Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 22883 |
| ensemblid | ENSG00000171603.18 |
| hgncid | 17447 |
| symbol | CLSTN1 |
| name | calsyntenin 1 |
| refseq_nuc | NM_001009566.3 |
| refseq_prot | NP_001009566.1 |
| ensembl_nuc | ENST00000377298.9 |
| ensembl_prot | ENSP00000366513.4 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 9728926 |
| end | 9823965 |
| strand | - |
| ver | v1.2 |
| region | chr1:9728926-9823965 |
| region5000 | chr1:9723926-9828965 |
| regionname0 | CLSTN1_chr1_9728926_9823965 |
| regionname5000 | CLSTN1_chr1_9723926_9828965 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 981 | 175 | 57 | 44 | 52 | 6 | 14 | 31 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | MLRRP others(976): Show |
chr1 | 9723926 | 9828965 |
| a0002 | 0/0 | 981 | 79 | 24 | 10 | 32 | 2 | 11 | 27 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | MLRRP others(976): Show |
chr1 | 9723926 | 9828965 |
| a0003 | 0/0 | 981 | 8 | 0 | 1 | 7 | 0 | 0 | 6 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | MLRRP others(976): Show |
chr1 | 9723926 | 9828965 |
| a0004 | 0/0 | 981 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | MLRRP others(976): Show |
chr1 | 9723926 | 9828965 |
| a0005 | 0/0 | 123 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | MLRRP others(118): Show |
chr1 | 9723926 | 9828965 |
| a0006 | 0/0 | 981 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | MLRRP others(976): Show |
chr1 | 9723926 | 9828965 |
| a0007 | 0/0 | 981 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | MLRRP others(976): Show |
chr1 | 9723926 | 9828965 |
| a0008 | 0/0 | 981 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | MLRRP others(976): Show |
chr1 | 9723926 | 9828965 |
| a0009 | 0/0 | 981 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | MLRRP others(976): Show |
chr1 | 9723926 | 9828965 |
| a0010 | 0/0 | 981 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | MLRRP others(976): Show |
chr1 | 9723926 | 9828965 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2943 | 139 | 30 | 39 | 48 | 6 | 14 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | ATGCT others(2938): Show |
chr1 | 9723926 | 9828965 | ||
| a0001c0003 | 0/0 | 2943 | 30 | 25 | 4 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | ATGCT others(2938): Show |
chr1 | 9723926 | 9828965 | ||
| a0001c0006 | 0/0 | 2943 | 2 | 1 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | ATGCT others(2938): Show |
chr1 | 9723926 | 9828965 | ||
| a0001c0008 | 0/0 | 2943 | 2 | 0 | 0 | 2 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | ATGCT others(2938): Show |
chr1 | 9723926 | 9828965 | ||
| a0001c0014 | 0/0 | 2943 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | ATGCT others(2938): Show |
chr1 | 9723926 | 9828965 | ||
| a0001c0016 | 0/0 | 2943 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | ATGCT others(2938): Show |
chr1 | 9723926 | 9828965 | ||
| a0002c0002 | 0/0 | 2943 | 74 | 22 | 10 | 29 | 2 | 11 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | ATGCT others(2938): Show |
chr1 | 9723926 | 9828965 | ||
| a0002c0007 | 0/0 | 2943 | 2 | 0 | 0 | 2 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | ATGCT others(2938): Show |
chr1 | 9723926 | 9828965 | ||
| a0002c0010 | 0/0 | 2943 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | ATGCT others(2938): Show |
chr1 | 9723926 | 9828965 | ||
| a0002c0013 | 0/0 | 2943 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | ATGCT others(2938): Show |
chr1 | 9723926 | 9828965 | ||
| a0002c0019 | 0/0 | 2943 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | ATGCT others(2938): Show |
chr1 | 9723926 | 9828965 | ||
| a0003c0004 | 0/0 | 2943 | 8 | 0 | 1 | 7 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | ATGCT others(2938): Show |
chr1 | 9723926 | 9828965 | ||
| a0004c0005 | 0/0 | 2943 | 2 | 0 | 2 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | ATGCT others(2938): Show |
chr1 | 9723926 | 9828965 | ||
| a0005c0011 | 0/0 | 2943 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | ATGCT others(2938): Show |
chr1 | 9723926 | 9828965 | ||
| a0006c0012 | 0/0 | 2943 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | ATGCT others(2938): Show |
chr1 | 9723926 | 9828965 | ||
| a0007c0017 | 0/0 | 2943 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | ATGCT others(2938): Show |
chr1 | 9723926 | 9828965 | ||
| a0008c0009 | 0/0 | 2943 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | ATGCT others(2938): Show |
chr1 | 9723926 | 9828965 | ||
| a0009c0018 | 0/0 | 2943 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | ATGCT others(2938): Show |
chr1 | 9723926 | 9828965 | ||
| a0010c0015 | 0/0 | 2943 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | ATGCT others(2938): Show |
chr1 | 9723926 | 9828965 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 4760 | 129 | 25 | 38 | 46 | 6 | 13 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | ATCTT others(4755): Show |
chr1 | 9723926 | 9828965 |
| a0001c0001t0004 | 0/0 | 4760 | 2 | 2 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | ATCTT others(4755): Show |
chr1 | 9723926 | 9828965 |
| a0001c0001t0008 | 0/0 | 4760 | 2 | 2 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | ATCTT others(4755): Show |
chr1 | 9723926 | 9828965 |
| a0001c0001t0013 | 1/0 | 4760 | 1 | 0 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | ATCTT others(4755): Show |
chr1 | 9723926 | 9828965 |
| a0001c0001t0015 | 0/0 | 4760 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | ATCTT others(4755): Show |
chr1 | 9723926 | 9828965 |
| a0001c0001t0016 | 0/0 | 4760 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | ATCTT others(4755): Show |
chr1 | 9723926 | 9828965 |
| a0001c0001t0018 | 0/0 | 4760 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | ATCTT others(4755): Show |
chr1 | 9723926 | 9828965 |
| a0001c0001t0019 | 0/0 | 4760 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | ATCTT others(4755): Show |
chr1 | 9723926 | 9828965 |
| a0001c0001t0020 | 0/0 | 4760 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | ATCTT others(4755): Show |
chr1 | 9723926 | 9828965 |
| a0001c0003t0004 | 0/0 | 4760 | 17 | 15 | 2 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | ATCTT others(4755): Show |
chr1 | 9723926 | 9828965 |
| a0001c0003t0005 | 0/0 | 4760 | 6 | 6 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | ATCTT others(4755): Show |
chr1 | 9723926 | 9828965 |
| a0001c0003t0006 | 0/0 | 4760 | 5 | 2 | 2 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | ATCTT others(4755): Show |
chr1 | 9723926 | 9828965 |
| a0001c0003t0007 | 0/0 | 4770 | 2 | 2 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | ATCTT others(4765): Show |
chr1 | 9723926 | 9828965 |
| a0001c0006t0009 | 0/0 | 4835 | 2 | 1 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | ATCTT others(4830): Show |
chr1 | 9723926 | 9828965 |
| a0001c0008t0001 | 0/0 | 4760 | 2 | 0 | 0 | 2 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | ATCTT others(4755): Show |
chr1 | 9723926 | 9828965 |
| a0001c0014t0001 | 0/0 | 4760 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | ATCTT others(4755): Show |
chr1 | 9723926 | 9828965 |
| a0001c0016t0001 | 0/0 | 4760 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | ATCTT others(4755): Show |
chr1 | 9723926 | 9828965 |
| a0002c0002t0002 | 0/0 | 4760 | 51 | 22 | 8 | 15 | 2 | 4 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | ATCTT others(4755): Show |
chr1 | 9723926 | 9828965 |
| a0002c0002t0003 | 0/0 | 4760 | 20 | 0 | 2 | 12 | 0 | 6 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | ATCTT others(4755): Show |
chr1 | 9723926 | 9828965 |
| a0002c0002t0011 | 0/0 | 4760 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | ATCTT others(4755): Show |
chr1 | 9723926 | 9828965 |
| a0002c0002t0012 | 0/0 | 4760 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | ATCTT others(4755): Show |
chr1 | 9723926 | 9828965 |
| a0002c0002t0017 | 0/0 | 4760 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | ATCTT others(4755): Show |
chr1 | 9723926 | 9828965 |
| a0002c0007t0002 | 0/0 | 4760 | 2 | 0 | 0 | 2 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | ATCTT others(4755): Show |
chr1 | 9723926 | 9828965 |
| a0002c0010t0002 | 0/0 | 4760 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | ATCTT others(4755): Show |
chr1 | 9723926 | 9828965 |
| a0002c0013t0002 | 0/0 | 4760 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | ATCTT others(4755): Show |
chr1 | 9723926 | 9828965 |
| a0002c0019t0002 | 0/0 | 4760 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | ATCTT others(4755): Show |
chr1 | 9723926 | 9828965 |
| a0003c0004t0002 | 0/0 | 4760 | 8 | 0 | 1 | 7 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | ATCTT others(4755): Show |
chr1 | 9723926 | 9828965 |
| a0004c0005t0001 | 0/0 | 4760 | 2 | 0 | 2 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | ATCTT others(4755): Show |
chr1 | 9723926 | 9828965 |
| a0005c0011t0021 | 0/0 | 4760 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | ATCTT others(4755): Show |
chr1 | 9723926 | 9828965 |
| a0006c0012t0003 | 0/0 | 4760 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | ATCTT others(4755): Show |
chr1 | 9723926 | 9828965 |
| a0007c0017t0010 | 0/0 | 4760 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | ATCTT others(4755): Show |
chr1 | 9723926 | 9828965 |
| a0008c0009t0002 | 0/0 | 4760 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | ATCTT others(4755): Show |
chr1 | 9723926 | 9828965 |
| a0009c0018t0001 | 0/0 | 4760 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | ATCTT others(4755): Show |
chr1 | 9723926 | 9828965 |
| a0010c0015t0014 | 0/0 | 4760 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | ATCTT others(4755): Show |
chr1 | 9723926 | 9828965 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0255 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0004g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0004g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0008g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0008g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0013g0103 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0015g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0016g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0018g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0019g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0001t0020g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0003t0004g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0003t0004g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0003t0004g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0003t0004g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0003t0004g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0003t0004g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0003t0004g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0003t0004g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0003t0004g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0003t0004g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0003t0004g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0003t0004g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0003t0004g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0003t0004g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0003t0004g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0003t0004g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0003t0004g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0003t0005g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0003t0005g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0003t0005g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0003t0005g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0003t0005g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0003t0005g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0003t0006g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0003t0006g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0003t0006g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0003t0006g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0003t0006g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0003t0007g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0003t0007g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0006t0009g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0006t0009g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0008t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0008t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0014t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0001c0016t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0002c0002t0002g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0002c0002t0002g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0002c0002t0002g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0002c0002t0002g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0002c0002t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0002c0002t0002g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0002c0002t0002g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0002c0002t0002g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0002c0002t0002g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0002c0002t0002g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0002c0002t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0002c0002t0002g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0002c0002t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0002c0002t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0002c0002t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0002c0002t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0002c0002t0002g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0002c0002t0002g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0002c0002t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0002c0002t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0002c0002t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0002c0002t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0002c0002t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0002c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0002c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0002c0002t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0002c0002t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0002c0002t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0002c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0002c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0002c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0002c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0002c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0002c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0002c0002t0002g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0002c0002t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0002c0002t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0002c0002t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0002c0002t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0002c0002t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0002c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0002c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0002c0002t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0002c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0002c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0002c0002t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0002c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0002c0002t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0002c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0002c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0002c0002t0003g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0002c0002t0003g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0002c0002t0003g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0002c0002t0003g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0002c0002t0003g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0002c0002t0003g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0002c0002t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0002c0002t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0002c0002t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0002c0002t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0002c0002t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0002c0002t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0002c0002t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0002c0002t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0002c0002t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0002c0002t0003g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0002c0002t0003g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0002c0002t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0002c0002t0003g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0002c0002t0003g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0002c0002t0011g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0002c0002t0012g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0002c0002t0017g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0002c0007t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0002c0007t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0002c0010t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0002c0013t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0002c0019t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0003c0004t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0003c0004t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0003c0004t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0003c0004t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0003c0004t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0003c0004t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0003c0004t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0003c0004t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0004c0005t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0004c0005t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0005c0011t0021g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0006c0012t0003g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0007c0017t0010g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0008c0009t0002g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0009c0018t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| a0010c0015t0014g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0245 | EUR | GBR | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0246 | EUR | GBR | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0242 | EUR | FIN | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0241 | EUR | FIN | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | CHS | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG00423 | hp2 | a0002 | c0002 | t0002 | g0073 | EAS | CHS | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG00558 | hp1 | a0003 | c0004 | t0002 | g0069 | EAS | CHS | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG00558 | hp2 | a0005 | c0011 | t0021 | g0268 | EAS | CHS | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | CHS | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | CHS | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | CHS | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | CHS | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0260 | AMR | PUR | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | PUR | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | PUR | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG00733 | hp2 | a0001 | c0003 | t0004 | g0112 | AMR | PUR | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0219 | AMR | PUR | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0263 | AMR | PUR | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG01081 | hp1 | a0002 | c0002 | t0003 | g0057 | AMR | PUR | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0256 | AMR | PUR | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG01109 | hp1 | a0001 | c0003 | t0004 | g0259 | AMR | PUR | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | PUR | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG01243 | hp2 | a0001 | c0006 | t0009 | g0264 | AMR | PUR | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG01255 | hp1 | a0001 | c0003 | t0006 | g0055 | AMR | CLM | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | CLM | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG01257 | hp1 | a0002 | c0002 | t0002 | g0094 | AMR | CLM | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | CLM | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG01258 | hp1 | a0002 | c0002 | t0002 | g0080 | AMR | CLM | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG01258 | hp2 | a0004 | c0005 | t0001 | g0202 | AMR | CLM | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | CLM | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG01261 | hp2 | a0006 | c0012 | t0003 | g0024 | AMR | CLM | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | CLM | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG01346 | hp2 | a0002 | c0002 | t0002 | g0081 | AMR | CLM | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG01361 | hp1 | a0002 | c0002 | t0002 | g0083 | AMR | CLM | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | CLM | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | CLM | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | CLM | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | CLM | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | CLM | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG01515 | hp1 | a0002 | c0002 | t0002 | g0102 | EUR | IBS | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0177 | EUR | IBS | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG01517 | hp1 | a0002 | c0002 | t0002 | g0101 | EUR | IBS | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0169 | EUR | IBS | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG01884 | hp1 | a0002 | c0013 | t0002 | g0012 | AFR | ACB | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG01884 | hp2 | a0007 | c0017 | t0010 | g0003 | AFR | ACB | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG01891 | hp1 | a0008 | c0009 | t0002 | g0004 | AFR | ACB | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG01891 | hp2 | a0001 | c0003 | t0004 | g0118 | AFR | ACB | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | PEL | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG01928 | hp2 | a0002 | c0002 | t0002 | g0079 | AMR | PEL | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0237 | AMR | PEL | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PEL | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG01975 | hp1 | a0002 | c0002 | t0002 | g0082 | AMR | PEL | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | PEL | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PEL | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0224 | AMR | PEL | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | PEL | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG01981 | hp2 | a0003 | c0004 | t0002 | g0063 | AMR | PEL | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | PEL | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | PEL | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG02004 | hp1 | a0004 | c0005 | t0001 | g0203 | AMR | PEL | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG02004 | hp2 | a0001 | c0001 | t0015 | g0235 | AMR | PEL | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG02027 | hp2 | a0001 | c0008 | t0001 | g0161 | EAS | KHV | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | KHV | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG02040 | hp2 | a0002 | c0002 | t0002 | g0091 | EAS | KHV | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG02071 | hp1 | a0001 | c0016 | t0001 | g0198 | EAS | KHV | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | KHV | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG02083 | hp1 | a0002 | c0002 | t0011 | g0053 | EAS | KHV | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG02083 | hp2 | a0001 | c0003 | t0006 | g0096 | EAS | KHV | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | KHV | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | KHV | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG02135 | hp1 | a0002 | c0002 | t0002 | g0075 | EAS | KHV | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | KHV | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | ACB | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG02145 | hp2 | a0001 | c0001 | t0004 | g0212 | AFR | ACB | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | PEL | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG02148 | hp2 | a0002 | c0002 | t0002 | g0078 | AMR | PEL | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | CDX | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | CDX | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | CDX | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | CDX | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG02258 | hp1 | a0001 | c0003 | t0006 | g0022 | AFR | ACB | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG02258 | hp2 | a0002 | c0002 | t0002 | g0062 | AFR | ACB | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG02280 | hp1 | a0001 | c0003 | t0005 | g0100 | AFR | ACB | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG02280 | hp2 | a0001 | c0014 | t0001 | g0251 | AFR | ACB | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PEL | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG02293 | hp2 | a0001 | c0003 | t0006 | g0042 | AMR | PEL | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG02300 | hp1 | a0002 | c0002 | t0002 | g0071 | AMR | PEL | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PEL | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG02451 | hp1 | a0001 | c0003 | t0004 | g0111 | AFR | ACB | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG02451 | hp2 | a0002 | c0002 | t0002 | g0015 | AFR | ACB | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | KHV | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG02523 | hp2 | a0002 | c0002 | t0002 | g0074 | EAS | KHV | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | GWD | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0254 | AFR | GWD | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG02602 | hp1 | a0002 | c0002 | t0003 | g0021 | SAS | PJL | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0205 | SAS | PJL | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG02615 | hp1 | a0001 | c0003 | t0004 | g0116 | AFR | GWD | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG02615 | hp2 | a0001 | c0003 | t0005 | g0098 | AFR | GWD | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG02622 | hp1 | a0001 | c0003 | t0005 | g0009 | AFR | GWD | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG02622 | hp2 | a0001 | c0003 | t0004 | g0120 | AFR | GWD | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG02630 | hp1 | a0002 | c0002 | t0002 | g0033 | AFR | GWD | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | GWD | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG02647 | hp1 | a0001 | c0001 | t0008 | g0185 | AFR | GWD | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG02647 | hp2 | a0001 | c0003 | t0004 | g0119 | AFR | GWD | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG02698 | hp1 | a0002 | c0002 | t0003 | g0051 | SAS | PJL | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0223 | SAS | PJL | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG02717 | hp1 | a0002 | c0002 | t0002 | g0001 | AFR | GWD | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG02717 | hp2 | a0002 | c0002 | t0002 | g0027 | AFR | GWD | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG02723 | hp1 | a0001 | c0001 | t0008 | g0238 | AFR | GWD | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG02723 | hp2 | a0001 | c0003 | t0005 | g0099 | AFR | GWD | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0149 | SAS | PJL | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | PJL | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | GWD | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | GWD | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | GWD | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG02886 | hp2 | a0002 | c0002 | t0002 | g0019 | AFR | GWD | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG02895 | hp1 | a0002 | c0002 | t0002 | g0020 | AFR | GWD | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | GWD | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG02897 | hp1 | a0002 | c0002 | t0002 | g0018 | AFR | GWD | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG02897 | hp2 | a0001 | c0003 | t0004 | g0109 | AFR | GWD | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG02922 | hp1 | a0002 | c0002 | t0002 | g0013 | AFR | ESN | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | ESN | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | ESN | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG02970 | hp2 | a0001 | c0006 | t0009 | g0265 | AFR | ESN | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0266 | AFR | ESN | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG02976 | hp2 | a0002 | c0002 | t0002 | g0010 | AFR | ESN | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0163 | SAS | PJL | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0157 | SAS | PJL | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | GWD | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG03041 | hp2 | a0001 | c0003 | t0004 | g0123 | AFR | GWD | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | ESN | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG03130 | hp2 | a0002 | c0002 | t0002 | g0026 | AFR | ESN | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG03139 | hp1 | a0001 | c0003 | t0007 | g0095 | AFR | ESN | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | ESN | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG03209 | hp1 | a0001 | c0003 | t0005 | g0008 | AFR | MSL | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | MSL | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG03225 | hp1 | a0001 | c0001 | t0004 | g0165 | AFR | MSL | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG03225 | hp2 | a0001 | c0003 | t0004 | g0122 | AFR | MSL | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0244 | SAS | PJL | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0249 | SAS | PJL | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG03453 | hp1 | a0002 | c0002 | t0002 | g0017 | AFR | MSL | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG03453 | hp2 | a0001 | c0003 | t0004 | g0110 | AFR | MSL | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG03486 | hp1 | a0001 | c0003 | t0004 | g0108 | AFR | MSL | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG03486 | hp2 | a0002 | c0002 | t0002 | g0005 | AFR | MSL | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0221 | SAS | PJL | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG03491 | hp2 | a0002 | c0002 | t0003 | g0052 | SAS | PJL | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG03516 | hp1 | a0002 | c0002 | t0002 | g0006 | AFR | ESN | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG03516 | hp2 | a0002 | c0002 | t0002 | g0016 | AFR | ESN | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG03540 | hp1 | a0001 | c0001 | t0020 | g0267 | AFR | GWD | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG03540 | hp2 | a0001 | c0003 | t0004 | g0114 | AFR | GWD | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG03579 | hp1 | a0002 | c0002 | t0002 | g0034 | AFR | MSL | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG03579 | hp2 | a0001 | c0003 | t0007 | g0032 | AFR | MSL | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0234 | SAS | STU | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG03688 | hp2 | a0002 | c0002 | t0003 | g0036 | SAS | STU | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG03831 | hp1 | a0002 | c0002 | t0003 | g0023 | SAS | BEB | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG03831 | hp2 | a0002 | c0002 | t0002 | g0030 | SAS | BEB | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG03834 | hp1 | a0009 | c0018 | t0001 | g0231 | SAS | BEB | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG03834 | hp2 | a0001 | c0001 | t0016 | g0257 | SAS | BEB | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG04199 | hp1 | a0002 | c0002 | t0002 | g0076 | SAS | STU | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG04199 | hp2 | a0002 | c0002 | t0003 | g0060 | SAS | STU | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0196 | SAS | STU | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG04204 | hp2 | a0002 | c0002 | t0017 | g0107 | SAS | STU | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG04228 | hp1 | a0002 | c0002 | t0002 | g0028 | SAS | STU | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0214 | SAS | STU | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| NA18522 | hp1 | a0001 | c0003 | t0004 | g0113 | AFR | YRI | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| NA18522 | hp2 | a0002 | c0002 | t0002 | g0001 | AFR | YRI | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | CHB | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | CHB | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | YRI | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | YRI | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| NA18940 | hp1 | a0002 | c0002 | t0003 | g0038 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| NA18940 | hp2 | a0003 | c0004 | t0002 | g0070 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| NA18942 | hp2 | a0002 | c0002 | t0003 | g0048 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| NA18943 | hp2 | a0002 | c0002 | t0003 | g0041 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| NA18948 | hp1 | a0001 | c0001 | t0019 | g0143 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| NA18948 | hp2 | a0002 | c0002 | t0002 | g0058 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| NA18951 | hp1 | a0002 | c0002 | t0003 | g0025 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| NA18956 | hp1 | a0002 | c0002 | t0002 | g0072 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| NA18963 | hp1 | a0002 | c0002 | t0003 | g0040 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| NA18964 | hp1 | a0001 | c0008 | t0001 | g0206 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| NA18968 | hp2 | a0003 | c0004 | t0002 | g0066 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| NA18971 | hp1 | a0002 | c0002 | t0003 | g0046 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| NA18971 | hp2 | a0002 | c0002 | t0002 | g0093 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| NA18979 | hp2 | a0002 | c0002 | t0002 | g0092 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| NA18983 | hp2 | a0003 | c0004 | t0002 | g0068 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| NA18984 | hp1 | a0002 | c0002 | t0002 | g0043 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| NA18985 | hp2 | a0002 | c0002 | t0003 | g0054 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| NA18990 | hp1 | a0003 | c0004 | t0002 | g0067 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| NA18990 | hp2 | a0002 | c0002 | t0003 | g0049 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| NA18995 | hp2 | a0003 | c0004 | t0002 | g0064 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| NA18999 | hp1 | a0002 | c0002 | t0003 | g0050 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| NA19000 | hp2 | a0002 | c0002 | t0003 | g0047 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| NA19005 | hp1 | a0002 | c0019 | t0002 | g0059 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| NA19010 | hp2 | a0002 | c0002 | t0002 | g0086 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| NA19030 | hp1 | a0002 | c0010 | t0002 | g0029 | AFR | LWK | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | LWK | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| NA19043 | hp1 | a0001 | c0003 | t0005 | g0097 | AFR | LWK | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| NA19043 | hp2 | a0002 | c0002 | t0002 | g0061 | AFR | LWK | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| NA19060 | hp1 | a0002 | c0002 | t0002 | g0077 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| NA19064 | hp1 | a0001 | c0001 | t0018 | g0148 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| NA19066 | hp1 | a0002 | c0007 | t0002 | g0085 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| NA19070 | hp1 | a0002 | c0002 | t0003 | g0044 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| NA19074 | hp1 | a0002 | c0002 | t0002 | g0090 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| NA19079 | hp2 | a0002 | c0002 | t0012 | g0088 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| NA19080 | hp2 | a0002 | c0007 | t0002 | g0084 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| NA19082 | hp1 | a0002 | c0002 | t0003 | g0045 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| NA19082 | hp2 | a0003 | c0004 | t0002 | g0065 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| NA19085 | hp2 | a0002 | c0002 | t0002 | g0089 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| NA19088 | hp1 | a0002 | c0002 | t0002 | g0087 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| NA19088 | hp2 | a0002 | c0002 | t0002 | g0037 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| NA19240 | hp1 | a0002 | c0002 | t0002 | g0011 | AFR | YRI | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | YRI | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0167 | SAS | GIH | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| NA20905 | hp2 | a0002 | c0002 | t0002 | g0007 | SAS | GIH | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | CLM | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG01123 | hp2 | a0002 | c0002 | t0003 | g0039 | AMR | CLM | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0253 | AFR | ACB | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG02109 | hp2 | a0002 | c0002 | t0002 | g0014 | AFR | ACB | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | ACB | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG02486 | hp2 | a0001 | c0003 | t0006 | g0056 | AFR | ACB | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG02559 | hp1 | a0001 | c0003 | t0004 | g0117 | AFR | ACB | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG02559 | hp2 | a0002 | c0002 | t0002 | g0035 | AFR | ACB | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | MSL | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG03471 | hp2 | a0001 | c0003 | t0004 | g0115 | AFR | MSL | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG06807 | hp1 | a0001 | c0003 | t0004 | g0121 | AFR | USA | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | USA | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | USA | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| NA20300 | hp2 | a0002 | c0002 | t0002 | g0031 | AFR | USA | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | LWK | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| NA21309 | hp2 | a0010 | c0015 | t0014 | g0104 | AFR | LWK | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0255 | REF | REF | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0013 | g0103 | REF | REF | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:9730584 | T | C | 1 | a0010 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.2870A>G | p.Glu957Gly | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 19/19 | 3102/4760 | 2870/2946 | 957/981 | chr1 | 9730584 | |||
