Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 9746 |
| ensemblid | ENSG00000139182.15 |
| hgncid | 18371 |
| symbol | CLSTN3 |
| name | calsyntenin 3 |
| refseq_nuc | NM_014718.4 |
| refseq_prot | NP_055533.2 |
| ensembl_nuc | ENST00000266546.11 |
| ensembl_prot | ENSP00000266546.6 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 7130371 |
| end | 7158945 |
| strand | + |
| ver | v1.2 |
| region | chr12:7130371-7158945 |
| region5000 | chr12:7125371-7163945 |
| regionname0 | CLSTN3_chr12_7130371_7158945 |
| regionname5000 | CLSTN3_chr12_7125371_7163945 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 956 | 375 | 82 | 62 | 175 | 16 | 38 | 132 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | MTLLL others(951): Show |
chr12 | 7125371 | 7163945 |
| a0002 | 0/0 | 956 | 5 | 3 | 1 | 0 | 0 | 1 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | MTLLL others(951): Show |
chr12 | 7125371 | 7163945 |
| a0003 | 0/0 | 956 | 4 | 2 | 1 | 0 | 0 | 1 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | MTLLL others(951): Show |
chr12 | 7125371 | 7163945 |
| a0004 | 0/0 | 956 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | MTLLL others(951): Show |
chr12 | 7125371 | 7163945 |
| a0005 | 0/0 | 956 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | MTLLL others(951): Show |
chr12 | 7125371 | 7163945 |
| a0006 | 0/0 | 956 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | MTLLL others(951): Show |
chr12 | 7125371 | 7163945 |
| a0007 | 0/0 | 956 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | MTLLL others(951): Show |
chr12 | 7125371 | 7163945 |
| a0008 | 0/0 | 956 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | MTLLL others(951): Show |
chr12 | 7125371 | 7163945 |
| a0009 | 0/0 | 956 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | MTLQL others(951): Show |
chr12 | 7125371 | 7163945 |
| a0010 | 0/0 | 956 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | MTLLL others(951): Show |
chr12 | 7125371 | 7163945 |
| a0011 | 0/0 | 956 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | MTLLL others(951): Show |
chr12 | 7125371 | 7163945 |
| a0012 | 0/0 | 956 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | MTLLL others(951): Show |
chr12 | 7125371 | 7163945 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2868 | 324 | 72 | 57 | 150 | 14 | 29 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | ATGAC others(2863): Show |
chr12 | 7125371 | 7163945 | ||
| a0001c0002 | 0/0 | 2868 | 37 | 2 | 4 | 21 | 2 | 8 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | ATGAC others(2863): Show |
chr12 | 7125371 | 7163945 | ||
| a0001c0003 | 0/0 | 2868 | 6 | 6 | 0 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | ATGAC others(2863): Show |
chr12 | 7125371 | 7163945 | ||
| a0001c0008 | 0/0 | 2868 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | ATGAC others(2863): Show |
chr12 | 7125371 | 7163945 | ||
| a0001c0010 | 0/0 | 2868 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | ATGAC others(2863): Show |
chr12 | 7125371 | 7163945 | ||
| a0001c0013 | 0/0 | 2868 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | ATGAC others(2863): Show |
chr12 | 7125371 | 7163945 | ||
| a0001c0015 | 0/0 | 2868 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | ATGAC others(2863): Show |
chr12 | 7125371 | 7163945 | ||
| a0001c0016 | 0/0 | 2868 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | ATGAC others(2863): Show |
chr12 | 7125371 | 7163945 | ||
| a0001c0017 | 0/0 | 2868 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | ATGAC others(2863): Show |
chr12 | 7125371 | 7163945 | ||
| a0001c0019 | 0/0 | 2868 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | ATGAC others(2863): Show |
chr12 | 7125371 | 7163945 | ||
| a0001c0022 | 0/0 | 2868 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | ATGAC others(2863): Show |
chr12 | 7125371 | 7163945 | ||
| a0002c0004 | 0/0 | 2868 | 5 | 3 | 1 | 0 | 0 | 1 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | ATGAC others(2863): Show |
chr12 | 7125371 | 7163945 | ||
| a0003c0005 | 0/0 | 2868 | 4 | 2 | 1 | 0 | 0 | 1 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | ATGAC others(2863): Show |
chr12 | 7125371 | 7163945 | ||
| a0004c0006 | 0/0 | 2868 | 2 | 0 | 2 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | ATGAC others(2863): Show |
chr12 | 7125371 | 7163945 | ||
| a0005c0021 | 0/0 | 2868 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | ATGAC others(2863): Show |
chr12 | 7125371 | 7163945 | ||
| a0006c0012 | 0/0 | 2868 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | ATGAC others(2863): Show |
chr12 | 7125371 | 7163945 | ||
| a0007c0014 | 0/0 | 2868 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | ATGAC others(2863): Show |
chr12 | 7125371 | 7163945 | ||
| a0008c0020 | 0/0 | 2868 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | ATGAC others(2863): Show |
chr12 | 7125371 | 7163945 | ||
| a0009c0007 | 0/0 | 2868 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | ATGAC others(2863): Show |
chr12 | 7125371 | 7163945 | ||
| a0010c0018 | 0/0 | 2868 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | ATGAC others(2863): Show |
chr12 | 7125371 | 7163945 | ||
| a0011c0009 | 0/0 | 2868 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | ATGAC others(2863): Show |
chr12 | 7125371 | 7163945 | ||
| a0012c0011 | 0/0 | 2868 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | ATGAC others(2863): Show |
chr12 | 7125371 | 7163945 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 4017 | 265 | 32 | 47 | 146 | 12 | 27 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | ATCCT others(4012): Show |
chr12 | 7125371 | 7163945 |
| a0001c0001t0002 | 0/0 | 4013 | 3 | 0 | 0 | 2 | 0 | 1 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | ATCCT others(4008): Show |
chr12 | 7125371 | 7163945 |
| a0001c0001t0003 | 1/0 | 4013 | 17 | 14 | 2 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | ATCCT others(4008): Show |
chr12 | 7125371 | 7163945 |
| a0001c0001t0004 | 0/0 | 4013 | 19 | 19 | 0 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | ATCCT others(4008): Show |
chr12 | 7125371 | 7163945 |
| a0001c0001t0005 | 0/0 | 4017 | 8 | 0 | 5 | 0 | 2 | 1 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | ATCCT others(4012): Show |
chr12 | 7125371 | 7163945 |
| a0001c0001t0006 | 0/0 | 4013 | 2 | 2 | 0 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | ATCCT others(4008): Show |
chr12 | 7125371 | 7163945 |
| a0001c0001t0008 | 0/0 | 4017 | 2 | 0 | 2 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | ATCCT others(4012): Show |
chr12 | 7125371 | 7163945 |
| a0001c0001t0009 | 0/0 | 4013 | 2 | 2 | 0 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | ATCCT others(4008): Show |
chr12 | 7125371 | 7163945 |
| a0001c0001t0010 | 0/0 | 4017 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | ATCCT others(4012): Show |
chr12 | 7125371 | 7163945 |
| a0001c0001t0011 | 0/0 | 4017 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | ATCCT others(4012): Show |
chr12 | 7125371 | 7163945 |
| a0001c0001t0012 | 0/0 | 4013 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | ATCCT others(4008): Show |
chr12 | 7125371 | 7163945 |
| a0001c0001t0013 | 0/0 | 4013 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | ATCCT others(4008): Show |
chr12 | 7125371 | 7163945 |
| a0001c0001t0014 | 0/0 | 4017 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | ATCCT others(4012): Show |
chr12 | 7125371 | 7163945 |
| a0001c0001t0016 | 0/0 | 4017 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | ATCCT others(4012): Show |
chr12 | 7125371 | 7163945 |
| a0001c0002t0001 | 0/0 | 4017 | 10 | 0 | 1 | 6 | 0 | 3 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | ATCCT others(4012): Show |
chr12 | 7125371 | 7163945 |
| a0001c0002t0002 | 0/0 | 4013 | 23 | 1 | 3 | 12 | 2 | 5 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | ATCCT others(4008): Show |
chr12 | 7125371 | 7163945 |
| a0001c0002t0004 | 0/0 | 4013 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | ATCCT others(4008): Show |
chr12 | 7125371 | 7163945 |
| a0001c0002t0007 | 0/0 | 4013 | 2 | 0 | 0 | 2 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | ATCCT others(4008): Show |
chr12 | 7125371 | 7163945 |
| a0001c0002t0015 | 0/0 | 4013 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | ATCCT others(4008): Show |
chr12 | 7125371 | 7163945 |
| a0001c0003t0003 | 0/0 | 4013 | 6 | 6 | 0 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | ATCCT others(4008): Show |
chr12 | 7125371 | 7163945 |
| a0001c0008t0003 | 0/0 | 4013 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | ATCCT others(4008): Show |
chr12 | 7125371 | 7163945 |
| a0001c0010t0001 | 0/0 | 4017 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | ATCCT others(4012): Show |
chr12 | 7125371 | 7163945 |
| a0001c0013t0001 | 0/0 | 4017 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | ATCCT others(4012): Show |
chr12 | 7125371 | 7163945 |
| a0001c0015t0001 | 0/0 | 4017 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | ATCCT others(4012): Show |
chr12 | 7125371 | 7163945 |
| a0001c0016t0001 | 0/0 | 4017 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | ATCCT others(4012): Show |
chr12 | 7125371 | 7163945 |
| a0001c0017t0001 | 0/0 | 4017 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | ATCCT others(4012): Show |
chr12 | 7125371 | 7163945 |
| a0001c0019t0001 | 0/0 | 4017 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | ATCCT others(4012): Show |
chr12 | 7125371 | 7163945 |
| a0001c0022t0002 | 0/0 | 4013 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | ATCCT others(4008): Show |
chr12 | 7125371 | 7163945 |
| a0002c0004t0001 | 0/0 | 4017 | 5 | 3 | 1 | 0 | 0 | 1 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | ATCCT others(4012): Show |
chr12 | 7125371 | 7163945 |
| a0003c0005t0001 | 0/0 | 4017 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | ATCCT others(4012): Show |
chr12 | 7125371 | 7163945 |
| a0003c0005t0002 | 0/0 | 4013 | 3 | 2 | 1 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | ATCCT others(4008): Show |
chr12 | 7125371 | 7163945 |
| a0004c0006t0001 | 0/0 | 4017 | 2 | 0 | 2 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | ATCCT others(4012): Show |
chr12 | 7125371 | 7163945 |
| a0005c0021t0003 | 0/0 | 4013 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | ATCCT others(4008): Show |
chr12 | 7125371 | 7163945 |
| a0006c0012t0001 | 0/0 | 4017 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | ATCCT others(4012): Show |
chr12 | 7125371 | 7163945 |
| a0007c0014t0001 | 0/0 | 4017 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | ATCCT others(4012): Show |
chr12 | 7125371 | 7163945 |
| a0008c0020t0004 | 0/0 | 4013 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | ATCCT others(4008): Show |
chr12 | 7125371 | 7163945 |
| a0009c0007t0001 | 0/0 | 4017 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | ATCCT others(4012): Show |
chr12 | 7125371 | 7163945 |
| a0010c0018t0004 | 0/0 | 4013 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | ATCCT others(4008): Show |
chr12 | 7125371 | 7163945 |
| a0011c0009t0001 | 0/0 | 4017 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | ATCCT others(4012): Show |
chr12 | 7125371 | 7163945 |
| a0012c0011t0001 | 0/0 | 4017 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | ATCCT others(4012): Show |
chr12 | 7125371 | 7163945 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 15 | 1 | 1 | 10 | 1 | 2 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0002 | 0/0 | 7 | 0 | 1 | 4 | 2 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0003 | 0/0 | 7 | 0 | 0 | 6 | 0 | 1 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0004 | 0/0 | 6 | 1 | 0 | 5 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0005 | 0/0 | 6 | 0 | 0 | 5 | 0 | 1 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0006 | 0/0 | 6 | 0 | 1 | 4 | 0 | 1 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0008 | 0/0 | 5 | 0 | 2 | 2 | 0 | 1 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0009 | 0/0 | 5 | 0 | 1 | 3 | 1 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0010 | 0/0 | 4 | 0 | 0 | 3 | 1 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0012 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0015 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0021 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0048 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0049 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0187 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0003g0026 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0003g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0003g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0003g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0003g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0003g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0003g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0003g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0003g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0003g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0003g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0003g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0003g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0003g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0003g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0004g0007 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0004g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0004g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0004g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0004g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0004g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0004g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0004g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0004g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0004g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0004g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0004g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0004g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0004g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0005g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0005g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0005g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0005g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0005g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0005g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0005g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0005g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0006g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0006g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0008g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0009g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0009g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0010g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0011g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0012g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0013g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0014g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0001t0016g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0002t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0002t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0002t0002g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0002t0002g0033 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0002t0002g0035 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0002t0002g0036 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0002t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0002t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0002t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0002t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0002t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0002t0002g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0002t0002g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0002t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0002t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0002t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0002t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0002t0002g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0002t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0002t0004g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0002t0007g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0002t0007g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0002t0015g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0003t0003g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0003t0003g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0003t0003g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0003t0003g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0003t0003g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0008t0003g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0010t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0013t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0015t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0016t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0017t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0019t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0001c0022t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0002c0004t0001g0013 