Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 1499 |
| ensemblid | ENSG00000168036.18 |
| hgncid | 2514 |
| symbol | CTNNB1 |
| name | catenin beta 1 |
| refseq_nuc | NM_001904.4 |
| refseq_prot | NP_001895.1 |
| ensembl_nuc | ENST00000349496.11 |
| ensembl_prot | ENSP00000344456.5 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 41199505 |
| end | 41240443 |
| strand | + |
| ver | v1.2 |
| region | chr3:41199505-41240443 |
| region5000 | chr3:41194505-41245443 |
| regionname0 | CTNNB1_chr3_41199505_41240443 |
| regionname5000 | CTNNB1_chr3_41194505_41245443 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2343 | 298 | 83 | 48 | 125 | 12 | 28 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | ATGGC others(2338): Show |
chr3 | 41194505 | 41245443 | ||
| a0001c0002 | 0/0 | 2343 | 27 | 0 | 7 | 20 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | ATGGC others(2338): Show |
chr3 | 41194505 | 41245443 | ||
| a0001c0003 | 0/0 | 2343 | 7 | 7 | 0 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | ATGGC others(2338): Show |
chr3 | 41194505 | 41245443 | ||
| a0001c0004 | 0/0 | 2343 | 3 | 3 | 0 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | ATGGC others(2338): Show |
chr3 | 41194505 | 41245443 | ||
| a0001c0005 | 0/0 | 2343 | 3 | 2 | 1 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | ATGGC others(2338): Show |
chr3 | 41194505 | 41245443 | ||
| a0001c0006 | 0/0 | 2343 | 2 | 0 | 0 | 2 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | ATGGC others(2338): Show |
chr3 | 41194505 | 41245443 | ||
| a0001c0007 | 0/0 | 2343 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | ATGGC others(2338): Show |
chr3 | 41194505 | 41245443 | ||
| a0001c0008 | 0/0 | 2343 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | ATGGC others(2338): Show |
chr3 | 41194505 | 41245443 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3662 | 114 | 19 | 16 | 64 | 2 | 13 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | AAGCC others(3657): Show |
chr3 | 41194505 | 41245443 |
| a0001c0001t0002 | 1/1 | 3661 | 87 | 42 | 13 | 24 | 4 | 2 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | AAGCC others(3656): Show |
chr3 | 41194505 | 41245443 |
| a0001c0001t0003 | 0/0 | 3665 | 50 | 4 | 14 | 20 | 4 | 8 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | AAGCC others(3660): Show |
chr3 | 41194505 | 41245443 |
| a0001c0001t0004 | 0/0 | 3665 | 12 | 3 | 1 | 6 | 0 | 2 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | AAGCC others(3660): Show |
chr3 | 41194505 | 41245443 |
| a0001c0001t0005 | 0/0 | 3660 | 8 | 6 | 0 | 1 | 1 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | AAGCC others(3655): Show |
chr3 | 41194505 | 41245443 |
| a0001c0001t0006 | 0/0 | 3663 | 9 | 1 | 1 | 5 | 0 | 2 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | AAGCC others(3658): Show |
chr3 | 41194505 | 41245443 |
| a0001c0001t0007 | 0/0 | 3664 | 5 | 1 | 1 | 1 | 1 | 1 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | AAGCC others(3659): Show |
chr3 | 41194505 | 41245443 |
| a0001c0001t0008 | 0/0 | 3666 | 5 | 4 | 1 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | AAGCC others(3661): Show |
chr3 | 41194505 | 41245443 |
| a0001c0001t0009 | 0/0 | 3666 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | AAGCC others(3661): Show |
chr3 | 41194505 | 41245443 |
| a0001c0001t0011 | 0/0 | 3662 | 2 | 0 | 0 | 2 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | AAGCC others(3657): Show |
chr3 | 41194505 | 41245443 |
| a0001c0001t0012 | 0/0 | 3664 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | AAGCC others(3659): Show |
chr3 | 41194505 | 41245443 |
| a0001c0001t0013 | 0/0 | 3661 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | AAGCC others(3656): Show |
chr3 | 41194505 | 41245443 |
| a0001c0001t0015 | 0/0 | 3661 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | AAGCC others(3656): Show |
chr3 | 41194505 | 41245443 |
| a0001c0001t0016 | 0/0 | 3662 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | AAGCC others(3657): Show |
chr3 | 41194505 | 41245443 |
| a0001c0001t0018 | 0/0 | 3662 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | AAGCC others(3657): Show |
chr3 | 41194505 | 41245443 |
| a0001c0002t0003 | 0/0 | 3665 | 22 | 0 | 5 | 17 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | AAGCC others(3660): Show |
chr3 | 41194505 | 41245443 |
| a0001c0002t0007 | 0/0 | 3664 | 2 | 0 | 2 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | AAGCC others(3659): Show |
chr3 | 41194505 | 41245443 |
| a0001c0002t0009 | 0/0 | 3666 | 2 | 0 | 0 | 2 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | AAGCC others(3661): Show |
chr3 | 41194505 | 41245443 |
| a0001c0002t0017 | 0/0 | 3665 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | AAGCC others(3660): Show |
chr3 | 41194505 | 41245443 |
| a0001c0003t0004 | 0/0 | 3665 | 6 | 6 | 0 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | AAGCC others(3660): Show |
chr3 | 41194505 | 41245443 |
| a0001c0003t0008 | 0/0 | 3666 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | AAGCC others(3661): Show |
chr3 | 41194505 | 41245443 |
| a0001c0004t0001 | 0/0 | 3662 | 2 | 2 | 0 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | AAGCC others(3657): Show |
chr3 | 41194505 | 41245443 |
| a0001c0004t0005 | 0/0 | 3660 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | AAGCC others(3655): Show |
chr3 | 41194505 | 41245443 |
| a0001c0005t0002 | 0/0 | 3661 | 3 | 2 | 1 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | AAGCC others(3656): Show |
chr3 | 41194505 | 41245443 |
| a0001c0006t0010 | 0/0 | 3665 | 2 | 0 | 0 | 2 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | AAGCC others(3660): Show |
chr3 | 41194505 | 41245443 |
| a0001c0007t0001 | 0/0 | 3662 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | AAGCC others(3657): Show |
chr3 | 41194505 | 41245443 |
| a0001c0008t0014 | 0/0 | 3665 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | AAGCC others(3660): Show |
chr3 | 41194505 | 41245443 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0001g0003 | 0/0 | 5 | 1 | 1 | 3 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0001g0004 | 0/0 | 3 | 1 | 0 | 0 | 0 | 2 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0001g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0002g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0002g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0002g0004 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0002g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0002g0007 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0002g0008 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0002g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0002g0014 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0002g0015 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0002g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0002g0025 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0002g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0002g0158 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0002g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0002g0212 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0002g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0002g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0003g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0003g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0003g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0003g0018 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0003g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0003g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0003g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0003g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0003g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0003g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0003g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0003g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0003g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0003g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0003g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0003g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0003g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0003g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0003g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0003g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0004g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0004g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0004g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0004g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0004g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0004g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0004g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0004g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0004g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0004g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0005g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0005g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0005g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0005g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0005g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0005g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0005g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0005g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0006g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0006g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0006g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0006g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0006g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0006g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0006g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0006g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0006g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0007g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0007g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0007g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0007g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0007g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0008g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0008g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0008g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0008g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0008g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0009g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0011g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0011g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0012g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0013g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0015g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0016g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0001t0018g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0002t0003g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0002t0003g0005 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0002t0003g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0002t0003g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0002t0003g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0002t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0002t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0002t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0002t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0002t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0002t0003g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0002t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0002t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0002t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0002t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0002t0003g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0002t0007g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0002t0007g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0002t0009g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0002t0009g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0002t0017g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0003t0004g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0003t0004g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0003t0004g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0003t0004g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0003t0004g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0003t0008g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0004t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0004t0005g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0005t0002g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0005t0002g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0005t0002g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0006t0010g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0006t0010g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0007t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| a0001c0008t0014g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0007 | EUR | GBR | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG00140 | hp2 | a0001 | c0001 | t0003 | g0058 | EUR | GBR | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG00280 | hp1 | a0001 | c0001 | t0003 | g0051 | EUR | FIN | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0223 | EUR | FIN | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG00323 | hp1 | a0001 | c0001 | t0003 | g0020 | EUR | FIN | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG00323 | hp2 | a0001 | c0001 | t0005 | g0027 | EUR | FIN | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | CHS | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG00408 | hp2 | a0001 | c0002 | t0003 | g0001 | EAS | CHS | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | CHS | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | CHS | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | CHS | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG00544 | hp2 | a0001 | c0002 | t0003 | g0091 | EAS | CHS | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | CHS | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | CHS | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | CHS | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | CHS | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG00621 | hp1 | a0001 | c0002 | t0003 | g0093 | EAS | CHS | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | CHS | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG00639 | hp1 | a0001 | c0001 | t0003 | g0018 | AMR | PUR | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG00673 | hp1 | a0001 | c0001 | t0004 | g0050 | EAS | CHS | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | CHS | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG00733 | hp1 | a0001 | c0001 | t0003 | g0011 | AMR | PUR | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0015 | AMR | PUR | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0064 | AMR | PUR | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0211 | AMR | PUR | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0262 | AMR | PUR | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0255 | AMR | PUR | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG01071 | hp2 | a0001 | c0001 | t0003 | g0018 | AMR | PUR | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG01074 | hp1 | a0001 | c0001 | t0008 | g0087 | AMR | PUR | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG01081 | hp1 | a0001 | c0001 | t0003 | g0011 | AMR | PUR | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | PUR | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG01099 | hp1 | a0001 | c0001 | t0003 | g0044 | AMR | PUR | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0149 | AMR | PUR | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0256 | AMR | PUR | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0121 | AMR | PUR | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG01167 | hp2 | a0001 | c0001 | t0004 | g0086 | AMR | PUR | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG01175 | hp1 | a0001 | c0001 | t0003 | g0261 | AMR | PUR | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG01175 | hp2 | a0001 | c0001 | t0006 | g0032 | AMR | PUR | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0141 | AMR | PUR | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0014 | AMR | PUR | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG01255 | hp1 | a0001 | c0002 | t0003 | g0089 | AMR | CLM | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0227 | AMR | CLM | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG01256 | hp1 | a0001 | c0002 | t0007 | g0005 | AMR | CLM | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0250 | AMR | CLM | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG01258 | hp1 | a0001 | c0002 | t0003 | g0005 | AMR | CLM | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG01258 | hp2 | a0001 | c0001 | t0003 | g0055 | AMR | CLM | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0253 | AMR | CLM | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG01261 | hp2 | a0001 | c0001 | t0003 | g0018 | AMR | CLM | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG01358 | hp1 | a0001 | c0002 | t0003 | g0047 | AMR | CLM | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0147 | AMR | CLM | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | CLM | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG01361 | hp2 | a0001 | c0001 | t0003 | g0104 | AMR | CLM | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0135 | AMR | CLM | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | CLM | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | CLM | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | CLM | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0015 | EUR | IBS | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG01515 | hp2 | a0001 | c0001 | t0007 | g0056 | EUR | IBS | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0004 | EUR | IBS | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0122 | EUR | IBS | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | ACB | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG01884 | hp2 | a0001 | c0001 | t0005 | g0270 | AFR | ACB | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG01891 | hp1 | a0001 | c0004 | t0001 | g0028 | AFR | ACB | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0016 | AFR | ACB | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG01928 | hp1 | a0001 | c0002 | t0003 | g0022 | AMR | PEL | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PEL | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PEL | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG01934 | hp2 | a0001 | c0005 | t0002 | g0152 | AMR | PEL | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PEL | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG01952 | hp2 | a0001 | c0002 | t0003 | g0096 | AMR | PEL | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0027 | AMR | PEL | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG01975 | hp2 | a0001 | c0002 | t0007 | g0097 | AMR | PEL | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0142 | AMR | PEL | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0148 | AMR | PEL | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG02004 | hp2 | a0001 | c0001 | t0007 | g0011 | AMR | PEL | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG02015 | hp1 | a0001 | c0001 | t0003 | g0094 | EAS | KHV | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | KHV | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | KHV | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG02027 | hp2 | a0001 | c0002 | t0003 | g0021 | EAS | KHV | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0060 | AFR | ACB | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | ACB | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | KHV | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG02056 | hp2 | a0001 | c0001 | t0006 | g0206 | EAS | KHV | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | KHV | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG02071 | hp2 | a0001 | c0002 | t0003 | g0079 | EAS | KHV | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | KHV | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | KHV | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG02129 | hp2 | a0001 | c0002 | t0003 | g0092 | EAS | KHV | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | KHV | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG02132 | hp2 | a0001 | c0001 | t0003 | g0232 | EAS | KHV | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0062 | AFR | ACB | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG02145 | hp2 | a0001 | c0001 | t0008 | g0059 | AFR | ACB | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG02155 | hp1 | a0001 | c0002 | t0003 | g0088 | EAS | CDX | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | CDX | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG02165 | hp1 | a0001 | c0001 | t0003 | g0045 | EAS | CDX | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | CDX | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | ACB | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG02258 | hp1 | a0001 | c0005 | t0002 | g0151 | AFR | ACB | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | PEL | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PEL | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG02280 | hp1 | a0001 | c0008 | t0014 | g0269 | AFR | ACB | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG02280 | hp2 | a0001 | c0001 | t0004 | g0103 | AFR | ACB | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | ACB | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG02572 | hp1 | a0001 | c0001 | t0006 | g0230 | AFR | GWD | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0222 | SAS | PJL | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG02602 | hp2 | a0001 | c0001 | t0007 | g0020 | SAS | PJL | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0016 | AFR | GWD | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG02615 | hp2 | a0001 | c0001 | t0018 | g0046 | AFR | GWD | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG02622 | hp1 | a0001 | c0001 | t0008 | g0057 | AFR | GWD | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0228 | AFR | GWD | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG02630 | hp1 | a0001 | c0001 | t0005 | g0268 | AFR | GWD | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG02630 | hp2 | a0001 | c0003 | t0004 | g0099 | AFR | GWD | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0129 | AFR | GWD | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0265 | AFR | GWD | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0202 | SAS | PJL | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0264 | SAS | PJL | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0123 | AFR | GWD | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG02717 | hp2 | a0001 | c0001 | t0008 | g0085 | AFR | GWD | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG02735 | hp2 | a0001 | c0001 | t0003 | g0067 | SAS | PJL | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG02738 | hp1 | a0001 | c0001 | t0003 | g0043 | SAS | PJL | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0178 | SAS | PJL | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG02809 | hp1 | a0001 | c0003 | t0008 | g0100 | AFR | GWD | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0134 | AFR | GWD | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG02818 | hp1 | a0001 | c0001 | t0005 | g0038 | AFR | GWD | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | GWD | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | GWD | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0154 | AFR | GWD | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG02895 | hp1 | a0001 | c0001 | t0005 | g0266 | AFR | GWD | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG02895 | hp2 | a0001 | c0001 | t0005 | g0132 | AFR | GWD | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0038 | AFR | GWD | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0013 | AFR | GWD | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0131 | AFR | ESN | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | ESN | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0016 | AFR | ESN | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0130 | AFR | ESN | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0155 | AFR | ESN | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | ESN | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG02976 | hp1 | a0001 | c0004 | t0005 | g0114 | AFR | ESN | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | ESN | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG03041 | hp1 | a0001 | c0001 | t0007 | g0259 | AFR | GWD | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0162 | AFR | GWD | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0220 | AFR | MSL | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0120 | AFR | MSL | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG03130 | hp1 | a0001 | c0001 | t0005 | g0160 | AFR | ESN | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG03130 | hp2 | a0001 | c0003 | t0004 | g0054 | AFR | ESN | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0150 | AFR | ESN | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG03139 | hp2 | a0001 | c0003 | t0004 | g0024 | AFR | ESN | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG03195 | hp2 | a0001 | c0003 | t0004 | g0024 | AFR | ESN | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0124 | AFR | MSL | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0219 | AFR | MSL | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | MSL | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG03225 | hp2 | a0001 | c0001 | t0008 | g0084 | AFR | MSL | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG03239 | hp2 | a0001 | c0001 | t0003 | g0263 | SAS | PJL | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG03453 | hp1 | a0001 | c0001 | t0016 | g0245 | AFR | MSL | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0136 | AFR | MSL | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | MSL | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG03486 | hp2 | a0001 | c0004 | t0001 | g0028 | AFR | MSL | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0126 | AFR | ESN | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0144 | AFR | ESN | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0153 | AFR | GWD | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0013 | AFR | GWD | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0026 | AFR | MSL | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | MSL | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG03669 | hp2 | a0001 | c0001 | t0003 | g0069 | SAS | PJL | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG03688 | hp1 | a0001 | c0001 | t0004 | g0075 | SAS | STU | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG03688 | hp2 | a0001 | c0001 | t0006 | g0215 | SAS | STU | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG03704 | hp1 | a0001 | c0001 | t0003 | g0065 | SAS | PJL | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0166 | SAS | PJL | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0185 | SAS | PJL | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG03831 | hp1 | a0001 | c0001 | t0003 | g0258 | SAS | BEB | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG03831 | hp2 | a0001 | c0001 | t0006 | g0033 | SAS | BEB | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0025 | SAS | BEB | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0168 | SAS | BEB | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0242 | SAS | BEB | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG03942 | hp2 | a0001 | c0001 | t0003 | g0066 | SAS | BEB | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG04184 | hp1 | a0001 | c0001 | t0003 | g0068 | SAS | BEB | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0213 | SAS | BEB | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0181 | SAS | STU | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG04199 | hp2 | a0001 | c0001 | t0004 | g0083 | SAS | STU | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0026 | AFR | YRI | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0013 | AFR | YRI | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | CHB | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | CHB | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0216 | AFR | YRI | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA18906 | hp2 | a0001 | c0001 | t0003 | g0082 | AFR | YRI | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA18941 | hp1 | a0001 | c0001 | t0011 | g0236 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA18943 | hp2 | a0001 | c0001 | t0004 | g0010 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA18946 | hp2 | a0001 | c0002 | t0003 | g0005 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA18951 | hp2 | a0001 | c0001 | t0005 | g0175 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA18953 | hp2 | a0001 | c0001 | t0003 | g0072 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA18956 | hp1 | a0001 | c0006 | t0010 | g0041 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA18957 | hp1 | a0001 | c0006 | t0010 | g0040 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA18957 | hp2 | a0001 | c0001 | t0003 | g0241 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA18959 | hp1 | a0001 | c0001 | t0011 | g0036 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA18961 | hp2 | a0001 | c0001 | t0003 | g0081 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA18963 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA18964 | hp1 | a0001 | c0002 | t0017 | g0022 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA18968 | hp1 | a0001 | c0001 | t0003 | g0238 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA18968 | hp2 | a0001 | c0001 | t0004 | g0019 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA18971 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA18975 | hp1 | a0001 | c0007 | t0001 | g0229 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA18975 | hp2 | a0001 | c0001 | t0003 | g0073 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA18981 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA18982 | hp2 | a0001 | c0001 | t0003 | g0023 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA18983 | hp1 | a0001 | c0001 | t0006 | g0037 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA18983 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA18984 | hp2 | a0001 | c0001 | t0003 | g0052 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA18985 | hp1 | a0001 | c0002 | t0003 | g0048 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA18988 | hp2 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA18992 | hp1 | a0001 | c0001 | t0003 | g0231 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA18993 | hp2 | a0001 | c0002 | t0003 | g0021 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA18999 | hp1 | a0001 | c0002 | t0003 | g0071 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA19000 | hp1 | a0001 | c0002 | t0003 | g0076 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA19001 | hp2 | a0001 | c0001 | t0004 | g0010 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA19002 | hp2 | a0001 | c0001 | t0003 | g0095 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA19003 | hp1 | a0001 | c0002 | t0003 | g0090 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA19004 | hp1 | a0001 | c0001 | t0003 | g0080 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA19006 | hp1 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA19007 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA19009 | hp2 | a0001 | c0001 | t0006 | g0184 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA19030 | hp1 | a0001 | c0001 | t0009 | g0070 | AFR | LWK | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA19030 | hp2 | a0001 | c0003 | t0004 | g0098 | AFR | LWK | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0161 | AFR | LWK | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0029 | AFR | LWK | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA19056 | hp2 | a0001 | c0001 | t0007 | g0023 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA19070 | hp1 | a0001 | c0002 | t0003 | g0005 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA19072 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA19072 | hp2 | a0001 | c0001 | t0012 | g0010 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA19074 | hp1 | a0001 | c0001 | t0006 | g0237 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA19075 | hp1 | a0001 | c0002 | t0009 | g0078 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA19075 | hp2 | a0001 | c0001 | t0006 | g0252 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA19076 | hp1 | a0001 | c0002 | t0009 | g0077 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA19076 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA19077 | hp1 | a0001 | c0001 | t0003 | g0074 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA19079 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA19079 | hp2 | a0001 | c0001 | t0004 | g0019 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA19084 | hp1 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA19089 | hp2 | a0001 | c0001 | t0013 | g0101 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA19090 | hp1 | a0001 | c0001 | t0004 | g0049 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0159 | AFR | YRI | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0157 | AFR | YRI | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0128 | AFR | ASW | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0156 | AFR | ASW | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0218 | EUR | TSI | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA20805 | hp2 | a0001 | c0001 | t0003 | g0061 | EUR | TSI | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG01123 | hp1 | a0001 | c0001 | t0003 | g0257 | AMR | CLM | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG01123 | hp2 | a0001 | c0001 | t0015 | g0015 | AMR | CLM | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG02109 | hp1 | a0001 | c0001 | t0004 | g0102 | AFR | ACB | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | ACB | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0209 | AFR | ACB | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG02559 | hp1 | a0001 | c0005 | t0002 | g0260 | AFR | ACB | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | ACB | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG03471 | hp1 | a0001 | c0001 | t0004 | g0267 | AFR | MSL | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0127 | AFR | MSL | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | USA | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0217 | AFR | USA | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA18955 | hp2 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA20300 | hp1 | a0001 | c0003 | t0004 | g0053 | AFR | USA | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | USA | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | LWK | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| NA21309 | hp2 | a0001 | c0001 | t0003 | g0063 | AFR | LWK | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0212 | REF | REF | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0158 | REF | REF | CTNNB1_chr3_41194505_41245443 | CTNNB1 | chr3 | 41194505 | 41245443 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:41225480 | C | G | 1 | a0001c0008 | 1 | HG02280.hp1 | synonymous_variant | LOW | c.642C>G | p.Thr214Thr | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 5/15 | 856/3661 | 642/2346 | 214/781 | chr3 | 41225480 | |||
| chr3:41225480 | C | T | 1 | a0001c0005 | 3 | HG01934.hp2 HG02258.hp1 HG02559.hp1 |
synonymous_variant | LOW | c.642C>T | p.Thr214Thr | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 5/15 | 856/3661 | 642/2346 | 214/781 | chr3 | 41225480 | |||
| chr3:41233414 | C | A | 1 | a0001c0006 | 2 | NA18956.hp1 NA18957.hp1 |
synonymous_variant | LOW | c.1155C>A | p.Leu385Leu | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 8/15 | 1369/3661 | 1155/2346 | 385/781 | chr3 | 41233414 | |||
| chr3:41233859 | C | T | 1 | a0001c0003 | 7 | HG02630.hp2 HG02809.hp1 HG03130.hp2 others(4): Show |
synonymous_variant | LOW | c.1516C>T | p.Leu506Leu | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 9/15 | 1730/3661 | 1516/2346 | 506/781 | chr3 | 41233859 | |||
| chr3:41236616 | A | C | 1 | a0001c0004 | 3 | HG01891.hp1 HG02976.hp1 HG03486.hp2 |
synonymous_variant | LOW | c.1983A>C | p.Arg661Arg | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 13/15 | 2197/3661 | 1983/2346 | 661/781 | chr3 | 41236616 | |||
| chr3:41239222 | C | T | 1 | a0001c0007 | 1 | NA18975.hp1 | synonymous_variant | LOW | c.2226C>T | p.His742His | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 15/15 | 2440/3661 | 2226/2346 | 742/781 | chr3 | 41239222 | |||
| chr3:41239336 | C | T | 1 | a0001c0002 | 27 | HG00408.hp2 HG00544.hp2 HG00621.hp1 others(24): Show |
synonymous_variant | LOW | c.2340C>T | p.Asp780Asp | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 15/15 | 2554/3661 | 2340/2346 | 780/781 | chr3 | 41239336 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:41199663 | C | G | 1 | a0001c0001t0018 | 1 | HG02615.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-56C>G | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/15 | chr3 | 41199663 | |||||||
| chr3:41239374 | C | T | 1 | a0001c0002t0017 | 1 | NA18964.hp1 | 3_prime_UTR_variant | MODIFIER | c.*32C>T | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 15/15 | 32 | chr3 | 41239374 | ||||||
| chr3:41239897 | T | G | 14 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0007 others(11): Show |
111 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(108): Show |
3_prime_UTR_variant | MODIFIER | c.*555T>G | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 15/15 | 555 | chr3 | 41239897 | ||||||
| chr3:41239918 | T | TA | 2 | a0001c0001t0009 a0001c0002t0009 |
3 | NA19030.hp1 NA19075.hp1 NA19076.hp1 |
3_prime_UTR_variant | MODIFIER | c.*579dupA | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 15/15 | 580 | INFO_REALIGN_3_PRIME | chr3 | 41239918 | |||||
| chr3:41239921 | A | AT | 8 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0011 others(5): Show |
127 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(124): Show |
3_prime_UTR_variant | MODIFIER | c.*598dupT | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 15/15 | 599 | INFO_REALIGN_3_PRIME | chr3 | 41239921 | |||||
| chr3:41239921 | A | ATT | 1 | a0001c0001t0006 | 9 | HG01175.hp2 HG02056.hp2 HG02572.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*597_*598dupTT | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 15/15 | 599 | INFO_REALIGN_3_PRIME | chr3 | 41239921 | |||||
| chr3:41239921 | A | T | 1 | a0001c0006t0010 | 2 | NA18956.hp1 NA18957.hp1 |
3_prime_UTR_variant | MODIFIER | c.*579A>T | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 15/15 | 579 | chr3 | 41239921 | ||||||
| chr3:41239921 | AT | A | 5 | a0001c0001t0005 a0001c0001t0007 a0001c0001t0012 others(2): Show |
17 | HG00323.hp2 HG01256.hp1 HG01515.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*598delT | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 15/15 | 598 | INFO_REALIGN_3_PRIME | chr3 | 41239921 | |||||
| chr3:41239922 | T | A | 3 | a0001c0001t0003 a0001c0002t0003 a0001c0002t0017 |
73 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(70): Show |
3_prime_UTR_variant | MODIFIER | c.*580T>A | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 15/15 | 580 | chr3 | 41239922 | ||||||
| chr3:41239923 | T | A | 2 | a0001c0001t0007 a0001c0002t0007 |
7 | HG01256.hp1 HG01515.hp2 HG01975.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*581T>A | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 15/15 | 581 | chr3 | 41239923 | ||||||
| chr3:41239986 | C | CT | 7 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(4): Show |
31 | HG00140.hp2 HG00544.hp2 HG00609.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*669dupT | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 15/15 | 670 | INFO_REALIGN_3_PRIME | chr3 | 41239986 | |||||
| chr3:41239986 | C | CTT | 8 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0006 others(5): Show |
61 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*668_*669dupTT | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 15/15 | 670 | INFO_REALIGN_3_PRIME | chr3 | 41239986 | |||||
| chr3:41239986 | C | CTTT | 6 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0008 others(3): Show |
20 | HG00323.hp1 HG01071.hp2 HG01175.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*667_*669dupTTT | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 15/15 | 670 | INFO_REALIGN_3_PRIME | chr3 | 41239986 | |||||
| chr3:41239986 | C | CTTTT | 5 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0007 others(2): Show |
7 | HG02145.hp2 HG02602.hp2 HG03688.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*666_*669dupTTTT | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 15/15 | 670 | INFO_REALIGN_3_PRIME | chr3 | 41239986 | |||||
| chr3:41239986 | CT | C | 7 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(4): Show |
38 | HG00639.hp2 HG00735.hp2 HG01074.hp2 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*669delT | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 15/15 | 669 | INFO_REALIGN_3_PRIME | chr3 | 41239986 | |||||
| chr3:41239986 | CTT | C | 3 | a0001c0001t0002 a0001c0001t0004 a0001c0008t0014 |
7 | HG01167.hp1 HG01167.hp2 HG02280.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*668_*669delTT | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 15/15 | 668 | INFO_REALIGN_3_PRIME | chr3 | 41239986 | |||||
| chr3:41239986 | CTTTT | C | 4 | a0001c0001t0002 a0001c0001t0004 a0001c0003t0004 others(1): Show |
7 | HG02004.hp1 HG02809.hp1 HG03139.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*666_*669delTTTT | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 15/15 | 666 | INFO_REALIGN_3_PRIME | chr3 | 41239986 | |||||
| chr3:41239986 | CTTTTT | C | 5 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(2): Show |
31 | HG00323.hp2 HG00733.hp2 HG01123.hp2 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*665_*669delTTTTT | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 15/15 | 665 | INFO_REALIGN_3_PRIME | chr3 | 41239986 | |||||
| chr3:41240109 | C | CTAAT | 14 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0007 others(11): Show |
111 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(108): Show |
3_prime_UTR_variant | MODIFIER | c.*769_*772dupAATT | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 15/15 | 773 | INFO_REALIGN_3_PRIME | chr3 | 41240109 | |||||
| chr3:41240247 | T | G | 1 | a0001c0001t0011 | 2 | NA18941.hp1 NA18959.hp1 |
3_prime_UTR_variant | MODIFIER | c.*905T>G | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 15/15 | 905 | chr3 | 41240247 | ||||||
| chr3:41240356 | C | T | 1 | a0001c0001t0016 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1014C>T | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 15/15 | 1014 | chr3 | 41240356 | ||||||
| chr3:41240382 | C | T | 1 | a0001c0001t0015 | 1 | HG01123.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1040C>T | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 15/15 | 1040 | chr3 | 41240382 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:41199703 | G | T | 1 | a0001c0001t0005g0270 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-49+33G>T | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41199703 | |||||||
| chr3:41199722 | C | T | 1 | a0001c0008t0014g0269 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-49+52C>T | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41199722 | |||||||
| chr3:41199792 | G | A | 1 | a0001c0008t0014g0269 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-49+122G>A | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41199792 | |||||||
| chr3:41199866 | G | A | 1 | a0001c0008t0014g0269 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-49+196G>A | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41199866 | |||||||
| chr3:41199869 | C | A | 1 | a0001c0001t0001g0039 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-49+199C>A | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41199869 | |||||||
| chr3:41199894 | C | T | 5 | a0001c0001t0002g0038 a0001c0001t0004g0267 a0001c0001t0005g0038 others(2): Show |
5 | HG02630.hp1 HG02818.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.-49+224C>T | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41199894 | |||||||
| chr3:41199902 | A | T | 1 | a0001c0001t0002g0265 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-49+232A>T | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41199902 | |||||||
| chr3:41199995 | C | T | 1 | a0001c0001t0002g0264 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-49+325C>T | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41199995 | |||||||
| chr3:41200013 | C | T | 3 | a0001c0001t0003g0261 a0001c0001t0003g0262 a0001c0001t0003g0263 |
3 | HG00741.hp1 HG01175.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.-49+343C>T | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41200013 | |||||||
| chr3:41200043 | G | T | 1 | a0001c0001t0002g0264 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-49+373G>T | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41200043 | |||||||
| chr3:41200144 | C | T | 1 | a0001c0005t0002g0260 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-49+474C>T | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41200144 | |||||||
| chr3:41200185 | T | C | 2 | a0001c0006t0010g0040 a0001c0006t0010g0041 |
2 | NA18956.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.-49+515T>C | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41200185 | |||||||
| chr3:41200249 | C | G | 1 | a0001c0001t0007g0259 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-49+579C>G | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41200249 | |||||||
