Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 8727 |
| ensemblid | ENSG00000119326.15 |
| hgncid | 2512 |
| symbol | CTNNAL1 |
| name | catenin alpha like 1 |
| refseq_nuc | NM_003798.4 |
| refseq_prot | NP_003789.1 |
| ensembl_nuc | ENST00000325551.9 |
| ensembl_prot | ENSP00000320434.4 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 108942577 |
| end | 109013499 |
| strand | - |
| ver | v1.2 |
| region | chr9:108942577-109013499 |
| region5000 | chr9:108937577-109018499 |
| regionname0 | CTNNAL1_chr9_108942577_109013499 |
| regionname5000 | CTNNAL1_chr9_108937577_109018499 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 734 | 324 | 82 | 48 | 150 | 10 | 32 | 122 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | MAASP others(729): Show |
chr9 | 108937577 | 109018499 |
| a0002 | 0/0 | 734 | 81 | 1 | 21 | 50 | 4 | 5 | 40 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | MAASP others(729): Show |
chr9 | 108937577 | 109018499 |
| a0003 | 0/0 | 734 | 9 | 7 | 2 | 0 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | MAASP others(729): Show |
chr9 | 108937577 | 109018499 |
| a0004 | 0/0 | 734 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | MAASP others(729): Show |
chr9 | 108937577 | 109018499 |
| a0005 | 0/0 | 734 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | MAASP others(729): Show |
chr9 | 108937577 | 109018499 |
| a0006 | 0/0 | 734 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | MAASP others(729): Show |
chr9 | 108937577 | 109018499 |
| a0007 | 0/0 | 734 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | MAASP others(729): Show |
chr9 | 108937577 | 109018499 |
| a0008 | 0/0 | 734 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | MAASP others(729): Show |
chr9 | 108937577 | 109018499 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2202 | 323 | 82 | 48 | 149 | 10 | 32 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | ATGGC others(2197): Show |
chr9 | 108937577 | 109018499 | ||
| a0001c0010 | 0/0 | 2202 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | ATGGC others(2197): Show |
chr9 | 108937577 | 109018499 | ||
| a0002c0002 | 0/0 | 2202 | 80 | 1 | 21 | 49 | 4 | 5 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | ATGGC others(2197): Show |
chr9 | 108937577 | 109018499 | ||
| a0002c0006 | 0/0 | 2202 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | ATGGC others(2197): Show |
chr9 | 108937577 | 109018499 | ||
| a0003c0003 | 0/0 | 2202 | 9 | 7 | 2 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | ATGGC others(2197): Show |
chr9 | 108937577 | 109018499 | ||
| a0004c0004 | 0/0 | 2202 | 2 | 0 | 0 | 0 | 0 | 2 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | ATGGC others(2197): Show |
chr9 | 108937577 | 109018499 | ||
| a0005c0005 | 0/0 | 2202 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | ATGGC others(2197): Show |
chr9 | 108937577 | 109018499 | ||
| a0006c0009 | 0/0 | 2202 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | ATGGC others(2197): Show |
chr9 | 108937577 | 109018499 | ||
| a0007c0007 | 0/0 | 2202 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | ATGGC others(2197): Show |
chr9 | 108937577 | 109018499 | ||
| a0008c0008 | 0/0 | 2202 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | ATGGC others(2197): Show |
chr9 | 108937577 | 109018499 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2454 | 288 | 62 | 43 | 149 | 6 | 26 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | GACTG others(2449): Show |
chr9 | 108937577 | 109018499 |
| a0001c0001t0002 | 0/0 | 2454 | 27 | 18 | 2 | 0 | 2 | 5 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | GACTG others(2449): Show |
chr9 | 108937577 | 109018499 |
| a0001c0001t0003 | 0/0 | 2454 | 5 | 0 | 2 | 0 | 2 | 1 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | GACTG others(2449): Show |
chr9 | 108937577 | 109018499 |
| a0001c0001t0004 | 0/0 | 2454 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | GACTG others(2449): Show |
chr9 | 108937577 | 109018499 |
| a0001c0001t0005 | 0/0 | 2454 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | GACTG others(2449): Show |
chr9 | 108937577 | 109018499 |
| a0001c0001t0006 | 0/0 | 2454 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | GACTG others(2449): Show |
chr9 | 108937577 | 109018499 |
| a0001c0010t0001 | 0/0 | 2454 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | GACTG others(2449): Show |
chr9 | 108937577 | 109018499 |
| a0002c0002t0001 | 0/0 | 2454 | 80 | 1 | 21 | 49 | 4 | 5 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | GACTG others(2449): Show |
chr9 | 108937577 | 109018499 |
| a0002c0006t0001 | 0/0 | 2454 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | GACTG others(2449): Show |
chr9 | 108937577 | 109018499 |
| a0003c0003t0001 | 0/0 | 2454 | 9 | 7 | 2 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | GACTG others(2449): Show |
chr9 | 108937577 | 109018499 |
| a0004c0004t0001 | 0/0 | 2454 | 2 | 0 | 0 | 0 | 0 | 2 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | GACTG others(2449): Show |
chr9 | 108937577 | 109018499 |
| a0005c0005t0001 | 0/0 | 2454 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | GACTG others(2449): Show |
chr9 | 108937577 | 109018499 |
| a0006c0009t0001 | 0/0 | 2454 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | GACTG others(2449): Show |
chr9 | 108937577 | 109018499 |
| a0007c0007t0001 | 0/0 | 2454 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | GACTG others(2449): Show |
chr9 | 108937577 | 109018499 |
| a0008c0008t0001 | 0/0 | 2454 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | GACTG others(2449): Show |
chr9 | 108937577 | 109018499 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 7 | 0 | 1 | 6 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0006 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0008 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0009 | 0/0 | 4 | 0 | 0 | 0 | 0 | 4 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0235 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0337 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0001g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0002g0003 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0002g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0002g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0003g0357 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0003g0358 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0003g0359 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0003g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0003g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0004g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0005g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0001t0006g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0001c0010t0001g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0002c0002t0001g0002 | 0/0 | 5 | 0 | 3 | 2 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0002c0002t0001g0004 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0002c0002t0001g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0002c0002t0001g0015 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0002c0002t0001g0016 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0002c0002t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0002c0002t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0002c0002t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0002c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0002c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0002c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0002c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0002c0002t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0002c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0002c0002t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0002c0002t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0002c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0002c0002t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0002c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0002c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0002c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0002c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0002c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0002c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0002c0002t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0002c0002t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0002c0002t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0002c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0002c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0002c0002t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0002c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0002c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0002c0002t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0002c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0002c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0002c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0002c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0002c0002t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0002c0002t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0002c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0002c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0002c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0002c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0002c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0002c0002t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0002c0002t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0002c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0002c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0002c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0002c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0002c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0002c0002t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0002c0002t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0002c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0002c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0002c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0002c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0002c0002t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0002c0002t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0002c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0002c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0002c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0002c0002t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0002c0002t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0002c0006t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0003c0003t0001g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0003c0003t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0003c0003t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0003c0003t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0003c0003t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0003c0003t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0003c0003t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0004c0004t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0004c0004t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0005c0005t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0006c0009t0001g0353 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0007c0007t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| a0008c0008t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0001 | g0015 | EUR | GBR | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0038 | EUR | GBR | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0136 | EUR | GBR | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0040 | EUR | GBR | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0177 | EUR | FIN | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0289 | EUR | FIN | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | CHS | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0335 | EAS | CHS | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | CHS | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG00438 | hp2 | a0002 | c0002 | t0001 | g0091 | EAS | CHS | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | CHS | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | CHS | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG00558 | hp2 | a0002 | c0002 | t0001 | g0025 | EAS | CHS | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | CHS | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG00621 | hp2 | a0002 | c0002 | t0001 | g0062 | EAS | CHS | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0237 | AMR | PUR | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0261 | AMR | PUR | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG00673 | hp1 | a0002 | c0002 | t0001 | g0097 | EAS | CHS | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | CHS | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG00733 | hp1 | a0003 | c0003 | t0001 | g0309 | AMR | PUR | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0250 | AMR | PUR | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG00735 | hp2 | a0002 | c0002 | t0001 | g0063 | AMR | PUR | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG00738 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG00741 | hp1 | a0002 | c0002 | t0001 | g0104 | AMR | PUR | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0271 | AMR | PUR | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG01070 | hp1 | a0002 | c0002 | t0001 | g0071 | AMR | PUR | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0211 | AMR | PUR | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0327 | AMR | PUR | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0265 | AMR | PUR | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0324 | AMR | PUR | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG01099 | hp2 | a0002 | c0002 | t0001 | g0092 | AMR | PUR | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0047 | AMR | PUR | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG01109 | hp2 | a0003 | c0003 | t0001 | g0311 | AMR | PUR | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG01167 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0345 | AMR | PUR | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0334 | AMR | PUR | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG01175 | hp1 | a0002 | c0002 | t0001 | g0073 | AMR | PUR | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG01192 | hp1 | a0002 | c0002 | t0001 | g0093 | AMR | PUR | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0299 | AMR | PUR | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG01243 | hp2 | a0001 | c0001 | t0004 | g0245 | AMR | PUR | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | CLM | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0281 | AMR | CLM | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | CLM | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0330 | AMR | CLM | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG01257 | hp2 | a0002 | c0002 | t0001 | g0086 | AMR | CLM | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG01261 | hp1 | a0002 | c0002 | t0001 | g0085 | AMR | CLM | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0315 | AMR | CLM | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG01346 | hp1 | a0002 | c0002 | t0001 | g0101 | AMR | CLM | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | CLM | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0039 | AMR | CLM | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG01358 | hp2 | a0002 | c0002 | t0001 | g0060 | AMR | CLM | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG01361 | hp1 | a0002 | c0002 | t0001 | g0072 | AMR | CLM | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | CLM | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG01433 | hp1 | a0002 | c0002 | t0001 | g0079 | AMR | CLM | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG01433 | hp2 | a0001 | c0001 | t0003 | g0360 | AMR | CLM | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG01496 | hp1 | a0001 | c0001 | t0003 | g0361 | AMR | CLM | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | CLM | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG01515 | hp1 | a0002 | c0002 | t0001 | g0084 | EUR | IBS | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG01515 | hp2 | a0001 | c0001 | t0003 | g0358 | EUR | IBS | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG01516 | hp1 | a0002 | c0002 | t0001 | g0078 | EUR | IBS | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | IBS | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG01517 | hp1 | a0001 | c0001 | t0003 | g0357 | EUR | IBS | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG01517 | hp2 | a0002 | c0002 | t0001 | g0015 | EUR | IBS | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0306 | AFR | ACB | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | ACB | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0331 | AFR | ACB | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG01934 | hp1 | a0002 | c0002 | t0001 | g0110 | AMR | PEL | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0323 | AMR | PEL | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PEL | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG01952 | hp2 | a0002 | c0002 | t0001 | g0061 | AMR | PEL | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG01978 | hp1 | a0002 | c0002 | t0001 | g0247 | AMR | PEL | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | PEL | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PEL | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG02004 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PEL | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | KHV | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | KHV | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | KHV | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | KHV | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | ACB | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0300 | AFR | ACB | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG02056 | hp1 | a0002 | c0002 | t0001 | g0075 | EAS | KHV | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | KHV | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | KHV | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | KHV | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | KHV | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG02074 | hp2 | a0002 | c0002 | t0001 | g0173 | EAS | KHV | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | KHV | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG02080 | hp2 | a0002 | c0002 | t0001 | g0081 | EAS | KHV | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | KHV | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0344 | EAS | KHV | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | KHV | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG02129 | hp2 | a0002 | c0002 | t0001 | g0064 | EAS | KHV | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | KHV | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG02145 | hp1 | a0003 | c0003 | t0001 | g0012 | AFR | ACB | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0249 | AFR | ACB | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0277 | AMR | PEL | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG02148 | hp2 | a0002 | c0002 | t0001 | g0076 | AMR | PEL | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG02165 | hp1 | a0002 | c0002 | t0001 | g0082 | EAS | CDX | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | CDX | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG02257 | hp1 | a0003 | c0003 | t0001 | g0312 | AFR | ACB | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0288 | AFR | ACB | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0266 | AFR | ACB | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0284 | AFR | ACB | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG02293 | hp1 | a0005 | c0005 | t0001 | g0094 | AMR | PEL | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0269 | AMR | PEL | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG02300 | hp1 | a0002 | c0002 | t0001 | g0058 | AMR | PEL | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0303 | AFR | ACB | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0051 | AFR | ACB | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | KHV | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0338 | EAS | KHV | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0314 | AFR | GWD | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0234 | AFR | GWD | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0044 | AFR | GWD | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0297 | AFR | GWD | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | GWD | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | GWD | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0053 | AFR | GWD | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0317 | AFR | GWD | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0326 | SAS | PJL | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0175 | SAS | PJL | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | GWD | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | GWD | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0287 | AFR | GWD | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG02735 | hp1 | a0002 | c0002 | t0001 | g0105 | SAS | PJL | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0286 | SAS | PJL | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0264 | AFR | GWD | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | GWD | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0278 | AFR | GWD | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG02818 | hp2 | a0002 | c0002 | t0001 | g0112 | AFR | GWD | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | GWD | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | GWD | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0049 | AFR | GWD | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG02922 | hp1 | a0003 | c0003 | t0001 | g0301 | AFR | ESN | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0251 | AFR | ESN | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | ESN | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0050 | AFR | ESN | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | ESN | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG02970 | hp2 | a0001 | c0001 | t0005 | g0305 | AFR | ESN | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | ESN | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0280 | AFR | ESN | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0042 | SAS | PJL | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | GWD | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0308 | AFR | GWD | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0316 | AFR | MSL | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | MSL | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0045 | AFR | ESN | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ESN | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | ESN | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | ESN | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0035 | AFR | ESN | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG03195 | hp2 | a0003 | c0003 | t0001 | g0012 | AFR | ESN | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | MSL | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0348 | AFR | MSL | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0304 | AFR | MSL | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0246 | AFR | MSL | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0048 | SAS | PJL | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG03239 | hp2 | a0002 | c0002 | t0001 | g0016 | SAS | PJL | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0014 | AFR | MSL | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG03453 | hp2 | a0003 | c0003 | t0001 | g0298 | AFR | MSL | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG03486 | hp1 | a0003 | c0003 | t0001 | g0012 | AFR | MSL | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | MSL | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG03490 | hp2 | a0002 | c0002 | t0001 | g0016 | SAS | PJL | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0275 | SAS | PJL | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0137 | SAS | PJL | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | ESN | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | ESN | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0052 | AFR | GWD | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0242 | AFR | GWD | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | MSL | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0349 | AFR | MSL | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0270 | SAS | PJL | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG03669 | hp1 | a0006 | c0009 | t0001 | g0353 | SAS | PJL | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0276 | SAS | PJL | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0126 | SAS | STU | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0329 | SAS | STU | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0043 | SAS | PJL | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG03710 | hp1 | a0002 | c0002 | t0001 | g0087 | SAS | PJL | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0041 | SAS | PJL | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | BEB | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0036 | SAS | BEB | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | BEB | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0226 | SAS | BEB | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0236 | SAS | BEB | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | BEB | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0359 | SAS | STU | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG04115 | hp2 | a0004 | c0004 | t0001 | g0184 | SAS | STU | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0127 | SAS | BEB | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0213 | SAS | BEB | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | STU | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG04204 | hp2 | a0004 | c0004 | t0001 | g0183 | SAS | STU | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0172 | SAS | STU | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0233 | SAS | STU | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA18522 | hp1 | a0003 | c0003 | t0001 | g0310 | AFR | YRI | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0013 | AFR | YRI | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | CHB | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | CHB | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA18747 | hp1 | a0002 | c0002 | t0001 | g0080 | EAS | CHB | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | CHB | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | YRI | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0313 | AFR | YRI | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0347 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA18941 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0346 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0340 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA18942 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA18944 | hp1 | a0007 | c0007 | t0001 | g0068 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA18946 | hp2 | a0002 | c0002 | t0001 | g0106 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA18949 | hp2 | a0002 | c0002 | t0001 | g0069 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0336 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA18956 | hp2 | a0002 | c0002 | t0001 | g0098 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0333 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA18959 | hp1 | a0002 | c0002 | t0001 | g0099 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA18961 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA18963 | hp1 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0352 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA18966 | hp1 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA18967 | hp1 | a0002 | c0002 | t0001 | g0054 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA18968 | hp2 | a0002 | c0002 | t0001 | g0107 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA18971 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA18973 | hp2 | a0002 | c0002 | t0001 | g0089 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA18974 | hp2 | a0002 | c0002 | t0001 | g0090 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0341 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0351 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA18983 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA18984 | hp1 | a0002 | c0002 | t0001 | g0077 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA18986 | hp1 | a0002 | c0002 | t0001 | g0088 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0343 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA18988 | hp1 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0342 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA18990 | hp2 | a0002 | c0002 | t0001 | g0083 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA18991 | hp1 | a0002 | c0002 | t0001 | g0350 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA18992 | hp2 | a0002 | c0002 | t0001 | g0025 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA18995 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA19000 | hp1 | a0002 | c0002 | t0001 | g0059 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA19002 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA19003 | hp2 | a0002 | c0002 | t0001 | g0108 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA19004 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA19005 | hp1 | a0002 | c0002 | t0001 | g0065 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA19006 | hp1 | a0002 | c0002 | t0001 | g0056 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA19007 | hp2 | a0002 | c0006 | t0001 | g0096 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA19010 | hp2 | a0008 | c0008 | t0001 | g0221 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0046 | AFR | LWK | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA19030 | hp2 | a0001 | c0001 | t0006 | g0356 | AFR | LWK | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0302 | AFR | LWK | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0354 | AFR | LWK | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA19054 | hp1 | a0002 | c0002 | t0001 | g0074 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA19055 | hp1 | a0002 | c0002 | t0001 | g0057 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA19062 | hp1 | a0002 | c0002 | t0001 | g0095 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA19062 | hp2 | a0002 | c0002 | t0001 | g0188 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA19064 | hp2 | a0002 | c0002 | t0001 | g0070 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA19065 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0332 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA19072 | hp2 | a0002 | c0002 | t0001 | g0100 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA19074 | hp1 | a0002 | c0002 | t0001 | g0185 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA19078 | hp1 | a0002 | c0002 | t0001 | g0066 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA19078 | hp2 | a0001 | c0010 | t0001 | g0355 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0339 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA19085 | hp2 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA19089 | hp1 | a0002 | c0002 | t0001 | g0067 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0282 | AFR | YRI | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | YRI | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0182 | EUR | TSI | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0292 | EUR | TSI | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | GIH | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA20905 | hp2 | a0002 | c0002 | t0001 | g0055 | SAS | GIH | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | CLM | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG01123 | hp2 | a0002 | c0002 | t0001 | g0004 | AMR | CLM | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | ACB | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0283 | AFR | ACB | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | ACB | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | ACB | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0037 | AFR | ACB | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0307 | AFR | USA | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0239 | AFR | USA | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | USA | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0267 | AFR | USA | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0320 | AFR | LWK | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | LWK | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0337 | REF | REF | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0235 | REF | REF | CTNNAL1_chr9_108937577_109018499 | CTNNAL1 | chr9 | 108937577 | 109018499 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:108942827 | A | C | 1 | a0006 | 1 | HG03669.hp1 | missense_variant | MODERATE | c.2147T>G | p.Met716Arg | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 19/19 | 2204/2454 | 2147/2205 | 716/734 | chr9 | 108942827 | |||
| chr9:108965390 | C | G | 3 | a0002 a0005 a0007 |
83 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(80): Show |
missense_variant | MODERATE | c.1579G>C | p.Glu527Gln | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 11/19 | 1636/2454 | 1579/2205 | 527/734 | chr9 | 108965390 | |||
| chr9:108972751 | G | C | 1 | a0003 | 9 | HG00733.hp1 HG01109.hp2 HG02145.hp1 others(6): Show |
missense_variant | MODERATE | c.1271C>G | p.Thr424Ser | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 9/19 | 1328/2454 | 1271/2205 | 424/734 | chr9 | 108972751 | |||
| chr9:108972784 | G | C | 1 | a0007 | 1 | NA18944.hp1 | missense_variant | MODERATE | c.1238C>G | p.Ala413Gly | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 9/19 | 1295/2454 | 1238/2205 | 413/734 | chr9 | 108972784 | |||
| chr9:108983267 | C | T | 1 | a0005 | 1 | HG02293.hp1 | missense_variant | MODERATE | c.778G>A | p.Gly260Arg | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 6/19 | 835/2454 | 778/2205 | 260/734 | chr9 | 108983267 | |||
| chr9:108990758 | C | T | 1 | a0004 | 2 | HG04115.hp2 HG04204.hp2 |
missense_variant | MODERATE | c.607G>A | p.Glu203Lys | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 4/19 | 664/2454 | 607/2205 | 203/734 | chr9 | 108990758 | |||
| chr9:108999122 | T | A | 1 | a0008 | 1 | NA19010.hp2 | missense_variant | MODERATE | c.276A>T | p.Glu92Asp | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 2/19 | 333/2454 | 276/2205 | 92/734 | chr9 | 108999122 | |||
| chr9:108999126 | T | G | 1 | a0006 | 1 | HG03669.hp1 | missense_variant | MODERATE | c.272A>C | p.Asn91Thr | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 2/19 | 329/2454 | 272/2205 | 91/734 | chr9 | 108999126 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:108976992 | G | A | 1 | a0006c0009 | 1 | HG03669.hp1 | synonymous_variant | LOW | c.1158C>T | p.Ile386Ile | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 8/19 | 1215/2454 | 1158/2205 | 386/734 | chr9 | 108976992 | |||
| chr9:108979323 | C | T | 1 | a0002c0006 | 1 | NA19007.hp2 | synonymous_variant | LOW | c.1059G>A | p.Ala353Ala | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 7/19 | 1116/2454 | 1059/2205 | 353/734 | chr9 | 108979323 | |||
| chr9:108992728 | C | T | 4 | a0002c0002 a0002c0006 a0005c0005 others(1): Show |
83 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(80): Show |
synonymous_variant | LOW | c.423G>A | p.Val141Val | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 3/19 | 480/2454 | 423/2205 | 141/734 | chr9 | 108992728 | |||
| chr9:109013428 | G | A | 1 | a0001c0010 | 1 | NA19078.hp2 | synonymous_variant | LOW | c.15C>T | p.Pro5Pro | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/19 | 72/2454 | 15/2205 | 5/734 | chr9 | 109013428 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:108942694 | G | C | 1 | a0001c0001t0005 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*75C>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 19/19 | 75 | chr9 | 108942694 | ||||||
| chr9:108942750 | A | C | 1 | a0001c0001t0004 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*19T>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 19/19 | 19 | chr9 | 108942750 | ||||||
| chr9:109013463 | G | C | 1 | a0001c0001t0006 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-21C>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/19 | 21 | chr9 | 109013463 | ||||||
| chr9:109013476 | G | C | 1 | a0001c0001t0003 | 5 | HG01433.hp2 HG01496.hp1 HG01515.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-34C>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/19 | 34 | chr9 | 109013476 | ||||||
| chr9:109013487 | C | T | 1 | a0001c0001t0002 | 27 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(24): Show |
5_prime_UTR_variant | MODIFIER | c.-45G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/19 | 45 | chr9 | 109013487 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:108943221 | A | C | 132 | a0001c0001t0001g0011 a0001c0001t0001g0019 a0001c0001t0001g0031 others(129): Show |
156 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(153): Show |
intron_variant | MODIFIER | c.2056-177T>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 17/18 | chr9 | 108943221 | |||||||
| chr9:108943413 | G | A | 1 | a0001c0001t0001g0111 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2055+290C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 17/18 | chr9 | 108943413 | |||||||
| chr9:108943450 | G | A | 1 | a0001c0001t0001g0282 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2055+253C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 17/18 | chr9 | 108943450 | |||||||
| chr9:108943462 | G | T | 1 | a0001c0001t0001g0117 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2055+241C>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 17/18 | chr9 | 108943462 | |||||||
| chr9:108943463 | A | T | 1 | a0001c0001t0001g0117 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2055+240T>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 17/18 | chr9 | 108943463 | |||||||
| chr9:108943670 | G | C | 1 | a0001c0001t0001g0327 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2055+33C>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 17/18 | chr9 | 108943670 | |||||||
| chr9:108944140 | T | G | 3 | a0001c0001t0002g0003 a0001c0001t0002g0045 a0001c0001t0002g0050 |
6 | HG02109.hp1 HG02717.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1885-122A>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 15/18 | chr9 | 108944140 | |||||||
| chr9:108944152 | A | G | 2 | a0002c0002t0001g0016 a0002c0002t0001g0084 |
3 | HG01515.hp1 HG03239.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.1885-134T>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 15/18 | chr9 | 108944152 | |||||||
| chr9:108944177 | A | C | 1 | a0003c0003t0001g0309 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1885-159T>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 15/18 | chr9 | 108944177 | |||||||
| chr9:108944370 | A | T | 1 | a0001c0001t0001g0209 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1885-352T>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 15/18 | chr9 | 108944370 | |||||||
| chr9:108944416 | AT | A | 44 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0020 others(41): Show |
56 | HG00140.hp1 HG00408.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.1885-399delA | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 15/18 | chr9 | 108944416 | |||||||
| chr9:108944618 | A | C | 1 | a0001c0001t0001g0225 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1885-600T>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 15/18 | chr9 | 108944618 | |||||||
| chr9:108945137 | C | G | 347 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(344): Show |
403 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(400): Show |
intron_variant | MODIFIER | c.1885-1119G>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 15/18 | chr9 | 108945137 | |||||||
| chr9:108945191 | C | A | 13 | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0001g0297 others(10): Show |
16 | HG01243.hp1 HG01884.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.1885-1173G>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 15/18 | chr9 | 108945191 | |||||||
| chr9:108945417 | G | A | 1 | a0001c0001t0001g0167 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1885-1399C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 15/18 | chr9 | 108945417 | |||||||
| chr9:108945425 | T | A | 41 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(38): Show |
44 | HG00408.hp2 HG01081.hp1 HG01099.hp1 others(41): Show |
intron_variant | MODIFIER | c.1885-1407A>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 15/18 | chr9 | 108945425 | |||||||
| chr9:108945425 | T | G | 1 | a0001c0001t0001g0187 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1885-1407A>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 15/18 | chr9 | 108945425 | |||||||
| chr9:108945463 | C | CT | 16 | a0001c0001t0001g0127 a0001c0001t0001g0155 a0001c0001t0001g0171 others(13): Show |
16 | HG01109.hp2 HG01243.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.1885-1446dupA | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 15/18 | chr9 | 108945463 | |||||||
| chr9:108945546 | T | G | 1 | a0006c0009t0001g0353 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1885-1528A>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 15/18 | chr9 | 108945546 | |||||||
| chr9:108945554 | C | A | 33 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(30): Show |
36 | HG00408.hp2 HG01081.hp1 HG01099.hp1 others(33): Show |
intron_variant | MODIFIER | c.1885-1536G>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 15/18 | chr9 | 108945554 | |||||||
| chr9:108945619 | G | A | 33 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(30): Show |
36 | HG00408.hp2 HG01081.hp1 HG01099.hp1 others(33): Show |
intron_variant | MODIFIER | c.1885-1601C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 15/18 | chr9 | 108945619 | |||||||
| chr9:108945628 | GT | G | 319 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(316): Show |
369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.1885-1611delA | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 15/18 | chr9 | 108945628 | |||||||
| chr9:108945638 | T | G | 49 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0021 others(46): Show |
55 | HG00280.hp1 HG00544.hp2 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.1885-1620A>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 15/18 | chr9 | 108945638 | |||||||
| chr9:108945639 | T | G | 4 | a0001c0001t0001g0109 a0001c0001t0001g0354 a0001c0001t0002g0037 others(1): Show |
4 | HG01109.hp1 HG02559.hp2 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.1885-1621A>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 15/18 | chr9 | 108945639 | |||||||
| chr9:108945640 | T | G | 1 | a0001c0001t0001g0339 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1885-1622A>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 15/18 | chr9 | 108945640 | |||||||
| chr9:108945641 | T | G | 32 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(29): Show |
35 | HG00408.hp2 HG01081.hp1 HG01099.hp1 others(32): Show |
intron_variant | MODIFIER | c.1885-1623A>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 15/18 | chr9 | 108945641 | |||||||
| chr9:108945642 | T | G | 21 | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0001g0297 others(18): Show |
26 | HG00733.hp1 HG01109.hp2 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.1885-1624A>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 15/18 | chr9 | 108945642 | |||||||
| chr9:108945643 | G | T | 21 | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0001g0297 others(18): Show |
26 | HG00733.hp1 HG01109.hp2 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.1885-1625C>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 15/18 | chr9 | 108945643 | |||||||
| chr9:108945646 | T | G | 7 | a0001c0001t0001g0031 a0001c0001t0001g0297 a0001c0001t0001g0299 others(4): Show |
8 | HG01243.hp1 HG01884.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.1885-1628A>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 15/18 | chr9 | 108945646 | |||||||
| chr9:108945648 | G | T | 60 | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0001g0032 others(57): Show |
68 | HG00408.hp2 HG01081.hp1 HG01099.hp1 others(65): Show |
intron_variant | MODIFIER | c.1885-1630C>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 15/18 | chr9 | 108945648 | |||||||
| chr9:108945650 | T | G | 4 | a0001c0001t0001g0299 a0001c0001t0001g0304 a0001c0001t0001g0307 others(1): Show |
4 | HG01243.hp1 HG03225.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1885-1632A>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 15/18 | chr9 | 108945650 | |||||||
| chr9:108945689 | G | A | 1 | a0001c0001t0001g0272 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1885-1671C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 15/18 | chr9 | 108945689 | |||||||
| chr9:108945692 | C | A | 1 | a0001c0001t0001g0236 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1885-1674G>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 15/18 | chr9 | 108945692 | |||||||
| chr9:108945821 | G | A | 1 | a0002c0002t0001g0063 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1885-1803C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 15/18 | chr9 | 108945821 | |||||||
| chr9:108946248 | G | A | 33 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(30): Show |
36 | HG00408.hp2 HG01081.hp1 HG01099.hp1 others(33): Show |
intron_variant | MODIFIER | c.1884+1938C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 15/18 | chr9 | 108946248 | |||||||
| chr9:108946297 | C | CA | 70 | a0001c0001t0001g0019 a0001c0001t0001g0119 a0001c0001t0001g0180 others(67): Show |
86 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.1884+1888dupT | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 15/18 | chr9 | 108946297 | |||||||
| chr9:108946297 | CA | C | 29 | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0001g0141 others(26): Show |
34 | HG00733.hp1 HG00733.hp2 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.1884+1888delT | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 15/18 | chr9 | 108946297 | |||||||
| chr9:108946458 | T | C | 2 | a0001c0001t0001g0118 a0001c0001t0001g0128 |
2 | HG00408.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.1884+1728A>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 15/18 | chr9 | 108946458 | |||||||
| chr9:108946502 | T | A | 1 | a0001c0001t0002g0047 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1884+1684A>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 15/18 | chr9 | 108946502 | |||||||
| chr9:108946507 | G | A | 1 | a0002c0002t0001g0058 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1884+1679C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 15/18 | chr9 | 108946507 | |||||||
| chr9:108946542 | T | C | 33 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(30): Show |
36 | HG00408.hp2 HG01081.hp1 HG01099.hp1 others(33): Show |
intron_variant | MODIFIER | c.1884+1644A>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 15/18 | chr9 | 108946542 | |||||||
| chr9:108946904 | C | T | 1 | a0001c0001t0001g0165 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1884+1282G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 15/18 | chr9 | 108946904 | |||||||
| chr9:108947112 | T | C | 1 | a0006c0009t0001g0353 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1884+1074A>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 15/18 | chr9 | 108947112 | |||||||
| chr9:108947115 | C | CT | 118 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0027 others(115): Show |
139 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(136): Show |
intron_variant | MODIFIER | c.1884+1070dupA | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 15/18 | chr9 | 108947115 | |||||||
| chr9:108947119 | T | C | 2 | a0001c0001t0002g0013 a0001c0001t0002g0046 |
3 | HG03041.hp1 NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1884+1067A>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 15/18 | chr9 | 108947119 | |||||||
| chr9:108947180 | C | T | 1 | a0001c0001t0001g0308 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1884+1006G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 15/18 | chr9 | 108947180 | |||||||
| chr9:108947271 | A | G | 41 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(38): Show |
44 | HG00408.hp2 HG01081.hp1 HG01099.hp1 others(41): Show |
intron_variant | MODIFIER | c.1884+915T>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 15/18 | chr9 | 108947271 | |||||||
| chr9:108947300 | A | C | 7 | a0001c0001t0001g0308 a0001c0001t0001g0354 a0001c0001t0003g0357 others(4): Show |
7 | HG01433.hp2 HG01496.hp1 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.1884+886T>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 15/18 | chr9 | 108947300 | |||||||
| chr9:108947348 | C | T | 44 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0020 others(41): Show |
56 | HG00140.hp1 HG00408.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.1884+838G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 15/18 | chr9 | 108947348 | |||||||
| chr9:108947379 | C | T | 69 | a0001c0001t0001g0019 a0002c0002t0001g0002 a0002c0002t0001g0004 others(66): Show |
85 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.1884+807G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 15/18 | chr9 | 108947379 | |||||||
| chr9:108947627 | G | C | 1 | a0006c0009t0001g0353 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1884+559C>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 15/18 | chr9 | 108947627 | |||||||
| chr9:108947796 | T | A | 1 | a0006c0009t0001g0353 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1884+390A>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 15/18 | chr9 | 108947796 | |||||||
| chr9:108947943 | C | T | 1 | a0001c0001t0001g0165 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1884+243G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 15/18 | chr9 | 108947943 | |||||||
| chr9:108948863 | G | A | 1 | a0006c0009t0001g0353 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1836-629C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 14/18 | chr9 | 108948863 | |||||||
| chr9:108948923 | A | T | 1 | a0006c0009t0001g0353 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1836-689T>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 14/18 | chr9 | 108948923 | |||||||
| chr9:108948928 | T | C | 20 | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0001g0297 others(17): Show |
25 | HG00733.hp1 HG01109.hp2 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.1836-694A>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 14/18 | chr9 | 108948928 | |||||||
| chr9:108948990 | C | T | 1 | a0006c0009t0001g0353 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1836-756G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 14/18 | chr9 | 108948990 | |||||||
| chr9:108949030 | A | C | 48 | a0001c0001t0001g0009 a0001c0001t0001g0026 a0001c0001t0001g0028 others(45): Show |
54 | HG00280.hp2 HG00558.hp1 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.1836-796T>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 14/18 | chr9 | 108949030 | |||||||
| chr9:108949115 | A | T | 2 | a0001c0001t0001g0246 a0001c0001t0004g0245 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1836-881T>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 14/18 | chr9 | 108949115 | |||||||
| chr9:108949235 | A | G | 41 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(38): Show |
44 | HG00408.hp2 HG01081.hp1 HG01099.hp1 others(41): Show |
intron_variant | MODIFIER | c.1836-1001T>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 14/18 | chr9 | 108949235 | |||||||
| chr9:108949251 | G | A | 8 | a0002c0002t0001g0060 a0002c0002t0001g0061 a0002c0002t0001g0071 others(5): Show |
8 | HG01070.hp1 HG01257.hp2 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.1836-1017C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 14/18 | chr9 | 108949251 | |||||||
| chr9:108949337 | C | T | 1 | a0001c0001t0001g0339 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1836-1103G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 14/18 | chr9 | 108949337 | |||||||
| chr9:108949433 | C | T | 10 | a0002c0002t0001g0005 a0002c0002t0001g0056 a0002c0002t0001g0057 others(7): Show |
13 | HG00673.hp1 NA18946.hp2 NA18956.hp2 others(10): Show |
intron_variant | MODIFIER | c.1836-1199G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 14/18 | chr9 | 108949433 | |||||||
| chr9:108949506 | G | C | 1 | a0001c0001t0006g0356 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1836-1272C>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 14/18 | chr9 | 108949506 | |||||||
| chr9:108949533 | C | T | 1 | a0001c0001t0001g0150 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1836-1299G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 14/18 | chr9 | 108949533 | |||||||
| chr9:108949543 | A | G | 33 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(30): Show |
36 | HG00408.hp2 HG01081.hp1 HG01099.hp1 others(33): Show |
intron_variant | MODIFIER | c.1836-1309T>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 14/18 | chr9 | 108949543 | |||||||
| chr9:108949581 | C | T | 68 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0005 others(65): Show |
83 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(80): Show |
intron_variant | MODIFIER | c.1836-1347G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 14/18 | chr9 | 108949581 | |||||||
| chr9:108949705 | G | A | 2 | a0001c0001t0001g0021 a0001c0001t0001g0143 |
3 | NA18954.hp1 NA18962.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.1836-1471C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 14/18 | chr9 | 108949705 | |||||||
| chr9:108949751 | G | A | 2 | a0001c0001t0001g0027 a0001c0001t0001g0218 |
3 | NA19011.hp1 NA19066.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.1836-1517C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 14/18 | chr9 | 108949751 | |||||||
| chr9:108949760 | C | T | 1 | a0001c0001t0001g0124 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1836-1526G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 14/18 | chr9 | 108949760 | |||||||
| chr9:108949790 | G | A | 1 | a0001c0001t0001g0354 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1836-1556C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 14/18 | chr9 | 108949790 | |||||||
| chr9:108949839 | G | A | 1 | a0001c0001t0001g0011 | 3 | HG02486.hp1 NA19240.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1836-1605C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 14/18 | chr9 | 108949839 | |||||||