| chr1:9730601 | C | G | 1 | a0006 | 1 | HG01261.hp2 | missense_variant | MODERATE | c.2853G>C | p.Glu951Asp | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 19/19 | 3085/4760 | 2853/2946 | 951/981 | chr1 | 9730601 | |||
| chr1:9743997 | G | A | 1 | a0007 | 1 | HG01884.hp2 | missense_variant | MODERATE | c.1243C>T | p.Arg415Trp | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 9/19 | 1475/4760 | 1243/2946 | 415/981 | chr1 | 9743997 | |||
| chr1:9744634 | G | A | 1 | a0002 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.995C>T | p.Ala332Val | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 8/19 | 1227/4760 | 995/2946 | 332/981 | chr1 | 9744634 | |||
| chr1:9744635 | C | T | 3 | a0002 a0006 a0008 |
81 | HG00423.hp2 HG01081.hp1 HG01123.hp2 others(78): Show |
missense_variant | MODERATE | c.994G>A | p.Ala332Thr | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 8/19 | 1226/4760 | 994/2946 | 332/981 | chr1 | 9744635 | |||
| chr1:9744640 | G | A | 1 | a0009 | 1 | HG03834.hp1 | missense_variant | MODERATE | c.989C>T | p.Ala330Val | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 8/19 | 1221/4760 | 989/2946 | 330/981 | chr1 | 9744640 | |||
| chr1:9751595 | C | T | 1 | a0004 | 2 | HG01258.hp2 HG02004.hp1 |
missense_variant | MODERATE | c.527G>A | p.Gly176Glu | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 5/19 | 759/4760 | 527/2946 | 176/981 | chr1 | 9751595 | |||
| chr1:9755182 | A | C | 1 | a0005 | 1 | HG00558.hp2 | stop_gained | HIGH | c.372T>G | p.Tyr124* | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 4/19 | 604/4760 | 372/2946 | 124/981 | chr1 | 9755182 | |||
| chr1:9773277 | A | T | 1 | a0003 | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
missense_variant | MODERATE | c.209T>A | p.Phe70Tyr | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/19 | 441/4760 | 209/2946 | 70/981 | chr1 | 9773277 | |||
| chr1:9823712 | C | T | 1 | a0008 | 1 | HG01891.hp1 | missense_variant | MODERATE | c.22G>A | p.Ala8Thr | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/19 | 254/4760 | 22/2946 | 8/981 | chr1 | 9823712 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:9730568 | G | A | 1 | a0001c0014 | 1 | HG02280.hp2 | synonymous_variant | LOW | c.2886C>T | p.Asp962Asp | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 19/19 | 3118/4760 | 2886/2946 | 962/981 | chr1 | 9730568 | |||
| chr1:9731894 | C | T | 1 | a0001c0016 | 1 | HG02071.hp1 | splice_region_variant&synonymous_variant | LOW | c.2430G>A | p.Val810Val | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 17/19 | 2662/4760 | 2430/2946 | 810/981 | chr1 | 9731894 | |||
| chr1:9749561 | T | C | 1 | a0001c0008 | 2 | HG02027.hp2 NA18964.hp1 |
synonymous_variant | LOW | c.885A>G | p.Pro295Pro | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/19 | 1117/4760 | 885/2946 | 295/981 | chr1 | 9749561 | |||
| chr1:9749618 | C | T | 1 | a0001c0006 | 2 | HG01243.hp2 HG02970.hp2 |
synonymous_variant | LOW | c.828G>A | p.Pro276Pro | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/19 | 1060/4760 | 828/2946 | 276/981 | chr1 | 9749618 | |||
| chr1:9749882 | G | A | 1 | a0002c0007 | 2 | NA19066.hp1 NA19080.hp2 |
synonymous_variant | LOW | c.681C>T | p.Tyr227Tyr | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 6/19 | 913/4760 | 681/2946 | 227/981 | chr1 | 9749882 | |||
| chr1:9751483 | A | G | 12 | a0001c0003 a0001c0006 a0001c0014 others(9): Show |
123 | HG00423.hp2 HG00558.hp1 HG00733.hp2 others(120): Show |
synonymous_variant | LOW | c.639T>C | p.Val213Val | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 5/19 | 871/4760 | 639/2946 | 213/981 | chr1 | 9751483 | |||
| chr1:9751600 | G | A | 1 | a0002c0019 | 1 | NA19005.hp1 | synonymous_variant | LOW | c.522C>T | p.Ile174Ile | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 5/19 | 754/4760 | 522/2946 | 174/981 | chr1 | 9751600 | |||
| chr1:9773393 | A | G | 1 | a0002c0010 | 1 | NA19030.hp1 | splice_region_variant&synonymous_variant | LOW | c.93T>C | p.Val31Val | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/19 | 325/4760 | 93/2946 | 31/981 | chr1 | 9773393 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:9729092 | C | T | 1 | a0001c0003t0005 | 6 | HG02280.hp1 HG02615.hp2 HG02622.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1416G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 19/19 | 1416 | chr1 | 9729092 | ||||||
| chr1:9729142 | G | A | 1 | a0010c0015t0014 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1366C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 19/19 | 1366 | chr1 | 9729142 | ||||||
| chr1:9729410 | C | G | 1 | a0001c0001t0008 | 2 | HG02647.hp1 HG02723.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1098G>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 19/19 | 1098 | chr1 | 9729410 | ||||||
| chr1:9729519 | G | A | 4 | a0002c0002t0003 a0002c0002t0011 a0002c0002t0017 others(1): Show |
23 | HG01081.hp1 HG01123.hp2 HG01261.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*989C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 19/19 | 989 | chr1 | 9729519 | ||||||
| chr1:9729523 | C | A | 1 | a0001c0001t0016 | 1 | HG03834.hp2 | 3_prime_UTR_variant | MODIFIER | c.*985G>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 19/19 | 985 | chr1 | 9729523 | ||||||
| chr1:9729544 | C | CCAAAAGG others(68): Show |
1 | a0001c0006t0009 | 2 | HG01243.hp2 HG02970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*889_*963dupCTTAAA others(69): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 19/19 | 963 | chr1 | 9729544 | ||||||
| chr1:9729833 | T | C | 18 | a0001c0001t0004 a0001c0003t0004 a0001c0003t0005 others(15): Show |
119 | HG00423.hp2 HG00558.hp1 HG00733.hp2 others(116): Show |
3_prime_UTR_variant | MODIFIER | c.*675A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 19/19 | 675 | chr1 | 9729833 | ||||||
| chr1:9729837 | C | G | 1 | a0002c0002t0012 | 1 | NA19079.hp2 | 3_prime_UTR_variant | MODIFIER | c.*671G>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 19/19 | 671 | chr1 | 9729837 | ||||||
| chr1:9729855 | G | GGGGCGGG others(3): Show |
1 | a0001c0003t0007 | 2 | HG03139.hp1 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*643_*652dupAGCCCC others(4): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 19/19 | 652 | chr1 | 9729855 | ||||||
| chr1:9729911 | G | A | 1 | a0001c0001t0018 | 1 | NA19064.hp1 | 3_prime_UTR_variant | MODIFIER | c.*597C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 19/19 | 597 | chr1 | 9729911 | ||||||
| chr1:9730027 | T | C | 1 | a0001c0001t0019 | 1 | NA18948.hp1 | 3_prime_UTR_variant | MODIFIER | c.*481A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 19/19 | 481 | chr1 | 9730027 | ||||||
| chr1:9730194 | G | C | 1 | a0001c0003t0005 | 6 | HG02280.hp1 HG02615.hp2 HG02622.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*314C>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 19/19 | 314 | chr1 | 9730194 | ||||||
| chr1:9730220 | G | A | 1 | a0001c0003t0005 | 6 | HG02280.hp1 HG02615.hp2 HG02622.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*288C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 19/19 | 288 | chr1 | 9730220 | ||||||
| chr1:9730305 | C | T | 1 | a0002c0002t0011 | 1 | HG02083.hp1 | 3_prime_UTR_variant | MODIFIER | c.*203G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 19/19 | 203 | chr1 | 9730305 | ||||||
| chr1:9730322 | C | T | 1 | a0005c0011t0021 | 1 | HG00558.hp2 | 3_prime_UTR_variant | MODIFIER | c.*186G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 19/19 | 186 | chr1 | 9730322 | ||||||
| chr1:9730362 | C | T | 1 | a0001c0001t0015 | 1 | HG02004.hp2 | 3_prime_UTR_variant | MODIFIER | c.*146G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 19/19 | 146 | chr1 | 9730362 | ||||||
| chr1:9823805 | C | A | 1 | a0001c0001t0020 | 1 | HG03540.hp1 | 5_prime_UTR_variant | MODIFIER | c.-72G>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/19 | 72 | chr1 | 9823805 | ||||||
| chr1:9823820 | T | C | 32 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0008 others(29): Show |
267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-87A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/19 | chr1 | 9823820 | |||||||
| chr1:9823902 | A | G | 14 | a0001c0003t0005 a0001c0003t0006 a0001c0003t0007 others(11): Show |
101 | HG00423.hp2 HG00558.hp1 HG01081.hp1 others(98): Show |
5_prime_UTR_variant | MODIFIER | c.-169T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/19 | 169 | chr1 | 9823902 | ||||||
| chr1:9823920 | C | T | 1 | a0007c0017t0010 | 1 | HG01884.hp2 | 5_prime_UTR_variant | MODIFIER | c.-187G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/19 | 187 | chr1 | 9823920 | ||||||
| chr1:9823930 | C | A | 1 | a0005c0011t0021 | 1 | HG00558.hp2 | 5_prime_UTR_variant | MODIFIER | c.-197G>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/19 | 197 | chr1 | 9823930 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:9730730 | A | G | 1 | a0010c0015t0014g0104 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2749-25T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 18/18 | chr1 | 9730730 | |||||||
| chr1:9730738 | G | A | 1 | a0001c0001t0001g0186 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2749-33C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 18/18 | chr1 | 9730738 | |||||||
| chr1:9730825 | G | A | 16 | a0001c0003t0004g0108 a0001c0003t0004g0109 a0001c0003t0004g0110 others(13): Show |
16 | HG00733.hp2 HG01891.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.2749-120C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 18/18 | chr1 | 9730825 | |||||||
| chr1:9730841 | C | T | 19 | a0001c0003t0004g0108 a0001c0003t0004g0109 a0001c0003t0004g0110 others(16): Show |
19 | HG00733.hp2 HG01109.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.2749-136G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 18/18 | chr1 | 9730841 | |||||||
| chr1:9730848 | G | A | 1 | a0002c0002t0003g0038 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.2749-143C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 18/18 | chr1 | 9730848 | |||||||
| chr1:9730903 | C | T | 2 | a0001c0001t0004g0165 a0001c0001t0004g0212 |
2 | HG02145.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2749-198G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 18/18 | chr1 | 9730903 | |||||||
| chr1:9730904 | A | G | 10 | a0001c0001t0004g0165 a0001c0001t0004g0212 a0003c0004t0002g0063 others(7): Show |
10 | HG00558.hp1 HG01981.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.2749-199T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 18/18 | chr1 | 9730904 | |||||||
| chr1:9730937 | A | G | 198 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0126 others(195): Show |
199 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(196): Show |
intron_variant | MODIFIER | c.2749-232T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 18/18 | chr1 | 9730937 | |||||||
| chr1:9730958 | T | G | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.2748+248A>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 18/18 | chr1 | 9730958 | |||||||
| chr1:9731404 | AG | A | 10 | a0001c0001t0004g0165 a0001c0001t0004g0212 a0003c0004t0002g0063 others(7): Show |
10 | HG00558.hp1 HG01981.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.2564-15delC | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 17/18 | chr1 | 9731404 | |||||||
| chr1:9731428 | G | A | 18 | a0001c0003t0004g0259 a0001c0003t0005g0008 a0001c0003t0005g0009 others(15): Show |
18 | HG00558.hp1 HG01109.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.2564-38C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 17/18 | chr1 | 9731428 | |||||||
| chr1:9731488 | C | A | 12 | a0002c0002t0002g0010 a0002c0002t0002g0011 a0002c0002t0002g0013 others(9): Show |
12 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.2564-98G>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 17/18 | chr1 | 9731488 | |||||||
| chr1:9731559 | G | A | 1 | a0001c0003t0006g0042 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.2564-169C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 17/18 | chr1 | 9731559 | |||||||
| chr1:9731581 | G | A | 88 | a0001c0003t0005g0008 a0001c0003t0005g0009 a0001c0003t0005g0097 others(85): Show |
89 | HG00423.hp2 HG01081.hp1 HG01123.hp2 others(86): Show |
intron_variant | MODIFIER | c.2563+180C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 17/18 | chr1 | 9731581 | |||||||
| chr1:9731920 | G | A | 1 | a0001c0003t0005g0097 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2428-24C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 16/18 | chr1 | 9731920 | |||||||
| chr1:9731993 | C | A | 2 | a0001c0001t0004g0165 a0001c0001t0004g0212 |
2 | HG02145.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2428-97G>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 16/18 | chr1 | 9731993 | |||||||
| chr1:9732026 | C | T | 1 | a0001c0001t0001g0139 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.2428-130G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 16/18 | chr1 | 9732026 | |||||||
| chr1:9732027 | G | A | 3 | a0001c0001t0004g0165 a0001c0001t0004g0212 a0002c0002t0003g0023 |
3 | HG02145.hp2 HG03225.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.2428-131C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 16/18 | chr1 | 9732027 | |||||||
| chr1:9732157 | T | C | 1 | a0001c0014t0001g0251 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2428-261A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 16/18 | chr1 | 9732157 | |||||||
| chr1:9732491 | G | A | 1 | a0001c0003t0006g0096 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2428-595C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 16/18 | chr1 | 9732491 | |||||||
| chr1:9732503 | G | A | 1 | a0001c0001t0001g0183 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.2428-607C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 16/18 | chr1 | 9732503 | |||||||
| chr1:9732579 | T | C | 2 | a0002c0002t0002g0010 a0002c0002t0002g0019 |
2 | HG02886.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.2428-683A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 16/18 | chr1 | 9732579 | |||||||
| chr1:9732707 | G | C | 12 | a0001c0001t0004g0165 a0001c0001t0004g0212 a0001c0006t0009g0264 others(9): Show |
12 | HG00558.hp1 HG01243.hp2 HG01981.hp2 others(9): Show |
intron_variant | MODIFIER | c.2427+694C>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 16/18 | chr1 | 9732707 | |||||||
| chr1:9732722 | C | T | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.2427+679G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 16/18 | chr1 | 9732722 | |||||||
| chr1:9732756 | A | G | 10 | a0001c0006t0009g0264 a0001c0006t0009g0265 a0003c0004t0002g0063 others(7): Show |
10 | HG00558.hp1 HG01243.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.2427+645T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 16/18 | chr1 | 9732756 | |||||||
| chr1:9732794 | C | T | 1 | a0001c0001t0008g0185 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2427+607G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 16/18 | chr1 | 9732794 | |||||||
| chr1:9733027 | A | AAAAT | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.2427+370_2427+373d others(6): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 16/18 | chr1 | 9733027 | |||||||
| chr1:9733158 | G | A | 1 | a0001c0001t0001g0128 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.2427+243C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 16/18 | chr1 | 9733158 | |||||||
| chr1:9733246 | C | G | 1 | a0001c0001t0001g0246 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2427+155G>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 16/18 | chr1 | 9733246 | |||||||
| chr1:9733300 | A | G | 12 | a0001c0001t0004g0165 a0001c0001t0004g0212 a0001c0006t0009g0264 others(9): Show |
12 | HG00558.hp1 HG01243.hp2 HG01981.hp2 others(9): Show |
intron_variant | MODIFIER | c.2427+101T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 16/18 | chr1 | 9733300 | |||||||
| chr1:9733394 | T | A | 29 | a0002c0002t0002g0037 a0002c0002t0002g0043 a0002c0002t0002g0058 others(26): Show |
29 | HG01081.hp1 HG01123.hp2 HG01261.hp2 others(26): Show |
splice_region_variant&intron_variant | LOW | c.2427+7A>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 16/18 | chr1 | 9733394 | |||||||
| chr1:9733601 | C | A | 1 | a0001c0001t0001g0172 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2282-55G>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 15/18 | chr1 | 9733601 | |||||||
| chr1:9733787 | T | A | 12 | a0002c0002t0002g0010 a0002c0002t0002g0011 a0002c0002t0002g0013 others(9): Show |
12 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.2281+185A>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 15/18 | chr1 | 9733787 | |||||||
| chr1:9733865 | T | C | 1 | a0001c0001t0001g0247 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2281+107A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 15/18 | chr1 | 9733865 | |||||||
| chr1:9733960 | C | T | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.2281+12G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 15/18 | chr1 | 9733960 | |||||||
| chr1:9734198 | C | T | 1 | a0002c0002t0003g0023 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2111-56G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 14/18 | chr1 | 9734198 | |||||||
| chr1:9734208 | T | C | 2 | a0001c0001t0004g0165 a0001c0001t0004g0212 |
2 | HG02145.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2111-66A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 14/18 | chr1 | 9734208 | |||||||
| chr1:9734225 | C | T | 1 | a0001c0001t0001g0260 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2111-83G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 14/18 | chr1 | 9734225 | |||||||
| chr1:9734247 | C | T | 117 | a0001c0001t0004g0165 a0001c0001t0004g0212 a0001c0003t0004g0108 others(114): Show |
118 | HG00423.hp2 HG00558.hp1 HG00733.hp2 others(115): Show |
intron_variant | MODIFIER | c.2111-105G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 14/18 | chr1 | 9734247 | |||||||
| chr1:9734281 | C | T | 1 | a0001c0003t0004g0259 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2111-139G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 14/18 | chr1 | 9734281 | |||||||
| chr1:9734419 | A | G | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.2111-277T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 14/18 | chr1 | 9734419 | |||||||
| chr1:9734574 | C | CAAAA | 7 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(4): Show |
7 | HG01981.hp2 NA18940.hp2 NA18968.hp2 others(4): Show |
intron_variant | MODIFIER | c.2110+370_2110+373d others(6): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 14/18 | chr1 | 9734574 | |||||||
| chr1:9734589 | A | G | 17 | a0001c0001t0001g0002 a0001c0001t0001g0129 a0001c0001t0001g0209 others(14): Show |
18 | HG00140.hp1 HG01109.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.2110+359T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 14/18 | chr1 | 9734589 | |||||||
| chr1:9734614 | G | C | 1 | a0002c0002t0003g0036 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2110+334C>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 14/18 | chr1 | 9734614 | |||||||
| chr1:9734640 | C | T | 1 | a0001c0001t0001g0210 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2110+308G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 14/18 | chr1 | 9734640 | |||||||
| chr1:9734924 | C | T | 88 | a0001c0003t0005g0008 a0001c0003t0005g0009 a0001c0003t0005g0097 others(85): Show |
89 | HG00423.hp2 HG01081.hp1 HG01123.hp2 others(86): Show |
intron_variant | MODIFIER | c.2110+24G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 14/18 | chr1 | 9734924 | |||||||
| chr1:9734937 | G | C | 5 | a0001c0001t0001g0124 a0001c0001t0001g0138 a0001c0001t0001g0139 others(2): Show |
5 | HG01346.hp1 HG01993.hp1 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.2110+11C>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 14/18 | chr1 | 9734937 | |||||||
| chr1:9735192 | G | A | 88 | a0001c0003t0005g0008 a0001c0003t0005g0009 a0001c0003t0005g0097 others(85): Show |
89 | HG00423.hp2 HG01081.hp1 HG01123.hp2 others(86): Show |
intron_variant | MODIFIER | c.1884-18C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 13/18 | chr1 | 9735192 | |||||||
| chr1:9735318 | C | T | 1 | a0001c0001t0001g0142 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1884-144G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 13/18 | chr1 | 9735318 | |||||||
| chr1:9735652 | G | T | 1 | a0001c0001t0001g0192 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1735-37C>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 12/18 | chr1 | 9735652 | |||||||
| chr1:9735661 | C | T | 118 | a0001c0001t0004g0165 a0001c0001t0004g0212 a0001c0003t0004g0108 others(115): Show |
119 | HG00423.hp2 HG00558.hp1 HG00733.hp2 others(116): Show |
intron_variant | MODIFIER | c.1735-46G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 12/18 | chr1 | 9735661 | |||||||
| chr1:9735847 | G | A | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.1734+38C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 12/18 | chr1 | 9735847 | |||||||
| chr1:9735861 | G | A | 5 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0174 others(2): Show |
5 | HG02922.hp2 HG03041.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1734+24C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 12/18 | chr1 | 9735861 | |||||||
| chr1:9736125 | G | A | 4 | a0001c0003t0005g0097 a0001c0003t0005g0098 a0001c0003t0005g0099 others(1): Show |
4 | HG02280.hp1 HG02615.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1577-83C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 11/18 | chr1 | 9736125 | |||||||
| chr1:9736280 | C | G | 1 | a0001c0001t0001g0246 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1577-238G>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 11/18 | chr1 | 9736280 | |||||||
| chr1:9736473 | G | A | 1 | a0001c0001t0001g0220 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1577-431C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 11/18 | chr1 | 9736473 | |||||||
| chr1:9736651 | G | A | 2 | a0001c0003t0007g0032 a0001c0003t0007g0095 |
2 | HG03139.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1577-609C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 11/18 | chr1 | 9736651 | |||||||
| chr1:9736756 | A | G | 24 | a0002c0002t0002g0071 a0002c0002t0002g0072 a0002c0002t0002g0073 others(21): Show |
24 | HG00423.hp2 HG01257.hp1 HG01258.hp1 others(21): Show |
intron_variant | MODIFIER | c.1577-714T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 11/18 | chr1 | 9736756 | |||||||
| chr1:9736937 | G | A | 1 | a0001c0001t0001g0249 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1576+561C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 11/18 | chr1 | 9736937 | |||||||
| chr1:9736965 | T | C | 12 | a0001c0001t0004g0165 a0001c0001t0004g0212 a0001c0006t0009g0264 others(9): Show |
12 | HG00558.hp1 HG01243.hp2 HG01981.hp2 others(9): Show |
intron_variant | MODIFIER | c.1576+533A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 11/18 | chr1 | 9736965 | |||||||
| chr1:9736968 | G | A | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.1576+530C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 11/18 | chr1 | 9736968 | |||||||
| chr1:9737094 | C | T | 2 | a0001c0001t0004g0165 a0001c0001t0004g0212 |
2 | HG02145.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1576+404G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 11/18 | chr1 | 9737094 | |||||||
| chr1:9737203 | C | CT | 6 | a0001c0003t0005g0008 a0001c0003t0005g0009 a0001c0003t0005g0097 others(3): Show |
6 | HG02280.hp1 HG02615.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1576+294dupA | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 11/18 | chr1 | 9737203 | |||||||
| chr1:9737258 | TG | T | 199 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0126 others(196): Show |
200 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(197): Show |
intron_variant | MODIFIER | c.1576+239delC | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 11/18 | chr1 | 9737258 | |||||||
| chr1:9737262 | G | C | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.1576+236C>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 11/18 | chr1 | 9737262 | |||||||
| chr1:9737657 | A | G | 16 | a0001c0003t0004g0108 a0001c0003t0004g0109 a0001c0003t0004g0110 others(13): Show |
16 | HG00733.hp2 HG01891.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.1520-103T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 10/18 | chr1 | 9737657 | |||||||
| chr1:9737788 | C | T | 3 | a0001c0001t0001g0159 a0001c0001t0008g0185 a0001c0001t0008g0238 |
3 | HG02647.hp1 HG02723.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1520-234G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 10/18 | chr1 | 9737788 | |||||||
| chr1:9737859 | C | T | 1 | a0001c0001t0001g0228 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1520-305G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 10/18 | chr1 | 9737859 | |||||||
| chr1:9737996 | A | C | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.1520-442T>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 10/18 | chr1 | 9737996 | |||||||
| chr1:9738009 | A | G | 6 | a0001c0003t0005g0008 a0001c0003t0005g0009 a0001c0003t0005g0097 others(3): Show |
6 | HG02280.hp1 HG02615.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1520-455T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 10/18 | chr1 | 9738009 | |||||||
| chr1:9738041 | C | A | 1 | a0001c0014t0001g0251 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1520-487G>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 10/18 | chr1 | 9738041 | |||||||
| chr1:9738041 | C | T | 1 | a0001c0001t0001g0243 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1520-487G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 10/18 | chr1 | 9738041 | |||||||
| chr1:9738123 | A | G | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.1520-569T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 10/18 | chr1 | 9738123 | |||||||
| chr1:9738188 | T | G | 1 | a0002c0002t0003g0060 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1520-634A>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 10/18 | chr1 | 9738188 | |||||||
| chr1:9738409 | G | C | 24 | a0002c0002t0002g0071 a0002c0002t0002g0072 a0002c0002t0002g0073 others(21): Show |
24 | HG00423.hp2 HG01257.hp1 HG01258.hp1 others(21): Show |
intron_variant | MODIFIER | c.1520-855C>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 10/18 | chr1 | 9738409 | |||||||
| chr1:9738451 | G | C | 2 | a0004c0005t0001g0202 a0004c0005t0001g0203 |
2 | HG01258.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.1520-897C>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 10/18 | chr1 | 9738451 | |||||||
| chr1:9738833 | G | A | 2 | a0001c0001t0004g0165 a0001c0001t0004g0212 |
2 | HG02145.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1520-1279C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 10/18 | chr1 | 9738833 | |||||||
| chr1:9738836 | G | A | 119 | a0001c0001t0004g0165 a0001c0001t0004g0212 a0001c0003t0004g0108 others(116): Show |
120 | HG00423.hp2 HG00558.hp1 HG00733.hp2 others(117): Show |
intron_variant | MODIFIER | c.1520-1282C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 10/18 | chr1 | 9738836 | |||||||
| chr1:9738904 | C | T | 3 | a0003c0004t0002g0065 a0003c0004t0002g0066 a0003c0004t0002g0070 |
3 | NA18940.hp2 NA18968.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.1520-1350G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 10/18 | chr1 | 9738904 | |||||||
| chr1:9738916 | T | C | 1 | a0001c0001t0001g0220 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1520-1362A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 10/18 | chr1 | 9738916 | |||||||
| chr1:9738949 | G | A | 2 | a0001c0001t0004g0165 a0001c0001t0004g0212 |
2 | HG02145.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1520-1395C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 10/18 | chr1 | 9738949 | |||||||
| chr1:9738996 | T | C | 2 | a0001c0006t0009g0264 a0001c0006t0009g0265 |
2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1520-1442A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 10/18 | chr1 | 9738996 | |||||||
| chr1:9739310 | C | T | 1 | a0001c0014t0001g0251 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1520-1756G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 10/18 | chr1 | 9739310 | |||||||
| chr1:9739328 | C | T | 1 | a0001c0001t0001g0150 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1519+1766G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 10/18 | chr1 | 9739328 | |||||||
| chr1:9739438 | G | C | 75 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0126 others(72): Show |
75 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.1519+1656C>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 10/18 | chr1 | 9739438 | |||||||
| chr1:9739606 | G | A | 2 | a0001c0006t0009g0264 a0001c0006t0009g0265 |
2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1519+1488C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 10/18 | chr1 | 9739606 | |||||||
| chr1:9739610 | G | A | 38 | a0001c0001t0001g0105 a0001c0001t0001g0126 a0001c0001t0001g0127 others(35): Show |
38 | HG00423.hp1 HG00558.hp2 HG00609.hp2 others(35): Show |
intron_variant | MODIFIER | c.1519+1484C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 10/18 | chr1 | 9739610 | |||||||
| chr1:9739635 | G | C | 1 | a0001c0014t0001g0251 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1519+1459C>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 10/18 | chr1 | 9739635 | |||||||
| chr1:9739752 | G | C | 5 | a0002c0002t0003g0045 a0002c0002t0003g0046 a0002c0002t0003g0047 others(2): Show |
5 | NA18942.hp2 NA18971.hp1 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.1519+1342C>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 10/18 | chr1 | 9739752 | |||||||
| chr1:9739766 | T | C | 1 | a0001c0001t0001g0183 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1519+1328A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 10/18 | chr1 | 9739766 | |||||||
| chr1:9739794 | G | A | 12 | a0002c0002t0002g0010 a0002c0002t0002g0011 a0002c0002t0002g0013 others(9): Show |
12 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1519+1300C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 10/18 | chr1 | 9739794 | |||||||
| chr1:9739814 | A | AT | 12 | a0001c0001t0001g0106 a0001c0001t0001g0142 a0001c0001t0001g0145 others(9): Show |
12 | HG00140.hp2 HG00735.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1519+1279dupA | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 10/18 | chr1 | 9739814 | |||||||
| chr1:9739814 | AT | A | 96 | a0001c0001t0001g0168 a0001c0001t0001g0178 a0001c0001t0001g0183 others(93): Show |
97 | HG00423.hp2 HG00558.hp1 HG01070.hp1 others(94): Show |
intron_variant | MODIFIER | c.1519+1279delA | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 10/18 | chr1 | 9739814 | |||||||
| chr1:9739814 | ATT | A | 21 | a0001c0003t0004g0108 a0001c0003t0004g0109 a0001c0003t0004g0110 others(18): Show |
21 | HG00733.hp2 HG01891.hp2 HG02559.hp1 others(18): Show |
intron_variant | MODIFIER | c.1519+1278_1519+127 others(6): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 10/18 | chr1 | 9739814 | |||||||
| chr1:9739817 | T | C | 1 | a0001c0006t0009g0265 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1519+1277A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 10/18 | chr1 | 9739817 | |||||||
| chr1:9739818 | T | C | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.1519+1276A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 10/18 | chr1 | 9739818 | |||||||
| chr1:9739845 | T | C | 122 | a0001c0001t0004g0165 a0001c0001t0004g0212 a0001c0003t0004g0108 others(119): Show |
123 | HG00423.hp2 HG00558.hp1 HG00733.hp2 others(120): Show |
intron_variant | MODIFIER | c.1519+1249A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 10/18 | chr1 | 9739845 | |||||||
| chr1:9739977 | T | C | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.1519+1117A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 10/18 | chr1 | 9739977 | |||||||
| chr1:9740083 | T | G | 1 | a0001c0003t0004g0259 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1519+1011A>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 10/18 | chr1 | 9740083 | |||||||
| chr1:9740112 | G | A | 1 | a0001c0003t0004g0259 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1519+982C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 10/18 | chr1 | 9740112 | |||||||
| chr1:9740124 | A | G | 4 | a0001c0001t0001g0211 a0001c0001t0001g0215 a0001c0001t0001g0216 others(1): Show |
4 | HG02630.hp2 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1519+970T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 10/18 | chr1 | 9740124 | |||||||
| chr1:9740187 | G | A | 2 | a0001c0006t0009g0264 a0001c0006t0009g0265 |
2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1519+907C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 10/18 | chr1 | 9740187 | |||||||
| chr1:9740349 | C | T | 7 | a0002c0002t0002g0007 a0002c0002t0002g0026 a0002c0002t0002g0027 others(4): Show |
7 | HG02717.hp2 HG03130.hp2 HG03831.hp2 others(4): Show |
intron_variant | MODIFIER | c.1519+745G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 10/18 | chr1 | 9740349 | |||||||
| chr1:9740350 | G | A | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.1519+744C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 10/18 | chr1 | 9740350 | |||||||
| chr1:9740493 | A | G | 10 | a0001c0006t0009g0264 a0001c0006t0009g0265 a0003c0004t0002g0063 others(7): Show |
10 | HG00558.hp1 HG01243.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.1519+601T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 10/18 | chr1 | 9740493 | |||||||
| chr1:9740529 | T | C | 1 | a0002c0013t0002g0012 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1519+565A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 10/18 | chr1 | 9740529 | |||||||
| chr1:9740679 | C | T | 4 | a0001c0001t0004g0165 a0001c0001t0004g0212 a0001c0006t0009g0264 others(1): Show |
4 | HG01243.hp2 HG02145.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1519+415G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 10/18 | chr1 | 9740679 | |||||||
| chr1:9740722 | C | T | 1 | a0002c0002t0002g0035 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1519+372G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 10/18 | chr1 | 9740722 | |||||||
| chr1:9741063 | C | T | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.1519+31G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 10/18 | chr1 | 9741063 | |||||||
| chr1:9741283 | G | A | 71 | a0001c0003t0006g0022 a0001c0003t0006g0042 a0001c0003t0006g0055 others(68): Show |
72 | HG00423.hp2 HG01081.hp1 HG01123.hp2 others(69): Show |
intron_variant | MODIFIER | c.1357-27C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 9/18 | chr1 | 9741283 | |||||||
| chr1:9741447 | G | A | 1 | a0001c0001t0001g0223 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1357-191C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 9/18 | chr1 | 9741447 | |||||||
| chr1:9741451 | G | C | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.1357-195C>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 9/18 | chr1 | 9741451 | |||||||
| chr1:9741480 | G | A | 1 | a0001c0001t0001g0159 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1357-224C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 9/18 | chr1 | 9741480 | |||||||
| chr1:9741649 | G | A | 4 | a0001c0001t0001g0157 a0001c0001t0001g0167 a0001c0001t0001g0169 others(1): Show |
4 | HG00738.hp2 HG01517.hp2 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.1357-393C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 9/18 | chr1 | 9741649 | |||||||
| chr1:9741703 | A | G | 122 | a0001c0001t0004g0165 a0001c0001t0004g0212 a0001c0003t0004g0108 others(119): Show |
123 | HG00423.hp2 HG00558.hp1 HG00733.hp2 others(120): Show |
intron_variant | MODIFIER | c.1357-447T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 9/18 | chr1 | 9741703 | |||||||
| chr1:9741817 | C | T | 1 | a0001c0001t0001g0183 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1357-561G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 9/18 | chr1 | 9741817 | |||||||
| chr1:9741921 | G | A | 2 | a0001c0001t0004g0165 a0001c0001t0004g0212 |
2 | HG02145.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1357-665C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 9/18 | chr1 | 9741921 | |||||||
| chr1:9741938 | T | C | 1 | a0001c0001t0001g0139 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1357-682A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 9/18 | chr1 | 9741938 | |||||||
| chr1:9741969 | A | G | 2 | a0001c0006t0009g0264 a0001c0006t0009g0265 |