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0002c0004t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0003c0005t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0003c0005t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0003c0005t0002g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0003c0005t0002g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0004c0006t0001g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0005c0021t0003g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0006c0012t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0007c0014t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0008c0020t0004g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0009c0007t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0010c0018t0004g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0011c0009t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| a0012c0011t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0212 | EUR | GBR | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG00099 | hp2 | a0001 | c0001 | t0005 | g0186 | EUR | GBR | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG00140 | hp1 | a0001 | c0001 | t0005 | g0183 | EUR | GBR | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0009 | EUR | GBR | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0010 | EUR | FIN | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG00280 | hp2 | a0001 | c0002 | t0002 | g0033 | EUR | FIN | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG00423 | hp1 | a0001 | c0002 | t0002 | g0159 | EAS | CHS | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | CHS | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG00438 | hp1 | a0001 | c0002 | t0002 | g0162 | EAS | CHS | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG00438 | hp2 | a0001 | c0001 | t0014 | g0135 | EAS | CHS | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | CHS | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG00544 | hp2 | a0001 | c0002 | t0001 | g0032 | EAS | CHS | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG00597 | hp1 | a0001 | c0002 | t0007 | g0034 | EAS | CHS | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | CHS | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | CHS | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG00621 | hp1 | a0001 | c0002 | t0002 | g0171 | EAS | CHS | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | CHS | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG00639 | hp2 | a0002 | c0004 | t0001 | g0013 | AMR | PUR | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG00642 | hp1 | a0001 | c0001 | t0005 | g0184 | AMR | PUR | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | CHS | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | CHS | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG00735 | hp2 | a0001 | c0002 | t0002 | g0035 | AMR | PUR | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0120 | AMR | PUR | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG00741 | hp2 | a0001 | c0002 | t0001 | g0178 | AMR | PUR | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG01069 | hp2 | a0001 | c0001 | t0008 | g0041 | AMR | PUR | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG01070 | hp2 | a0001 | c0002 | t0002 | g0164 | AMR | PUR | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0270 | AMR | PUR | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0271 | AMR | PUR | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG01109 | hp1 | a0003 | c0005 | t0002 | g0273 | AMR | PUR | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0257 | AMR | PUR | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0255 | AMR | PUR | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG01168 | hp2 | a0004 | c0006 | t0001 | g0025 | AMR | PUR | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG01169 | hp2 | a0004 | c0006 | t0001 | g0025 | AMR | PUR | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG01175 | hp2 | a0001 | c0001 | t0005 | g0188 | AMR | PUR | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0274 | AMR | PUR | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG01243 | hp1 | a0001 | c0001 | t0005 | g0182 | AMR | PUR | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0276 | AMR | CLM | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | CLM | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG01256 | hp2 | a0001 | c0001 | t0005 | g0185 | AMR | CLM | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0235 | AMR | CLM | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG01346 | hp1 | a0001 | c0001 | t0011 | g0091 | AMR | CLM | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG01346 | hp2 | a0001 | c0002 | t0002 | g0168 | AMR | CLM | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG01358 | hp1 | a0001 | c0001 | t0003 | g0121 | AMR | CLM | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | CLM | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0259 | AMR | CLM | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | CLM | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG01496 | hp1 | a0001 | c0001 | t0005 | g0147 | AMR | CLM | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG01496 | hp2 | a0001 | c0019 | t0001 | g0001 | AMR | CLM | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0219 | EUR | IBS | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0090 | EUR | IBS | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0220 | EUR | IBS | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0012 | EUR | IBS | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | ACB | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG01884 | hp2 | a0001 | c0001 | t0006 | g0201 | AFR | ACB | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG01891 | hp1 | a0005 | c0021 | t0003 | g0195 | AFR | ACB | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | ACB | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0275 | AMR | PEL | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG01943 | hp1 | a0001 | c0001 | t0008 | g0041 | AMR | PEL | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | PEL | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0247 | AMR | PEL | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | PEL | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG02015 | hp2 | a0006 | c0012 | t0001 | g0050 | EAS | KHV | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | KHV | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | KHV | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | KHV | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | KHV | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | ACB | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG02055 | hp2 | a0001 | c0001 | t0004 | g0153 | AFR | ACB | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG02056 | hp1 | a0001 | c0002 | t0002 | g0102 | EAS | KHV | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | KHV | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG02080 | hp2 | a0001 | c0017 | t0001 | g0214 | EAS | KHV | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | KHV | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG02083 | hp2 | a0001 | c0022 | t0002 | g0034 | EAS | KHV | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG02129 | hp2 | a0001 | c0002 | t0002 | g0176 | EAS | KHV | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | KHV | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG02135 | hp1 | a0001 | c0002 | t0001 | g0160 | EAS | KHV | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG02145 | hp1 | a0001 | c0001 | t0004 | g0030 | AFR | ACB | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0269 | AFR | ACB | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG02155 | hp1 | a0001 | c0002 | t0007 | g0177 | EAS | CDX | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | CDX | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0095 | EAS | CDX | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | CDX | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG02280 | hp1 | a0003 | c0005 | t0002 | g0254 | AFR | ACB | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | ACB | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0243 | AMR | PEL | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PEL | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | PEL | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG02451 | hp1 | a0003 | c0005 | t0002 | g0272 | AFR | ACB | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG02451 | hp2 | a0001 | c0001 | t0004 | g0007 | AFR | ACB | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG02572 | hp1 | a0001 | c0001 | t0013 | g0089 | AFR | GWD | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | GWD | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG02602 | hp1 | a0001 | c0001 | t0005 | g0146 | SAS | PJL | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG02602 | hp2 | a0002 | c0004 | t0001 | g0238 | SAS | PJL | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | GWD | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0027 | AFR | GWD | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG02622 | hp1 | a0001 | c0001 | t0012 | g0140 | AFR | GWD | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | GWD | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG02630 | hp2 | a0001 | c0001 | t0004 | g0157 | AFR | GWD | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG02647 | hp2 | a0001 | c0002 | t0004 | g0175 | AFR | GWD | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0266 | SAS | PJL | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG02698 | hp2 | a0001 | c0002 | t0001 | g0172 | SAS | PJL | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0119 | AFR | GWD | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG02717 | hp2 | a0001 | c0001 | t0016 | g0101 | AFR | GWD | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG02723 | hp1 | a0001 | c0001 | t0004 | g0031 | AFR | GWD | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG02723 | hp2 | a0001 | c0001 | t0004 | g0007 | AFR | GWD | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG02735 | hp2 | a0001 | c0002 | t0002 | g0179 | SAS | PJL | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0240 | SAS | PJL | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | PJL | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG02809 | hp2 | a0001 | c0001 | t0004 | g0100 | AFR | GWD | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | GWD | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG02818 | hp2 | a0001 | c0003 | t0003 | g0197 | AFR | GWD | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG02886 | hp1 | a0001 | c0008 | t0003 | g0279 | AFR | GWD | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG02886 | hp2 | a0002 | c0004 | t0001 | g0013 | AFR | GWD | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG02895 | hp1 | a0001 | c0003 | t0003 | g0037 | AFR | GWD | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG02895 | hp2 | a0001 | c0001 | t0003 | g0190 | AFR | GWD | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG02896 | hp1 | a0001 | c0003 | t0003 | g0196 | AFR | GWD | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG02897 | hp2 | a0001 | c0003 | t0003 | g0198 | AFR | GWD | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG02922 | hp1 | a0001 | c0001 | t0004 | g0007 | AFR | ESN | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0200 | AFR | ESN | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0118 | AFR | ESN | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0246 | AFR | ESN | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | ESN | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG02976 | hp2 | a0007 | c0014 | t0001 | g0156 | AFR | ESN | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0253 | SAS | PJL | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | GWD | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | GWD | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | MSL | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG03098 | hp2 | a0001 | c0001 | t0004 | g0030 | AFR | MSL | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0242 | AFR | ESN | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG03139 | hp1 | a0002 | c0004 | t0001 | g0013 | AFR | ESN | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0189 | AFR | ESN | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG03195 | hp1 | a0001 | c0001 | t0004 | g0007 | AFR | ESN | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG03195 | hp2 | a0001 | c0001 | t0006 | g0203 | AFR | ESN | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0123 | AFR | MSL | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG03209 | hp2 | a0001 | c0001 | t0004 | g0007 | AFR | MSL | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0027 | AFR | MSL | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG03225 | hp2 | a0001 | c0001 | t0009 | g0193 | AFR | MSL | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0250 | SAS | PJL | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0045 | SAS | PJL | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | MSL | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG03453 | hp2 | a0001 | c0001 | t0004 | g0110 | AFR | MSL | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG03486 | hp1 | a0001 | c0001 | t0003 | g0278 | AFR | MSL | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0117 | AFR | MSL | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0268 | SAS | PJL | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0267 | SAS | PJL | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG03516 | hp1 | a0001 | c0001 | t0004 | g0151 | AFR | ESN | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | ESN | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG03540 | hp1 | a0001 | c0001 | t0004 | g0111 | AFR | GWD | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | GWD | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG03579 | hp1 | a0001 | c0013 | t0001 | g0136 | AFR | MSL | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG03579 | hp2 | a0008 | c0020 | t0004 | g0199 | AFR | MSL | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0258 | SAS | PJL | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0251 | SAS | PJL | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0042 | SAS | PJL | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0262 | SAS | PJL | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0256 | SAS | PJL | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG03710 | hp2 | a0001 | c0002 | t0002 | g0180 | SAS | PJL | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0181 | SAS | BEB | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG03831 | hp2 | a0009 | c0007 | t0001 | g0230 | SAS | BEB | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0231 | SAS | BEB | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG03927 | hp2 | a0001 | c0002 | t0002 | g0036 | SAS | BEB | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0234 | SAS | BEB | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG03942 | hp2 | a0001 | c0002 | t0002 | g0167 | SAS | BEB | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0127 | SAS | STU | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG04115 | hp2 | a0001 | c0002 | t0001 | g0174 | SAS | STU | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0148 | SAS | BEB | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | BEB | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | STU | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | STU | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG04204 | hp1 | a0001 | c0002 | t0001 | g0165 | SAS | STU | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG04204 | hp2 | a0001 | c0002 | t0002 | g0036 | SAS | STU | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG04228 | hp1 | a0001 | c0010 | t0001 | g0029 | SAS | STU | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0122 | AFR | YRI | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA18522 | hp2 | a0010 | c0018 | t0004 | g0031 | AFR | YRI | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | CHB | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | CHB | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | CHB | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA18747 | hp2 | a0001 | c0002 | t0002 | g0170 | EAS | CHB | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA18947 | hp1 | a0001 | c0002 | t0001 | g0032 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA18964 | hp1 | a0001 | c0016 | t0001 | g0216 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA18978 | hp2 | a0001 | c0002 | t0015 | g0169 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA18989 | hp1 | a0001 | c0001 | t0010 | g0206 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA18991 | hp2 | a0001 | c0002 | t0001 | g0161 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA19002 | hp1 | a0001 | c0002 | t0001 | g0158 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA19004 | hp1 | a0001 | c0002 | t0002 | g0173 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA19006 | hp1 | a0001 | c0002 | t0001 | g0163 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA19012 | hp1 | a0001 | c0015 | t0001 | g0084 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | LWK | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA19030 | hp2 | a0001 | c0001 | t0009 | g0202 | AFR | LWK | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA19043 | hp1 | a0001 | c0001 | t0004 | g0115 | AFR | LWK | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA19043 | hp2 | a0011 | c0009 | t0001 | g0045 | AFR | LWK | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA19066 | hp2 | a0001 | c0002 | t0002 | g0022 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA19068 | hp2 | a0001 | c0002 | t0002 | g0022 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA19079 | hp1 | a0001 | c0002 | t0002 | g0022 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA19083 | hp1 | a0001 | c0002 | t0002 | g0166 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA19085 | hp2 | a0001 | c0002 | t0002 | g0033 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA19240 | hp1 | a0001 | c0001 | t0003 | g0124 | AFR | YRI | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | YRI | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA20129 | hp1 | a0001 | c0001 | t0004 | g0116 | AFR | ASW | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA20129 | hp2 | a0001 | c0001 | t0004 | g0113 | AFR | ASW | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA20752 | hp1 | a0001 | c0002 | t0002 | g0035 | EUR | TSI | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0012 | EUR | TSI | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0277 | EUR | TSI | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA20905 | hp1 | a0003 | c0005 | t0001 | g0248 | SAS | GIH | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA20905 | hp2 | a0012 | c0011 | t0001 | g0104 | SAS | GIH | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | CLM | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | CLM | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG02109 | hp1 | a0002 | c0004 | t0001 | g0013 | AFR | ACB | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0026 | AFR | ACB | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG02486 | hp1 | a0001 | c0001 | t0004 | g0114 | AFR | ACB | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | ACB | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG02559 | hp1 | a0001 | c0002 | t0002 | g0112 | AFR | ACB | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | ACB | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG03471 | hp1 | a0001 | c0003 | t0003 | g0088 | AFR | MSL | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0265 | AFR | MSL | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | USA | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0280 | AFR | USA | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0241 | AFR | USA | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | USA | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA21309 | hp1 | a0001 | c0003 | t0003 | g0037 | AFR | LWK | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| NA21309 | hp2 | a0001 | c0001 | t0004 | g0152 | AFR | LWK | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0187 | REF | REF | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0026 | REF | REF | CLSTN3_chr12_7125371_7163945 | CLSTN3 | chr12 | 7125371 | 7163945 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:7130659 | T | A | 1 | a0009 | 1 | HG03831.hp2 | missense_variant | MODERATE | c.11T>A | p.Leu4Gln | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 1/18 | 289/4013 | 11/2871 | 4/956 | chr12 | 7130659 | |||
| chr12:7130691 | G | T | 1 | a0003 | 4 | HG01109.hp1 HG02280.hp1 HG02451.hp1 others(1): Show |
missense_variant | MODERATE | c.43G>T | p.Ala15Ser | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 1/18 | 321/4013 | 43/2871 | 15/956 | chr12 | 7130691 | |||
| chr12:7133660 | G | A | 1 | a0011 | 1 | NA19043.hp2 | missense_variant | MODERATE | c.275G>A | p.Arg92Gln | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 3/18 | 553/4013 | 275/2871 | 92/956 | chr12 | 7133660 | |||
| chr12:7135836 | A | G | 1 | a0002 | 5 | HG00639.hp2 HG02109.hp1 HG02602.hp2 others(2): Show |
missense_variant | MODERATE | c.625A>G | p.Ser209Gly | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 5/18 | 903/4013 | 625/2871 | 209/956 | chr12 | 7135836 | |||
| chr12:7136241 | G | A | 1 | a0012 | 1 | NA20905.hp2 | missense_variant | MODERATE | c.778G>A | p.Gly260Arg | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 6/18 | 1056/4013 | 778/2871 | 260/956 | chr12 | 7136241 | |||
| chr12:7137089 | G | A | 1 | a0008 | 1 | HG03579.hp2 | missense_variant | MODERATE | c.1189G>A | p.Val397Ile | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 7/18 | 1467/4013 | 1189/2871 | 397/956 | chr12 | 7137089 | |||
| chr12:7137990 | G | A | 1 | a0006 | 1 | HG02015.hp2 | missense_variant | MODERATE | c.1246G>A | p.Gly416Ser | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 8/18 | 1524/4013 | 1246/2871 | 416/956 | chr12 | 7137990 | |||
| chr12:7149534 | C | T | 1 | a0010 | 1 | NA18522.hp2 | missense_variant | MODERATE | c.2086C>T | p.Arg696Cys | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 14/18 | 2364/4013 | 2086/2871 | 696/956 | chr12 | 7149534 | |||
| chr12:7151023 | G | C | 1 | a0004 | 2 | HG01168.hp2 HG01169.hp2 |
missense_variant | MODERATE | c.2487G>C | p.Glu829Asp | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 16/18 | 2765/4013 | 2487/2871 | 829/956 | chr12 | 7151023 | |||
| chr12:7158014 | C | T | 1 | a0005 | 1 | HG01891.hp1 | missense_variant | MODERATE | c.2804C>T | p.Ser935Leu | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 18/18 | 3082/4013 | 2804/2871 | 935/956 | chr12 | 7158014 | |||
| chr12:7158062 | C | A | 1 | a0007 | 1 | HG02976.hp2 | missense_variant | MODERATE | c.2852C>A | p.Thr951Asn | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 18/18 | 3130/4013 | 2852/2871 | 951/956 | chr12 | 7158062 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:7133133 | G | A | 1 | a0001c0008 | 1 | HG02886.hp1 | synonymous_variant | LOW | c.174G>A | p.Pro58Pro | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 2/18 | 452/4013 | 174/2871 | 58/956 | chr12 | 7133133 | |||
| chr12:7135360 | C | T | 5 | a0001c0002 a0001c0003 a0001c0022 others(2): Show |
46 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(43): Show |
synonymous_variant | LOW | c.417C>T | p.Asn139Asn | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 4/18 | 695/4013 | 417/2871 | 139/956 | chr12 | 7135360 | |||
| chr12:7136213 | C | T | 1 | a0001c0022 | 1 | HG02083.hp2 | synonymous_variant | LOW | c.750C>T | p.Asn250Asn | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 6/18 | 1028/4013 | 750/2871 | 250/956 | chr12 | 7136213 | |||
| chr12:7136240 | T | C | 1 | a0001c0010 | 1 | HG04228.hp1 | synonymous_variant | LOW | c.777T>C | p.Ala259Ala | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 6/18 | 1055/4013 | 777/2871 | 259/956 | chr12 | 7136240 | |||
| chr12:7141268 | C | T | 1 | a0001c0019 | 1 | HG01496.hp2 | synonymous_variant | LOW | c.1350C>T | p.Tyr450Tyr | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 9/18 | 1628/4013 | 1350/2871 | 450/956 | chr12 | 7141268 | |||
| chr12:7143276 | C | T | 2 | a0001c0003 a0005c0021 |
7 | HG01891.hp1 HG02818.hp2 HG02895.hp1 others(4): Show |
synonymous_variant | LOW | c.1812C>T | p.Pro604Pro | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 12/18 | 2090/4013 | 1812/2871 | 604/956 | chr12 | 7143276 | |||
| chr12:7149623 | C | T | 1 | a0001c0017 | 1 | HG02080.hp2 | synonymous_variant | LOW | c.2175C>T | p.Leu725Leu | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 14/18 | 2453/4013 | 2175/2871 | 725/956 | chr12 | 7149623 | |||
| chr12:7150617 | C | T | 1 | a0001c0016 | 1 | NA18964.hp1 | synonymous_variant | LOW | c.2319C>T | p.Leu773Leu | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 15/18 | 2597/4013 | 2319/2871 | 773/956 | chr12 | 7150617 | |||
| chr12:7157601 | C | T | 1 | a0001c0015 | 1 | NA19012.hp1 | synonymous_variant | LOW | c.2640C>T | p.Ala880Ala | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 17/18 | 2918/4013 | 2640/2871 | 880/956 | chr12 | 7157601 | |||
| chr12:7158015 | G | A | 1 | a0001c0013 | 1 | HG03579.hp1 | synonymous_variant | LOW | c.2805G>A | p.Ser935Ser | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 18/18 | 3083/4013 | 2805/2871 | 935/956 | chr12 | 7158015 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:7130497 | G | T | 1 | a0001c0001t0016 | 1 | HG02717.hp2 | 5_prime_UTR_variant | MODIFIER | c.-152G>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 1/18 | 152 | chr12 | 7130497 | ||||||
| chr12:7130538 | T | A | 2 | a0001c0001t0005 a0001c0001t0006 |
10 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(7): Show |
5_prime_UTR_variant | MODIFIER | c.-111T>A | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 1/18 | 111 | chr12 | 7130538 | ||||||
| chr12:7130614 | C | G | 1 | a0001c0002t0015 | 1 | NA18978.hp2 | 5_prime_UTR_variant | MODIFIER | c.-35C>G | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 1/18 | 35 | chr12 | 7130614 | ||||||
| chr12:7130615 | A | C | 1 | a0001c0002t0015 | 1 | NA18978.hp2 | 5_prime_UTR_variant | MODIFIER | c.-34A>C | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 1/18 | 34 | chr12 | 7130615 | ||||||
| chr12:7158178 | G | C | 6 | a0001c0001t0002 a0001c0002t0002 a0001c0002t0007 others(3): Show |
33 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*97G>C | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 18/18 | 97 | chr12 | 7158178 | ||||||
| chr12:7158183 | A | T | 1 | a0001c0001t0014 | 1 | HG00438.hp2 | 3_prime_UTR_variant | MODIFIER | c.*102A>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 18/18 | 102 | chr12 | 7158183 | ||||||
| chr12:7158259 | C | T | 1 | a0001c0001t0013 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*178C>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 18/18 | 178 | chr12 | 7158259 | ||||||
| chr12:7158421 | T | TGGCTGG | 22 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0008 others(19): Show |
307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
3_prime_UTR_variant | MODIFIER | c.*355_*360dupCTGGGG | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 18/18 | 361 | INFO_REALIGN_3_PRIME | chr12 | 7158421 | |||||
| chr12:7158495 | G | T | 1 | a0001c0002t0007 | 2 | HG00597.hp1 HG02155.hp1 |
3_prime_UTR_variant | MODIFIER | c.*414G>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 18/18 | 414 | chr12 | 7158495 | ||||||
| chr12:7158539 | G | A | 1 | a0001c0001t0009 | 2 | HG03225.hp2 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*458G>A | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 18/18 | 458 | chr12 | 7158539 | ||||||
| chr12:7158663 | G | A | 1 | a0001c0001t0010 | 1 | NA18989.hp1 | 3_prime_UTR_variant | MODIFIER | c.*582G>A | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 18/18 | 582 | chr12 | 7158663 | ||||||
| chr12:7158664 | T | C | 1 | a0001c0001t0010 | 1 | NA18989.hp1 | 3_prime_UTR_variant | MODIFIER | c.*583T>C | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 18/18 | 583 | chr12 | 7158664 | ||||||
| chr12:7158667 | T | C | 1 | a0001c0001t0010 | 1 | NA18989.hp1 | 3_prime_UTR_variant | MODIFIER | c.*586T>C | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 18/18 | 586 | chr12 | 7158667 | ||||||
| chr12:7158668 | G | C | 1 | a0001c0001t0010 | 1 | NA18989.hp1 | 3_prime_UTR_variant | MODIFIER | c.*587G>C | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 18/18 | 587 | chr12 | 7158668 | ||||||
| chr12:7158670 | A | T | 1 | a0001c0001t0010 | 1 | NA18989.hp1 | 3_prime_UTR_variant | MODIFIER | c.*589A>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 18/18 | 589 | chr12 | 7158670 | ||||||
| chr12:7158675 | C | T | 1 | a0001c0001t0008 | 2 | HG01069.hp2 HG01943.hp1 |
3_prime_UTR_variant | MODIFIER | c.*594C>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 18/18 | 594 | chr12 | 7158675 | ||||||
| chr12:7158676 | G | T | 1 | a0001c0001t0010 | 1 | NA18989.hp1 | 3_prime_UTR_variant | MODIFIER | c.*595G>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 18/18 | 595 | chr12 | 7158676 | ||||||
| chr12:7158677 | G | C | 1 | a0001c0001t0010 | 1 | NA18989.hp1 | 3_prime_UTR_variant | MODIFIER | c.*596G>C | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 18/18 | 596 | chr12 | 7158677 | ||||||
| chr12:7158685 | T | A | 1 | a0001c0001t0010 | 1 | NA18989.hp1 | 3_prime_UTR_variant | MODIFIER | c.*604T>A | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 18/18 | 604 | chr12 | 7158685 | ||||||
| chr12:7158690 | G | C | 1 | a0001c0001t0010 | 1 | NA18989.hp1 | 3_prime_UTR_variant | MODIFIER | c.*609G>C | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 18/18 | 609 | chr12 | 7158690 | ||||||
| chr12:7158691 | A | C | 1 | a0001c0001t0010 | 1 | NA18989.hp1 | 3_prime_UTR_variant | MODIFIER | c.*610A>C | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 18/18 | 610 | chr12 | 7158691 | ||||||
| chr12:7158695 | G | C | 1 | a0001c0001t0010 | 1 | NA18989.hp1 | 3_prime_UTR_variant | MODIFIER | c.*614G>C | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 18/18 | 614 | chr12 | 7158695 | ||||||
| chr12:7158698 | G | T | 1 | a0001c0001t0010 | 1 | NA18989.hp1 | 3_prime_UTR_variant | MODIFIER | c.*617G>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 18/18 | 617 | chr12 | 7158698 | ||||||
| chr12:7158699 | T | C | 1 | a0001c0001t0010 | 1 | NA18989.hp1 | 3_prime_UTR_variant | MODIFIER | c.*618T>C | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 18/18 | 618 | chr12 | 7158699 | ||||||
| chr12:7158700 | G | T | 1 | a0001c0001t0010 | 1 | NA18989.hp1 | 3_prime_UTR_variant | MODIFIER | c.*619G>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 18/18 | 619 | chr12 | 7158700 | ||||||
| chr12:7158701 | G | C | 1 | a0001c0001t0010 | 1 | NA18989.hp1 | 3_prime_UTR_variant | MODIFIER | c.*620G>C | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 18/18 | 620 | chr12 | 7158701 | ||||||
| chr12:7158708 | T | C | 1 | a0001c0001t0010 | 1 | NA18989.hp1 | 3_prime_UTR_variant | MODIFIER | c.*627T>C | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 18/18 | 627 | chr12 | 7158708 | ||||||
| chr12:7158709 | G | C | 1 | a0001c0001t0010 | 1 | NA18989.hp1 | 3_prime_UTR_variant | MODIFIER | c.*628G>C | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 18/18 | 628 | chr12 | 7158709 | ||||||
| chr12:7158711 | G | C | 1 | a0001c0001t0010 | 1 | NA18989.hp1 | 3_prime_UTR_variant | MODIFIER | c.*630G>C | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 18/18 | 630 | chr12 | 7158711 | ||||||
| chr12:7158712 | G | C | 1 | a0001c0001t0010 | 1 | NA18989.hp1 | 3_prime_UTR_variant | MODIFIER | c.*631G>C | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 18/18 | 631 | chr12 | 7158712 | ||||||
| chr12:7158713 | G | T | 1 | a0001c0001t0010 | 1 | NA18989.hp1 | 3_prime_UTR_variant | MODIFIER | c.*632G>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 18/18 | 632 | chr12 | 7158713 | ||||||
| chr12:7158715 | A | T | 1 | a0001c0001t0010 | 1 | NA18989.hp1 | 3_prime_UTR_variant | MODIFIER | c.*634A>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 18/18 | 634 | chr12 | 7158715 | ||||||
| chr12:7158717 | G | T | 1 | a0001c0001t0010 | 1 | NA18989.hp1 | 3_prime_UTR_variant | MODIFIER | c.*636G>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 18/18 | 636 | chr12 | 7158717 | ||||||
| chr12:7158719 | G | T | 1 | a0001c0001t0010 | 1 | NA18989.hp1 | 3_prime_UTR_variant | MODIFIER | c.*638G>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 18/18 | 638 | chr12 | 7158719 | ||||||
| chr12:7158720 | A | C | 1 | a0001c0001t0010 | 1 | NA18989.hp1 | 3_prime_UTR_variant | MODIFIER | c.*639A>C | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 18/18 | 639 | chr12 | 7158720 | ||||||
| chr12:7158722 | G | C | 1 | a0001c0001t0010 | 1 | NA18989.hp1 | 3_prime_UTR_variant | MODIFIER | c.*641G>C | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 18/18 | 641 | chr12 | 7158722 | ||||||
| chr12:7158723 | G | A | 1 | a0001c0001t0010 | 1 | NA18989.hp1 | 3_prime_UTR_variant | MODIFIER | c.*642G>A | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 18/18 | 642 | chr12 | 7158723 | ||||||
| chr12:7158724 | G | C | 1 | a0001c0001t0010 | 1 | NA18989.hp1 | 3_prime_UTR_variant | MODIFIER | c.*643G>C | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 18/18 | 643 | chr12 | 7158724 | ||||||
| chr12:7158725 | A | C | 1 | a0001c0001t0010 | 1 | NA18989.hp1 | 3_prime_UTR_variant | MODIFIER | c.*644A>C | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 18/18 | 644 | chr12 | 7158725 | ||||||
| chr12:7158727 | G | C | 1 | a0001c0001t0010 | 1 | NA18989.hp1 | 3_prime_UTR_variant | MODIFIER | c.*646G>C | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 18/18 | 646 | chr12 | 7158727 | ||||||
| chr12:7158728 | T | C | 1 | a0001c0001t0010 | 1 | NA18989.hp1 | 3_prime_UTR_variant | MODIFIER | c.*647T>C | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 18/18 | 647 | chr12 | 7158728 | ||||||
| chr12:7158729 | G | C | 1 | a0001c0001t0010 | 1 | NA18989.hp1 | 3_prime_UTR_variant | MODIFIER | c.*648G>C | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 18/18 | 648 | chr12 | 7158729 | ||||||
| chr12:7158730 | G | C | 1 | a0001c0001t0010 | 1 | NA18989.hp1 | 3_prime_UTR_variant | MODIFIER | c.*649G>C | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 18/18 | 649 | chr12 | 7158730 | ||||||
| chr12:7158731 | G | C | 1 | a0001c0001t0010 | 1 | NA18989.hp1 | 3_prime_UTR_variant | MODIFIER | c.*650G>C | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 18/18 | 650 | chr12 | 7158731 | ||||||
| chr12:7158732 | G | C | 1 | a0001c0001t0010 | 1 | NA18989.hp1 | 3_prime_UTR_variant | MODIFIER | c.*651G>C | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 18/18 | 651 | chr12 | 7158732 | ||||||