| chr9:108949863 | G | C | 7 | a0001c0001t0001g0308 a0001c0001t0001g0354 a0001c0001t0003g0357 others(4): Show |
7 | HG01433.hp2 HG01496.hp1 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.1836-1629C>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 14/18 | chr9 | 108949863 | |||||||
| chr9:108949895 | G | A | 1 | a0001c0001t0001g0109 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1836-1661C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 14/18 | chr9 | 108949895 | |||||||
| chr9:108949928 | G | C | 1 | a0002c0002t0001g0080 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1836-1694C>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 14/18 | chr9 | 108949928 | |||||||
| chr9:108949992 | C | T | 1 | a0002c0002t0001g0071 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1836-1758G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 14/18 | chr9 | 108949992 | |||||||
| chr9:108950023 | C | CA | 54 | a0001c0001t0001g0009 a0001c0001t0001g0024 a0001c0001t0001g0029 others(51): Show |
63 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.1836-1790dupT | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 14/18 | chr9 | 108950023 | |||||||
| chr9:108950023 | CA | C | 57 | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0001g0032 others(54): Show |
65 | HG00408.hp2 HG00733.hp1 HG01081.hp1 others(62): Show |
intron_variant | MODIFIER | c.1836-1790delT | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 14/18 | chr9 | 108950023 | |||||||
| chr9:108950387 | T | C | 7 | a0001c0001t0001g0308 a0001c0001t0001g0354 a0001c0001t0003g0357 others(4): Show |
7 | HG01433.hp2 HG01496.hp1 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.1835+1822A>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 14/18 | chr9 | 108950387 | |||||||
| chr9:108950627 | C | T | 7 | a0003c0003t0001g0012 a0003c0003t0001g0298 a0003c0003t0001g0301 others(4): Show |
9 | HG00733.hp1 HG01109.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.1835+1582G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 14/18 | chr9 | 108950627 | |||||||
| chr9:108950630 | G | C | 345 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(342): Show |
401 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(398): Show |
intron_variant | MODIFIER | c.1835+1579C>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 14/18 | chr9 | 108950630 | |||||||
| chr9:108950644 | G | C | 128 | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0001g0032 others(125): Show |
151 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(148): Show |
intron_variant | MODIFIER | c.1835+1565C>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 14/18 | chr9 | 108950644 | |||||||
| chr9:108950858 | GA | G | 104 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0026 others(101): Show |
114 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(111): Show |
intron_variant | MODIFIER | c.1835+1350delT | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 14/18 | chr9 | 108950858 | |||||||
| chr9:108951040 | C | T | 1 | a0002c0002t0001g0110 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1835+1169G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 14/18 | chr9 | 108951040 | |||||||
| chr9:108951072 | G | A | 26 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0111 others(23): Show |
30 | HG02132.hp1 HG02622.hp1 HG02647.hp2 others(27): Show |
intron_variant | MODIFIER | c.1835+1137C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 14/18 | chr9 | 108951072 | |||||||
| chr9:108951073 | C | T | 15 | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0001g0135 others(12): Show |
18 | HG01069.hp2 HG01071.hp2 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.1835+1136G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 14/18 | chr9 | 108951073 | |||||||
| chr9:108951101 | C | T | 33 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(30): Show |
36 | HG00408.hp2 HG01081.hp1 HG01099.hp1 others(33): Show |
intron_variant | MODIFIER | c.1835+1108G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 14/18 | chr9 | 108951101 | |||||||
| chr9:108951167 | C | T | 1 | a0001c0001t0001g0198 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1835+1042G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 14/18 | chr9 | 108951167 | |||||||
| chr9:108951240 | C | T | 67 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0005 others(64): Show |
82 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.1835+969G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 14/18 | chr9 | 108951240 | |||||||
| chr9:108951585 | G | A | 19 | a0001c0001t0001g0300 a0001c0001t0002g0003 a0001c0001t0002g0013 others(16): Show |
24 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.1835+624C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 14/18 | chr9 | 108951585 | |||||||
| chr9:108951658 | T | C | 1 | a0001c0001t0002g0037 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1835+551A>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 14/18 | chr9 | 108951658 | |||||||
| chr9:108951758 | T | C | 32 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(29): Show |
35 | HG00408.hp2 HG01081.hp1 HG01099.hp1 others(32): Show |
intron_variant | MODIFIER | c.1835+451A>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 14/18 | chr9 | 108951758 | |||||||
| chr9:108951901 | G | A | 6 | a0001c0001t0001g0354 a0001c0001t0003g0357 a0001c0001t0003g0358 others(3): Show |
6 | HG01433.hp2 HG01496.hp1 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.1835+308C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 14/18 | chr9 | 108951901 | |||||||
| chr9:108951988 | C | T | 1 | a0006c0009t0001g0353 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1835+221G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 14/18 | chr9 | 108951988 | |||||||
| chr9:108952616 | A | C | 9 | a0001c0001t0001g0031 a0001c0001t0001g0297 a0001c0001t0001g0299 others(6): Show |
10 | HG01243.hp1 HG01884.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.1630-122T>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 12/18 | chr9 | 108952616 | |||||||
| chr9:108952632 | AC | A | 20 | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0001g0297 others(17): Show |
25 | HG00733.hp1 HG01109.hp2 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.1630-139delG | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 12/18 | chr9 | 108952632 | |||||||
| chr9:108952645 | A | T | 6 | a0001c0001t0001g0354 a0001c0001t0003g0357 a0001c0001t0003g0358 others(3): Show |
6 | HG01433.hp2 HG01496.hp1 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.1630-151T>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 12/18 | chr9 | 108952645 | |||||||
| chr9:108952758 | T | A | 1 | a0001c0001t0001g0300 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1630-264A>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 12/18 | chr9 | 108952758 | |||||||
| chr9:108952759 | C | T | 1 | a0002c0002t0001g0067 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1630-265G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 12/18 | chr9 | 108952759 | |||||||
| chr9:108952870 | T | C | 6 | a0001c0001t0001g0354 a0001c0001t0003g0357 a0001c0001t0003g0358 others(3): Show |
6 | HG01433.hp2 HG01496.hp1 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.1630-376A>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 12/18 | chr9 | 108952870 | |||||||
| chr9:108952927 | T | C | 49 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0019 others(46): Show |
62 | HG00140.hp1 HG00408.hp1 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.1630-433A>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 12/18 | chr9 | 108952927 | |||||||
| chr9:108953016 | T | C | 4 | a0001c0001t0001g0152 a0001c0001t0001g0161 a0001c0001t0001g0162 others(1): Show |
4 | HG01261.hp2 HG02809.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1630-522A>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 12/18 | chr9 | 108953016 | |||||||
| chr9:108953019 | A | T | 1 | a0001c0001t0001g0136 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1630-525T>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 12/18 | chr9 | 108953019 | |||||||
| chr9:108953440 | A | G | 40 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(37): Show |
43 | HG00408.hp2 HG01081.hp1 HG01099.hp1 others(40): Show |
intron_variant | MODIFIER | c.1630-946T>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 12/18 | chr9 | 108953440 | |||||||
| chr9:108953470 | C | T | 32 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(29): Show |
35 | HG00408.hp2 HG01081.hp1 HG01099.hp1 others(32): Show |
intron_variant | MODIFIER | c.1630-976G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 12/18 | chr9 | 108953470 | |||||||
| chr9:108953496 | C | T | 1 | a0001c0001t0001g0256 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1630-1002G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 12/18 | chr9 | 108953496 | |||||||
| chr9:108953520 | T | TAAAAC | 67 | a0001c0001t0001g0019 a0002c0002t0001g0002 a0002c0002t0001g0004 others(64): Show |
82 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.1630-1031_1630-102 others(9): Show |
CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 12/18 | chr9 | 108953520 | |||||||
| chr9:108953569 | C | G | 1 | a0006c0009t0001g0353 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1630-1075G>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 12/18 | chr9 | 108953569 | |||||||
| chr9:108953600 | C | T | 22 | a0001c0001t0001g0024 a0001c0001t0001g0102 a0001c0001t0001g0147 others(19): Show |
23 | HG00280.hp1 HG00544.hp2 HG00673.hp2 others(20): Show |
intron_variant | MODIFIER | c.1630-1106G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 12/18 | chr9 | 108953600 | |||||||
| chr9:108953668 | C | T | 1 | a0002c0002t0001g0092 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1630-1174G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 12/18 | chr9 | 108953668 | |||||||
| chr9:108953701 | C | A | 1 | a0002c0002t0001g0081 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1630-1207G>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 12/18 | chr9 | 108953701 | |||||||
| chr9:108953816 | A | G | 7 | a0003c0003t0001g0012 a0003c0003t0001g0298 a0003c0003t0001g0301 others(4): Show |
9 | HG00733.hp1 HG01109.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.1630-1322T>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 12/18 | chr9 | 108953816 | |||||||
| chr9:108953818 | AC | A | 43 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0020 others(40): Show |
55 | HG00140.hp1 HG00408.hp1 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.1630-1325delG | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 12/18 | chr9 | 108953818 | |||||||
| chr9:108953843 | C | CAG | 6 | a0001c0001t0002g0003 a0001c0001t0002g0013 a0001c0001t0002g0045 others(3): Show |
10 | HG02109.hp1 HG02451.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.1630-1351_1630-135 others(6): Show |
CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 12/18 | chr9 | 108953843 | |||||||
| chr9:108953874 | A | G | 1 | a0001c0001t0001g0340 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1630-1380T>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 12/18 | chr9 | 108953874 | |||||||
| chr9:108954185 | T | C | 1 | a0001c0001t0001g0132 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1629+1605A>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 12/18 | chr9 | 108954185 | |||||||
| chr9:108954236 | G | A | 40 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(37): Show |
43 | HG00408.hp2 HG01081.hp1 HG01099.hp1 others(40): Show |
intron_variant | MODIFIER | c.1629+1554C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 12/18 | chr9 | 108954236 | |||||||
| chr9:108954555 | C | A | 1 | a0002c0002t0001g0173 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1629+1235G>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 12/18 | chr9 | 108954555 | |||||||
| chr9:108954655 | T | C | 2 | a0001c0001t0001g0341 a0001c0001t0001g0342 |
2 | NA18979.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.1629+1135A>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 12/18 | chr9 | 108954655 | |||||||
| chr9:108954766 | A | C | 3 | a0001c0001t0001g0133 a0001c0001t0001g0196 a0001c0001t0001g0223 |
3 | NA18998.hp1 NA19083.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.1629+1024T>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 12/18 | chr9 | 108954766 | |||||||
| chr9:108954827 | C | CGTGT | 18 | a0001c0001t0002g0003 a0001c0001t0002g0013 a0001c0001t0002g0014 others(15): Show |
23 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.1629+962_1629+963i others(6): Show |
CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 12/18 | chr9 | 108954827 | |||||||
| chr9:108954832 | A | G | 129 | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0001g0032 others(126): Show |
151 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(148): Show |
intron_variant | MODIFIER | c.1629+958T>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 12/18 | chr9 | 108954832 | |||||||
| chr9:108954858 | T | C | 129 | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0001g0032 others(126): Show |
151 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(148): Show |
intron_variant | MODIFIER | c.1629+932A>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 12/18 | chr9 | 108954858 | |||||||
| chr9:108954868 | A | C | 2 | a0001c0001t0001g0175 a0001c0001t0001g0261 |
2 | HG00639.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.1629+922T>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 12/18 | chr9 | 108954868 | |||||||
| chr9:108954875 | T | C | 1 | a0006c0009t0001g0353 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1629+915A>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 12/18 | chr9 | 108954875 | |||||||
| chr9:108954967 | TA | T | 4 | a0001c0001t0001g0147 a0001c0001t0001g0169 a0001c0001t0001g0176 others(1): Show |
4 | HG00544.hp2 NA19067.hp1 NA19067.hp2 others(1): Show |
intron_variant | MODIFIER | c.1629+822delT | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 12/18 | chr9 | 108954967 | |||||||
| chr9:108954968 | A | AT | 42 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0020 others(39): Show |
54 | HG00140.hp1 HG00408.hp1 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.1629+821dupA | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 12/18 | chr9 | 108954968 | |||||||
| chr9:108954968 | AT | A | 130 | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0001g0032 others(127): Show |
151 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(148): Show |
intron_variant | MODIFIER | c.1629+821delA | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 12/18 | chr9 | 108954968 | |||||||
| chr9:108954974 | T | A | 33 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(30): Show |
36 | HG00408.hp2 HG01081.hp1 HG01099.hp1 others(33): Show |
intron_variant | MODIFIER | c.1629+816A>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 12/18 | chr9 | 108954974 | |||||||
| chr9:108955008 | G | A | 23 | a0001c0001t0001g0024 a0001c0001t0001g0102 a0001c0001t0001g0147 others(20): Show |
24 | HG00280.hp1 HG00544.hp2 HG00639.hp2 others(21): Show |
intron_variant | MODIFIER | c.1629+782C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 12/18 | chr9 | 108955008 | |||||||
| chr9:108955119 | C | T | 4 | a0001c0001t0001g0031 a0001c0001t0001g0297 a0001c0001t0001g0304 others(1): Show |
5 | HG01884.hp1 HG02615.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1629+671G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 12/18 | chr9 | 108955119 | |||||||
| chr9:108955178 | G | T | 1 | a0001c0001t0001g0200 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1629+612C>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 12/18 | chr9 | 108955178 | |||||||
| chr9:108955181 | T | A | 1 | a0001c0001t0001g0200 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1629+609A>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 12/18 | chr9 | 108955181 | |||||||
| chr9:108955233 | A | G | 347 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(344): Show |
403 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(400): Show |
intron_variant | MODIFIER | c.1629+557T>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 12/18 | chr9 | 108955233 | |||||||
| chr9:108955329 | C | A | 1 | a0001c0001t0001g0200 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1629+461G>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 12/18 | chr9 | 108955329 | |||||||
| chr9:108955569 | T | C | 1 | a0001c0001t0003g0359 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1629+221A>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 12/18 | chr9 | 108955569 | |||||||
| chr9:108955689 | T | C | 1 | a0001c0001t0001g0011 | 3 | HG02486.hp1 NA19240.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1629+101A>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 12/18 | chr9 | 108955689 | |||||||
| chr9:108955783 | T | C | 20 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0151 others(17): Show |
24 | HG02132.hp1 HG02809.hp2 HG02818.hp1 others(21): Show |
splice_region_variant&intron_variant | LOW | c.1629+7A>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 12/18 | chr9 | 108955783 | |||||||
| chr9:108956041 | C | T | 1 | a0003c0003t0001g0298 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1592-214G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 11/18 | chr9 | 108956041 | |||||||
| chr9:108956045 | T | C | 40 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(37): Show |
43 | HG00408.hp2 HG01081.hp1 HG01099.hp1 others(40): Show |
intron_variant | MODIFIER | c.1592-218A>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 11/18 | chr9 | 108956045 | |||||||
| chr9:108956063 | A | T | 1 | a0001c0001t0001g0232 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1592-236T>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 11/18 | chr9 | 108956063 | |||||||
| chr9:108956068 | T | A | 131 | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0001g0032 others(128): Show |
154 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(151): Show |
intron_variant | MODIFIER | c.1592-241A>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 11/18 | chr9 | 108956068 | |||||||
| chr9:108956104 | G | A | 1 | a0001c0001t0001g0240 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1592-277C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 11/18 | chr9 | 108956104 | |||||||
| chr9:108956384 | G | A | 1 | a0001c0001t0002g0045 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1592-557C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 11/18 | chr9 | 108956384 | |||||||
| chr9:108956629 | T | C | 2 | a0001c0001t0001g0246 a0001c0001t0004g0245 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1592-802A>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 11/18 | chr9 | 108956629 | |||||||
| chr9:108956722 | G | A | 4 | a0002c0002t0001g0017 a0002c0002t0001g0081 a0002c0002t0001g0107 others(1): Show |
5 | HG02080.hp2 NA18968.hp2 NA18988.hp1 others(2): Show |
intron_variant | MODIFIER | c.1592-895C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 11/18 | chr9 | 108956722 | |||||||
| chr9:108956819 | A | G | 13 | a0001c0001t0001g0006 a0001c0001t0001g0022 a0001c0001t0001g0116 others(10): Show |
17 | HG00140.hp1 HG00733.hp2 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.1592-992T>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 11/18 | chr9 | 108956819 | |||||||
| chr9:108956909 | G | A | 1 | a0001c0001t0001g0354 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1592-1082C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 11/18 | chr9 | 108956909 | |||||||
| chr9:108956934 | T | C | 1 | a0001c0001t0001g0172 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1592-1107A>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 11/18 | chr9 | 108956934 | |||||||
| chr9:108957081 | C | A | 1 | a0001c0001t0001g0175 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1592-1254G>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 11/18 | chr9 | 108957081 | |||||||
| chr9:108957094 | A | C | 3 | a0001c0001t0001g0265 a0001c0001t0001g0266 a0001c0001t0006g0356 |
3 | HG01081.hp2 HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1592-1267T>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 11/18 | chr9 | 108957094 | |||||||
| chr9:108957116 | A | AT | 17 | a0001c0001t0001g0123 a0001c0001t0001g0129 a0001c0001t0001g0140 others(14): Show |
17 | HG01070.hp1 HG01978.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.1592-1290dupA | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 11/18 | chr9 | 108957116 | |||||||
| chr9:108957116 | AT | A | 81 | a0001c0001t0001g0009 a0001c0001t0001g0026 a0001c0001t0001g0028 others(78): Show |
90 | HG00280.hp2 HG00408.hp2 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.1592-1290delA | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 11/18 | chr9 | 108957116 | |||||||
| chr9:108957277 | A | C | 39 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(36): Show |
42 | HG00408.hp2 HG01081.hp1 HG01099.hp1 others(39): Show |
intron_variant | MODIFIER | c.1592-1450T>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 11/18 | chr9 | 108957277 | |||||||
| chr9:108957300 | T | A | 4 | a0001c0001t0001g0008 a0001c0001t0001g0241 a0001c0001t0001g0242 others(1): Show |
7 | HG01192.hp2 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1592-1473A>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 11/18 | chr9 | 108957300 | |||||||
| chr9:108957412 | GC | G | 22 | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0001g0297 others(19): Show |
27 | HG00733.hp1 HG01109.hp2 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.1592-1586delG | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 11/18 | chr9 | 108957412 | |||||||
| chr9:108957450 | C | T | 14 | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0001g0297 others(11): Show |
17 | HG01243.hp1 HG01884.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.1592-1623G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 11/18 | chr9 | 108957450 | |||||||
| chr9:108957506 | G | C | 1 | a0002c0002t0001g0065 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1592-1679C>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 11/18 | chr9 | 108957506 | |||||||
| chr9:108957611 | A | G | 1 | a0001c0001t0001g0193 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1592-1784T>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 11/18 | chr9 | 108957611 | |||||||
| chr9:108957905 | G | C | 1 | a0006c0009t0001g0353 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1592-2078C>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 11/18 | chr9 | 108957905 | |||||||
| chr9:108957985 | G | A | 1 | a0001c0001t0001g0300 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1592-2158C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 11/18 | chr9 | 108957985 | |||||||
| chr9:108958062 | T | A | 8 | a0001c0001t0002g0036 a0001c0001t0002g0038 a0001c0001t0002g0039 others(5): Show |
8 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.1592-2235A>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 11/18 | chr9 | 108958062 | |||||||
| chr9:108958063 | C | CA | 8 | a0001c0001t0001g0246 a0002c0002t0001g0065 a0002c0002t0001g0088 others(5): Show |
8 | HG01934.hp1 HG03225.hp2 HG03669.hp1 others(5): Show |
intron_variant | MODIFIER | c.1592-2237dupT | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 11/18 | chr9 | 108958063 | |||||||
| chr9:108958063 | C | CAAA | 21 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(18): Show |
24 | HG00408.hp2 HG01081.hp1 HG01099.hp1 others(21): Show |
intron_variant | MODIFIER | c.1592-2239_1592-223 others(7): Show |
CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 11/18 | chr9 | 108958063 | |||||||
| chr9:108958063 | C | CAAAA | 6 | a0001c0001t0001g0103 a0001c0001t0001g0320 a0001c0001t0001g0323 others(3): Show |
6 | HG01891.hp1 HG01934.hp2 HG03688.hp2 others(3): Show |
intron_variant | MODIFIER | c.1592-2240_1592-223 others(8): Show |
CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 11/18 | chr9 | 108958063 | |||||||
| chr9:108958063 | C | CAAAAAAA others(4): Show |
2 | a0001c0001t0003g0357 a0001c0001t0003g0358 |
2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1592-2247_1592-223 others(15): Show |
CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 11/18 | chr9 | 108958063 | |||||||
| chr9:108958063 | C | CAAAAAAA others(5): Show |
1 | a0001c0001t0003g0360 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1592-2248_1592-223 others(16): Show |
CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 11/18 | chr9 | 108958063 | |||||||
| chr9:108958063 | C | CAAAAAAA others(6): Show |
2 | a0001c0001t0003g0359 a0001c0001t0003g0361 |
2 | HG01496.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1592-2249_1592-223 others(17): Show |
CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 11/18 | chr9 | 108958063 | |||||||
| chr9:108958063 | CA | C | 156 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(153): Show |
178 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(175): Show |
intron_variant | MODIFIER | c.1592-2237delT | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 11/18 | chr9 | 108958063 | |||||||
| chr9:108958063 | CAA | C | 56 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0021 others(53): Show |
65 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.1592-2238_1592-223 others(6): Show |
CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 11/18 | chr9 | 108958063 | |||||||
| chr9:108958120 | A | C | 2 | a0002c0002t0001g0025 a0002c0002t0001g0173 |
3 | HG00558.hp2 HG02074.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.1592-2293T>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 11/18 | chr9 | 108958120 | |||||||
| chr9:108958128 | A | G | 1 | a0001c0001t0001g0335 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1592-2301T>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 11/18 | chr9 | 108958128 | |||||||
| chr9:108958469 | T | C | 1 | a0002c0002t0001g0082 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1592-2642A>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 11/18 | chr9 | 108958469 | |||||||
| chr9:108958646 | A | C | 2 | a0004c0004t0001g0183 a0004c0004t0001g0184 |
2 | HG04115.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1592-2819T>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 11/18 | chr9 | 108958646 | |||||||
| chr9:108958733 | C | CT | 10 | a0001c0001t0001g0200 a0001c0001t0002g0053 a0002c0002t0001g0060 others(7): Show |
10 | HG01070.hp1 HG01257.hp2 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.1592-2907dupA | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 11/18 | chr9 | 108958733 | |||||||
| chr9:108958774 | A | G | 36 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(33): Show |
39 | HG00408.hp2 HG01081.hp1 HG01099.hp1 others(36): Show |
intron_variant | MODIFIER | c.1592-2947T>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 11/18 | chr9 | 108958774 | |||||||
| chr9:108958891 | G | T | 6 | a0001c0001t0001g0354 a0001c0001t0003g0357 a0001c0001t0003g0358 others(3): Show |
6 | HG01433.hp2 HG01496.hp1 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.1592-3064C>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 11/18 | chr9 | 108958891 | |||||||
| chr9:108958943 | T | G | 1 | a0006c0009t0001g0353 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1592-3116A>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 11/18 | chr9 | 108958943 | |||||||
| chr9:108958952 | G | GA | 11 | a0001c0001t0001g0193 a0001c0001t0001g0222 a0001c0001t0001g0234 others(8): Show |