2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1357-713T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 9/18 | chr1 | 9741969 | |||||||
| chr1:9742000 | A | G | 1 | a0002c0002t0002g0031 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1357-744T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 9/18 | chr1 | 9742000 | |||||||
| chr1:9742195 | G | A | 1 | a0002c0002t0002g0075 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1357-939C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 9/18 | chr1 | 9742195 | |||||||
| chr1:9742277 | T | C | 5 | a0001c0001t0001g0124 a0001c0001t0001g0138 a0001c0001t0001g0139 others(2): Show |
5 | HG01346.hp1 HG01993.hp1 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.1357-1021A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 9/18 | chr1 | 9742277 | |||||||
| chr1:9742336 | C | G | 10 | a0001c0006t0009g0264 a0001c0006t0009g0265 a0003c0004t0002g0063 others(7): Show |
10 | HG00558.hp1 HG01243.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.1357-1080G>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 9/18 | chr1 | 9742336 | |||||||
| chr1:9742348 | G | A | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.1357-1092C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 9/18 | chr1 | 9742348 | |||||||
| chr1:9742355 | T | C | 4 | a0001c0003t0005g0097 a0001c0003t0005g0098 a0001c0003t0005g0099 others(1): Show |
4 | HG02280.hp1 HG02615.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1357-1099A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 9/18 | chr1 | 9742355 | |||||||
| chr1:9742680 | A | T | 2 | a0001c0006t0009g0264 a0001c0006t0009g0265 |
2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1356+1204T>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 9/18 | chr1 | 9742680 | |||||||
| chr1:9742730 | G | A | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.1356+1154C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 9/18 | chr1 | 9742730 | |||||||
| chr1:9742761 | A | G | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.1356+1123T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 9/18 | chr1 | 9742761 | |||||||
| chr1:9742764 | C | T | 1 | a0001c0001t0001g0147 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1356+1120G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 9/18 | chr1 | 9742764 | |||||||
| chr1:9742777 | G | A | 1 | a0002c0002t0002g0034 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1356+1107C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 9/18 | chr1 | 9742777 | |||||||
| chr1:9742883 | G | T | 1 | a0001c0001t0001g0177 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1356+1001C>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 9/18 | chr1 | 9742883 | |||||||
| chr1:9742919 | A | G | 11 | a0002c0002t0002g0010 a0002c0002t0002g0011 a0002c0002t0002g0013 others(8): Show |
11 | HG01884.hp1 HG01891.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.1356+965T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 9/18 | chr1 | 9742919 | |||||||
| chr1:9742964 | A | G | 1 | a0003c0004t0002g0063 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1356+920T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 9/18 | chr1 | 9742964 | |||||||
| chr1:9743145 | C | A | 1 | a0001c0001t0001g0244 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1356+739G>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 9/18 | chr1 | 9743145 | |||||||
| chr1:9743369 | G | A | 1 | a0001c0001t0016g0257 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1356+515C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 9/18 | chr1 | 9743369 | |||||||
| chr1:9743499 | C | T | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.1356+385G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 9/18 | chr1 | 9743499 | |||||||
| chr1:9743536 | A | G | 24 | a0002c0002t0002g0071 a0002c0002t0002g0072 a0002c0002t0002g0073 others(21): Show |
24 | HG00423.hp2 HG01257.hp1 HG01258.hp1 others(21): Show |
intron_variant | MODIFIER | c.1356+348T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 9/18 | chr1 | 9743536 | |||||||
| chr1:9743570 | C | T | 17 | a0001c0003t0004g0108 a0001c0003t0004g0109 a0001c0003t0004g0110 others(14): Show |
17 | HG00733.hp2 HG01109.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.1356+314G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 9/18 | chr1 | 9743570 | |||||||
| chr1:9743604 | G | A | 1 | a0001c0001t0001g0224 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1356+280C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 9/18 | chr1 | 9743604 | |||||||
| chr1:9743664 | C | T | 1 | a0001c0001t0001g0138 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1356+220G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 9/18 | chr1 | 9743664 | |||||||
| chr1:9743724 | G | GT | 26 | a0001c0001t0001g0142 a0001c0001t0001g0216 a0001c0001t0001g0262 others(23): Show |
26 | HG00423.hp1 HG00733.hp2 HG01981.hp2 others(23): Show |
intron_variant | MODIFIER | c.1356+159dupA | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 9/18 | chr1 | 9743724 | |||||||
| chr1:9743724 | G | T | 2 | a0001c0001t0001g0186 a0001c0001t0001g0192 |
2 | HG00735.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.1356+160C>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 9/18 | chr1 | 9743724 | |||||||
| chr1:9743786 | G | A | 1 | a0001c0001t0001g0245 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1356+98C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 9/18 | chr1 | 9743786 | |||||||
| chr1:9744094 | A | G | 2 | a0001c0001t0001g0174 a0001c0001t0001g0175 |
2 | HG02922.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1235-89T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 8/18 | chr1 | 9744094 | |||||||
| chr1:9744128 | C | A | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.1235-123G>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 8/18 | chr1 | 9744128 | |||||||
| chr1:9744190 | G | A | 6 | a0001c0003t0005g0008 a0001c0003t0005g0009 a0001c0003t0005g0097 others(3): Show |
6 | HG02280.hp1 HG02615.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1235-185C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 8/18 | chr1 | 9744190 | |||||||
| chr1:9744196 | C | T | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.1235-191G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 8/18 | chr1 | 9744196 | |||||||
| chr1:9744257 | C | T | 2 | a0004c0005t0001g0202 a0004c0005t0001g0203 |
2 | HG01258.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.1234+138G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 8/18 | chr1 | 9744257 | |||||||
| chr1:9744268 | C | G | 1 | a0001c0001t0001g0205 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1234+127G>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 8/18 | chr1 | 9744268 | |||||||
| chr1:9744312 | T | C | 12 | a0002c0002t0002g0010 a0002c0002t0002g0011 a0002c0002t0002g0013 others(9): Show |
12 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1234+83A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 8/18 | chr1 | 9744312 | |||||||
| chr1:9744661 | G | A | 1 | a0001c0003t0004g0259 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.986-18C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9744661 | |||||||
| chr1:9744672 | T | C | 10 | a0001c0006t0009g0264 a0001c0006t0009g0265 a0003c0004t0002g0063 others(7): Show |
10 | HG00558.hp1 HG01243.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.986-29A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9744672 | |||||||
| chr1:9744696 | A | G | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.986-53T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9744696 | |||||||
| chr1:9744775 | G | A | 2 | a0001c0006t0009g0264 a0001c0006t0009g0265 |
2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.986-132C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9744775 | |||||||
| chr1:9744973 | G | T | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.986-330C>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9744973 | |||||||
| chr1:9745132 | G | A | 5 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0174 others(2): Show |
5 | HG02922.hp2 HG03041.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.986-489C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9745132 | |||||||
| chr1:9745145 | C | T | 1 | a0001c0001t0001g0260 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.986-502G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9745145 | |||||||
| chr1:9745216 | G | A | 2 | a0001c0006t0009g0264 a0001c0006t0009g0265 |
2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.986-573C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9745216 | |||||||
| chr1:9745228 | CA | C | 107 | a0001c0001t0001g0105 a0001c0001t0001g0126 a0001c0001t0001g0127 others(104): Show |
107 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.986-586delT | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9745228 | |||||||
| chr1:9745228 | CAA | C | 79 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0004g0165 others(76): Show |
79 | HG00733.hp2 HG00738.hp1 HG01081.hp1 others(76): Show |
intron_variant | MODIFIER | c.986-587_986-586del others(2): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9745228 | |||||||
| chr1:9745351 | G | A | 2 | a0001c0006t0009g0264 a0001c0006t0009g0265 |
2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.986-708C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9745351 | |||||||
| chr1:9745380 | G | A | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.986-737C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9745380 | |||||||
| chr1:9745396 | C | T | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.986-753G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9745396 | |||||||
| chr1:9745636 | G | A | 1 | a0002c0002t0003g0060 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.986-993C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9745636 | |||||||
| chr1:9745694 | T | G | 2 | a0001c0006t0009g0264 a0001c0006t0009g0265 |
2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.986-1051A>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9745694 | |||||||
| chr1:9745765 | G | GT | 53 | a0001c0001t0001g0002 a0001c0001t0001g0106 a0001c0001t0001g0126 others(50): Show |
54 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(51): Show |
intron_variant | MODIFIER | c.986-1123dupA | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9745765 | |||||||
| chr1:9745765 | G | GTT | 7 | a0001c0001t0001g0209 a0001c0001t0001g0222 a0001c0001t0001g0225 others(4): Show |
7 | HG00733.hp1 HG01981.hp1 HG02083.hp2 others(4): Show |
intron_variant | MODIFIER | c.986-1124_986-1123d others(4): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9745765 | |||||||
| chr1:9745765 | GT | G | 59 | a0001c0001t0001g0201 a0001c0001t0001g0253 a0001c0001t0001g0260 others(56): Show |
60 | HG00423.hp2 HG00639.hp1 HG01243.hp2 others(57): Show |
intron_variant | MODIFIER | c.986-1123delA | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9745765 | |||||||
| chr1:9745846 | G | A | 2 | a0002c0007t0002g0084 a0002c0007t0002g0085 |
2 | NA19066.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.986-1203C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9745846 | |||||||
| chr1:9745915 | T | C | 2 | a0001c0003t0006g0055 a0001c0003t0006g0056 |
2 | HG01255.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.986-1272A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9745915 | |||||||
| chr1:9745931 | G | A | 1 | a0001c0003t0007g0032 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.986-1288C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9745931 | |||||||
| chr1:9746293 | T | A | 17 | a0001c0003t0004g0108 a0001c0003t0004g0109 a0001c0003t0004g0110 others(14): Show |
17 | HG00733.hp2 HG01109.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.986-1650A>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9746293 | |||||||
| chr1:9746359 | G | A | 4 | a0001c0001t0001g0234 a0001c0001t0001g0236 a0001c0001t0001g0237 others(1): Show |
4 | HG00621.hp2 HG01952.hp1 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.986-1716C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9746359 | |||||||
| chr1:9746453 | C | T | 2 | a0001c0001t0001g0188 a0001c0001t0001g0222 |
2 | HG00733.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.986-1810G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9746453 | |||||||
| chr1:9746527 | C | T | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.986-1884G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9746527 | |||||||
| chr1:9746566 | G | T | 245 | a0001c0001t0001g0002 a0001c0001t0001g0105 a0001c0001t0001g0106 others(242): Show |
247 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.986-1923C>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9746566 | |||||||
| chr1:9746618 | G | A | 6 | a0002c0002t0002g0007 a0002c0002t0002g0026 a0002c0002t0002g0027 others(3): Show |
6 | HG02717.hp2 HG03130.hp2 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.986-1975C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9746618 | |||||||
| chr1:9746886 | T | C | 4 | a0001c0003t0005g0097 a0001c0003t0005g0098 a0001c0003t0005g0099 others(1): Show |
4 | HG02280.hp1 HG02615.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.986-2243A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9746886 | |||||||
| chr1:9746963 | T | C | 2 | a0001c0001t0001g0261 a0001c0001t0001g0262 |
2 | HG00423.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.986-2320A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9746963 | |||||||
| chr1:9747095 | G | A | 1 | a0002c0002t0002g0091 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.985+2366C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9747095 | |||||||
| chr1:9747126 | G | A | 2 | a0001c0003t0005g0097 a0001c0003t0005g0099 |
2 | HG02723.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.985+2335C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9747126 | |||||||
| chr1:9747135 | C | T | 1 | a0001c0001t0001g0260 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.985+2326G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9747135 | |||||||
| chr1:9747176 | C | CA | 21 | a0001c0001t0001g0142 a0001c0001t0001g0145 a0001c0001t0001g0149 others(18): Show |
21 | HG00558.hp2 HG01258.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.985+2284dupT | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9747176 | |||||||
| chr1:9747176 | C | CAAAAAAA others(8): Show |
2 | a0003c0004t0002g0063 a0003c0004t0002g0068 |
2 | HG01981.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.985+2270_985+2284d others(17): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9747176 | |||||||
| chr1:9747176 | C | CAAAAAAA others(9): Show |
1 | a0003c0004t0002g0064 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.985+2269_985+2284d others(18): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9747176 | |||||||
| chr1:9747176 | C | CAAAAAAA others(11): Show |
2 | a0003c0004t0002g0066 a0003c0004t0002g0067 |
2 | NA18968.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.985+2267_985+2284d others(20): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9747176 | |||||||
| chr1:9747176 | C | CAAAAAAA others(16): Show |
1 | a0003c0004t0002g0070 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.985+2262_985+2284d others(25): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9747176 | |||||||
| chr1:9747176 | C | CAAAAAAA others(21): Show |
1 | a0003c0004t0002g0069 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.985+2284_985+2285i others(30): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9747176 | |||||||
| chr1:9747176 | CA | C | 68 | a0001c0001t0001g0105 a0001c0001t0001g0124 a0001c0001t0001g0126 others(65): Show |
68 | HG00423.hp2 HG01081.hp1 HG01099.hp1 others(65): Show |
intron_variant | MODIFIER | c.985+2284delT | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9747176 | |||||||
| chr1:9747176 | CAA | C | 7 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0006 others(4): Show |
8 | HG02559.hp2 HG02717.hp1 HG03486.hp2 others(5): Show |
intron_variant | MODIFIER | c.985+2283_985+2284d others(4): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9747176 | |||||||
| chr1:9747176 | CAAAAAA | C | 13 | a0001c0003t0004g0108 a0001c0003t0004g0109 a0001c0003t0004g0110 others(10): Show |
13 | HG00733.hp2 HG01891.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.985+2279_985+2284d others(8): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9747176 | |||||||
| chr1:9747222 | G | A | 1 | a0001c0014t0001g0251 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.985+2239C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9747222 | |||||||
| chr1:9747253 | T | C | 2 | a0001c0006t0009g0264 a0001c0006t0009g0265 |
2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.985+2208A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9747253 | |||||||
| chr1:9747297 | C | A | 1 | a0001c0001t0001g0183 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.985+2164G>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9747297 | |||||||
| chr1:9747325 | A | G | 14 | a0001c0003t0004g0108 a0001c0003t0004g0109 a0001c0003t0004g0110 others(11): Show |
14 | HG00733.hp2 HG01891.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.985+2136T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9747325 | |||||||
| chr1:9747607 | C | A | 1 | a0002c0002t0017g0107 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.985+1854G>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9747607 | |||||||
| chr1:9747731 | A | C | 2 | a0001c0006t0009g0264 a0001c0006t0009g0265 |
2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.985+1730T>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9747731 | |||||||
| chr1:9747772 | G | A | 1 | a0001c0001t0001g0217 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.985+1689C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9747772 | |||||||
| chr1:9747819 | G | A | 7 | a0002c0002t0002g0007 a0002c0002t0002g0026 a0002c0002t0002g0027 others(4): Show |
7 | HG02717.hp2 HG03130.hp2 HG03831.hp2 others(4): Show |
intron_variant | MODIFIER | c.985+1642C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9747819 | |||||||
| chr1:9747860 | G | A | 1 | a0001c0001t0001g0260 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.985+1601C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9747860 | |||||||
| chr1:9747950 | G | A | 1 | a0002c0010t0002g0029 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.985+1511C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9747950 | |||||||
| chr1:9748042 | T | TA | 32 | a0001c0003t0004g0108 a0001c0003t0004g0109 a0001c0003t0004g0110 others(29): Show |
32 | HG00733.hp2 HG01109.hp1 HG01515.hp1 others(29): Show |
intron_variant | MODIFIER | c.985+1418dupT | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9748042 | |||||||
| chr1:9748042 | TA | T | 9 | a0001c0001t0001g0178 a0003c0004t0002g0063 a0003c0004t0002g0064 others(6): Show |
9 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(6): Show |
intron_variant | MODIFIER | c.985+1418delT | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9748042 | |||||||
| chr1:9748244 | A | G | 121 | a0001c0003t0004g0108 a0001c0003t0004g0109 a0001c0003t0004g0110 others(118): Show |
122 | HG00423.hp2 HG00558.hp1 HG00733.hp2 others(119): Show |
intron_variant | MODIFIER | c.985+1217T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9748244 | |||||||
| chr1:9748400 | A | G | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.985+1061T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9748400 | |||||||
| chr1:9748411 | T | A | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.985+1050A>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9748411 | |||||||
| chr1:9748545 | C | T | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.985+916G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9748545 | |||||||
| chr1:9748546 | G | A | 2 | a0001c0006t0009g0264 a0001c0006t0009g0265 |
2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.985+915C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9748546 | |||||||
| chr1:9748619 | T | C | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.985+842A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9748619 | |||||||
| chr1:9748679 | G | C | 1 | a0002c0002t0002g0086 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.985+782C>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9748679 | |||||||
| chr1:9748687 | C | T | 5 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0006 others(2): Show |
6 | HG02559.hp2 HG02717.hp1 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.985+774G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9748687 | |||||||
| chr1:9748956 | G | A | 1 | a0001c0003t0004g0119 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.985+505C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9748956 | |||||||
| chr1:9749016 | C | CA | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.985+444_985+445ins others(1): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9749016 | |||||||
| chr1:9749017 | G | C | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.985+444C>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9749017 | |||||||
| chr1:9749100 | C | T | 2 | a0002c0002t0002g0071 a0002c0002t0002g0081 |
2 | HG01346.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.985+361G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9749100 | |||||||
| chr1:9749197 | T | C | 1 | a0001c0003t0007g0032 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.985+264A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9749197 | |||||||
| chr1:9749284 | C | T | 1 | a0010c0015t0014g0104 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.985+177G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9749284 | |||||||
| chr1:9749988 | C | T | 1 | a0002c0002t0003g0036 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.650-75G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 5/18 | chr1 | 9749988 | |||||||
| chr1:9750040 | G | A | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.650-127C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 5/18 | chr1 | 9750040 | |||||||
| chr1:9750226 | T | C | 16 | a0001c0003t0004g0108 a0001c0003t0004g0109 a0001c0003t0004g0110 others(13): Show |
16 | HG00733.hp2 HG01891.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.650-313A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 5/18 | chr1 | 9750226 | |||||||
| chr1:9750412 | G | A | 10 | a0001c0006t0009g0264 a0001c0006t0009g0265 a0003c0004t0002g0063 others(7): Show |
10 | HG00558.hp1 HG01243.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.650-499C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 5/18 | chr1 | 9750412 | |||||||
| chr1:9750458 | C | T | 3 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0006 |
4 | HG02717.hp1 HG03486.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.650-545G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 5/18 | chr1 | 9750458 | |||||||
| chr1:9750634 | C | T | 1 | a0001c0014t0001g0251 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.650-721G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 5/18 | chr1 | 9750634 | |||||||
| chr1:9750715 | C | CAAAAAAA others(1): Show |
22 | a0001c0001t0001g0253 a0001c0001t0001g0254 a0001c0001t0001g0260 others(19): Show |
22 | HG00639.hp1 HG00733.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.649+750_649+757dup others(8): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 5/18 | chr1 | 9750715 | |||||||
| chr1:9750715 | C | CAAAAAAA others(2): Show |
90 | a0001c0001t0004g0165 a0001c0003t0004g0115 a0001c0003t0004g0117 others(87): Show |
91 | HG00423.hp2 HG00558.hp1 HG01081.hp1 others(88): Show |
intron_variant | MODIFIER | c.649+749_649+757dup others(9): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 5/18 | chr1 | 9750715 | |||||||
| chr1:9750715 | C | CAAAAAAA others(3): Show |
12 | a0001c0003t0006g0022 a0001c0003t0006g0055 a0001c0003t0006g0056 others(9): Show |
12 | HG01255.hp1 HG01891.hp1 HG01981.hp2 others(9): Show |
intron_variant | MODIFIER | c.649+748_649+757dup others(10): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 5/18 | chr1 | 9750715 | |||||||
| chr1:9750715 | CA | C | 8 | a0001c0001t0001g0162 a0001c0001t0001g0234 a0001c0001t0001g0236 others(5): Show |
8 | HG00621.hp2 HG01952.hp1 HG02004.hp2 others(5): Show |
intron_variant | MODIFIER | c.649+757delT | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 5/18 | chr1 | 9750715 | |||||||
| chr1:9750909 | C | A | 1 | a0002c0002t0003g0049 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.649+564G>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 5/18 | chr1 | 9750909 | |||||||
| chr1:9751019 | C | T | 1 | a0007c0017t0010g0003 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.649+454G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 5/18 | chr1 | 9751019 | |||||||
| chr1:9751377 | A | G | 122 | a0001c0003t0004g0108 a0001c0003t0004g0109 a0001c0003t0004g0110 others(119): Show |
123 | HG00423.hp2 HG00558.hp1 HG00733.hp2 others(120): Show |
intron_variant | MODIFIER | c.649+96T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 5/18 | chr1 | 9751377 | |||||||
| chr1:9751428 | C | A | 1 | a0001c0003t0007g0032 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.649+45G>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 5/18 | chr1 | 9751428 | |||||||
| chr1:9751458 | C | G | 1 | a0001c0001t0001g0150 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.649+15G>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 5/18 | chr1 | 9751458 | |||||||
| chr1:9751752 | T | C | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.441-71A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 4/18 | chr1 | 9751752 | |||||||
| chr1:9751856 | C | T | 4 | a0001c0001t0001g0211 a0001c0001t0001g0215 a0001c0001t0001g0216 others(1): Show |
4 | HG02630.hp2 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.441-175G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 4/18 | chr1 | 9751856 | |||||||
| chr1:9752241 | C | G | 2 | a0001c0006t0009g0264 a0001c0006t0009g0265 |
2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.441-560G>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 4/18 | chr1 | 9752241 | |||||||
| chr1:9752414 | C | T | 1 | a0001c0001t0001g0136 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.441-733G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 4/18 | chr1 | 9752414 | |||||||
| chr1:9752810 | C | T | 1 | a0001c0001t0001g0266 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.441-1129G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 4/18 | chr1 | 9752810 | |||||||
| chr1:9752835 | C | G | 17 | a0001c0003t0004g0108 a0001c0003t0004g0109 a0001c0003t0004g0110 others(14): Show |
17 | HG00733.hp2 HG01109.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.441-1154G>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 4/18 | chr1 | 9752835 | |||||||
| chr1:9752871 | G | GTAAA | 7 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(4): Show |
7 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(4): Show |
intron_variant | MODIFIER | c.441-1194_441-1191d others(6): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 4/18 | chr1 | 9752871 | |||||||
| chr1:9753077 | G | A | 1 | a0001c0001t0001g0155 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.441-1396C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 4/18 | chr1 | 9753077 | |||||||
| chr1:9753132 | C | T | 7 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(4): Show |
7 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(4): Show |
intron_variant | MODIFIER | c.441-1451G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 4/18 | chr1 | 9753132 | |||||||
| chr1:9753187 | C | T | 7 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(4): Show |
7 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(4): Show |
intron_variant | MODIFIER | c.441-1506G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 4/18 | chr1 | 9753187 | |||||||
| chr1:9753210 | C | T | 7 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(4): Show |
7 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(4): Show |
intron_variant | MODIFIER | c.441-1529G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 4/18 | chr1 | 9753210 | |||||||
| chr1:9753211 | G | C | 7 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(4): Show |
7 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(4): Show |
intron_variant | MODIFIER | c.441-1530C>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 4/18 | chr1 | 9753211 | |||||||
| chr1:9753341 | C | G | 1 | a0001c0001t0001g0155 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.441-1660G>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 4/18 | chr1 | 9753341 | |||||||
| chr1:9753345 | C | A | 7 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(4): Show |
7 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(4): Show |
intron_variant | MODIFIER | c.441-1664G>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 4/18 | chr1 | 9753345 | |||||||
| chr1:9753365 | G | A | 3 | a0001c0001t0001g0138 a0001c0001t0001g0144 a0001c0001t0001g0147 |
3 | HG01346.hp1 HG01993.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.441-1684C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 4/18 | chr1 | 9753365 | |||||||
| chr1:9753424 | T | C | 1 | a0001c0001t0019g0143 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.440+1690A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 4/18 | chr1 | 9753424 | |||||||
| chr1:9753493 | A | AT | 10 | a0001c0001t0019g0143 a0001c0006t0009g0264 a0001c0006t0009g0265 others(7): Show |
10 | HG00558.hp1 HG01243.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.440+1620dupA | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 4/18 | chr1 | 9753493 | |||||||
| chr1:9753567 | G | C | 9 | a0001c0006t0009g0264 a0001c0006t0009g0265 a0003c0004t0002g0063 others(6): Show |
9 | HG00558.hp1 HG01243.hp2 HG01981.hp2 others(6): Show |
intron_variant | MODIFIER | c.440+1547C>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 4/18 | chr1 | 9753567 | |||||||
| chr1:9753585 | A | C | 66 | a0001c0003t0006g0022 a0001c0003t0006g0042 a0001c0003t0006g0055 others(63): Show |
67 | HG00423.hp2 HG01081.hp1 HG01123.hp2 others(64): Show |
intron_variant | MODIFIER | c.440+1529T>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 4/18 | chr1 | 9753585 | |||||||
| chr1:9753797 | G | T | 1 | a0001c0003t0007g0095 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.440+1317C>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 4/18 | chr1 | 9753797 | |||||||
| chr1:9754244 | A | C | 2 | a0001c0001t0001g0106 a0001c0001t0001g0244 |
2 | HG02738.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.440+870T>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 4/18 | chr1 | 9754244 | |||||||
| chr1:9754283 | C | T | 1 | a0001c0016t0001g0198 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.440+831G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 4/18 | chr1 | 9754283 | |||||||
| chr1:9754341 | G | A | 7 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(4): Show |
7 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(4): Show |
intron_variant | MODIFIER | c.440+773C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 4/18 | chr1 | 9754341 | |||||||
| chr1:9754491 | G | A | 14 | a0001c0003t0004g0108 a0001c0003t0004g0109 a0001c0003t0004g0110 others(11): Show |
14 | HG00733.hp2 HG01891.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.440+623C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 4/18 | chr1 | 9754491 | |||||||
| chr1:9754787 | G | A | 1 | a0001c0003t0004g0259 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.440+327C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 4/18 | chr1 | 9754787 | |||||||
| chr1:9754906 | A | G | 127 | a0001c0001t0001g0253 a0001c0001t0001g0254 a0001c0001t0001g0260 others(124): Show |
128 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(125): Show |
intron_variant | MODIFIER | c.440+208T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 4/18 | chr1 | 9754906 | |||||||
| chr1:9755041 | T | C | 1 | a0004c0005t0001g0202 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.440+73A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 4/18 | chr1 | 9755041 | |||||||
| chr1:9755314 | G | A | 25 | a0001c0003t0006g0096 a0002c0002t0002g0071 a0002c0002t0002g0072 others(22): Show |
25 | HG00423.hp2 HG01257.hp1 HG01258.hp1 others(22): Show |
splice_region_variant&intron_variant | LOW | c.245-5C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 3/18 | chr1 | 9755314 | |||||||
| chr1:9755341 | C | G | 6 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0174 others(3): Show |
6 | HG02922.hp2 HG03041.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.245-32G>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 3/18 | chr1 | 9755341 | |||||||
| chr1:9755485 | C | G | 123 | a0001c0001t0001g0253 a0001c0001t0001g0254 a0001c0001t0001g0260 others(120): Show |
124 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(121): Show |
intron_variant | MODIFIER | c.245-176G>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 3/18 | chr1 | 9755485 | |||||||
| chr1:9755555 | G | A | 1 | a0007c0017t0010g0003 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.245-246C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 3/18 | chr1 | 9755555 | |||||||
| chr1:9755762 | G | GATATAGG others(12): Show |
1 | a0003c0004t0002g0066 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.245-472_245-454dup others(19): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 3/18 | chr1 | 9755762 | |||||||
| chr1:9755798 | C | CA | 244 | a0001c0001t0001g0002 a0001c0001t0001g0105 a0001c0001t0001g0106 others(241): Show |
245 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.245-490dupT | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 3/18 | chr1 | 9755798 | |||||||
| chr1:9755798 | C | CAA | 5 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0006 others(2): Show |
6 | HG02559.hp2 HG02717.hp1 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.245-491_245-490dup others(2): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 3/18 | chr1 | 9755798 | |||||||
| chr1:9755873 | C | T | 2 | a0001c0001t0001g0213 a0001c0001t0001g0217 |
2 | HG02145.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.245-564G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 3/18 | chr1 | 9755873 | |||||||
| chr1:9755939 | G | A | 1 | a0001c0001t0001g0228 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.244+542C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 3/18 | chr1 | 9755939 | |||||||
| chr1:9755946 | A | C | 1 | a0001c0008t0001g0206 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.244+535T>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 3/18 | chr1 | 9755946 | |||||||
| chr1:9755980 | T | C | 1 | a0002c0002t0002g0017 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.244+501A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 3/18 | chr1 | 9755980 | |||||||
| chr1:9755993 | G | A | 1 | a0007c0017t0010g0003 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.244+488C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 3/18 | chr1 | 9755993 | |||||||
| chr1:9756062 | A | AG | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.244+418_244+419ins others(1): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 3/18 | chr1 | 9756062 | |||||||
| chr1:9756112 | C | T | 4 | a0001c0001t0001g0234 a0001c0001t0001g0236 a0001c0001t0001g0237 others(1): Show |
4 | HG00621.hp2 HG01952.hp1 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.244+369G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 3/18 | chr1 | 9756112 | |||||||
| chr1:9756214 | T | C | 265 | a0001c0001t0001g0002 a0001c0001t0001g0105 a0001c0001t0001g0106 others(262): Show |
267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.244+267A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 3/18 | chr1 | 9756214 | |||||||
| chr1:9756224 | C | G | 1 | a0001c0003t0007g0032 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.244+257G>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 3/18 | chr1 | 9756224 | |||||||
| chr1:9756384 | C | T | 1 | a0002c0002t0003g0046 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.244+97G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 3/18 | chr1 | 9756384 | |||||||
| chr1:9756533 | C | G | 1 | a0001c0001t0001g0220 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.215-23G>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9756533 | |||||||
| chr1:9756563 | G | A | 1 | a0002c0002t0002g0014 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.215-53C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9756563 | |||||||
| chr1:9756692 | T | A | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.215-182A>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9756692 | |||||||
| chr1:9756709 | A | G | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.215-199T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9756709 | |||||||
| chr1:9756790 | C | CT | 6 | a0001c0003t0005g0008 a0001c0003t0005g0009 a0001c0003t0005g0097 others(3): Show |
6 | HG02280.hp1 HG02615.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.215-281dupA | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9756790 | |||||||
| chr1:9757008 | G | T | 1 | a0001c0001t0001g0146 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.215-498C>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9757008 | |||||||
| chr1:9757019 | C | A | 87 | a0001c0003t0005g0008 a0001c0003t0005g0009 a0001c0003t0005g0097 others(84): Show |
88 | HG00423.hp2 HG01081.hp1 HG01123.hp2 others(85): Show |
intron_variant | MODIFIER | c.215-509G>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9757019 | |||||||
| chr1:9757205 | C | T | 2 | a0001c0001t0001g0253 a0001c0001t0001g0254 |
2 | HG02109.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.215-695G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9757205 | |||||||
| chr1:9757211 | T | C | 1 | a0001c0001t0001g0224 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.215-701A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9757211 | |||||||
| chr1:9757244 | G | GT | 13 | a0001c0001t0001g0106 a0001c0001t0001g0141 a0001c0001t0001g0162 others(10): Show |
