a0001c0001t0001g0229 a0007c0017t0001g0152 |
3 | HG00741.hp1 HG01106.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1324+3841_1324+384 others(23): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89536472 | ||||||
| chr16:89536481 | T | C | 4 | a0001c0001t0001g0097 a0001c0001t0001g0229 a0001c0001t0002g0224 others(1): Show |
4 | HG00741.hp1 HG01106.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1324+3845T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536481 | |||||||
| chr16:89536486 | T | C | 4 | a0001c0001t0001g0097 a0001c0001t0001g0229 a0001c0001t0002g0224 others(1): Show |
4 | HG00741.hp1 HG01106.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1324+3850T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536486 | |||||||
| chr16:89536488 | A | G | 1 | a0001c0001t0001g0183 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1324+3852A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536488 | |||||||
| chr16:89536491 | T | C | 1 | a0001c0001t0001g0183 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1324+3855T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536491 | |||||||
| chr16:89536497 | A | G | 2 | a0001c0001t0001g0183 a0001c0001t0002g0224 |
2 | HG01175.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1324+3861A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536497 | |||||||
| chr16:89536500 | T | C | 1 | a0001c0001t0001g0183 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1324+3864T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536500 | |||||||
| chr16:89536505 | T | C | 1 | a0001c0001t0001g0183 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1324+3869T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536505 | |||||||
| chr16:89536506 | G | C | 2 | a0001c0001t0001g0183 a0001c0001t0002g0224 |
2 | HG01175.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1324+3870G>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536506 | |||||||
| chr16:89536510 | C | T | 2 | a0001c0001t0001g0183 a0001c0001t0002g0224 |
2 | HG01175.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1324+3874C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536510 | |||||||
| chr16:89536512 | G | A | 2 | a0001c0001t0001g0183 a0001c0001t0002g0224 |
2 | HG01175.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1324+3876G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536512 | |||||||
| chr16:89536514 | T | C | 4 | a0003c0003t0002g0234 a0003c0003t0002g0235 a0003c0003t0002g0236 others(1): Show |
4 | HG02451.hp2 HG02717.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1324+3878T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536514 | |||||||
| chr16:89536514 | T | G | 2 | a0001c0001t0001g0183 a0001c0001t0002g0224 |
2 | HG01175.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1324+3878T>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536514 | |||||||
| chr16:89536515 | G | C | 2 | a0001c0001t0001g0183 a0001c0001t0002g0224 |
2 | HG01175.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1324+3879G>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536515 | |||||||
| chr16:89536519 | T | C | 4 | a0003c0003t0002g0234 a0003c0003t0002g0235 a0003c0003t0002g0236 others(1): Show |
4 | HG02451.hp2 HG02717.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1324+3883T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536519 | |||||||
| chr16:89536520 | C | CAGGTGAA others(7): Show |
2 | a0001c0001t0001g0052 a0001c0001t0001g0188 |
2 | NA18957.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.1324+3890_1324+389 others(18): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89536520 | ||||||
| chr16:89536520 | C | CAGGTGAG others(7): Show |
184 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0013 others(181): Show |
185 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.1324+3893_1324+389 others(18): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89536520 | ||||||
| chr16:89536520 | C | CAGGTGAG others(40): Show |
2 | a0001c0001t0001g0144 a0001c0006t0001g0058 |
2 | HG01074.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.1324+3893_1324+389 others(51): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89536520 | ||||||
| chr16:89536520 | C | G | 2 | a0001c0001t0001g0183 a0001c0001t0002g0224 |
2 | HG01175.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1324+3884C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536520 | |||||||
| chr16:89536530 | G | A | 1 | a0001c0001t0002g0224 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1324+3894G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536530 | |||||||
| chr16:89536549 | A | G | 2 | a0001c0001t0001g0144 a0001c0001t0002g0224 |
2 | HG02809.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.1324+3913A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536549 | |||||||
| chr16:89536550 | G | T | 1 | a0001c0001t0002g0224 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1324+3914G>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536550 | |||||||
| chr16:89536561 | GCGGGTGA others(3): Show |
G | 1 | a0001c0001t0002g0224 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1324+3927_1324+393 others(14): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89536561 | ||||||
| chr16:89536563 | G | A | 4 | a0003c0003t0002g0234 a0003c0003t0002g0235 a0003c0003t0002g0236 others(1): Show |
4 | HG02451.hp2 HG02717.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1324+3927G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536563 | |||||||
| chr16:89536577 | G | C | 13 | a0001c0001t0001g0243 a0001c0001t0001g0324 a0001c0001t0001g0325 others(10): Show |
13 | HG01192.hp1 HG02280.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.1324+3941G>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536577 | |||||||
| chr16:89536582 | G | A | 5 | a0001c0001t0001g0097 a0001c0001t0001g0183 a0001c0001t0002g0224 others(2): Show |
5 | HG00741.hp1 HG01074.hp1 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.1324+3946G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536582 | |||||||
| chr16:89536583 | G | T | 4 | a0003c0003t0002g0234 a0003c0003t0002g0235 a0003c0003t0002g0236 others(1): Show |
4 | HG02451.hp2 HG02717.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1324+3947G>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536583 | |||||||
| chr16:89536586 | G | GAGGTGAG others(2): Show |
4 | a0003c0003t0002g0234 a0003c0003t0002g0235 a0003c0003t0002g0236 others(1): Show |
4 | HG02451.hp2 HG02717.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1324+3959_1324+396 others(13): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89536586 | ||||||
| chr16:89536586 | G | GAGGTGAG others(12): Show |
1 | a0001c0001t0001g0183 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1324+3959_1324+396 others(23): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89536586 | ||||||
| chr16:89536596 | A | AGGTGAGG others(7): Show |
1 | a0001c0001t0001g0183 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1324+3972_1324+397 others(18): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89536596 | ||||||
| chr16:89536596 | A | G | 3 | a0001c0001t0001g0097 a0001c0006t0001g0058 a0007c0017t0001g0152 |
3 | HG00741.hp1 HG01074.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.1324+3960A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536596 | |||||||
| chr16:89536605 | G | C | 1 | a0001c0006t0001g0058 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1324+3969G>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536605 | |||||||
| chr16:89536618 | C | T | 4 | a0003c0003t0002g0234 a0003c0003t0002g0235 a0003c0003t0002g0236 others(1): Show |
4 | HG02451.hp2 HG02717.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1324+3982C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536618 | |||||||
| chr16:89536624 | AG | A | 4 | a0003c0003t0002g0234 a0003c0003t0002g0235 a0003c0003t0002g0236 others(1): Show |
4 | HG02451.hp2 HG02717.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1324+3991delG | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89536624 | ||||||
| chr16:89536634 | A | AG | 4 | a0003c0003t0002g0234 a0003c0003t0002g0235 a0003c0003t0002g0236 others(1): Show |
4 | HG02451.hp2 HG02717.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1324+4000dupG | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89536634 | ||||||
| chr16:89536641 | C | T | 4 | a0003c0003t0002g0234 a0003c0003t0002g0235 a0003c0003t0002g0236 others(1): Show |
4 | HG02451.hp2 HG02717.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1324+4005C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536641 | |||||||
| chr16:89536646 | T | C | 4 | a0003c0003t0002g0234 a0003c0003t0002g0235 a0003c0003t0002g0236 others(1): Show |
4 | HG02451.hp2 HG02717.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1324+4010T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536646 | |||||||
| chr16:89536647 | G | GAGGCAGG others(3): Show |
1 | a0001c0001t0001g0320 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1324+4011_1324+401 others(14): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536647 | |||||||
| chr16:89536650 | C | T | 1 | a0001c0001t0001g0320 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1324+4014C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536650 | |||||||
| chr16:89536656 | A | G | 197 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0013 others(194): Show |
198 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(195): Show |
intron_variant | MODIFIER | c.1324+4020A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536656 | |||||||
| chr16:89536659 | C | T | 2 | a0001c0001t0001g0103 a0001c0001t0001g0229 |
2 | HG01361.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1324+4023C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536659 | |||||||
| chr16:89536722 | A | G | 5 | a0001c0001t0002g0224 a0003c0003t0002g0234 a0003c0003t0002g0235 others(2): Show |
5 | HG02451.hp2 HG02717.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1324+4086A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536722 | |||||||
| chr16:89536809 | C | T | 1 | a0001c0001t0001g0206 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1324+4173C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536809 | |||||||
| chr16:89536860 | C | T | 4 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(1): Show |
4 | HG02523.hp2 NA18945.hp1 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.1324+4224C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536860 | |||||||
| chr16:89536948 | G | T | 5 | a0001c0001t0002g0224 a0003c0003t0002g0234 a0003c0003t0002g0235 others(2): Show |
5 | HG02451.hp2 HG02717.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1324+4312G>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536948 | |||||||
| chr16:89536978 | A | G | 1 | a0002c0002t0002g0020 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1324+4342A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536978 | |||||||
| chr16:89536982 | C | T | 1 | a0001c0001t0001g0221 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1324+4346C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536982 | |||||||
| chr16:89537007 | C | A | 1 | a0001c0001t0001g0087 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1324+4371C>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89537007 | |||||||