| chr3:41200333 | G | A | 1 | a0001c0001t0001g0042 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-49+663G>A | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41200333 | |||||||
| chr3:41200403 | T | C | 2 | a0001c0006t0010g0040 a0001c0006t0010g0041 |
2 | NA18956.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.-49+733T>C | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41200403 | |||||||
| chr3:41200419 | T | C | 2 | a0001c0001t0003g0043 a0001c0001t0003g0044 |
2 | HG01099.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.-49+749T>C | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41200419 | |||||||
| chr3:41200424 | T | A | 1 | a0001c0001t0003g0045 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-49+754T>A | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41200424 | |||||||
| chr3:41200427 | T | C | 1 | a0001c0001t0018g0046 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-49+757T>C | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41200427 | |||||||
| chr3:41200502 | A | G | 5 | a0001c0001t0003g0018 a0001c0001t0003g0255 a0001c0001t0003g0256 others(2): Show |
7 | HG00639.hp1 HG00741.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.-49+832A>G | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41200502 | |||||||
| chr3:41200847 | C | A | 90 | a0001c0001t0003g0001 a0001c0001t0003g0011 a0001c0001t0003g0018 others(87): Show |
103 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.-49+1177C>A | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41200847 | |||||||
| chr3:41200853 | T | C | 1 | a0001c0008t0014g0269 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-49+1183T>C | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41200853 | |||||||
| chr3:41200876 | C | T | 120 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(117): Show |
142 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.-49+1206C>T | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41200876 | |||||||
| chr3:41201139 | C | A | 9 | a0001c0001t0001g0106 a0001c0001t0001g0108 a0001c0001t0001g0110 others(6): Show |
10 | HG01928.hp2 HG01934.hp1 HG01952.hp1 others(7): Show |
intron_variant | MODIFIER | c.-49+1469C>A | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41201139 | |||||||
| chr3:41201166 | C | G | 1 | a0001c0001t0002g0162 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-49+1496C>G | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41201166 | |||||||
| chr3:41201186 | C | T | 3 | a0001c0001t0003g0011 a0001c0001t0003g0104 a0001c0001t0007g0011 |
4 | HG00733.hp1 HG01081.hp1 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.-49+1516C>T | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41201186 | |||||||
| chr3:41201372 | A | G | 92 | a0001c0001t0002g0161 a0001c0001t0003g0001 a0001c0001t0003g0011 others(89): Show |
105 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.-49+1702A>G | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41201372 | |||||||
| chr3:41201453 | C | G | 2 | a0001c0001t0002g0161 a0001c0001t0005g0160 |
2 | HG03130.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-49+1783C>G | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41201453 | |||||||
| chr3:41201519 | G | A | 1 | a0001c0001t0002g0162 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-49+1849G>A | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41201519 | |||||||
| chr3:41201554 | T | G | 8 | a0001c0001t0001g0012 a0001c0001t0001g0113 a0001c0001t0001g0115 others(5): Show |
10 | HG02055.hp2 HG02486.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.-49+1884T>G | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41201554 | |||||||
| chr3:41201860 | C | G | 2 | a0001c0001t0002g0161 a0001c0001t0005g0160 |
2 | HG03130.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-49+2190C>G | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41201860 | |||||||
| chr3:41202141 | A | G | 1 | a0001c0001t0001g0254 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-49+2471A>G | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41202141 | |||||||
| chr3:41202147 | T | C | 1 | a0001c0002t0003g0047 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-49+2477T>C | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41202147 | |||||||
| chr3:41202251 | T | G | 93 | a0001c0001t0002g0120 a0001c0001t0002g0161 a0001c0001t0003g0001 others(90): Show |
106 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.-49+2581T>G | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41202251 | |||||||
| chr3:41202582 | C | T | 1 | a0001c0001t0001g0253 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-49+2912C>T | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41202582 | |||||||
| chr3:41202614 | T | C | 1 | a0001c0002t0003g0048 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-49+2944T>C | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41202614 | |||||||
| chr3:41202663 | CTATT | C | 5 | a0001c0001t0004g0010 a0001c0001t0004g0019 a0001c0001t0004g0049 others(2): Show |
7 | HG00673.hp1 NA18943.hp2 NA18968.hp2 others(4): Show |
intron_variant | MODIFIER | c.-49+2997_-49+3000d others(6): Show |
CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr3 | 41202663 | ||||||
| chr3:41202816 | CAG | C | 4 | a0001c0001t0001g0037 a0001c0001t0001g0251 a0001c0001t0006g0037 others(1): Show |
4 | NA18971.hp1 NA18981.hp1 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.-49+3147_-49+3148d others(4): Show |
CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41202816 | |||||||
| chr3:41202885 | T | G | 1 | a0001c0001t0003g0051 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-49+3215T>G | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41202885 | |||||||
| chr3:41203035 | CT | C | 25 | a0001c0001t0001g0029 a0001c0001t0001g0248 a0001c0001t0001g0249 others(22): Show |
28 | HG01256.hp2 HG01891.hp1 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.-49+3385delT | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr3 | 41203035 | ||||||
| chr3:41203035 | CTT | C | 251 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(248): Show |
298 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.-49+3384_-49+3385d others(4): Show |
CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr3 | 41203035 | ||||||
| chr3:41203035 | CTTT | C | 8 | a0001c0001t0001g0106 a0001c0001t0001g0164 a0001c0001t0001g0165 others(5): Show |
8 | HG01167.hp1 HG01517.hp2 HG01934.hp1 others(5): Show |
intron_variant | MODIFIER | c.-49+3383_-49+3385d others(5): Show |
CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr3 | 41203035 | ||||||
| chr3:41203055 | T | A | 1 | a0001c0001t0001g0163 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-49+3385T>A | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41203055 | |||||||
| chr3:41203067 | A | C | 1 | a0001c0001t0002g0159 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-49+3397A>C | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41203067 | |||||||
| chr3:41203193 | T | G | 2 | a0001c0003t0004g0053 a0001c0003t0004g0054 |
2 | HG03130.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-49+3523T>G | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41203193 | |||||||
| chr3:41203209 | AT | A | 32 | a0001c0001t0003g0011 a0001c0001t0003g0018 a0001c0001t0003g0020 others(29): Show |
35 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(32): Show |
intron_variant | MODIFIER | c.-49+3552delT | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr3 | 41203209 | ||||||
| chr3:41203281 | A | G | 1 | a0001c0001t0001g0247 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.-49+3611A>G | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41203281 | |||||||
| chr3:41203312 | A | G | 4 | a0001c0001t0001g0042 a0001c0001t0001g0254 a0001c0001t0002g0161 others(1): Show |
4 | HG03130.hp1 NA18969.hp1 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.-49+3642A>G | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41203312 | |||||||
| chr3:41203355 | T | G | 1 | a0001c0001t0002g0123 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-49+3685T>G | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41203355 | |||||||
| chr3:41203356 | C | A | 1 | a0001c0001t0002g0123 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-49+3686C>A | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41203356 | |||||||
| chr3:41203848 | G | A | 1 | a0001c0001t0002g0124 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-49+4178G>A | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41203848 | |||||||
| chr3:41203970 | G | A | 2 | a0001c0003t0004g0053 a0001c0003t0004g0054 |
2 | HG03130.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-49+4300G>A | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41203970 | |||||||
| chr3:41204106 | T | A | 1 | a0001c0001t0001g0167 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-49+4436T>A | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41204106 | |||||||
| chr3:41204190 | A | G | 1 | a0001c0001t0001g0246 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-49+4520A>G | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41204190 | |||||||
| chr3:41204199 | A | G | 6 | a0001c0003t0004g0024 a0001c0003t0004g0053 a0001c0003t0004g0054 others(3): Show |
7 | HG02630.hp2 HG02809.hp1 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.-49+4529A>G | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41204199 | |||||||
| chr3:41204240 | A | C | 56 | a0001c0001t0001g0012 a0001c0001t0001g0106 a0001c0001t0001g0108 others(53): Show |
68 | HG00323.hp2 HG00733.hp2 HG01109.hp1 others(65): Show |
intron_variant | MODIFIER | c.-49+4570A>C | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41204240 | |||||||
| chr3:41204250 | G | A | 1 | a0001c0008t0014g0269 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-49+4580G>A | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41204250 | |||||||
| chr3:41204313 | T | C | 2 | a0001c0001t0003g0055 a0001c0001t0007g0056 |
2 | HG01258.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.-49+4643T>C | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41204313 | |||||||
| chr3:41204321 | C | G | 1 | a0001c0008t0014g0269 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-49+4651C>G | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41204321 | |||||||
| chr3:41204690 | A | G | 1 | a0001c0001t0016g0245 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-49+5020A>G | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41204690 | |||||||
| chr3:41204900 | C | T | 2 | a0001c0002t0003g0096 a0001c0002t0007g0097 |
2 | HG01952.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.-49+5230C>T | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41204900 | |||||||
| chr3:41204917 | G | A | 3 | a0001c0005t0002g0151 a0001c0005t0002g0152 a0001c0005t0002g0260 |
3 | HG01934.hp2 HG02258.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.-49+5247G>A | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41204917 | |||||||
| chr3:41204950 | C | T | 2 | a0001c0002t0003g0096 a0001c0002t0007g0097 |
2 | HG01952.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.-49+5280C>T | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41204950 | |||||||
| chr3:41205009 | G | C | 1 | a0001c0001t0005g0160 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-49+5339G>C | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41205009 | |||||||
| chr3:41205045 | A | G | 3 | a0001c0001t0002g0156 a0001c0001t0002g0157 a0001c0001t0002g0265 |
3 | HG02647.hp2 NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-49+5375A>G | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41205045 | |||||||
| chr3:41205049 | ACTTT | A | 3 | a0001c0005t0002g0151 a0001c0005t0002g0152 a0001c0005t0002g0260 |
3 | HG01934.hp2 HG02258.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.-49+5383_-49+5386d others(6): Show |
CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr3 | 41205049 | ||||||
| chr3:41205372 | T | C | 1 | a0001c0001t0001g0168 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-49+5702T>C | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41205372 | |||||||
| chr3:41205460 | T | C | 2 | a0001c0006t0010g0040 a0001c0006t0010g0041 |
2 | NA18956.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.-49+5790T>C | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41205460 | |||||||
| chr3:41205508 | G | C | 1 | a0001c0001t0002g0153 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-49+5838G>C | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41205508 | |||||||
| chr3:41205633 | G | A | 4 | a0001c0001t0001g0030 a0001c0001t0001g0169 a0001c0001t0001g0170 others(1): Show |
4 | HG00609.hp1 NA18747.hp2 NA18956.hp2 others(1): Show |
intron_variant | MODIFIER | c.-49+5963G>A | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41205633 | |||||||
| chr3:41205687 | G | A | 1 | a0001c0001t0001g0171 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-49+6017G>A | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41205687 | |||||||
| chr3:41205852 | C | T | 1 | a0001c0008t0014g0269 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-49+6182C>T | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41205852 | |||||||
| chr3:41205862 | T | C | 1 | a0001c0001t0003g0043 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-49+6192T>C | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41205862 | |||||||
| chr3:41205897 | C | T | 1 | a0001c0001t0006g0252 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-49+6227C>T | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41205897 | |||||||
| chr3:41206237 | T | A | 1 | a0001c0001t0013g0101 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-49+6567T>A | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41206237 | |||||||
| chr3:41206991 | A | G | 47 | a0001c0001t0001g0012 a0001c0001t0001g0106 a0001c0001t0001g0108 others(44): Show |
55 | HG00323.hp2 HG00733.hp2 HG01109.hp1 others(52): Show |
intron_variant | MODIFIER | c.-49+7321A>G | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41206991 | |||||||
| chr3:41207044 | A | G | 2 | a0001c0001t0002g0161 a0001c0001t0005g0160 |
2 | HG03130.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-49+7374A>G | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41207044 | |||||||
| chr3:41207271 | G | A | 1 | a0001c0001t0003g0104 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-49+7601G>A | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41207271 | |||||||
| chr3:41207379 | A | G | 3 | a0001c0001t0003g0023 a0001c0001t0003g0052 a0001c0001t0007g0023 |
3 | NA18982.hp2 NA18984.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.-49+7709A>G | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41207379 | |||||||
| chr3:41207438 | C | A | 1 | a0001c0001t0001g0172 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-49+7768C>A | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41207438 | |||||||
| chr3:41207590 | A | G | 2 | a0001c0001t0001g0163 a0001c0001t0002g0244 |
2 | HG00423.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.-49+7920A>G | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41207590 | |||||||
| chr3:41207616 | T | C | 1 | a0001c0001t0005g0132 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-49+7946T>C | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41207616 | |||||||
| chr3:41207678 | T | G | 2 | a0001c0001t0001g0125 a0001c0004t0001g0028 |
3 | HG01891.hp1 HG02976.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-49+8008T>G | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41207678 | |||||||