13 | HG00423.hp1 HG01261.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.215-735dupA | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9757244 | |||||||
| chr1:9757248 | T | TTG | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.215-739_215-738ins others(2): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9757248 | |||||||
| chr1:9757328 | G | A | 3 | a0001c0001t0001g0138 a0001c0001t0001g0144 a0001c0001t0001g0147 |
3 | HG01346.hp1 HG01993.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.215-818C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9757328 | |||||||
| chr1:9757537 | A | G | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.215-1027T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9757537 | |||||||
| chr1:9757836 | C | T | 1 | a0001c0001t0001g0249 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.215-1326G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9757836 | |||||||
| chr1:9757955 | G | A | 1 | a0007c0017t0010g0003 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.215-1445C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9757955 | |||||||
| chr1:9758006 | G | A | 1 | a0007c0017t0010g0003 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.215-1496C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9758006 | |||||||
| chr1:9758006 | G | C | 2 | a0004c0005t0001g0202 a0004c0005t0001g0203 |
2 | HG01258.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.215-1496C>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9758006 | |||||||
| chr1:9758014 | T | G | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.215-1504A>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9758014 | |||||||
| chr1:9758018 | A | G | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.215-1508T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9758018 | |||||||
| chr1:9758134 | C | T | 4 | a0001c0001t0001g0211 a0001c0001t0001g0215 a0001c0001t0001g0216 others(1): Show |
4 | HG02630.hp2 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.215-1624G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9758134 | |||||||
| chr1:9758229 | G | A | 1 | a0001c0001t0001g0214 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.215-1719C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9758229 | |||||||
| chr1:9758270 | G | A | 2 | a0001c0006t0009g0264 a0001c0006t0009g0265 |
2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.215-1760C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9758270 | |||||||
| chr1:9758395 | C | A | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.215-1885G>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9758395 | |||||||
| chr1:9758441 | G | A | 1 | a0001c0003t0005g0009 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.215-1931C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9758441 | |||||||
| chr1:9758516 | A | G | 1 | a0002c0002t0002g0037 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.215-2006T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9758516 | |||||||
| chr1:9758566 | C | A | 116 | a0001c0003t0004g0108 a0001c0003t0004g0109 a0001c0003t0004g0110 others(113): Show |
117 | HG00423.hp2 HG00558.hp1 HG00733.hp2 others(114): Show |
intron_variant | MODIFIER | c.215-2056G>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9758566 | |||||||
| chr1:9758593 | C | T | 6 | a0001c0003t0005g0008 a0001c0003t0005g0009 a0001c0003t0005g0097 others(3): Show |
6 | HG02280.hp1 HG02615.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.215-2083G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9758593 | |||||||
| chr1:9758686 | T | C | 2 | a0001c0006t0009g0264 a0001c0006t0009g0265 |
2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.215-2176A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9758686 | |||||||
| chr1:9758723 | G | A | 2 | a0001c0001t0001g0213 a0001c0001t0001g0217 |
2 | HG02145.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.215-2213C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9758723 | |||||||
| chr1:9758922 | C | T | 1 | a0001c0001t0001g0210 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.215-2412G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9758922 | |||||||
| chr1:9759054 | T | C | 1 | a0003c0004t0002g0066 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.215-2544A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9759054 | |||||||
| chr1:9759473 | G | A | 1 | a0007c0017t0010g0003 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.215-2963C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9759473 | |||||||
| chr1:9759534 | G | A | 1 | a0001c0003t0004g0259 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.215-3024C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9759534 | |||||||
| chr1:9759802 | T | C | 1 | a0001c0003t0007g0095 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.215-3292A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9759802 | |||||||
| chr1:9759806 | T | C | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.215-3296A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9759806 | |||||||
| chr1:9760253 | C | G | 10 | a0001c0006t0009g0264 a0001c0006t0009g0265 a0003c0004t0002g0063 others(7): Show |
10 | HG00558.hp1 HG01243.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.215-3743G>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9760253 | |||||||
| chr1:9760364 | C | A | 2 | a0001c0003t0007g0032 a0001c0003t0007g0095 |
2 | HG03139.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.215-3854G>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9760364 | |||||||
| chr1:9760407 | G | A | 2 | a0002c0002t0002g0101 a0002c0002t0002g0102 |
2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.215-3897C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9760407 | |||||||
| chr1:9760682 | G | A | 1 | a0001c0003t0007g0095 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.215-4172C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9760682 | |||||||
| chr1:9760684 | G | GT | 99 | a0001c0001t0001g0002 a0001c0001t0001g0125 a0001c0001t0001g0130 others(96): Show |
101 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.215-4175dupA | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9760684 | |||||||
| chr1:9760684 | G | GTT | 40 | a0001c0001t0001g0106 a0001c0001t0001g0260 a0001c0003t0004g0122 others(37): Show |
40 | HG00639.hp1 HG01081.hp1 HG01123.hp2 others(37): Show |
intron_variant | MODIFIER | c.215-4176_215-4175d others(4): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9760684 | |||||||
| chr1:9760684 | G | GTTT | 10 | a0002c0002t0002g0033 a0002c0002t0002g0073 a0002c0002t0002g0074 others(7): Show |
10 | HG00423.hp2 HG02040.hp2 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.215-4177_215-4175d others(5): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9760684 | |||||||
| chr1:9760684 | GT | G | 6 | a0001c0001t0001g0169 a0003c0004t0002g0064 a0003c0004t0002g0065 others(3): Show |
6 | HG01517.hp2 NA18940.hp2 NA18968.hp2 others(3): Show |
intron_variant | MODIFIER | c.215-4175delA | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9760684 | |||||||
| chr1:9760795 | C | T | 1 | a0001c0001t0001g0155 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.215-4285G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9760795 | |||||||
| chr1:9760836 | T | C | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.215-4326A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9760836 | |||||||
| chr1:9760845 | A | G | 2 | a0001c0006t0009g0264 a0001c0006t0009g0265 |
2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.215-4335T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9760845 | |||||||
| chr1:9761365 | T | A | 1 | a0001c0001t0018g0148 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.215-4855A>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9761365 | |||||||
| chr1:9761371 | A | T | 10 | a0001c0006t0009g0264 a0001c0006t0009g0265 a0003c0004t0002g0063 others(7): Show |
10 | HG00558.hp1 HG01243.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.215-4861T>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9761371 | |||||||
| chr1:9761415 | T | C | 248 | a0001c0001t0001g0002 a0001c0001t0001g0105 a0001c0001t0001g0106 others(245): Show |
250 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.215-4905A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9761415 | |||||||
| chr1:9761506 | TTTTTTTA others(4): Show |
T | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.215-5007_215-4997d others(13): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9761506 | |||||||
| chr1:9761512 | T | A | 1 | a0001c0003t0004g0122 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.215-5002A>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9761512 | |||||||
| chr1:9761524 | T | A | 2 | a0001c0001t0001g0171 a0001c0001t0001g0179 |
2 | HG01433.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.215-5014A>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9761524 | |||||||
| chr1:9761601 | T | C | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.215-5091A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9761601 | |||||||
| chr1:9761697 | G | A | 2 | a0001c0006t0009g0264 a0001c0006t0009g0265 |
2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.215-5187C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9761697 | |||||||
| chr1:9761705 | G | A | 1 | a0001c0001t0001g0139 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.215-5195C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9761705 | |||||||
| chr1:9761747 | T | A | 81 | a0001c0003t0006g0096 a0002c0002t0002g0001 a0002c0002t0002g0005 others(78): Show |
82 | HG00423.hp2 HG01081.hp1 HG01123.hp2 others(79): Show |
intron_variant | MODIFIER | c.215-5237A>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9761747 | |||||||
| chr1:9761763 | G | A | 1 | a0002c0002t0003g0039 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.215-5253C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9761763 | |||||||
| chr1:9761764 | G | C | 1 | a0002c0002t0003g0039 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.215-5254C>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9761764 | |||||||
| chr1:9761786 | T | C | 1 | a0002c0002t0002g0033 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.215-5276A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9761786 | |||||||
| chr1:9761884 | A | G | 1 | a0002c0002t0003g0023 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.215-5374T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9761884 | |||||||
| chr1:9761927 | A | G | 2 | a0001c0003t0007g0032 a0001c0003t0007g0095 |
2 | HG03139.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.215-5417T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9761927 | |||||||
| chr1:9761930 | T | G | 1 | a0002c0002t0002g0033 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.215-5420A>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9761930 | |||||||
| chr1:9761953 | G | A | 1 | a0001c0001t0001g0250 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.215-5443C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9761953 | |||||||
| chr1:9761977 | C | T | 1 | a0002c0002t0002g0033 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.215-5467G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9761977 | |||||||
| chr1:9761984 | G | A | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.215-5474C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9761984 | |||||||
| chr1:9762106 | G | A | 1 | a0001c0003t0007g0095 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.215-5596C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9762106 | |||||||
| chr1:9762273 | T | C | 119 | a0001c0001t0001g0260 a0001c0003t0004g0108 a0001c0003t0004g0109 others(116): Show |
120 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(117): Show |
intron_variant | MODIFIER | c.215-5763A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9762273 | |||||||
| chr1:9762287 | C | T | 2 | a0001c0006t0009g0264 a0001c0006t0009g0265 |
2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.215-5777G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9762287 | |||||||
| chr1:9762417 | C | T | 5 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0006 others(2): Show |
6 | HG02559.hp2 HG02717.hp1 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.215-5907G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9762417 | |||||||
| chr1:9762455 | T | C | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.215-5945A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9762455 | |||||||
| chr1:9762460 | CA | C | 115 | a0001c0001t0001g0253 a0001c0001t0001g0254 a0001c0001t0001g0260 others(112): Show |
116 | HG00423.hp2 HG00639.hp1 HG00733.hp2 others(113): Show |
intron_variant | MODIFIER | c.215-5951delT | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9762460 | |||||||
| chr1:9762523 | G | GCACTCGG others(141): Show |
16 | a0001c0003t0004g0108 a0001c0003t0004g0109 a0001c0003t0004g0110 others(13): Show |
16 | HG00733.hp2 HG01891.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.215-6014_215-6013i others(150): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9762523 | |||||||
| chr1:9762523 | GCACTCGG others(30): Show |
G | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.215-6050_215-6014d others(39): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9762523 | |||||||
| chr1:9762542 | A | ACACTCAA others(141): Show |
1 | a0001c0003t0004g0259 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.215-6033_215-6032i others(150): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9762542 | |||||||
| chr1:9762579 | G | A | 2 | a0001c0006t0009g0264 a0001c0006t0009g0265 |
2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.215-6069C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9762579 | |||||||
| chr1:9762593 | T | C | 2 | a0001c0006t0009g0264 a0001c0006t0009g0265 |
2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.215-6083A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9762593 | |||||||
| chr1:9762597 | C | CCACTCGG others(212): Show |
2 | a0001c0006t0009g0264 a0001c0006t0009g0265 |
2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.215-6088_215-6087i others(221): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9762597 | |||||||
| chr1:9762664 | T | C | 3 | a0003c0004t0002g0063 a0003c0004t0002g0067 a0003c0004t0002g0069 |
3 | HG00558.hp1 HG01981.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.215-6154A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9762664 | |||||||
| chr1:9762696 | C | G | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.215-6186G>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9762696 | |||||||
| chr1:9762698 | C | T | 2 | a0001c0003t0007g0032 a0001c0003t0007g0095 |
2 | HG03139.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.215-6188G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9762698 | |||||||
| chr1:9762771 | C | T | 1 | a0001c0001t0001g0249 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.215-6261G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9762771 | |||||||
| chr1:9762853 | G | A | 1 | a0002c0002t0003g0038 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.215-6343C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9762853 | |||||||
| chr1:9762932 | T | C | 2 | a0001c0006t0009g0264 a0001c0006t0009g0265 |
2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.215-6422A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9762932 | |||||||
| chr1:9762960 | CT | C | 81 | a0001c0003t0006g0096 a0002c0002t0002g0001 a0002c0002t0002g0005 others(78): Show |
82 | HG00423.hp2 HG01081.hp1 HG01123.hp2 others(79): Show |
intron_variant | MODIFIER | c.215-6451delA | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9762960 | |||||||
| chr1:9763075 | C | T | 1 | a0001c0001t0001g0177 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.215-6565G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9763075 | |||||||
| chr1:9763087 | G | C | 1 | a0001c0001t0001g0218 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.215-6577C>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9763087 | |||||||
| chr1:9763123 | G | A | 1 | a0002c0002t0002g0007 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.215-6613C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9763123 | |||||||
| chr1:9763547 | C | T | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.215-7037G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9763547 | |||||||
| chr1:9763624 | A | T | 1 | a0002c0002t0002g0014 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.215-7114T>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9763624 | |||||||
| chr1:9763652 | G | A | 1 | a0001c0003t0007g0095 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.215-7142C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9763652 | |||||||
| chr1:9763661 | T | C | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.215-7151A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9763661 | |||||||
| chr1:9763726 | T | C | 119 | a0001c0001t0001g0260 a0001c0003t0004g0108 a0001c0003t0004g0109 others(116): Show |
120 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(117): Show |
intron_variant | MODIFIER | c.215-7216A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9763726 | |||||||
| chr1:9763862 | A | G | 10 | a0001c0006t0009g0264 a0001c0006t0009g0265 a0003c0004t0002g0063 others(7): Show |
10 | HG00558.hp1 HG01243.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.215-7352T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9763862 | |||||||
| chr1:9763866 | A | G | 119 | a0001c0003t0004g0108 a0001c0003t0004g0109 a0001c0003t0004g0110 others(116): Show |
120 | HG00423.hp2 HG00558.hp1 HG00733.hp2 others(117): Show |
intron_variant | MODIFIER | c.215-7356T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9763866 | |||||||
| chr1:9764000 | G | T | 1 | a0001c0001t0001g0249 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.215-7490C>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9764000 | |||||||
| chr1:9764102 | AAGAAAG | A | 82 | a0001c0003t0006g0096 a0002c0002t0002g0001 a0002c0002t0002g0005 others(79): Show |
83 | HG00423.hp2 HG01081.hp1 HG01123.hp2 others(80): Show |
intron_variant | MODIFIER | c.215-7598_215-7593d others(8): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9764102 | |||||||
| chr1:9764106 | AAG | A | 25 | a0001c0003t0004g0108 a0001c0003t0004g0109 a0001c0003t0004g0110 others(22): Show |
25 | HG00733.hp2 HG01109.hp1 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.215-7598_215-7597d others(4): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9764106 | |||||||
| chr1:9764198 | T | A | 1 | a0001c0001t0001g0258 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.215-7688A>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9764198 | |||||||
| chr1:9764200 | G | C | 1 | a0001c0003t0005g0009 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.215-7690C>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9764200 | |||||||
| chr1:9764452 | C | T | 1 | a0001c0001t0001g0175 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.215-7942G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9764452 | |||||||
| chr1:9764613 | G | A | 38 | a0001c0001t0001g0105 a0001c0001t0001g0126 a0001c0001t0001g0127 others(35): Show |
38 | HG00423.hp1 HG00558.hp2 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.215-8103C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9764613 | |||||||
| chr1:9764637 | T | TA | 7 | a0001c0001t0001g0125 a0001c0001t0001g0156 a0001c0001t0001g0229 others(4): Show |
7 | HG01928.hp1 HG02027.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.215-8128dupT | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9764637 | |||||||
| chr1:9764637 | TA | T | 146 | a0001c0001t0001g0105 a0001c0001t0001g0126 a0001c0001t0001g0127 others(143): Show |
147 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(144): Show |
intron_variant | MODIFIER | c.215-8128delT | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9764637 | |||||||
| chr1:9764637 | TAA | T | 30 | a0001c0001t0001g0164 a0001c0001t0001g0174 a0001c0001t0001g0184 others(27): Show |
30 | HG00558.hp2 HG00733.hp2 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.215-8129_215-8128d others(4): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9764637 | |||||||
| chr1:9764637 | TAAAAAAA others(4): Show |
T | 2 | a0001c0006t0009g0264 a0001c0006t0009g0265 |
2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.215-8138_215-8128d others(13): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9764637 | |||||||
| chr1:9764637 | TAAAAAAA others(6): Show |
T | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.215-8140_215-8128d others(15): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9764637 | |||||||
| chr1:9764638 | A | T | 1 | a0001c0001t0001g0136 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.215-8128T>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9764638 | |||||||
| chr1:9764649 | A | T | 2 | a0001c0006t0009g0264 a0001c0006t0009g0265 |
2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.215-8139T>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9764649 | |||||||
| chr1:9764716 | T | C | 2 | a0001c0001t0004g0165 a0001c0001t0004g0212 |
2 | HG02145.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.215-8206A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9764716 | |||||||
| chr1:9764830 | A | G | 2 | a0001c0006t0009g0264 a0001c0006t0009g0265 |
2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.215-8320T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9764830 | |||||||
| chr1:9764920 | C | T | 2 | a0001c0001t0001g0253 a0001c0001t0001g0254 |
2 | HG02109.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.214+8352G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9764920 | |||||||
| chr1:9765117 | G | A | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.214+8155C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9765117 | |||||||
| chr1:9765240 | C | A | 1 | a0001c0001t0001g0241 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.214+8032G>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9765240 | |||||||
| chr1:9765260 | T | C | 1 | a0001c0001t0001g0128 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.214+8012A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9765260 | |||||||
| chr1:9765298 | C | A | 3 | a0001c0001t0001g0159 a0001c0001t0008g0185 a0001c0001t0008g0238 |
3 | HG02647.hp1 HG02723.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.214+7974G>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9765298 | |||||||
| chr1:9765319 | G | C | 17 | a0001c0003t0004g0108 a0001c0003t0004g0109 a0001c0003t0004g0110 others(14): Show |
17 | HG00733.hp2 HG01109.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.214+7953C>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9765319 | |||||||
| chr1:9765479 | T | C | 4 | a0001c0001t0001g0211 a0001c0001t0001g0215 a0001c0001t0001g0216 others(1): Show |
4 | HG02630.hp2 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.214+7793A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9765479 | |||||||
| chr1:9765485 | C | G | 81 | a0001c0003t0006g0096 a0002c0002t0002g0001 a0002c0002t0002g0005 others(78): Show |
82 | HG00423.hp2 HG01081.hp1 HG01123.hp2 others(79): Show |
intron_variant | MODIFIER | c.214+7787G>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9765485 | |||||||
| chr1:9765583 | GA | G | 6 | a0001c0003t0005g0008 a0001c0003t0005g0009 a0001c0003t0005g0097 others(3): Show |
6 | HG02280.hp1 HG02615.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.214+7688delT | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9765583 | |||||||
| chr1:9765736 | C | T | 1 | a0001c0001t0001g0245 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.214+7536G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9765736 | |||||||
| chr1:9766034 | G | T | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.214+7238C>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9766034 | |||||||
| chr1:9766046 | G | C | 1 | a0002c0002t0003g0060 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.214+7226C>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9766046 | |||||||
| chr1:9766072 | TCTAA | T | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.214+7196_214+7199d others(6): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9766072 | |||||||
| chr1:9766255 | A | G | 10 | a0001c0006t0009g0264 a0001c0006t0009g0265 a0003c0004t0002g0063 others(7): Show |
10 | HG00558.hp1 HG01243.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.214+7017T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9766255 | |||||||
| chr1:9766430 | G | A | 4 | a0001c0003t0005g0097 a0001c0003t0005g0098 a0001c0003t0005g0099 others(1): Show |
4 | HG02280.hp1 HG02615.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.214+6842C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9766430 | |||||||
| chr1:9766552 | C | T | 5 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0006 others(2): Show |
6 | HG02559.hp2 HG02717.hp1 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.214+6720G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9766552 | |||||||
| chr1:9766817 | A | T | 4 | a0001c0003t0005g0097 a0001c0003t0005g0098 a0001c0003t0005g0099 others(1): Show |
4 | HG02280.hp1 HG02615.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.214+6455T>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9766817 | |||||||
| chr1:9766818 | C | T | 1 | a0001c0001t0001g0160 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.214+6454G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9766818 | |||||||
| chr1:9766886 | G | A | 1 | a0001c0001t0001g0134 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.214+6386C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9766886 | |||||||
| chr1:9766976 | C | T | 1 | a0001c0001t0001g0260 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.214+6296G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9766976 | |||||||
| chr1:9767027 | C | A | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.214+6245G>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9767027 | |||||||
| chr1:9767034 | C | T | 1 | a0001c0003t0005g0097 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.214+6238G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9767034 | |||||||
| chr1:9767119 | C | A | 2 | a0002c0002t0002g0061 a0002c0002t0002g0062 |
2 | HG02258.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.214+6153G>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9767119 | |||||||
| chr1:9767143 | A | C | 2 | a0001c0006t0009g0264 a0001c0006t0009g0265 |
2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.214+6129T>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9767143 | |||||||
| chr1:9767190 | C | T | 2 | a0001c0006t0009g0264 a0001c0006t0009g0265 |
2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.214+6082G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9767190 | |||||||
| chr1:9767280 | C | T | 1 | a0001c0001t0001g0164 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.214+5992G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9767280 | |||||||
| chr1:9767528 | G | C | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.214+5744C>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9767528 | |||||||
| chr1:9767544 | C | CA | 101 | a0001c0001t0001g0132 a0001c0001t0001g0137 a0001c0001t0001g0151 others(98): Show |
102 | HG00423.hp2 HG00609.hp1 HG01081.hp1 others(99): Show |
intron_variant | MODIFIER | c.214+5727dupT | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9767544 | |||||||
| chr1:9767544 | CA | C | 10 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0221 others(7): Show |
10 | HG00558.hp1 HG01515.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.214+5727delT | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9767544 | |||||||
| chr1:9767577 | G | A | 1 | a0001c0003t0004g0259 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.214+5695C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9767577 | |||||||
| chr1:9767651 | A | G | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.214+5621T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9767651 | |||||||
| chr1:9767779 | T | C | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.214+5493A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9767779 | |||||||
| chr1:9767805 | G | A | 2 | a0001c0006t0009g0264 a0001c0006t0009g0265 |
2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.214+5467C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9767805 | |||||||
| chr1:9767911 | T | G | 1 | a0001c0003t0007g0032 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.214+5361A>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9767911 | |||||||
| chr1:9767975 | C | A | 2 | a0002c0002t0003g0044 a0002c0002t0003g0054 |
2 | NA18985.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.214+5297G>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9767975 | |||||||
| chr1:9768044 | T | C | 10 | a0001c0006t0009g0264 a0001c0006t0009g0265 a0003c0004t0002g0063 others(7): Show |
10 | HG00558.hp1 HG01243.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.214+5228A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9768044 | |||||||
| chr1:9768265 | T | C | 122 | a0001c0003t0004g0108 a0001c0003t0004g0109 a0001c0003t0004g0110 others(119): Show |
123 | HG00423.hp2 HG00558.hp1 HG00733.hp2 others(120): Show |
intron_variant | MODIFIER | c.214+5007A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9768265 | |||||||
| chr1:9768308 | C | CTGGGCGG others(24): Show |
1 | a0001c0014t0001g0251 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.214+4933_214+4963d others(33): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9768308 | |||||||
| chr1:9768358 | C | T | 2 | a0001c0006t0009g0264 a0001c0006t0009g0265 |
2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.214+4914G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9768358 | |||||||
| chr1:9768382 | ATGGGGGC others(23): Show |
A | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.214+4860_214+4889d others(32): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9768382 | |||||||
| chr1:9768391 | G | C | 1 | a0001c0001t0001g0140 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.214+4881C>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9768391 | |||||||
| chr1:9768401 | T | C | 1 | a0001c0001t0001g0139 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.214+4871A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9768401 | |||||||
| chr1:9768401 | TTGGGCGG others(23): Show |
T | 2 | a0001c0001t0001g0253 a0001c0001t0001g0254 |
2 | HG02109.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.214+4841_214+4870d others(32): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9768401 | |||||||
| chr1:9768412 | C | CA | 113 | a0001c0003t0004g0108 a0001c0003t0004g0109 a0001c0003t0004g0110 others(110): Show |
114 | HG00423.hp2 HG00733.hp2 HG01081.hp1 others(111): Show |
intron_variant | MODIFIER | c.214+4859_214+4860i others(3): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9768412 | |||||||
| chr1:9768419 | C | G | 1 | a0001c0001t0001g0177 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.214+4853G>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9768419 | |||||||
| chr1:9768437 | G | A | 6 | a0001c0003t0005g0008 a0001c0003t0005g0009 a0001c0003t0005g0097 others(3): Show |
6 | HG02280.hp1 HG02615.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.214+4835C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9768437 | |||||||
| chr1:9768491 | T | C | 1 | a0001c0001t0001g0197 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.214+4781A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9768491 | |||||||
| chr1:9768498 | T | C | 4 | a0001c0003t0006g0022 a0001c0003t0006g0042 a0001c0003t0006g0055 others(1): Show |
4 | HG01255.hp1 HG02258.hp1 HG02293.hp2 others(1): Show |
intron_variant | MODIFIER | c.214+4774A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9768498 | |||||||
| chr1:9768577 | G | T | 1 | a0001c0001t0001g0210 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.214+4695C>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9768577 | |||||||
| chr1:9768586 | C | CTGGGTGG others(25): Show |
1 | a0002c0002t0002g0092 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.214+4685_214+4686i others(34): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9768586 | |||||||
| chr1:9768586 | C | CTGGGTGG others(24): Show |
111 | a0001c0003t0004g0108 a0001c0003t0004g0109 a0001c0003t0004g0110 others(108): Show |
112 | HG00423.hp2 HG00733.hp2 HG01081.hp1 others(109): Show |
intron_variant | MODIFIER | c.214+4655_214+4685d others(33): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9768586 | |||||||
| chr1:9768586 | C | T | 2 | a0001c0006t0009g0264 a0001c0006t0009g0265 |
2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.214+4686G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9768586 | |||||||
| chr1:9768606 | GGGGTTCT others(24): Show |
G | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.214+4635_214+4665d others(33): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9768606 | |||||||
| chr1:9768667 | CGGGGTTC others(22): Show |
C | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.214+4576_214+4604d others(31): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9768667 | |||||||
| chr1:9768708 | C | T | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.214+4564G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9768708 | |||||||
| chr1:9768715 | G | A | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.214+4557C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9768715 | |||||||
| chr1:9768728 | G | A | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.214+4544C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9768728 | |||||||
| chr1:9768732 | T | TTC | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.214+4539_214+4540i others(4): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9768732 | |||||||
| chr1:9768810 | T | C | 128 | a0001c0001t0001g0253 a0001c0001t0001g0254 a0001c0001t0001g0260 others(125): Show |
129 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(126): Show |
intron_variant | MODIFIER | c.214+4462A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9768810 | |||||||
| chr1:9768864 | G | T | 1 | a0007c0017t0010g0003 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.214+4408C>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9768864 | |||||||
| chr1:9768932 | G | A | 2 | a0001c0006t0009g0264 a0001c0006t0009g0265 |
2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.214+4340C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9768932 | |||||||
| chr1:9768941 | G | GAGGGAGG others(9): Show |
8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.214+4330_214+4331i others(18): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9768941 | |||||||
| chr1:9768992 | T | G | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.214+4280A>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9768992 | |||||||
| chr1:9769048 | GGAGGGAG others(3): Show |
G | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.214+4214_214+4223d others(12): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9769048 | |||||||
| chr1:9769099 | G | C | 2 | a0002c0007t0002g0084 a0002c0007t0002g0085 |
2 | NA19066.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.214+4173C>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9769099 | |||||||
| chr1:9769111 | G | A | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.214+4161C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9769111 | |||||||
| chr1:9769130 | T | TGAGAGGG others(1): Show |
8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.214+4134_214+4141d others(10): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9769130 | |||||||
| chr1:9769196 | C | T | 9 | a0002c0002t0002g0010 a0002c0002t0002g0011 a0002c0002t0002g0013 others(6): Show |
9 | HG01884.hp1 HG02109.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.214+4076G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9769196 | |||||||
| chr1:9769293 | T | G | 1 | a0001c0014t0001g0251 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.214+3979A>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9769293 | |||||||
| chr1:9769366 | T | C | 2 | a0001c0003t0007g0032 a0001c0003t0007g0095 |
2 | HG03139.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.214+3906A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9769366 | |||||||
| chr1:9769669 | A | G | 17 | a0001c0003t0004g0108 a0001c0003t0004g0109 a0001c0003t0004g0110 others(14): Show |
17 | HG00733.hp2 HG01109.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.214+3603T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9769669 | |||||||
| chr1:9769785 | A | G | 10 | a0001c0006t0009g0264 a0001c0006t0009g0265 a0003c0004t0002g0063 others(7): Show |
10 | HG00558.hp1 HG01243.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.214+3487T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9769785 | |||||||
| chr1:9769899 | G | A | 1 | a0002c0010t0002g0029 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.214+3373C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9769899 | |||||||
| chr1:9769903 | T | G | 10 | a0001c0006t0009g0264 a0001c0006t0009g0265 a0003c0004t0002g0063 others(7): Show |
10 | HG00558.hp1 HG01243.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.214+3369A>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9769903 | |||||||
| chr1:9769918 | T | G | 6 | a0001c0003t0005g0008 a0001c0003t0005g0009 a0001c0003t0005g0097 others(3): Show |
6 | HG02280.hp1 HG02615.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.214+3354A>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9769918 | |||||||
| chr1:9769963 | G | A | 12 | a0002c0002t0002g0010 a0002c0002t0002g0011 a0002c0002t0002g0013 others(9): Show |
12 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.214+3309C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9769963 | |||||||
| chr1:9770016 | T | C | 10 | a0001c0006t0009g0264 a0001c0006t0009g0265 a0003c0004t0002g0063 others(7): Show |
10 | HG00558.hp1 HG01243.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.214+3256A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9770016 | |||||||