| chr16:89537050 | CTGAAGGC others(7): Show |
C | 4 | a0001c0001t0001g0110 a0001c0001t0001g0117 a0001c0001t0001g0118 others(1): Show |
4 | HG01928.hp1 HG01943.hp1 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.1324+4418_1324+443 others(18): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89537050 | ||||||
| chr16:89537178 | A | G | 198 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0013 others(195): Show |
199 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.1324+4542A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89537178 | |||||||
| chr16:89537290 | C | CT | 145 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(142): Show |
149 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.1324+4654_1324+465 others(5): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89537290 | |||||||
| chr16:89537318 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1324+4682G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89537318 | |||||||
| chr16:89537344 | G | A | 2 | a0001c0001t0001g0159 a0001c0001t0001g0185 |
2 | NA18984.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.1324+4708G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89537344 | |||||||
| chr16:89537358 | T | G | 1 | a0001c0001t0001g0146 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1324+4722T>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89537358 | |||||||
| chr16:89537375 | GGGGAGCG others(18): Show |
G | 5 | a0001c0001t0001g0257 a0001c0001t0001g0285 a0001c0001t0001g0286 others(2): Show |
5 | HG00408.hp1 HG00438.hp1 HG02155.hp1 others(2): Show |
intron_variant | MODIFIER | c.1324+4746_1324+477 others(29): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89537375 | ||||||
| chr16:89537454 | C | T | 5 | a0001c0001t0002g0224 a0003c0003t0002g0234 a0003c0003t0002g0235 others(2): Show |
5 | HG02451.hp2 HG02717.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1324+4818C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89537454 | |||||||
| chr16:89537532 | C | T | 1 | a0001c0001t0001g0221 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1324+4896C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89537532 | |||||||
| chr16:89537733 | C | T | 1 | a0001c0001t0001g0154 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1324+5097C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89537733 | |||||||
| chr16:89537972 | T | A | 1 | a0001c0001t0001g0352 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1324+5336T>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89537972 | |||||||
| chr16:89538202 | A | G | 197 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0013 others(194): Show |
198 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(195): Show |
intron_variant | MODIFIER | c.1324+5566A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89538202 | |||||||
| chr16:89538235 | C | T | 1 | a0001c0001t0001g0221 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1324+5599C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89538235 | |||||||
| chr16:89538339 | C | G | 1 | a0001c0001t0002g0224 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1324+5703C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89538339 | |||||||
| chr16:89538429 | C | T | 1 | a0001c0001t0001g0004 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1324+5793C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89538429 | |||||||
| chr16:89538617 | C | G | 1 | a0001c0001t0001g0147 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1324+5981C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89538617 | |||||||
| chr16:89538663 | C | T | 1 | a0001c0001t0002g0224 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1325-5985C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89538663 | |||||||
| chr16:89538700 | T | G | 1 | a0001c0001t0002g0224 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1325-5948T>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89538700 | |||||||
| chr16:89538747 | C | T | 1 | a0001c0001t0002g0224 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1325-5901C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89538747 | |||||||
| chr16:89538846 | G | A | 1 | a0001c0001t0002g0224 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1325-5802G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89538846 | |||||||
| chr16:89538955 | T | TGAACACT others(14): Show |
7 | a0001c0001t0001g0231 a0001c0001t0002g0222 a0001c0001t0002g0230 others(4): Show |
7 | HG01081.hp1 HG02109.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.1325-5692_1325-567 others(25): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89538955 | ||||||
| chr16:89538961 | C | T | 1 | a0002c0002t0002g0038 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1325-5687C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89538961 | |||||||
| chr16:89538996 | G | T | 7 | a0001c0001t0001g0231 a0001c0001t0002g0222 a0001c0001t0002g0230 others(4): Show |
7 | HG01081.hp1 HG02109.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.1325-5652G>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89538996 | |||||||
| chr16:89539087 | C | T | 140 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(137): Show |
144 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.1325-5561C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89539087 | |||||||
| chr16:89539157 | C | T | 1 | a0001c0001t0002g0224 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1325-5491C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89539157 | |||||||
| chr16:89539300 | G | A | 1 | a0001c0001t0001g0214 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1325-5348G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89539300 | |||||||
| chr16:89539325 | C | A | 2 | a0002c0002t0002g0011 a0002c0002t0002g0034 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1325-5323C>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89539325 | |||||||
| chr16:89539488 | G | A | 6 | a0001c0001t0001g0045 a0001c0001t0001g0126 a0001c0001t0001g0127 others(3): Show |
6 | HG00642.hp1 HG00735.hp1 HG01069.hp1 others(3): Show |
intron_variant | MODIFIER | c.1325-5160G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89539488 | |||||||
| chr16:89539556 | C | T | 2 | a0001c0001t0001g0070 a0001c0001t0001g0089 |
2 | HG00621.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.1325-5092C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89539556 | |||||||
| chr16:89539630 | G | A | 1 | a0001c0001t0001g0281 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1325-5018G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89539630 | |||||||
| chr16:89539688 | T | G | 3 | a0001c0001t0002g0224 a0001c0013t0003g0341 a0001c0019t0003g0220 |
3 | HG01891.hp2 HG02809.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1325-4960T>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89539688 | |||||||
| chr16:89539706 | A | G | 1 | a0001c0001t0001g0270 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1325-4942A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89539706 | |||||||
| chr16:89539950 | G | A | 4 | a0001c0001t0002g0023 a0001c0001t0002g0026 a0001c0001t0002g0031 others(1): Show |
4 | HG02071.hp1 HG02602.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.1325-4698G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89539950 | |||||||
| chr16:89540118 | C | T | 1 | a0001c0001t0001g0254 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1325-4530C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89540118 | |||||||
| chr16:89540376 | C | T | 1 | a0001c0001t0001g0270 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1325-4272C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89540376 | |||||||
| chr16:89540420 | C | G | 3 | a0001c0001t0002g0224 a0001c0013t0003g0341 a0001c0019t0003g0220 |
3 | HG01891.hp2 HG02809.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1325-4228C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89540420 | |||||||
| chr16:89540547 | C | T | 1 | a0001c0001t0001g0167 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1325-4101C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89540547 | |||||||
| chr16:89540734 | G | A | 53 | a0001c0001t0001g0002 a0001c0001t0001g0044 a0001c0001t0001g0045 others(50): Show |
54 | HG00099.hp2 HG00597.hp2 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.1325-3914G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89540734 | |||||||
| chr16:89540755 | G | A | 1 | a0001c0012t0001g0063 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1325-3893G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89540755 | |||||||
| chr16:89540836 | C | T | 2 | a0001c0001t0001g0013 a0001c0001t0001g0054 |
2 | HG01433.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1325-3812C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89540836 | |||||||
| chr16:89540849 | C | T | 1 | a0001c0001t0001g0043 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1325-3799C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89540849 | |||||||
| chr16:89540950 | A | G | 1 | a0001c0001t0002g0224 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1325-3698A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89540950 | |||||||
| chr16:89541006 | G | A | 191 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0013 others(188): Show |
192 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.1325-3642G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89541006 | |||||||
| chr16:89541006 | G | GACTAGAA others(191): Show |
1 | a0001c0001t0001g0217 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1325-3557_1325-355 others(202): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89541006 | ||||||
| chr16:89541006 | G | GACTAGAA others(288): Show |
1 | a0003c0003t0002g0056 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1325-3412_1325-341 others(299): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89541006 | ||||||
| chr16:89541008 | C | CTAGAAGA others(42): Show |
3 | a0001c0001t0001g0226 a0001c0001t0001g0243 a0001c0001t0001g0328 |
3 | HG02886.hp1 HG03225.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1325-3552_1325-350 others(53): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89541008 | ||||||
| chr16:89541008 | CTAGAAGA others(42): Show |
C | 1 | a0001c0001t0002g0224 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1325-3552_1325-350 others(53): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89541008 | ||||||
| chr16:89541047 | GTACGCAG others(91): Show |
G | 1 | a0001c0001t0001g0275 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1325-3552_1325-345 others(102): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89541047 | ||||||
| chr16:89541096 | GTACGCAG others(42): Show |
G | 139 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(136): Show |
143 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.1325-3446_1325-339 others(53): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89541096 | ||||||
| chr16:89541100 | G | A | 13 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0075 others(10): Show |
13 | HG00621.hp2 HG01243.hp2 HG01346.hp2 others(10): Show |
intron_variant | MODIFIER | c.1325-3548G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89541100 | |||||||
| chr16:89541145 | C | CTACGCAG others(42): Show |