11 | HG01433.hp2 HG01496.hp1 HG01515.hp2 others(8): Show |
intron_variant | MODIFIER | c.1592-3126dupT | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 11/18 | chr9 | 108958952 | |||||||
| chr9:108958952 | GA | G | 6 | a0001c0001t0001g0204 a0001c0001t0001g0265 a0002c0002t0001g0058 others(3): Show |
6 | HG01081.hp2 HG01433.hp1 HG02300.hp1 others(3): Show |
intron_variant | MODIFIER | c.1592-3126delT | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 11/18 | chr9 | 108958952 | |||||||
| chr9:108959221 | C | T | 66 | a0001c0001t0001g0019 a0001c0001t0001g0175 a0002c0002t0001g0002 others(63): Show |
81 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.1592-3394G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 11/18 | chr9 | 108959221 | |||||||
| chr9:108959222 | G | A | 35 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(32): Show |
38 | HG00408.hp2 HG01081.hp1 HG01099.hp1 others(35): Show |
intron_variant | MODIFIER | c.1592-3395C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 11/18 | chr9 | 108959222 | |||||||
| chr9:108959317 | A | G | 1 | a0002c0002t0001g0083 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1592-3490T>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 11/18 | chr9 | 108959317 | |||||||
| chr9:108959364 | C | CA | 10 | a0001c0001t0001g0169 a0001c0001t0001g0240 a0001c0001t0001g0334 others(7): Show |
10 | HG00544.hp2 HG01169.hp1 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.1592-3538dupT | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 11/18 | chr9 | 108959364 | |||||||
| chr9:108959364 | CA | C | 194 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
227 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.1592-3538delT | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 11/18 | chr9 | 108959364 | |||||||
| chr9:108959364 | CAA | C | 61 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0002c0002t0001g0002 others(58): Show |
75 | HG00099.hp1 HG00558.hp2 HG00621.hp2 others(72): Show |
intron_variant | MODIFIER | c.1592-3539_1592-353 others(6): Show |
CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 11/18 | chr9 | 108959364 | |||||||
| chr9:108959364 | CAAAAAAA others(7): Show |
C | 1 | a0001c0001t0001g0300 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1592-3551_1592-353 others(18): Show |
CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 11/18 | chr9 | 108959364 | |||||||
| chr9:108959438 | A | T | 1 | a0002c0002t0001g0112 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1592-3611T>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 11/18 | chr9 | 108959438 | |||||||
| chr9:108959582 | TATA | T | 21 | a0001c0001t0001g0024 a0001c0001t0001g0102 a0001c0001t0001g0147 others(18): Show |
22 | HG00280.hp1 HG00544.hp2 HG00673.hp2 others(19): Show |
intron_variant | MODIFIER | c.1592-3758_1592-375 others(7): Show |
CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 11/18 | chr9 | 108959582 | |||||||
| chr9:108959687 | G | C | 1 | a0001c0001t0001g0335 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1592-3860C>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 11/18 | chr9 | 108959687 | |||||||
| chr9:108959765 | C | T | 1 | a0001c0001t0001g0155 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1592-3938G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 11/18 | chr9 | 108959765 | |||||||
| chr9:108959975 | A | C | 1 | a0001c0001t0002g0037 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1592-4148T>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 11/18 | chr9 | 108959975 | |||||||
| chr9:108960153 | T | A | 1 | a0001c0001t0001g0232 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1592-4326A>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 11/18 | chr9 | 108960153 | |||||||
| chr9:108960353 | G | A | 345 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(342): Show |
401 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(398): Show |
intron_variant | MODIFIER | c.1592-4526C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 11/18 | chr9 | 108960353 | |||||||
| chr9:108960478 | C | T | 6 | a0001c0001t0001g0249 a0001c0001t0001g0252 a0001c0001t0001g0281 others(3): Show |
6 | HG01255.hp2 HG02109.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.1592-4651G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 11/18 | chr9 | 108960478 | |||||||
| chr9:108960718 | A | G | 6 | a0001c0001t0001g0354 a0001c0001t0003g0357 a0001c0001t0003g0358 others(3): Show |
6 | HG01433.hp2 HG01496.hp1 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.1591+4660T>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 11/18 | chr9 | 108960718 | |||||||
| chr9:108960887 | A | G | 1 | a0001c0001t0001g0212 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1591+4491T>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 11/18 | chr9 | 108960887 | |||||||
| chr9:108960950 | C | T | 8 | a0001c0001t0001g0010 a0001c0001t0001g0197 a0001c0001t0001g0209 others(5): Show |
10 | HG00544.hp1 HG02523.hp1 NA18962.hp1 others(7): Show |
intron_variant | MODIFIER | c.1591+4428G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 11/18 | chr9 | 108960950 | |||||||
| chr9:108961071 | ATACT | A | 107 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0026 others(104): Show |
117 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(114): Show |
intron_variant | MODIFIER | c.1591+4303_1591+430 others(8): Show |
CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 11/18 | chr9 | 108961071 | |||||||
| chr9:108961441 | C | T | 1 | a0001c0001t0001g0265 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1591+3937G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 11/18 | chr9 | 108961441 | |||||||
| chr9:108961496 | A | G | 1 | a0001c0001t0001g0251 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1591+3882T>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 11/18 | chr9 | 108961496 | |||||||
| chr9:108962152 | T | A | 345 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(342): Show |
401 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(398): Show |
intron_variant | MODIFIER | c.1591+3226A>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 11/18 | chr9 | 108962152 | |||||||
| chr9:108962525 | T | C | 1 | a0001c0001t0001g0348 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1591+2853A>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 11/18 | chr9 | 108962525 | |||||||
| chr9:108962560 | C | T | 35 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(32): Show |
38 | HG00408.hp2 HG01081.hp1 HG01099.hp1 others(35): Show |
intron_variant | MODIFIER | c.1591+2818G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 11/18 | chr9 | 108962560 | |||||||
| chr9:108962639 | G | C | 36 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(33): Show |
39 | HG00408.hp2 HG01081.hp1 HG01099.hp1 others(36): Show |
intron_variant | MODIFIER | c.1591+2739C>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 11/18 | chr9 | 108962639 | |||||||
| chr9:108962679 | A | T | 14 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0151 others(11): Show |
18 | HG02132.hp1 NA18943.hp2 NA18946.hp1 others(15): Show |
intron_variant | MODIFIER | c.1591+2699T>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 11/18 | chr9 | 108962679 | |||||||
| chr9:108962756 | T | C | 1 | a0002c0002t0001g0071 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1591+2622A>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 11/18 | chr9 | 108962756 | |||||||
| chr9:108963215 | C | G | 1 | a0001c0001t0001g0354 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1591+2163G>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 11/18 | chr9 | 108963215 | |||||||
| chr9:108963286 | C | T | 1 | a0001c0001t0001g0279 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1591+2092G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 11/18 | chr9 | 108963286 | |||||||
| chr9:108963413 | C | T | 1 | a0002c0002t0001g0112 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1591+1965G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 11/18 | chr9 | 108963413 | |||||||
| chr9:108963528 | G | C | 1 | a0001c0001t0001g0354 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1591+1850C>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 11/18 | chr9 | 108963528 | |||||||
| chr9:108963604 | T | A | 2 | a0002c0002t0001g0104 a0002c0002t0001g0105 |
2 | HG00741.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.1591+1774A>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 11/18 | chr9 | 108963604 | |||||||
| chr9:108963618 | G | A | 5 | a0001c0001t0003g0357 a0001c0001t0003g0358 a0001c0001t0003g0359 others(2): Show |
5 | HG01433.hp2 HG01496.hp1 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.1591+1760C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 11/18 | chr9 | 108963618 | |||||||
| chr9:108963790 | A | G | 22 | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0001g0297 others(19): Show |
27 | HG00733.hp1 HG01109.hp2 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.1591+1588T>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 11/18 | chr9 | 108963790 | |||||||
| chr9:108963904 | G | A | 28 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(25): Show |
31 | HG00408.hp2 HG01081.hp1 HG01099.hp1 others(28): Show |
intron_variant | MODIFIER | c.1591+1474C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 11/18 | chr9 | 108963904 | |||||||
| chr9:108964135 | T | C | 1 | a0001c0001t0001g0303 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1591+1243A>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 11/18 | chr9 | 108964135 | |||||||
| chr9:108964442 | T | C | 47 | a0001c0001t0001g0010 a0001c0001t0001g0027 a0001c0001t0001g0193 others(44): Show |
50 | HG00438.hp1 HG00544.hp1 HG01070.hp2 others(47): Show |
intron_variant | MODIFIER | c.1591+936A>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 11/18 | chr9 | 108964442 | |||||||
| chr9:108964650 | A | G | 1 | a0001c0001t0001g0267 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1591+728T>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 11/18 | chr9 | 108964650 | |||||||
| chr9:108964712 | T | C | 1 | a0001c0001t0002g0040 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1591+666A>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 11/18 | chr9 | 108964712 | |||||||
| chr9:108964750 | T | C | 35 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(32): Show |
38 | HG00408.hp2 HG01081.hp1 HG01099.hp1 others(35): Show |
intron_variant | MODIFIER | c.1591+628A>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 11/18 | chr9 | 108964750 | |||||||
| chr9:108964784 | T | A | 1 | a0002c0002t0001g0083 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1591+594A>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 11/18 | chr9 | 108964784 | |||||||
| chr9:108964842 | T | TTTTA | 91 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0019 others(88): Show |
108 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.1591+532_1591+535d others(6): Show |
CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 11/18 | chr9 | 108964842 | |||||||
| chr9:108964842 | T | TTTTATTT others(1): Show |
23 | a0001c0001t0001g0011 a0001c0001t0001g0109 a0001c0001t0001g0131 others(20): Show |
25 | HG01109.hp1 HG01243.hp1 HG01256.hp2 others(22): Show |
intron_variant | MODIFIER | c.1591+528_1591+535d others(10): Show |
CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 11/18 | chr9 | 108964842 | |||||||
| chr9:108964842 | T | TTTTATTT others(5): Show |
23 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(20): Show |
26 | HG01081.hp1 HG01099.hp1 HG01168.hp1 others(23): Show |
intron_variant | MODIFIER | c.1591+524_1591+535d others(14): Show |
CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 11/18 | chr9 | 108964842 | |||||||
| chr9:108964842 | T | TTTTATTT others(9): Show |
3 | a0001c0001t0001g0335 a0001c0001t0001g0336 a0001c0001t0001g0339 |
3 | HG00408.hp2 NA18956.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.1591+520_1591+535d others(18): Show |
CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 11/18 | chr9 | 108964842 | |||||||
| chr9:108964848 | T | C | 1 | a0001c0001t0001g0205 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1591+530A>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 11/18 | chr9 | 108964848 | |||||||
| chr9:108964863 | T | C | 1 | a0001c0001t0001g0210 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1591+515A>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 11/18 | chr9 | 108964863 | |||||||
| chr9:108964878 | T | A | 21 | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0001g0297 others(18): Show |
26 | HG00733.hp1 HG01109.hp2 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.1591+500A>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 11/18 | chr9 | 108964878 | |||||||
| chr9:108964955 | C | T | 1 | a0006c0009t0001g0353 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1591+423G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 11/18 | chr9 | 108964955 | |||||||
| chr9:108965034 | A | G | 21 | a0001c0001t0001g0024 a0001c0001t0001g0102 a0001c0001t0001g0167 others(18): Show |
22 | HG00280.hp1 HG00544.hp2 HG00673.hp2 others(19): Show |
intron_variant | MODIFIER | c.1591+344T>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 11/18 | chr9 | 108965034 | |||||||
| chr9:108965072 | T | C | 1 | a0002c0002t0001g0059 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1591+306A>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 11/18 | chr9 | 108965072 | |||||||
| chr9:108965126 | G | A | 1 | a0001c0001t0001g0348 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1591+252C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 11/18 | chr9 | 108965126 | |||||||
| chr9:108965229 | T | C | 2 | a0001c0001t0002g0037 a0001c0001t0002g0044 |
2 | HG02559.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.1591+149A>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 11/18 | chr9 | 108965229 | |||||||
| chr9:108965249 | T | C | 68 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0005 others(65): Show |
83 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(80): Show |
intron_variant | MODIFIER | c.1591+129A>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 11/18 | chr9 | 108965249 | |||||||
| chr9:108965593 | A | G | 1 | a0001c0001t0001g0034 | 2 | NA18968.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.1441-65T>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 10/18 | chr9 | 108965593 | |||||||
| chr9:108965787 | C | T | 123 | a0001c0001t0001g0011 a0001c0001t0001g0019 a0001c0001t0001g0031 others(120): Show |
146 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(143): Show |
intron_variant | MODIFIER | c.1441-259G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 10/18 | chr9 | 108965787 | |||||||
| chr9:108965889 | C | T | 1 | a0001c0001t0001g0161 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1441-361G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 10/18 | chr9 | 108965889 | |||||||
| chr9:108965950 | T | A | 43 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0023 others(40): Show |
52 | HG00733.hp1 HG01081.hp2 HG01109.hp2 others(49): Show |
intron_variant | MODIFIER | c.1441-422A>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 10/18 | chr9 | 108965950 | |||||||
| chr9:108966019 | A | C | 1 | a0003c0003t0001g0309 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1441-491T>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 10/18 | chr9 | 108966019 | |||||||
| chr9:108966274 | G | A | 1 | a0001c0001t0002g0041 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1441-746C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 10/18 | chr9 | 108966274 | |||||||
| chr9:108966297 | A | G | 48 | a0001c0001t0001g0009 a0001c0001t0001g0026 a0001c0001t0001g0028 others(45): Show |
54 | HG00280.hp2 HG00558.hp1 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.1441-769T>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 10/18 | chr9 | 108966297 | |||||||
| chr9:108966303 | T | C | 21 | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0001g0297 others(18): Show |
26 | HG00733.hp1 HG01109.hp2 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.1441-775A>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 10/18 | chr9 | 108966303 | |||||||
| chr9:108966337 | T | C | 36 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(33): Show |
39 | HG00408.hp2 HG01081.hp1 HG01099.hp1 others(36): Show |
intron_variant | MODIFIER | c.1441-809A>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 10/18 | chr9 | 108966337 | |||||||
| chr9:108966438 | C | T | 90 | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0001g0297 others(87): Show |
110 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(107): Show |
intron_variant | MODIFIER | c.1441-910G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 10/18 | chr9 | 108966438 | |||||||
| chr9:108966545 | AG | A | 19 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0151 others(16): Show |
23 | HG01261.hp2 HG02132.hp1 HG02809.hp2 others(20): Show |
intron_variant | MODIFIER | c.1441-1018delC | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 10/18 | chr9 | 108966545 | |||||||
| chr9:108966559 | G | T | 19 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0151 others(16): Show |
23 | HG01261.hp2 HG02132.hp1 HG02809.hp2 others(20): Show |
intron_variant | MODIFIER | c.1441-1031C>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 10/18 | chr9 | 108966559 | |||||||
| chr9:108966737 | T | TC | 348 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(345): Show |
404 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(401): Show |
intron_variant | MODIFIER | c.1441-1210_1441-120 others(5): Show |
CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 10/18 | chr9 | 108966737 | |||||||
| chr9:108966986 | A | G | 1 | a0006c0009t0001g0353 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1441-1458T>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 10/18 | chr9 | 108966986 | |||||||
| chr9:108967101 | G | A | 1 | a0001c0001t0001g0300 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1441-1573C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 10/18 | chr9 | 108967101 | |||||||
| chr9:108967237 | G | A | 9 | a0001c0001t0001g0031 a0001c0001t0001g0297 a0001c0001t0001g0299 others(6): Show |
10 | HG01243.hp1 HG01884.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.1441-1709C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 10/18 | chr9 | 108967237 | |||||||
| chr9:108967384 | T | TCA | 69 | a0001c0001t0001g0019 a0002c0002t0001g0002 a0002c0002t0001g0004 others(66): Show |
85 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.1441-1858_1441-185 others(6): Show |
CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 10/18 | chr9 | 108967384 | |||||||
| chr9:108967432 | A | G | 1 | a0006c0009t0001g0353 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1441-1904T>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 10/18 | chr9 | 108967432 | |||||||
| chr9:108967485 | G | C | 1 | a0001c0001t0001g0153 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1441-1957C>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 10/18 | chr9 | 108967485 | |||||||
| chr9:108967913 | T | G | 22 | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0001g0297 others(19): Show |
27 | HG00733.hp1 HG01109.hp2 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.1441-2385A>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 10/18 | chr9 | 108967913 | |||||||
| chr9:108968227 | A | T | 1 | a0002c0002t0001g0085 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1440+2175T>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 10/18 | chr9 | 108968227 | |||||||
| chr9:108968241 | A | G | 1 | a0001c0001t0001g0204 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1440+2161T>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 10/18 | chr9 | 108968241 | |||||||
| chr9:108968248 | C | A | 15 | a0001c0001t0001g0196 a0001c0001t0001g0198 a0001c0001t0001g0199 others(12): Show |
15 | HG01070.hp2 HG01071.hp1 HG01256.hp1 others(12): Show |
intron_variant | MODIFIER | c.1440+2154G>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 10/18 | chr9 | 108968248 | |||||||
| chr9:108968307 | A | C | 1 | a0001c0001t0002g0049 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1440+2095T>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 10/18 | chr9 | 108968307 | |||||||
| chr9:108968408 | C | T | 1 | a0001c0001t0001g0326 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1440+1994G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 10/18 | chr9 | 108968408 | |||||||
| chr9:108968705 | G | A | 3 | a0001c0001t0001g0265 a0001c0001t0001g0266 a0001c0001t0006g0356 |
3 | HG01081.hp2 HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1440+1697C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 10/18 | chr9 | 108968705 | |||||||
| chr9:108968721 | T | C | 1 | a0001c0001t0001g0203 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1440+1681A>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 10/18 | chr9 | 108968721 | |||||||
| chr9:108968887 | T | C | 44 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0020 others(41): Show |
56 | HG00140.hp1 HG00408.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.1440+1515A>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 10/18 | chr9 | 108968887 | |||||||
| chr9:108968922 | A | T | 2 | a0001c0001t0001g0175 a0001c0001t0001g0261 |
2 | HG00639.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.1440+1480T>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 10/18 | chr9 | 108968922 | |||||||
| chr9:108969056 | G | C | 1 | a0001c0001t0001g0232 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1440+1346C>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 10/18 | chr9 | 108969056 | |||||||
| chr9:108969056 | G | T | 1 | a0001c0001t0001g0269 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1440+1346C>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 10/18 | chr9 | 108969056 | |||||||
| chr9:108969168 | G | A | 33 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(30): Show |
36 | HG00408.hp2 HG01081.hp1 HG01099.hp1 others(33): Show |
intron_variant | MODIFIER | c.1440+1234C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 10/18 | chr9 | 108969168 | |||||||
| chr9:108969227 | G | A | 5 | a0001c0001t0003g0357 a0001c0001t0003g0358 a0001c0001t0003g0359 others(2): Show |
5 | HG01433.hp2 HG01496.hp1 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.1440+1175C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 10/18 | chr9 | 108969227 | |||||||
| chr9:108969269 | C | CA | 16 | a0001c0001t0001g0008 a0001c0001t0001g0234 a0001c0001t0001g0236 others(13): Show |
19 | HG00639.hp1 HG01192.hp2 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.1440+1132dupT | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 10/18 | chr9 | 108969269 | |||||||
| chr9:108969269 | CA | C | 6 | a0001c0001t0001g0137 a0002c0002t0001g0025 a0002c0002t0001g0173 others(3): Show |
7 | HG00558.hp2 HG02074.hp2 HG03491.hp2 others(4): Show |
intron_variant | MODIFIER | c.1440+1132delT | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 10/18 | chr9 | 108969269 | |||||||
| chr9:108969269 | CAA | C | 7 | a0003c0003t0001g0012 a0003c0003t0001g0298 a0003c0003t0001g0301 others(4): Show |
9 | HG00733.hp1 HG01109.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.1440+1131_1440+113 others(6): Show |
CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 10/18 | chr9 | 108969269 | |||||||
| chr9:108969505 | T | C | 69 | a0001c0001t0001g0019 a0002c0002t0001g0002 a0002c0002t0001g0004 others(66): Show |
85 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.1440+897A>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 10/18 | chr9 | 108969505 | |||||||
| chr9:108969574 | A | G | 1 | a0001c0001t0001g0011 | 3 | HG02486.hp1 NA19240.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1440+828T>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 10/18 | chr9 | 108969574 | |||||||
| chr9:108969690 | T | A | 2 | a0001c0001t0001g0283 a0001c0001t0001g0284 |
2 | HG02109.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.1440+712A>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 10/18 | chr9 | 108969690 | |||||||
| chr9:108969821 | TTTTG | T | 12 | a0001c0001t0001g0011 a0001c0001t0001g0297 a0001c0001t0001g0299 others(9): Show |
14 | HG01243.hp1 HG01884.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1440+577_1440+580d others(6): Show |
CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 10/18 | chr9 | 108969821 | |||||||
| chr9:108969860 | G | C | 128 | a0001c0001t0001g0011 a0001c0001t0001g0032 a0001c0001t0001g0033 others(125): Show |
150 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(147): Show |
intron_variant | MODIFIER | c.1440+542C>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 10/18 | chr9 | 108969860 | |||||||
| chr9:108970095 | C | T | 4 | a0001c0001t0001g0297 a0001c0001t0001g0304 a0001c0001t0001g0306 others(1): Show |
4 | HG01884.hp1 HG02615.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1440+307G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 10/18 | chr9 | 108970095 | |||||||
| chr9:108970144 | T | C | 6 | a0002c0002t0001g0062 a0002c0002t0001g0065 a0002c0002t0001g0077 others(3): Show |
6 | HG00621.hp2 NA18973.hp2 NA18974.hp2 others(3): Show |
intron_variant | MODIFIER | c.1440+258A>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 10/18 | chr9 | 108970144 | |||||||
| chr9:108970308 | G | A | 20 | a0001c0001t0001g0011 a0001c0001t0001g0297 a0001c0001t0001g0299 others(17): Show |
24 | HG00733.hp1 HG01109.hp2 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.1440+94C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 10/18 | chr9 | 108970308 | |||||||
| chr9:108970328 | C | T | 1 | a0001c0001t0001g0213 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1440+74G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 10/18 | chr9 | 108970328 | |||||||
| chr9:108970364 | G | C | 33 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(30): Show |
36 | HG00408.hp2 HG01081.hp1 HG01099.hp1 others(33): Show |
intron_variant | MODIFIER | c.1440+38C>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 10/18 | chr9 | 108970364 | |||||||
| chr9:108970531 | C | T | 1 | a0001c0001t0001g0329 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1348-37G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 9/18 | chr9 | 108970531 | |||||||
| chr9:108970790 | C | T | 18 | a0001c0001t0002g0003 a0001c0001t0002g0013 a0001c0001t0002g0014 others(15): Show |
23 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.1348-296G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 9/18 | chr9 | 108970790 | |||||||
| chr9:108970809 | G | T | 1 | a0001c0001t0001g0157 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1348-315C>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 9/18 | chr9 | 108970809 | |||||||
| chr9:108970936 | T | C | 216 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(213): Show |
249 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(246): Show |
intron_variant | MODIFIER | c.1348-442A>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 9/18 | chr9 | 108970936 | |||||||
| chr9:108971002 | C | T | 12 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0151 others(9): Show |
16 | HG02132.hp1 NA18943.hp2 NA18946.hp1 others(13): Show |
intron_variant | MODIFIER | c.1348-508G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 9/18 | chr9 | 108971002 | |||||||
| chr9:108971027 | AT | A | 4 | a0001c0001t0001g0008 a0001c0001t0001g0241 a0001c0001t0001g0242 others(1): Show |
7 | HG01192.hp2 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1348-534delA | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 9/18 | chr9 | 108971027 | |||||||