| chr1:9770029 | CA | C | 235 | a0001c0001t0001g0002 a0001c0001t0001g0105 a0001c0001t0001g0106 others(232): Show |
237 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.214+3242delT | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9770029 | |||||||
| chr1:9770029 | CAA | C | 11 | a0001c0001t0001g0221 a0002c0002t0002g0031 a0002c0002t0002g0074 others(8): Show |
11 | HG00558.hp1 HG01981.hp2 HG02523.hp2 others(8): Show |
intron_variant | MODIFIER | c.214+3241_214+3242d others(4): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9770029 | |||||||
| chr1:9770044 | A | G | 1 | a0001c0001t0001g0142 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.214+3228T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9770044 | |||||||
| chr1:9770151 | T | C | 13 | a0001c0003t0004g0108 a0001c0003t0004g0109 a0001c0003t0004g0110 others(10): Show |
13 | HG00733.hp2 HG01891.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.214+3121A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9770151 | |||||||
| chr1:9770261 | T | C | 1 | a0002c0002t0003g0060 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.214+3011A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9770261 | |||||||
| chr1:9770528 | C | T | 1 | a0001c0001t0001g0245 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.214+2744G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9770528 | |||||||
| chr1:9770655 | T | C | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.214+2617A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9770655 | |||||||
| chr1:9770661 | G | T | 1 | a0001c0001t0001g0146 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.214+2611C>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9770661 | |||||||
| chr1:9770733 | C | T | 1 | a0001c0001t0001g0252 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.214+2539G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9770733 | |||||||
| chr1:9770751 | C | T | 2 | a0001c0006t0009g0264 a0001c0006t0009g0265 |
2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.214+2521G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9770751 | |||||||
| chr1:9770769 | G | A | 1 | a0010c0015t0014g0104 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.214+2503C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9770769 | |||||||
| chr1:9770788 | G | A | 1 | a0002c0002t0003g0039 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.214+2484C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9770788 | |||||||
| chr1:9770863 | G | C | 1 | a0001c0001t0001g0155 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.214+2409C>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9770863 | |||||||
| chr1:9770872 | T | C | 2 | a0001c0003t0007g0032 a0001c0003t0007g0095 |
2 | HG03139.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.214+2400A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9770872 | |||||||
| chr1:9770938 | A | C | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.214+2334T>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9770938 | |||||||
| chr1:9770987 | C | T | 2 | a0001c0006t0009g0264 a0001c0006t0009g0265 |
2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.214+2285G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9770987 | |||||||
| chr1:9771120 | A | G | 2 | a0002c0002t0003g0021 a0002c0002t0003g0052 |
2 | HG02602.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.214+2152T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9771120 | |||||||
| chr1:9771308 | C | T | 1 | a0010c0015t0014g0104 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.214+1964G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9771308 | |||||||
| chr1:9771397 | C | G | 5 | a0001c0001t0001g0158 a0001c0001t0001g0180 a0001c0001t0001g0181 others(2): Show |
5 | HG02809.hp1 HG02970.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.214+1875G>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9771397 | |||||||
| chr1:9771420 | C | A | 1 | a0002c0002t0003g0023 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.214+1852G>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9771420 | |||||||
| chr1:9771423 | G | A | 5 | a0001c0001t0001g0125 a0001c0001t0001g0141 a0001c0001t0001g0142 others(2): Show |
5 | HG02027.hp1 HG02071.hp2 HG02165.hp2 others(2): Show |
intron_variant | MODIFIER | c.214+1849C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9771423 | |||||||
| chr1:9771556 | G | C | 1 | a0002c0002t0002g0035 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.214+1716C>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9771556 | |||||||
| chr1:9771629 | T | C | 2 | a0001c0001t0001g0253 a0001c0001t0001g0254 |
2 | HG02109.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.214+1643A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9771629 | |||||||
| chr1:9771641 | C | T | 2 | a0001c0006t0009g0264 a0001c0006t0009g0265 |
2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.214+1631G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9771641 | |||||||
| chr1:9771657 | G | A | 1 | a0001c0003t0005g0009 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.214+1615C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9771657 | |||||||
| chr1:9771920 | CAT | C | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.214+1350_214+1351d others(4): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9771920 | |||||||
| chr1:9771941 | T | A | 17 | a0001c0003t0004g0108 a0001c0003t0004g0109 a0001c0003t0004g0110 others(14): Show |
17 | HG00733.hp2 HG01109.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.214+1331A>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9771941 | |||||||
| chr1:9772016 | G | A | 1 | a0002c0002t0002g0071 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.214+1256C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9772016 | |||||||
| chr1:9772140 | CT | C | 135 | a0001c0001t0001g0002 a0001c0001t0001g0105 a0001c0001t0001g0125 others(132): Show |
136 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.214+1131delA | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9772140 | |||||||
| chr1:9772140 | CTT | C | 92 | a0001c0001t0001g0164 a0001c0001t0001g0167 a0001c0001t0001g0168 others(89): Show |
93 | HG00280.hp1 HG00733.hp2 HG00735.hp2 others(90): Show |
intron_variant | MODIFIER | c.214+1130_214+1131d others(4): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9772140 | |||||||
| chr1:9772166 | T | A | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.214+1106A>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9772166 | |||||||
| chr1:9772277 | C | T | 1 | a0001c0001t0001g0248 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.214+995G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9772277 | |||||||
| chr1:9772537 | C | T | 1 | a0001c0003t0005g0009 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.214+735G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9772537 | |||||||
| chr1:9772635 | A | G | 1 | a0002c0002t0002g0034 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.214+637T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9772635 | |||||||
| chr1:9772836 | T | C | 1 | a0001c0001t0001g0140 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.214+436A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9772836 | |||||||
| chr1:9772847 | C | T | 2 | a0001c0006t0009g0264 a0001c0006t0009g0265 |
2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.214+425G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9772847 | |||||||
| chr1:9772874 | G | C | 25 | a0001c0003t0006g0096 a0002c0002t0002g0071 a0002c0002t0002g0072 others(22): Show |
25 | HG00423.hp2 HG01257.hp1 HG01258.hp1 others(22): Show |
intron_variant | MODIFIER | c.214+398C>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9772874 | |||||||
| chr1:9773088 | C | G | 1 | a0010c0015t0014g0104 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.214+184G>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9773088 | |||||||
| chr1:9773186 | A | G | 1 | a0003c0004t0002g0068 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.214+86T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9773186 | |||||||
| chr1:9773212 | T | G | 1 | a0010c0015t0014g0104 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.214+60A>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9773212 | |||||||
| chr1:9773412 | G | C | 1 | a0010c0015t0014g0104 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.92-18C>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9773412 | |||||||
| chr1:9773500 | T | C | 1 | a0001c0001t0001g0248 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.92-106A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9773500 | |||||||
| chr1:9773676 | G | A | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.92-282C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9773676 | |||||||
| chr1:9773758 | G | C | 2 | a0001c0003t0007g0032 a0001c0003t0007g0095 |
2 | HG03139.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.92-364C>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9773758 | |||||||
| chr1:9773793 | G | T | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.92-399C>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9773793 | |||||||
| chr1:9773863 | G | A | 3 | a0001c0003t0004g0115 a0001c0003t0004g0116 a0001c0003t0004g0119 |
3 | HG02615.hp1 HG02647.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.92-469C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9773863 | |||||||
| chr1:9773870 | C | G | 1 | a0001c0001t0001g0182 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.92-476G>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9773870 | |||||||
| chr1:9773899 | A | AT | 11 | a0002c0002t0002g0010 a0002c0002t0002g0011 a0002c0002t0002g0013 others(8): Show |
11 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.92-506dupA | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9773899 | |||||||
| chr1:9773977 | A | C | 1 | a0001c0003t0007g0095 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.92-583T>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9773977 | |||||||
| chr1:9773999 | C | G | 2 | a0001c0003t0004g0120 a0001c0003t0004g0121 |
2 | HG02622.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.92-605G>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9773999 | |||||||
| chr1:9774045 | G | A | 2 | a0001c0006t0009g0264 a0001c0006t0009g0265 |
2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.92-651C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9774045 | |||||||
| chr1:9774225 | T | C | 1 | a0001c0001t0001g0160 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.92-831A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9774225 | |||||||
| chr1:9774288 | G | A | 1 | a0010c0015t0014g0104 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.92-894C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9774288 | |||||||
| chr1:9774292 | G | A | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.92-898C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9774292 | |||||||
| chr1:9774334 | C | T | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.92-940G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9774334 | |||||||
| chr1:9774384 | G | T | 1 | a0001c0001t0001g0182 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.92-990C>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9774384 | |||||||
| chr1:9774467 | G | C | 2 | a0001c0006t0009g0264 a0001c0006t0009g0265 |
2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.92-1073C>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9774467 | |||||||
| chr1:9774560 | C | T | 1 | a0001c0003t0004g0259 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.92-1166G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9774560 | |||||||
| chr1:9774565 | C | CA | 8 | a0001c0001t0001g0136 a0001c0001t0001g0157 a0001c0001t0001g0167 others(5): Show |
8 | HG00738.hp2 HG01243.hp2 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.92-1172dupT | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9774565 | |||||||
| chr1:9774565 | CA | C | 9 | a0002c0002t0002g0094 a0003c0004t0002g0063 a0003c0004t0002g0064 others(6): Show |
9 | HG00558.hp1 HG01257.hp1 HG01981.hp2 others(6): Show |
intron_variant | MODIFIER | c.92-1172delT | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9774565 | |||||||
| chr1:9774811 | C | G | 3 | a0001c0003t0005g0097 a0001c0003t0005g0099 a0001c0003t0005g0100 |
3 | HG02280.hp1 HG02723.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.92-1417G>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9774811 | |||||||
| chr1:9774862 | C | T | 1 | a0005c0011t0021g0268 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.92-1468G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9774862 | |||||||
| chr1:9774889 | A | C | 1 | a0001c0003t0005g0097 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.92-1495T>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9774889 | |||||||
| chr1:9775031 | T | A | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.92-1637A>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9775031 | |||||||
| chr1:9775312 | G | A | 1 | a0001c0001t0001g0154 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.92-1918C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9775312 | |||||||
| chr1:9775432 | C | T | 12 | a0002c0002t0002g0010 a0002c0002t0002g0011 a0002c0002t0002g0013 others(9): Show |
12 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.92-2038G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9775432 | |||||||
| chr1:9775473 | CCT | C | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.92-2081_92-2080del others(2): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9775473 | |||||||
| chr1:9775559 | A | C | 248 | a0001c0001t0001g0002 a0001c0001t0001g0105 a0001c0001t0001g0106 others(245): Show |
250 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.92-2165T>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9775559 | |||||||
| chr1:9775971 | C | T | 1 | a0001c0001t0001g0134 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.92-2577G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9775971 | |||||||
| chr1:9775976 | C | CT | 8 | a0002c0002t0002g0075 a0003c0004t0002g0063 a0003c0004t0002g0064 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 HG02135.hp1 others(5): Show |
intron_variant | MODIFIER | c.92-2583dupA | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9775976 | |||||||
| chr1:9776049 | T | C | 2 | a0001c0006t0009g0264 a0001c0006t0009g0265 |
2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.92-2655A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9776049 | |||||||
| chr1:9776067 | G | A | 1 | a0001c0001t0001g0220 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.92-2673C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9776067 | |||||||
| chr1:9776098 | G | A | 9 | a0002c0002t0002g0010 a0002c0002t0002g0011 a0002c0002t0002g0013 others(6): Show |
9 | HG01884.hp1 HG02109.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.92-2704C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9776098 | |||||||
| chr1:9776127 | C | T | 2 | a0001c0001t0001g0106 a0001c0001t0001g0244 |
2 | HG02738.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.92-2733G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9776127 | |||||||
| chr1:9776172 | C | T | 123 | a0001c0001t0001g0260 a0001c0003t0004g0108 a0001c0003t0004g0109 others(120): Show |
124 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(121): Show |
intron_variant | MODIFIER | c.92-2778G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9776172 | |||||||
| chr1:9776247 | G | A | 1 | a0001c0003t0004g0114 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.92-2853C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9776247 | |||||||
| chr1:9776498 | A | G | 123 | a0001c0001t0001g0260 a0001c0003t0004g0108 a0001c0003t0004g0109 others(120): Show |
124 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(121): Show |
intron_variant | MODIFIER | c.92-3104T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9776498 | |||||||
| chr1:9776524 | T | TA | 14 | a0001c0001t0001g0160 a0001c0001t0001g0162 a0001c0001t0001g0178 others(11): Show |
14 | HG00609.hp1 HG02027.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.92-3131dupT | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9776524 | |||||||
| chr1:9776571 | T | C | 1 | a0002c0002t0011g0053 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.92-3177A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9776571 | |||||||
| chr1:9776650 | G | A | 1 | a0001c0001t0001g0138 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.92-3256C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9776650 | |||||||
| chr1:9776719 | G | C | 1 | a0001c0001t0001g0177 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.92-3325C>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9776719 | |||||||
| chr1:9776788 | C | CTCTA | 7 | a0001c0001t0001g0211 a0001c0001t0001g0215 a0001c0001t0001g0216 others(4): Show |
7 | HG00423.hp2 HG02523.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.92-3398_92-3395dup others(4): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9776788 | |||||||
| chr1:9776788 | C | CTCTATCT others(1): Show |
3 | a0001c0003t0007g0032 a0001c0006t0009g0264 a0001c0006t0009g0265 |
3 | HG01243.hp2 HG02970.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.92-3402_92-3395dup others(8): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9776788 | |||||||
| chr1:9776788 | C | CTCTATCT others(13): Show |
4 | a0003c0004t0002g0064 a0003c0004t0002g0065 a0003c0004t0002g0066 others(1): Show |
4 | NA18940.hp2 NA18968.hp2 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.92-3414_92-3395dup others(20): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9776788 | |||||||
| chr1:9776788 | C | CTCTATCT others(17): Show |
3 | a0003c0004t0002g0063 a0003c0004t0002g0068 a0003c0004t0002g0069 |
3 | HG00558.hp1 HG01981.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.92-3418_92-3395dup others(24): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9776788 | |||||||
| chr1:9776788 | C | CTCTATCT others(21): Show |
1 | a0003c0004t0002g0067 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.92-3395_92-3394ins others(28): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9776788 | |||||||
| chr1:9776788 | CTCTA | C | 4 | a0001c0001t0001g0253 a0001c0001t0001g0254 a0002c0002t0002g0010 others(1): Show |
4 | HG02109.hp1 HG02572.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.92-3398_92-3395del others(4): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9776788 | |||||||
| chr1:9776807 | T | TATCTATC others(14): Show |
1 | a0001c0003t0004g0115 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.92-3434_92-3414dup others(21): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9776807 | |||||||
| chr1:9776845 | CTATCATC others(10): Show |
C | 1 | a0002c0002t0003g0060 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.92-3468_92-3452del others(17): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9776845 | |||||||
| chr1:9776862 | T | TTATC | 93 | a0001c0001t0001g0002 a0001c0001t0001g0105 a0001c0001t0001g0106 others(90): Show |
93 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.92-3472_92-3469dup others(4): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9776862 | |||||||
| chr1:9776862 | T | TTATCTAT others(1): Show |
50 | a0001c0001t0001g0002 a0001c0001t0001g0126 a0001c0001t0001g0133 others(47): Show |
50 | HG00609.hp1 HG00639.hp1 HG00735.hp2 others(47): Show |
intron_variant | MODIFIER | c.92-3476_92-3469dup others(8): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9776862 | |||||||
| chr1:9776862 | T | TTATCTAT others(18): Show |
8 | a0001c0003t0004g0110 a0001c0003t0004g0113 a0001c0003t0004g0116 others(5): Show |
8 | HG02559.hp1 HG02615.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.92-3469_92-3468ins others(25): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9776862 | |||||||
| chr1:9776862 | T | TTATCTAT others(22): Show |
7 | a0001c0003t0004g0108 a0001c0003t0004g0109 a0001c0003t0004g0111 others(4): Show |
7 | HG00733.hp2 HG01891.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.92-3469_92-3468ins others(29): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9776862 | |||||||
| chr1:9776862 | T | TTATCTAT others(5): Show |
10 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0187 others(7): Show |
10 | HG00621.hp1 HG01081.hp2 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.92-3480_92-3469dup others(12): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9776862 | |||||||
| chr1:9776862 | T | TTATCTAT others(9): Show |
1 | a0001c0001t0001g0199 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.92-3484_92-3469dup others(16): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9776862 | |||||||
| chr1:9776862 | TTATC | T | 33 | a0001c0001t0001g0145 a0001c0001t0001g0166 a0001c0001t0001g0177 others(30): Show |
33 | HG00280.hp2 HG00639.hp2 HG01515.hp2 others(30): Show |
intron_variant | MODIFIER | c.92-3472_92-3469del others(4): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9776862 | |||||||
| chr1:9776862 | TTATCTAT others(1): Show |
T | 8 | a0001c0001t0001g0163 a0001c0001t0001g0214 a0001c0001t0001g0221 others(5): Show |
9 | HG01070.hp2 HG02559.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.92-3476_92-3469del others(8): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9776862 | |||||||
| chr1:9776974 | T | C | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.92-3580A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9776974 | |||||||
| chr1:9777094 | C | G | 1 | a0001c0001t0001g0139 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.92-3700G>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9777094 | |||||||
| chr1:9777155 | G | A | 8 | a0001c0001t0001g0136 a0001c0001t0001g0157 a0001c0001t0001g0164 others(5): Show |
8 | HG00735.hp2 HG00738.hp2 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.92-3761C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9777155 | |||||||
| chr1:9777217 | C | CA | 87 | a0001c0001t0001g0149 a0001c0001t0001g0162 a0001c0003t0004g0259 others(84): Show |
88 | HG00423.hp2 HG00558.hp2 HG01081.hp1 others(85): Show |
intron_variant | MODIFIER | c.92-3824dupT | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9777217 | |||||||
| chr1:9777217 | C | CAA | 13 | a0001c0001t0001g0236 a0001c0006t0009g0264 a0001c0006t0009g0265 others(10): Show |
13 | HG00621.hp2 HG01243.hp2 HG01361.hp1 others(10): Show |
intron_variant | MODIFIER | c.92-3825_92-3824dup others(2): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9777217 | |||||||
| chr1:9777252 | G | A | 1 | a0001c0001t0001g0204 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.92-3858C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9777252 | |||||||
| chr1:9777345 | T | C | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.92-3951A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9777345 | |||||||
| chr1:9777501 | C | A | 3 | a0001c0003t0004g0115 a0001c0003t0004g0116 a0001c0003t0004g0119 |
3 | HG02615.hp1 HG02647.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.92-4107G>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9777501 | |||||||
| chr1:9777526 | AAAC | A | 7 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0066 others(4): Show |
7 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(4): Show |
intron_variant | MODIFIER | c.92-4135_92-4133del others(3): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9777526 | |||||||
| chr1:9777759 | T | G | 1 | a0010c0015t0014g0104 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.92-4365A>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9777759 | |||||||
| chr1:9777793 | G | A | 1 | a0001c0001t0001g0140 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.92-4399C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9777793 | |||||||
| chr1:9777823 | C | T | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.92-4429G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9777823 | |||||||
| chr1:9777942 | C | T | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.92-4548G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9777942 | |||||||
| chr1:9777946 | C | T | 2 | a0002c0002t0002g0061 a0002c0002t0002g0062 |
2 | HG02258.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.92-4552G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9777946 | |||||||
| chr1:9778041 | A | C | 1 | a0001c0008t0001g0161 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.92-4647T>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9778041 | |||||||
| chr1:9778223 | A | AAC | 43 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0132 others(40): Show |
43 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(40): Show |
intron_variant | MODIFIER | c.92-4831_92-4830dup others(2): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9778223 | |||||||
| chr1:9778223 | A | AACAC | 49 | a0001c0001t0001g0105 a0001c0001t0001g0126 a0001c0001t0001g0127 others(46): Show |
49 | HG00621.hp1 HG00735.hp1 HG01099.hp1 others(46): Show |
intron_variant | MODIFIER | c.92-4833_92-4830dup others(4): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9778223 | |||||||
| chr1:9778223 | A | AACACAC | 14 | a0001c0001t0001g0106 a0001c0001t0001g0128 a0001c0001t0001g0180 others(11): Show |
15 | HG02258.hp2 HG02280.hp2 HG02717.hp1 others(12): Show |
intron_variant | MODIFIER | c.92-4835_92-4830dup others(6): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9778223 | |||||||
| chr1:9778223 | A | AACACACA others(1): Show |
5 | a0001c0001t0001g0210 a0001c0001t0001g0253 a0001c0001t0004g0212 others(2): Show |
5 | HG02109.hp1 HG02109.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.92-4837_92-4830dup others(8): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9778223 | |||||||
| chr1:9778223 | A | AACACACA others(3): Show |
1 | a0001c0001t0001g0147 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.92-4839_92-4830dup others(10): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9778223 | |||||||
| chr1:9778223 | A | AACACACA others(13): Show |
1 | a0001c0003t0007g0032 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.92-4849_92-4830dup others(20): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9778223 | |||||||
| chr1:9778223 | A | AACACACA others(23): Show |
1 | a0001c0003t0005g0009 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.92-4859_92-4830dup others(30): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9778223 | |||||||
| chr1:9778223 | AAC | A | 32 | a0001c0001t0001g0142 a0001c0001t0001g0166 a0001c0001t0001g0168 others(29): Show |
32 | HG00140.hp2 HG00621.hp2 HG00639.hp2 others(29): Show |
intron_variant | MODIFIER | c.92-4831_92-4830del others(2): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9778223 | |||||||
| chr1:9778223 | AACAC | A | 48 | a0001c0001t0001g0175 a0001c0001t0001g0227 a0001c0001t0001g0228 others(45): Show |
48 | HG00733.hp2 HG01109.hp1 HG01123.hp2 others(45): Show |
intron_variant | MODIFIER | c.92-4833_92-4830del others(4): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9778223 | |||||||
| chr1:9778223 | AACACAC | A | 33 | a0001c0003t0006g0022 a0001c0003t0006g0055 a0001c0003t0006g0056 others(30): Show |
33 | HG00423.hp2 HG00558.hp1 HG01255.hp1 others(30): Show |
intron_variant | MODIFIER | c.92-4835_92-4830del others(6): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9778223 | |||||||
| chr1:9778223 | AACACACA others(1): Show |
A | 3 | a0001c0003t0004g0114 a0001c0003t0004g0120 a0001c0003t0004g0121 |
3 | HG02622.hp2 HG03540.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.92-4837_92-4830del others(8): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9778223 | |||||||
| chr1:9778223 | AACACACA others(3): Show |
A | 2 | a0001c0001t0001g0260 a0001c0003t0004g0108 |
2 | HG00639.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.92-4839_92-4830del others(10): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9778223 | |||||||
| chr1:9778382 | G | A | 10 | a0001c0006t0009g0264 a0001c0006t0009g0265 a0003c0004t0002g0063 others(7): Show |
10 | HG00558.hp1 HG01243.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.92-4988C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9778382 | |||||||
| chr1:9778423 | G | C | 2 | a0001c0001t0001g0105 a0001c0001t0001g0256 |
2 | HG01099.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.92-5029C>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9778423 | |||||||
| chr1:9778727 | A | G | 2 | a0001c0003t0004g0120 a0001c0003t0004g0121 |
2 | HG02622.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.92-5333T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9778727 | |||||||
| chr1:9778733 | G | A | 1 | a0001c0001t0001g0260 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.92-5339C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9778733 | |||||||
| chr1:9778742 | C | T | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.92-5348G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9778742 | |||||||
| chr1:9778743 | G | A | 3 | a0001c0003t0004g0115 a0001c0003t0004g0116 a0001c0003t0004g0119 |
3 | HG02615.hp1 HG02647.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.92-5349C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9778743 | |||||||
| chr1:9778897 | A | T | 10 | a0001c0006t0009g0264 a0001c0006t0009g0265 a0003c0004t0002g0063 others(7): Show |
10 | HG00558.hp1 HG01243.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.92-5503T>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9778897 | |||||||
| chr1:9779023 | C | CA | 49 | a0001c0001t0001g0105 a0001c0001t0001g0126 a0001c0001t0001g0127 others(46): Show |
49 | HG00423.hp1 HG00558.hp2 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.92-5630dupT | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9779023 | |||||||
| chr1:9779023 | CA | C | 8 | a0001c0003t0007g0095 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG03139.hp1 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.92-5630delT | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9779023 | |||||||
| chr1:9779072 | G | A | 1 | a0001c0014t0001g0251 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.92-5678C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9779072 | |||||||
| chr1:9779193 | T | C | 10 | a0001c0006t0009g0264 a0001c0006t0009g0265 a0003c0004t0002g0063 others(7): Show |
10 | HG00558.hp1 HG01243.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.92-5799A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9779193 | |||||||
| chr1:9779260 | T | A | 2 | a0001c0006t0009g0264 a0001c0006t0009g0265 |
2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.92-5866A>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9779260 | |||||||
| chr1:9779271 | T | G | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.92-5877A>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9779271 | |||||||
| chr1:9779294 | C | T | 2 | a0001c0003t0005g0008 a0001c0003t0005g0009 |
2 | HG02622.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.92-5900G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9779294 | |||||||
| chr1:9779415 | A | T | 1 | a0001c0003t0004g0259 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.92-6021T>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9779415 | |||||||
| chr1:9779810 | A | G | 1 | a0001c0001t0001g0155 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.92-6416T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9779810 | |||||||
| chr1:9779812 | A | C | 1 | a0001c0001t0001g0155 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.92-6418T>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9779812 | |||||||
| chr1:9779855 | C | CTTTTT | 7 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0066 others(4): Show |
7 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(4): Show |
intron_variant | MODIFIER | c.92-6466_92-6462dup others(5): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9779855 | |||||||
| chr1:9780064 | A | G | 2 | a0001c0001t0001g0218 a0001c0001t0001g0219 |
2 | HG00738.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.92-6670T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9780064 | |||||||
| chr1:9780080 | T | C | 123 | a0001c0001t0001g0260 a0001c0003t0004g0108 a0001c0003t0004g0109 others(120): Show |
124 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(121): Show |
intron_variant | MODIFIER | c.92-6686A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9780080 | |||||||
| chr1:9780150 | C | T | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.92-6756G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9780150 | |||||||
| chr1:9780161 | C | A | 5 | a0001c0001t0001g0158 a0001c0001t0001g0180 a0001c0001t0001g0181 others(2): Show |
5 | HG02809.hp1 HG02970.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.92-6767G>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9780161 | |||||||
| chr1:9780202 | A | C | 2 | a0001c0001t0001g0253 a0001c0001t0001g0254 |
2 | HG02109.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.92-6808T>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9780202 | |||||||
| chr1:9780225 | AT | A | 93 | a0001c0003t0005g0008 a0001c0003t0005g0009 a0001c0003t0005g0097 others(90): Show |
94 | HG00423.hp2 HG01081.hp1 HG01123.hp2 others(91): Show |
intron_variant | MODIFIER | c.92-6832delA | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9780225 | |||||||
| chr1:9780311 | A | C | 1 | a0001c0001t0001g0205 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.92-6917T>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9780311 | |||||||
| chr1:9780420 | C | T | 12 | a0002c0002t0002g0010 a0002c0002t0002g0011 a0002c0002t0002g0013 others(9): Show |
12 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.92-7026G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9780420 | |||||||
| chr1:9780590 | C | G | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.92-7196G>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9780590 | |||||||
| chr1:9780618 | A | G | 1 | a0001c0001t0001g0266 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.92-7224T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9780618 | |||||||
| chr1:9780661 | T | C | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.92-7267A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9780661 | |||||||
| chr1:9780680 | G | A | 1 | a0001c0003t0007g0095 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.92-7286C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9780680 | |||||||
| chr1:9780705 | A | C | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.92-7311T>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9780705 | |||||||
| chr1:9780771 | C | T | 1 | a0001c0001t0001g0232 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.92-7377G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9780771 | |||||||
| chr1:9780828 | C | T | 1 | a0001c0001t0001g0149 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.92-7434G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9780828 | |||||||
| chr1:9780863 | T | C | 2 | a0001c0006t0009g0264 a0001c0006t0009g0265 |
2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.92-7469A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9780863 | |||||||
| chr1:9781021 | T | C | 6 | a0001c0003t0005g0008 a0001c0003t0005g0009 a0001c0003t0005g0097 others(3): Show |
6 | HG02280.hp1 HG02615.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.92-7627A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9781021 | |||||||
| chr1:9781060 | G | T | 1 | a0007c0017t0010g0003 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.92-7666C>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9781060 | |||||||
| chr1:9781629 | G | A | 1 | a0001c0001t0001g0252 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.92-8235C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9781629 | |||||||
| chr1:9781680 | T | C | 5 | a0001c0003t0005g0008 a0001c0003t0005g0009 a0001c0003t0005g0097 others(2): Show |
5 | HG02280.hp1 HG02622.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.92-8286A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9781680 | |||||||
| chr1:9781814 | C | T | 2 | a0001c0006t0009g0264 a0001c0006t0009g0265 |
2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.92-8420G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9781814 | |||||||
| chr1:9781958 | A | C | 1 | a0001c0003t0004g0116 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.92-8564T>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9781958 | |||||||
| chr1:9782271 | G | A | 2 | a0001c0006t0009g0264 a0001c0006t0009g0265 |
2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.92-8877C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9782271 | |||||||
| chr1:9782403 | C | A | 1 | a0001c0001t0001g0149 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.92-9009G>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9782403 | |||||||
| chr1:9782518 | C | T | 202 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0126 others(199): Show |
203 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(200): Show |
intron_variant | MODIFIER | c.92-9124G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9782518 | |||||||
| chr1:9782790 | T | C | 6 | a0002c0002t0002g0007 a0002c0002t0002g0026 a0002c0002t0002g0027 others(3): Show |
6 | HG02717.hp2 HG03130.hp2 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.92-9396A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9782790 | |||||||
| chr1:9782908 | G | T | 93 | a0001c0003t0005g0008 a0001c0003t0005g0009 a0001c0003t0005g0097 others(90): Show |
94 | HG00423.hp2 HG01081.hp1 HG01123.hp2 others(91): Show |
intron_variant | MODIFIER | c.92-9514C>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9782908 | |||||||
| chr1:9782988 | C | T | 1 | a0002c0002t0002g0086 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.92-9594G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9782988 | |||||||
| chr1:9783128 | G | A | 123 | a0001c0001t0001g0260 a0001c0003t0004g0108 a0001c0003t0004g0109 others(120): Show |
124 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(121): Show |
intron_variant | MODIFIER | c.92-9734C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9783128 | |||||||
| chr1:9783172 | T | A | 1 | a0001c0001t0001g0178 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.92-9778A>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9783172 | |||||||