| chr3:41208389 | A | G | 1 | a0001c0001t0001g0243 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-49+8719A>G | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41208389 | |||||||
| chr3:41208433 | C | A | 1 | a0001c0001t0001g0173 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-49+8763C>A | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41208433 | |||||||
| chr3:41208535 | T | C | 1 | a0001c0001t0003g0255 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-49+8865T>C | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41208535 | |||||||
| chr3:41208578 | A | C | 2 | a0001c0001t0002g0014 a0001c0001t0002g0131 |
4 | HG01243.hp2 HG02257.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.-49+8908A>C | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41208578 | |||||||
| chr3:41208638 | G | T | 55 | a0001c0001t0001g0012 a0001c0001t0001g0106 a0001c0001t0001g0108 others(52): Show |
67 | HG00323.hp2 HG00733.hp2 HG01109.hp1 others(64): Show |
intron_variant | MODIFIER | c.-49+8968G>T | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41208638 | |||||||
| chr3:41208684 | G | C | 1 | a0001c0008t0014g0269 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-49+9014G>C | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41208684 | |||||||
| chr3:41208810 | G | T | 1 | a0001c0001t0006g0252 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-49+9140G>T | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41208810 | |||||||
| chr3:41208882 | T | C | 1 | a0001c0001t0002g0159 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-49+9212T>C | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41208882 | |||||||
| chr3:41208891 | C | T | 1 | a0001c0001t0001g0172 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-49+9221C>T | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41208891 | |||||||
| chr3:41208990 | G | A | 92 | a0001c0001t0002g0161 a0001c0001t0003g0001 a0001c0001t0003g0011 others(89): Show |
105 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.-49+9320G>A | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41208990 | |||||||
| chr3:41209439 | G | C | 2 | a0001c0006t0010g0040 a0001c0006t0010g0041 |
2 | NA18956.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.-49+9769G>C | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41209439 | |||||||
| chr3:41209672 | A | G | 28 | a0001c0001t0001g0030 a0001c0001t0001g0035 a0001c0001t0001g0036 others(25): Show |
31 | HG00558.hp1 HG00609.hp1 HG01255.hp2 others(28): Show |
intron_variant | MODIFIER | c.-49+10002A>G | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41209672 | |||||||
| chr3:41209975 | A | G | 1 | a0001c0001t0001g0226 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.-49+10305A>G | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41209975 | |||||||
| chr3:41210180 | G | A | 4 | a0001c0003t0004g0024 a0001c0003t0004g0098 a0001c0003t0004g0099 others(1): Show |
5 | HG02630.hp2 HG02809.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.-49+10510G>A | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41210180 | |||||||
| chr3:41210229 | G | A | 1 | a0001c0001t0002g0133 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-49+10559G>A | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41210229 | |||||||
| chr3:41210235 | C | T | 4 | a0001c0001t0003g0066 a0001c0001t0003g0067 a0001c0001t0003g0068 others(1): Show |
4 | HG02735.hp2 HG03669.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.-49+10565C>T | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41210235 | |||||||
| chr3:41210289 | C | T | 2 | a0001c0001t0001g0166 a0001c0001t0001g0225 |
2 | HG01099.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.-49+10619C>T | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41210289 | |||||||
| chr3:41210364 | G | C | 1 | a0001c0001t0008g0057 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-49+10694G>C | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41210364 | |||||||
| chr3:41210385 | C | T | 1 | a0001c0001t0001g0224 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-49+10715C>T | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41210385 | |||||||
| chr3:41210402 | C | T | 1 | a0001c0001t0005g0160 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-49+10732C>T | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41210402 | |||||||
| chr3:41210796 | C | A | 8 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0121 others(5): Show |
12 | HG01167.hp1 HG01243.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.-49+11126C>A | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41210796 | |||||||
| chr3:41210828 | C | A | 1 | a0001c0001t0001g0253 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-49+11158C>A | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41210828 | |||||||
| chr3:41210968 | T | A | 2 | a0001c0001t0001g0125 a0001c0004t0001g0028 |
3 | HG01891.hp1 HG02976.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-49+11298T>A | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41210968 | |||||||
| chr3:41210985 | G | T | 3 | a0001c0001t0003g0023 a0001c0001t0003g0052 a0001c0001t0007g0023 |
3 | NA18982.hp2 NA18984.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.-49+11315G>T | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41210985 | |||||||
| chr3:41211035 | C | G | 1 | a0001c0001t0003g0045 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-49+11365C>G | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41211035 | |||||||
| chr3:41211088 | T | C | 1 | a0001c0001t0002g0107 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-49+11418T>C | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41211088 | |||||||
| chr3:41211207 | A | T | 1 | a0001c0001t0001g0225 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-49+11537A>T | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41211207 | |||||||
| chr3:41211210 | T | C | 1 | a0001c0001t0001g0225 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-49+11540T>C | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41211210 | |||||||
| chr3:41211592 | T | A | 1 | a0001c0001t0001g0174 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-49+11922T>A | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41211592 | |||||||
| chr3:41211850 | T | C | 7 | a0001c0001t0008g0057 a0001c0003t0004g0024 a0001c0003t0004g0053 others(4): Show |
8 | HG02622.hp1 HG02630.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.-48-12171T>C | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41211850 | |||||||
| chr3:41212060 | G | A | 1 | a0001c0001t0005g0175 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.-48-11961G>A | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41212060 | |||||||
| chr3:41212252 | G | A | 1 | a0001c0001t0004g0267 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-48-11769G>A | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41212252 | |||||||
| chr3:41212353 | T | G | 2 | a0001c0001t0007g0259 a0001c0001t0009g0070 |
2 | HG03041.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-48-11668T>G | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41212353 | |||||||
| chr3:41212729 | C | T | 1 | a0001c0001t0003g0043 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-48-11292C>T | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41212729 | |||||||
| chr3:41212783 | A | G | 7 | a0001c0001t0008g0057 a0001c0003t0004g0024 a0001c0003t0004g0053 others(4): Show |
8 | HG02622.hp1 HG02630.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.-48-11238A>G | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41212783 | |||||||
| chr3:41212954 | C | T | 1 | a0001c0001t0001g0242 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-48-11067C>T | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41212954 | |||||||
| chr3:41213100 | T | C | 1 | a0001c0001t0001g0242 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-48-10921T>C | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41213100 | |||||||
| chr3:41213155 | G | T | 89 | a0001c0001t0003g0001 a0001c0001t0003g0011 a0001c0001t0003g0018 others(86): Show |
102 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.-48-10866G>T | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41213155 | |||||||
| chr3:41213188 | C | G | 1 | a0001c0008t0014g0269 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-48-10833C>G | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41213188 | |||||||
| chr3:41213576 | A | G | 1 | a0001c0001t0005g0132 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-48-10445A>G | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41213576 | |||||||
| chr3:41213685 | C | T | 8 | a0001c0001t0001g0029 a0001c0001t0002g0016 a0001c0001t0002g0029 others(5): Show |
10 | HG01891.hp2 HG02572.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.-48-10336C>T | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41213685 | |||||||
| chr3:41213762 | A | G | 1 | a0001c0001t0001g0119 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-48-10259A>G | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41213762 | |||||||
| chr3:41213854 | G | T | 2 | a0001c0006t0010g0040 a0001c0006t0010g0041 |
2 | NA18956.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.-48-10167G>T | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41213854 | |||||||
| chr3:41213867 | T | G | 120 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(117): Show |
142 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.-48-10154T>G | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41213867 | |||||||
| chr3:41214139 | A | G | 2 | a0001c0001t0002g0161 a0001c0001t0005g0160 |
2 | HG03130.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-48-9882A>G | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41214139 | |||||||
| chr3:41214394 | T | TA | 263 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(260): Show |
311 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.-48-9614dupA | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr3 | 41214394 | ||||||
| chr3:41214394 | T | TAA | 14 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0176 others(11): Show |
15 | HG00423.hp2 HG00733.hp2 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.-48-9615_-48-9614d others(4): Show |
CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr3 | 41214394 | ||||||
| chr3:41214506 | T | C | 1 | a0001c0001t0002g0134 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-48-9515T>C | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41214506 | |||||||
| chr3:41214554 | C | T | 1 | a0001c0001t0005g0132 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-48-9467C>T | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41214554 | |||||||
| chr3:41214555 | G | C | 1 | a0001c0001t0001g0168 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-48-9466G>C | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41214555 | |||||||
| chr3:41214605 | A | C | 2 | a0001c0006t0010g0040 a0001c0006t0010g0041 |
2 | NA18956.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.-48-9416A>C | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41214605 | |||||||
| chr3:41214670 | C | T | 5 | a0001c0001t0002g0038 a0001c0001t0004g0267 a0001c0001t0005g0038 others(2): Show |
5 | HG02630.hp1 HG02818.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.-48-9351C>T | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41214670 | |||||||
| chr3:41214775 | T | C | 1 | a0001c0004t0001g0028 | 2 | HG01891.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-48-9246T>C | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41214775 | |||||||
| chr3:41214779 | T | TA | 7 | a0001c0001t0001g0012 a0001c0001t0001g0113 a0001c0001t0001g0115 others(4): Show |
9 | HG02055.hp2 HG02486.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.-48-9231dupA | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr3 | 41214779 | ||||||
| chr3:41214893 | G | A | 3 | a0001c0001t0001g0007 a0001c0001t0001g0177 a0001c0001t0002g0007 |
5 | HG00140.hp1 HG01071.hp1 HG01074.hp2 others(2): Show |
intron_variant | MODIFIER | c.-48-9128G>A | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41214893 | |||||||
| chr3:41214925 | T | C | 1 | a0001c0001t0005g0160 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-48-9096T>C | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41214925 | |||||||
| chr3:41215213 | TA | T | 175 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(172): Show |
209 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(206): Show |
intron_variant | MODIFIER | c.-48-8783delA | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr3 | 41215213 | ||||||
| chr3:41215213 | TAA | T | 87 | a0001c0001t0001g0118 a0001c0001t0001g0222 a0001c0001t0001g0223 others(84): Show |
100 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.-48-8784_-48-8783d others(4): Show |
CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr3 | 41215213 | ||||||
| chr3:41215213 | TAAAAAAA others(3): Show |
T | 1 | a0001c0001t0004g0267 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-48-8792_-48-8783d others(12): Show |
CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr3 | 41215213 | ||||||
| chr3:41215321 | T | G | 1 | a0001c0001t0001g0181 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-48-8700T>G | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41215321 | |||||||
| chr3:41215337 | C | T | 1 | a0001c0001t0001g0221 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-48-8684C>T | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41215337 | |||||||
| chr3:41215347 | C | T | 1 | a0001c0001t0003g0080 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.-48-8674C>T | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41215347 | |||||||
| chr3:41215382 | C | CA | 140 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0032 others(137): Show |
160 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.-48-8617dupA | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr3 | 41215382 | ||||||
| chr3:41215382 | C | CAA | 22 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0031 others(19): Show |
29 | HG00140.hp1 HG00609.hp2 HG00621.hp2 others(26): Show |
intron_variant | MODIFIER | c.-48-8618_-48-8617d others(4): Show |
CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr3 | 41215382 | ||||||
| chr3:41215402 | A | AAC | 6 | a0001c0003t0004g0024 a0001c0003t0004g0053 a0001c0003t0004g0054 others(3): Show |
7 | HG02630.hp2 HG02809.hp1 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.-48-8618_-48-8617i others(4): Show |
CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr3 | 41215402 | ||||||
| chr3:41215470 | C | G | 2 | a0001c0001t0004g0102 a0001c0001t0004g0103 |
2 | HG02109.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.-48-8551C>G | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41215470 | |||||||
| chr3:41215507 | C | T | 2 | a0001c0001t0003g0094 a0001c0001t0003g0095 |
2 | HG02015.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.-48-8514C>T | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41215507 | |||||||
| chr3:41215581 | T | G | 12 | a0001c0001t0004g0010 a0001c0001t0004g0019 a0001c0001t0004g0049 others(9): Show |
14 | HG00673.hp1 HG01074.hp1 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.-48-8440T>G | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41215581 | |||||||
| chr3:41215649 | G | T | 1 | a0001c0008t0014g0269 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-48-8372G>T | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41215649 | |||||||