| chr9:108971080 | T | C | 1 | a0001c0001t0001g0274 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1348-586A>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 9/18 | chr9 | 108971080 | |||||||
| chr9:108971162 | T | C | 1 | a0001c0001t0001g0134 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1348-668A>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 9/18 | chr9 | 108971162 | |||||||
| chr9:108971195 | A | G | 22 | a0001c0001t0001g0024 a0001c0001t0001g0102 a0001c0001t0001g0167 others(19): Show |
23 | HG00280.hp1 HG00544.hp2 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.1348-701T>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 9/18 | chr9 | 108971195 | |||||||
| chr9:108971212 | A | G | 1 | a0001c0001t0001g0153 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1348-718T>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 9/18 | chr9 | 108971212 | |||||||
| chr9:108971317 | A | G | 6 | a0001c0001t0001g0354 a0001c0001t0003g0357 a0001c0001t0003g0358 others(3): Show |
6 | HG01433.hp2 HG01496.hp1 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.1348-823T>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 9/18 | chr9 | 108971317 | |||||||
| chr9:108971382 | G | A | 1 | a0001c0001t0001g0326 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1348-888C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 9/18 | chr9 | 108971382 | |||||||
| chr9:108971396 | T | C | 1 | a0001c0001t0001g0348 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1348-902A>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 9/18 | chr9 | 108971396 | |||||||
| chr9:108971405 | G | C | 9 | a0001c0001t0001g0031 a0001c0001t0001g0297 a0001c0001t0001g0299 others(6): Show |
10 | HG01243.hp1 HG01884.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.1348-911C>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 9/18 | chr9 | 108971405 | |||||||
| chr9:108971490 | A | G | 5 | a0001c0001t0003g0357 a0001c0001t0003g0358 a0001c0001t0003g0359 others(2): Show |
5 | HG01433.hp2 HG01496.hp1 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.1348-996T>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 9/18 | chr9 | 108971490 | |||||||
| chr9:108971500 | G | C | 6 | a0001c0001t0001g0354 a0001c0001t0003g0357 a0001c0001t0003g0358 others(3): Show |
6 | HG01433.hp2 HG01496.hp1 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.1348-1006C>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 9/18 | chr9 | 108971500 | |||||||
| chr9:108971578 | C | A | 1 | a0003c0003t0001g0310 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1348-1084G>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 9/18 | chr9 | 108971578 | |||||||
| chr9:108971949 | C | T | 1 | a0001c0001t0001g0299 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1347+726G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 9/18 | chr9 | 108971949 | |||||||
| chr9:108971956 | C | T | 1 | a0006c0009t0001g0353 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1347+719G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 9/18 | chr9 | 108971956 | |||||||
| chr9:108972394 | C | T | 32 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(29): Show |
35 | HG00408.hp2 HG01081.hp1 HG01099.hp1 others(32): Show |
intron_variant | MODIFIER | c.1347+281G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 9/18 | chr9 | 108972394 | |||||||
| chr9:108972422 | G | T | 6 | a0001c0001t0001g0354 a0001c0001t0003g0357 a0001c0001t0003g0358 others(3): Show |
6 | HG01433.hp2 HG01496.hp1 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.1347+253C>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 9/18 | chr9 | 108972422 | |||||||
| chr9:108972439 | G | T | 1 | a0006c0009t0001g0353 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1347+236C>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 9/18 | chr9 | 108972439 | |||||||
| chr9:108972507 | C | T | 1 | a0001c0001t0001g0255 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1347+168G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 9/18 | chr9 | 108972507 | |||||||
| chr9:108972840 | ATG | A | 13 | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0001g0297 others(10): Show |
16 | HG01243.hp1 HG01884.hp1 HG02451.hp1 others(13): Show |
splice_region_variant&intron_variant | LOW | c.1189-9_1189-8delCA | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 8/18 | chr9 | 108972840 | |||||||
| chr9:108972853 | T | TG | 18 | a0001c0001t0001g0102 a0001c0001t0001g0115 a0001c0001t0001g0123 others(15): Show |
18 | HG00673.hp2 HG01109.hp2 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.1189-21dupC | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 8/18 | chr9 | 108972853 | |||||||
| chr9:108972883 | G | A | 13 | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0001g0297 others(10): Show |
16 | HG01243.hp1 HG01884.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.1189-50C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 8/18 | chr9 | 108972883 | |||||||
| chr9:108972895 | A | G | 2 | a0001c0001t0001g0267 a0001c0001t0001g0268 |
2 | NA18965.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1189-62T>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 8/18 | chr9 | 108972895 | |||||||
| chr9:108973030 | G | T | 32 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(29): Show |
35 | HG00408.hp2 HG01081.hp1 HG01099.hp1 others(32): Show |
intron_variant | MODIFIER | c.1189-197C>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 8/18 | chr9 | 108973030 | |||||||
| chr9:108973046 | G | A | 3 | a0001c0001t0001g0225 a0001c0001t0001g0231 a0001c0001t0001g0232 |
3 | HG00438.hp1 HG02071.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.1189-213C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 8/18 | chr9 | 108973046 | |||||||
| chr9:108973082 | T | C | 1 | a0001c0001t0001g0136 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1189-249A>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 8/18 | chr9 | 108973082 | |||||||
| chr9:108973092 | T | A | 1 | a0001c0001t0001g0236 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1189-259A>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 8/18 | chr9 | 108973092 | |||||||
| chr9:108973239 | T | C | 1 | a0001c0001t0001g0229 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1189-406A>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 8/18 | chr9 | 108973239 | |||||||
| chr9:108973312 | G | A | 18 | a0001c0001t0002g0003 a0001c0001t0002g0013 a0001c0001t0002g0014 others(15): Show |
23 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.1189-479C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 8/18 | chr9 | 108973312 | |||||||
| chr9:108973486 | T | A | 1 | a0001c0001t0001g0296 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1189-653A>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 8/18 | chr9 | 108973486 | |||||||
| chr9:108973605 | T | G | 40 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(37): Show |
43 | HG00408.hp2 HG01081.hp1 HG01099.hp1 others(40): Show |
intron_variant | MODIFIER | c.1189-772A>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 8/18 | chr9 | 108973605 | |||||||
| chr9:108973680 | C | CT | 9 | a0001c0001t0001g0208 a0001c0001t0001g0246 a0001c0001t0001g0249 others(6): Show |
9 | HG01243.hp2 HG01255.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1189-848dupA | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 8/18 | chr9 | 108973680 | |||||||
| chr9:108973680 | CT | C | 44 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(41): Show |
47 | HG00408.hp2 HG01081.hp1 HG01099.hp1 others(44): Show |
intron_variant | MODIFIER | c.1189-848delA | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 8/18 | chr9 | 108973680 | |||||||
| chr9:108973727 | A | G | 1 | a0001c0001t0004g0245 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1189-894T>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 8/18 | chr9 | 108973727 | |||||||
| chr9:108974039 | G | A | 19 | a0001c0001t0001g0024 a0001c0001t0001g0102 a0001c0001t0001g0167 others(16): Show |
20 | HG00280.hp1 HG00544.hp2 HG00673.hp2 others(17): Show |
intron_variant | MODIFIER | c.1189-1206C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 8/18 | chr9 | 108974039 | |||||||
| chr9:108974059 | G | A | 6 | a0001c0001t0001g0354 a0001c0001t0003g0357 a0001c0001t0003g0358 others(3): Show |
6 | HG01433.hp2 HG01496.hp1 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.1189-1226C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 8/18 | chr9 | 108974059 | |||||||
| chr9:108974613 | T | C | 2 | a0001c0001t0001g0114 a0001c0001t0001g0115 |
2 | HG02056.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.1189-1780A>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 8/18 | chr9 | 108974613 | |||||||
| chr9:108974694 | G | C | 1 | a0001c0001t0001g0246 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1189-1861C>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 8/18 | chr9 | 108974694 | |||||||
| chr9:108974872 | C | T | 213 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(210): Show |
244 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.1189-2039G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 8/18 | chr9 | 108974872 | |||||||
| chr9:108974892 | A | T | 1 | a0001c0001t0002g0050 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1189-2059T>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 8/18 | chr9 | 108974892 | |||||||
| chr9:108975055 | C | T | 1 | a0001c0001t0001g0174 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1188+1907G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 8/18 | chr9 | 108975055 | |||||||
| chr9:108975109 | G | A | 20 | a0001c0001t0001g0024 a0001c0001t0001g0102 a0001c0001t0001g0167 others(17): Show |
21 | HG00280.hp1 HG00544.hp2 HG00673.hp2 others(18): Show |
intron_variant | MODIFIER | c.1188+1853C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 8/18 | chr9 | 108975109 | |||||||
| chr9:108975124 | C | T | 16 | a0001c0001t0002g0003 a0001c0001t0002g0013 a0001c0001t0002g0014 others(13): Show |
21 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.1188+1838G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 8/18 | chr9 | 108975124 | |||||||
| chr9:108975373 | C | T | 2 | a0002c0002t0001g0104 a0002c0002t0001g0105 |
2 | HG00741.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.1188+1589G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 8/18 | chr9 | 108975373 | |||||||
| chr9:108975501 | A | G | 44 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(41): Show |
49 | HG00280.hp1 HG00544.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.1188+1461T>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 8/18 | chr9 | 108975501 | |||||||
| chr9:108975845 | C | T | 33 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(30): Show |
36 | HG00408.hp2 HG01081.hp1 HG01099.hp1 others(33): Show |
intron_variant | MODIFIER | c.1188+1117G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 8/18 | chr9 | 108975845 | |||||||
| chr9:108975909 | C | T | 1 | a0006c0009t0001g0353 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1188+1053G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 8/18 | chr9 | 108975909 | |||||||
| chr9:108975987 | T | A | 1 | a0001c0001t0001g0332 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1188+975A>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 8/18 | chr9 | 108975987 | |||||||
| chr9:108976062 | A | C | 1 | a0001c0001t0001g0224 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1188+900T>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 8/18 | chr9 | 108976062 | |||||||
| chr9:108976456 | A | G | 1 | a0001c0001t0001g0354 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1188+506T>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 8/18 | chr9 | 108976456 | |||||||
| chr9:108976666 | G | C | 10 | a0002c0002t0001g0005 a0002c0002t0001g0056 a0002c0002t0001g0057 others(7): Show |
13 | HG00673.hp1 NA18946.hp2 NA18956.hp2 others(10): Show |
intron_variant | MODIFIER | c.1188+296C>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 8/18 | chr9 | 108976666 | |||||||
| chr9:108977060 | A | T | 33 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(30): Show |
36 | HG00408.hp2 HG01081.hp1 HG01099.hp1 others(33): Show |
intron_variant | MODIFIER | c.1102-12T>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 7/18 | chr9 | 108977060 | |||||||
| chr9:108977091 | T | C | 1 | a0001c0001t0001g0109 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1102-43A>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 7/18 | chr9 | 108977091 | |||||||
| chr9:108977270 | A | T | 1 | a0001c0001t0001g0175 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1102-222T>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 7/18 | chr9 | 108977270 | |||||||
| chr9:108977271 | T | A | 1 | a0001c0001t0001g0175 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1102-223A>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 7/18 | chr9 | 108977271 | |||||||
| chr9:108977360 | ATC | A | 66 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0005 others(63): Show |
81 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.1102-314_1102-313d others(4): Show |
CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 7/18 | chr9 | 108977360 | |||||||
| chr9:108977635 | C | T | 2 | a0002c0002t0001g0015 a0002c0002t0001g0078 |
3 | HG00099.hp1 HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1102-587G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 7/18 | chr9 | 108977635 | |||||||
| chr9:108977684 | T | C | 39 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(36): Show |
42 | HG00408.hp2 HG01081.hp1 HG01099.hp1 others(39): Show |
intron_variant | MODIFIER | c.1102-636A>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 7/18 | chr9 | 108977684 | |||||||
| chr9:108977691 | G | A | 1 | a0001c0001t0001g0212 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1102-643C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 7/18 | chr9 | 108977691 | |||||||
| chr9:108977835 | C | T | 1 | a0001c0001t0001g0128 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1102-787G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 7/18 | chr9 | 108977835 | |||||||
| chr9:108977992 | A | G | 1 | a0001c0001t0001g0103 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1102-944T>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 7/18 | chr9 | 108977992 | |||||||
| chr9:108978053 | G | A | 1 | a0001c0001t0001g0140 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1102-1005C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 7/18 | chr9 | 108978053 | |||||||
| chr9:108978212 | A | G | 1 | a0001c0001t0001g0308 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1101+1069T>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 7/18 | chr9 | 108978212 | |||||||
| chr9:108978258 | C | T | 1 | a0001c0001t0001g0299 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1101+1023G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 7/18 | chr9 | 108978258 | |||||||
| chr9:108978428 | C | G | 33 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(30): Show |
36 | HG00408.hp2 HG01081.hp1 HG01099.hp1 others(33): Show |
intron_variant | MODIFIER | c.1101+853G>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 7/18 | chr9 | 108978428 | |||||||
| chr9:108978462 | G | C | 1 | a0001c0001t0001g0251 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1101+819C>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 7/18 | chr9 | 108978462 | |||||||
| chr9:108978541 | A | T | 1 | a0001c0001t0001g0119 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1101+740T>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 7/18 | chr9 | 108978541 | |||||||
| chr9:108978580 | C | T | 68 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0005 others(65): Show |
83 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(80): Show |
intron_variant | MODIFIER | c.1101+701G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 7/18 | chr9 | 108978580 | |||||||
| chr9:108978688 | A | G | 3 | a0001c0001t0002g0003 a0001c0001t0002g0045 a0001c0001t0002g0050 |
6 | HG02109.hp1 HG02717.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1101+593T>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 7/18 | chr9 | 108978688 | |||||||
| chr9:108979147 | A | G | 4 | a0001c0001t0001g0299 a0001c0001t0001g0303 a0001c0001t0001g0307 others(1): Show |
4 | HG01243.hp1 HG02451.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1101+134T>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 7/18 | chr9 | 108979147 | |||||||
| chr9:108979207 | A | C | 1 | a0001c0001t0001g0119 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1101+74T>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 7/18 | chr9 | 108979207 | |||||||
| chr9:108979251 | A | T | 1 | a0001c0001t0001g0119 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1101+30T>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 7/18 | chr9 | 108979251 | |||||||
| chr9:108979252 | T | A | 1 | a0001c0001t0001g0119 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1101+29A>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 7/18 | chr9 | 108979252 | |||||||
| chr9:108979697 | G | T | 1 | a0001c0001t0001g0119 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.901-216C>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 6/18 | chr9 | 108979697 | |||||||
| chr9:108979770 | T | A | 1 | a0001c0010t0001g0355 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.901-289A>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 6/18 | chr9 | 108979770 | |||||||
| chr9:108979799 | A | T | 1 | a0001c0001t0001g0119 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.901-318T>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 6/18 | chr9 | 108979799 | |||||||
| chr9:108979956 | A | T | 1 | a0001c0001t0001g0119 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.901-475T>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 6/18 | chr9 | 108979956 | |||||||
| chr9:108980100 | T | C | 40 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(37): Show |
43 | HG00408.hp2 HG01081.hp1 HG01099.hp1 others(40): Show |
intron_variant | MODIFIER | c.901-619A>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 6/18 | chr9 | 108980100 | |||||||
| chr9:108980184 | C | T | 1 | a0001c0001t0001g0354 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.901-703G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 6/18 | chr9 | 108980184 | |||||||
| chr9:108980308 | C | T | 1 | a0005c0005t0001g0094 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.901-827G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 6/18 | chr9 | 108980308 | |||||||
| chr9:108980430 | A | T | 2 | a0001c0001t0001g0246 a0001c0001t0004g0245 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.901-949T>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 6/18 | chr9 | 108980430 | |||||||
| chr9:108980435 | G | C | 1 | a0001c0001t0001g0279 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.901-954C>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 6/18 | chr9 | 108980435 | |||||||
| chr9:108980560 | T | C | 4 | a0001c0001t0001g0027 a0001c0001t0001g0214 a0001c0001t0001g0217 others(1): Show |
5 | HG02015.hp1 NA19011.hp1 NA19066.hp2 others(2): Show |
intron_variant | MODIFIER | c.901-1079A>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 6/18 | chr9 | 108980560 | |||||||
| chr9:108980676 | G | A | 1 | a0001c0001t0001g0205 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.901-1195C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 6/18 | chr9 | 108980676 | |||||||
| chr9:108980688 | C | T | 2 | a0001c0001t0001g0215 a0001c0001t0001g0220 |
2 | NA18955.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.901-1207G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 6/18 | chr9 | 108980688 | |||||||
| chr9:108980698 | C | A | 1 | a0001c0001t0001g0213 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.901-1217G>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 6/18 | chr9 | 108980698 | |||||||
| chr9:108980905 | T | C | 2 | a0003c0003t0001g0298 a0003c0003t0001g0301 |
2 | HG02922.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.901-1424A>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 6/18 | chr9 | 108980905 | |||||||
| chr9:108981070 | C | A | 1 | a0001c0001t0001g0150 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.901-1589G>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 6/18 | chr9 | 108981070 | |||||||
| chr9:108981145 | C | T | 5 | a0001c0001t0001g0111 a0001c0001t0001g0189 a0001c0001t0001g0190 others(2): Show |
5 | HG02622.hp1 HG02717.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.901-1664G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 6/18 | chr9 | 108981145 | |||||||
| chr9:108981146 | T | C | 63 | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0001g0032 others(60): Show |
71 | HG00408.hp2 HG00733.hp1 HG01081.hp1 others(68): Show |
intron_variant | MODIFIER | c.901-1665A>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 6/18 | chr9 | 108981146 | |||||||
| chr9:108981160 | C | G | 2 | a0001c0001t0001g0262 a0001c0001t0001g0263 |
2 | HG02132.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.901-1679G>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 6/18 | chr9 | 108981160 | |||||||
| chr9:108981464 | C | CA | 23 | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0001g0297 others(20): Show |
28 | HG00733.hp1 HG01109.hp2 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.900+1680dupT | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 6/18 | chr9 | 108981464 | |||||||
| chr9:108981464 | CA | C | 68 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0166 others(65): Show |
83 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(80): Show |
intron_variant | MODIFIER | c.900+1680delT | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 6/18 | chr9 | 108981464 | |||||||
| chr9:108981484 | CA | C | 70 | a0001c0001t0001g0354 a0001c0001t0003g0357 a0001c0001t0003g0358 others(67): Show |
85 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.900+1660delT | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 6/18 | chr9 | 108981484 | |||||||
| chr9:108981484 | CAA | C | 22 | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0001g0297 others(19): Show |
27 | HG00733.hp1 HG01109.hp2 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.900+1659_900+1660d others(4): Show |
CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 6/18 | chr9 | 108981484 | |||||||
| chr9:108981489 | A | C | 217 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(214): Show |
250 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(247): Show |
intron_variant | MODIFIER | c.900+1656T>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 6/18 | chr9 | 108981489 | |||||||
| chr9:108981492 | A | C | 1 | a0002c0002t0001g0095 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.900+1653T>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 6/18 | chr9 | 108981492 | |||||||
| chr9:108981517 | A | C | 66 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0005 others(63): Show |
81 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.900+1628T>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 6/18 | chr9 | 108981517 | |||||||
| chr9:108981555 | A | G | 40 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(37): Show |
43 | HG00408.hp2 HG01081.hp1 HG01099.hp1 others(40): Show |
intron_variant | MODIFIER | c.900+1590T>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 6/18 | chr9 | 108981555 | |||||||
| chr9:108981663 | G | A | 1 | a0001c0001t0001g0191 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.900+1482C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 6/18 | chr9 | 108981663 | |||||||
| chr9:108981699 | C | G | 6 | a0001c0001t0001g0354 a0001c0001t0003g0357 a0001c0001t0003g0358 others(3): Show |
6 | HG01433.hp2 HG01496.hp1 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.900+1446G>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 6/18 | chr9 | 108981699 | |||||||
| chr9:108981716 | G | A | 8 | a0002c0002t0001g0060 a0002c0002t0001g0061 a0002c0002t0001g0071 others(5): Show |
8 | HG01070.hp1 HG01257.hp2 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.900+1429C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 6/18 | chr9 | 108981716 | |||||||
| chr9:108981792 | G | C | 1 | a0001c0001t0001g0141 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.900+1353C>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 6/18 | chr9 | 108981792 | |||||||
| chr9:108981879 | C | G | 9 | a0001c0001t0001g0031 a0001c0001t0001g0297 a0001c0001t0001g0299 others(6): Show |
10 | HG01243.hp1 HG01884.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.900+1266G>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 6/18 | chr9 | 108981879 | |||||||
| chr9:108981963 | A | G | 1 | a0001c0001t0001g0109 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.900+1182T>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 6/18 | chr9 | 108981963 | |||||||
| chr9:108982139 | C | T | 2 | a0001c0001t0001g0117 a0001c0001t0001g0125 |
2 | HG01175.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.900+1006G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 6/18 | chr9 | 108982139 | |||||||
| chr9:108982169 | A | G | 1 | a0001c0001t0001g0307 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.900+976T>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 6/18 | chr9 | 108982169 | |||||||
| chr9:108982264 | G | C | 1 | a0001c0001t0001g0164 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.900+881C>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 6/18 | chr9 | 108982264 | |||||||
| chr9:108982343 | C | G | 1 | a0002c0002t0001g0185 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.900+802G>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 6/18 | chr9 | 108982343 | |||||||
| chr9:108982347 | A | C | 40 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(37): Show |
43 | HG00408.hp2 HG01081.hp1 HG01099.hp1 others(40): Show |
intron_variant | MODIFIER | c.900+798T>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 6/18 | chr9 | 108982347 | |||||||
| chr9:108982433 | C | T | 62 | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0001g0032 others(59): Show |
70 | HG00408.hp2 HG00733.hp1 HG01081.hp1 others(67): Show |
intron_variant | MODIFIER | c.900+712G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 6/18 | chr9 | 108982433 | |||||||
| chr9:108982491 | A | C | 41 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(38): Show |
46 | HG00280.hp1 HG00544.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.900+654T>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 6/18 | chr9 | 108982491 | |||||||
| chr9:108982524 | T | A | 1 | a0001c0001t0001g0165 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.900+621A>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 6/18 | chr9 | 108982524 | |||||||
| chr9:108982613 | T | C | 2 | a0001c0001t0001g0246 a0001c0001t0004g0245 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.900+532A>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 6/18 | chr9 | 108982613 | |||||||
| chr9:108982717 | T | C | 1 | a0001c0001t0001g0120 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.900+428A>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 6/18 | chr9 | 108982717 | |||||||
| chr9:108982732 | C | G | 1 | a0001c0001t0001g0324 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.900+413G>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 6/18 | chr9 | 108982732 | |||||||
| chr9:108982815 | T | C | 33 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(30): Show |
36 | HG00408.hp2 HG01081.hp1 HG01099.hp1 others(33): Show |
intron_variant | MODIFIER | c.900+330A>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 6/18 | chr9 | 108982815 | |||||||