1 | a0001c0001t0001g0239 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1325-3455_1325-345 others(53): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89541145 | ||||||
| chr16:89541145 | C | G | 2 | a0001c0001t0001g0101 a0001c0001t0001g0119 |
2 | HG02965.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1325-3503C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89541145 | |||||||
| chr16:89541147 | A | G | 1 | a0001c0001t0002g0224 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1325-3501A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89541147 | |||||||
| chr16:89541197 | C | T | 1 | a0001c0001t0001g0139 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1325-3451C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89541197 | |||||||
| chr16:89541202 | A | C | 2 | a0001c0013t0003g0341 a0001c0019t0003g0220 |
2 | HG01891.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1325-3446A>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89541202 | |||||||
| chr16:89541258 | A | G | 1 | a0001c0001t0002g0224 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1325-3390A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89541258 | |||||||
| chr16:89541271 | G | A | 141 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(138): Show |
145 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.1325-3377G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89541271 | |||||||
| chr16:89541295 | T | C | 2 | a0001c0013t0003g0341 a0001c0019t0003g0220 |
2 | HG01891.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1325-3353T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89541295 | |||||||
| chr16:89541427 | G | A | 1 | a0001c0001t0001g0229 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1325-3221G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89541427 | |||||||
| chr16:89541521 | T | C | 1 | a0001c0001t0002g0224 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1325-3127T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89541521 | |||||||
| chr16:89541532 | G | A | 1 | a0001c0001t0001g0004 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1325-3116G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89541532 | |||||||
| chr16:89541560 | A | G | 1 | a0001c0005t0010g0238 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1325-3088A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89541560 | |||||||
| chr16:89541561 | C | G | 1 | a0001c0001t0002g0224 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1325-3087C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89541561 | |||||||
| chr16:89541758 | G | A | 1 | a0001c0001t0001g0186 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1325-2890G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89541758 | |||||||
| chr16:89541827 | A | G | 234 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(231): Show |
238 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.1325-2821A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89541827 | |||||||
| chr16:89541887 | A | G | 1 | a0001c0001t0001g0269 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1325-2761A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89541887 | |||||||
| chr16:89541897 | G | A | 1 | a0001c0001t0001g0285 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1325-2751G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89541897 | |||||||
| chr16:89541934 | T | C | 143 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(140): Show |
147 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.1325-2714T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89541934 | |||||||
| chr16:89542035 | CAT | C | 9 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 others(6): Show |
9 | HG00597.hp2 NA18946.hp2 NA18974.hp1 others(6): Show |
intron_variant | MODIFIER | c.1325-2611_1325-261 others(6): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89542035 | ||||||
| chr16:89542052 | C | G | 1 | a0001c0001t0001g0102 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1325-2596C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89542052 | |||||||
| chr16:89542062 | G | A | 1 | a0001c0001t0002g0224 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1325-2586G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89542062 | |||||||
| chr16:89542125 | A | T | 1 | a0001c0001t0002g0224 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1325-2523A>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89542125 | |||||||
| chr16:89542150 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1325-2498G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89542150 | |||||||
| chr16:89542170 | A | C | 1 | a0001c0001t0001g0335 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1325-2478A>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89542170 | |||||||
| chr16:89542289 | G | A | 2 | a0001c0001t0001g0051 a0001c0001t0001g0206 |
2 | HG02145.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.1325-2359G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89542289 | |||||||
| chr16:89542294 | G | A | 98 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(95): Show |
102 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.1325-2354G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89542294 | |||||||
| chr16:89542359 | C | T | 1 | a0001c0001t0001g0183 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1325-2289C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89542359 | |||||||
| chr16:89542435 | G | A | 1 | a0001c0001t0002g0224 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1325-2213G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89542435 | |||||||
| chr16:89542589 | C | G | 1 | a0001c0001t0002g0224 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1325-2059C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89542589 | |||||||
| chr16:89542622 | T | C | 1 | a0001c0001t0001g0078 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1325-2026T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89542622 | |||||||
| chr16:89542705 | C | T | 3 | a0001c0001t0001g0226 a0001c0001t0001g0243 a0001c0001t0001g0328 |
3 | HG02886.hp1 HG03225.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1325-1943C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89542705 | |||||||
| chr16:89542833 | C | G | 154 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(151): Show |
158 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.1325-1815C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89542833 | |||||||
| chr16:89542900 | C | T | 4 | a0001c0001t0001g0323 a0001c0001t0001g0334 a0005c0007t0001g0297 others(1): Show |
4 | HG01884.hp2 HG02145.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.1325-1748C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89542900 | |||||||
| chr16:89542941 | C | CT | 12 | a0001c0001t0001g0051 a0001c0001t0001g0071 a0001c0001t0001g0087 others(9): Show |
12 | HG01106.hp2 HG01192.hp1 HG02027.hp1 others(9): Show |
intron_variant | MODIFIER | c.1325-1683dupT | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89542941 | ||||||
| chr16:89542941 | CT | C | 10 | a0001c0001t0001g0043 a0001c0001t0001g0064 a0001c0001t0001g0086 others(7): Show |
10 | HG00140.hp2 HG01167.hp2 HG01168.hp2 others(7): Show |
intron_variant | MODIFIER | c.1325-1683delT | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89542941 | ||||||
| chr16:89542941 | CTT | C | 104 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(101): Show |
108 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.1325-1684_1325-168 others(6): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89542941 | ||||||
| chr16:89542941 | CTTT | C | 57 | a0001c0001t0001g0069 a0001c0001t0001g0075 a0001c0001t0001g0076 others(54): Show |
57 | HG00323.hp1 HG00621.hp1 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.1325-1685_1325-168 others(7): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89542941 | ||||||
| chr16:89542978 | T | C | 1 | a0001c0001t0001g0229 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1325-1670T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89542978 | |||||||
| chr16:89543010 | T | G | 118 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(115): Show |
122 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.1325-1638T>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89543010 | |||||||
| chr16:89543017 | G | A | 1 | a0001c0001t0002g0224 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1325-1631G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89543017 | |||||||
| chr16:89543022 | C | A | 1 | a0001c0001t0001g0229 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1325-1626C>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89543022 | |||||||
| chr16:89543032 | C | G | 1 | a0001c0001t0002g0224 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1325-1616C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89543032 | |||||||
| chr16:89543034 | A | G | 172 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(169): Show |
176 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.1325-1614A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89543034 | |||||||
| chr16:89543048 | C | T | 35 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(32): Show |
38 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.1325-1600C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89543048 | |||||||
| chr16:89543080 | T | C | 1 | a0001c0001t0001g0084 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1325-1568T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89543080 | |||||||
| chr16:89543096 | C | T | 13 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0075 others(10): Show |
13 | HG00621.hp2 HG01243.hp2 HG01346.hp2 others(10): Show |
intron_variant | MODIFIER | c.1325-1552C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89543096 | |||||||
| chr16:89543097 | G | A | 1 | a0001c0001t0001g0052 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1325-1551G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89543097 | |||||||
| chr16:89543100 | A | G | 1 | a0002c0002t0002g0015 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1325-1548A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89543100 | |||||||
| chr16:89543105 | G | A | 2 | a0001c0001t0001g0099 a0001c0001t0001g0100 |
2 | HG02717.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1325-1543G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89543105 | |||||||
| chr16:89543109 | A | G | 2 | a0001c0001t0001g0299 a0001c0013t0003g0341 |
2 | HG01891.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.1325-1539A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89543109 | |||||||
| chr16:89543136 | A | G | 2 | a0001c0001t0001g0106 a0008c0009t0001g0120 |
2 | NA18747.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.1325-1512A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89543136 | |||||||
| chr16:89543148 | T | C | 10 | a0001c0001t0001g0051 a0001c0001t0001g0106 a0001c0001t0001g0192 others(7): Show |
10 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.1325-1500T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89543148 | |||||||
| chr16:89543149 | G | A | 2 | a0001c0001t0001g0106 a0008c0009t0001g0120 |
2 | NA18747.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.1325-1499G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89543149 | |||||||
| chr16:89543154 | A | G | 4 | a0001c0001t0001g0332 a0001c0001t0001g0344 a0001c0001t0001g0350 others(1): Show |