| chr3:41215660 | G | C | 7 | a0001c0001t0004g0010 a0001c0001t0004g0019 a0001c0001t0004g0049 others(4): Show |
9 | HG00673.hp1 HG03688.hp1 HG04199.hp2 others(6): Show |
intron_variant | MODIFIER | c.-48-8361G>C | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41215660 | |||||||
| chr3:41215680 | C | G | 1 | a0001c0001t0001g0210 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-48-8341C>G | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41215680 | |||||||
| chr3:41215755 | C | G | 4 | a0001c0001t0003g0018 a0001c0001t0003g0256 a0001c0001t0003g0257 others(1): Show |
6 | HG00639.hp1 HG01071.hp2 HG01109.hp2 others(3): Show |
intron_variant | MODIFIER | c.-48-8266C>G | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41215755 | |||||||
| chr3:41215925 | T | G | 1 | a0001c0001t0002g0161 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-48-8096T>G | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41215925 | |||||||
| chr3:41216492 | A | G | 2 | a0001c0001t0002g0227 a0001c0001t0002g0228 |
2 | HG01255.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-48-7529A>G | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41216492 | |||||||
| chr3:41216557 | A | G | 94 | a0001c0001t0001g0222 a0001c0001t0002g0120 a0001c0001t0002g0161 others(91): Show |
107 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.-48-7464A>G | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41216557 | |||||||
| chr3:41216755 | A | G | 1 | a0001c0003t0004g0054 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-48-7266A>G | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41216755 | |||||||
| chr3:41216816 | A | C | 3 | a0001c0001t0003g0055 a0001c0001t0003g0064 a0001c0001t0007g0056 |
3 | HG00735.hp1 HG01258.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.-48-7205A>C | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41216816 | |||||||
| chr3:41217084 | A | C | 4 | a0001c0001t0001g0008 a0001c0001t0002g0008 a0001c0001t0002g0209 others(1): Show |
6 | HG00639.hp2 HG01884.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-48-6937A>C | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41217084 | |||||||
| chr3:41217145 | C | T | 1 | a0001c0001t0002g0219 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-48-6876C>T | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41217145 | |||||||
| chr3:41217263 | G | C | 1 | a0001c0001t0003g0067 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-48-6758G>C | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41217263 | |||||||
| chr3:41217399 | C | G | 1 | a0001c0001t0002g0162 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-48-6622C>G | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41217399 | |||||||
| chr3:41217665 | A | T | 12 | a0001c0001t0004g0010 a0001c0001t0004g0019 a0001c0001t0004g0049 others(9): Show |
14 | HG00673.hp1 HG01074.hp1 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.-48-6356A>T | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41217665 | |||||||
| chr3:41217671 | T | C | 1 | a0001c0001t0002g0120 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-48-6350T>C | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41217671 | |||||||
| chr3:41217724 | A | G | 1 | a0001c0001t0001g0208 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-48-6297A>G | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41217724 | |||||||
| chr3:41217821 | T | C | 1 | a0001c0002t0003g0088 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-48-6200T>C | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41217821 | |||||||
| chr3:41218020 | G | A | 92 | a0001c0001t0002g0161 a0001c0001t0003g0001 a0001c0001t0003g0011 others(89): Show |
105 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.-48-6001G>A | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41218020 | |||||||
| chr3:41218103 | G | A | 92 | a0001c0001t0002g0161 a0001c0001t0003g0001 a0001c0001t0003g0011 others(89): Show |
105 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.-48-5918G>A | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41218103 | |||||||
| chr3:41218366 | T | C | 1 | a0001c0001t0005g0160 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-48-5655T>C | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41218366 | |||||||
| chr3:41218526 | G | A | 66 | a0001c0001t0003g0001 a0001c0001t0003g0011 a0001c0001t0003g0018 others(63): Show |
76 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.-48-5495G>A | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41218526 | |||||||
| chr3:41218833 | A | G | 6 | a0001c0003t0004g0024 a0001c0003t0004g0053 a0001c0003t0004g0054 others(3): Show |
7 | HG02630.hp2 HG02809.hp1 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.-48-5188A>G | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41218833 | |||||||
| chr3:41218878 | C | T | 80 | a0001c0001t0003g0001 a0001c0001t0003g0011 a0001c0001t0003g0018 others(77): Show |
92 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.-48-5143C>T | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41218878 | |||||||
| chr3:41218908 | C | T | 1 | a0001c0001t0001g0165 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-48-5113C>T | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41218908 | |||||||
| chr3:41218911 | G | A | 87 | a0001c0001t0003g0001 a0001c0001t0003g0011 a0001c0001t0003g0018 others(84): Show |
100 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.-48-5110G>A | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41218911 | |||||||
| chr3:41219082 | A | G | 10 | a0001c0001t0001g0017 a0001c0001t0001g0042 a0001c0001t0001g0203 others(7): Show |
12 | HG00423.hp1 HG00673.hp2 HG02056.hp2 others(9): Show |
intron_variant | MODIFIER | c.-48-4939A>G | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41219082 | |||||||
| chr3:41219551 | G | T | 2 | a0001c0001t0004g0102 a0001c0001t0004g0103 |
2 | HG02109.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.-48-4470G>T | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41219551 | |||||||
| chr3:41219604 | T | G | 4 | a0001c0003t0004g0024 a0001c0003t0004g0098 a0001c0003t0004g0099 others(1): Show |
5 | HG02630.hp2 HG02809.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.-48-4417T>G | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41219604 | |||||||
| chr3:41219628 | A | C | 1 | a0001c0001t0008g0087 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-48-4393A>C | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41219628 | |||||||
| chr3:41219911 | A | T | 1 | a0001c0001t0005g0160 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-48-4110A>T | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41219911 | |||||||
| chr3:41220119 | G | A | 1 | a0001c0001t0003g0232 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-48-3902G>A | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41220119 | |||||||
| chr3:41220223 | T | A | 1 | a0001c0001t0001g0174 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-48-3798T>A | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41220223 | |||||||
| chr3:41220322 | A | G | 3 | a0001c0001t0001g0181 a0001c0001t0001g0202 a0001c0001t0001g0218 |
3 | HG02698.hp1 HG04199.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-48-3699A>G | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41220322 | |||||||
| chr3:41220366 | C | G | 1 | a0001c0001t0002g0159 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-48-3655C>G | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41220366 | |||||||
| chr3:41220371 | A | AGAACAC | 7 | a0001c0001t0008g0057 a0001c0003t0004g0024 a0001c0003t0004g0053 others(4): Show |
8 | HG02622.hp1 HG02630.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.-48-3649_-48-3644d others(8): Show |
CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr3 | 41220371 | ||||||
| chr3:41220378 | ACACACC | A | 5 | a0001c0001t0002g0027 a0001c0001t0002g0147 a0001c0001t0002g0148 others(2): Show |
5 | HG00323.hp2 HG01358.hp2 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.-48-3623_-48-3618d others(8): Show |
CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr3 | 41220378 | ||||||
| chr3:41220398 | A | ACACCCT | 12 | a0001c0001t0004g0010 a0001c0001t0004g0019 a0001c0001t0004g0049 others(9): Show |
14 | HG00673.hp1 HG01074.hp1 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.-48-3617_-48-3612d others(8): Show |
CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr3 | 41220398 | ||||||
| chr3:41220488 | A | G | 126 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(123): Show |
148 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(145): Show |
intron_variant | MODIFIER | c.-48-3533A>G | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41220488 | |||||||
| chr3:41220953 | T | C | 91 | a0001c0001t0002g0120 a0001c0001t0003g0001 a0001c0001t0003g0011 others(88): Show |
104 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.-48-3068T>C | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41220953 | |||||||
| chr3:41220988 | C | T | 1 | a0001c0001t0001g0111 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-48-3033C>T | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41220988 | |||||||
| chr3:41221030 | G | A | 1 | a0001c0001t0005g0160 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-48-2991G>A | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41221030 | |||||||
| chr3:41221069 | C | G | 1 | a0001c0001t0008g0057 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-48-2952C>G | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41221069 | |||||||
| chr3:41221132 | A | G | 8 | a0001c0001t0002g0120 a0001c0001t0008g0057 a0001c0003t0004g0024 others(5): Show |
9 | HG02622.hp1 HG02630.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.-48-2889A>G | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41221132 | |||||||
| chr3:41221206 | C | T | 1 | a0001c0001t0001g0201 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-48-2815C>T | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41221206 | |||||||
| chr3:41221267 | C | T | 1 | a0001c0001t0009g0070 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-48-2754C>T | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41221267 | |||||||
| chr3:41221339 | C | CT | 86 | a0001c0001t0001g0200 a0001c0001t0002g0120 a0001c0001t0003g0001 others(83): Show |
99 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.-48-2668dupT | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr3 | 41221339 | ||||||
| chr3:41221353 | T | A | 4 | a0001c0001t0002g0126 a0001c0005t0002g0151 a0001c0005t0002g0152 others(1): Show |
4 | HG01934.hp2 HG02258.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.-48-2668T>A | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41221353 | |||||||
| chr3:41221559 | G | A | 4 | a0001c0003t0004g0024 a0001c0003t0004g0098 a0001c0003t0004g0099 others(1): Show |
5 | HG02630.hp2 HG02809.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.-48-2462G>A | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41221559 | |||||||
| chr3:41221657 | C | G | 5 | a0001c0001t0003g0009 a0001c0001t0003g0231 a0001c0001t0003g0232 others(2): Show |
8 | HG02132.hp2 NA18957.hp2 NA18968.hp1 others(5): Show |
intron_variant | MODIFIER | c.-48-2364C>G | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41221657 | |||||||
| chr3:41222129 | C | T | 1 | a0001c0001t0001g0199 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.-48-1892C>T | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41222129 | |||||||
| chr3:41222179 | G | A | 1 | a0001c0001t0001g0187 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-48-1842G>A | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41222179 | |||||||
| chr3:41222196 | T | A | 12 | a0001c0001t0004g0010 a0001c0001t0004g0019 a0001c0001t0004g0049 others(9): Show |
14 | HG00673.hp1 HG01074.hp1 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.-48-1825T>A | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41222196 | |||||||
| chr3:41222216 | G | C | 1 | a0001c0001t0007g0259 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-48-1805G>C | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41222216 | |||||||
| chr3:41222352 | G | A | 1 | a0001c0001t0001g0201 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-48-1669G>A | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41222352 | |||||||
| chr3:41222453 | G | A | 1 | a0001c0001t0001g0188 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-48-1568G>A | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41222453 | |||||||
| chr3:41222962 | G | C | 3 | a0001c0001t0002g0038 a0001c0001t0005g0038 a0001c0001t0005g0266 |
3 | HG02818.hp1 HG02895.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.-48-1059G>C | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41222962 | |||||||
| chr3:41222995 | T | C | 4 | a0001c0001t0008g0059 a0001c0001t0008g0084 a0001c0001t0008g0085 others(1): Show |
4 | HG01074.hp1 HG02145.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.-48-1026T>C | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41222995 | |||||||
| chr3:41223041 | A | G | 8 | a0001c0001t0002g0120 a0001c0001t0008g0057 a0001c0003t0004g0024 others(5): Show |
9 | HG02622.hp1 HG02630.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.-48-980A>G | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41223041 | |||||||
| chr3:41223074 | C | CA | 8 | a0001c0001t0002g0120 a0001c0001t0008g0057 a0001c0003t0004g0024 others(5): Show |
9 | HG02622.hp1 HG02630.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.-48-938dupA | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr3 | 41223074 | ||||||
| chr3:41223382 | T | C | 12 | a0001c0001t0004g0010 a0001c0001t0004g0019 a0001c0001t0004g0049 others(9): Show |
14 | HG00673.hp1 HG01074.hp1 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.-48-639T>C | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41223382 | |||||||
| chr3:41223510 | A | C | 1 | a0001c0001t0001g0201 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-48-511A>C | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41223510 | |||||||
| chr3:41223519 | A | C | 1 | a0001c0001t0001g0165 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-48-502A>C | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41223519 | |||||||
| chr3:41223742 | C | T | 1 | a0001c0001t0004g0267 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-48-279C>T | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41223742 | |||||||
| chr3:41223838 | T | A | 1 | a0001c0001t0008g0057 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-48-183T>A | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41223838 | |||||||
| chr3:41223860 | T | A | 1 | a0001c0001t0002g0153 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-48-161T>A | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 1/14 | chr3 | 41223860 | |||||||
| chr3:41224359 | A | T | 1 | a0001c0003t0004g0053 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.14-167A>T | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 2/14 | chr3 | 41224359 | |||||||
| chr3:41224522 | A | G | 2 | a0001c0001t0004g0102 a0001c0001t0004g0103 |
2 | HG02109.hp1 HG02280.hp2 |
splice_region_variant&intron_variant | LOW | c.14-4A>G | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 2/14 | chr3 | 41224522 | |||||||
| chr3:41224767 | T | C | 1 | a0001c0001t0001g0169 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.241+14T>C | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 3/14 | chr3 | 41224767 | |||||||