| chr1:9783179 | G | A | 1 | a0010c0015t0014g0104 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.92-9785C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9783179 | |||||||
| chr1:9783289 | C | T | 2 | a0001c0006t0009g0264 a0001c0006t0009g0265 |
2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.92-9895G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9783289 | |||||||
| chr1:9783420 | A | C | 1 | a0008c0009t0002g0004 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.92-10026T>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9783420 | |||||||
| chr1:9783539 | G | A | 2 | a0001c0006t0009g0264 a0001c0006t0009g0265 |
2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.92-10145C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9783539 | |||||||
| chr1:9783593 | C | T | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.92-10199G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9783593 | |||||||
| chr1:9783730 | C | T | 1 | a0001c0003t0007g0032 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.92-10336G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9783730 | |||||||
| chr1:9784172 | C | CA | 51 | a0001c0001t0001g0128 a0001c0001t0001g0133 a0001c0001t0001g0137 others(48): Show |
51 | HG00280.hp2 HG00733.hp1 HG01081.hp1 others(48): Show |
intron_variant | MODIFIER | c.92-10779dupT | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9784172 | |||||||
| chr1:9784172 | CAAA | C | 7 | a0003c0004t0002g0064 a0003c0004t0002g0065 a0003c0004t0002g0066 others(4): Show |
7 | HG00558.hp1 NA18940.hp2 NA18968.hp2 others(4): Show |
intron_variant | MODIFIER | c.92-10781_92-10779d others(5): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9784172 | |||||||
| chr1:9784204 | G | A | 2 | a0001c0006t0009g0264 a0001c0006t0009g0265 |
2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.92-10810C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9784204 | |||||||
| chr1:9784578 | T | C | 2 | a0001c0001t0001g0253 a0001c0001t0001g0254 |
2 | HG02109.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.92-11184A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9784578 | |||||||
| chr1:9784610 | G | T | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.92-11216C>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9784610 | |||||||
| chr1:9784675 | A | C | 2 | a0001c0006t0009g0264 a0001c0006t0009g0265 |
2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.92-11281T>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9784675 | |||||||
| chr1:9784682 | A | G | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.92-11288T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9784682 | |||||||
| chr1:9784704 | C | A | 5 | a0001c0001t0001g0124 a0001c0001t0001g0138 a0001c0001t0001g0139 others(2): Show |
5 | HG01346.hp1 HG01993.hp1 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.92-11310G>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9784704 | |||||||
| chr1:9784983 | C | G | 2 | a0001c0006t0009g0264 a0001c0006t0009g0265 |
2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.92-11589G>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9784983 | |||||||
| chr1:9784996 | C | CT | 12 | a0001c0001t0001g0002 a0001c0001t0001g0191 a0001c0001t0001g0209 others(9): Show |
13 | HG00140.hp1 HG01261.hp2 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.92-11603dupA | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9784996 | |||||||
| chr1:9784996 | CT | C | 27 | a0001c0001t0001g0125 a0001c0001t0001g0162 a0001c0001t0001g0173 others(24): Show |
27 | HG00639.hp1 HG00733.hp2 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.92-11603delA | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9784996 | |||||||
| chr1:9785158 | C | T | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.92-11764G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9785158 | |||||||
| chr1:9785439 | T | C | 1 | a0001c0001t0001g0260 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.92-12045A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9785439 | |||||||
| chr1:9785566 | G | T | 1 | a0003c0004t0002g0064 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.92-12172C>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9785566 | |||||||
| chr1:9785591 | G | A | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.92-12197C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9785591 | |||||||
| chr1:9785633 | A | G | 1 | a0002c0002t0002g0087 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.92-12239T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9785633 | |||||||
| chr1:9785795 | CT | C | 11 | a0001c0001t0001g0126 a0001c0001t0001g0141 a0001c0003t0005g0008 others(8): Show |
11 | HG01243.hp2 HG02280.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.92-12402delA | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9785795 | |||||||
| chr1:9785795 | CTT | C | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.92-12403_92-12402d others(4): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9785795 | |||||||
| chr1:9785889 | A | C | 3 | a0002c0002t0002g0007 a0002c0002t0002g0028 a0002c0002t0002g0030 |
3 | HG03831.hp2 HG04228.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.92-12495T>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9785889 | |||||||
| chr1:9785903 | C | T | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.92-12509G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9785903 | |||||||
| chr1:9785940 | T | C | 1 | a0002c0002t0002g0090 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.92-12546A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9785940 | |||||||
| chr1:9785970 | G | A | 1 | a0002c0002t0002g0026 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.92-12576C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9785970 | |||||||
| chr1:9786103 | C | T | 2 | a0001c0003t0004g0120 a0001c0003t0004g0121 |
2 | HG02622.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.92-12709G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9786103 | |||||||
| chr1:9786209 | A | G | 85 | a0001c0003t0006g0022 a0001c0003t0006g0042 a0001c0003t0006g0055 others(82): Show |
86 | HG00423.hp2 HG01081.hp1 HG01123.hp2 others(83): Show |
intron_variant | MODIFIER | c.92-12815T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9786209 | |||||||
| chr1:9786283 | T | C | 73 | a0001c0003t0006g0022 a0001c0003t0006g0042 a0001c0003t0006g0055 others(70): Show |
74 | HG00423.hp2 HG01081.hp1 HG01123.hp2 others(71): Show |
intron_variant | MODIFIER | c.92-12889A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9786283 | |||||||
| chr1:9786433 | G | A | 9 | a0002c0002t0002g0010 a0002c0002t0002g0011 a0002c0002t0002g0013 others(6): Show |
9 | HG01884.hp1 HG02109.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.92-13039C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9786433 | |||||||
| chr1:9786563 | G | A | 121 | a0001c0003t0004g0108 a0001c0003t0004g0109 a0001c0003t0004g0110 others(118): Show |
122 | HG00423.hp2 HG00558.hp1 HG00733.hp2 others(119): Show |
intron_variant | MODIFIER | c.92-13169C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9786563 | |||||||
| chr1:9786575 | G | A | 17 | a0001c0003t0004g0108 a0001c0003t0004g0109 a0001c0003t0004g0110 others(14): Show |
17 | HG00733.hp2 HG01109.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.92-13181C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9786575 | |||||||
| chr1:9786592 | GAGATTGT others(10034): Show |
G | 25 | a0001c0003t0006g0096 a0002c0002t0002g0071 a0002c0002t0002g0072 others(22): Show |
25 | HG00423.hp2 HG01257.hp1 HG01258.hp1 others(22): Show |
intron_variant | MODIFIER | c.92-23239_92-13199d others(2): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9786592 | |||||||
| chr1:9786644 | G | A | 2 | a0004c0005t0001g0202 a0004c0005t0001g0203 |
2 | HG01258.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.92-13250C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9786644 | |||||||
| chr1:9786648 | C | CA | 51 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0125 others(48): Show |
51 | HG00423.hp1 HG00558.hp2 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.92-13255dupT | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9786648 | |||||||
| chr1:9786648 | C | CAA | 38 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0207 others(35): Show |
38 | HG01081.hp1 HG01255.hp1 HG01517.hp1 others(35): Show |
intron_variant | MODIFIER | c.92-13256_92-13255d others(4): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9786648 | |||||||
| chr1:9786648 | C | CAAA | 32 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0176 others(29): Show |
32 | HG01123.hp2 HG01261.hp2 HG01515.hp1 others(29): Show |
intron_variant | MODIFIER | c.92-13257_92-13255d others(5): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9786648 | |||||||
| chr1:9786648 | CAAAA | C | 6 | a0003c0004t0002g0063 a0003c0004t0002g0066 a0003c0004t0002g0067 others(3): Show |
6 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(3): Show |
intron_variant | MODIFIER | c.92-13258_92-13255d others(6): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9786648 | |||||||
| chr1:9786665 | A | C | 4 | a0001c0001t0001g0002 a0001c0001t0001g0191 a0001c0001t0001g0209 others(1): Show |
5 | HG02135.hp2 HG02155.hp2 NA18984.hp2 others(2): Show |
intron_variant | MODIFIER | c.92-13271T>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9786665 | |||||||
| chr1:9786666 | A | C | 1 | a0001c0001t0001g0261 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.92-13272T>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9786666 | |||||||
| chr1:9786819 | C | T | 1 | a0001c0003t0004g0114 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.92-13425G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9786819 | |||||||
| chr1:9787178 | CAGA | C | 68 | a0001c0003t0005g0008 a0001c0003t0005g0009 a0001c0003t0005g0097 others(65): Show |
69 | HG01081.hp1 HG01123.hp2 HG01255.hp1 others(66): Show |
intron_variant | MODIFIER | c.92-13787_92-13785d others(5): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9787178 | |||||||
| chr1:9787189 | GCTTCTGT others(6): Show |
G | 1 | a0002c0002t0003g0038 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.92-13808_92-13796d others(15): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9787189 | |||||||
| chr1:9787232 | G | A | 4 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0006 others(1): Show |
5 | HG02717.hp1 HG03486.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.92-13838C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9787232 | |||||||
| chr1:9787263 | A | T | 6 | a0001c0001t0001g0162 a0001c0001t0001g0190 a0001c0001t0001g0200 others(3): Show |
6 | HG00609.hp1 HG02027.hp2 NA18964.hp1 others(3): Show |
intron_variant | MODIFIER | c.92-13869T>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9787263 | |||||||
| chr1:9787402 | A | AT | 26 | a0001c0001t0001g0106 a0001c0001t0001g0125 a0001c0001t0001g0128 others(23): Show |
26 | HG01109.hp2 HG01884.hp2 HG02027.hp1 others(23): Show |
intron_variant | MODIFIER | c.92-14009dupA | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9787402 | |||||||
| chr1:9787402 | A | ATTTTT | 5 | a0003c0004t0002g0063 a0003c0004t0002g0065 a0003c0004t0002g0066 others(2): Show |
5 | HG00558.hp1 HG01981.hp2 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.92-14013_92-14009d others(7): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9787402 | |||||||
| chr1:9787427 | G | A | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.92-14033C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9787427 | |||||||
| chr1:9787442 | C | T | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.92-14048G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9787442 | |||||||
| chr1:9787496 | C | T | 1 | a0001c0003t0004g0109 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.92-14102G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9787496 | |||||||
| chr1:9787529 | G | A | 2 | a0002c0002t0003g0023 a0002c0002t0003g0039 |
2 | HG01123.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.92-14135C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9787529 | |||||||
| chr1:9787558 | C | T | 1 | a0001c0001t0001g0260 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.92-14164G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9787558 | |||||||
| chr1:9787594 | G | A | 1 | a0001c0003t0004g0259 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.92-14200C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9787594 | |||||||
| chr1:9787704 | C | T | 17 | a0001c0003t0004g0108 a0001c0003t0004g0109 a0001c0003t0004g0110 others(14): Show |
17 | HG00733.hp2 HG01109.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.92-14310G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9787704 | |||||||
| chr1:9787715 | C | G | 2 | a0001c0003t0007g0032 a0001c0003t0007g0095 |
2 | HG03139.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.92-14321G>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9787715 | |||||||
| chr1:9787913 | C | G | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.92-14519G>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9787913 | |||||||
| chr1:9788024 | G | A | 2 | a0002c0002t0002g0061 a0002c0002t0002g0062 |
2 | HG02258.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.92-14630C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9788024 | |||||||
| chr1:9788063 | C | T | 2 | a0001c0001t0004g0165 a0001c0001t0004g0212 |
2 | HG02145.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.92-14669G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9788063 | |||||||
| chr1:9788075 | C | T | 10 | a0001c0006t0009g0264 a0001c0006t0009g0265 a0003c0004t0002g0063 others(7): Show |
10 | HG00558.hp1 HG01243.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.92-14681G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9788075 | |||||||
| chr1:9788088 | C | T | 1 | a0001c0001t0001g0134 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.92-14694G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9788088 | |||||||
| chr1:9788291 | C | T | 1 | a0001c0003t0004g0110 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.92-14897G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9788291 | |||||||
| chr1:9788302 | A | G | 10 | a0001c0006t0009g0264 a0001c0006t0009g0265 a0003c0004t0002g0063 others(7): Show |
10 | HG00558.hp1 HG01243.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.92-14908T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9788302 | |||||||
| chr1:9788442 | A | G | 1 | a0001c0014t0001g0251 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.92-15048T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9788442 | |||||||
| chr1:9788445 | C | T | 2 | a0001c0006t0009g0264 a0001c0006t0009g0265 |
2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.92-15051G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9788445 | |||||||
| chr1:9788541 | C | T | 1 | a0001c0003t0004g0109 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.92-15147G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9788541 | |||||||
| chr1:9788566 | CA | C | 9 | a0001c0001t0001g0191 a0003c0004t0002g0063 a0003c0004t0002g0064 others(6): Show |
9 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(6): Show |
intron_variant | MODIFIER | c.92-15173delT | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9788566 | |||||||
| chr1:9788734 | G | A | 2 | a0001c0003t0004g0109 a0001c0003t0004g0110 |
2 | HG02897.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.92-15340C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9788734 | |||||||
| chr1:9788855 | G | A | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.92-15461C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9788855 | |||||||
| chr1:9788867 | CA | C | 203 | a0001c0001t0001g0002 a0001c0001t0001g0105 a0001c0001t0001g0124 others(200): Show |
205 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.92-15474delT | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9788867 | |||||||
| chr1:9788867 | CAAA | C | 7 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(4): Show |
7 | HG00558.hp1 HG01981.hp2 NA18968.hp2 others(4): Show |
intron_variant | MODIFIER | c.92-15476_92-15474d others(5): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9788867 | |||||||
| chr1:9788875 | A | C | 2 | a0001c0006t0009g0264 a0001c0006t0009g0265 |
2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.92-15481T>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9788875 | |||||||
| chr1:9788879 | A | C | 1 | a0001c0014t0001g0251 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.92-15485T>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9788879 | |||||||
| chr1:9788885 | A | C | 1 | a0001c0003t0004g0115 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.92-15491T>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9788885 | |||||||
| chr1:9789014 | C | CCTTT | 10 | a0001c0006t0009g0264 a0001c0006t0009g0265 a0003c0004t0002g0063 others(7): Show |
10 | HG00558.hp1 HG01243.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.92-15624_92-15621d others(6): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9789014 | |||||||
| chr1:9789148 | C | T | 1 | a0001c0001t0001g0180 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.92-15754G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9789148 | |||||||
| chr1:9789193 | G | A | 1 | a0001c0003t0007g0095 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.92-15799C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9789193 | |||||||
| chr1:9789300 | C | T | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.92-15906G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9789300 | |||||||
| chr1:9789346 | T | C | 2 | a0001c0006t0009g0264 a0001c0006t0009g0265 |
2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.92-15952A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9789346 | |||||||
| chr1:9789364 | T | C | 1 | a0001c0003t0005g0098 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.92-15970A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9789364 | |||||||
| chr1:9789586 | A | G | 2 | a0002c0002t0003g0048 a0002c0002t0003g0049 |
2 | NA18942.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.92-16192T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9789586 | |||||||
| chr1:9789796 | T | C | 1 | a0001c0001t0001g0205 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.92-16402A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9789796 | |||||||
| chr1:9789894 | G | A | 1 | a0001c0003t0007g0095 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.92-16500C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9789894 | |||||||
| chr1:9789954 | G | T | 2 | a0001c0006t0009g0264 a0001c0006t0009g0265 |
2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.92-16560C>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9789954 | |||||||
| chr1:9790009 | C | T | 1 | a0002c0002t0002g0062 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.92-16615G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9790009 | |||||||
| chr1:9790155 | A | G | 3 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0001g0207 |
3 | HG01255.hp2 HG03130.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.92-16761T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9790155 | |||||||
| chr1:9790171 | T | C | 2 | a0002c0002t0002g0018 a0002c0002t0002g0020 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.92-16777A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9790171 | |||||||
| chr1:9790189 | A | G | 2 | a0002c0002t0003g0021 a0002c0002t0003g0052 |
2 | HG02602.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.92-16795T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9790189 | |||||||
| chr1:9790354 | T | C | 1 | a0001c0001t0001g0246 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.92-16960A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9790354 | |||||||
| chr1:9790437 | C | A | 1 | a0001c0016t0001g0198 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.92-17043G>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9790437 | |||||||
| chr1:9790440 | T | G | 5 | a0002c0002t0003g0025 a0002c0002t0003g0040 a0002c0002t0003g0041 others(2): Show |
5 | HG02698.hp1 NA18943.hp2 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.92-17046A>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9790440 | |||||||
| chr1:9790451 | AAC | A | 60 | a0001c0003t0006g0022 a0001c0003t0006g0042 a0001c0003t0006g0055 others(57): Show |
61 | HG01081.hp1 HG01123.hp2 HG01255.hp1 others(58): Show |
intron_variant | MODIFIER | c.92-17059_92-17058d others(4): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9790451 | |||||||
| chr1:9790483 | C | T | 1 | a0002c0002t0002g0043 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.92-17089G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9790483 | |||||||
| chr1:9790521 | T | C | 1 | a0001c0003t0007g0095 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.92-17127A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9790521 | |||||||
| chr1:9790565 | A | G | 1 | a0001c0001t0001g0246 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.92-17171T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9790565 | |||||||
| chr1:9790617 | A | G | 1 | a0001c0001t0001g0164 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.92-17223T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9790617 | |||||||
| chr1:9790769 | G | A | 2 | a0002c0002t0002g0061 a0002c0002t0002g0062 |
2 | HG02258.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.92-17375C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9790769 | |||||||
| chr1:9790855 | C | T | 1 | a0001c0014t0001g0251 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.92-17461G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9790855 | |||||||
| chr1:9790865 | G | A | 60 | a0001c0003t0006g0022 a0001c0003t0006g0042 a0001c0003t0006g0055 others(57): Show |
61 | HG01081.hp1 HG01123.hp2 HG01255.hp1 others(58): Show |
intron_variant | MODIFIER | c.92-17471C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9790865 | |||||||
| chr1:9790915 | T | C | 97 | a0001c0003t0004g0108 a0001c0003t0004g0109 a0001c0003t0004g0110 others(94): Show |
98 | HG00558.hp1 HG00733.hp2 HG01081.hp1 others(95): Show |
intron_variant | MODIFIER | c.92-17521A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9790915 | |||||||
| chr1:9790916 | G | A | 12 | a0002c0002t0002g0010 a0002c0002t0002g0011 a0002c0002t0002g0013 others(9): Show |
12 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.92-17522C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9790916 | |||||||
| chr1:9790930 | G | A | 1 | a0001c0001t0001g0245 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.92-17536C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9790930 | |||||||
| chr1:9790960 | C | T | 1 | a0002c0002t0003g0025 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.92-17566G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9790960 | |||||||
| chr1:9791064 | G | A | 4 | a0001c0003t0005g0097 a0001c0003t0005g0098 a0001c0003t0005g0099 others(1): Show |
4 | HG02280.hp1 HG02615.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.92-17670C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9791064 | |||||||
| chr1:9791096 | C | T | 1 | a0001c0001t0018g0148 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.92-17702G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9791096 | |||||||
| chr1:9791141 | C | CA | 6 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0142 others(3): Show |
6 | HG01243.hp2 HG02027.hp1 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.92-17748dupT | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9791141 | |||||||
| chr1:9791141 | CA | C | 76 | a0001c0001t0001g0253 a0001c0001t0001g0254 a0001c0001t0004g0165 others(73): Show |
77 | HG00558.hp2 HG00733.hp2 HG01081.hp1 others(74): Show |
intron_variant | MODIFIER | c.92-17748delT | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9791141 | |||||||
| chr1:9791141 | CAA | C | 13 | a0001c0001t0001g0260 a0001c0003t0004g0121 a0001c0003t0004g0122 others(10): Show |
13 | HG00639.hp1 HG01884.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.92-17749_92-17748d others(4): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9791141 | |||||||
| chr1:9791170 | T | TTAA | 10 | a0001c0006t0009g0264 a0001c0006t0009g0265 a0003c0004t0002g0063 others(7): Show |
10 | HG00558.hp1 HG01243.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.92-17777_92-17776i others(5): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9791170 | |||||||
| chr1:9791209 | T | C | 10 | a0001c0006t0009g0264 a0001c0006t0009g0265 a0003c0004t0002g0063 others(7): Show |
10 | HG00558.hp1 HG01243.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.92-17815A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9791209 | |||||||
| chr1:9791382 | C | A | 1 | a0002c0002t0002g0015 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.92-17988G>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9791382 | |||||||
| chr1:9791532 | C | T | 1 | a0007c0017t0010g0003 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.92-18138G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9791532 | |||||||
| chr1:9791619 | C | T | 2 | a0002c0002t0002g0018 a0002c0002t0002g0020 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.92-18225G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9791619 | |||||||
| chr1:9791656 | T | C | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.92-18262A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9791656 | |||||||
| chr1:9791660 | A | T | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.92-18266T>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9791660 | |||||||
| chr1:9791663 | T | C | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.92-18269A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9791663 | |||||||
| chr1:9791676 | T | C | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.92-18282A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9791676 | |||||||
| chr1:9791677 | G | A | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.92-18283C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9791677 | |||||||
| chr1:9791755 | A | C | 1 | a0006c0012t0003g0024 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.92-18361T>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9791755 | |||||||
| chr1:9791829 | C | T | 1 | a0001c0003t0005g0099 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.92-18435G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9791829 | |||||||
| chr1:9791848 | G | A | 6 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0174 others(3): Show |
6 | HG02922.hp2 HG03041.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.92-18454C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9791848 | |||||||
| chr1:9792033 | C | T | 2 | a0001c0003t0005g0008 a0001c0003t0005g0009 |
2 | HG02622.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.92-18639G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9792033 | |||||||
| chr1:9792084 | G | T | 1 | a0001c0001t0001g0133 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.92-18690C>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9792084 | |||||||
| chr1:9792141 | G | T | 2 | a0001c0006t0009g0264 a0001c0006t0009g0265 |
2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.92-18747C>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9792141 | |||||||
| chr1:9792164 | C | T | 1 | a0001c0001t0001g0177 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.92-18770G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9792164 | |||||||
| chr1:9792171 | G | A | 1 | a0001c0003t0005g0100 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.92-18777C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9792171 | |||||||
| chr1:9792185 | A | G | 10 | a0001c0006t0009g0264 a0001c0006t0009g0265 a0003c0004t0002g0063 others(7): Show |
10 | HG00558.hp1 HG01243.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.92-18791T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9792185 | |||||||
| chr1:9792213 | C | A | 34 | a0001c0001t0001g0125 a0001c0001t0001g0168 a0001c0001t0001g0178 others(31): Show |
34 | HG00558.hp1 HG01243.hp2 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.92-18819G>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9792213 | |||||||
| chr1:9792216 | A | C | 1 | a0007c0017t0010g0003 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.92-18822T>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9792216 | |||||||
| chr1:9792263 | A | G | 2 | a0001c0006t0009g0264 a0001c0006t0009g0265 |
2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.92-18869T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9792263 | |||||||
| chr1:9792272 | G | A | 1 | a0002c0002t0002g0027 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.92-18878C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9792272 | |||||||
| chr1:9792306 | A | G | 10 | a0001c0006t0009g0264 a0001c0006t0009g0265 a0003c0004t0002g0063 others(7): Show |
10 | HG00558.hp1 HG01243.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.92-18912T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9792306 | |||||||
| chr1:9792339 | T | C | 10 | a0001c0006t0009g0264 a0001c0006t0009g0265 a0003c0004t0002g0063 others(7): Show |
10 | HG00558.hp1 HG01243.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.92-18945A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9792339 | |||||||
| chr1:9792434 | C | G | 1 | a0001c0003t0005g0009 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.92-19040G>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9792434 | |||||||
| chr1:9792705 | A | G | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.92-19311T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9792705 | |||||||
| chr1:9792770 | C | G | 2 | a0001c0003t0007g0032 a0001c0003t0007g0095 |
2 | HG03139.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.92-19376G>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9792770 | |||||||
| chr1:9792794 | G | T | 1 | a0001c0003t0005g0009 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.92-19400C>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9792794 | |||||||
| chr1:9793461 | G | A | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.92-20067C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9793461 | |||||||
| chr1:9793494 | G | A | 3 | a0002c0002t0002g0016 a0002c0002t0002g0017 a0008c0009t0002g0004 |
3 | HG01891.hp1 HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.92-20100C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9793494 | |||||||
| chr1:9794058 | G | T | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.92-20664C>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9794058 | |||||||
| chr1:9794068 | T | C | 1 | a0001c0001t0001g0170 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.92-20674A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9794068 | |||||||
| chr1:9794143 | G | A | 6 | a0001c0003t0005g0008 a0001c0003t0005g0009 a0001c0003t0005g0097 others(3): Show |
6 | HG02280.hp1 HG02615.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.92-20749C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9794143 | |||||||
| chr1:9794180 | A | G | 222 | a0001c0001t0001g0002 a0001c0001t0001g0105 a0001c0001t0001g0106 others(219): Show |
224 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.92-20786T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9794180 | |||||||
| chr1:9794212 | C | T | 1 | a0001c0003t0007g0095 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.92-20818G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9794212 | |||||||
| chr1:9794427 | A | G | 10 | a0001c0006t0009g0264 a0001c0006t0009g0265 a0003c0004t0002g0063 others(7): Show |
10 | HG00558.hp1 HG01243.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.92-21033T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9794427 | |||||||
| chr1:9794714 | T | C | 10 | a0001c0006t0009g0264 a0001c0006t0009g0265 a0003c0004t0002g0063 others(7): Show |
10 | HG00558.hp1 HG01243.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.92-21320A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9794714 | |||||||
| chr1:9794715 | G | A | 2 | a0001c0006t0009g0264 a0001c0006t0009g0265 |
2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.92-21321C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9794715 | |||||||
| chr1:9794734 | C | A | 15 | a0001c0003t0004g0108 a0001c0003t0004g0109 a0001c0003t0004g0110 others(12): Show |
15 | HG00733.hp2 HG01891.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.92-21340G>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9794734 | |||||||
| chr1:9794837 | T | C | 1 | a0001c0014t0001g0251 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.92-21443A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9794837 | |||||||
| chr1:9794918 | G | A | 1 | a0001c0001t0001g0232 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.92-21524C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9794918 | |||||||
| chr1:9795021 | GA | G | 86 | a0001c0003t0004g0108 a0001c0003t0004g0109 a0001c0003t0004g0110 others(83): Show |
87 | HG00733.hp2 HG01081.hp1 HG01109.hp1 others(84): Show |
intron_variant | MODIFIER | c.92-21628delT | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9795021 | |||||||
| chr1:9795025 | A | G | 6 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0174 others(3): Show |
6 | HG02922.hp2 HG03041.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.92-21631T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9795025 | |||||||
| chr1:9795032 | A | G | 1 | a0003c0004t0002g0069 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.92-21638T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9795032 | |||||||
| chr1:9795033 | A | G | 7 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(4): Show |
7 | HG01981.hp2 NA18940.hp2 NA18968.hp2 others(4): Show |
intron_variant | MODIFIER | c.92-21639T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9795033 | |||||||
| chr1:9795034 | G | A | 7 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(4): Show |
7 | HG01981.hp2 NA18940.hp2 NA18968.hp2 others(4): Show |
intron_variant | MODIFIER | c.92-21640C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9795034 | |||||||
| chr1:9795167 | CT | C | 14 | a0001c0006t0009g0264 a0001c0006t0009g0265 a0002c0002t0002g0010 others(11): Show |
14 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.92-21774delA | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9795167 | |||||||
| chr1:9795205 | G | A | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.92-21811C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9795205 | |||||||
| chr1:9795326 | C | T | 1 | a0001c0003t0004g0113 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.92-21932G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9795326 | |||||||
| chr1:9795354 | C | T | 6 | a0001c0003t0005g0008 a0001c0003t0005g0009 a0001c0003t0005g0097 others(3): Show |
6 | HG02280.hp1 HG02615.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.92-21960G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9795354 | |||||||
| chr1:9795413 | G | A | 1 | a0001c0008t0001g0161 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.92-22019C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9795413 | |||||||
| chr1:9795441 | T | C | 10 | a0001c0006t0009g0264 a0001c0006t0009g0265 a0003c0004t0002g0063 others(7): Show |
10 | HG00558.hp1 HG01243.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.92-22047A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9795441 | |||||||
| chr1:9795471 | C | T | 241 | a0001c0001t0001g0002 a0001c0001t0001g0105 a0001c0001t0001g0106 others(238): Show |
243 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.92-22077G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9795471 | |||||||
| chr1:9795503 | G | T | 2 | a0001c0003t0005g0008 a0001c0003t0005g0009 |
2 | HG02622.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.92-22109C>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9795503 | |||||||
| chr1:9795632 | T | G | 2 | a0002c0002t0003g0044 a0002c0002t0003g0054 |
2 | NA18985.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.92-22238A>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9795632 | |||||||
| chr1:9795957 | C | T | 1 | a0001c0001t0001g0260 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.92-22563G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9795957 | |||||||
| chr1:9795961 | CA | C | 173 | a0001c0001t0001g0002 a0001c0001t0001g0105 a0001c0001t0001g0124 others(170): Show |
174 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.92-22568delT | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9795961 | |||||||
| chr1:9796122 | C | T | 1 | a0001c0001t0001g0219 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.92-22728G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9796122 | |||||||
| chr1:9796154 | C | T | 1 | a0001c0001t0008g0238 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.92-22760G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9796154 | |||||||
| chr1:9796225 | G | A | 6 | a0001c0001t0001g0201 a0001c0003t0005g0008 a0001c0003t0005g0009 others(3): Show |
6 | HG02615.hp2 HG02622.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.92-22831C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9796225 | |||||||
| chr1:9796240 | C | T | 2 | a0002c0002t0002g0061 a0002c0002t0002g0062 |
2 | HG02258.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.92-22846G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9796240 | |||||||
| chr1:9796260 | CAAAAACA others(5): Show |
C | 12 | a0002c0002t0002g0010 a0002c0002t0002g0011 a0002c0002t0002g0013 others(9): Show |
12 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.92-22878_92-22867d others(14): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9796260 | |||||||
| chr1:9796262 | A | G | 5 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0006 others(2): Show |
6 | HG02559.hp2 HG02717.hp1 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.92-22868T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9796262 | |||||||
| chr1:9796266 | CA | C | 159 | a0001c0001t0001g0002 a0001c0001t0001g0105 a0001c0001t0001g0125 others(156): Show |
160 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.92-22873delT | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9796266 | |||||||