4 | HG02280.hp1 HG02572.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1325-1494A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89543154 | |||||||
| chr16:89543161 | A | C | 3 | a0001c0001t0001g0226 a0001c0001t0002g0222 a0001c0005t0010g0238 |
3 | HG01081.hp1 HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1325-1487A>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89543161 | |||||||
| chr16:89543164 | C | G | 103 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0051 others(100): Show |
105 | HG00323.hp1 HG00408.hp2 HG00558.hp1 others(102): Show |
intron_variant | MODIFIER | c.1325-1484C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89543164 | |||||||
| chr16:89543169 | C | A | 2 | a0001c0001t0001g0094 a0001c0001t0001g0109 |
2 | HG02074.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.1325-1479C>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89543169 | |||||||
| chr16:89543182 | T | A | 2 | a0001c0001t0002g0026 a0002c0002t0002g0033 |
2 | HG02602.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.1325-1466T>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89543182 | |||||||
| chr16:89543182 | T | C | 4 | a0001c0001t0001g0106 a0001c0001t0001g0217 a0001c0001t0002g0224 others(1): Show |
4 | HG01256.hp1 HG02809.hp2 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.1325-1466T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89543182 | |||||||
| chr16:89543190 | G | A | 2 | a0001c0001t0001g0183 a0001c0005t0010g0238 |
2 | HG01175.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.1325-1458G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89543190 | |||||||
| chr16:89543193 | C | T | 1 | a0001c0001t0001g0239 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1325-1455C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89543193 | |||||||
| chr16:89543194 | T | G | 2 | a0001c0001t0001g0239 a0001c0001t0001g0249 |
2 | HG02976.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1325-1454T>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89543194 | |||||||
| chr16:89543225 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1325-1423G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89543225 | |||||||
| chr16:89543232 | C | A | 1 | a0001c0001t0001g0299 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1325-1416C>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89543232 | |||||||
| chr16:89543237 | G | A | 3 | a0001c0001t0001g0134 a0001c0001t0001g0176 a0001c0001t0001g0346 |
3 | HG00642.hp1 HG00735.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1325-1411G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89543237 | |||||||
| chr16:89543238 | C | T | 10 | a0001c0001t0001g0069 a0001c0001t0001g0075 a0001c0001t0001g0076 others(7): Show |
10 | HG00621.hp2 HG01243.hp2 HG01346.hp2 others(7): Show |
intron_variant | MODIFIER | c.1325-1410C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89543238 | |||||||
| chr16:89543239 | G | A | 34 | a0001c0001t0001g0046 a0001c0001t0001g0095 a0001c0001t0001g0221 others(31): Show |
34 | HG00099.hp1 HG00280.hp1 HG00673.hp1 others(31): Show |
intron_variant | MODIFIER | c.1325-1409G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89543239 | |||||||
| chr16:89543242 | T | C | 1 | a0001c0001t0001g0265 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1325-1406T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89543242 | |||||||
| chr16:89543270 | C | CGGT | 57 | a0001c0001t0001g0069 a0001c0001t0001g0075 a0001c0001t0001g0076 others(54): Show |
57 | HG00408.hp2 HG00621.hp1 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.1325-1376_1325-137 others(7): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89543270 | ||||||
| chr16:89543286 | A | G | 37 | a0001c0001t0001g0214 a0001c0001t0002g0023 a0001c0001t0002g0026 others(34): Show |
37 | HG00323.hp1 HG00408.hp2 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.1325-1362A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89543286 | |||||||
| chr16:89543347 | C | CTTTTTTT others(3): Show |
4 | a0002c0002t0002g0025 a0002c0002t0002g0036 a0002c0002t0002g0040 others(1): Show |
4 | HG01515.hp2 HG01517.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1325-1293_1325-128 others(14): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89543347 | ||||||
| chr16:89543347 | C | CTTTTTTT others(4): Show |
52 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0075 others(49): Show |
52 | HG00323.hp1 HG00621.hp1 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.1325-1294_1325-128 others(15): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89543347 | ||||||
| chr16:89543347 | C | CTTTTTTT others(5): Show |
8 | a0001c0001t0001g0081 a0001c0001t0001g0088 a0001c0001t0001g0216 others(5): Show |
8 | HG01243.hp2 HG02148.hp1 HG02300.hp1 others(5): Show |
intron_variant | MODIFIER | c.1325-1295_1325-128 others(16): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89543347 | ||||||
| chr16:89543347 | C | CTTTTTTT others(6): Show |
3 | a0001c0005t0005g0302 a0001c0005t0005g0305 a0002c0002t0002g0028 |
3 | HG02559.hp1 NA18940.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1325-1296_1325-128 others(17): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89543347 | ||||||
| chr16:89543347 | C | CTTTTTTT others(7): Show |
3 | a0003c0003t0002g0055 a0003c0003t0002g0056 a0003c0003t0002g0057 |
3 | HG02615.hp2 HG02970.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1325-1297_1325-128 others(18): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89543347 | ||||||
| chr16:89543347 | CT | C | 8 | a0001c0001t0001g0047 a0001c0001t0001g0090 a0001c0001t0001g0139 others(5): Show |
8 | HG01109.hp2 HG01169.hp2 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.1325-1284delT | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89543347 | ||||||
| chr16:89543365 | G | T | 1 | a0001c0001t0001g0258 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1325-1283G>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89543365 | |||||||
| chr16:89543367 | G | C | 13 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0075 others(10): Show |
13 | HG00621.hp2 HG01243.hp2 HG01346.hp2 others(10): Show |
intron_variant | MODIFIER | c.1325-1281G>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89543367 | |||||||
| chr16:89543445 | G | A | 35 | a0001c0001t0002g0023 a0001c0001t0002g0026 a0001c0001t0002g0031 others(32): Show |
35 | HG00323.hp1 HG00621.hp1 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.1325-1203G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89543445 | |||||||
| chr16:89543613 | C | T | 67 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0075 others(64): Show |
67 | HG00323.hp1 HG00621.hp1 HG00621.hp2 others(64): Show |
intron_variant | MODIFIER | c.1325-1035C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89543613 | |||||||
| chr16:89543646 | ATTCTTTT others(2): Show |
A | 30 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0075 others(27): Show |
30 | HG00621.hp2 HG01081.hp1 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.1325-999_1325-991d others(11): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89543646 | ||||||
| chr16:89543646 | ATTCTTTT others(3): Show |
A | 36 | a0001c0001t0002g0023 a0001c0001t0002g0026 a0001c0001t0002g0031 others(33): Show |
36 | HG00323.hp1 HG00621.hp1 HG00673.hp2 others(33): Show |
intron_variant | MODIFIER | c.1325-999_1325-990d others(12): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89543646 | ||||||
| chr16:89543649 | C | CT | 18 | a0001c0001t0001g0005 a0001c0001t0001g0097 a0001c0001t0001g0103 others(15): Show |
18 | HG00140.hp1 HG00280.hp2 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.1325-978dupT | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89543649 | ||||||
| chr16:89543649 | CT | C | 6 | a0001c0001t0001g0064 a0001c0001t0001g0067 a0001c0001t0001g0121 others(3): Show |
6 | HG01943.hp1 HG02895.hp2 NA18941.hp1 others(3): Show |
intron_variant | MODIFIER | c.1325-978delT | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89543649 | ||||||
| chr16:89543699 | G | C | 4 | a0001c0001t0002g0023 a0001c0001t0002g0026 a0001c0001t0002g0031 others(1): Show |
4 | HG02071.hp1 HG02602.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.1325-949G>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89543699 | |||||||
| chr16:89543776 | C | G | 2 | a0001c0001t0001g0226 a0001c0001t0001g0243 |
2 | HG03225.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1325-872C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89543776 | |||||||
| chr16:89543784 | A | G | 1 | a0001c0001t0001g0335 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1325-864A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89543784 | |||||||
| chr16:89543796 | G | A | 1 | a0001c0001t0002g0224 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1325-852G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89543796 | |||||||
| chr16:89543836 | G | C | 1 | a0001c0001t0002g0224 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1325-812G>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89543836 | |||||||
| chr16:89543938 | C | T | 2 | a0001c0001t0001g0153 a0001c0001t0001g0213 |
2 | HG00140.hp1 HG00280.hp2 |
intron_variant | MODIFIER | c.1325-710C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89543938 | |||||||
| chr16:89543974 | A | T | 3 | a0001c0001t0001g0128 a0001c0001t0001g0175 a0001c0001t0001g0198 |
3 | HG01099.hp2 HG03704.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.1325-674A>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89543974 | |||||||
| chr16:89544100 | C | T | 1 | a0001c0001t0002g0224 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1325-548C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89544100 | |||||||
| chr16:89544162 | G | T | 1 | a0001c0001t0001g0315 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1325-486G>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89544162 | |||||||
| chr16:89544256 | C | G | 2 | a0001c0001t0001g0070 a0001c0001t0001g0089 |
2 | HG00621.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.1325-392C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89544256 | |||||||
| chr16:89544346 | G | A | 1 | a0001c0005t0005g0302 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1325-302G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89544346 | |||||||
| chr16:89544355 | A | G | 1 | a0002c0002t0002g0039 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1325-293A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89544355 | |||||||
| chr16:89544438 | C | T | 1 | a0001c0005t0010g0238 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1325-210C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89544438 | |||||||
| chr16:89544791 | G | A | 47 | a0001c0001t0001g0007 a0001c0001t0001g0046 a0001c0001t0001g0059 others(44): Show |
47 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.1449+19G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 10/16 | chr16 | 89544791 | |||||||
| chr16:89544827 | C | G | 1 | a0001c0001t0002g0224 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1449+55C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 10/16 | chr16 | 89544827 | |||||||
| chr16:89544856 | C | T | 1 | a0001c0005t0009g0340 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1449+84C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 10/16 | chr16 | 89544856 | |||||||