| chr12:7158733 | G | C | 1 | a0001c0001t0010 | 1 | NA18989.hp1 | 3_prime_UTR_variant | MODIFIER | c.*652G>C | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 18/18 | 652 | chr12 | 7158733 | ||||||
| chr12:7158734 | C | T | 1 | a0001c0001t0010 | 1 | NA18989.hp1 | 3_prime_UTR_variant | MODIFIER | c.*653C>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 18/18 | 653 | chr12 | 7158734 | ||||||
| chr12:7158736 | C | T | 1 | a0001c0001t0010 | 1 | NA18989.hp1 | 3_prime_UTR_variant | MODIFIER | c.*655C>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 18/18 | 655 | chr12 | 7158736 | ||||||
| chr12:7158738 | G | A | 12 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 others(9): Show |
59 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*657G>A | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 18/18 | 657 | chr12 | 7158738 | ||||||
| chr12:7158740 | G | T | 1 | a0001c0001t0010 | 1 | NA18989.hp1 | 3_prime_UTR_variant | MODIFIER | c.*659G>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 18/18 | 659 | chr12 | 7158740 | ||||||
| chr12:7158742 | G | C | 1 | a0001c0001t0010 | 1 | NA18989.hp1 | 3_prime_UTR_variant | MODIFIER | c.*661G>C | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 18/18 | 661 | chr12 | 7158742 | ||||||
| chr12:7158746 | A | C | 1 | a0001c0001t0010 | 1 | NA18989.hp1 | 3_prime_UTR_variant | MODIFIER | c.*665A>C | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 18/18 | 665 | chr12 | 7158746 | ||||||
| chr12:7158748 | A | C | 1 | a0001c0001t0010 | 1 | NA18989.hp1 | 3_prime_UTR_variant | MODIFIER | c.*667A>C | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 18/18 | 667 | chr12 | 7158748 | ||||||
| chr12:7158751 | T | C | 1 | a0001c0001t0010 | 1 | NA18989.hp1 | 3_prime_UTR_variant | MODIFIER | c.*670T>C | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 18/18 | 670 | chr12 | 7158751 | ||||||
| chr12:7158753 | A | T | 1 | a0001c0001t0010 | 1 | NA18989.hp1 | 3_prime_UTR_variant | MODIFIER | c.*672A>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 18/18 | 672 | chr12 | 7158753 | ||||||
| chr12:7158754 | T | G | 1 | a0001c0001t0010 | 1 | NA18989.hp1 | 3_prime_UTR_variant | MODIFIER | c.*673T>G | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 18/18 | 673 | chr12 | 7158754 | ||||||
| chr12:7158758 | T | G | 1 | a0001c0001t0010 | 1 | NA18989.hp1 | 3_prime_UTR_variant | MODIFIER | c.*677T>G | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 18/18 | 677 | chr12 | 7158758 | ||||||
| chr12:7158760 | T | G | 1 | a0001c0001t0010 | 1 | NA18989.hp1 | 3_prime_UTR_variant | MODIFIER | c.*679T>G | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 18/18 | 679 | chr12 | 7158760 | ||||||
| chr12:7158761 | T | C | 1 | a0001c0001t0010 | 1 | NA18989.hp1 | 3_prime_UTR_variant | MODIFIER | c.*680T>C | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 18/18 | 680 | chr12 | 7158761 | ||||||
| chr12:7158822 | ATG | A | 22 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0008 others(19): Show |
307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
3_prime_UTR_variant | MODIFIER | c.*762_*763delTG | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 18/18 | 762 | INFO_REALIGN_3_PRIME | chr12 | 7158822 | |||||
| chr12:7158887 | G | A | 1 | a0001c0001t0012 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*806G>A | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 18/18 | 806 | chr12 | 7158887 | ||||||
| chr12:7158912 | G | C | 1 | a0001c0001t0011 | 1 | HG01346.hp1 | 3_prime_UTR_variant | MODIFIER | c.*831G>C | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 18/18 | 831 | chr12 | 7158912 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:7130845 | C | G | 2 | a0001c0001t0001g0281 a0001c0001t0001g0282 |
2 | NA18990.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.64+133C>G | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 1/17 | chr12 | 7130845 | |||||||
| chr12:7130926 | G | T | 3 | a0001c0001t0003g0278 a0001c0001t0003g0280 a0001c0008t0003g0279 |
3 | HG02886.hp1 HG03486.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.64+214G>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 1/17 | chr12 | 7130926 | |||||||
| chr12:7131050 | G | A | 66 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(63): Show |
96 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.64+338G>A | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 1/17 | chr12 | 7131050 | |||||||
| chr12:7131093 | C | T | 1 | a0001c0001t0001g0049 | 2 | HG01243.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.64+381C>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 1/17 | chr12 | 7131093 | |||||||
| chr12:7131310 | A | G | 5 | a0001c0001t0001g0048 a0001c0001t0001g0274 a0001c0001t0001g0275 others(2): Show |
6 | HG00642.hp2 HG01192.hp2 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.64+598A>G | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 1/17 | chr12 | 7131310 | |||||||
| chr12:7131485 | G | A | 65 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(62): Show |
96 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.64+773G>A | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 1/17 | chr12 | 7131485 | |||||||
| chr12:7131705 | C | T | 176 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(173): Show |
250 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.64+993C>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 1/17 | chr12 | 7131705 | |||||||
| chr12:7131744 | C | CGCCTCCT others(1): Show |
76 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(73): Show |
109 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.64+1040_64+1047dup others(8): Show |
CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 7131744 | ||||||
| chr12:7131765 | T | G | 1 | a0008c0020t0004g0199 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.64+1053T>G | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 1/17 | chr12 | 7131765 | |||||||
| chr12:7131888 | A | C | 272 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(269): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.65-1136A>C | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 1/17 | chr12 | 7131888 | |||||||
| chr12:7131898 | ATCAGGGT others(7): Show |
A | 2 | a0001c0001t0001g0051 a0006c0012t0001g0050 |
2 | HG02015.hp2 HG02040.hp2 |
intron_variant | MODIFIER | c.65-1122_65-1109del others(14): Show |
CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 7131898 | ||||||
| chr12:7131909 | T | C | 1 | a0001c0001t0001g0019 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.65-1115T>C | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 1/17 | chr12 | 7131909 | |||||||
| chr12:7131918 | G | A | 1 | a0006c0012t0001g0050 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.65-1106G>A | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 1/17 | chr12 | 7131918 | |||||||
| chr12:7132024 | G | A | 1 | a0001c0001t0001g0038 | 2 | HG01106.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.65-1000G>A | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 1/17 | chr12 | 7132024 | |||||||
| chr12:7132041 | G | C | 3 | a0001c0001t0006g0201 a0001c0001t0006g0203 a0001c0001t0009g0202 |
3 | HG01884.hp2 HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.65-983G>C | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 1/17 | chr12 | 7132041 | |||||||
| chr12:7132097 | C | G | 3 | a0001c0001t0003g0189 a0001c0001t0003g0190 a0001c0001t0004g0113 |
3 | HG02895.hp2 HG03139.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.65-927C>G | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 1/17 | chr12 | 7132097 | |||||||
| chr12:7132212 | A | G | 2 | a0001c0001t0003g0189 a0001c0001t0003g0190 |
2 | HG02895.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.65-812A>G | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 1/17 | chr12 | 7132212 | |||||||
| chr12:7132339 | G | A | 35 | a0001c0001t0001g0023 a0001c0001t0001g0039 a0001c0001t0001g0040 others(32): Show |
43 | HG00099.hp1 HG00597.hp2 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.65-685G>A | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 1/17 | chr12 | 7132339 | |||||||
| chr12:7132745 | T | C | 8 | a0001c0001t0003g0278 a0001c0001t0003g0280 a0001c0001t0004g0113 others(5): Show |
8 | HG01884.hp2 HG02886.hp1 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.65-279T>C | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 1/17 | chr12 | 7132745 | |||||||
| chr12:7132886 | C | T | 6 | a0001c0001t0005g0182 a0001c0001t0005g0183 a0001c0001t0005g0184 others(3): Show |
6 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(3): Show |
intron_variant | MODIFIER | c.65-138C>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 1/17 | chr12 | 7132886 | |||||||
| chr12:7132931 | T | C | 8 | a0001c0001t0003g0278 a0001c0001t0003g0280 a0001c0001t0004g0113 others(5): Show |
8 | HG01884.hp2 HG02886.hp1 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.65-93T>C | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 1/17 | chr12 | 7132931 | |||||||
| chr12:7132970 | G | A | 2 | a0001c0001t0004g0110 a0001c0001t0004g0111 |
2 | HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.65-54G>A | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 1/17 | chr12 | 7132970 | |||||||
| chr12:7133300 | A | G | 2 | a0001c0001t0001g0106 a0001c0001t0001g0107 |
2 | HG00738.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.187+154A>G | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 2/17 | chr12 | 7133300 | |||||||
| chr12:7133323 | A | C | 1 | a0001c0001t0001g0181 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.187+177A>C | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 2/17 | chr12 | 7133323 | |||||||
| chr12:7133356 | A | G | 1 | a0001c0001t0001g0049 | 2 | HG01243.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.187+210A>G | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 2/17 | chr12 | 7133356 | |||||||
| chr12:7133515 | A | G | 8 | a0001c0001t0003g0278 a0001c0001t0003g0280 a0001c0001t0004g0113 others(5): Show |
8 | HG01884.hp2 HG02886.hp1 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.188-58A>G | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 2/17 | chr12 | 7133515 | |||||||
| chr12:7133550 | C | G | 3 | a0001c0001t0001g0049 a0001c0001t0004g0110 a0001c0001t0004g0111 |
4 | HG01243.hp2 HG03453.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.188-23C>G | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 2/17 | chr12 | 7133550 | |||||||
| chr12:7133995 | C | T | 2 | a0001c0001t0001g0090 a0001c0001t0011g0091 |
2 | HG01346.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.383+227C>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 3/17 | chr12 | 7133995 | |||||||
| chr12:7134025 | C | T | 1 | a0001c0001t0013g0089 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.383+257C>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 3/17 | chr12 | 7134025 | |||||||
| chr12:7134108 | T | C | 1 | a0001c0001t0004g0113 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.383+340T>C | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 3/17 | chr12 | 7134108 | |||||||
| chr12:7134205 | A | C | 1 | a0001c0001t0005g0188 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.383+437A>C | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 3/17 | chr12 | 7134205 | |||||||
| chr12:7134288 | C | T | 2 | a0001c0001t0004g0110 a0001c0001t0004g0111 |
2 | HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.383+520C>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 3/17 | chr12 | 7134288 | |||||||
| chr12:7134338 | G | T | 2 | a0003c0005t0002g0272 a0003c0005t0002g0273 |
2 | HG01109.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.383+570G>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 3/17 | chr12 | 7134338 | |||||||
| chr12:7134447 | T | C | 1 | a0001c0001t0001g0125 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.383+679T>C | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 3/17 | chr12 | 7134447 | |||||||
| chr12:7134587 | G | T | 3 | a0001c0001t0003g0278 a0001c0001t0003g0280 a0001c0008t0003g0279 |
3 | HG02886.hp1 HG03486.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.384-740G>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 3/17 | chr12 | 7134587 | |||||||
| chr12:7134638 | A | G | 6 | a0001c0001t0003g0278 a0001c0001t0003g0280 a0001c0001t0006g0201 others(3): Show |
6 | HG01884.hp2 HG02886.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.384-689A>G | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 3/17 | chr12 | 7134638 | |||||||
| chr12:7134804 | G | A | 6 | a0001c0001t0003g0278 a0001c0001t0003g0280 a0001c0001t0006g0201 others(3): Show |
6 | HG01884.hp2 HG02886.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.384-523G>A | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 3/17 | chr12 | 7134804 | |||||||
| chr12:7134816 | G | A | 3 | a0001c0001t0006g0201 a0001c0001t0006g0203 a0001c0001t0009g0202 |
3 | HG01884.hp2 HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.384-511G>A | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 3/17 | chr12 | 7134816 | |||||||
| chr12:7134858 | C | T | 1 | a0009c0007t0001g0230 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.384-469C>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 3/17 | chr12 | 7134858 | |||||||
| chr12:7135026 | C | T | 39 | a0001c0002t0001g0032 a0001c0002t0001g0158 a0001c0002t0001g0160 others(36): Show |
46 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(43): Show |
intron_variant | MODIFIER | c.384-301C>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 3/17 | chr12 | 7135026 | |||||||
| chr12:7135100 | C | T | 6 | a0001c0003t0003g0037 a0001c0003t0003g0088 a0001c0003t0003g0196 others(3): Show |
7 | HG01891.hp1 HG02818.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.384-227C>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 3/17 | chr12 | 7135100 | |||||||
| chr12:7135157 | A | G | 10 | a0001c0001t0003g0278 a0001c0001t0003g0280 a0001c0001t0004g0110 others(7): Show |
10 | HG01884.hp2 HG02886.hp1 HG03195.hp2 others(7): Show |
intron_variant | MODIFIER | c.384-170A>G | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 3/17 | chr12 | 7135157 | |||||||
| chr12:7135187 | C | T | 2 | a0001c0001t0001g0090 a0001c0001t0011g0091 |
2 | HG01346.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.384-140C>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 3/17 | chr12 | 7135187 | |||||||
| chr12:7135222 | G | A | 1 | a0001c0001t0001g0181 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.384-105G>A | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 3/17 | chr12 | 7135222 | |||||||
| chr12:7135290 | A | C | 164 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(161): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.384-37A>C | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 3/17 | chr12 | 7135290 | |||||||
| chr12:7135318 | C | T | 194 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(191): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.384-9C>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 3/17 | chr12 | 7135318 | |||||||
| chr12:7135323 | G | T | 2 | a0001c0001t0001g0228 a0001c0001t0001g0229 |
2 | NA18968.hp1 NA19078.hp2 |
splice_region_variant&intron_variant | LOW | c.384-4G>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 3/17 | chr12 | 7135323 | |||||||
| chr12:7135636 | C | T | 1 | a0001c0001t0009g0193 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.592+101C>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 4/17 | chr12 | 7135636 | |||||||
| chr12:7135652 | T | C | 1 | a0001c0001t0001g0204 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.592+117T>C | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 4/17 | chr12 | 7135652 | |||||||
| chr12:7135673 | T | C | 1 | a0001c0001t0001g0232 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.593-131T>C | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 4/17 | chr12 | 7135673 | |||||||
| chr12:7135674 | C | T | 1 | a0001c0001t0001g0232 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.593-130C>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 4/17 | chr12 | 7135674 | |||||||
| chr12:7135682 | C | G | 2 | a0001c0001t0003g0189 a0001c0001t0003g0190 |
2 | HG02895.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.593-122C>G | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 4/17 | chr12 | 7135682 | |||||||
| chr12:7135696 | G | A | 1 | a0001c0001t0004g0113 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.593-108G>A | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 4/17 | chr12 | 7135696 | |||||||
| chr12:7135723 | C | T | 15 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0154 others(12): Show |
20 | HG02055.hp1 HG02055.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.593-81C>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 4/17 | chr12 | 7135723 | |||||||
| chr12:7135998 | C | T | 1 | a0001c0001t0001g0227 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.742+45C>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 5/17 | chr12 | 7135998 | |||||||
| chr12:7136078 | A | G | 1 | a0001c0001t0001g0271 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.742+125A>G | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 5/17 | chr12 | 7136078 | |||||||
| chr12:7136090 | C | A | 41 | a0001c0001t0003g0189 a0001c0001t0003g0190 a0001c0002t0001g0032 others(38): Show |
48 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(45): Show |
intron_variant | MODIFIER | c.743-116C>A | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 5/17 | chr12 | 7136090 | |||||||
| chr12:7136138 | G | A | 73 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(70): Show |