| chr9:108982832 | C | A | 2 | a0003c0003t0001g0298 a0003c0003t0001g0301 |
2 | HG02922.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.900+313G>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 6/18 | chr9 | 108982832 | |||||||
| chr9:108983030 | A | G | 40 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(37): Show |
43 | HG00408.hp2 HG01081.hp1 HG01099.hp1 others(40): Show |
intron_variant | MODIFIER | c.900+115T>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 6/18 | chr9 | 108983030 | |||||||
| chr9:108983084 | TTAAAA | T | 3 | a0001c0001t0001g0265 a0001c0001t0002g0036 a0001c0001t0006g0356 |
3 | HG01081.hp2 HG03831.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.900+56_900+60delTT others(3): Show |
CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 6/18 | chr9 | 108983084 | |||||||
| chr9:108983457 | T | A | 1 | a0001c0001t0001g0318 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.730-142A>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 5/18 | chr9 | 108983457 | |||||||
| chr9:108983489 | G | A | 1 | a0001c0001t0001g0259 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.730-174C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 5/18 | chr9 | 108983489 | |||||||
| chr9:108983662 | A | G | 1 | a0001c0001t0001g0226 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.730-347T>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 5/18 | chr9 | 108983662 | |||||||
| chr9:108983669 | C | A | 1 | a0001c0001t0001g0300 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.730-354G>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 5/18 | chr9 | 108983669 | |||||||
| chr9:108983755 | G | A | 6 | a0001c0001t0001g0354 a0001c0001t0003g0357 a0001c0001t0003g0358 others(3): Show |
6 | HG01433.hp2 HG01496.hp1 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.730-440C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 5/18 | chr9 | 108983755 | |||||||
| chr9:108983789 | T | A | 2 | a0001c0001t0001g0343 a0001c0001t0001g0344 |
2 | HG02083.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.730-474A>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 5/18 | chr9 | 108983789 | |||||||
| chr9:108983789 | T | C | 39 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(36): Show |
42 | HG00408.hp2 HG01081.hp1 HG01099.hp1 others(39): Show |
intron_variant | MODIFIER | c.730-474A>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 5/18 | chr9 | 108983789 | |||||||
| chr9:108983817 | T | G | 174 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(171): Show |
202 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.730-502A>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 5/18 | chr9 | 108983817 | |||||||
| chr9:108983819 | T | C | 1 | a0001c0001t0001g0176 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.730-504A>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 5/18 | chr9 | 108983819 | |||||||
| chr9:108983987 | A | G | 131 | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0001g0032 others(128): Show |
154 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(151): Show |
intron_variant | MODIFIER | c.729+360T>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 5/18 | chr9 | 108983987 | |||||||
| chr9:108984139 | T | C | 1 | a0001c0001t0001g0277 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.729+208A>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 5/18 | chr9 | 108984139 | |||||||
| chr9:108984262 | A | T | 1 | a0001c0001t0001g0149 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.729+85T>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 5/18 | chr9 | 108984262 | |||||||
| chr9:108984327 | T | C | 45 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0019 others(42): Show |
58 | HG00140.hp1 HG00408.hp1 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.729+20A>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 5/18 | chr9 | 108984327 | |||||||
| chr9:108984548 | G | GA | 31 | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0001g0111 others(28): Show |
36 | HG00733.hp1 HG01109.hp2 HG01243.hp1 others(33): Show |
intron_variant | MODIFIER | c.640-113dupT | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 4/18 | chr9 | 108984548 | |||||||
| chr9:108984901 | G | A | 1 | a0001c0001t0001g0308 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.640-465C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 4/18 | chr9 | 108984901 | |||||||
| chr9:108984920 | G | A | 1 | a0001c0001t0001g0343 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.640-484C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 4/18 | chr9 | 108984920 | |||||||
| chr9:108984921 | T | A | 1 | a0001c0001t0001g0344 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.640-485A>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 4/18 | chr9 | 108984921 | |||||||
| chr9:108984932 | C | G | 2 | a0001c0001t0001g0196 a0001c0001t0001g0223 |
2 | NA18998.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.640-496G>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 4/18 | chr9 | 108984932 | |||||||
| chr9:108984998 | G | C | 1 | a0001c0001t0002g0044 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.640-562C>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 4/18 | chr9 | 108984998 | |||||||
| chr9:108985008 | G | T | 1 | a0001c0001t0002g0036 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.640-572C>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 4/18 | chr9 | 108985008 | |||||||
| chr9:108985030 | T | C | 9 | a0001c0001t0001g0006 a0001c0001t0001g0022 a0001c0001t0001g0120 others(6): Show |
13 | HG00140.hp1 HG00741.hp2 HG01069.hp2 others(10): Show |
intron_variant | MODIFIER | c.640-594A>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 4/18 | chr9 | 108985030 | |||||||
| chr9:108985077 | A | G | 1 | a0001c0001t0001g0251 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.640-641T>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 4/18 | chr9 | 108985077 | |||||||
| chr9:108985079 | T | C | 5 | a0001c0001t0003g0357 a0001c0001t0003g0358 a0001c0001t0003g0359 others(2): Show |
5 | HG01433.hp2 HG01496.hp1 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.640-643A>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 4/18 | chr9 | 108985079 | |||||||
| chr9:108985571 | A | G | 1 | a0001c0001t0001g0280 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.640-1135T>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 4/18 | chr9 | 108985571 | |||||||
| chr9:108985721 | T | G | 69 | a0001c0001t0001g0019 a0002c0002t0001g0002 a0002c0002t0001g0004 others(66): Show |
85 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.640-1285A>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 4/18 | chr9 | 108985721 | |||||||
| chr9:108985854 | A | G | 1 | a0001c0001t0001g0267 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.640-1418T>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 4/18 | chr9 | 108985854 | |||||||
| chr9:108985883 | C | T | 1 | a0001c0001t0001g0214 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.640-1447G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 4/18 | chr9 | 108985883 | |||||||
| chr9:108986032 | T | A | 1 | a0002c0002t0001g0087 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.640-1596A>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 4/18 | chr9 | 108986032 | |||||||
| chr9:108986134 | G | A | 1 | a0001c0001t0001g0240 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.640-1698C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 4/18 | chr9 | 108986134 | |||||||
| chr9:108986164 | C | T | 4 | a0002c0002t0001g0057 a0002c0002t0001g0095 a0002c0002t0001g0097 others(1): Show |
4 | HG00673.hp1 NA19007.hp2 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.640-1728G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 4/18 | chr9 | 108986164 | |||||||
| chr9:108986176 | C | A | 23 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0151 others(20): Show |
27 | HG01261.hp2 HG02132.hp1 HG02145.hp2 others(24): Show |
intron_variant | MODIFIER | c.640-1740G>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 4/18 | chr9 | 108986176 | |||||||
| chr9:108986347 | G | A | 40 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(37): Show |
43 | HG00408.hp2 HG01081.hp1 HG01099.hp1 others(40): Show |
intron_variant | MODIFIER | c.640-1911C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 4/18 | chr9 | 108986347 | |||||||
| chr9:108986492 | G | A | 12 | a0001c0001t0001g0027 a0001c0001t0001g0194 a0001c0001t0001g0195 others(9): Show |
13 | HG01978.hp2 HG02015.hp1 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.640-2056C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 4/18 | chr9 | 108986492 | |||||||
| chr9:108986527 | G | C | 40 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(37): Show |
43 | HG00408.hp2 HG01081.hp1 HG01099.hp1 others(40): Show |
intron_variant | MODIFIER | c.640-2091C>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 4/18 | chr9 | 108986527 | |||||||
| chr9:108986603 | A | C | 20 | a0001c0001t0001g0024 a0001c0001t0001g0102 a0001c0001t0001g0167 others(17): Show |
21 | HG00280.hp1 HG00544.hp2 HG00673.hp2 others(18): Show |
intron_variant | MODIFIER | c.640-2167T>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 4/18 | chr9 | 108986603 | |||||||
| chr9:108986606 | G | A | 1 | a0001c0001t0001g0011 | 3 | HG02486.hp1 NA19240.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.640-2170C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 4/18 | chr9 | 108986606 | |||||||
| chr9:108986661 | C | T | 4 | a0001c0001t0001g0116 a0001c0001t0001g0126 a0001c0001t0001g0127 others(1): Show |
4 | HG00733.hp2 HG03688.hp1 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.640-2225G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 4/18 | chr9 | 108986661 | |||||||
| chr9:108986901 | T | G | 7 | a0003c0003t0001g0012 a0003c0003t0001g0298 a0003c0003t0001g0301 others(4): Show |
9 | HG00733.hp1 HG01109.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.640-2465A>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 4/18 | chr9 | 108986901 | |||||||
| chr9:108986990 | G | C | 42 | a0001c0001t0001g0010 a0001c0001t0001g0027 a0001c0001t0001g0193 others(39): Show |
45 | HG00438.hp1 HG00544.hp1 HG01070.hp2 others(42): Show |
intron_variant | MODIFIER | c.640-2554C>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 4/18 | chr9 | 108986990 | |||||||
| chr9:108987093 | A | C | 347 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(344): Show |
403 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(400): Show |
intron_variant | MODIFIER | c.640-2657T>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 4/18 | chr9 | 108987093 | |||||||
| chr9:108987168 | C | T | 5 | a0001c0001t0001g0111 a0001c0001t0001g0189 a0001c0001t0001g0190 others(2): Show |
5 | HG02622.hp1 HG02717.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.640-2732G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 4/18 | chr9 | 108987168 | |||||||
| chr9:108987186 | G | A | 40 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(37): Show |
43 | HG00408.hp2 HG01081.hp1 HG01099.hp1 others(40): Show |
intron_variant | MODIFIER | c.640-2750C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 4/18 | chr9 | 108987186 | |||||||
| chr9:108987347 | A | G | 2 | a0001c0001t0001g0246 a0001c0001t0004g0245 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.640-2911T>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 4/18 | chr9 | 108987347 | |||||||
| chr9:108987386 | A | G | 1 | a0001c0001t0001g0354 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.640-2950T>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 4/18 | chr9 | 108987386 | |||||||
| chr9:108987426 | C | A | 3 | a0001c0001t0001g0029 a0001c0001t0001g0276 a0001c0001t0001g0277 |
4 | HG01346.hp2 HG02148.hp1 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.640-2990G>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 4/18 | chr9 | 108987426 | |||||||
| chr9:108987451 | G | A | 3 | a0001c0001t0001g0313 a0001c0001t0001g0314 a0001c0001t0001g0316 |
3 | HG02572.hp1 HG03098.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.640-3015C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 4/18 | chr9 | 108987451 | |||||||
| chr9:108987505 | A | G | 5 | a0003c0003t0001g0012 a0003c0003t0001g0309 a0003c0003t0001g0310 others(2): Show |
7 | HG00733.hp1 HG01109.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.640-3069T>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 4/18 | chr9 | 108987505 | |||||||
| chr9:108987535 | C | T | 21 | a0001c0001t0001g0024 a0001c0001t0001g0102 a0001c0001t0001g0167 others(18): Show |
22 | HG00280.hp1 HG00544.hp2 HG00673.hp2 others(19): Show |
intron_variant | MODIFIER | c.640-3099G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 4/18 | chr9 | 108987535 | |||||||
| chr9:108987636 | A | T | 2 | a0001c0001t0003g0357 a0001c0001t0003g0358 |
2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.639+3090T>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 4/18 | chr9 | 108987636 | |||||||
| chr9:108987864 | T | A | 20 | a0001c0001t0001g0024 a0001c0001t0001g0102 a0001c0001t0001g0167 others(17): Show |
21 | HG00280.hp1 HG00544.hp2 HG00673.hp2 others(18): Show |
intron_variant | MODIFIER | c.639+2862A>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 4/18 | chr9 | 108987864 | |||||||
| chr9:108987885 | T | C | 1 | a0002c0002t0001g0061 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.639+2841A>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 4/18 | chr9 | 108987885 | |||||||
| chr9:108987890 | C | G | 42 | a0001c0001t0001g0009 a0001c0001t0001g0028 a0001c0001t0001g0029 others(39): Show |
47 | HG00280.hp2 HG00558.hp1 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.639+2836G>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 4/18 | chr9 | 108987890 | |||||||
| chr9:108987937 | G | A | 40 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(37): Show |
43 | HG00408.hp2 HG01081.hp1 HG01099.hp1 others(40): Show |
intron_variant | MODIFIER | c.639+2789C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 4/18 | chr9 | 108987937 | |||||||
| chr9:108987941 | G | A | 1 | a0001c0001t0001g0019 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.639+2785C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 4/18 | chr9 | 108987941 | |||||||
| chr9:108987977 | G | A | 1 | a0001c0001t0001g0203 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.639+2749C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 4/18 | chr9 | 108987977 | |||||||
| chr9:108988137 | G | A | 67 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0005 others(64): Show |
82 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.639+2589C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 4/18 | chr9 | 108988137 | |||||||
| chr9:108988243 | T | C | 130 | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0001g0032 others(127): Show |
153 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.639+2483A>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 4/18 | chr9 | 108988243 | |||||||
| chr9:108988533 | T | C | 1 | a0001c0001t0001g0122 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.639+2193A>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 4/18 | chr9 | 108988533 | |||||||
| chr9:108988548 | G | A | 1 | a0006c0009t0001g0353 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.639+2178C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 4/18 | chr9 | 108988548 | |||||||
| chr9:108988636 | G | A | 1 | a0002c0002t0001g0062 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.639+2090C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 4/18 | chr9 | 108988636 | |||||||
| chr9:108988690 | C | T | 32 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(29): Show |
35 | HG00408.hp2 HG01081.hp1 HG01099.hp1 others(32): Show |
intron_variant | MODIFIER | c.639+2036G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 4/18 | chr9 | 108988690 | |||||||
| chr9:108988727 | T | C | 2 | a0001c0001t0001g0033 a0001c0001t0001g0327 |
3 | HG01081.hp1 HG01257.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.639+1999A>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 4/18 | chr9 | 108988727 | |||||||
| chr9:108988764 | C | T | 1 | a0001c0001t0001g0290 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.639+1962G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 4/18 | chr9 | 108988764 | |||||||
| chr9:108988774 | A | G | 1 | a0001c0001t0001g0279 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.639+1952T>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 4/18 | chr9 | 108988774 | |||||||
| chr9:108988805 | A | G | 32 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(29): Show |
35 | HG00408.hp2 HG01081.hp1 HG01099.hp1 others(32): Show |
intron_variant | MODIFIER | c.639+1921T>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 4/18 | chr9 | 108988805 | |||||||
| chr9:108988857 | T | G | 1 | a0001c0001t0001g0263 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.639+1869A>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 4/18 | chr9 | 108988857 | |||||||
| chr9:108988982 | T | C | 1 | a0001c0001t0001g0354 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.639+1744A>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 4/18 | chr9 | 108988982 | |||||||
| chr9:108989039 | G | A | 1 | a0001c0001t0001g0354 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.639+1687C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 4/18 | chr9 | 108989039 | |||||||
| chr9:108989051 | A | G | 1 | a0001c0001t0001g0323 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.639+1675T>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 4/18 | chr9 | 108989051 | |||||||
| chr9:108989055 | T | C | 1 | a0001c0001t0001g0300 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.639+1671A>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 4/18 | chr9 | 108989055 | |||||||
| chr9:108989160 | T | C | 1 | a0006c0009t0001g0353 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.639+1566A>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 4/18 | chr9 | 108989160 | |||||||
| chr9:108989331 | A | G | 1 | a0002c0002t0001g0077 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.639+1395T>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 4/18 | chr9 | 108989331 | |||||||
| chr9:108989437 | T | C | 347 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(344): Show |
403 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(400): Show |
intron_variant | MODIFIER | c.639+1289A>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 4/18 | chr9 | 108989437 | |||||||
| chr9:108989440 | A | G | 347 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(344): Show |
403 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(400): Show |
intron_variant | MODIFIER | c.639+1286T>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 4/18 | chr9 | 108989440 | |||||||
| chr9:108989883 | C | G | 1 | a0002c0002t0001g0076 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.639+843G>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 4/18 | chr9 | 108989883 | |||||||
| chr9:108989911 | C | T | 1 | a0001c0001t0001g0300 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.639+815G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 4/18 | chr9 | 108989911 | |||||||
| chr9:108990292 | CAAAT | C | 67 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0005 others(64): Show |
82 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.639+430_639+433del others(4): Show |
CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 4/18 | chr9 | 108990292 | |||||||
| chr9:108990332 | C | T | 2 | a0001c0001t0001g0287 a0001c0001t0001g0288 |
2 | HG02257.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.639+394G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 4/18 | chr9 | 108990332 | |||||||
| chr9:108990588 | C | G | 1 | a0001c0001t0001g0199 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.639+138G>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 4/18 | chr9 | 108990588 | |||||||
| chr9:108990602 | C | T | 1 | a0006c0009t0001g0353 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.639+124G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 4/18 | chr9 | 108990602 | |||||||
| chr9:108990669 | A | G | 3 | a0001c0001t0001g0177 a0001c0001t0001g0182 a0001c0001t0001g0186 |
3 | HG00280.hp1 HG01255.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.639+57T>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 4/18 | chr9 | 108990669 | |||||||
| chr9:108990879 | G | T | 40 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(37): Show |
43 | HG00408.hp2 HG01081.hp1 HG01099.hp1 others(40): Show |
intron_variant | MODIFIER | c.520-34C>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 3/18 | chr9 | 108990879 | |||||||
| chr9:108990903 | T | G | 1 | a0001c0001t0001g0226 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.520-58A>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 3/18 | chr9 | 108990903 | |||||||
| chr9:108990929 | G | C | 9 | a0001c0001t0001g0031 a0001c0001t0001g0297 a0001c0001t0001g0299 others(6): Show |
10 | HG01243.hp1 HG01884.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.520-84C>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 3/18 | chr9 | 108990929 | |||||||
| chr9:108991093 | A | G | 6 | a0001c0001t0001g0354 a0001c0001t0003g0357 a0001c0001t0003g0358 others(3): Show |
6 | HG01433.hp2 HG01496.hp1 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.520-248T>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 3/18 | chr9 | 108991093 | |||||||
| chr9:108991257 | T | C | 358 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(355): Show |
417 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(414): Show |
intron_variant | MODIFIER | c.520-412A>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 3/18 | chr9 | 108991257 | |||||||
| chr9:108991299 | A | C | 1 | a0001c0001t0001g0307 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.520-454T>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 3/18 | chr9 | 108991299 | |||||||
| chr9:108991402 | T | C | 12 | a0001c0001t0002g0014 a0001c0001t0002g0036 a0001c0001t0002g0038 others(9): Show |
13 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.520-557A>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 3/18 | chr9 | 108991402 | |||||||
| chr9:108991417 | C | A | 2 | a0001c0001t0002g0013 a0001c0001t0002g0046 |
3 | HG03041.hp1 NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.520-572G>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 3/18 | chr9 | 108991417 | |||||||
| chr9:108991541 | TA | T | 40 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(37): Show |
43 | HG00408.hp2 HG01081.hp1 HG01099.hp1 others(40): Show |
intron_variant | MODIFIER | c.520-697delT | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 3/18 | chr9 | 108991541 | |||||||
| chr9:108992008 | T | C | 347 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(344): Show |
403 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(400): Show |
intron_variant | MODIFIER | c.519+624A>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 3/18 | chr9 | 108992008 | |||||||
| chr9:108992390 | C | CT | 17 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0125 others(14): Show |
19 | HG01081.hp1 HG01099.hp1 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.519+241dupA | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 3/18 | chr9 | 108992390 | |||||||
| chr9:108992533 | A | G | 1 | a0001c0001t0001g0160 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.519+99T>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 3/18 | chr9 | 108992533 | |||||||
| chr9:108992833 | C | T | 1 | a0001c0001t0001g0354 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.332-14G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 2/18 | chr9 | 108992833 | |||||||
| chr9:108992984 | G | A | 40 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(37): Show |
43 | HG00408.hp2 HG01081.hp1 HG01099.hp1 others(40): Show |
intron_variant | MODIFIER | c.332-165C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 2/18 | chr9 | 108992984 | |||||||
| chr9:108993004 | TA | T | 40 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(37): Show |
43 | HG00408.hp2 HG01081.hp1 HG01099.hp1 others(40): Show |
intron_variant | MODIFIER | c.332-186delT | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 2/18 | chr9 | 108993004 | |||||||
| chr9:108993211 | G | A | 39 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(36): Show |
42 | HG00408.hp2 HG01081.hp1 HG01099.hp1 others(39): Show |
intron_variant | MODIFIER | c.332-392C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 2/18 | chr9 | 108993211 | |||||||
| chr9:108993452 | C | T | 1 | a0001c0001t0001g0019 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.332-633G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 2/18 | chr9 | 108993452 | |||||||
| chr9:108993702 | G | T | 5 | a0001c0001t0003g0357 a0001c0001t0003g0358 a0001c0001t0003g0359 others(2): Show |
5 | HG01433.hp2 HG01496.hp1 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.332-883C>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 2/18 | chr9 | 108993702 | |||||||
| chr9:108993744 | A | G | 33 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(30): Show |
36 | HG00408.hp2 HG01081.hp1 HG01099.hp1 others(33): Show |
intron_variant | MODIFIER | c.332-925T>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 2/18 | chr9 | 108993744 | |||||||
| chr9:108993955 | C | T | 1 | a0001c0001t0001g0322 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.332-1136G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 2/18 | chr9 | 108993955 | |||||||
| chr9:108994057 | C | T | 1 | a0001c0001t0001g0169 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.332-1238G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 2/18 | chr9 | 108994057 | |||||||
| chr9:108994058 | G | A | 6 | a0001c0001t0001g0354 a0001c0001t0003g0357 a0001c0001t0003g0358 others(3): Show |
6 | HG01433.hp2 HG01496.hp1 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.332-1239C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 2/18 | chr9 | 108994058 | |||||||
| chr9:108994146 | G | A | 1 | a0006c0009t0001g0353 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.332-1327C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 2/18 | chr9 | 108994146 | |||||||
| chr9:108994162 | C | T | 2 | a0001c0001t0001g0113 a0001c0001t0001g0138 |
2 | HG01106.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.332-1343G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 2/18 | chr9 | 108994162 | |||||||
| chr9:108994329 | T | C | 1 | a0001c0001t0001g0152 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.332-1510A>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 2/18 | chr9 | 108994329 | |||||||
| chr9:108994609 | G | A | 3 | a0001c0001t0002g0037 a0001c0001t0002g0041 a0001c0001t0002g0044 |
3 | HG02559.hp2 HG02615.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.332-1790C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 2/18 | chr9 | 108994609 | |||||||
| chr9:108994614 | T | C | 1 | a0003c0003t0001g0298 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.332-1795A>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 2/18 | chr9 | 108994614 | |||||||
| chr9:108994656 | G | A | 1 | a0001c0001t0002g0046 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.332-1837C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 2/18 | chr9 | 108994656 | |||||||
| chr9:108994675 | G | A | 1 | a0001c0001t0001g0300 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.332-1856C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 2/18 | chr9 | 108994675 | |||||||