| chr16:89544946 | C | T | 2 | a0001c0013t0003g0341 a0001c0019t0003g0220 |
2 | HG01891.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1449+174C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 10/16 | chr16 | 89544946 | |||||||
| chr16:89544950 | CGGCTGCA others(54): Show |
C | 1 | a0001c0001t0001g0192 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1449+195_1449+255d others(63): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr16 | 89544950 | ||||||
| chr16:89544956 | C | T | 1 | a0001c0016t0001g0288 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1449+184C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 10/16 | chr16 | 89544956 | |||||||
| chr16:89545039 | A | G | 1 | a0001c0001t0001g0346 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1449+267A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 10/16 | chr16 | 89545039 | |||||||
| chr16:89545153 | T | G | 1 | a0001c0001t0001g0069 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1449+381T>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 10/16 | chr16 | 89545153 | |||||||
| chr16:89545378 | C | T | 5 | a0001c0001t0002g0204 a0001c0001t0004g0201 a0001c0001t0004g0202 others(2): Show |
5 | HG02723.hp2 HG02896.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1449+606C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 10/16 | chr16 | 89545378 | |||||||
| chr16:89545540 | C | T | 1 | a0001c0012t0001g0063 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1449+768C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 10/16 | chr16 | 89545540 | |||||||
| chr16:89545549 | T | C | 1 | a0001c0001t0001g0013 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1449+777T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 10/16 | chr16 | 89545549 | |||||||
| chr16:89545588 | CTTCTCCA others(11): Show |
C | 1 | a0001c0001t0008g0306 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1449+847_1449+864d others(20): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr16 | 89545588 | ||||||
| chr16:89545649 | C | G | 1 | a0001c0001t0002g0224 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1449+877C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 10/16 | chr16 | 89545649 | |||||||
| chr16:89545697 | G | A | 5 | a0001c0001t0001g0257 a0001c0001t0001g0285 a0001c0001t0001g0286 others(2): Show |
5 | HG00408.hp1 HG00438.hp1 HG02155.hp1 others(2): Show |
intron_variant | MODIFIER | c.1449+925G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 10/16 | chr16 | 89545697 | |||||||
| chr16:89545795 | C | T | 1 | a0003c0003t0002g0211 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1450-863C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 10/16 | chr16 | 89545795 | |||||||
| chr16:89545850 | T | C | 1 | a0001c0001t0001g0206 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1450-808T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 10/16 | chr16 | 89545850 | |||||||
| chr16:89545852 | A | AT | 65 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0075 others(62): Show |
65 | HG00323.hp1 HG00621.hp1 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.1450-801dupT | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr16 | 89545852 | ||||||
| chr16:89545866 | T | A | 1 | a0001c0001t0001g0119 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1450-792T>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 10/16 | chr16 | 89545866 | |||||||
| chr16:89545910 | T | C | 17 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(14): Show |
17 | HG00408.hp2 HG01934.hp2 HG02074.hp1 others(14): Show |
intron_variant | MODIFIER | c.1450-748T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 10/16 | chr16 | 89545910 | |||||||
| chr16:89545990 | G | A | 13 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0075 others(10): Show |
13 | HG00621.hp2 HG01243.hp2 HG01346.hp2 others(10): Show |
intron_variant | MODIFIER | c.1450-668G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 10/16 | chr16 | 89545990 | |||||||
| chr16:89546103 | T | G | 27 | a0001c0001t0001g0007 a0001c0001t0001g0046 a0001c0001t0001g0073 others(24): Show |
27 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(24): Show |
intron_variant | MODIFIER | c.1450-555T>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 10/16 | chr16 | 89546103 | |||||||
| chr16:89546144 | C | T | 1 | a0001c0001t0001g0256 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1450-514C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 10/16 | chr16 | 89546144 | |||||||
| chr16:89546227 | C | T | 2 | a0001c0005t0005g0302 a0001c0005t0005g0305 |
2 | HG02559.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1450-431C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 10/16 | chr16 | 89546227 | |||||||
| chr16:89546230 | G | A | 62 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0075 others(59): Show |
62 | HG00323.hp1 HG00621.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.1450-428G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 10/16 | chr16 | 89546230 | |||||||
| chr16:89546236 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1450-422G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 10/16 | chr16 | 89546236 | |||||||
| chr16:89546571 | A | AC | 91 | a0001c0001t0001g0046 a0001c0001t0001g0050 a0001c0001t0001g0052 others(88): Show |
91 | HG00140.hp1 HG00597.hp1 HG00597.hp2 others(88): Show |
intron_variant | MODIFIER | c.1450-75dupC | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr16 | 89546571 | ||||||
| chr16:89546571 | AC | A | 79 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(76): Show |
83 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(80): Show |
intron_variant | MODIFIER | c.1450-75delC | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr16 | 89546571 | ||||||
| chr16:89546574 | C | T | 3 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0001t0001g0187 |
3 | NA18941.hp1 NA18964.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.1450-84C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 10/16 | chr16 | 89546574 | |||||||
| chr16:89546578 | C | A | 1 | a0001c0001t0001g0186 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1450-80C>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 10/16 | chr16 | 89546578 | |||||||
| chr16:89546580 | C | T | 2 | a0001c0013t0003g0341 a0001c0019t0003g0220 |
2 | HG01891.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1450-78C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 10/16 | chr16 | 89546580 | |||||||
| chr16:89546583 | C | A | 2 | a0001c0005t0005g0302 a0001c0005t0005g0305 |
2 | HG02559.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1450-75C>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 10/16 | chr16 | 89546583 | |||||||
| chr16:89546584 | A | C | 1 | a0001c0005t0010g0238 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1450-74A>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 10/16 | chr16 | 89546584 | |||||||
| chr16:89546629 | G | A | 65 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0075 others(62): Show |
65 | HG00323.hp1 HG00621.hp1 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.1450-29G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 10/16 | chr16 | 89546629 | |||||||
| chr16:89546810 | G | A | 3 | a0001c0001t0001g0047 a0001c0001t0001g0049 a0001c0001t0001g0136 |
3 | HG00639.hp1 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1552+50G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 11/16 | chr16 | 89546810 | |||||||
| chr16:89546825 | A | C | 63 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0075 others(60): Show |
63 | HG00323.hp1 HG00621.hp1 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.1552+65A>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 11/16 | chr16 | 89546825 | |||||||
| chr16:89546863 | C | T | 2 | a0001c0005t0005g0302 a0001c0005t0005g0305 |
2 | HG02559.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1552+103C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 11/16 | chr16 | 89546863 | |||||||
| chr16:89546939 | G | A | 1 | a0001c0001t0001g0067 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1552+179G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 11/16 | chr16 | 89546939 | |||||||
| chr16:89546965 | G | A | 45 | a0001c0001t0001g0002 a0001c0001t0001g0044 a0001c0001t0001g0045 others(42): Show |
46 | HG00099.hp2 HG00597.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.1552+205G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 11/16 | chr16 | 89546965 | |||||||
| chr16:89546991 | C | T | 2 | a0001c0013t0003g0341 a0001c0019t0003g0220 |
2 | HG01891.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1552+231C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 11/16 | chr16 | 89546991 | |||||||
| chr16:89547004 | T | C | 336 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(333): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.1552+244T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 11/16 | chr16 | 89547004 | |||||||
| chr16:89547057 | G | A | 1 | a0001c0001t0002g0224 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1552+297G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 11/16 | chr16 | 89547057 | |||||||
| chr16:89547113 | G | C | 2 | a0001c0001t0001g0099 a0001c0001t0001g0275 |
2 | HG02258.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1552+353G>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 11/16 | chr16 | 89547113 | |||||||
| chr16:89547122 | G | A | 64 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0075 others(61): Show |
64 | HG00323.hp1 HG00621.hp1 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.1552+362G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 11/16 | chr16 | 89547122 | |||||||
| chr16:89547312 | A | G | 2 | a0001c0001t0001g0051 a0001c0001t0001g0206 |
2 | HG02145.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.1552+552A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 11/16 | chr16 | 89547312 | |||||||
| chr16:89547315 | C | T | 1 | a0001c0001t0001g0221 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1552+555C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 11/16 | chr16 | 89547315 | |||||||
| chr16:89547362 | A | G | 2 | a0001c0005t0005g0302 a0001c0005t0005g0305 |
2 | HG02559.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1552+602A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 11/16 | chr16 | 89547362 | |||||||
| chr16:89547416 | G | T | 2 | a0001c0005t0005g0302 a0001c0005t0005g0305 |
2 | HG02559.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1553-587G>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 11/16 | chr16 | 89547416 | |||||||
| chr16:89547490 | G | T | 1 | a0001c0001t0001g0280 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1553-513G>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 11/16 | chr16 | 89547490 | |||||||
| chr16:89547538 | G | T | 1 | a0001c0001t0001g0239 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1553-465G>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 11/16 | chr16 | 89547538 | |||||||
| chr16:89547552 | G | C | 335 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(332): Show |
340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.1553-451G>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 11/16 | chr16 | 89547552 | |||||||