| chr1:9796266 | CAA | C | 15 | a0001c0001t0001g0207 a0001c0003t0005g0097 a0001c0003t0005g0098 others(12): Show |
15 | HG00558.hp1 HG01243.hp2 HG01981.hp2 others(12): Show |
intron_variant | MODIFIER | c.92-22874_92-22873d others(4): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9796266 | |||||||
| chr1:9796272 | AAAAAACA others(6): Show |
A | 4 | a0001c0003t0004g0109 a0001c0003t0004g0110 a0001c0003t0007g0032 others(1): Show |
4 | HG02897.hp2 HG03139.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.92-22891_92-22879d others(15): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9796272 | |||||||
| chr1:9796298 | A | C | 3 | a0001c0003t0004g0109 a0001c0003t0004g0110 a0001c0003t0007g0032 |
3 | HG02897.hp2 HG03453.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.92-22904T>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9796298 | |||||||
| chr1:9796300 | A | C | 2 | a0001c0001t0001g0184 a0001c0001t0001g0260 |
2 | HG00639.hp1 NA18942.hp1 |
intron_variant | MODIFIER | c.92-22906T>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9796300 | |||||||
| chr1:9796403 | G | A | 3 | a0001c0003t0004g0259 a0001c0006t0009g0264 a0001c0006t0009g0265 |
3 | HG01109.hp1 HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.92-23009C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9796403 | |||||||
| chr1:9796414 | C | T | 6 | a0001c0003t0005g0008 a0001c0003t0005g0009 a0001c0003t0005g0097 others(3): Show |
6 | HG02280.hp1 HG02615.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.92-23020G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9796414 | |||||||
| chr1:9796447 | C | T | 2 | a0001c0006t0009g0264 a0001c0006t0009g0265 |
2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.92-23053G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9796447 | |||||||
| chr1:9796556 | C | T | 4 | a0001c0001t0001g0234 a0001c0001t0001g0236 a0001c0001t0001g0237 others(1): Show |
4 | HG00621.hp2 HG01952.hp1 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.92-23162G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9796556 | |||||||
| chr1:9796557 | G | A | 1 | a0001c0001t0001g0151 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.92-23163C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9796557 | |||||||
| chr1:9796569 | A | G | 9 | a0001c0001t0001g0142 a0003c0004t0002g0063 a0003c0004t0002g0064 others(6): Show |
9 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(6): Show |
intron_variant | MODIFIER | c.92-23175T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9796569 | |||||||
| chr1:9796577 | A | G | 181 | a0001c0001t0001g0002 a0001c0001t0001g0105 a0001c0001t0001g0124 others(178): Show |
182 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.92-23183T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9796577 | |||||||
| chr1:9796641 | G | A | 25 | a0001c0003t0006g0096 a0002c0002t0002g0071 a0002c0002t0002g0072 others(22): Show |
25 | HG00423.hp2 HG01257.hp1 HG01258.hp1 others(22): Show |
intron_variant | MODIFIER | c.92-23247C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9796641 | |||||||
| chr1:9796657 | C | T | 4 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0006 others(1): Show |
5 | HG02717.hp1 HG03486.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.92-23263G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9796657 | |||||||
| chr1:9796768 | T | G | 17 | a0001c0003t0004g0108 a0001c0003t0004g0109 a0001c0003t0004g0110 others(14): Show |
17 | HG00733.hp2 HG01109.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.92-23374A>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9796768 | |||||||
| chr1:9796804 | G | C | 2 | a0002c0002t0003g0040 a0002c0002t0003g0041 |
2 | NA18943.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.92-23410C>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9796804 | |||||||
| chr1:9796933 | C | T | 1 | a0002c0002t0002g0074 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.92-23539G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9796933 | |||||||
| chr1:9796934 | G | A | 1 | a0001c0001t0001g0253 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.92-23540C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9796934 | |||||||
| chr1:9796993 | C | T | 1 | a0001c0001t0001g0144 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.92-23599G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9796993 | |||||||
| chr1:9797072 | A | G | 2 | a0001c0003t0004g0120 a0001c0003t0004g0121 |
2 | HG02622.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.92-23678T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9797072 | |||||||
| chr1:9797268 | G | A | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.92-23874C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9797268 | |||||||
| chr1:9797320 | G | C | 1 | a0001c0001t0001g0201 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.92-23926C>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9797320 | |||||||
| chr1:9797581 | C | T | 1 | a0001c0001t0001g0248 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.92-24187G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9797581 | |||||||
| chr1:9797684 | A | C | 1 | a0006c0012t0003g0024 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.92-24290T>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9797684 | |||||||
| chr1:9797716 | G | C | 1 | a0001c0003t0005g0009 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.92-24322C>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9797716 | |||||||
| chr1:9797722 | T | G | 2 | a0004c0005t0001g0202 a0004c0005t0001g0203 |
2 | HG01258.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.92-24328A>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9797722 | |||||||
| chr1:9797744 | T | C | 1 | a0002c0002t0002g0076 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.92-24350A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9797744 | |||||||
| chr1:9797954 | C | T | 2 | a0001c0003t0005g0097 a0001c0003t0005g0099 |
2 | HG02723.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.92-24560G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9797954 | |||||||
| chr1:9798085 | G | A | 3 | a0001c0001t0001g0160 a0001c0001t0001g0184 a0001c0001t0001g0204 |
3 | NA18942.hp1 NA18943.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.92-24691C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9798085 | |||||||
| chr1:9798105 | AGAGAGAG others(1): Show |
A | 10 | a0001c0006t0009g0264 a0001c0006t0009g0265 a0003c0004t0002g0063 others(7): Show |
10 | HG00558.hp1 HG01243.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.92-24719_92-24712d others(10): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9798105 | |||||||
| chr1:9798124 | G | GAGAGGGG others(9): Show |
1 | a0002c0002t0002g0091 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.92-24746_92-24731d others(18): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9798124 | |||||||
| chr1:9798274 | C | T | 1 | a0002c0002t0002g0031 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.92-24880G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9798274 | |||||||
| chr1:9798356 | G | A | 2 | a0001c0001t0001g0253 a0001c0001t0001g0254 |
2 | HG02109.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.92-24962C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9798356 | |||||||
| chr1:9798742 | C | A | 1 | a0002c0002t0003g0040 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.91+24901G>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9798742 | |||||||
| chr1:9798799 | G | A | 1 | a0002c0002t0002g0031 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.91+24844C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9798799 | |||||||
| chr1:9798845 | C | A | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.91+24798G>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9798845 | |||||||
| chr1:9799030 | A | G | 1 | a0002c0002t0003g0039 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.91+24613T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9799030 | |||||||
| chr1:9799280 | C | T | 1 | a0001c0003t0005g0009 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.91+24363G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9799280 | |||||||
| chr1:9799327 | T | C | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.91+24316A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9799327 | |||||||
| chr1:9799370 | G | C | 1 | a0001c0003t0005g0098 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.91+24273C>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9799370 | |||||||
| chr1:9799670 | C | T | 2 | a0001c0003t0005g0008 a0001c0003t0005g0009 |
2 | HG02622.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.91+23973G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9799670 | |||||||
| chr1:9799681 | G | A | 2 | a0001c0006t0009g0264 a0001c0006t0009g0265 |
2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.91+23962C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9799681 | |||||||
| chr1:9799766 | A | C | 98 | a0001c0001t0001g0106 a0001c0003t0004g0108 a0001c0003t0004g0109 others(95): Show |
99 | HG00558.hp1 HG00733.hp2 HG01081.hp1 others(96): Show |
intron_variant | MODIFIER | c.91+23877T>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9799766 | |||||||
| chr1:9799802 | G | A | 3 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0176 |
3 | HG02922.hp2 HG03209.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.91+23841C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9799802 | |||||||
| chr1:9799820 | A | C | 1 | a0007c0017t0010g0003 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.91+23823T>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9799820 | |||||||
| chr1:9799962 | A | T | 1 | a0001c0003t0004g0259 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.91+23681T>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9799962 | |||||||
| chr1:9799982 | C | G | 2 | a0002c0002t0002g0073 a0002c0002t0002g0074 |
2 | HG00423.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.91+23661G>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9799982 | |||||||
| chr1:9799992 | C | A | 194 | a0001c0001t0001g0002 a0001c0001t0001g0105 a0001c0001t0001g0124 others(191): Show |
195 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.91+23651G>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9799992 | |||||||
| chr1:9800120 | GA | G | 4 | a0001c0003t0005g0097 a0001c0003t0005g0098 a0001c0003t0005g0099 others(1): Show |
4 | HG02280.hp1 HG02615.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.91+23522delT | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9800120 | |||||||
| chr1:9800462 | G | A | 1 | a0002c0002t0002g0093 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.91+23181C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9800462 | |||||||
| chr1:9800504 | G | A | 1 | a0001c0001t0001g0164 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.91+23139C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9800504 | |||||||
| chr1:9800557 | G | GAAA | 6 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0066 others(3): Show |
6 | HG01981.hp2 NA18940.hp2 NA18968.hp2 others(3): Show |
intron_variant | MODIFIER | c.91+23083_91+23085d others(5): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9800557 | |||||||
| chr1:9800557 | GA | G | 118 | a0001c0001t0001g0002 a0001c0001t0001g0105 a0001c0001t0001g0124 others(115): Show |
119 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.91+23085delT | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9800557 | |||||||
| chr1:9800607 | G | A | 2 | a0001c0006t0009g0264 a0001c0006t0009g0265 |
2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.91+23036C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9800607 | |||||||
| chr1:9800627 | G | C | 1 | a0001c0001t0001g0230 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.91+23016C>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9800627 | |||||||
| chr1:9800645 | A | G | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.91+22998T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9800645 | |||||||
| chr1:9800662 | G | A | 2 | a0001c0001t0001g0261 a0001c0001t0001g0262 |
2 | HG00423.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.91+22981C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9800662 | |||||||
| chr1:9800729 | CA | C | 82 | a0001c0001t0001g0106 a0001c0001t0001g0253 a0001c0001t0001g0254 others(79): Show |
83 | HG00558.hp1 HG01081.hp1 HG01123.hp2 others(80): Show |
intron_variant | MODIFIER | c.91+22913delT | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9800729 | |||||||
| chr1:9800740 | T | A | 1 | a0001c0001t0001g0246 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.91+22903A>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9800740 | |||||||
| chr1:9800767 | G | GA | 9 | a0001c0003t0004g0122 a0003c0004t0002g0063 a0003c0004t0002g0064 others(6): Show |
9 | HG00558.hp1 HG01981.hp2 HG03225.hp2 others(6): Show |
intron_variant | MODIFIER | c.91+22875dupT | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9800767 | |||||||
| chr1:9800841 | A | C | 1 | a0001c0001t0001g0250 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.91+22802T>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9800841 | |||||||
| chr1:9800886 | C | T | 50 | a0001c0001t0001g0106 a0001c0003t0006g0022 a0001c0003t0006g0042 others(47): Show |
51 | HG01081.hp1 HG01123.hp2 HG01255.hp1 others(48): Show |
intron_variant | MODIFIER | c.91+22757G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9800886 | |||||||
| chr1:9800909 | A | G | 1 | a0001c0001t0001g0127 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.91+22734T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9800909 | |||||||
| chr1:9800940 | A | AAAAG | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.91+22702_91+22703i others(6): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9800940 | |||||||
| chr1:9800974 | C | T | 1 | a0001c0001t0001g0164 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.91+22669G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9800974 | |||||||
| chr1:9800979 | G | A | 1 | a0001c0001t0001g0166 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.91+22664C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9800979 | |||||||
| chr1:9801079 | T | C | 73 | a0001c0001t0001g0106 a0001c0001t0001g0253 a0001c0001t0001g0254 others(70): Show |
74 | HG01081.hp1 HG01123.hp2 HG01255.hp1 others(71): Show |
intron_variant | MODIFIER | c.91+22564A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9801079 | |||||||
| chr1:9801231 | G | A | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.91+22412C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9801231 | |||||||
| chr1:9801313 | TTA | T | 6 | a0002c0002t0002g0037 a0002c0002t0002g0043 a0002c0002t0002g0058 others(3): Show |
6 | NA18948.hp2 NA18984.hp1 NA18985.hp2 others(3): Show |
intron_variant | MODIFIER | c.91+22328_91+22329d others(4): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9801313 | |||||||
| chr1:9801321 | T | A | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.91+22322A>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9801321 | |||||||
| chr1:9801548 | CATT | C | 6 | a0001c0003t0005g0008 a0001c0003t0005g0009 a0001c0003t0005g0097 others(3): Show |
6 | HG02280.hp1 HG02615.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.91+22092_91+22094d others(5): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9801548 | |||||||
| chr1:9801578 | G | C | 9 | a0002c0002t0002g0071 a0002c0002t0002g0078 a0002c0002t0002g0079 others(6): Show |
9 | HG01257.hp1 HG01258.hp1 HG01346.hp2 others(6): Show |
intron_variant | MODIFIER | c.91+22065C>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9801578 | |||||||
| chr1:9801716 | G | A | 3 | a0002c0002t0002g0007 a0002c0002t0002g0028 a0002c0002t0002g0030 |
3 | HG03831.hp2 HG04228.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.91+21927C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9801716 | |||||||
| chr1:9801986 | T | C | 1 | a0002c0010t0002g0029 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.91+21657A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9801986 | |||||||
| chr1:9802010 | T | C | 1 | a0001c0003t0005g0097 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.91+21633A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9802010 | |||||||
| chr1:9802314 | C | T | 164 | a0001c0001t0001g0002 a0001c0001t0001g0105 a0001c0001t0001g0124 others(161): Show |
165 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.91+21329G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9802314 | |||||||
| chr1:9802423 | T | C | 1 | a0001c0001t0001g0247 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.91+21220A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9802423 | |||||||
| chr1:9802424 | G | A | 1 | a0001c0001t0001g0260 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.91+21219C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9802424 | |||||||
| chr1:9802536 | A | C | 1 | a0002c0002t0003g0038 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.91+21107T>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9802536 | |||||||
| chr1:9802702 | C | T | 2 | a0001c0001t0001g0163 a0001c0001t0001g0221 |
2 | HG03017.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.91+20941G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9802702 | |||||||
| chr1:9802710 | G | A | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.91+20933C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9802710 | |||||||
| chr1:9802713 | AC | A | 3 | a0001c0001t0001g0002 a0001c0001t0001g0209 a0001c0001t0001g0247 |
4 | HG02135.hp2 HG02155.hp2 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.91+20929delG | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9802713 | |||||||
| chr1:9802804 | A | C | 10 | a0001c0006t0009g0264 a0001c0006t0009g0265 a0003c0004t0002g0063 others(7): Show |
10 | HG00558.hp1 HG01243.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.91+20839T>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9802804 | |||||||
| chr1:9802823 | A | AT | 158 | a0001c0001t0001g0002 a0001c0001t0001g0105 a0001c0001t0001g0124 others(155): Show |
159 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.91+20819dupA | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9802823 | |||||||
| chr1:9802823 | A | ATT | 15 | a0001c0001t0001g0159 a0001c0001t0001g0162 a0001c0001t0001g0164 others(12): Show |
15 | HG00733.hp1 HG00735.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.91+20818_91+20819d others(4): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9802823 | |||||||
| chr1:9802823 | AT | A | 10 | a0002c0002t0002g0010 a0002c0002t0002g0011 a0002c0002t0002g0013 others(7): Show |
10 | HG00558.hp1 HG01884.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.91+20819delA | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9802823 | |||||||
| chr1:9803072 | C | T | 2 | a0001c0006t0009g0264 a0001c0006t0009g0265 |
2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.91+20571G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9803072 | |||||||
| chr1:9803158 | C | A | 3 | a0001c0001t0001g0236 a0001c0001t0001g0237 a0001c0001t0015g0235 |
3 | HG00621.hp2 HG01952.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.91+20485G>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9803158 | |||||||
| chr1:9803263 | A | C | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.91+20380T>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9803263 | |||||||
| chr1:9803402 | C | T | 2 | a0002c0002t0003g0040 a0002c0002t0003g0041 |
2 | NA18943.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.91+20241G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9803402 | |||||||
| chr1:9803470 | C | T | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.91+20173G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9803470 | |||||||
| chr1:9803524 | C | T | 2 | a0001c0001t0001g0253 a0001c0001t0001g0254 |
2 | HG02109.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.91+20119G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9803524 | |||||||
| chr1:9803631 | C | T | 1 | a0001c0001t0001g0126 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.91+20012G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9803631 | |||||||
| chr1:9803632 | G | A | 1 | a0001c0003t0007g0032 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.91+20011C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9803632 | |||||||
| chr1:9803792 | A | G | 7 | a0001c0003t0005g0008 a0001c0003t0005g0009 a0001c0003t0005g0097 others(4): Show |
7 | HG02280.hp1 HG02615.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.91+19851T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9803792 | |||||||
| chr1:9803825 | T | A | 1 | a0001c0001t0001g0243 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.91+19818A>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9803825 | |||||||
| chr1:9803832 | T | A | 6 | a0001c0003t0004g0115 a0001c0003t0004g0116 a0001c0003t0004g0117 others(3): Show |
6 | HG01243.hp2 HG02559.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.91+19811A>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9803832 | |||||||
| chr1:9803976 | A | G | 3 | a0001c0001t0001g0159 a0001c0001t0008g0185 a0001c0001t0008g0238 |
3 | HG02647.hp1 HG02723.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.91+19667T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9803976 | |||||||
| chr1:9804055 | T | C | 17 | a0001c0003t0004g0108 a0001c0003t0004g0109 a0001c0003t0004g0110 others(14): Show |
17 | HG00733.hp2 HG01109.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.91+19588A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9804055 | |||||||
| chr1:9804088 | T | C | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.91+19555A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9804088 | |||||||
| chr1:9804147 | G | A | 2 | a0001c0006t0009g0264 a0001c0006t0009g0265 |
2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.91+19496C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9804147 | |||||||
| chr1:9804220 | G | A | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.91+19423C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9804220 | |||||||
| chr1:9804256 | A | G | 1 | a0003c0004t0002g0067 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.91+19387T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9804256 | |||||||
| chr1:9804323 | A | C | 1 | a0002c0002t0002g0086 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.91+19320T>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9804323 | |||||||
| chr1:9804340 | C | T | 1 | a0003c0004t0002g0063 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.91+19303G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9804340 | |||||||
| chr1:9804361 | C | CA | 21 | a0001c0001t0001g0162 a0001c0001t0001g0168 a0001c0001t0001g0170 others(18): Show |
21 | HG00558.hp1 HG01261.hp1 HG02135.hp2 others(18): Show |
intron_variant | MODIFIER | c.91+19281dupT | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9804361 | |||||||
| chr1:9804361 | CA | C | 105 | a0001c0001t0001g0166 a0001c0001t0001g0177 a0001c0001t0001g0184 others(102): Show |
105 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.91+19281delT | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9804361 | |||||||
| chr1:9804361 | CAA | C | 16 | a0001c0003t0004g0108 a0001c0003t0004g0109 a0001c0003t0004g0110 others(13): Show |
16 | HG00733.hp2 HG01109.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.91+19280_91+19281d others(4): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9804361 | |||||||
| chr1:9804394 | A | G | 75 | a0001c0001t0001g0106 a0001c0003t0006g0022 a0001c0003t0006g0042 others(72): Show |
76 | HG00423.hp2 HG01081.hp1 HG01123.hp2 others(73): Show |
intron_variant | MODIFIER | c.91+19249T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9804394 | |||||||
| chr1:9804407 | G | A | 1 | a0001c0003t0007g0095 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.91+19236C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9804407 | |||||||
| chr1:9804435 | C | T | 93 | a0001c0001t0001g0106 a0001c0003t0005g0008 a0001c0003t0005g0009 others(90): Show |
94 | HG00423.hp2 HG01081.hp1 HG01123.hp2 others(91): Show |
intron_variant | MODIFIER | c.91+19208G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9804435 | |||||||
| chr1:9804769 | C | T | 1 | a0001c0003t0006g0096 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.91+18874G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9804769 | |||||||
| chr1:9804867 | G | C | 1 | a0001c0001t0001g0171 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.91+18776C>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9804867 | |||||||
| chr1:9805058 | T | C | 1 | a0007c0017t0010g0003 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.91+18585A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9805058 | |||||||
| chr1:9805206 | C | A | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.91+18437G>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9805206 | |||||||
| chr1:9805556 | G | A | 1 | a0002c0002t0017g0107 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.91+18087C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9805556 | |||||||
| chr1:9805575 | G | A | 170 | a0001c0001t0001g0002 a0001c0001t0001g0105 a0001c0001t0001g0124 others(167): Show |
171 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.91+18068C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9805575 | |||||||
| chr1:9805591 | G | A | 1 | a0001c0001t0001g0232 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.91+18052C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9805591 | |||||||
| chr1:9805633 | G | A | 1 | a0002c0002t0002g0015 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.91+18010C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9805633 | |||||||
| chr1:9805740 | G | A | 1 | a0001c0001t0001g0254 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.91+17903C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9805740 | |||||||
| chr1:9805745 | T | A | 1 | a0001c0003t0004g0259 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.91+17898A>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9805745 | |||||||
| chr1:9805866 | C | CA | 96 | a0001c0001t0001g0106 a0001c0001t0001g0132 a0001c0001t0001g0149 others(93): Show |
97 | HG00423.hp2 HG00738.hp1 HG01081.hp1 others(94): Show |
intron_variant | MODIFIER | c.91+17776dupT | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9805866 | |||||||
| chr1:9805866 | C | CAA | 7 | a0001c0003t0005g0009 a0002c0002t0002g0030 a0002c0002t0002g0072 others(4): Show |
7 | HG01884.hp2 HG02622.hp1 HG03831.hp2 others(4): Show |
intron_variant | MODIFIER | c.91+17775_91+17776d others(4): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9805866 | |||||||
| chr1:9805866 | CA | C | 13 | a0001c0001t0001g0157 a0001c0001t0001g0163 a0001c0001t0001g0183 others(10): Show |
13 | HG00558.hp1 HG01070.hp1 HG01257.hp2 others(10): Show |
intron_variant | MODIFIER | c.91+17776delT | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9805866 | |||||||
| chr1:9806205 | G | A | 1 | a0001c0001t0001g0220 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.91+17438C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9806205 | |||||||
| chr1:9806223 | G | A | 160 | a0001c0001t0001g0002 a0001c0001t0001g0105 a0001c0001t0001g0124 others(157): Show |
161 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.91+17420C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9806223 | |||||||
| chr1:9806379 | G | T | 46 | a0001c0001t0001g0105 a0001c0001t0001g0124 a0001c0001t0001g0125 others(43): Show |
46 | HG00609.hp2 HG00621.hp1 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.91+17264C>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9806379 | |||||||
| chr1:9806600 | C | T | 9 | a0002c0002t0002g0071 a0002c0002t0002g0078 a0002c0002t0002g0079 others(6): Show |
9 | HG01257.hp1 HG01258.hp1 HG01346.hp2 others(6): Show |
intron_variant | MODIFIER | c.91+17043G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9806600 | |||||||
| chr1:9806662 | G | A | 1 | a0001c0001t0001g0260 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.91+16981C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9806662 | |||||||
| chr1:9806704 | C | T | 1 | a0001c0001t0001g0164 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.91+16939G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9806704 | |||||||
| chr1:9806740 | G | A | 3 | a0001c0001t0001g0002 a0001c0001t0001g0209 a0001c0001t0001g0247 |
4 | HG02135.hp2 HG02155.hp2 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.91+16903C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9806740 | |||||||
| chr1:9806898 | C | T | 10 | a0001c0006t0009g0264 a0001c0006t0009g0265 a0003c0004t0002g0063 others(7): Show |
10 | HG00558.hp1 HG01243.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.91+16745G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9806898 | |||||||
| chr1:9806917 | C | T | 6 | a0001c0003t0005g0008 a0001c0003t0005g0009 a0001c0003t0005g0097 others(3): Show |
6 | HG02280.hp1 HG02615.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.91+16726G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9806917 | |||||||
| chr1:9807009 | C | T | 2 | a0002c0002t0003g0023 a0002c0002t0003g0039 |
2 | HG01123.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.91+16634G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9807009 | |||||||
| chr1:9807012 | G | C | 3 | a0002c0002t0002g0007 a0002c0002t0002g0028 a0002c0002t0002g0030 |
3 | HG03831.hp2 HG04228.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.91+16631C>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9807012 | |||||||
| chr1:9807227 | C | G | 2 | a0001c0006t0009g0264 a0001c0006t0009g0265 |
2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.91+16416G>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9807227 | |||||||
| chr1:9807341 | C | T | 1 | a0001c0001t0001g0178 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.91+16302G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9807341 | |||||||
| chr1:9807367 | C | A | 1 | a0001c0003t0004g0122 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.91+16276G>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9807367 | |||||||
| chr1:9807368 | G | C | 10 | a0001c0006t0009g0264 a0001c0006t0009g0265 a0003c0004t0002g0063 others(7): Show |
10 | HG00558.hp1 HG01243.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.91+16275C>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9807368 | |||||||
| chr1:9807893 | C | T | 1 | a0002c0002t0002g0005 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.91+15750G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9807893 | |||||||
| chr1:9808002 | C | T | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.91+15641G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9808002 | |||||||
| chr1:9808005 | C | T | 6 | a0001c0003t0005g0008 a0001c0003t0005g0009 a0001c0003t0005g0097 others(3): Show |
6 | HG02280.hp1 HG02615.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.91+15638G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9808005 | |||||||
| chr1:9808036 | C | T | 3 | a0001c0001t0001g0125 a0001c0001t0001g0141 a0001c0001t0001g0142 |
3 | HG02027.hp1 HG02523.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.91+15607G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9808036 | |||||||
| chr1:9808047 | G | A | 3 | a0002c0002t0002g0016 a0002c0002t0002g0017 a0008c0009t0002g0004 |
3 | HG01891.hp1 HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.91+15596C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9808047 | |||||||
| chr1:9808054 | C | T | 1 | a0001c0001t0001g0215 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.91+15589G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9808054 | |||||||
| chr1:9808330 | G | A | 3 | a0001c0003t0006g0022 a0001c0003t0006g0055 a0001c0003t0006g0056 |
3 | HG01255.hp1 HG02258.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.91+15313C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9808330 | |||||||
| chr1:9808529 | A | G | 1 | a0001c0014t0001g0251 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.91+15114T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9808529 | |||||||
| chr1:9808601 | C | T | 1 | a0002c0002t0002g0077 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.91+15042G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9808601 | |||||||
| chr1:9808602 | G | T | 16 | a0001c0003t0004g0108 a0001c0003t0004g0109 a0001c0003t0004g0110 others(13): Show |
16 | HG00733.hp2 HG01891.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.91+15041C>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9808602 | |||||||
| chr1:9808638 | G | A | 1 | a0001c0001t0001g0169 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.91+15005C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9808638 | |||||||
| chr1:9808692 | G | A | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.91+14951C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9808692 | |||||||
| chr1:9808698 | G | A | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.91+14945C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9808698 | |||||||
| chr1:9808743 | C | G | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.91+14900G>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9808743 | |||||||
| chr1:9808748 | A | G | 1 | a0001c0001t0001g0242 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.91+14895T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9808748 | |||||||
| chr1:9809182 | T | C | 1 | a0001c0001t0001g0154 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.91+14461A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9809182 | |||||||
| chr1:9809188 | C | T | 1 | a0001c0001t0001g0182 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.91+14455G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9809188 | |||||||
| chr1:9809272 | C | A | 2 | a0001c0001t0001g0253 a0001c0001t0001g0254 |
2 | HG02109.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.91+14371G>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9809272 | |||||||
| chr1:9809289 | A | G | 1 | a0001c0001t0001g0214 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.91+14354T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9809289 | |||||||
| chr1:9809808 | G | A | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.91+13835C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9809808 | |||||||
| chr1:9809863 | C | T | 195 | a0001c0001t0001g0002 a0001c0001t0001g0105 a0001c0001t0001g0124 others(192): Show |
196 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.91+13780G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9809863 | |||||||
| chr1:9809984 | A | G | 1 | a0001c0001t0001g0130 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.91+13659T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9809984 | |||||||
| chr1:9810071 | A | G | 1 | a0001c0014t0001g0251 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.91+13572T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9810071 | |||||||
| chr1:9810091 | A | AGGAG | 9 | a0002c0002t0002g0010 a0002c0002t0002g0011 a0002c0002t0002g0013 others(6): Show |
9 | HG01884.hp1 HG02109.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.91+13548_91+13551d others(6): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9810091 | |||||||
| chr1:9810141 | A | AAGGGAAG others(136): Show |
1 | a0001c0003t0007g0032 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.91+13501_91+13502i others(145): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9810141 | |||||||
| chr1:9810141 | A | AAGGGAAG others(111): Show |
2 | a0001c0006t0009g0264 a0001c0006t0009g0265 |
2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.91+13501_91+13502i others(120): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9810141 | |||||||
| chr1:9810141 | A | AAGGGAAG others(153): Show |
8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.91+13501_91+13502i others(162): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9810141 | |||||||
| chr1:9810141 | A | AAGGGAAG others(134): Show |
1 | a0001c0001t0001g0258 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.91+13501_91+13502i others(143): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9810141 | |||||||
| chr1:9810141 | A | AAGGGAAG others(133): Show |
2 | a0001c0001t0001g0162 a0001c0001t0001g0213 |
2 | HG02145.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.91+13501_91+13502i others(142): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9810141 | |||||||
| chr1:9810141 | A | AAGGGAAG others(134): Show |
1 | a0002c0002t0003g0038 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.91+13501_91+13502i others(143): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9810141 | |||||||
| chr1:9810141 | A | AAGGGAAG others(133): Show |
3 | a0001c0003t0005g0008 a0002c0002t0002g0037 a0002c0002t0002g0092 |
3 | HG03209.hp1 NA18979.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.91+13501_91+13502i others(142): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9810141 | |||||||
| chr1:9810141 | A | AAGGGAAG others(132): Show |
1 | a0002c0002t0002g0027 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.91+13501_91+13502i others(141): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9810141 | |||||||
| chr1:9810141 | A | AAGGGAAG others(132): Show |
2 | a0001c0001t0001g0253 a0001c0001t0001g0254 |
2 | HG02109.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.91+13501_91+13502i others(141): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9810141 | |||||||
| chr1:9810141 | A | AAGGGAAG others(133): Show |
4 | a0001c0001t0001g0106 a0001c0001t0001g0256 a0002c0002t0002g0073 others(1): Show |
4 | HG00423.hp2 HG01099.hp2 HG02135.hp1 others(1): Show |
intron_variant | MODIFIER | c.91+13501_91+13502i others(142): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9810141 | |||||||
| chr1:9810141 | A | AAGGGAAG others(153): Show |
2 | a0001c0001t0001g0244 a0002c0002t0002g0076 |
2 | HG03239.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.91+13501_91+13502i others(162): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9810141 | |||||||
| chr1:9810141 | A | AAGGGAAG others(195): Show |