104 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.743-68G>A | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 5/17 | chr12 | 7136138 | |||||||
| chr12:7136405 | C | T | 2 | a0001c0001t0004g0110 a0001c0001t0004g0111 |
2 | HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.928+14C>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 6/17 | chr12 | 7136405 | |||||||
| chr12:7136564 | A | G | 39 | a0001c0002t0001g0032 a0001c0002t0001g0158 a0001c0002t0001g0160 others(36): Show |
46 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(43): Show |
intron_variant | MODIFIER | c.928+173A>G | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 6/17 | chr12 | 7136564 | |||||||
| chr12:7136592 | T | A | 6 | a0001c0001t0001g0039 a0001c0001t0001g0205 a0001c0001t0001g0207 others(3): Show |
7 | HG02027.hp2 NA18612.hp1 NA18941.hp2 others(4): Show |
intron_variant | MODIFIER | c.928+201T>A | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 6/17 | chr12 | 7136592 | |||||||
| chr12:7136596 | C | T | 6 | a0001c0001t0004g0030 a0001c0001t0004g0031 a0001c0001t0004g0157 others(3): Show |
7 | HG02145.hp1 HG02630.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.928+205C>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 6/17 | chr12 | 7136596 | |||||||
| chr12:7137163 | G | A | 4 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0094 others(1): Show |
4 | HG02165.hp1 NA18962.hp2 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.1210+53G>A | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 7/17 | chr12 | 7137163 | |||||||
| chr12:7137228 | C | T | 2 | a0001c0002t0002g0036 a0001c0002t0002g0180 |
3 | HG03710.hp2 HG03927.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1210+118C>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 7/17 | chr12 | 7137228 | |||||||
| chr12:7137604 | T | G | 73 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(70): Show |
104 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.1211-351T>G | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 7/17 | chr12 | 7137604 | |||||||
| chr12:7137625 | G | T | 1 | a0001c0001t0004g0113 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1211-330G>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 7/17 | chr12 | 7137625 | |||||||
| chr12:7137756 | A | ATG | 14 | a0001c0001t0001g0266 a0001c0001t0001g0267 a0001c0001t0001g0268 others(11): Show |
15 | HG00738.hp1 HG01358.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.1211-160_1211-159d others(4): Show |
CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 7137756 | ||||||
| chr12:7137756 | A | ATGTG | 4 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0269 others(1): Show |
4 | HG01081.hp1 HG02055.hp1 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.1211-162_1211-159d others(6): Show |
CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 7137756 | ||||||
| chr12:7137756 | A | ATGTGTG | 3 | a0001c0001t0001g0086 a0001c0001t0003g0123 a0001c0001t0003g0124 |
3 | HG03098.hp1 HG03209.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1211-164_1211-159d others(8): Show |
CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 7137756 | ||||||
| chr12:7137756 | A | ATGTGTGT others(3): Show |
1 | a0001c0001t0001g0049 | 2 | HG01243.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1211-168_1211-159d others(12): Show |
CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 7137756 | ||||||
| chr12:7137756 | A | ATGTGTGT others(7): Show |
1 | a0001c0001t0001g0087 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1211-172_1211-159d others(16): Show |
CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 7137756 | ||||||
| chr12:7137756 | ATG | A | 4 | a0001c0001t0004g0007 a0001c0001t0004g0100 a0001c0001t0005g0182 others(1): Show |
8 | HG00140.hp1 HG01243.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1211-160_1211-159d others(4): Show |
CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 7137756 | ||||||
| chr12:7137781 | TGTGTGTG others(9): Show |
T | 1 | a0001c0001t0013g0089 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1211-172_1211-157d others(18): Show |
CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 7137781 | ||||||
| chr12:7137787 | T | A | 2 | a0001c0001t0003g0189 a0001c0001t0003g0190 |
2 | HG02895.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1211-168T>A | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 7/17 | chr12 | 7137787 | |||||||
| chr12:7137789 | T | A | 2 | a0001c0001t0003g0189 a0001c0001t0003g0190 |
2 | HG02895.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1211-166T>A | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 7/17 | chr12 | 7137789 | |||||||
| chr12:7137791 | T | A | 2 | a0001c0001t0003g0189 a0001c0001t0003g0190 |
2 | HG02895.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1211-164T>A | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 7/17 | chr12 | 7137791 | |||||||
| chr12:7137793 | T | A | 2 | a0001c0001t0003g0189 a0001c0001t0003g0190 |
2 | HG02895.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1211-162T>A | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 7/17 | chr12 | 7137793 | |||||||
| chr12:7137793 | T | TGA | 6 | a0001c0001t0001g0012 a0001c0001t0001g0127 a0001c0001t0001g0129 others(3): Show |
8 | HG00639.hp1 HG01070.hp1 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.1211-161_1211-160i others(4): Show |
CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 7137793 | ||||||
| chr12:7137795 | T | A | 10 | a0001c0001t0001g0012 a0001c0001t0001g0127 a0001c0001t0001g0129 others(7): Show |
13 | HG00140.hp1 HG00639.hp1 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.1211-160T>A | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 7/17 | chr12 | 7137795 | |||||||
| chr12:7137795 | T | TGA | 31 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(28): Show |
54 | HG00438.hp2 HG00558.hp1 HG00738.hp2 others(51): Show |
intron_variant | MODIFIER | c.1211-134_1211-133d others(4): Show |
CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 7137795 | ||||||
| chr12:7137795 | T | TGTGA | 16 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0029 others(13): Show |
17 | HG00099.hp2 HG00323.hp1 HG00621.hp1 others(14): Show |
intron_variant | MODIFIER | c.1211-159_1211-158i others(6): Show |
CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 7137795 | ||||||
| chr12:7137795 | T | TGTGAGA | 27 | a0001c0001t0001g0255 a0001c0001t0001g0271 a0001c0002t0001g0158 others(24): Show |
31 | HG00423.hp1 HG00597.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.1211-159_1211-158i others(8): Show |
CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 7137795 | ||||||
| chr12:7137795 | T | TGTGTGA | 26 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(23): Show |
32 | HG01081.hp2 HG01167.hp2 HG01192.hp1 others(29): Show |
intron_variant | MODIFIER | c.1211-159_1211-158i others(8): Show |
CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 7137795 | ||||||
| chr12:7137795 | T | TGTGTGAG others(1): Show |
31 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(28): Show |
33 | HG00140.hp2 HG00280.hp2 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.1211-159_1211-158i others(10): Show |
CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 7137795 | ||||||
| chr12:7137795 | T | TGTGTGAG others(3): Show |
2 | a0001c0001t0001g0010 a0002c0004t0001g0013 |
2 | HG00280.hp1 HG00639.hp2 |
intron_variant | MODIFIER | c.1211-159_1211-158i others(12): Show |
CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 7137795 | ||||||
| chr12:7137795 | T | TGTGTGAG others(5): Show |
1 | a0001c0001t0001g0150 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1211-159_1211-158i others(14): Show |
CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 7137795 | ||||||
| chr12:7137795 | T | TGTGTGTG others(1): Show |
14 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(11): Show |
19 | HG00735.hp1 HG01109.hp1 HG01358.hp2 others(16): Show |
intron_variant | MODIFIER | c.1211-159_1211-158i others(10): Show |
CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 7137795 | ||||||
| chr12:7137795 | T | TGTGTGTG others(3): Show |
8 | a0001c0001t0001g0010 a0001c0001t0001g0016 a0001c0001t0001g0051 others(5): Show |
8 | HG01099.hp2 HG02015.hp2 HG02040.hp2 others(5): Show |
intron_variant | MODIFIER | c.1211-159_1211-158i others(12): Show |
CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 7137795 | ||||||
| chr12:7137795 | T | TGTGTGTG others(5): Show |
10 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0015 others(7): Show |
15 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(12): Show |
intron_variant | MODIFIER | c.1211-159_1211-158i others(14): Show |
CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 7137795 | ||||||
| chr12:7137795 | T | TGTGTGTG others(7): Show |
2 | a0001c0001t0001g0014 a0008c0020t0004g0199 |
2 | HG03579.hp2 NA18949.hp1 |
intron_variant | MODIFIER | c.1211-159_1211-158i others(16): Show |
CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 7137795 | ||||||
| chr12:7137795 | T | TGTGTGTG others(3): Show |
6 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0096 others(3): Show |
7 | HG00544.hp2 HG01934.hp2 HG03540.hp2 others(4): Show |
intron_variant | MODIFIER | c.1211-159_1211-158i others(12): Show |
CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 7137795 | ||||||
| chr12:7137795 | T | TGTGTGTG others(5): Show |
32 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(29): Show |
43 | HG00323.hp2 HG00558.hp2 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.1211-159_1211-158i others(14): Show |
CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 7137795 | ||||||
| chr12:7137795 | T | TGTGTGTG others(7): Show |
6 | a0001c0001t0001g0010 a0001c0001t0001g0052 a0001c0001t0001g0065 others(3): Show |
6 | HG03017.hp2 NA18956.hp1 NA18959.hp2 others(3): Show |
intron_variant | MODIFIER | c.1211-159_1211-158i others(16): Show |
CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 7137795 | ||||||
| chr12:7137795 | T | TGTGTGTG others(5): Show |
2 | a0001c0001t0001g0038 a0001c0001t0002g0251 |
3 | HG01106.hp2 HG01109.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.1211-159_1211-158i others(14): Show |
CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 7137795 | ||||||
| chr12:7137795 | T | TGTGTGTG others(7): Show |
6 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0054 others(3): Show |
6 | HG02027.hp1 HG02074.hp2 HG02293.hp2 others(3): Show |
intron_variant | MODIFIER | c.1211-159_1211-158i others(16): Show |
CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 7137795 | ||||||
| chr12:7137795 | T | TGTGTGTG others(7): Show |
2 | a0001c0001t0001g0015 a0001c0001t0001g0066 |
2 | HG01952.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1211-159_1211-158i others(16): Show |
CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 7137795 | ||||||
| chr12:7137795 | T | TGTGTGTG others(9): Show |
4 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0074 others(1): Show |
4 | HG02083.hp1 HG03130.hp2 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.1211-159_1211-158i others(18): Show |
CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 7137795 | ||||||
| chr12:7137795 | T | TGTGTGTG others(11): Show |
3 | a0001c0001t0001g0018 a0001c0001t0001g0059 a0001c0001t0001g0076 |
4 | HG00741.hp1 HG01361.hp1 HG01943.hp2 others(1): Show |
intron_variant | MODIFIER | c.1211-159_1211-158i others(20): Show |
CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 7137795 | ||||||
| chr12:7137795 | T | TGTGTGTG others(13): Show |
1 | a0001c0001t0001g0017 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1211-159_1211-158i others(22): Show |
CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 7137795 | ||||||
| chr12:7137795 | TGA | T | 31 | a0001c0001t0001g0023 a0001c0001t0001g0039 a0001c0001t0001g0040 others(28): Show |
39 | HG00099.hp1 HG00597.hp2 HG00609.hp2 others(36): Show |
intron_variant | MODIFIER | c.1211-134_1211-133d others(4): Show |
CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 7137795 | ||||||
| chr12:7137795 | TGAGA | T | 5 | a0001c0001t0001g0205 a0001c0001t0001g0210 a0001c0001t0001g0227 others(2): Show |
5 | HG02486.hp2 NA18612.hp1 NA18989.hp1 others(2): Show |
intron_variant | MODIFIER | c.1211-136_1211-133d others(6): Show |
CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 7137795 | ||||||
| chr12:7137797 | A | T | 12 | a0001c0001t0001g0223 a0001c0001t0001g0266 a0001c0001t0001g0268 others(9): Show |
12 | HG01884.hp2 HG02080.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1211-158A>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 7/17 | chr12 | 7137797 | |||||||
| chr12:7137799 | A | T | 32 | a0001c0001t0001g0023 a0001c0001t0001g0039 a0001c0001t0001g0040 others(29): Show |
40 | HG00099.hp1 HG00597.hp2 HG00609.hp2 others(37): Show |
intron_variant | MODIFIER | c.1211-156A>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 7/17 | chr12 | 7137799 | |||||||
| chr12:7137801 | A | T | 34 | a0001c0001t0001g0023 a0001c0001t0001g0039 a0001c0001t0001g0040 others(31): Show |
42 | HG00597.hp2 HG00609.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.1211-154A>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 7/17 | chr12 | 7137801 | |||||||
| chr12:7137803 | A | T | 8 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0223 others(5): Show |
10 | HG00597.hp2 HG00621.hp2 NA18945.hp2 others(7): Show |
intron_variant | MODIFIER | c.1211-152A>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 7/17 | chr12 | 7137803 | |||||||
| chr12:7137843 | C | T | 3 | a0001c0001t0006g0201 a0001c0001t0006g0203 a0001c0001t0009g0202 |
3 | HG01884.hp2 HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1211-112C>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 7/17 | chr12 | 7137843 | |||||||
| chr12:7137880 | T | C | 1 | a0001c0001t0001g0233 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1211-75T>C | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 7/17 | chr12 | 7137880 | |||||||
| chr12:7138096 | G | A | 1 | a0001c0001t0004g0113 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1323+29G>A | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 8/17 | chr12 | 7138096 | |||||||
| chr12:7138273 | T | TAAAAAAA others(5): Show |
1 | a0001c0001t0003g0280 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1323+216_1323+217i others(14): Show |
CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr12 | 7138273 | ||||||
| chr12:7138273 | T | TAAAAAAA others(6): Show |
6 | a0001c0001t0003g0278 a0001c0001t0004g0113 a0001c0001t0004g0114 others(3): Show |
6 | HG02486.hp1 HG02886.hp1 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1323+216_1323+217i others(15): Show |
CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr12 | 7138273 | ||||||
| chr12:7138273 | T | TAAAAAAA others(7): Show |
1 | a0009c0007t0001g0230 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1323+216_1323+217i others(16): Show |
CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr12 | 7138273 | ||||||
| chr12:7138342 | T | TTC | 6 | a0001c0001t0005g0182 a0001c0001t0005g0183 a0001c0001t0005g0184 others(3): Show |
6 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(3): Show |
intron_variant | MODIFIER | c.1323+287_1323+288d others(4): Show |
CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr12 | 7138342 | ||||||
| chr12:7138518 | A | G | 2 | a0001c0001t0003g0189 a0001c0001t0003g0190 |
2 | HG02895.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1323+451A>G | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 8/17 | chr12 | 7138518 | |||||||
| chr12:7138564 | G | A | 3 | a0001c0001t0006g0201 a0001c0001t0006g0203 a0001c0001t0009g0202 |
3 | HG01884.hp2 HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1323+497G>A | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 8/17 | chr12 | 7138564 | |||||||
| chr12:7138598 | C | T | 1 | a0001c0001t0001g0265 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1323+531C>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 8/17 | chr12 | 7138598 | |||||||
| chr12:7138610 | C | T | 35 | a0001c0001t0001g0023 a0001c0001t0001g0039 a0001c0001t0001g0040 others(32): Show |
43 | HG00099.hp1 HG00597.hp2 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.1323+543C>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 8/17 | chr12 | 7138610 | |||||||
| chr12:7138829 | C | CA | 35 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0024 others(32): Show |
42 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(39): Show |
intron_variant | MODIFIER | c.1323+789dupA | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr12 | 7138829 | ||||||
| chr12:7138829 | CA | C | 43 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0020 others(40): Show |
58 | HG00140.hp2 HG00621.hp2 HG00735.hp1 others(55): Show |
intron_variant | MODIFIER | c.1323+789delA | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr12 | 7138829 | ||||||
| chr12:7138829 | CAA | C | 116 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(113): Show |
166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.1323+788_1323+789d others(4): Show |
CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr12 | 7138829 | ||||||
| chr12:7138829 | CAAA | C | 6 | a0001c0001t0004g0113 a0001c0001t0004g0115 a0001c0001t0004g0116 others(3): Show |
6 | HG01884.hp2 HG03195.hp2 NA19030.hp2 others(3): Show |
intron_variant | MODIFIER | c.1323+787_1323+789d others(5): Show |
CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr12 | 7138829 | ||||||