| chr16:89547711 | C | T | 1 | a0001c0001t0007g0010 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1553-292C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 11/16 | chr16 | 89547711 | |||||||
| chr16:89547753 | C | G | 1 | a0003c0003t0002g0211 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1553-250C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 11/16 | chr16 | 89547753 | |||||||
| chr16:89547788 | T | G | 1 | a0001c0001t0002g0338 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1553-215T>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 11/16 | chr16 | 89547788 | |||||||
| chr16:89547872 | C | G | 1 | a0001c0001t0002g0224 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1553-131C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 11/16 | chr16 | 89547872 | |||||||
| chr16:89547975 | C | G | 1 | a0001c0001t0001g0270 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1553-28C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 11/16 | chr16 | 89547975 | |||||||
| chr16:89548126 | C | T | 2 | a0001c0001t0001g0290 a0006c0014t0001g0262 |
2 | HG00099.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.1663+13C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 12/16 | chr16 | 89548126 | |||||||
| chr16:89548170 | A | G | 1 | a0001c0001t0001g0275 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1663+57A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 12/16 | chr16 | 89548170 | |||||||
| chr16:89548225 | C | T | 1 | a0001c0001t0001g0295 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1663+112C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 12/16 | chr16 | 89548225 | |||||||
| chr16:89548274 | T | C | 1 | a0001c0001t0001g0242 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1663+161T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 12/16 | chr16 | 89548274 | |||||||
| chr16:89548296 | T | C | 1 | a0001c0001t0001g0090 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1663+183T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 12/16 | chr16 | 89548296 | |||||||
| chr16:89548481 | C | T | 1 | a0001c0001t0004g0205 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1663+368C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 12/16 | chr16 | 89548481 | |||||||
| chr16:89548509 | C | T | 1 | a0001c0001t0002g0230 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1663+396C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 12/16 | chr16 | 89548509 | |||||||
| chr16:89548583 | C | G | 1 | a0001c0001t0001g0198 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1663+470C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 12/16 | chr16 | 89548583 | |||||||
| chr16:89548653 | G | A | 7 | a0001c0001t0001g0225 a0001c0001t0001g0245 a0001c0001t0001g0291 others(4): Show |
7 | HG00280.hp1 NA18612.hp2 NA18747.hp2 others(4): Show |
intron_variant | MODIFIER | c.1663+540G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 12/16 | chr16 | 89548653 | |||||||
| chr16:89548800 | C | T | 1 | a0001c0001t0001g0279 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1663+687C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 12/16 | chr16 | 89548800 | |||||||
| chr16:89548844 | G | A | 1 | a0001c0001t0001g0270 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1663+731G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 12/16 | chr16 | 89548844 | |||||||
| chr16:89548905 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1663+792C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 12/16 | chr16 | 89548905 | |||||||
| chr16:89548924 | C | T | 1 | a0001c0001t0002g0224 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1663+811C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 12/16 | chr16 | 89548924 | |||||||
| chr16:89548925 | C | T | 52 | a0001c0001t0001g0231 a0001c0001t0002g0222 a0001c0001t0002g0224 others(49): Show |
52 | HG00323.hp1 HG00621.hp1 HG00673.hp2 others(49): Show |
intron_variant | MODIFIER | c.1663+812C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 12/16 | chr16 | 89548925 | |||||||
| chr16:89549045 | A | C | 50 | a0001c0001t0001g0231 a0001c0001t0002g0222 a0001c0001t0002g0224 others(47): Show |
50 | HG00323.hp1 HG00621.hp1 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.1663+932A>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 12/16 | chr16 | 89549045 | |||||||
| chr16:89549058 | C | T | 2 | a0001c0005t0005g0302 a0001c0005t0005g0305 |
2 | HG02559.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1663+945C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 12/16 | chr16 | 89549058 | |||||||
| chr16:89549134 | G | A | 4 | a0001c0001t0001g0110 a0001c0001t0001g0117 a0001c0001t0001g0118 others(1): Show |
4 | HG01928.hp1 HG01943.hp1 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.1663+1021G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 12/16 | chr16 | 89549134 | |||||||
| chr16:89549141 | C | T | 2 | a0001c0001t0001g0106 a0008c0009t0001g0120 |
2 | NA18747.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.1663+1028C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 12/16 | chr16 | 89549141 | |||||||
| chr16:89549271 | C | G | 1 | a0003c0003t0002g0211 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1663+1158C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 12/16 | chr16 | 89549271 | |||||||
| chr16:89549357 | T | G | 35 | a0001c0005t0005g0302 a0001c0005t0005g0305 a0002c0002t0002g0001 others(32): Show |
35 | HG00323.hp1 HG00621.hp1 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.1664-1137T>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 12/16 | chr16 | 89549357 | |||||||
| chr16:89549631 | G | A | 147 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(144): Show |
151 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.1664-863G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 12/16 | chr16 | 89549631 | |||||||
| chr16:89549747 | G | T | 33 | a0002c0002t0002g0001 a0002c0002t0002g0009 a0002c0002t0002g0011 others(30): Show |
33 | HG00323.hp1 HG00621.hp1 HG00673.hp2 others(30): Show |
intron_variant | MODIFIER | c.1664-747G>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 12/16 | chr16 | 89549747 | |||||||
| chr16:89549755 | G | A | 1 | a0003c0003t0002g0211 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1664-739G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 12/16 | chr16 | 89549755 | |||||||
| chr16:89549759 | T | C | 49 | a0001c0001t0001g0231 a0001c0001t0002g0222 a0001c0001t0002g0224 others(46): Show |
49 | HG00323.hp1 HG00621.hp1 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.1664-735T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 12/16 | chr16 | 89549759 | |||||||
| chr16:89549770 | G | A | 49 | a0001c0001t0001g0231 a0001c0001t0002g0222 a0001c0001t0002g0224 others(46): Show |
49 | HG00323.hp1 HG00621.hp1 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.1664-724G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 12/16 | chr16 | 89549770 | |||||||
| chr16:89549824 | G | A | 48 | a0001c0001t0001g0231 a0001c0001t0002g0222 a0001c0001t0002g0230 others(45): Show |
48 | HG00323.hp1 HG00621.hp1 HG00673.hp2 others(45): Show |
intron_variant | MODIFIER | c.1664-670G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 12/16 | chr16 | 89549824 | |||||||
| chr16:89549894 | C | G | 1 | a0002c0002t0002g0012 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1664-600C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 12/16 | chr16 | 89549894 | |||||||
| chr16:89550033 | C | T | 8 | a0003c0003t0002g0055 a0003c0003t0002g0056 a0003c0003t0002g0057 others(5): Show |
8 | HG01891.hp1 HG02451.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1664-461C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 12/16 | chr16 | 89550033 | |||||||
| chr16:89550150 | T | C | 50 | a0001c0001t0001g0231 a0001c0001t0002g0222 a0001c0001t0002g0224 others(47): Show |
50 | HG00323.hp1 HG00621.hp1 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.1664-344T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 12/16 | chr16 | 89550150 | |||||||
| chr16:89550166 | C | G | 1 | a0001c0005t0005g0305 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1664-328C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 12/16 | chr16 | 89550166 | |||||||
| chr16:89550317 | C | T | 50 | a0001c0001t0001g0007 a0001c0001t0001g0231 a0001c0001t0002g0222 others(47): Show |
50 | HG00323.hp1 HG00621.hp1 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.1664-177C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 12/16 | chr16 | 89550317 | |||||||
| chr16:89550364 | G | T | 50 | a0001c0001t0001g0231 a0001c0001t0002g0222 a0001c0001t0002g0224 others(47): Show |
50 | HG00323.hp1 HG00621.hp1 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.1664-130G>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 12/16 | chr16 | 89550364 | |||||||
| chr16:89550382 | G | A | 49 | a0001c0001t0001g0231 a0001c0001t0002g0222 a0001c0001t0002g0230 others(46): Show |
49 | HG00323.hp1 HG00621.hp1 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.1664-112G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 12/16 | chr16 | 89550382 | |||||||
| chr16:89550392 | C | T | 5 | a0001c0001t0001g0006 a0001c0001t0001g0309 a0001c0001t0001g0311 others(2): Show |
6 | HG01168.hp1 HG01169.hp2 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.1664-102C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 12/16 | chr16 | 89550392 | |||||||
| chr16:89550440 | T | G | 1 | a0001c0001t0001g0156 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1664-54T>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 12/16 | chr16 | 89550440 | |||||||
| chr16:89550479 | C | A | 2 | a0001c0013t0003g0341 a0001c0019t0003g0220 |
2 | HG01891.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1664-15C>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 12/16 | chr16 | 89550479 | |||||||
| chr16:89550656 | G | C | 52 | a0001c0001t0001g0231 a0001c0001t0002g0222 a0001c0001t0002g0224 others(49): Show |
52 | HG00323.hp1 HG00621.hp1 HG00673.hp2 others(49): Show |
intron_variant | MODIFIER | c.1779+47G>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 13/16 | chr16 | 89550656 | |||||||
| chr16:89550656 | GTGGGGAG others(23): Show |
G | 1 | a0001c0001t0001g0107 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1779+103_1779+132d others(32): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr16 | 89550656 | ||||||
| chr16:89550847 | A | G | 17 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(14): Show |
17 | HG00597.hp1 HG01934.hp2 HG02040.hp2 others(14): Show |
intron_variant | MODIFIER | c.1779+238A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 13/16 | chr16 | 89550847 | |||||||
| chr16:89550901 | G | A | 1 | a0001c0001t0001g0143 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1779+292G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 13/16 | chr16 | 89550901 | |||||||
| chr16:89551065 | TCAAA | T | 50 | a0001c0001t0001g0112 a0001c0001t0001g0231 a0001c0001t0002g0222 others(47): Show |
50 | HG00323.hp1 HG00621.hp1 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.1779+469_1779+472d others(6): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr16 | 89551065 | ||||||
| chr16:89551110 | C | T | 34 | a0002c0002t0002g0001 a0002c0002t0002g0009 a0002c0002t0002g0011 others(31): Show |