5 | a0001c0001t0001g0158 a0001c0001t0001g0180 a0001c0001t0001g0181 others(2): Show |
5 | HG02809.hp1 HG02970.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.91+13501_91+13502i others(204): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9810141 | |||||||
| chr1:9810141 | A | AAGGGAAG others(131): Show |
1 | a0002c0002t0003g0021 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.91+13501_91+13502i others(140): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9810141 | |||||||
| chr1:9810141 | A | AAGGGAAG others(111): Show |
1 | a0002c0002t0002g0034 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.91+13501_91+13502i others(120): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9810141 | |||||||
| chr1:9810141 | A | AAGGGAAG others(127): Show |
1 | a0001c0003t0004g0123 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.91+13501_91+13502i others(136): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9810141 | |||||||
| chr1:9810141 | A | AAGGGAAG others(131): Show |
15 | a0001c0003t0004g0108 a0001c0003t0004g0109 a0001c0003t0004g0110 others(12): Show |
15 | HG00733.hp2 HG01891.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.91+13501_91+13502i others(140): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9810141 | |||||||
| chr1:9810141 | A | AAGGGAAG others(105): Show |
2 | a0001c0001t0004g0165 a0001c0001t0004g0212 |
2 | HG02145.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.91+13501_91+13502i others(114): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9810141 | |||||||
| chr1:9810141 | A | AAGGGAAG others(156): Show |
1 | a0001c0003t0004g0259 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.91+13501_91+13502i others(165): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9810141 | |||||||
| chr1:9810141 | A | AAGGGAAG others(134): Show |
1 | a0001c0001t0001g0170 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.91+13501_91+13502i others(143): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9810141 | |||||||
| chr1:9810141 | A | AAGGGAAG others(134): Show |
2 | a0001c0001t0001g0125 a0002c0002t0003g0036 |
2 | HG02027.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.91+13501_91+13502i others(143): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9810141 | |||||||
| chr1:9810141 | A | AAGGGAAG others(133): Show |
5 | a0001c0001t0001g0141 a0001c0001t0001g0178 a0001c0001t0001g0234 others(2): Show |
5 | HG00558.hp2 HG02523.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.91+13501_91+13502i others(142): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9810141 | |||||||
| chr1:9810230 | C | T | 3 | a0001c0003t0005g0097 a0001c0003t0005g0099 a0001c0003t0005g0100 |
3 | HG02280.hp1 HG02723.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.91+13413G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9810230 | |||||||
| chr1:9810272 | ACGAGACC others(292): Show |
A | 1 | a0001c0003t0004g0117 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.91+13072_91+13370d others(2): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9810272 | |||||||
| chr1:9810731 | C | T | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.91+12912G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9810731 | |||||||
| chr1:9810903 | A | T | 69 | a0001c0001t0001g0106 a0001c0003t0005g0008 a0001c0003t0005g0009 others(66): Show |
70 | HG01081.hp1 HG01123.hp2 HG01255.hp1 others(67): Show |
intron_variant | MODIFIER | c.91+12740T>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9810903 | |||||||
| chr1:9810946 | T | C | 1 | a0002c0002t0002g0031 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.91+12697A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9810946 | |||||||
| chr1:9810957 | C | T | 69 | a0001c0001t0001g0106 a0001c0003t0005g0008 a0001c0003t0005g0009 others(66): Show |
70 | HG01081.hp1 HG01123.hp2 HG01255.hp1 others(67): Show |
intron_variant | MODIFIER | c.91+12686G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9810957 | |||||||
| chr1:9811167 | G | A | 5 | a0001c0001t0001g0002 a0001c0001t0001g0209 a0001c0001t0001g0244 others(2): Show |
6 | HG00140.hp1 HG02135.hp2 HG02155.hp2 others(3): Show |
intron_variant | MODIFIER | c.91+12476C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9811167 | |||||||
| chr1:9811173 | G | C | 1 | a0002c0002t0002g0031 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.91+12470C>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9811173 | |||||||
| chr1:9811214 | T | C | 5 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0006 others(2): Show |
6 | HG02559.hp2 HG02717.hp1 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.91+12429A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9811214 | |||||||
| chr1:9811224 | T | A | 1 | a0001c0001t0001g0233 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.91+12419A>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9811224 | |||||||
| chr1:9811225 | C | A | 1 | a0001c0001t0001g0233 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.91+12418G>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9811225 | |||||||
| chr1:9811252 | G | A | 1 | a0002c0002t0002g0031 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.91+12391C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9811252 | |||||||
| chr1:9811542 | TA | T | 5 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0006 others(2): Show |
6 | HG02559.hp2 HG02717.hp1 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.91+12100delT | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9811542 | |||||||
| chr1:9811731 | C | CA | 30 | a0001c0001t0001g0125 a0001c0001t0001g0133 a0001c0001t0001g0134 others(27): Show |
30 | HG00609.hp1 HG00733.hp2 HG01361.hp2 others(27): Show |
intron_variant | MODIFIER | c.91+11911dupT | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9811731 | |||||||
| chr1:9811731 | CA | C | 49 | a0001c0001t0001g0177 a0001c0001t0001g0179 a0001c0001t0001g0211 others(46): Show |
50 | HG00558.hp1 HG01109.hp1 HG01243.hp2 others(47): Show |
intron_variant | MODIFIER | c.91+11911delT | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9811731 | |||||||
| chr1:9811747 | A | G | 1 | a0001c0001t0001g0129 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.91+11896T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9811747 | |||||||
| chr1:9811802 | G | GT | 37 | a0001c0001t0001g0002 a0001c0001t0001g0172 a0001c0001t0001g0173 others(34): Show |
38 | HG00140.hp1 HG00423.hp2 HG01257.hp1 others(35): Show |
intron_variant | MODIFIER | c.91+11840dupA | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9811802 | |||||||
| chr1:9812143 | A | C | 1 | a0001c0001t0001g0178 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.91+11500T>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9812143 | |||||||
| chr1:9812144 | C | A | 1 | a0001c0001t0001g0178 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.91+11499G>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9812144 | |||||||
| chr1:9812260 | G | A | 1 | a0001c0001t0001g0170 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.91+11383C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9812260 | |||||||
| chr1:9812296 | G | A | 3 | a0001c0003t0005g0097 a0001c0003t0005g0099 a0001c0003t0005g0100 |
3 | HG02280.hp1 HG02723.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.91+11347C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9812296 | |||||||
| chr1:9812314 | T | C | 10 | a0001c0006t0009g0264 a0001c0006t0009g0265 a0003c0004t0002g0063 others(7): Show |
10 | HG00558.hp1 HG01243.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.91+11329A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9812314 | |||||||
| chr1:9812351 | C | T | 16 | a0001c0003t0004g0108 a0001c0003t0004g0109 a0001c0003t0004g0110 others(13): Show |
16 | HG00733.hp2 HG01891.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.91+11292G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9812351 | |||||||
| chr1:9812455 | G | C | 2 | a0001c0003t0005g0008 a0001c0003t0005g0009 |
2 | HG02622.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.91+11188C>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9812455 | |||||||
| chr1:9812494 | G | C | 2 | a0001c0001t0001g0253 a0001c0001t0001g0254 |
2 | HG02109.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.91+11149C>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9812494 | |||||||
| chr1:9812613 | G | A | 12 | a0002c0002t0002g0010 a0002c0002t0002g0011 a0002c0002t0002g0013 others(9): Show |
12 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.91+11030C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9812613 | |||||||
| chr1:9812667 | A | G | 1 | a0002c0002t0002g0033 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.91+10976T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9812667 | |||||||
| chr1:9812671 | A | G | 2 | a0001c0001t0001g0253 a0001c0001t0001g0254 |
2 | HG02109.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.91+10972T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9812671 | |||||||
| chr1:9812713 | T | C | 1 | a0007c0017t0010g0003 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.91+10930A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9812713 | |||||||
| chr1:9812848 | C | CA | 10 | a0001c0001t0001g0162 a0001c0001t0001g0207 a0001c0001t0001g0237 others(7): Show |
10 | HG01081.hp1 HG01243.hp2 HG01952.hp1 others(7): Show |
intron_variant | MODIFIER | c.91+10794dupT | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9812848 | |||||||
| chr1:9812848 | C | CAAAA | 7 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0066 others(4): Show |
7 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(4): Show |
intron_variant | MODIFIER | c.91+10791_91+10794d others(6): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9812848 | |||||||
| chr1:9812866 | C | A | 10 | a0001c0006t0009g0264 a0001c0006t0009g0265 a0003c0004t0002g0063 others(7): Show |
10 | HG00558.hp1 HG01243.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.91+10777G>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9812866 | |||||||
| chr1:9812993 | A | G | 265 | a0001c0001t0001g0002 a0001c0001t0001g0105 a0001c0001t0001g0106 others(262): Show |
267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.91+10650T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9812993 | |||||||
| chr1:9813004 | A | T | 1 | a0002c0002t0002g0033 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.91+10639T>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9813004 | |||||||
| chr1:9813114 | G | A | 4 | a0001c0001t0001g0234 a0001c0001t0001g0236 a0001c0001t0001g0237 others(1): Show |
4 | HG00621.hp2 HG01952.hp1 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.91+10529C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9813114 | |||||||
| chr1:9813199 | A | T | 1 | a0001c0001t0001g0260 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.91+10444T>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9813199 | |||||||
| chr1:9813362 | G | A | 1 | a0001c0001t0001g0208 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.91+10281C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9813362 | |||||||
| chr1:9813493 | T | A | 105 | a0001c0001t0001g0002 a0001c0001t0001g0105 a0001c0001t0001g0124 others(102): Show |
106 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.91+10150A>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9813493 | |||||||
| chr1:9813494 | G | A | 104 | a0001c0001t0001g0002 a0001c0001t0001g0105 a0001c0001t0001g0124 others(101): Show |
105 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.91+10149C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9813494 | |||||||
| chr1:9813497 | T | C | 1 | a0001c0001t0001g0178 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.91+10146A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9813497 | |||||||
| chr1:9813498 | C | CA | 16 | a0001c0001t0001g0151 a0001c0001t0001g0260 a0001c0001t0008g0238 others(13): Show |
16 | HG00558.hp1 HG00639.hp1 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.91+10144dupT | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9813498 | |||||||
| chr1:9813498 | C | T | 1 | a0001c0001t0001g0178 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.91+10145G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9813498 | |||||||
| chr1:9813499 | A | C | 1 | a0001c0001t0001g0178 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.91+10144T>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9813499 | |||||||
| chr1:9813509 | A | C | 1 | a0007c0017t0010g0003 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.91+10134T>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9813509 | |||||||
| chr1:9813836 | G | A | 1 | a0001c0003t0004g0118 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.91+9807C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9813836 | |||||||
| chr1:9813840 | C | T | 1 | a0001c0001t0001g0242 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.91+9803G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9813840 | |||||||
| chr1:9813881 | C | T | 1 | a0001c0001t0001g0138 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.91+9762G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9813881 | |||||||
| chr1:9813887 | G | C | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.91+9756C>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9813887 | |||||||
| chr1:9814032 | A | G | 1 | a0001c0001t0001g0177 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.91+9611T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9814032 | |||||||
| chr1:9814074 | C | G | 2 | a0002c0002t0002g0073 a0002c0002t0002g0074 |
2 | HG00423.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.91+9569G>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9814074 | |||||||
| chr1:9814100 | T | C | 17 | a0001c0003t0004g0108 a0001c0003t0004g0109 a0001c0003t0004g0110 others(14): Show |
17 | HG00733.hp2 HG01109.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.91+9543A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9814100 | |||||||
| chr1:9814137 | T | C | 1 | a0001c0003t0007g0032 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.91+9506A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9814137 | |||||||
| chr1:9814240 | T | C | 1 | a0001c0001t0001g0242 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.91+9403A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9814240 | |||||||
| chr1:9814247 | C | CA | 47 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0129 others(44): Show |
47 | HG00609.hp1 HG00621.hp1 HG00733.hp2 others(44): Show |
intron_variant | MODIFIER | c.91+9395dupT | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9814247 | |||||||
| chr1:9814247 | C | CAAAAAAA others(3): Show |
6 | a0003c0004t0002g0063 a0003c0004t0002g0065 a0003c0004t0002g0066 others(3): Show |
6 | HG00558.hp1 HG01981.hp2 NA18968.hp2 others(3): Show |
intron_variant | MODIFIER | c.91+9386_91+9395dup others(10): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9814247 | |||||||
| chr1:9814247 | C | CAAAAAAA others(4): Show |
2 | a0003c0004t0002g0064 a0003c0004t0002g0070 |
2 | NA18940.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.91+9385_91+9395dup others(11): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9814247 | |||||||
| chr1:9814345 | C | T | 13 | a0001c0003t0004g0108 a0001c0003t0004g0109 a0001c0003t0004g0110 others(10): Show |
13 | HG00733.hp2 HG01891.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.91+9298G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9814345 | |||||||
| chr1:9814488 | A | C | 2 | a0001c0006t0009g0264 a0001c0006t0009g0265 |
2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.91+9155T>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9814488 | |||||||
| chr1:9814620 | G | A | 1 | a0002c0002t0003g0023 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.91+9023C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9814620 | |||||||
| chr1:9814744 | T | C | 168 | a0001c0001t0001g0002 a0001c0001t0001g0105 a0001c0001t0001g0124 others(165): Show |
169 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.91+8899A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9814744 | |||||||
| chr1:9814774 | C | T | 16 | a0001c0003t0004g0108 a0001c0003t0004g0109 a0001c0003t0004g0110 others(13): Show |
16 | HG00733.hp2 HG01891.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.91+8869G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9814774 | |||||||
| chr1:9814812 | T | C | 1 | a0001c0003t0004g0122 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.91+8831A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9814812 | |||||||
| chr1:9814899 | CA | C | 202 | a0001c0001t0001g0002 a0001c0001t0001g0105 a0001c0001t0001g0124 others(199): Show |
203 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.91+8743delT | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9814899 | |||||||
| chr1:9814918 | A | T | 1 | a0001c0003t0007g0095 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.91+8725T>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9814918 | |||||||
| chr1:9815034 | G | C | 1 | a0001c0001t0001g0242 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.91+8609C>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9815034 | |||||||
| chr1:9815123 | C | G | 1 | a0001c0003t0004g0119 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.91+8520G>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9815123 | |||||||
| chr1:9815245 | TA | T | 5 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0174 others(2): Show |
5 | HG02922.hp2 HG03041.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.91+8397delT | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9815245 | |||||||
| chr1:9815283 | C | T | 204 | a0001c0001t0001g0002 a0001c0001t0001g0105 a0001c0001t0001g0124 others(201): Show |
205 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.91+8360G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9815283 | |||||||
| chr1:9815289 | C | T | 204 | a0001c0001t0001g0002 a0001c0001t0001g0105 a0001c0001t0001g0124 others(201): Show |
205 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.91+8354G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9815289 | |||||||
| chr1:9815429 | A | T | 1 | a0001c0001t0001g0139 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.91+8214T>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9815429 | |||||||
| chr1:9815430 | T | A | 1 | a0001c0001t0001g0139 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.91+8213A>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9815430 | |||||||
| chr1:9815460 | T | C | 1 | a0001c0014t0001g0251 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.91+8183A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9815460 | |||||||
| chr1:9815510 | A | G | 3 | a0002c0002t0002g0033 a0002c0002t0002g0061 a0002c0002t0002g0062 |
3 | HG02258.hp2 HG02630.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.91+8133T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9815510 | |||||||
| chr1:9815575 | C | T | 216 | a0001c0001t0001g0002 a0001c0001t0001g0105 a0001c0001t0001g0124 others(213): Show |
217 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.91+8068G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9815575 | |||||||
| chr1:9815697 | A | G | 1 | a0001c0001t0001g0139 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.91+7946T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9815697 | |||||||
| chr1:9815698 | G | C | 1 | a0001c0001t0001g0155 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.91+7945C>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9815698 | |||||||
| chr1:9815699 | G | C | 1 | a0001c0001t0001g0139 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.91+7944C>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9815699 | |||||||
| chr1:9815893 | A | G | 169 | a0001c0001t0001g0002 a0001c0001t0001g0105 a0001c0001t0001g0124 others(166): Show |
170 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.91+7750T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9815893 | |||||||
| chr1:9815944 | A | T | 9 | a0001c0001t0001g0157 a0001c0001t0001g0164 a0001c0001t0001g0167 others(6): Show |
9 | HG00735.hp2 HG00738.hp2 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.91+7699T>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9815944 | |||||||
| chr1:9815964 | T | A | 1 | a0001c0001t0001g0139 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.91+7679A>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9815964 | |||||||
| chr1:9815981 | C | T | 4 | a0001c0003t0004g0108 a0001c0003t0004g0109 a0001c0003t0004g0110 others(1): Show |
4 | HG02451.hp1 HG02897.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.91+7662G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9815981 | |||||||
| chr1:9816050 | G | A | 1 | a0001c0003t0004g0259 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.91+7593C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9816050 | |||||||
| chr1:9816110 | T | C | 1 | a0001c0001t0001g0243 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.91+7533A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9816110 | |||||||
| chr1:9816536 | TA | T | 29 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0156 others(26): Show |
29 | HG00558.hp2 HG01884.hp1 HG01891.hp1 others(26): Show |
intron_variant | MODIFIER | c.91+7106delT | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9816536 | |||||||
| chr1:9816537 | A | T | 166 | a0001c0001t0001g0002 a0001c0001t0001g0105 a0001c0001t0001g0124 others(163): Show |
167 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.91+7106T>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9816537 | |||||||
| chr1:9816538 | A | T | 14 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0156 others(11): Show |
14 | HG00558.hp1 HG00558.hp2 HG01981.hp2 others(11): Show |
intron_variant | MODIFIER | c.91+7105T>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9816538 | |||||||
| chr1:9816577 | GTTTT | G | 143 | a0001c0001t0001g0002 a0001c0001t0001g0105 a0001c0001t0001g0124 others(140): Show |
144 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.91+7062_91+7065del others(4): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9816577 | |||||||
| chr1:9816590 | T | C | 2 | a0001c0001t0001g0244 a0001c0001t0001g0245 |
2 | HG00140.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.91+7053A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9816590 | |||||||
| chr1:9816675 | T | C | 1 | a0001c0001t0001g0156 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.91+6968A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9816675 | |||||||
| chr1:9816820 | A | G | 1 | a0001c0001t0004g0165 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.91+6823T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9816820 | |||||||
| chr1:9816906 | C | T | 5 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0135 others(2): Show |
5 | HG01361.hp2 HG01433.hp2 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.91+6737G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9816906 | |||||||
| chr1:9816936 | C | T | 2 | a0001c0006t0009g0264 a0001c0006t0009g0265 |
2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.91+6707G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9816936 | |||||||
| chr1:9817094 | C | T | 10 | a0001c0006t0009g0264 a0001c0006t0009g0265 a0003c0004t0002g0063 others(7): Show |
10 | HG00558.hp1 HG01243.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.91+6549G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9817094 | |||||||
| chr1:9817121 | C | T | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.91+6522G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9817121 | |||||||
| chr1:9817130 | G | A | 1 | a0002c0002t0002g0093 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.91+6513C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9817130 | |||||||
| chr1:9817222 | T | C | 1 | a0001c0001t0001g0246 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.91+6421A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9817222 | |||||||
| chr1:9817247 | A | C | 1 | a0001c0001t0001g0127 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.91+6396T>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9817247 | |||||||
| chr1:9817367 | G | T | 1 | a0006c0012t0003g0024 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.91+6276C>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9817367 | |||||||
| chr1:9817686 | G | A | 2 | a0001c0001t0001g0253 a0001c0001t0001g0254 |
2 | HG02109.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.91+5957C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9817686 | |||||||
| chr1:9817849 | A | G | 1 | a0001c0001t0001g0164 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.91+5794T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9817849 | |||||||
| chr1:9817864 | G | A | 6 | a0001c0003t0005g0008 a0001c0003t0005g0009 a0001c0003t0005g0097 others(3): Show |
6 | HG02280.hp1 HG02615.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.91+5779C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9817864 | |||||||
| chr1:9817920 | G | C | 1 | a0002c0002t0003g0060 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.91+5723C>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9817920 | |||||||
| chr1:9817924 | G | A | 1 | a0001c0003t0004g0122 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.91+5719C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9817924 | |||||||
| chr1:9817930 | C | T | 7 | a0001c0001t0001g0105 a0001c0001t0001g0127 a0001c0001t0001g0128 others(4): Show |
7 | HG01099.hp1 HG01978.hp1 HG02155.hp1 others(4): Show |
intron_variant | MODIFIER | c.91+5713G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9817930 | |||||||
| chr1:9818003 | CT | C | 236 | a0001c0001t0001g0002 a0001c0001t0001g0105 a0001c0001t0001g0106 others(233): Show |
238 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.91+5639delA | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9818003 | |||||||
| chr1:9818003 | CTT | C | 11 | a0001c0001t0001g0247 a0001c0003t0005g0100 a0001c0006t0009g0264 others(8): Show |
11 | HG00558.hp1 HG01243.hp2 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.91+5638_91+5639del others(2): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9818003 | |||||||
| chr1:9818105 | T | G | 2 | a0002c0002t0002g0061 a0002c0002t0002g0062 |
2 | HG02258.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.91+5538A>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9818105 | |||||||
| chr1:9818211 | T | C | 1 | a0001c0001t0001g0266 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.91+5432A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9818211 | |||||||
| chr1:9818249 | G | A | 10 | a0001c0006t0009g0264 a0001c0006t0009g0265 a0003c0004t0002g0063 others(7): Show |
10 | HG00558.hp1 HG01243.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.91+5394C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9818249 | |||||||
| chr1:9818326 | G | A | 6 | a0001c0003t0005g0008 a0001c0003t0005g0009 a0001c0003t0005g0097 others(3): Show |
6 | HG02280.hp1 HG02615.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.91+5317C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9818326 | |||||||
| chr1:9818386 | C | T | 36 | a0001c0001t0001g0105 a0001c0001t0001g0124 a0001c0001t0001g0125 others(33): Show |
36 | HG00609.hp2 HG00621.hp1 HG01081.hp2 others(33): Show |
intron_variant | MODIFIER | c.91+5257G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9818386 | |||||||
| chr1:9818492 | CTAATTTT others(2): Show |
C | 6 | a0001c0003t0005g0008 a0001c0003t0005g0009 a0001c0003t0005g0097 others(3): Show |
6 | HG02280.hp1 HG02615.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.91+5142_91+5150del others(9): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9818492 | |||||||
| chr1:9818504 | T | A | 2 | a0001c0006t0009g0264 a0001c0006t0009g0265 |
2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.91+5139A>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9818504 | |||||||
| chr1:9818532 | T | C | 2 | a0001c0006t0009g0264 a0001c0006t0009g0265 |
2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.91+5111A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9818532 | |||||||
| chr1:9818647 | G | A | 1 | a0001c0001t0001g0248 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.91+4996C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9818647 | |||||||
| chr1:9818777 | C | CT | 66 | a0001c0001t0001g0002 a0001c0001t0001g0125 a0001c0001t0001g0127 others(63): Show |
66 | HG00140.hp1 HG00423.hp1 HG00735.hp2 others(63): Show |
intron_variant | MODIFIER | c.91+4865dupA | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9818777 | |||||||
| chr1:9818777 | CT | C | 19 | a0001c0001t0001g0166 a0001c0001t0001g0249 a0001c0003t0004g0108 others(16): Show |
19 | HG00733.hp2 HG01257.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.91+4865delA | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9818777 | |||||||
| chr1:9818777 | CTTT | C | 7 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(4): Show |
7 | HG00558.hp1 HG01981.hp2 NA18968.hp2 others(4): Show |
intron_variant | MODIFIER | c.91+4863_91+4865del others(3): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9818777 | |||||||
| chr1:9818850 | G | A | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.91+4793C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9818850 | |||||||
| chr1:9818856 | G | A | 2 | a0001c0006t0009g0264 a0001c0006t0009g0265 |
2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.91+4787C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9818856 | |||||||
| chr1:9818912 | G | T | 12 | a0002c0002t0002g0010 a0002c0002t0002g0011 a0002c0002t0002g0013 others(9): Show |
12 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.91+4731C>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9818912 | |||||||
| chr1:9818943 | C | T | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.91+4700G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9818943 | |||||||
| chr1:9818962 | A | AT | 164 | a0001c0001t0001g0002 a0001c0001t0001g0105 a0001c0001t0001g0124 others(161): Show |
165 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.91+4680dupA | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9818962 | |||||||
| chr1:9819026 | C | A | 1 | a0001c0001t0001g0249 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.91+4617G>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9819026 | |||||||
| chr1:9819291 | A | G | 2 | a0001c0003t0005g0008 a0001c0003t0005g0009 |
2 | HG02622.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.91+4352T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9819291 | |||||||
| chr1:9819444 | A | G | 1 | a0003c0004t0002g0063 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.91+4199T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9819444 | |||||||
| chr1:9819559 | A | G | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.91+4084T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9819559 | |||||||
| chr1:9819683 | C | A | 1 | a0001c0001t0001g0250 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.91+3960G>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9819683 | |||||||
| chr1:9819686 | G | C | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.91+3957C>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9819686 | |||||||
| chr1:9819707 | T | C | 1 | a0001c0014t0001g0251 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.91+3936A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9819707 | |||||||
| chr1:9819754 | T | C | 10 | a0001c0006t0009g0264 a0001c0006t0009g0265 a0003c0004t0002g0063 others(7): Show |
10 | HG00558.hp1 HG01243.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.91+3889A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9819754 | |||||||
| chr1:9819896 | C | A | 1 | a0001c0003t0004g0119 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.91+3747G>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9819896 | |||||||
| chr1:9819975 | A | G | 13 | a0001c0003t0004g0108 a0001c0003t0004g0109 a0001c0003t0004g0110 others(10): Show |
13 | HG00733.hp2 HG01891.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.91+3668T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9819975 | |||||||
| chr1:9820159 | C | A | 1 | a0001c0001t0001g0252 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.91+3484G>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9820159 | |||||||
| chr1:9820322 | C | T | 1 | a0005c0011t0021g0268 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.91+3321G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9820322 | |||||||
| chr1:9820495 | G | A | 2 | a0001c0001t0001g0253 a0001c0001t0001g0254 |
2 | HG02109.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.91+3148C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9820495 | |||||||
| chr1:9820517 | A | T | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.91+3126T>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9820517 | |||||||
| chr1:9820538 | A | C | 1 | a0001c0001t0001g0124 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.91+3105T>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9820538 | |||||||
| chr1:9820569 | A | G | 1 | a0002c0002t0002g0007 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.91+3074T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9820569 | |||||||
| chr1:9820572 | T | G | 1 | a0001c0003t0004g0259 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.91+3071A>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9820572 | |||||||
| chr1:9820628 | G | T | 2 | a0001c0001t0001g0261 a0001c0001t0001g0262 |
2 | HG00423.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.91+3015C>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9820628 | |||||||
| chr1:9820911 | G | C | 2 | a0001c0001t0001g0256 a0001c0001t0016g0257 |
2 | HG01099.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.91+2732C>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9820911 | |||||||
| chr1:9820917 | T | C | 8 | a0003c0004t0002g0063 a0003c0004t0002g0064 a0003c0004t0002g0065 others(5): Show |
8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.91+2726A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9820917 | |||||||
| chr1:9820983 | G | A | 1 | a0001c0003t0004g0123 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.91+2660C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9820983 | |||||||
| chr1:9821054 | C | T | 3 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0006 |
4 | HG02717.hp1 HG03486.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.91+2589G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9821054 | |||||||
| chr1:9821246 | C | T | 2 | a0001c0006t0009g0264 a0001c0006t0009g0265 |
2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.91+2397G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9821246 | |||||||
| chr1:9821314 | G | A | 1 | a0001c0001t0001g0260 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.91+2329C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9821314 | |||||||
| chr1:9821484 | G | A | 144 | a0001c0001t0001g0002 a0001c0001t0001g0105 a0001c0001t0001g0124 others(141): Show |
145 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.91+2159C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9821484 | |||||||
| chr1:9821555 | G | A | 1 | a0001c0001t0001g0258 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.91+2088C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9821555 | |||||||
| chr1:9821636 | T | C | 1 | a0001c0003t0004g0259 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.91+2007A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9821636 | |||||||
| chr1:9821907 | C | T | 163 | a0001c0001t0001g0002 a0001c0001t0001g0105 a0001c0001t0001g0124 others(160): Show |
164 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.91+1736G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9821907 | |||||||
| chr1:9821997 | T | C | 1 | a0001c0001t0001g0260 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.91+1646A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9821997 | |||||||
| chr1:9822049 | C | A | 163 | a0001c0001t0001g0002 a0001c0001t0001g0105 a0001c0001t0001g0124 others(160): Show |
164 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.91+1594G>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9822049 | |||||||
| chr1:9822607 | T | G | 2 | a0001c0001t0001g0261 a0001c0001t0001g0262 |
2 | HG00423.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.91+1036A>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9822607 | |||||||
| chr1:9822608 | C | T | 77 | a0001c0001t0001g0106 a0001c0003t0005g0008 a0001c0003t0005g0009 others(74): Show |
78 | HG00558.hp1 HG01081.hp1 HG01123.hp2 others(75): Show |
intron_variant | MODIFIER | c.91+1035G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9822608 | |||||||
| chr1:9823208 | G | C | 1 | a0001c0003t0007g0095 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.91+435C>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9823208 | |||||||
| chr1:9823226 | T | A | 1 | a0001c0003t0006g0096 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.91+417A>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9823226 | |||||||
| chr1:9823287 | G | A | 1 | a0001c0001t0001g0263 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.91+356C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9823287 | |||||||
| chr1:9823395 | C | T | 1 | a0001c0001t0001g0105 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.91+248G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9823395 | |||||||
| chr1:9823419 | T | C | 2 | a0001c0006t0009g0264 a0001c0006t0009g0265 |
2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.91+224A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9823419 | |||||||
| chr1:9823437 | G | A | 4 | a0001c0003t0005g0097 a0001c0003t0005g0098 a0001c0003t0005g0099 others(1): Show |
4 | HG02280.hp1 HG02615.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.91+206C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9823437 | |||||||
| chr1:9823484 | T | C | 1 | a0001c0001t0001g0266 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.91+159A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9823484 | |||||||
| chr1:9823609 | C | A | 2 | a0002c0002t0002g0101 a0002c0002t0002g0102 |
2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.91+34G>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9823609 |