| chr12:7138888 | A | G | 1 | a0001c0001t0006g0203 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1323+821A>G | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 8/17 | chr12 | 7138888 | |||||||
| chr12:7138898 | C | T | 1 | a0001c0001t0001g0063 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1323+831C>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 8/17 | chr12 | 7138898 | |||||||
| chr12:7138964 | T | C | 3 | a0001c0001t0006g0201 a0001c0001t0006g0203 a0001c0001t0009g0202 |
3 | HG01884.hp2 HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1323+897T>C | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 8/17 | chr12 | 7138964 | |||||||
| chr12:7139074 | A | G | 55 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0012 others(52): Show |
80 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.1323+1007A>G | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 8/17 | chr12 | 7139074 | |||||||
| chr12:7139256 | G | C | 3 | a0001c0001t0006g0201 a0001c0001t0006g0203 a0001c0001t0009g0202 |
3 | HG01884.hp2 HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1323+1189G>C | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 8/17 | chr12 | 7139256 | |||||||
| chr12:7139340 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1323+1273G>A | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 8/17 | chr12 | 7139340 | |||||||
| chr12:7139637 | T | C | 8 | a0001c0001t0003g0278 a0001c0001t0003g0280 a0001c0001t0004g0113 others(5): Show |
8 | HG02486.hp1 HG02886.hp1 HG03486.hp1 others(5): Show |
intron_variant | MODIFIER | c.1323+1570T>C | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 8/17 | chr12 | 7139637 | |||||||
| chr12:7139640 | T | C | 4 | a0001c0001t0004g0113 a0001c0001t0004g0114 a0001c0001t0004g0115 others(1): Show |
4 | HG02486.hp1 NA19043.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.1323+1573T>C | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 8/17 | chr12 | 7139640 | |||||||
| chr12:7139652 | TA | T | 6 | a0001c0003t0003g0037 a0001c0003t0003g0088 a0001c0003t0003g0196 others(3): Show |
7 | HG01891.hp1 HG02818.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1323+1586delA | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 8/17 | chr12 | 7139652 | |||||||
| chr12:7139655 | TA | T | 47 | a0001c0001t0001g0029 a0001c0001t0001g0046 a0001c0001t0001g0047 others(44): Show |
55 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(52): Show |
intron_variant | MODIFIER | c.1324-1586delA | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 8/17 | chr12 | 7139655 | |||||||
| chr12:7139656 | A | T | 55 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0016 others(52): Show |
75 | HG00323.hp2 HG00558.hp2 HG00642.hp2 others(72): Show |
intron_variant | MODIFIER | c.1324-1586A>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 8/17 | chr12 | 7139656 | |||||||
| chr12:7139656 | AT | A | 145 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(142): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.1324-1575delT | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr12 | 7139656 | ||||||
| chr12:7139659 | T | A | 19 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0014 others(16): Show |
31 | HG00280.hp1 HG00423.hp2 HG00544.hp1 others(28): Show |
intron_variant | MODIFIER | c.1324-1583T>A | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 8/17 | chr12 | 7139659 | |||||||
| chr12:7139660 | T | A | 3 | a0001c0001t0003g0278 a0001c0001t0003g0280 a0001c0008t0003g0279 |
3 | HG02886.hp1 HG03486.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1324-1582T>A | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 8/17 | chr12 | 7139660 | |||||||
| chr12:7139683 | T | C | 3 | a0001c0001t0006g0201 a0001c0001t0006g0203 a0001c0001t0009g0202 |
3 | HG01884.hp2 HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1324-1559T>C | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 8/17 | chr12 | 7139683 | |||||||
| chr12:7139805 | C | T | 93 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(90): Show |
134 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.1324-1437C>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 8/17 | chr12 | 7139805 | |||||||
| chr12:7140115 | A | G | 39 | a0001c0002t0001g0032 a0001c0002t0001g0158 a0001c0002t0001g0160 others(36): Show |
46 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(43): Show |
intron_variant | MODIFIER | c.1324-1127A>G | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 8/17 | chr12 | 7140115 | |||||||
| chr12:7140202 | C | T | 2 | a0001c0001t0001g0233 a0001c0001t0001g0261 |
2 | HG02080.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.1324-1040C>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 8/17 | chr12 | 7140202 | |||||||
| chr12:7140300 | G | C | 6 | a0001c0003t0003g0037 a0001c0003t0003g0088 a0001c0003t0003g0196 others(3): Show |
7 | HG01891.hp1 HG02818.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1324-942G>C | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 8/17 | chr12 | 7140300 | |||||||
| chr12:7140399 | A | C | 1 | a0001c0001t0001g0260 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1324-843A>C | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 8/17 | chr12 | 7140399 | |||||||
| chr12:7140455 | A | G | 2 | a0001c0001t0001g0082 a0001c0001t0001g0083 |
2 | NA18946.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.1324-787A>G | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 8/17 | chr12 | 7140455 | |||||||
| chr12:7140506 | T | G | 1 | a0001c0001t0001g0241 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1324-736T>G | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 8/17 | chr12 | 7140506 | |||||||
| chr12:7140742 | C | T | 3 | a0001c0002t0001g0165 a0001c0002t0002g0035 a0001c0002t0002g0179 |
4 | HG00735.hp2 HG02735.hp2 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.1324-500C>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 8/17 | chr12 | 7140742 | |||||||
| chr12:7140835 | G | A | 53 | a0001c0001t0001g0049 a0001c0001t0003g0189 a0001c0001t0003g0190 others(50): Show |
61 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.1324-407G>A | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 8/17 | chr12 | 7140835 | |||||||
| chr12:7141093 | G | C | 3 | a0001c0001t0004g0114 a0001c0001t0004g0115 a0001c0001t0004g0116 |
3 | HG02486.hp1 NA19043.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1324-149G>C | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 8/17 | chr12 | 7141093 | |||||||
| chr12:7141094 | A | T | 3 | a0001c0001t0004g0114 a0001c0001t0004g0115 a0001c0001t0004g0116 |
3 | HG02486.hp1 NA19043.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1324-148A>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 8/17 | chr12 | 7141094 | |||||||
| chr12:7141151 | C | T | 8 | a0001c0001t0003g0278 a0001c0001t0003g0280 a0001c0001t0004g0113 others(5): Show |
8 | HG02486.hp1 HG02886.hp1 HG03486.hp1 others(5): Show |
intron_variant | MODIFIER | c.1324-91C>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 8/17 | chr12 | 7141151 | |||||||
| chr12:7141159 | C | T | 3 | a0001c0001t0006g0201 a0001c0001t0006g0203 a0001c0001t0009g0202 |
3 | HG01884.hp2 HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1324-83C>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 8/17 | chr12 | 7141159 | |||||||
| chr12:7141200 | C | G | 129 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(126): Show |
168 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(165): Show |
intron_variant | MODIFIER | c.1324-42C>G | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 8/17 | chr12 | 7141200 | |||||||
| chr12:7141570 | T | A | 1 | a0009c0007t0001g0230 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1486+166T>A | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 9/17 | chr12 | 7141570 | |||||||
| chr12:7141631 | C | G | 55 | a0001c0001t0001g0049 a0001c0001t0003g0189 a0001c0001t0003g0190 others(52): Show |
63 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.1486+227C>G | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 9/17 | chr12 | 7141631 | |||||||
| chr12:7141749 | C | T | 1 | a0009c0007t0001g0230 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1487-337C>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 9/17 | chr12 | 7141749 | |||||||
| chr12:7142009 | A | T | 1 | a0009c0007t0001g0230 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1487-77A>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 9/17 | chr12 | 7142009 | |||||||
| chr12:7142061 | G | GT | 47 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0016 others(44): Show |
66 | HG00323.hp2 HG00544.hp1 HG00558.hp2 others(63): Show |
splice_region_variant&intron_variant | LOW | c.1487-9dupT | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr12 | 7142061 | ||||||
| chr12:7142061 | GT | G | 182 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(179): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.1487-9delT | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr12 | 7142061 | ||||||
| chr12:7142256 | G | A | 3 | a0001c0001t0006g0201 a0001c0001t0006g0203 a0001c0001t0009g0202 |
3 | HG01884.hp2 HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1540+117G>A | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 10/17 | chr12 | 7142256 | |||||||
| chr12:7142300 | G | A | 3 | a0001c0001t0004g0114 a0001c0001t0004g0115 a0001c0001t0004g0116 |
3 | HG02486.hp1 NA19043.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1540+161G>A | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 10/17 | chr12 | 7142300 | |||||||
| chr12:7142335 | A | G | 1 | a0009c0007t0001g0230 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1540+196A>G | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 10/17 | chr12 | 7142335 | |||||||
| chr12:7142369 | C | T | 1 | a0001c0001t0001g0240 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1540+230C>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 10/17 | chr12 | 7142369 | |||||||
| chr12:7142525 | C | T | 1 | a0001c0001t0001g0067 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1541-344C>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 10/17 | chr12 | 7142525 | |||||||
| chr12:7142676 | C | G | 1 | a0001c0001t0001g0081 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1541-193C>G | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 10/17 | chr12 | 7142676 | |||||||
| chr12:7142676 | C | T | 1 | a0001c0001t0001g0240 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1541-193C>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 10/17 | chr12 | 7142676 | |||||||
| chr12:7142718 | C | CT | 48 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0017 others(45): Show |
65 | HG00323.hp2 HG00642.hp2 HG00673.hp1 others(62): Show |
intron_variant | MODIFIER | c.1541-134dupT | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr12 | 7142718 | ||||||
| chr12:7142718 | C | CTT | 35 | a0001c0001t0001g0011 a0001c0001t0001g0062 a0001c0001t0001g0073 others(32): Show |
44 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(41): Show |
intron_variant | MODIFIER | c.1541-135_1541-134d others(4): Show |
CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr12 | 7142718 | ||||||
| chr12:7143101 | C | T | 1 | a0001c0001t0003g0190 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1699-62C>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 11/17 | chr12 | 7143101 | |||||||
| chr12:7143108 | C | T | 3 | a0001c0001t0006g0201 a0001c0001t0006g0203 a0001c0001t0009g0202 |
3 | HG01884.hp2 HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1699-55C>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 11/17 | chr12 | 7143108 | |||||||
| chr12:7143157 | G | T | 1 | a0001c0001t0001g0225 | 1 | NA18945.hp2 | splice_region_variant&intron_variant | LOW | c.1699-6G>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 11/17 | chr12 | 7143157 | |||||||
| chr12:7143332 | G | A | 9 | a0001c0002t0001g0165 a0001c0002t0001g0178 a0001c0002t0002g0035 others(6): Show |
11 | HG00735.hp2 HG00741.hp2 HG01346.hp2 others(8): Show |
intron_variant | MODIFIER | c.1847+21G>A | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 12/17 | chr12 | 7143332 | |||||||
| chr12:7143583 | C | G | 3 | a0001c0001t0006g0201 a0001c0001t0006g0203 a0001c0001t0009g0202 |
3 | HG01884.hp2 HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1847+272C>G | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 12/17 | chr12 | 7143583 | |||||||
| chr12:7143846 | G | A | 1 | a0001c0001t0001g0098 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1847+535G>A | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 12/17 | chr12 | 7143846 | |||||||
| chr12:7143851 | T | C | 4 | a0001c0002t0002g0159 a0001c0002t0002g0166 a0001c0002t0002g0170 others(1): Show |
4 | HG00423.hp1 NA18747.hp2 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.1847+540T>C | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 12/17 | chr12 | 7143851 | |||||||
| chr12:7143853 | G | A | 146 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(143): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.1847+542G>A | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 12/17 | chr12 | 7143853 | |||||||
| chr12:7143870 | G | A | 2 | a0001c0001t0004g0110 a0001c0001t0004g0111 |
2 | HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1847+559G>A | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 12/17 | chr12 | 7143870 | |||||||
| chr12:7143897 | G | T | 1 | a0001c0001t0001g0239 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1847+586G>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 12/17 | chr12 | 7143897 | |||||||
| chr12:7143899 | T | C | 1 | a0001c0001t0001g0239 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1847+588T>C | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 12/17 | chr12 | 7143899 | |||||||
| chr12:7143955 | C | T | 8 | a0001c0001t0003g0278 a0001c0001t0003g0280 a0001c0001t0004g0113 others(5): Show |
8 | HG02486.hp1 HG02886.hp1 HG03486.hp1 others(5): Show |
intron_variant | MODIFIER | c.1847+644C>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 12/17 | chr12 | 7143955 | |||||||
| chr12:7143962 | G | A | 8 | a0001c0001t0003g0278 a0001c0001t0003g0280 a0001c0001t0004g0113 others(5): Show |
8 | HG02486.hp1 HG02886.hp1 HG03486.hp1 others(5): Show |
intron_variant | MODIFIER | c.1847+651G>A | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 12/17 | chr12 | 7143962 | |||||||
| chr12:7144177 | G | A | 1 | a0001c0001t0001g0049 | 2 | HG01243.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1847+866G>A | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 12/17 | chr12 | 7144177 | |||||||
| chr12:7144181 | C | T | 2 | a0001c0001t0001g0213 a0001c0001t0001g0217 |
2 | NA18980.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.1847+870C>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 12/17 | chr12 | 7144181 | |||||||
| chr12:7144213 | A | G | 1 | a0001c0001t0001g0258 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1847+902A>G | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 12/17 | chr12 | 7144213 | |||||||
| chr12:7144232 | C | CA | 21 | a0001c0001t0001g0052 a0001c0001t0001g0058 a0001c0001t0001g0062 others(18): Show |
21 | HG01891.hp1 HG02027.hp1 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.1847+944dupA | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr12 | 7144232 | ||||||
| chr12:7144232 | CA | C | 64 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0020 others(61): Show |
86 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.1847+944delA | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr12 | 7144232 | ||||||
| chr12:7144254 | A | T | 2 | a0001c0001t0003g0120 a0001c0001t0003g0122 |
2 | HG00738.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1847+943A>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 12/17 | chr12 | 7144254 | |||||||
| chr12:7144299 | T | C | 1 | a0001c0001t0001g0087 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1847+988T>C | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 12/17 | chr12 | 7144299 | |||||||
| chr12:7144656 | C | T | 146 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(143): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.1847+1345C>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 12/17 | chr12 | 7144656 | |||||||
| chr12:7144823 | G | T | 146 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(143): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.1847+1512G>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 12/17 | chr12 | 7144823 | |||||||
| chr12:7144824 | A | T | 146 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(143): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.1847+1513A>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 12/17 | chr12 | 7144824 | |||||||
| chr12:7144839 | C | G | 1 | a0001c0001t0001g0256 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1847+1528C>G | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 12/17 | chr12 | 7144839 | |||||||
| chr12:7144926 | T | C | 1 | a0001c0001t0001g0244 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1847+1615T>C | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 12/17 | chr12 | 7144926 | |||||||
| chr12:7144955 | G | C | 3 | a0001c0001t0006g0201 a0001c0001t0006g0203 a0001c0001t0009g0202 |
3 | HG01884.hp2 HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1847+1644G>C | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 12/17 | chr12 | 7144955 | |||||||
| chr12:7145164 | A | G | 2 | a0001c0001t0003g0119 a0001c0001t0003g0200 |
2 | HG02717.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1847+1853A>G | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 12/17 | chr12 | 7145164 | |||||||