34 | HG00323.hp1 HG00621.hp1 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.1779+501C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 13/16 | chr16 | 89551110 | |||||||
| chr16:89551182 | G | A | 1 | a0001c0001t0002g0224 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1779+573G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 13/16 | chr16 | 89551182 | |||||||
| chr16:89551194 | G | C | 2 | a0001c0005t0009g0340 a0001c0005t0010g0238 |
2 | HG02258.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1779+585G>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 13/16 | chr16 | 89551194 | |||||||
| chr16:89551334 | C | T | 1 | a0001c0001t0001g0219 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1779+725C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 13/16 | chr16 | 89551334 | |||||||
| chr16:89551363 | T | G | 2 | a0001c0001t0002g0224 a0001c0001t0007g0010 |
2 | HG02809.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.1779+754T>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 13/16 | chr16 | 89551363 | |||||||
| chr16:89551757 | G | A | 2 | a0001c0001t0002g0224 a0001c0001t0007g0010 |
2 | HG02809.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.1779+1148G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 13/16 | chr16 | 89551757 | |||||||
| chr16:89551978 | A | G | 2 | a0001c0001t0001g0241 a0001c0001t0001g0242 |
2 | HG01243.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.1780-1001A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 13/16 | chr16 | 89551978 | |||||||
| chr16:89552063 | T | G | 1 | a0001c0001t0001g0139 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1780-916T>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 13/16 | chr16 | 89552063 | |||||||
| chr16:89552064 | C | T | 7 | a0001c0001t0002g0224 a0001c0001t0007g0010 a0001c0005t0005g0302 others(4): Show |
7 | HG01891.hp2 HG02258.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1780-915C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 13/16 | chr16 | 89552064 | |||||||
| chr16:89552086 | T | G | 1 | a0001c0001t0001g0268 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1780-893T>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 13/16 | chr16 | 89552086 | |||||||
| chr16:89552087 | C | G | 1 | a0001c0001t0001g0268 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1780-892C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 13/16 | chr16 | 89552087 | |||||||
| chr16:89552122 | G | A | 46 | a0001c0001t0001g0002 a0001c0001t0001g0044 a0001c0001t0001g0045 others(43): Show |
47 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(44): Show |
intron_variant | MODIFIER | c.1780-857G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 13/16 | chr16 | 89552122 | |||||||
| chr16:89552194 | G | A | 1 | a0001c0001t0001g0274 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1780-785G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 13/16 | chr16 | 89552194 | |||||||
| chr16:89552214 | G | T | 2 | a0001c0013t0003g0341 a0001c0019t0003g0220 |
2 | HG01891.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1780-765G>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 13/16 | chr16 | 89552214 | |||||||
| chr16:89552267 | C | T | 1 | a0001c0001t0001g0121 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1780-712C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 13/16 | chr16 | 89552267 | |||||||
| chr16:89552275 | A | T | 2 | a0001c0001t0002g0224 a0001c0001t0007g0010 |
2 | HG02809.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.1780-704A>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 13/16 | chr16 | 89552275 | |||||||
| chr16:89552324 | G | A | 4 | a0001c0005t0005g0302 a0001c0005t0005g0305 a0001c0013t0003g0341 others(1): Show |
4 | HG01891.hp2 HG02559.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1780-655G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 13/16 | chr16 | 89552324 | |||||||
| chr16:89552341 | G | A | 1 | a0001c0019t0003g0220 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1780-638G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 13/16 | chr16 | 89552341 | |||||||
| chr16:89552467 | C | G | 2 | a0001c0005t0010g0238 a0001c0019t0003g0220 |
2 | HG02258.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1780-512C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 13/16 | chr16 | 89552467 | |||||||
| chr16:89552468 | G | A | 2 | a0001c0001t0001g0290 a0006c0014t0001g0262 |
2 | HG00099.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.1780-511G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 13/16 | chr16 | 89552468 | |||||||
| chr16:89552523 | C | T | 5 | a0001c0001t0002g0233 a0001c0005t0005g0302 a0001c0005t0005g0305 others(2): Show |
5 | HG01891.hp2 HG02559.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1780-456C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 13/16 | chr16 | 89552523 | |||||||
| chr16:89552720 | T | G | 3 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0186 |
3 | HG02717.hp2 HG03471.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1780-259T>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 13/16 | chr16 | 89552720 | |||||||
| chr16:89552791 | G | A | 1 | a0001c0001t0001g0051 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1780-188G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 13/16 | chr16 | 89552791 | |||||||
| chr16:89552885 | C | T | 1 | a0001c0005t0010g0238 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1780-94C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 13/16 | chr16 | 89552885 | |||||||
| chr16:89553162 | A | C | 2 | a0001c0001t0001g0282 a0010c0010t0001g0240 |
2 | HG00673.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.1936+27A>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 14/16 | chr16 | 89553162 | |||||||
| chr16:89553289 | G | T | 7 | a0001c0001t0002g0224 a0001c0001t0007g0010 a0001c0005t0005g0302 others(4): Show |
7 | HG01891.hp2 HG02258.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1936+154G>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 14/16 | chr16 | 89553289 | |||||||
| chr16:89553390 | A | T | 1 | a0001c0001t0001g0208 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1936+255A>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 14/16 | chr16 | 89553390 | |||||||
| chr16:89553667 | G | A | 8 | a0001c0001t0001g0073 a0001c0001t0001g0148 a0001c0001t0001g0149 others(5): Show |
8 | HG00597.hp1 HG02040.hp2 HG02083.hp1 others(5): Show |
intron_variant | MODIFIER | c.1937-127G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 14/16 | chr16 | 89553667 | |||||||
| chr16:89553740 | A | G | 58 | a0001c0001t0001g0101 a0001c0001t0002g0023 a0001c0001t0002g0026 others(55): Show |
58 | HG00323.hp1 HG00621.hp1 HG00673.hp2 others(55): Show |
intron_variant | MODIFIER | c.1937-54A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 14/16 | chr16 | 89553740 | |||||||
| chr16:89553750 | G | A | 6 | a0001c0001t0001g0324 a0001c0001t0001g0325 a0001c0001t0001g0326 others(3): Show |
6 | HG01192.hp1 HG02615.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1937-44G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 14/16 | chr16 | 89553750 | |||||||
| chr16:89553778 | C | G | 2 | a0001c0001t0002g0224 a0001c0001t0007g0010 |
2 | HG02809.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.1937-16C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 14/16 | chr16 | 89553778 | |||||||
| chr16:89553792 | A | G | 1 | a0001c0001t0001g0334 | 1 | HG02647.hp2 | splice_acceptor_variant&intron_variant | HIGH | c.1937-2A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 14/16 | chr16 | 89553792 | |||||||
| chr16:89554043 | G | A | 1 | a0001c0001t0001g0091 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.2103+83G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 15/16 | chr16 | 89554043 | |||||||
| chr16:89554055 | G | T | 2 | a0001c0005t0005g0302 a0001c0005t0005g0305 |
2 | HG02559.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2103+95G>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 15/16 | chr16 | 89554055 | |||||||
| chr16:89554255 | C | T | 1 | a0001c0019t0003g0220 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2104-231C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 15/16 | chr16 | 89554255 | |||||||
| chr16:89554447 | G | A | 3 | a0001c0001t0001g0329 a0001c0001t0001g0333 a0001c0005t0009g0340 |
3 | HG03098.hp2 HG03195.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2104-39G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 15/16 | chr16 | 89554447 | |||||||
| chr16:89554474 | C | G | 1 | a0001c0001t0001g0335 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2104-12C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 15/16 | chr16 | 89554474 | |||||||
| chr16:89554681 | A | G | 1 | a0001c0005t0010g0238 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2181+118A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89554681 | |||||||
| chr16:89554761 | C | T | 1 | a0001c0001t0001g0139 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2181+198C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89554761 | |||||||
| chr16:89554798 | C | G | 1 | a0001c0005t0010g0238 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2181+235C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89554798 | |||||||
| chr16:89554818 | C | G | 2 | a0001c0001t0002g0224 a0001c0001t0007g0010 |
2 | HG02809.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.2181+255C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89554818 | |||||||
| chr16:89554856 | C | T | 1 | a0001c0001t0001g0129 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.2181+293C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89554856 | |||||||
| chr16:89554893 | C | T | 1 | a0001c0005t0010g0238 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2181+330C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89554893 | |||||||
| chr16:89554971 | G | A | 1 | a0001c0005t0010g0238 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2181+408G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89554971 | |||||||
| chr16:89554982 | C | G | 2 | a0001c0001t0001g0094 a0001c0001t0001g0109 |
2 | HG02074.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.2181+419C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89554982 | |||||||
| chr16:89554986 | G | C | 1 | a0001c0001t0007g0010 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2181+423G>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89554986 | |||||||
| chr16:89555008 | C | T | 1 | a0001c0001t0001g0123 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2181+445C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89555008 | |||||||
| chr16:89555075 | T | C | 1 | a0001c0005t0010g0238 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2181+512T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89555075 | |||||||
| chr16:89555084 | C | CT | 12 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0085 others(9): Show |
12 | HG01346.hp2 HG01891.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.2181+537dupT | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr16 | 89555084 | ||||||
| chr16:89555084 | C | T | 1 | a0001c0005t0010g0238 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2181+521C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89555084 | |||||||
| chr16:89555084 | CT | C | 11 | a0001c0001t0001g0068 a0001c0001t0001g0114 a0001c0001t0001g0159 others(8): Show |