| chr9:108994838 | A | G | 33 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(30): Show |
36 | HG00408.hp2 HG01081.hp1 HG01099.hp1 others(33): Show |
intron_variant | MODIFIER | c.332-2019T>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 2/18 | chr9 | 108994838 | |||||||
| chr9:108994884 | G | A | 1 | a0001c0001t0001g0300 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.332-2065C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 2/18 | chr9 | 108994884 | |||||||
| chr9:108994891 | G | A | 2 | a0001c0001t0001g0333 a0001c0001t0001g0339 |
2 | NA18957.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.332-2072C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 2/18 | chr9 | 108994891 | |||||||
| chr9:108995028 | C | T | 5 | a0001c0001t0003g0357 a0001c0001t0003g0358 a0001c0001t0003g0359 others(2): Show |
5 | HG01433.hp2 HG01496.hp1 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.332-2209G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 2/18 | chr9 | 108995028 | |||||||
| chr9:108995029 | A | T | 3 | a0001c0001t0002g0037 a0001c0001t0002g0041 a0001c0001t0002g0044 |
3 | HG02559.hp2 HG02615.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.332-2210T>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 2/18 | chr9 | 108995029 | |||||||
| chr9:108995965 | G | GT | 92 | a0001c0001t0001g0011 a0001c0001t0001g0019 a0001c0001t0001g0031 others(89): Show |
113 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(110): Show |
intron_variant | MODIFIER | c.331+3101dupA | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 2/18 | chr9 | 108995965 | |||||||
| chr9:108996105 | G | A | 1 | a0002c0002t0001g0064 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.331+2962C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 2/18 | chr9 | 108996105 | |||||||
| chr9:108996202 | G | A | 80 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0023 others(77): Show |
88 | HG00438.hp1 HG00544.hp1 HG01070.hp2 others(85): Show |
intron_variant | MODIFIER | c.331+2865C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 2/18 | chr9 | 108996202 | |||||||
| chr9:108996210 | C | T | 1 | a0001c0001t0001g0261 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.331+2857G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 2/18 | chr9 | 108996210 | |||||||
| chr9:108996310 | A | G | 267 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(264): Show |
306 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(303): Show |
intron_variant | MODIFIER | c.331+2757T>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 2/18 | chr9 | 108996310 | |||||||
| chr9:108996337 | G | A | 3 | a0001c0001t0001g0265 a0001c0001t0001g0266 a0001c0001t0006g0356 |
3 | HG01081.hp2 HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.331+2730C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 2/18 | chr9 | 108996337 | |||||||
| chr9:108996374 | T | C | 2 | a0001c0001t0002g0013 a0001c0001t0002g0046 |
3 | HG03041.hp1 NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.331+2693A>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 2/18 | chr9 | 108996374 | |||||||
| chr9:108996456 | C | G | 5 | a0002c0002t0001g0072 a0002c0002t0001g0073 a0002c0002t0001g0092 others(2): Show |
5 | HG01099.hp2 HG01175.hp1 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.331+2611G>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 2/18 | chr9 | 108996456 | |||||||
| chr9:108996511 | C | A | 1 | a0001c0001t0001g0335 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.331+2556G>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 2/18 | chr9 | 108996511 | |||||||
| chr9:108996633 | A | T | 5 | a0001c0001t0001g0111 a0001c0001t0001g0189 a0001c0001t0001g0190 others(2): Show |
5 | HG02622.hp1 HG02717.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.331+2434T>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 2/18 | chr9 | 108996633 | |||||||
| chr9:108996643 | G | A | 5 | a0001c0001t0001g0313 a0001c0001t0001g0314 a0001c0001t0001g0315 others(2): Show |
5 | HG01261.hp2 HG02572.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.331+2424C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 2/18 | chr9 | 108996643 | |||||||
| chr9:108996669 | T | C | 1 | a0002c0002t0001g0091 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.331+2398A>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 2/18 | chr9 | 108996669 | |||||||
| chr9:108996720 | CT | C | 28 | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0001g0220 others(25): Show |
33 | HG00733.hp1 HG01109.hp2 HG01243.hp1 others(30): Show |
intron_variant | MODIFIER | c.331+2346delA | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 2/18 | chr9 | 108996720 | |||||||
| chr9:108996859 | A | G | 6 | a0001c0001t0001g0354 a0001c0001t0003g0357 a0001c0001t0003g0358 others(3): Show |
6 | HG01433.hp2 HG01496.hp1 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.331+2208T>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 2/18 | chr9 | 108996859 | |||||||
| chr9:108996931 | A | AT | 358 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(355): Show |
417 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(414): Show |
intron_variant | MODIFIER | c.331+2135dupA | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 2/18 | chr9 | 108996931 | |||||||
| chr9:108997197 | G | T | 14 | a0001c0001t0001g0011 a0001c0001t0001g0300 a0001c0001t0001g0313 others(11): Show |
18 | HG00733.hp1 HG01109.hp2 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.331+1870C>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 2/18 | chr9 | 108997197 | |||||||
| chr9:108997444 | T | C | 23 | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0001g0297 others(20): Show |
28 | HG00733.hp1 HG01109.hp2 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.331+1623A>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 2/18 | chr9 | 108997444 | |||||||
| chr9:108997580 | C | T | 1 | a0001c0001t0001g0313 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.331+1487G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 2/18 | chr9 | 108997580 | |||||||
| chr9:108997785 | T | C | 1 | a0002c0002t0001g0091 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.331+1282A>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 2/18 | chr9 | 108997785 | |||||||
| chr9:108997904 | C | T | 14 | a0001c0001t0001g0030 a0001c0001t0001g0248 a0001c0001t0001g0249 others(11): Show |
15 | HG01081.hp2 HG01255.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.331+1163G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 2/18 | chr9 | 108997904 | |||||||
| chr9:108998388 | C | CT | 26 | a0001c0001t0001g0024 a0001c0001t0001g0102 a0001c0001t0001g0167 others(23): Show |
27 | HG00280.hp1 HG00544.hp2 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.331+678dupA | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 2/18 | chr9 | 108998388 | |||||||
| chr9:108998388 | CT | C | 44 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(41): Show |
48 | HG00408.hp2 HG00558.hp2 HG01081.hp1 others(45): Show |
intron_variant | MODIFIER | c.331+678delA | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 2/18 | chr9 | 108998388 | |||||||
| chr9:108998732 | A | C | 62 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0005 others(59): Show |
76 | HG00099.hp1 HG00438.hp2 HG00621.hp2 others(73): Show |
intron_variant | MODIFIER | c.331+335T>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 2/18 | chr9 | 108998732 | |||||||
| chr9:108998749 | C | G | 12 | a0001c0001t0002g0014 a0001c0001t0002g0036 a0001c0001t0002g0038 others(9): Show |
13 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.331+318G>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 2/18 | chr9 | 108998749 | |||||||
| chr9:108998757 | T | C | 1 | a0001c0001t0001g0292 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.331+310A>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 2/18 | chr9 | 108998757 | |||||||
| chr9:108998908 | C | G | 45 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(42): Show |
49 | HG00408.hp2 HG00558.hp2 HG01081.hp1 others(46): Show |
intron_variant | MODIFIER | c.331+159G>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 2/18 | chr9 | 108998908 | |||||||
| chr9:108998922 | G | A | 45 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(42): Show |
49 | HG00408.hp2 HG00558.hp2 HG01081.hp1 others(46): Show |
intron_variant | MODIFIER | c.331+145C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 2/18 | chr9 | 108998922 | |||||||
| chr9:108998924 | G | A | 21 | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0001g0297 others(18): Show |
26 | HG00733.hp1 HG01109.hp2 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.331+143C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 2/18 | chr9 | 108998924 | |||||||
| chr9:108998949 | C | T | 45 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(42): Show |
49 | HG00408.hp2 HG00558.hp2 HG01081.hp1 others(46): Show |
intron_variant | MODIFIER | c.331+118G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 2/18 | chr9 | 108998949 | |||||||
| chr9:108999300 | C | T | 45 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(42): Show |
49 | HG00408.hp2 HG00558.hp2 HG01081.hp1 others(46): Show |
intron_variant | MODIFIER | c.142-44G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 108999300 | |||||||
| chr9:108999488 | C | A | 1 | a0001c0001t0001g0197 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.142-232G>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 108999488 | |||||||
| chr9:108999504 | T | C | 45 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0019 others(42): Show |
58 | HG00140.hp1 HG00408.hp1 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.142-248A>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 108999504 | |||||||
| chr9:108999560 | C | T | 2 | a0001c0001t0001g0260 a0001c0001t0001g0279 |
2 | HG00558.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.142-304G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 108999560 | |||||||
| chr9:108999576 | T | A | 6 | a0001c0001t0001g0354 a0001c0001t0003g0357 a0001c0001t0003g0358 others(3): Show |
6 | HG01433.hp2 HG01496.hp1 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.142-320A>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 108999576 | |||||||
| chr9:108999730 | A | T | 62 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0005 others(59): Show |
76 | HG00099.hp1 HG00438.hp2 HG00621.hp2 others(73): Show |
intron_variant | MODIFIER | c.142-474T>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 108999730 | |||||||
| chr9:108999781 | G | C | 1 | a0001c0001t0001g0279 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.142-525C>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 108999781 | |||||||
| chr9:108999813 | C | T | 45 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(42): Show |
49 | HG00408.hp2 HG00558.hp2 HG01081.hp1 others(46): Show |
intron_variant | MODIFIER | c.142-557G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 108999813 | |||||||
| chr9:108999822 | G | A | 62 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0005 others(59): Show |
76 | HG00099.hp1 HG00438.hp2 HG00621.hp2 others(73): Show |
intron_variant | MODIFIER | c.142-566C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 108999822 | |||||||
| chr9:109000039 | G | A | 5 | a0001c0001t0001g0111 a0001c0001t0001g0189 a0001c0001t0001g0190 others(2): Show |
5 | HG02622.hp1 HG02717.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.142-783C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109000039 | |||||||
| chr9:109000105 | T | C | 63 | a0001c0001t0001g0019 a0002c0002t0001g0002 a0002c0002t0001g0004 others(60): Show |
78 | HG00099.hp1 HG00438.hp2 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.142-849A>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109000105 | |||||||
| chr9:109000107 | T | C | 8 | a0001c0001t0001g0030 a0001c0001t0001g0249 a0001c0001t0001g0252 others(5): Show |
9 | HG01255.hp2 HG01891.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.142-851A>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109000107 | |||||||
| chr9:109000127 | T | A | 45 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(42): Show |
49 | HG00408.hp2 HG00558.hp2 HG01081.hp1 others(46): Show |
intron_variant | MODIFIER | c.142-871A>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109000127 | |||||||
| chr9:109000232 | C | T | 1 | a0001c0001t0001g0205 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.142-976G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109000232 | |||||||
| chr9:109000313 | G | A | 1 | a0001c0001t0001g0296 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.142-1057C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109000313 | |||||||
| chr9:109000383 | A | G | 1 | a0001c0001t0001g0124 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.142-1127T>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109000383 | |||||||
| chr9:109000436 | C | T | 2 | a0001c0001t0001g0114 a0001c0001t0001g0115 |
2 | HG02056.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.142-1180G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109000436 | |||||||
| chr9:109000457 | C | G | 3 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0166 |
3 | NA18977.hp1 NA18997.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.142-1201G>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109000457 | |||||||
| chr9:109000548 | T | C | 1 | a0001c0001t0001g0150 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.142-1292A>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109000548 | |||||||
| chr9:109000606 | C | G | 2 | a0001c0001t0001g0246 a0001c0001t0004g0245 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.142-1350G>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109000606 | |||||||
| chr9:109000607 | A | G | 68 | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0001g0032 others(65): Show |
77 | HG00408.hp2 HG00558.hp2 HG00733.hp1 others(74): Show |
intron_variant | MODIFIER | c.142-1351T>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109000607 | |||||||
| chr9:109000645 | C | T | 126 | a0001c0001t0001g0011 a0001c0001t0001g0019 a0001c0001t0001g0031 others(123): Show |
150 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(147): Show |
intron_variant | MODIFIER | c.142-1389G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109000645 | |||||||
| chr9:109000730 | T | C | 63 | a0001c0001t0001g0019 a0002c0002t0001g0002 a0002c0002t0001g0004 others(60): Show |
78 | HG00099.hp1 HG00438.hp2 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.142-1474A>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109000730 | |||||||
| chr9:109000764 | G | A | 13 | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0001g0297 others(10): Show |
16 | HG01243.hp1 HG01884.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.142-1508C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109000764 | |||||||
| chr9:109000769 | T | A | 18 | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0001g0297 others(15): Show |
23 | HG00733.hp1 HG01109.hp2 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.142-1513A>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109000769 | |||||||
| chr9:109000825 | G | C | 3 | a0002c0002t0001g0092 a0002c0002t0001g0093 a0002c0002t0001g0101 |
3 | HG01099.hp2 HG01192.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.142-1569C>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109000825 | |||||||
| chr9:109000834 | C | T | 45 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(42): Show |
49 | HG00408.hp2 HG00558.hp2 HG01081.hp1 others(46): Show |
intron_variant | MODIFIER | c.142-1578G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109000834 | |||||||
| chr9:109000847 | T | A | 340 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(337): Show |
396 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(393): Show |
intron_variant | MODIFIER | c.142-1591A>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109000847 | |||||||
| chr9:109001006 | C | CA | 56 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(53): Show |
60 | HG00408.hp2 HG00558.hp2 HG01081.hp1 others(57): Show |
intron_variant | MODIFIER | c.142-1751dupT | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109001006 | |||||||
| chr9:109001006 | CA | C | 6 | a0001c0001t0001g0189 a0001c0001t0001g0255 a0001c0001t0001g0256 others(3): Show |
6 | HG02165.hp2 HG03098.hp2 NA18949.hp1 others(3): Show |
intron_variant | MODIFIER | c.142-1751delT | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109001006 | |||||||
| chr9:109001006 | CAA | C | 63 | a0001c0001t0001g0019 a0002c0002t0001g0002 a0002c0002t0001g0004 others(60): Show |
78 | HG00099.hp1 HG00438.hp2 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.142-1752_142-1751d others(4): Show |
CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109001006 | |||||||
| chr9:109001121 | G | A | 1 | a0001c0001t0001g0300 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.142-1865C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109001121 | |||||||
| chr9:109001172 | C | CA | 31 | a0001c0001t0001g0011 a0001c0001t0001g0026 a0001c0001t0001g0031 others(28): Show |
37 | HG00621.hp1 HG00733.hp1 HG01070.hp1 others(34): Show |
intron_variant | MODIFIER | c.142-1917dupT | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109001172 | |||||||
| chr9:109001172 | C | CAA | 61 | a0001c0001t0001g0019 a0001c0001t0001g0300 a0001c0001t0001g0306 others(58): Show |
76 | HG00099.hp1 HG00438.hp2 HG00621.hp2 others(73): Show |
intron_variant | MODIFIER | c.142-1918_142-1917d others(4): Show |
CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109001172 | |||||||
| chr9:109001172 | CA | C | 14 | a0001c0001t0001g0023 a0001c0001t0001g0151 a0001c0001t0001g0153 others(11): Show |
15 | HG02132.hp1 HG02965.hp1 NA18963.hp2 others(12): Show |
intron_variant | MODIFIER | c.142-1917delT | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109001172 | |||||||
| chr9:109001262 | A | T | 347 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(344): Show |
403 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(400): Show |
intron_variant | MODIFIER | c.142-2006T>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109001262 | |||||||
| chr9:109001304 | G | C | 1 | a0005c0005t0001g0094 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.142-2048C>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109001304 | |||||||
| chr9:109001310 | G | C | 22 | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0001g0297 others(19): Show |
27 | HG00733.hp1 HG01109.hp2 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.142-2054C>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109001310 | |||||||
| chr9:109001381 | G | C | 1 | a0001c0001t0001g0182 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.142-2125C>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109001381 | |||||||
| chr9:109001569 | G | A | 2 | a0001c0001t0001g0346 a0001c0001t0001g0347 |
2 | NA18939.hp1 NA18941.hp2 |
intron_variant | MODIFIER | c.142-2313C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109001569 | |||||||
| chr9:109001723 | A | C | 1 | a0002c0002t0001g0058 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.142-2467T>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109001723 | |||||||
| chr9:109001831 | A | G | 21 | a0001c0001t0001g0024 a0001c0001t0001g0102 a0001c0001t0001g0167 others(18): Show |
22 | HG00280.hp1 HG00544.hp2 HG00673.hp2 others(19): Show |
intron_variant | MODIFIER | c.142-2575T>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109001831 | |||||||
| chr9:109001843 | C | A | 1 | a0001c0001t0001g0146 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.142-2587G>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109001843 | |||||||
| chr9:109001990 | C | T | 63 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0005 others(60): Show |
77 | HG00099.hp1 HG00438.hp2 HG00621.hp2 others(74): Show |
intron_variant | MODIFIER | c.142-2734G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109001990 | |||||||
| chr9:109001991 | G | A | 10 | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0001g0297 others(7): Show |
13 | HG01243.hp1 HG01884.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.142-2735C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109001991 | |||||||
| chr9:109002016 | G | A | 5 | a0001c0001t0003g0357 a0001c0001t0003g0358 a0001c0001t0003g0359 others(2): Show |
5 | HG01433.hp2 HG01496.hp1 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.142-2760C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109002016 | |||||||
| chr9:109002018 | G | A | 6 | a0001c0001t0001g0354 a0001c0001t0003g0357 a0001c0001t0003g0358 others(3): Show |
6 | HG01433.hp2 HG01496.hp1 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.142-2762C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109002018 | |||||||
| chr9:109002598 | T | A | 1 | a0001c0001t0001g0348 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.142-3342A>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109002598 | |||||||
| chr9:109002821 | T | TA | 11 | a0001c0001t0001g0307 a0002c0002t0001g0005 a0002c0002t0001g0056 others(8): Show |
14 | HG00673.hp1 HG06807.hp1 NA18946.hp2 others(11): Show |
intron_variant | MODIFIER | c.142-3566dupT | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109002821 | |||||||
| chr9:109002835 | AG | A | 40 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(37): Show |
44 | HG00408.hp2 HG00558.hp2 HG01081.hp1 others(41): Show |
intron_variant | MODIFIER | c.142-3580delC | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109002835 | |||||||
| chr9:109002836 | G | A | 20 | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0001g0297 others(17): Show |
25 | HG00733.hp1 HG01109.hp2 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.142-3580C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109002836 | |||||||
| chr9:109002907 | C | T | 1 | a0001c0001t0001g0300 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.142-3651G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109002907 | |||||||
| chr9:109002993 | CA | C | 18 | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0001g0297 others(15): Show |
23 | HG00733.hp1 HG01109.hp2 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.142-3738delT | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109002993 | |||||||
| chr9:109003106 | T | G | 1 | a0001c0001t0001g0300 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.142-3850A>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109003106 | |||||||
| chr9:109003108 | C | T | 5 | a0001c0001t0001g0111 a0001c0001t0001g0189 a0001c0001t0001g0190 others(2): Show |
5 | HG02622.hp1 HG02717.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.142-3852G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109003108 | |||||||
| chr9:109003207 | C | G | 38 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(35): Show |
42 | HG00408.hp2 HG00558.hp2 HG01081.hp1 others(39): Show |
intron_variant | MODIFIER | c.142-3951G>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109003207 | |||||||
| chr9:109003457 | C | T | 61 | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0001g0032 others(58): Show |
70 | HG00408.hp2 HG00558.hp2 HG00733.hp1 others(67): Show |
intron_variant | MODIFIER | c.142-4201G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109003457 | |||||||
| chr9:109003682 | G | A | 1 | a0001c0001t0001g0338 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.142-4426C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109003682 | |||||||
| chr9:109003804 | G | A | 1 | a0006c0009t0001g0353 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.142-4548C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109003804 | |||||||
| chr9:109003877 | A | G | 1 | a0001c0001t0001g0198 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.142-4621T>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109003877 | |||||||
| chr9:109004084 | G | T | 44 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(41): Show |
48 | HG00408.hp2 HG00558.hp2 HG01081.hp1 others(45): Show |
intron_variant | MODIFIER | c.142-4828C>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109004084 | |||||||
| chr9:109004157 | G | A | 9 | a0001c0001t0001g0031 a0001c0001t0001g0297 a0001c0001t0001g0299 others(6): Show |
10 | HG01243.hp1 HG01884.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.142-4901C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109004157 | |||||||
| chr9:109004178 | C | A | 353 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(350): Show |
412 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(409): Show |
intron_variant | MODIFIER | c.142-4922G>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109004178 | |||||||
| chr9:109004258 | G | A | 1 | a0001c0001t0001g0150 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.142-5002C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109004258 | |||||||
| chr9:109004285 | C | T | 1 | a0001c0001t0001g0354 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.142-5029G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109004285 | |||||||
| chr9:109004286 | G | A | 18 | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0001g0297 others(15): Show |
23 | HG00733.hp1 HG01109.hp2 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.142-5030C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109004286 | |||||||
| chr9:109004346 | T | A | 2 | a0001c0001t0001g0246 a0001c0001t0004g0245 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.142-5090A>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109004346 | |||||||
| chr9:109004347 | G | T | 1 | a0001c0001t0001g0299 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.142-5091C>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109004347 | |||||||
| chr9:109004379 | G | A | 38 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(35): Show |
42 | HG00408.hp2 HG00558.hp2 HG01081.hp1 others(39): Show |
intron_variant | MODIFIER | c.142-5123C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109004379 | |||||||
| chr9:109004429 | T | C | 1 | a0002c0002t0001g0101 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.142-5173A>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109004429 | |||||||
| chr9:109004473 | C | G | 5 | a0003c0003t0001g0012 a0003c0003t0001g0309 a0003c0003t0001g0310 others(2): Show |
7 | HG00733.hp1 HG01109.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.142-5217G>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109004473 | |||||||
| chr9:109004492 | T | C | 1 | a0001c0001t0001g0121 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.142-5236A>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109004492 | |||||||
| chr9:109004510 | G | A | 45 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(42): Show |
49 | HG00408.hp2 HG00558.hp2 HG01081.hp1 others(46): Show |
intron_variant | MODIFIER | c.142-5254C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109004510 | |||||||
| chr9:109004556 | G | C | 1 | a0001c0001t0001g0299 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.142-5300C>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109004556 | |||||||
| chr9:109004721 | G | C | 6 | a0001c0001t0001g0008 a0001c0001t0001g0239 a0001c0001t0001g0240 others(3): Show |
9 | HG01192.hp2 HG02486.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.142-5465C>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109004721 | |||||||
| chr9:109004760 | C | T | 64 | a0001c0001t0001g0019 a0002c0002t0001g0002 a0002c0002t0001g0004 others(61): Show |
79 | HG00099.hp1 HG00438.hp2 HG00621.hp2 others(76): Show |
intron_variant | MODIFIER | c.142-5504G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109004760 | |||||||