| chr12:7145204 | G | A | 1 | a0001c0001t0001g0131 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1847+1893G>A | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 12/17 | chr12 | 7145204 | |||||||
| chr12:7145314 | C | T | 3 | a0001c0001t0006g0201 a0001c0001t0006g0203 a0001c0001t0009g0202 |
3 | HG01884.hp2 HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1847+2003C>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 12/17 | chr12 | 7145314 | |||||||
| chr12:7145346 | GGT | G | 223 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(220): Show |
320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.1847+2059_1847+206 others(6): Show |
CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr12 | 7145346 | ||||||
| chr12:7145346 | GGTGT | G | 45 | a0001c0001t0001g0049 a0001c0001t0001g0262 a0001c0001t0004g0110 others(42): Show |
53 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.1847+2057_1847+206 others(8): Show |
CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr12 | 7145346 | ||||||
| chr12:7145346 | GGTGTGTG others(5): Show |
G | 1 | a0001c0001t0003g0027 | 2 | HG02615.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1847+2049_1847+206 others(16): Show |
CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr12 | 7145346 | ||||||
| chr12:7145370 | T | C | 6 | a0001c0001t0001g0139 a0001c0001t0001g0141 a0001c0001t0006g0201 others(3): Show |
6 | HG01884.hp1 HG01884.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1847+2059T>C | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 12/17 | chr12 | 7145370 | |||||||
| chr12:7145374 | C | T | 1 | a0001c0001t0001g0240 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1847+2063C>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 12/17 | chr12 | 7145374 | |||||||
| chr12:7145523 | A | C | 1 | a0001c0001t0001g0125 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1847+2212A>C | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 12/17 | chr12 | 7145523 | |||||||
| chr12:7145529 | T | G | 5 | a0001c0001t0004g0113 a0001c0001t0004g0114 a0001c0001t0004g0115 others(2): Show |
5 | HG02486.hp1 HG03831.hp2 NA19043.hp1 others(2): Show |
intron_variant | MODIFIER | c.1847+2218T>G | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 12/17 | chr12 | 7145529 | |||||||
| chr12:7145532 | G | A | 1 | a0001c0001t0001g0240 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1847+2221G>A | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 12/17 | chr12 | 7145532 | |||||||
| chr12:7145561 | G | GT | 7 | a0001c0001t0001g0057 a0001c0001t0004g0113 a0001c0001t0004g0114 others(4): Show |
7 | HG02486.hp1 HG02602.hp2 HG03831.hp2 others(4): Show |
intron_variant | MODIFIER | c.1847+2264dupT | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr12 | 7145561 | ||||||
| chr12:7145609 | A | C | 53 | a0001c0001t0001g0049 a0001c0001t0003g0278 a0001c0001t0003g0280 others(50): Show |
61 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.1847+2298A>C | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 12/17 | chr12 | 7145609 | |||||||
| chr12:7145670 | C | G | 1 | a0001c0001t0004g0116 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1847+2359C>G | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 12/17 | chr12 | 7145670 | |||||||
| chr12:7145731 | G | A | 144 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(141): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.1847+2420G>A | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 12/17 | chr12 | 7145731 | |||||||
| chr12:7145752 | A | G | 1 | a0001c0002t0002g0176 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1847+2441A>G | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 12/17 | chr12 | 7145752 | |||||||
| chr12:7145780 | T | C | 53 | a0001c0001t0001g0049 a0001c0001t0003g0278 a0001c0001t0003g0280 others(50): Show |
61 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.1847+2469T>C | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 12/17 | chr12 | 7145780 | |||||||
| chr12:7146001 | T | C | 1 | a0009c0007t0001g0230 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1847+2690T>C | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 12/17 | chr12 | 7146001 | |||||||
| chr12:7146035 | C | T | 5 | a0001c0001t0001g0055 a0001c0001t0001g0071 a0001c0001t0001g0103 others(2): Show |
5 | HG02615.hp1 HG02647.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1847+2724C>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 12/17 | chr12 | 7146035 | |||||||
| chr12:7146063 | C | A | 39 | a0001c0002t0001g0032 a0001c0002t0001g0158 a0001c0002t0001g0160 others(36): Show |
46 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(43): Show |
intron_variant | MODIFIER | c.1847+2752C>A | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 12/17 | chr12 | 7146063 | |||||||
| chr12:7146417 | AG | A | 8 | a0001c0001t0003g0278 a0001c0001t0003g0280 a0001c0001t0004g0114 others(5): Show |
8 | HG01891.hp1 HG02486.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1848-2554delG | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 12/17 | chr12 | 7146417 | |||||||
| chr12:7146418 | G | A | 43 | a0001c0001t0001g0049 a0001c0001t0004g0113 a0001c0001t0006g0201 others(40): Show |
51 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.1848-2554G>A | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 12/17 | chr12 | 7146418 | |||||||
| chr12:7146632 | T | G | 3 | a0001c0001t0003g0278 a0001c0001t0003g0280 a0001c0008t0003g0279 |
3 | HG02886.hp1 HG03486.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1848-2340T>G | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 12/17 | chr12 | 7146632 | |||||||
| chr12:7146683 | G | A | 1 | a0001c0001t0001g0097 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1848-2289G>A | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 12/17 | chr12 | 7146683 | |||||||
| chr12:7146702 | C | G | 51 | a0001c0001t0001g0049 a0001c0001t0003g0278 a0001c0001t0003g0280 others(48): Show |
59 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(56): Show |
intron_variant | MODIFIER | c.1848-2270C>G | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 12/17 | chr12 | 7146702 | |||||||
| chr12:7146967 | A | C | 1 | a0008c0020t0004g0199 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1848-2005A>C | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 12/17 | chr12 | 7146967 | |||||||
| chr12:7147268 | C | T | 3 | a0001c0001t0001g0255 a0001c0001t0001g0257 a0001c0001t0001g0271 |
3 | HG01106.hp1 HG01167.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.1848-1704C>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 12/17 | chr12 | 7147268 | |||||||
| chr12:7147395 | C | CAAA | 4 | a0001c0002t0001g0158 a0001c0002t0001g0163 a0001c0002t0002g0170 others(1): Show |
4 | HG00621.hp1 NA18747.hp2 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.1848-1577_1848-157 others(7): Show |
CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 12/17 | chr12 | 7147395 | |||||||
| chr12:7147395 | C | CAAAA | 8 | a0001c0002t0001g0032 a0001c0002t0001g0160 a0001c0002t0001g0161 others(5): Show |
11 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(8): Show |
intron_variant | MODIFIER | c.1848-1577_1848-157 others(8): Show |
CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 12/17 | chr12 | 7147395 | |||||||
| chr12:7147396 | C | A | 12 | a0001c0002t0001g0032 a0001c0002t0001g0158 a0001c0002t0001g0160 others(9): Show |
15 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(12): Show |
intron_variant | MODIFIER | c.1848-1576C>A | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 12/17 | chr12 | 7147396 | |||||||
| chr12:7147396 | C | CA | 30 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0016 others(27): Show |
41 | HG00544.hp1 HG00609.hp1 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.1848-1547dupA | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr12 | 7147396 | ||||||
| chr12:7147396 | C | CAA | 9 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0052 others(6): Show |
14 | HG00280.hp1 HG00423.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.1848-1548_1848-154 others(6): Show |
CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr12 | 7147396 | ||||||
| chr12:7147396 | C | CAAAA | 8 | a0001c0002t0001g0165 a0001c0002t0002g0033 a0001c0002t0002g0035 others(5): Show |
10 | HG00280.hp2 HG00735.hp2 HG01346.hp2 others(7): Show |
intron_variant | MODIFIER | c.1848-1550_1848-154 others(8): Show |
CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr12 | 7147396 | ||||||
| chr12:7147396 | C | CAAAAA | 6 | a0001c0002t0001g0172 a0001c0002t0001g0178 a0001c0002t0002g0036 others(3): Show |
7 | HG00741.hp2 HG01070.hp2 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.1848-1551_1848-154 others(9): Show |
CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr12 | 7147396 | ||||||
| chr12:7147396 | CA | C | 68 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0020 others(65): Show |
86 | HG00597.hp2 HG00609.hp2 HG00738.hp1 others(83): Show |
intron_variant | MODIFIER | c.1848-1547delA | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr12 | 7147396 | ||||||
| chr12:7147396 | CAA | C | 93 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(90): Show |
143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.1848-1548_1848-154 others(6): Show |
CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr12 | 7147396 | ||||||
| chr12:7147518 | C | CTT | 41 | a0001c0001t0001g0049 a0001c0001t0003g0189 a0001c0001t0003g0190 others(38): Show |
49 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(46): Show |
intron_variant | MODIFIER | c.1848-1444_1848-144 others(6): Show |
CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr12 | 7147518 | ||||||
| chr12:7147554 | C | T | 1 | a0001c0001t0001g0049 | 2 | HG01243.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1848-1418C>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 12/17 | chr12 | 7147554 | |||||||
| chr12:7147573 | C | A | 42 | a0001c0001t0001g0049 a0001c0001t0006g0201 a0001c0001t0006g0203 others(39): Show |
50 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.1848-1399C>A | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 12/17 | chr12 | 7147573 | |||||||
| chr12:7147668 | C | T | 31 | a0001c0002t0001g0032 a0001c0002t0001g0158 a0001c0002t0001g0160 others(28): Show |
37 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(34): Show |
intron_variant | MODIFIER | c.1848-1304C>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 12/17 | chr12 | 7147668 | |||||||
| chr12:7147883 | G | A | 2 | a0001c0001t0001g0058 a0001c0001t0001g0077 |
2 | NA19000.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.1848-1089G>A | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 12/17 | chr12 | 7147883 | |||||||
| chr12:7147925 | C | T | 1 | a0009c0007t0001g0230 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1848-1047C>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 12/17 | chr12 | 7147925 | |||||||
| chr12:7147931 | GATCACCT others(13): Show |
G | 1 | a0001c0001t0001g0061 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1848-1040_1848-102 others(24): Show |
CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 12/17 | chr12 | 7147931 | |||||||
| chr12:7148028 | G | A | 2 | a0001c0001t0003g0189 a0001c0001t0003g0190 |
2 | HG02895.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1848-944G>A | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 12/17 | chr12 | 7148028 | |||||||
| chr12:7148156 | A | AAAAG | 34 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(31): Show |
41 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.1848-760_1848-757d others(6): Show |
CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr12 | 7148156 | ||||||
| chr12:7148156 | A | AAAAGAAA others(1): Show |
19 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(16): Show |
23 | HG00558.hp1 HG01123.hp2 HG01256.hp1 others(20): Show |
intron_variant | MODIFIER | c.1848-764_1848-757d others(10): Show |
CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr12 | 7148156 | ||||||
| chr12:7148156 | A | AAAAGAAA others(5): Show |
7 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(4): Show |
9 | HG02896.hp2 HG02897.hp1 HG03209.hp1 others(6): Show |
intron_variant | MODIFIER | c.1848-768_1848-757d others(14): Show |
CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr12 | 7148156 | ||||||
| chr12:7148156 | A | AAAAGAAA others(9): Show |
2 | a0001c0001t0001g0001 a0001c0001t0001g0012 |
3 | HG02056.hp2 NA19090.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1848-772_1848-757d others(18): Show |
CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr12 | 7148156 | ||||||
| chr12:7148156 | A | AAAAGAAA others(17): Show |
2 | a0001c0001t0001g0001 a0001c0001t0001g0209 |
2 | NA18941.hp1 NA18941.hp2 |
intron_variant | MODIFIER | c.1848-780_1848-757d others(26): Show |
CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr12 | 7148156 | ||||||
| chr12:7148156 | A | AAAAGAAA others(169): Show |
1 | a0001c0001t0001g0242 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1848-757_1848-756i others(178): Show |
CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr12 | 7148156 | ||||||
| chr12:7148156 | A | AAAAGAAA others(181): Show |
2 | a0001c0001t0001g0246 a0001c0001t0001g0252 |
2 | HG02965.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1848-757_1848-756i others(190): Show |
CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr12 | 7148156 | ||||||
| chr12:7148156 | A | AAAAGAAA others(221): Show |
1 | a0001c0001t0001g0245 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1848-757_1848-756i others(230): Show |
CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr12 | 7148156 | ||||||
| chr12:7148156 | A | AAG | 3 | a0001c0001t0001g0129 a0001c0001t0001g0142 a0001c0001t0004g0030 |
3 | HG01123.hp1 HG01175.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.1848-815_1848-814i others(4): Show |
CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr12 | 7148156 | ||||||
| chr12:7148156 | AAAAG | A | 54 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(51): Show |
58 | HG00597.hp2 HG00621.hp2 HG00741.hp2 others(55): Show |
intron_variant | MODIFIER | c.1848-760_1848-757d others(6): Show |
CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr12 | 7148156 | ||||||
| chr12:7148156 | AAAAGAAA others(1): Show |
A | 61 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(58): Show |
82 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.1848-764_1848-757d others(10): Show |
CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr12 | 7148156 | ||||||
| chr12:7148156 | AAAAGAAA others(5): Show |
A | 16 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0042 others(13): Show |
17 | HG00323.hp2 HG00609.hp2 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.1848-768_1848-757d others(14): Show |
CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr12 | 7148156 | ||||||
| chr12:7148156 | AAAAGAAA others(9): Show |
A | 2 | a0001c0001t0001g0097 a0001c0001t0001g0098 |
2 | HG02300.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.1848-772_1848-757d others(18): Show |
CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr12 | 7148156 | ||||||
| chr12:7148156 | AAAAGAAA others(13): Show |
A | 6 | a0001c0001t0001g0265 a0001c0001t0006g0201 a0001c0001t0006g0203 others(3): Show |
6 | HG01884.hp2 HG02647.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.1848-776_1848-757d others(22): Show |
CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr12 | 7148156 | ||||||
| chr12:7148156 | AAAAGAAA others(17): Show |
A | 4 | a0001c0001t0001g0049 a0001c0001t0001g0192 a0001c0001t0009g0193 others(1): Show |
5 | HG01243.hp2 HG02976.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.1848-780_1848-757d others(26): Show |
CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr12 | 7148156 | ||||||
| chr12:7148156 | AAAAGAAA others(21): Show |
A | 10 | a0001c0001t0004g0007 a0001c0001t0004g0100 a0001c0001t0004g0113 others(7): Show |
14 | HG02055.hp2 HG02451.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.1848-784_1848-757d others(30): Show |
CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr12 | 7148156 | ||||||
| chr12:7148156 | AAAAGAAA others(25): Show |
A | 32 | a0001c0001t0003g0278 a0001c0001t0003g0280 a0001c0002t0001g0032 others(29): Show |
38 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(35): Show |
intron_variant | MODIFIER | c.1848-788_1848-757d others(34): Show |
CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr12 | 7148156 | ||||||
| chr12:7148178 | A | AAGAAAGA others(5): Show |
1 | a0001c0001t0001g0231 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1848-783_1848-782i others(14): Show |
CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr12 | 7148178 | ||||||
| chr12:7148213 | A | AAAGAAAG others(4): Show |
1 | a0001c0001t0001g0236 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1848-757_1848-756i others(13): Show |
CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr12 | 7148213 | ||||||
| chr12:7148216 | T | G | 1 | a0001c0001t0001g0242 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1848-756T>G | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 12/17 | chr12 | 7148216 | |||||||
| chr12:7148287 | G | A | 6 | a0001c0001t0001g0045 a0001c0001t0001g0133 a0001c0001t0001g0256 others(3): Show |
6 | HG01081.hp2 HG02647.hp2 HG03239.hp2 others(3): Show |
intron_variant | MODIFIER | c.1848-685G>A | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 12/17 | chr12 | 7148287 | |||||||
| chr12:7148304 | G | A | 256 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(253): Show |