11 | HG01515.hp2 HG02735.hp1 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.2181+537delT | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr16 | 89555084 | ||||||
| chr16:89555185 | A | G | 1 | a0001c0005t0010g0238 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2181+622A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89555185 | |||||||
| chr16:89555270 | G | T | 1 | a0001c0013t0003g0341 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2181+707G>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89555270 | |||||||
| chr16:89555283 | A | G | 3 | a0001c0005t0005g0302 a0001c0005t0005g0305 a0001c0005t0010g0238 |
3 | HG02258.hp2 HG02559.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2181+720A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89555283 | |||||||
| chr16:89555305 | T | C | 3 | a0001c0001t0001g0324 a0001c0001t0001g0330 a0001c0001t0001g0331 |
3 | HG02615.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2181+742T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89555305 | |||||||
| chr16:89555333 | G | A | 4 | a0001c0001t0002g0224 a0001c0001t0007g0010 a0001c0013t0003g0341 others(1): Show |
4 | HG01891.hp2 HG02809.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.2181+770G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89555333 | |||||||
| chr16:89555339 | C | A | 9 | a0001c0001t0001g0101 a0001c0001t0002g0224 a0001c0001t0003g0296 others(6): Show |
9 | HG01891.hp2 HG02055.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.2181+776C>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89555339 | |||||||
| chr16:89555462 | C | G | 3 | a0001c0001t0001g0337 a0001c0005t0009g0340 a0001c0005t0010g0238 |
3 | HG02258.hp2 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2181+899C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89555462 | |||||||
| chr16:89555500 | C | A | 1 | a0001c0001t0007g0010 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2181+937C>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89555500 | |||||||
| chr16:89555520 | C | T | 1 | a0001c0005t0005g0305 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2181+957C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89555520 | |||||||
| chr16:89555528 | A | G | 7 | a0001c0001t0001g0101 a0001c0001t0003g0296 a0001c0001t0003g0345 others(4): Show |
7 | HG01891.hp2 HG02055.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.2181+965A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89555528 | |||||||
| chr16:89555537 | G | C | 7 | a0001c0001t0001g0101 a0001c0001t0003g0296 a0001c0001t0003g0345 others(4): Show |
7 | HG01891.hp2 HG02055.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.2181+974G>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89555537 | |||||||
| chr16:89555565 | G | C | 2 | a0001c0005t0005g0302 a0001c0005t0005g0305 |
2 | HG02559.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2181+1002G>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89555565 | |||||||
| chr16:89555574 | C | T | 1 | a0001c0001t0004g0205 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2181+1011C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89555574 | |||||||
| chr16:89555575 | A | G | 350 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(347): Show |
355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.2181+1012A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89555575 | |||||||
| chr16:89555589 | C | T | 2 | a0001c0001t0002g0230 a0001c0001t0002g0233 |
2 | HG02572.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.2181+1026C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89555589 | |||||||
| chr16:89555649 | C | T | 4 | a0001c0005t0005g0302 a0001c0005t0005g0305 a0001c0005t0009g0340 others(1): Show |
4 | HG02258.hp2 HG02559.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2181+1086C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89555649 | |||||||
| chr16:89555699 | C | G | 4 | a0001c0005t0005g0302 a0001c0005t0005g0305 a0001c0005t0009g0340 others(1): Show |
4 | HG02258.hp2 HG02559.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2181+1136C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89555699 | |||||||
| chr16:89555709 | A | G | 4 | a0001c0005t0005g0302 a0001c0005t0005g0305 a0001c0005t0009g0340 others(1): Show |
4 | HG02258.hp2 HG02559.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2181+1146A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89555709 | |||||||
| chr16:89555748 | T | G | 4 | a0001c0005t0005g0302 a0001c0005t0005g0305 a0001c0005t0009g0340 others(1): Show |
4 | HG02258.hp2 HG02559.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2182-1139T>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89555748 | |||||||
| chr16:89555795 | C | T | 1 | a0001c0001t0001g0231 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2182-1092C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89555795 | |||||||
| chr16:89555800 | CTTTGTCC others(2): Show |
C | 4 | a0001c0005t0005g0302 a0001c0005t0005g0305 a0001c0005t0009g0340 others(1): Show |
4 | HG02258.hp2 HG02559.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2182-1085_2182-107 others(13): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr16 | 89555800 | ||||||
| chr16:89555860 | C | T | 1 | a0001c0001t0001g0183 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2182-1027C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89555860 | |||||||
| chr16:89555917 | T | C | 4 | a0001c0005t0005g0302 a0001c0005t0005g0305 a0001c0005t0009g0340 others(1): Show |
4 | HG02258.hp2 HG02559.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2182-970T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89555917 | |||||||
| chr16:89555934 | G | A | 4 | a0001c0005t0005g0302 a0001c0005t0005g0305 a0001c0005t0009g0340 others(1): Show |
4 | HG02258.hp2 HG02559.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2182-953G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89555934 | |||||||
| chr16:89555946 | C | T | 4 | a0001c0005t0005g0302 a0001c0005t0005g0305 a0001c0005t0009g0340 others(1): Show |
4 | HG02258.hp2 HG02559.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2182-941C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89555946 | |||||||
| chr16:89556044 | G | A | 2 | a0001c0001t0002g0224 a0001c0001t0007g0010 |
2 | HG02809.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.2182-843G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89556044 | |||||||
| chr16:89556088 | A | G | 14 | a0001c0001t0002g0204 a0001c0001t0002g0222 a0001c0001t0002g0230 others(11): Show |
14 | HG01081.hp1 HG01891.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.2182-799A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89556088 | |||||||
| chr16:89556092 | C | G | 1 | a0002c0002t0002g0038 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2182-795C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89556092 | |||||||
| chr16:89556099 | C | T | 2 | a0001c0005t0005g0302 a0001c0005t0005g0305 |
2 | HG02559.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2182-788C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89556099 | |||||||
| chr16:89556116 | T | G | 38 | a0001c0001t0002g0023 a0001c0001t0002g0026 a0001c0001t0002g0031 others(35): Show |
38 | HG00323.hp1 HG00621.hp1 HG00673.hp2 others(35): Show |
intron_variant | MODIFIER | c.2182-771T>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89556116 | |||||||
| chr16:89556209 | T | C | 4 | a0001c0005t0005g0302 a0001c0005t0005g0305 a0001c0005t0009g0340 others(1): Show |
4 | HG02258.hp2 HG02559.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2182-678T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89556209 | |||||||
| chr16:89556219 | A | C | 1 | a0001c0001t0002g0204 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2182-668A>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89556219 | |||||||
| chr16:89556305 | TAAC | T | 4 | a0001c0005t0005g0302 a0001c0005t0005g0305 a0001c0005t0009g0340 others(1): Show |
4 | HG02258.hp2 HG02559.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2182-567_2182-565d others(5): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr16 | 89556305 | ||||||
| chr16:89556320 | C | A | 4 | a0001c0001t0002g0222 a0001c0001t0002g0230 a0001c0001t0002g0232 others(1): Show |
4 | HG01081.hp1 HG02572.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.2182-567C>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89556320 | |||||||
| chr16:89556354 | C | A | 6 | a0001c0001t0001g0070 a0001c0001t0001g0075 a0001c0001t0001g0089 others(3): Show |
6 | HG00621.hp2 NA18980.hp2 NA19054.hp2 others(3): Show |
intron_variant | MODIFIER | c.2182-533C>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89556354 | |||||||
| chr16:89556366 | G | A | 4 | a0001c0005t0005g0302 a0001c0005t0005g0305 a0001c0005t0009g0340 others(1): Show |
4 | HG02258.hp2 HG02559.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2182-521G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89556366 | |||||||
| chr16:89556391 | T | G | 4 | a0001c0005t0005g0302 a0001c0005t0005g0305 a0001c0005t0009g0340 others(1): Show |
4 | HG02258.hp2 HG02559.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2182-496T>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89556391 | |||||||
| chr16:89556453 | C | T | 9 | a0001c0001t0002g0204 a0001c0001t0002g0224 a0001c0001t0003g0296 others(6): Show |
9 | HG01891.hp2 HG02055.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.2182-434C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89556453 | |||||||
| chr16:89556468 | A | T | 4 | a0001c0005t0005g0302 a0001c0005t0005g0305 a0001c0005t0009g0340 others(1): Show |
4 | HG02258.hp2 HG02559.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2182-419A>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89556468 | |||||||
| chr16:89556469 | A | G | 4 | a0001c0005t0005g0302 a0001c0005t0005g0305 a0001c0005t0009g0340 others(1): Show |
4 | HG02258.hp2 HG02559.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2182-418A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89556469 | |||||||
| chr16:89556480 | T | C | 1 | a0001c0001t0001g0229 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2182-407T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89556480 | |||||||
| chr16:89556603 | C | T | 1 | a0001c0004t0001g0179 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2182-284C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89556603 | |||||||
| chr16:89556604 | G | A | 4 | a0001c0005t0005g0302 a0001c0005t0005g0305 a0001c0005t0009g0340 others(1): Show |
4 | HG02258.hp2 HG02559.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2182-283G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89556604 | |||||||
| chr16:89556729 | T | C | 5 | a0001c0001t0001g0006 a0001c0001t0001g0309 a0001c0001t0001g0311 others(2): Show |
6 | HG01168.hp1 HG01169.hp2 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.2182-158T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89556729 | |||||||
| chr16:89556815 | C | G | 1 | a0001c0001t0001g0335 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2182-72C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89556815 | |||||||
| chr16:89556839 | C | T | 1 | a0001c0005t0010g0238 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2182-48C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89556839 |