| chr3:41224794 | T | C | 1 | a0001c0001t0002g0264 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.241+41T>C | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 3/14 | chr3 | 41224794 | |||||||
| chr3:41224856 | A | G | 1 | a0001c0001t0001g0198 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.242-98A>G | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 3/14 | chr3 | 41224856 | |||||||
| chr3:41224909 | A | G | 1 | a0001c0001t0005g0268 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.242-45A>G | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 3/14 | chr3 | 41224909 | |||||||
| chr3:41225259 | G | A | 2 | a0001c0006t0010g0040 a0001c0006t0010g0041 |
2 | NA18956.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.495+52G>A | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 4/14 | chr3 | 41225259 | |||||||
| chr3:41226034 | A | G | 64 | a0001c0001t0003g0001 a0001c0001t0003g0011 a0001c0001t0003g0018 others(61): Show |
74 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.936+173A>G | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 6/14 | chr3 | 41226034 | |||||||
| chr3:41226261 | C | T | 2 | a0001c0001t0003g0020 a0001c0001t0007g0020 |
2 | HG00323.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.936+400C>T | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 6/14 | chr3 | 41226261 | |||||||
| chr3:41226309 | T | C | 2 | a0001c0001t0004g0102 a0001c0001t0004g0103 |
2 | HG02109.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.936+448T>C | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 6/14 | chr3 | 41226309 | |||||||
| chr3:41226523 | C | T | 2 | a0001c0001t0001g0030 a0001c0001t0002g0030 |
2 | NA18956.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.936+662C>T | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 6/14 | chr3 | 41226523 | |||||||
| chr3:41226666 | T | G | 1 | a0001c0001t0001g0233 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.937-542T>G | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 6/14 | chr3 | 41226666 | |||||||
| chr3:41226863 | T | G | 5 | a0001c0001t0003g0011 a0001c0001t0003g0043 a0001c0001t0003g0044 others(2): Show |
6 | HG00733.hp1 HG01081.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.937-345T>G | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 6/14 | chr3 | 41226863 | |||||||
| chr3:41226937 | G | A | 1 | a0001c0001t0001g0202 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.937-271G>A | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 6/14 | chr3 | 41226937 | |||||||
| chr3:41226944 | C | A | 1 | a0001c0001t0002g0154 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.937-264C>A | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 6/14 | chr3 | 41226944 | |||||||
| chr3:41227075 | C | T | 1 | a0001c0008t0014g0269 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.937-133C>T | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 6/14 | chr3 | 41227075 | |||||||
| chr3:41227541 | T | G | 2 | a0001c0001t0001g0017 a0001c0001t0001g0203 |
4 | NA18992.hp2 NA19012.hp2 NA19074.hp2 others(1): Show |
intron_variant | MODIFIER | c.1081+189T>G | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 7/14 | chr3 | 41227541 | |||||||
| chr3:41227594 | T | G | 1 | a0001c0001t0001g0208 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1081+242T>G | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 7/14 | chr3 | 41227594 | |||||||
| chr3:41227636 | CAG | C | 3 | a0001c0001t0002g0013 a0001c0001t0002g0121 a0001c0001t0002g0124 |
5 | HG01167.hp1 HG02896.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1081+287_1081+288d others(4): Show |
CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr3 | 41227636 | ||||||
| chr3:41227661 | A | T | 91 | a0001c0001t0002g0120 a0001c0001t0003g0001 a0001c0001t0003g0011 others(88): Show |
104 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.1081+309A>T | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 7/14 | chr3 | 41227661 | |||||||
| chr3:41227728 | TTTTTG | T | 12 | a0001c0001t0004g0010 a0001c0001t0004g0019 a0001c0001t0004g0049 others(9): Show |
14 | HG00673.hp1 HG01074.hp1 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.1081+386_1081+390d others(7): Show |
CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr3 | 41227728 | ||||||
| chr3:41227802 | G | A | 1 | a0001c0001t0001g0211 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1081+450G>A | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 7/14 | chr3 | 41227802 | |||||||
| chr3:41227837 | T | C | 1 | a0001c0008t0014g0269 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1081+485T>C | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 7/14 | chr3 | 41227837 | |||||||
| chr3:41228211 | ATTTC | A | 12 | a0001c0001t0004g0010 a0001c0001t0004g0019 a0001c0001t0004g0049 others(9): Show |
14 | HG00673.hp1 HG01074.hp1 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.1081+863_1081+866d others(6): Show |
CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr3 | 41228211 | ||||||
| chr3:41228308 | A | G | 1 | a0001c0001t0002g0162 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1081+956A>G | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 7/14 | chr3 | 41228308 | |||||||
| chr3:41228387 | T | G | 1 | a0001c0001t0002g0182 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1081+1035T>G | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 7/14 | chr3 | 41228387 | |||||||
| chr3:41228427 | C | T | 2 | a0001c0001t0008g0059 a0001c0001t0008g0084 |
2 | HG02145.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1081+1075C>T | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 7/14 | chr3 | 41228427 | |||||||
| chr3:41228782 | G | A | 1 | a0001c0001t0001g0208 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1081+1430G>A | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 7/14 | chr3 | 41228782 | |||||||
| chr3:41228904 | T | G | 2 | a0001c0001t0002g0014 a0001c0001t0002g0131 |
4 | HG01243.hp2 HG02257.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.1081+1552T>G | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 7/14 | chr3 | 41228904 | |||||||
| chr3:41229031 | T | G | 1 | a0001c0001t0001g0189 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1081+1679T>G | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 7/14 | chr3 | 41229031 | |||||||
| chr3:41229079 | C | T | 2 | a0001c0001t0001g0180 a0001c0001t0001g0217 |
2 | HG03486.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1081+1727C>T | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 7/14 | chr3 | 41229079 | |||||||
| chr3:41229112 | A | G | 1 | a0001c0001t0002g0157 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1081+1760A>G | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 7/14 | chr3 | 41229112 | |||||||
| chr3:41229230 | T | A | 1 | a0001c0001t0003g0081 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1081+1878T>A | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 7/14 | chr3 | 41229230 | |||||||
| chr3:41229539 | C | A | 1 | a0001c0008t0014g0269 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1081+2187C>A | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 7/14 | chr3 | 41229539 | |||||||
| chr3:41229760 | A | G | 2 | a0001c0001t0002g0014 a0001c0001t0002g0131 |
4 | HG01243.hp2 HG02257.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.1081+2408A>G | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 7/14 | chr3 | 41229760 | |||||||
| chr3:41229876 | C | CTG | 17 | a0001c0001t0001g0039 a0001c0001t0001g0166 a0001c0001t0001g0188 others(14): Show |
19 | HG01074.hp1 HG01167.hp2 HG01261.hp1 others(16): Show |
intron_variant | MODIFIER | c.1081+2554_1081+255 others(6): Show |
CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr3 | 41229876 | ||||||
| chr3:41229876 | C | CTGTG | 15 | a0001c0001t0001g0029 a0001c0001t0001g0210 a0001c0001t0002g0016 others(12): Show |
17 | HG00673.hp1 HG01891.hp2 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.1081+2552_1081+255 others(8): Show |
CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr3 | 41229876 | ||||||
| chr3:41229876 | C | CTGTGTG | 59 | a0001c0001t0003g0001 a0001c0001t0003g0011 a0001c0001t0003g0018 others(56): Show |
69 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(66): Show |
intron_variant | MODIFIER | c.1081+2550_1081+255 others(10): Show |
CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr3 | 41229876 | ||||||
| chr3:41229876 | C | CTGTGTGT others(1): Show |
6 | a0001c0001t0003g0051 a0001c0001t0003g0060 a0001c0002t0003g0079 others(3): Show |
6 | HG00280.hp1 HG00544.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.1081+2548_1081+255 others(12): Show |
CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr3 | 41229876 | ||||||
| chr3:41229876 | C | CTGTGTGT others(3): Show |
4 | a0001c0001t0002g0120 a0001c0001t0003g0063 a0001c0001t0003g0074 others(1): Show |
4 | HG03098.hp2 NA19030.hp2 NA19077.hp1 others(1): Show |
intron_variant | MODIFIER | c.1081+2546_1081+255 others(14): Show |
CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr3 | 41229876 | ||||||
| chr3:41229876 | C | CTGTGTGT others(5): Show |
6 | a0001c0001t0003g0065 a0001c0001t0008g0057 a0001c0002t0003g0093 others(3): Show |
7 | HG00621.hp1 HG02622.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1081+2544_1081+255 others(16): Show |
CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr3 | 41229876 | ||||||
| chr3:41229876 | C | CTGTGTGT others(7): Show |
2 | a0001c0003t0004g0054 a0001c0003t0008g0100 |
2 | HG02809.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1081+2542_1081+255 others(18): Show |
CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr3 | 41229876 | ||||||
| chr3:41229876 | CTG | C | 56 | a0001c0001t0001g0012 a0001c0001t0001g0106 a0001c0001t0001g0108 others(53): Show |
68 | HG00323.hp2 HG00733.hp2 HG01109.hp1 others(65): Show |
intron_variant | MODIFIER | c.1081+2554_1081+255 others(6): Show |
CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr3 | 41229876 | ||||||
| chr3:41229908 | C | G | 6 | a0001c0003t0004g0024 a0001c0003t0004g0053 a0001c0003t0004g0054 others(3): Show |
7 | HG02630.hp2 HG02809.hp1 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.1081+2556C>G | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 7/14 | chr3 | 41229908 | |||||||
| chr3:41229962 | A | G | 2 | a0001c0001t0004g0102 a0001c0001t0004g0103 |
2 | HG02109.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.1081+2610A>G | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 7/14 | chr3 | 41229962 | |||||||
| chr3:41230037 | T | G | 2 | a0001c0001t0002g0016 a0001c0001t0002g0155 |
4 | HG01891.hp2 HG02615.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1081+2685T>G | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 7/14 | chr3 | 41230037 | |||||||
| chr3:41230063 | G | C | 1 | a0001c0001t0002g0126 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1081+2711G>C | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 7/14 | chr3 | 41230063 | |||||||
| chr3:41230116 | G | T | 1 | a0001c0001t0001g0240 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1081+2764G>T | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 7/14 | chr3 | 41230116 | |||||||
| chr3:41230512 | G | A | 1 | a0001c0001t0002g0135 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1082-2829G>A | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 7/14 | chr3 | 41230512 | |||||||
| chr3:41230590 | C | A | 91 | a0001c0001t0002g0120 a0001c0001t0003g0001 a0001c0001t0003g0011 others(88): Show |
104 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.1082-2751C>A | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 7/14 | chr3 | 41230590 | |||||||
| chr3:41230927 | G | C | 1 | a0001c0001t0001g0190 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1082-2414G>C | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 7/14 | chr3 | 41230927 | |||||||
| chr3:41230983 | G | C | 1 | a0001c0001t0002g0109 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1082-2358G>C | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 7/14 | chr3 | 41230983 | |||||||
| chr3:41231326 | C | CA | 96 | a0001c0001t0001g0031 a0001c0001t0001g0171 a0001c0001t0001g0181 others(93): Show |
110 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.1082-2001dupA | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr3 | 41231326 | ||||||
| chr3:41231351 | T | G | 1 | a0001c0008t0014g0269 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1082-1990T>G | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 7/14 | chr3 | 41231351 | |||||||
| chr3:41231618 | A | G | 12 | a0001c0001t0004g0010 a0001c0001t0004g0019 a0001c0001t0004g0049 others(9): Show |
14 | HG00673.hp1 HG01074.hp1 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.1082-1723A>G | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 7/14 | chr3 | 41231618 | |||||||
| chr3:41231886 | G | C | 3 | a0001c0005t0002g0151 a0001c0005t0002g0152 a0001c0005t0002g0260 |
3 | HG01934.hp2 HG02258.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1082-1455G>C | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 7/14 | chr3 | 41231886 | |||||||
| chr3:41231938 | A | C | 1 | a0001c0001t0003g0095 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1082-1403A>C | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 7/14 | chr3 | 41231938 | |||||||
| chr3:41232136 | C | CT | 12 | a0001c0001t0004g0010 a0001c0001t0004g0019 a0001c0001t0004g0049 others(9): Show |
14 | HG00673.hp1 HG01074.hp1 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.1082-1195dupT | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr3 | 41232136 | ||||||
| chr3:41232255 | G | A | 3 | a0001c0001t0002g0138 a0001c0001t0002g0139 a0001c0001t0002g0140 |
3 | NA18991.hp2 NA18993.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.1082-1086G>A | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 7/14 | chr3 | 41232255 | |||||||
| chr3:41232497 | G | A | 1 | a0001c0008t0014g0269 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1082-844G>A | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 7/14 | chr3 | 41232497 | |||||||
| chr3:41232538 | C | A | 2 | a0001c0001t0002g0161 a0001c0001t0005g0160 |
2 | HG03130.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1082-803C>A | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 7/14 | chr3 | 41232538 | |||||||
| chr3:41232569 | G | A | 2 | a0001c0001t0001g0183 a0001c0001t0002g0191 |
2 | HG00621.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.1082-772G>A | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 7/14 | chr3 | 41232569 | |||||||
| chr3:41232581 | C | G | 93 | a0001c0001t0003g0001 a0001c0001t0003g0009 a0001c0001t0003g0011 others(90): Show |
109 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.1082-760C>G | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 7/14 | chr3 | 41232581 | |||||||
| chr3:41232779 | A | T | 92 | a0001c0001t0003g0001 a0001c0001t0003g0009 a0001c0001t0003g0011 others(89): Show |
108 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.1082-562A>T | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 7/14 | chr3 | 41232779 | |||||||
| chr3:41232877 | T | G | 1 | a0001c0002t0003g0089 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1082-464T>G | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 7/14 | chr3 | 41232877 | |||||||
| chr3:41232946 | C | G | 1 | a0001c0001t0002g0239 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1082-395C>G | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 7/14 | chr3 | 41232946 | |||||||
| chr3:41232982 | G | T | 8 | a0001c0002t0003g0005 a0001c0002t0003g0022 a0001c0002t0003g0047 others(5): Show |