359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.1848-668G>A | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 12/17 | chr12 | 7148304 | |||||||
| chr12:7148561 | C | T | 1 | a0001c0003t0003g0197 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1848-411C>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 12/17 | chr12 | 7148561 | |||||||
| chr12:7148938 | G | A | 4 | a0001c0001t0004g0113 a0001c0001t0004g0114 a0001c0001t0004g0115 others(1): Show |
4 | HG02486.hp1 NA19043.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.1848-34G>A | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 12/17 | chr12 | 7148938 | |||||||
| chr12:7149277 | G | A | 1 | a0001c0001t0008g0041 | 2 | HG01069.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.2074+79G>A | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 13/17 | chr12 | 7149277 | |||||||
| chr12:7149386 | A | G | 30 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0012 others(27): Show |
50 | HG00438.hp2 HG00639.hp1 HG00738.hp2 others(47): Show |
intron_variant | MODIFIER | c.2075-137A>G | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 13/17 | chr12 | 7149386 | |||||||
| chr12:7149796 | G | T | 1 | a0001c0001t0001g0247 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.2245+103G>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 14/17 | chr12 | 7149796 | |||||||
| chr12:7149850 | C | T | 1 | a0001c0002t0002g0176 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2245+157C>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 14/17 | chr12 | 7149850 | |||||||
| chr12:7149928 | C | A | 1 | a0007c0014t0001g0156 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2245+235C>A | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 14/17 | chr12 | 7149928 | |||||||
| chr12:7150147 | G | T | 1 | a0001c0001t0001g0053 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2246-397G>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 14/17 | chr12 | 7150147 | |||||||
| chr12:7150180 | C | T | 1 | a0001c0016t0001g0216 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.2246-364C>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 14/17 | chr12 | 7150180 | |||||||
| chr12:7150294 | CTTCTTTC others(30): Show |
C | 1 | a0001c0001t0001g0099 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2246-249_2246-213d others(39): Show |
CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 14/17 | chr12 | 7150294 | |||||||
| chr12:7150311 | T | C | 1 | a0001c0001t0001g0019 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.2246-233T>C | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 14/17 | chr12 | 7150311 | |||||||
| chr12:7150777 | A | C | 1 | a0001c0016t0001g0216 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.2391+88A>C | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 15/17 | chr12 | 7150777 | |||||||
| chr12:7150778 | T | A | 1 | a0001c0016t0001g0216 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.2391+89T>A | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 15/17 | chr12 | 7150778 | |||||||
| chr12:7150779 | G | T | 1 | a0001c0016t0001g0216 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.2391+90G>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 15/17 | chr12 | 7150779 | |||||||
| chr12:7151291 | C | G | 5 | a0001c0001t0004g0007 a0001c0001t0004g0100 a0001c0001t0004g0151 others(2): Show |
9 | HG02055.hp2 HG02451.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.2527+228C>G | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 16/17 | chr12 | 7151291 | |||||||
| chr12:7151439 | C | T | 1 | a0001c0001t0001g0262 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2527+376C>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 16/17 | chr12 | 7151439 | |||||||
| chr12:7151449 | G | T | 2 | a0001c0001t0001g0192 a0001c0001t0009g0193 |
2 | HG02976.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.2527+386G>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 16/17 | chr12 | 7151449 | |||||||
| chr12:7151612 | TGCTGCCC others(6): Show |
T | 1 | a0001c0001t0001g0049 | 2 | HG01243.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2527+565_2527+577d others(15): Show |
CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr12 | 7151612 | ||||||
| chr12:7151908 | G | T | 1 | a0001c0001t0006g0203 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2527+845G>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 16/17 | chr12 | 7151908 | |||||||
| chr12:7151985 | C | A | 1 | a0001c0001t0001g0233 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.2527+922C>A | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 16/17 | chr12 | 7151985 | |||||||
| chr12:7151993 | G | T | 1 | a0001c0001t0001g0093 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.2527+930G>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 16/17 | chr12 | 7151993 | |||||||
| chr12:7152058 | G | GA | 13 | a0001c0001t0001g0058 a0001c0001t0001g0155 a0001c0001t0001g0231 others(10): Show |
16 | HG00438.hp2 HG00639.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.2527+1013dupA | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr12 | 7152058 | ||||||
| chr12:7152061 | A | G | 1 | a0001c0001t0001g0237 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.2527+998A>G | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 16/17 | chr12 | 7152061 | |||||||
| chr12:7152492 | G | A | 6 | a0001c0001t0003g0278 a0001c0001t0003g0280 a0001c0001t0006g0201 others(3): Show |
6 | HG01884.hp2 HG02886.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.2527+1429G>A | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 16/17 | chr12 | 7152492 | |||||||
| chr12:7152706 | A | G | 5 | a0001c0001t0004g0007 a0001c0001t0004g0100 a0001c0001t0004g0151 others(2): Show |
9 | HG02055.hp2 HG02451.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.2527+1643A>G | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 16/17 | chr12 | 7152706 | |||||||
| chr12:7152710 | C | T | 5 | a0001c0001t0001g0192 a0001c0001t0004g0110 a0001c0001t0004g0111 others(2): Show |
5 | HG02976.hp1 HG03225.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.2527+1647C>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 16/17 | chr12 | 7152710 | |||||||
| chr12:7152825 | C | T | 3 | a0001c0001t0001g0019 a0001c0001t0001g0057 a0001c0001t0001g0081 |
5 | HG02015.hp1 HG02132.hp2 NA18953.hp2 others(2): Show |
intron_variant | MODIFIER | c.2527+1762C>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 16/17 | chr12 | 7152825 | |||||||
| chr12:7153431 | C | T | 13 | a0001c0001t0004g0007 a0001c0001t0004g0100 a0001c0001t0004g0110 others(10): Show |
17 | HG02055.hp2 HG02451.hp2 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.2527+2368C>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 16/17 | chr12 | 7153431 | |||||||
| chr12:7153434 | C | T | 1 | a0001c0001t0001g0069 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.2527+2371C>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 16/17 | chr12 | 7153434 | |||||||
| chr12:7153486 | G | T | 1 | a0001c0001t0004g0115 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2527+2423G>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 16/17 | chr12 | 7153486 | |||||||
| chr12:7153868 | C | T | 1 | a0001c0002t0001g0178 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2527+2805C>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 16/17 | chr12 | 7153868 | |||||||
| chr12:7153908 | C | T | 2 | a0001c0001t0001g0086 a0001c0001t0001g0149 |
2 | HG02818.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2527+2845C>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 16/17 | chr12 | 7153908 | |||||||
| chr12:7154024 | A | C | 5 | a0001c0001t0004g0007 a0001c0001t0004g0100 a0001c0001t0004g0151 others(2): Show |
9 | HG02055.hp2 HG02451.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.2527+2961A>C | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 16/17 | chr12 | 7154024 | |||||||
| chr12:7154147 | C | T | 1 | a0001c0001t0009g0193 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2527+3084C>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 16/17 | chr12 | 7154147 | |||||||
| chr12:7154185 | C | A | 24 | a0001c0002t0001g0172 a0001c0002t0001g0174 a0001c0002t0002g0022 others(21): Show |
29 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(26): Show |
intron_variant | MODIFIER | c.2527+3122C>A | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 16/17 | chr12 | 7154185 | |||||||
| chr12:7154236 | G | C | 1 | a0001c0002t0001g0161 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.2527+3173G>C | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 16/17 | chr12 | 7154236 | |||||||
| chr12:7154247 | A | T | 25 | a0001c0001t0001g0109 a0001c0001t0001g0262 a0001c0001t0005g0188 others(22): Show |
30 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(27): Show |
intron_variant | MODIFIER | c.2527+3184A>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 16/17 | chr12 | 7154247 | |||||||
| chr12:7154369 | C | CAGGCGTG others(29): Show |
1 | a0001c0001t0001g0099 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2528-3120_2528-311 others(40): Show |
CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 16/17 | chr12 | 7154369 | |||||||
| chr12:7154370 | C | T | 1 | a0001c0001t0001g0099 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2528-3119C>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 16/17 | chr12 | 7154370 | |||||||
| chr12:7154549 | A | G | 9 | a0001c0001t0004g0007 a0001c0001t0004g0100 a0001c0001t0004g0114 others(6): Show |
13 | HG02055.hp2 HG02451.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.2528-2940A>G | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 16/17 | chr12 | 7154549 | |||||||
| chr12:7154553 | C | T | 3 | a0001c0001t0004g0114 a0001c0001t0004g0115 a0001c0001t0004g0116 |
3 | HG02486.hp1 NA19043.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2528-2936C>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 16/17 | chr12 | 7154553 | |||||||
| chr12:7154620 | C | T | 1 | a0001c0001t0003g0200 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2528-2869C>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 16/17 | chr12 | 7154620 | |||||||
| chr12:7154677 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2528-2812C>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 16/17 | chr12 | 7154677 | |||||||
| chr12:7154885 | G | A | 14 | a0001c0001t0001g0096 a0001c0001t0004g0007 a0001c0001t0004g0100 others(11): Show |
19 | HG01891.hp1 HG02055.hp2 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.2528-2604G>A | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 16/17 | chr12 | 7154885 | |||||||
| chr12:7154915 | C | T | 1 | a0001c0001t0013g0089 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2528-2574C>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 16/17 | chr12 | 7154915 | |||||||
| chr12:7154970 | G | T | 2 | a0001c0001t0009g0193 a0001c0001t0009g0202 |
2 | HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2528-2519G>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 16/17 | chr12 | 7154970 | |||||||
| chr12:7154984 | C | T | 1 | a0001c0001t0001g0087 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.2528-2505C>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 16/17 | chr12 | 7154984 | |||||||
| chr12:7155028 | CG | C | 6 | a0001c0001t0003g0278 a0001c0001t0003g0280 a0001c0001t0009g0193 others(3): Show |
6 | HG02572.hp1 HG02886.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.2528-2455delG | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr12 | 7155028 | ||||||
| chr12:7155112 | G | A | 1 | a0001c0001t0001g0072 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.2528-2377G>A | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 16/17 | chr12 | 7155112 | |||||||
| chr12:7155223 | C | G | 1 | a0001c0001t0005g0186 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2528-2266C>G | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 16/17 | chr12 | 7155223 | |||||||
| chr12:7155428 | T | G | 30 | a0001c0001t0002g0095 a0001c0001t0002g0249 a0001c0001t0009g0193 others(27): Show |
35 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(32): Show |
intron_variant | MODIFIER | c.2528-2061T>G | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 16/17 | chr12 | 7155428 | |||||||
| chr12:7155831 | T | C | 156 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(153): Show |
213 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.2528-1658T>C | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 16/17 | chr12 | 7155831 | |||||||
| chr12:7156332 | C | T | 3 | a0001c0001t0003g0278 a0001c0001t0003g0280 a0001c0008t0003g0279 |
3 | HG02886.hp1 HG03486.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2528-1157C>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 16/17 | chr12 | 7156332 | |||||||
| chr12:7156603 | G | A | 142 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(139): Show |
197 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.2528-886G>A | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 16/17 | chr12 | 7156603 | |||||||
| chr12:7156707 | C | T | 1 | a0001c0017t0001g0214 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2528-782C>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 16/17 | chr12 | 7156707 | |||||||
| chr12:7156723 | C | T | 6 | a0001c0001t0004g0030 a0001c0001t0004g0031 a0001c0001t0004g0157 others(3): Show |
7 | HG01884.hp2 HG02145.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.2528-766C>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 16/17 | chr12 | 7156723 | |||||||
| chr12:7156730 | C | T | 4 | a0001c0001t0001g0242 a0001c0001t0001g0245 a0001c0001t0001g0246 others(1): Show |
4 | HG02965.hp2 HG03041.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.2528-759C>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 16/17 | chr12 | 7156730 | |||||||
| chr12:7156816 | C | T | 4 | a0001c0001t0001g0018 a0001c0001t0001g0059 a0001c0001t0001g0076 others(1): Show |
6 | HG00741.hp1 HG01361.hp1 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.2528-673C>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 16/17 | chr12 | 7156816 | |||||||
| chr12:7156817 | G | A | 4 | a0001c0001t0001g0242 a0001c0001t0001g0245 a0001c0001t0001g0246 others(1): Show |
4 | HG02965.hp2 HG03041.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.2528-672G>A | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 16/17 | chr12 | 7156817 | |||||||
| chr12:7156870 | C | A | 1 | a0001c0001t0001g0079 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2528-619C>A | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 16/17 | chr12 | 7156870 | |||||||
| chr12:7156875 | C | A | 196 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(193): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.2528-614C>A | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 16/17 | chr12 | 7156875 | |||||||
| chr12:7156877 | G | C | 147 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(144): Show |
202 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.2528-612G>C | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 16/17 | chr12 | 7156877 | |||||||
| chr12:7157017 | C | G | 1 | a0001c0001t0004g0157 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2528-472C>G | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 16/17 | chr12 | 7157017 | |||||||
| chr12:7157017 | C | T | 84 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0020 others(81): Show |
110 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.2528-472C>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 16/17 | chr12 | 7157017 | |||||||
| chr12:7157088 | C | A | 1 | a0001c0001t0001g0063 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2528-401C>A | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 16/17 | chr12 | 7157088 | |||||||
| chr12:7157109 | G | A | 1 | a0001c0001t0001g0247 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.2528-380G>A | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 16/17 | chr12 | 7157109 | |||||||
| chr12:7157176 | A | G | 6 | a0001c0001t0001g0039 a0001c0001t0001g0143 a0001c0001t0001g0205 others(3): Show |
7 | HG00438.hp1 HG02027.hp2 NA18612.hp1 others(4): Show |
intron_variant | MODIFIER | c.2528-313A>G | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 16/17 | chr12 | 7157176 | |||||||
| chr12:7157196 | T | A | 1 | a0001c0001t0001g0069 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.2528-293T>A | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 16/17 | chr12 | 7157196 | |||||||
| chr12:7157369 | C | T | 50 | a0001c0001t0002g0095 a0001c0001t0002g0249 a0001c0001t0002g0251 others(47): Show |
60 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.2528-120C>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 16/17 | chr12 | 7157369 | |||||||
| chr12:7157373 | T | C | 6 | a0001c0001t0003g0189 a0001c0001t0003g0190 a0001c0001t0003g0200 others(3): Show |
6 | HG02895.hp2 HG02922.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.2528-116T>C | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 16/17 | chr12 | 7157373 | |||||||
| chr12:7157476 | G | A | 2 | a0001c0001t0001g0137 a0001c0001t0001g0144 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.2528-13G>A | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 16/17 | chr12 | 7157476 | |||||||
| chr12:7157710 | C | T | 1 | a0001c0001t0001g0250 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2730+19C>T | CLSTN3 | ENSG00000139182.15 | transcript | ENST00000266546.11 | protein_coding | 17/17 | chr12 | 7157710 |