| chr9:109004772 | C | T | 1 | a0002c0002t0001g0070 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.142-5516G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109004772 | |||||||
| chr9:109004793 | AT | A | 20 | a0001c0001t0001g0024 a0001c0001t0001g0102 a0001c0001t0001g0167 others(17): Show |
21 | HG00280.hp1 HG00544.hp2 HG00673.hp2 others(18): Show |
intron_variant | MODIFIER | c.142-5538delA | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109004793 | |||||||
| chr9:109004794 | T | A | 24 | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0001g0175 others(21): Show |
27 | HG01243.hp1 HG01433.hp2 HG01496.hp1 others(24): Show |
intron_variant | MODIFIER | c.142-5538A>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109004794 | |||||||
| chr9:109004798 | T | A | 6 | a0001c0001t0003g0357 a0001c0001t0003g0358 a0001c0001t0003g0359 others(3): Show |
6 | HG01433.hp2 HG01496.hp1 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.142-5542A>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109004798 | |||||||
| chr9:109004801 | A | T | 1 | a0006c0009t0001g0353 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.142-5545T>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109004801 | |||||||
| chr9:109004802 | T | A | 3 | a0001c0001t0003g0360 a0001c0001t0003g0361 a0006c0009t0001g0353 |
3 | HG01433.hp2 HG01496.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.142-5546A>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109004802 | |||||||
| chr9:109005200 | T | G | 2 | a0001c0001t0001g0196 a0001c0001t0001g0223 |
2 | NA18998.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.142-5944A>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109005200 | |||||||
| chr9:109005391 | C | T | 10 | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0001g0297 others(7): Show |
13 | HG01243.hp1 HG01884.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.142-6135G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109005391 | |||||||
| chr9:109005411 | T | TAAAATCC others(292): Show |
1 | a0004c0004t0001g0183 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.142-6156_142-6155i others(301): Show |
CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109005411 | |||||||
| chr9:109005411 | T | TAAAATCC others(293): Show |
1 | a0004c0004t0001g0184 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.142-6156_142-6155i others(302): Show |
CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109005411 | |||||||
| chr9:109005429 | T | C | 7 | a0003c0003t0001g0012 a0003c0003t0001g0298 a0003c0003t0001g0301 others(4): Show |
9 | HG00733.hp1 HG01109.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.142-6173A>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109005429 | |||||||
| chr9:109005463 | C | T | 1 | a0001c0001t0001g0203 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.142-6207G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109005463 | |||||||
| chr9:109005696 | T | A | 1 | a0001c0001t0001g0316 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.142-6440A>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109005696 | |||||||
| chr9:109005821 | C | T | 7 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0001g0200 others(4): Show |
7 | NA18949.hp2 NA18986.hp2 NA18992.hp1 others(4): Show |
intron_variant | MODIFIER | c.142-6565G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109005821 | |||||||
| chr9:109006020 | T | G | 2 | a0001c0001t0001g0224 a0001c0001t0001g0230 |
2 | HG02040.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.142-6764A>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109006020 | |||||||
| chr9:109006174 | C | T | 1 | a0003c0003t0001g0298 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.142-6918G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109006174 | |||||||
| chr9:109006279 | C | T | 3 | a0002c0002t0001g0066 a0002c0002t0001g0067 a0007c0007t0001g0068 |
3 | NA18944.hp1 NA19078.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.141+7023G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109006279 | |||||||
| chr9:109006418 | G | A | 37 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(34): Show |
41 | HG00408.hp2 HG00558.hp2 HG01081.hp1 others(38): Show |
intron_variant | MODIFIER | c.141+6884C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109006418 | |||||||
| chr9:109006448 | T | C | 4 | a0001c0001t0002g0042 a0001c0001t0002g0043 a0001c0001t0002g0047 others(1): Show |
4 | HG01106.hp1 HG03017.hp2 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.141+6854A>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109006448 | |||||||
| chr9:109006598 | A | G | 1 | a0001c0001t0001g0348 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.141+6704T>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109006598 | |||||||
| chr9:109006800 | C | T | 1 | a0001c0001t0001g0237 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.141+6502G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109006800 | |||||||
| chr9:109006920 | T | A | 10 | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0001g0297 others(7): Show |
13 | HG01243.hp1 HG01884.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.141+6382A>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109006920 | |||||||
| chr9:109006920 | T | TA | 44 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(41): Show |
48 | HG00408.hp2 HG00558.hp2 HG01081.hp1 others(45): Show |
intron_variant | MODIFIER | c.141+6381dupT | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109006920 | |||||||
| chr9:109007072 | AAAAAATT others(26): Show |
A | 1 | a0001c0001t0001g0234 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.141+6197_141+6229d others(35): Show |
CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109007072 | |||||||
| chr9:109007126 | T | C | 1 | a0002c0002t0001g0104 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.141+6176A>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109007126 | |||||||
| chr9:109007263 | G | A | 51 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0019 others(48): Show |
64 | HG00140.hp1 HG00408.hp1 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.141+6039C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109007263 | |||||||
| chr9:109007516 | G | A | 1 | a0001c0001t0001g0243 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.141+5786C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109007516 | |||||||
| chr9:109007755 | C | T | 19 | a0001c0001t0002g0003 a0001c0001t0002g0013 a0001c0001t0002g0014 others(16): Show |
24 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.141+5547G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109007755 | |||||||
| chr9:109007794 | T | C | 12 | a0001c0001t0001g0031 a0001c0001t0001g0287 a0001c0001t0001g0288 others(9): Show |
13 | HG01243.hp1 HG01884.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.141+5508A>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109007794 | |||||||
| chr9:109008152 | C | CT | 15 | a0001c0001t0001g0113 a0001c0001t0001g0123 a0001c0001t0001g0197 others(12): Show |
15 | HG00099.hp2 HG00140.hp2 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.141+5149dupA | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109008152 | |||||||
| chr9:109008152 | CT | C | 96 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(93): Show |
113 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.141+5149delA | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109008152 | |||||||
| chr9:109008152 | CTT | C | 25 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0151 others(22): Show |
29 | HG00438.hp1 HG01168.hp1 HG01515.hp2 others(26): Show |
intron_variant | MODIFIER | c.141+5148_141+5149d others(4): Show |
CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109008152 | |||||||
| chr9:109008190 | A | T | 1 | a0002c0002t0001g0062 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.141+5112T>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109008190 | |||||||
| chr9:109008213 | A | G | 1 | a0001c0001t0001g0142 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.141+5089T>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109008213 | |||||||
| chr9:109008219 | ACAATCTC others(17): Show |
A | 1 | a0001c0010t0001g0355 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.141+5059_141+5082d others(26): Show |
CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109008219 | |||||||
| chr9:109008238 | A | G | 2 | a0001c0001t0001g0334 a0001c0001t0001g0345 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.141+5064T>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109008238 | |||||||
| chr9:109008325 | T | C | 2 | a0003c0003t0001g0012 a0003c0003t0001g0312 |
4 | HG02145.hp1 HG02257.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.141+4977A>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109008325 | |||||||
| chr9:109008346 | G | C | 66 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0226 others(63): Show |
80 | HG00099.hp1 HG00438.hp2 HG00621.hp2 others(77): Show |
intron_variant | MODIFIER | c.141+4956C>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109008346 | |||||||
| chr9:109008374 | C | T | 20 | a0001c0001t0002g0003 a0001c0001t0002g0013 a0001c0001t0002g0014 others(17): Show |
25 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.141+4928G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109008374 | |||||||
| chr9:109008534 | C | G | 4 | a0001c0001t0001g0313 a0001c0001t0001g0314 a0001c0001t0001g0315 others(1): Show |
4 | HG01261.hp2 HG02572.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.141+4768G>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109008534 | |||||||
| chr9:109008584 | G | A | 1 | a0001c0001t0001g0165 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.141+4718C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109008584 | |||||||
| chr9:109008724 | T | C | 1 | a0001c0001t0001g0244 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.141+4578A>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109008724 | |||||||
| chr9:109008729 | C | T | 2 | a0001c0001t0001g0346 a0001c0001t0001g0347 |
2 | NA18939.hp1 NA18941.hp2 |
intron_variant | MODIFIER | c.141+4573G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109008729 | |||||||
| chr9:109008818 | G | T | 1 | a0006c0009t0001g0353 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.141+4484C>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109008818 | |||||||
| chr9:109008876 | C | CT | 33 | a0001c0001t0001g0026 a0001c0001t0001g0113 a0001c0001t0001g0114 others(30): Show |
34 | HG00735.hp1 HG01106.hp2 HG01358.hp2 others(31): Show |
intron_variant | MODIFIER | c.141+4425dupA | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109008876 | |||||||
| chr9:109008876 | CT | C | 45 | a0001c0001t0001g0008 a0001c0001t0001g0024 a0001c0001t0001g0142 others(42): Show |
50 | HG00280.hp1 HG00438.hp1 HG00558.hp2 others(47): Show |
intron_variant | MODIFIER | c.141+4425delA | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109008876 | |||||||
| chr9:109008876 | CTT | C | 6 | a0001c0001t0001g0167 a0001c0001t0001g0186 a0001c0001t0001g0187 others(3): Show |
6 | HG01255.hp1 NA18972.hp2 NA18984.hp2 others(3): Show |
intron_variant | MODIFIER | c.141+4424_141+4425d others(4): Show |
CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109008876 | |||||||
| chr9:109008876 | CTTT | C | 27 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(24): Show |
30 | HG00408.hp2 HG01081.hp1 HG01099.hp1 others(27): Show |
intron_variant | MODIFIER | c.141+4423_141+4425d others(5): Show |
CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109008876 | |||||||
| chr9:109008876 | CTTTT | C | 46 | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0001g0297 others(43): Show |
56 | HG00099.hp2 HG00140.hp2 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.141+4422_141+4425d others(6): Show |
CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109008876 | |||||||
| chr9:109008876 | CTTTTT | C | 7 | a0001c0001t0001g0314 a0001c0001t0001g0315 a0001c0001t0001g0316 others(4): Show |
7 | HG01261.hp2 HG01433.hp2 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.141+4421_141+4425d others(7): Show |
CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109008876 | |||||||
| chr9:109008876 | CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0001g0145 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.141+4414_141+4425d others(14): Show |
CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109008876 | |||||||
| chr9:109008961 | C | T | 18 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0151 others(15): Show |
22 | HG02132.hp1 HG02809.hp2 HG02886.hp2 others(19): Show |
intron_variant | MODIFIER | c.141+4341G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109008961 | |||||||
| chr9:109009010 | T | G | 3 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 |
3 | HG03927.hp1 NA18747.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.141+4292A>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109009010 | |||||||
| chr9:109009220 | G | A | 1 | a0001c0001t0001g0192 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.141+4082C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109009220 | |||||||
| chr9:109009225 | T | C | 1 | a0002c0002t0001g0112 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.141+4077A>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109009225 | |||||||
| chr9:109009279 | A | G | 1 | a0001c0001t0002g0035 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.141+4023T>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109009279 | |||||||
| chr9:109009303 | C | A | 3 | a0001c0001t0003g0359 a0001c0001t0003g0360 a0001c0001t0003g0361 |
3 | HG01433.hp2 HG01496.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.141+3999G>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109009303 | |||||||
| chr9:109009306 | AT | A | 356 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(353): Show |
415 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(412): Show |
intron_variant | MODIFIER | c.141+3995delA | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109009306 | |||||||
| chr9:109009498 | G | A | 4 | a0001c0001t0001g0293 a0001c0001t0001g0294 a0001c0001t0001g0295 others(1): Show |
4 | NA18612.hp2 NA19011.hp2 NA19054.hp2 others(1): Show |
intron_variant | MODIFIER | c.141+3804C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109009498 | |||||||
| chr9:109009708 | T | C | 23 | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0001g0297 others(20): Show |
28 | HG00733.hp1 HG01109.hp2 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.141+3594A>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109009708 | |||||||
| chr9:109009745 | T | A | 1 | a0001c0001t0001g0149 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.141+3557A>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109009745 | |||||||
| chr9:109009746 | G | A | 23 | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0001g0297 others(20): Show |
28 | HG00733.hp1 HG01109.hp2 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.141+3556C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109009746 | |||||||
| chr9:109009764 | A | T | 1 | a0006c0009t0001g0353 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.141+3538T>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109009764 | |||||||
| chr9:109009893 | C | T | 18 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0151 others(15): Show |
22 | HG02132.hp1 HG02809.hp2 HG02886.hp2 others(19): Show |
intron_variant | MODIFIER | c.141+3409G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109009893 | |||||||
| chr9:109010007 | T | A | 1 | a0001c0001t0001g0233 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.141+3295A>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109010007 | |||||||
| chr9:109010033 | T | A | 5 | a0003c0003t0001g0012 a0003c0003t0001g0309 a0003c0003t0001g0310 others(2): Show |
7 | HG00733.hp1 HG01109.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.141+3269A>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109010033 | |||||||
| chr9:109010068 | G | T | 61 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(58): Show |
69 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(66): Show |
intron_variant | MODIFIER | c.141+3234C>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109010068 | |||||||
| chr9:109010116 | G | A | 1 | a0002c0002t0001g0108 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.141+3186C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109010116 | |||||||
| chr9:109010196 | C | T | 42 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0020 others(39): Show |
54 | HG00140.hp1 HG00408.hp1 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.141+3106G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109010196 | |||||||
| chr9:109010358 | T | G | 1 | a0001c0001t0001g0244 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.141+2944A>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109010358 | |||||||
| chr9:109010516 | A | T | 1 | a0001c0001t0001g0234 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.141+2786T>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109010516 | |||||||
| chr9:109010517 | A | T | 1 | a0001c0001t0001g0234 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.141+2785T>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109010517 | |||||||
| chr9:109010525 | C | T | 1 | a0001c0001t0001g0234 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.141+2777G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109010525 | |||||||
| chr9:109010534 | C | T | 43 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0020 others(40): Show |
55 | HG00140.hp1 HG00408.hp1 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.141+2768G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109010534 | |||||||
| chr9:109010541 | A | T | 1 | a0001c0001t0001g0234 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.141+2761T>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109010541 | |||||||
| chr9:109010542 | G | A | 1 | a0001c0001t0001g0234 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.141+2760C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109010542 | |||||||
| chr9:109010550 | A | T | 1 | a0001c0001t0001g0234 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.141+2752T>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109010550 | |||||||
| chr9:109010551 | C | T | 1 | a0001c0001t0001g0234 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.141+2751G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109010551 | |||||||
| chr9:109010558 | T | A | 1 | a0001c0001t0001g0234 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.141+2744A>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109010558 | |||||||
| chr9:109010560 | C | A | 1 | a0001c0001t0001g0234 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.141+2742G>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109010560 | |||||||
| chr9:109010563 | A | T | 1 | a0001c0001t0001g0234 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.141+2739T>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109010563 | |||||||
| chr9:109010565 | A | T | 1 | a0001c0001t0001g0234 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.141+2737T>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109010565 | |||||||
| chr9:109010566 | C | T | 1 | a0001c0001t0001g0234 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.141+2736G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109010566 | |||||||
| chr9:109010577 | A | T | 1 | a0001c0001t0001g0234 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.141+2725T>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109010577 | |||||||
| chr9:109010580 | G | T | 1 | a0001c0001t0001g0234 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.141+2722C>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109010580 | |||||||
| chr9:109010584 | C | A | 1 | a0001c0001t0001g0234 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.141+2718G>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109010584 | |||||||
| chr9:109010589 | C | T | 1 | a0001c0001t0001g0234 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.141+2713G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109010589 | |||||||
| chr9:109010638 | G | T | 149 | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0001g0032 others(146): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.141+2664C>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109010638 | |||||||
| chr9:109010883 | C | T | 1 | a0002c0002t0001g0055 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.141+2419G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109010883 | |||||||
| chr9:109010905 | A | C | 1 | a0001c0010t0001g0355 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.141+2397T>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109010905 | |||||||
| chr9:109010906 | T | A | 1 | a0001c0010t0001g0355 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.141+2396A>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109010906 | |||||||
| chr9:109010943 | T | C | 1 | a0006c0009t0001g0353 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.141+2359A>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109010943 | |||||||
| chr9:109010974 | A | C | 1 | a0002c0002t0001g0054 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.141+2328T>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109010974 | |||||||
| chr9:109011037 | T | C | 64 | a0001c0001t0001g0019 a0001c0001t0001g0102 a0001c0001t0001g0103 others(61): Show |
79 | HG00099.hp1 HG00438.hp2 HG00621.hp2 others(76): Show |
intron_variant | MODIFIER | c.141+2265A>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109011037 | |||||||
| chr9:109011266 | A | T | 1 | a0003c0003t0001g0298 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.141+2036T>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109011266 | |||||||
| chr9:109011319 | G | A | 3 | a0001c0001t0001g0034 a0001c0001t0001g0346 a0001c0001t0001g0347 |
4 | NA18939.hp1 NA18941.hp2 NA18968.hp1 others(1): Show |
intron_variant | MODIFIER | c.141+1983C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109011319 | |||||||
| chr9:109011356 | C | T | 1 | a0001c0001t0001g0354 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.141+1946G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109011356 | |||||||
| chr9:109011371 | GA | G | 86 | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0001g0032 others(83): Show |
98 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.141+1930delT | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109011371 | |||||||
| chr9:109011409 | T | C | 5 | a0001c0001t0001g0313 a0001c0001t0001g0314 a0001c0001t0001g0315 others(2): Show |
5 | HG01261.hp2 HG02572.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.141+1893A>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109011409 | |||||||
| chr9:109011463 | C | T | 21 | a0001c0001t0002g0003 a0001c0001t0002g0013 a0001c0001t0002g0014 others(18): Show |
26 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.141+1839G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109011463 | |||||||
| chr9:109011534 | T | C | 5 | a0001c0001t0001g0111 a0001c0001t0001g0189 a0001c0001t0001g0190 others(2): Show |
5 | HG02622.hp1 HG02717.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.141+1768A>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109011534 | |||||||
| chr9:109011728 | A | G | 85 | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0001g0032 others(82): Show |
98 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.141+1574T>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109011728 | |||||||
| chr9:109011747 | G | C | 348 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(345): Show |
404 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(401): Show |
intron_variant | MODIFIER | c.141+1555C>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109011747 | |||||||
| chr9:109011885 | A | T | 46 | a0001c0001t0001g0010 a0001c0001t0001g0026 a0001c0001t0001g0027 others(43): Show |
50 | HG00438.hp1 HG00544.hp1 HG01070.hp2 others(47): Show |
intron_variant | MODIFIER | c.141+1417T>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109011885 | |||||||
| chr9:109011957 | G | A | 2 | a0001c0001t0003g0360 a0001c0001t0003g0361 |
2 | HG01433.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.141+1345C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109011957 | |||||||
| chr9:109012030 | C | T | 1 | a0001c0001t0001g0111 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.141+1272G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109012030 | |||||||
| chr9:109012076 | A | G | 2 | a0001c0001t0001g0031 a0001c0001t0001g0297 |
3 | HG02615.hp2 HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.141+1226T>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109012076 | |||||||
| chr9:109012113 | C | T | 243 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(240): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.141+1189G>A | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109012113 | |||||||
| chr9:109012183 | T | G | 39 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(36): Show |
42 | HG00408.hp2 HG01081.hp1 HG01099.hp1 others(39): Show |
intron_variant | MODIFIER | c.141+1119A>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109012183 | |||||||
| chr9:109012220 | G | GGA | 24 | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0001g0297 others(21): Show |
29 | HG00733.hp1 HG01109.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.141+1080_141+1081d others(4): Show |
CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109012220 | |||||||
| chr9:109012356 | T | A | 61 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(58): Show |
69 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(66): Show |
intron_variant | MODIFIER | c.141+946A>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109012356 | |||||||
| chr9:109012745 | G | A | 21 | a0001c0001t0002g0003 a0001c0001t0002g0013 a0001c0001t0002g0014 others(18): Show |
26 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.141+557C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109012745 | |||||||
| chr9:109012809 | T | C | 1 | a0001c0001t0001g0348 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.141+493A>G | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109012809 | |||||||
| chr9:109012822 | C | A | 1 | a0002c0002t0001g0110 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.141+480G>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109012822 | |||||||
| chr9:109012974 | G | A | 1 | a0001c0001t0001g0349 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.141+328C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109012974 | |||||||
| chr9:109012995 | G | A | 1 | a0002c0002t0001g0350 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.141+307C>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109012995 | |||||||
| chr9:109013053 | C | A | 2 | a0001c0001t0001g0351 a0001c0001t0001g0352 |
2 | NA18965.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.141+249G>T | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109013053 | |||||||
| chr9:109013222 | C | G | 65 | a0001c0001t0001g0019 a0001c0001t0001g0102 a0001c0001t0001g0103 others(62): Show |
80 | HG00099.hp1 HG00438.hp2 HG00621.hp2 others(77): Show |
intron_variant | MODIFIER | c.141+80G>C | CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109013222 | |||||||
| chr9:109013267 | AAGG | A | 29 | a0001c0001t0001g0354 a0001c0001t0002g0003 a0001c0001t0002g0013 others(26): Show |
34 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.141+32_141+34delCC others(1): Show |
CTNNAL1 | ENSG00000119326.15 | transcript | ENST00000325551.9 | protein_coding | 1/18 | chr9 | 109013267 |