10 | HG01255.hp1 HG01256.hp1 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1082-359G>T | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 7/14 | chr3 | 41232982 | |||||||
| chr3:41232986 | A | G | 73 | a0001c0001t0003g0001 a0001c0001t0003g0009 a0001c0001t0003g0011 others(70): Show |
86 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.1082-355A>G | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 7/14 | chr3 | 41232986 | |||||||
| chr3:41233108 | C | T | 3 | a0001c0001t0002g0026 a0001c0001t0002g0144 a0001c0001t0005g0270 |
4 | HG01884.hp2 HG03516.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1082-233C>T | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 7/14 | chr3 | 41233108 | |||||||
| chr3:41233138 | G | C | 2 | a0001c0006t0010g0040 a0001c0006t0010g0041 |
2 | NA18956.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.1082-203G>C | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 7/14 | chr3 | 41233138 | |||||||
| chr3:41233165 | C | G | 1 | a0001c0001t0006g0215 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1082-176C>G | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 7/14 | chr3 | 41233165 | |||||||
| chr3:41233247 | C | G | 1 | a0001c0001t0004g0075 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1082-94C>G | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 7/14 | chr3 | 41233247 | |||||||
| chr3:41233253 | G | T | 1 | a0001c0001t0001g0207 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1082-88G>T | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 7/14 | chr3 | 41233253 | |||||||
| chr3:41233324 | C | G | 12 | a0001c0001t0004g0010 a0001c0001t0004g0019 a0001c0001t0004g0049 others(9): Show |
14 | HG00673.hp1 HG01074.hp1 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.1082-17C>G | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 7/14 | chr3 | 41233324 | |||||||
| chr3:41234001 | G | A | 2 | a0001c0006t0010g0040 a0001c0006t0010g0041 |
2 | NA18956.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.1524+134G>A | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 9/14 | chr3 | 41234001 | |||||||
| chr3:41234314 | A | G | 1 | a0001c0001t0006g0206 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1683+17A>G | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 10/14 | chr3 | 41234314 | |||||||
| chr3:41234449 | A | G | 1 | a0001c0001t0001g0196 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1683+152A>G | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 10/14 | chr3 | 41234449 | |||||||
| chr3:41234513 | A | G | 2 | a0001c0003t0004g0053 a0001c0003t0004g0054 |
2 | HG03130.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1683+216A>G | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 10/14 | chr3 | 41234513 | |||||||
| chr3:41234553 | G | A | 1 | a0001c0004t0001g0028 | 2 | HG01891.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1683+256G>A | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 10/14 | chr3 | 41234553 | |||||||
| chr3:41234675 | A | T | 63 | a0001c0001t0003g0001 a0001c0001t0003g0011 a0001c0001t0003g0018 others(60): Show |
73 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(70): Show |
intron_variant | MODIFIER | c.1683+378A>T | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 10/14 | chr3 | 41234675 | |||||||
| chr3:41234681 | T | C | 1 | a0001c0001t0003g0072 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1683+384T>C | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 10/14 | chr3 | 41234681 | |||||||
| chr3:41234685 | A | C | 1 | a0001c0001t0003g0255 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1683+388A>C | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 10/14 | chr3 | 41234685 | |||||||
| chr3:41234796 | G | A | 4 | a0001c0001t0002g0123 a0001c0001t0002g0141 a0001c0001t0002g0149 others(1): Show |
4 | HG01109.hp1 HG01243.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1683+499G>A | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 10/14 | chr3 | 41234796 | |||||||
| chr3:41234916 | A | G | 1 | a0001c0001t0001g0187 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1683+619A>G | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 10/14 | chr3 | 41234916 | |||||||
| chr3:41234973 | T | G | 1 | a0001c0001t0018g0046 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1683+676T>G | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 10/14 | chr3 | 41234973 | |||||||
| chr3:41235098 | C | T | 5 | a0001c0001t0002g0015 a0001c0001t0002g0122 a0001c0001t0002g0135 others(2): Show |
6 | HG00733.hp2 HG01123.hp2 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.1684-626C>T | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 10/14 | chr3 | 41235098 | |||||||
| chr3:41235203 | T | C | 1 | a0001c0002t0003g0071 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1684-521T>C | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 10/14 | chr3 | 41235203 | |||||||
| chr3:41235473 | T | C | 1 | a0001c0001t0008g0057 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1684-251T>C | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 10/14 | chr3 | 41235473 | |||||||
| chr3:41235487 | C | T | 1 | a0001c0001t0003g0063 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1684-237C>T | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 10/14 | chr3 | 41235487 | |||||||
| chr3:41235549 | C | T | 65 | a0001c0001t0003g0001 a0001c0001t0003g0011 a0001c0001t0003g0018 others(62): Show |
75 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.1684-175C>T | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 10/14 | chr3 | 41235549 | |||||||
| chr3:41236015 | G | T | 1 | a0001c0001t0002g0131 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1803+172G>T | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 11/14 | chr3 | 41236015 | |||||||
| chr3:41236232 | T | C | 1 | a0001c0001t0007g0259 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1804-117T>C | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 11/14 | chr3 | 41236232 | |||||||
| chr3:41236291 | G | A | 1 | a0001c0001t0001g0163 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1804-58G>A | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 11/14 | chr3 | 41236291 | |||||||
| chr3:41236300 | A | G | 1 | a0001c0008t0014g0269 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1804-49A>G | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 11/14 | chr3 | 41236300 | |||||||
| chr3:41236541 | T | C | 2 | a0001c0001t0002g0227 a0001c0001t0002g0228 |
2 | HG01255.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1954+42T>C | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 12/14 | chr3 | 41236541 | |||||||
| chr3:41236802 | T | C | 1 | a0001c0001t0003g0261 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2076+93T>C | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 13/14 | chr3 | 41236802 | |||||||
| chr3:41237010 | C | T | 1 | a0001c0001t0003g0051 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2076+301C>T | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 13/14 | chr3 | 41237010 | |||||||
| chr3:41237054 | C | T | 2 | a0001c0001t0004g0102 a0001c0001t0004g0103 |
2 | HG02109.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.2076+345C>T | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 13/14 | chr3 | 41237054 | |||||||
| chr3:41237177 | A | G | 2 | a0001c0003t0004g0053 a0001c0003t0004g0054 |
2 | HG03130.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2076+468A>G | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 13/14 | chr3 | 41237177 | |||||||
| chr3:41237186 | A | G | 1 | a0001c0001t0001g0017 | 3 | NA18992.hp2 NA19012.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.2076+477A>G | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 13/14 | chr3 | 41237186 | |||||||
| chr3:41237207 | C | T | 1 | a0001c0001t0002g0153 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2076+498C>T | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 13/14 | chr3 | 41237207 | |||||||
| chr3:41237268 | G | A | 9 | a0001c0001t0001g0192 a0001c0001t0004g0267 a0001c0001t0008g0057 others(6): Show |
10 | HG02622.hp1 HG02630.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.2076+559G>A | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 13/14 | chr3 | 41237268 | |||||||
| chr3:41237285 | C | T | 4 | a0001c0001t0002g0006 a0001c0001t0002g0133 a0001c0001t0002g0137 others(1): Show |
7 | NA18959.hp2 NA18965.hp2 NA18966.hp2 others(4): Show |
intron_variant | MODIFIER | c.2076+576C>T | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 13/14 | chr3 | 41237285 | |||||||
| chr3:41237446 | C | CA | 37 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0115 others(34): Show |
37 | HG00423.hp2 HG00544.hp1 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.2077-549dupA | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr3 | 41237446 | ||||||
| chr3:41237446 | C | CAA | 6 | a0001c0001t0001g0030 a0001c0001t0001g0169 a0001c0001t0001g0170 others(3): Show |
6 | HG00423.hp1 HG00609.hp1 NA18747.hp2 others(3): Show |
intron_variant | MODIFIER | c.2077-550_2077-549d others(4): Show |
CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr3 | 41237446 | ||||||
| chr3:41237446 | C | CAAAA | 13 | a0001c0001t0004g0019 a0001c0001t0004g0050 a0001c0001t0004g0075 others(10): Show |
15 | HG00673.hp1 HG01074.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.2077-552_2077-549d others(6): Show |
CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr3 | 41237446 | ||||||
| chr3:41237446 | C | CAAAAA | 58 | a0001c0001t0003g0001 a0001c0001t0003g0009 a0001c0001t0003g0011 others(55): Show |
71 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.2077-553_2077-549d others(7): Show |
CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr3 | 41237446 | ||||||
| chr3:41237446 | C | CAAAAAA | 20 | a0001c0001t0003g0043 a0001c0001t0003g0055 a0001c0001t0003g0060 others(17): Show |
21 | HG00735.hp1 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.2077-554_2077-549d others(8): Show |
CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr3 | 41237446 | ||||||
| chr3:41237446 | C | CAAAAAAA others(3): Show |
1 | a0001c0001t0004g0102 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2077-558_2077-549d others(12): Show |
CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr3 | 41237446 | ||||||
| chr3:41237446 | CA | C | 6 | a0001c0001t0001g0171 a0001c0001t0001g0195 a0001c0001t0001g0203 others(3): Show |
6 | HG02015.hp2 HG02976.hp1 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.2077-549delA | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr3 | 41237446 | ||||||
| chr3:41237550 | T | A | 8 | a0001c0001t0001g0012 a0001c0001t0001g0113 a0001c0001t0001g0115 others(5): Show |
10 | HG02055.hp2 HG02486.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.2077-466T>A | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 13/14 | chr3 | 41237550 | |||||||
| chr3:41237605 | G | A | 1 | a0001c0001t0002g0126 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2077-411G>A | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 13/14 | chr3 | 41237605 | |||||||
| chr3:41237637 | A | T | 12 | a0001c0001t0004g0010 a0001c0001t0004g0019 a0001c0001t0004g0049 others(9): Show |
14 | HG00673.hp1 HG01074.hp1 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.2077-379A>T | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 13/14 | chr3 | 41237637 | |||||||
| chr3:41237697 | C | CT | 27 | a0001c0001t0001g0029 a0001c0001t0001g0033 a0001c0001t0001g0116 others(24): Show |
29 | HG00423.hp1 HG00423.hp2 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.2077-298dupT | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr3 | 41237697 | ||||||
| chr3:41237697 | CT | C | 70 | a0001c0001t0001g0037 a0001c0001t0001g0251 a0001c0001t0002g0014 others(67): Show |
84 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.2077-298delT | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr3 | 41237697 | ||||||
| chr3:41237718 | T | A | 1 | a0001c0001t0003g0081 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.2077-298T>A | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 13/14 | chr3 | 41237718 | |||||||
| chr3:41237719 | A | T | 1 | a0001c0001t0003g0081 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.2077-297A>T | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 13/14 | chr3 | 41237719 | |||||||
| chr3:41237949 | A | G | 75 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(72): Show |
89 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.2077-67A>G | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 13/14 | chr3 | 41237949 | |||||||
| chr3:41238291 | C | G | 2 | a0001c0006t0010g0040 a0001c0006t0010g0041 |
2 | NA18956.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.2137+215C>G | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 14/14 | chr3 | 41238291 | |||||||
| chr3:41238431 | A | G | 1 | a0001c0001t0002g0142 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.2137+355A>G | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 14/14 | chr3 | 41238431 | |||||||
| chr3:41238484 | T | C | 1 | a0001c0001t0002g0131 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2137+408T>C | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 14/14 | chr3 | 41238484 | |||||||
| chr3:41238490 | A | T | 1 | a0001c0001t0002g0131 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2137+414A>T | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 14/14 | chr3 | 41238490 | |||||||
| chr3:41238492 | C | A | 1 | a0001c0001t0002g0131 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2137+416C>A | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 14/14 | chr3 | 41238492 | |||||||
| chr3:41238497 | T | G | 1 | a0001c0001t0002g0131 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2137+421T>G | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 14/14 | chr3 | 41238497 | |||||||
| chr3:41238498 | T | C | 1 | a0001c0001t0002g0131 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2137+422T>C | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 14/14 | chr3 | 41238498 | |||||||
| chr3:41238505 | G | A | 1 | a0001c0001t0002g0131 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2137+429G>A | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 14/14 | chr3 | 41238505 | |||||||
| chr3:41238506 | G | T | 1 | a0001c0001t0002g0131 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2137+430G>T | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 14/14 | chr3 | 41238506 | |||||||
| chr3:41238511 | T | A | 1 | a0001c0001t0002g0131 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2137+435T>A | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 14/14 | chr3 | 41238511 | |||||||
| chr3:41238512 | G | A | 1 | a0001c0001t0002g0131 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2137+436G>A | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 14/14 | chr3 | 41238512 | |||||||
| chr3:41238513 | A | C | 1 | a0001c0001t0002g0131 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2137+437A>C | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 14/14 | chr3 | 41238513 | |||||||
| chr3:41238514 | A | C | 1 | a0001c0001t0002g0131 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2137+438A>C | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 14/14 | chr3 | 41238514 | |||||||
| chr3:41238517 | T | C | 1 | a0001c0001t0002g0131 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2137+441T>C | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 14/14 | chr3 | 41238517 | |||||||
| chr3:41238518 | G | C | 1 | a0001c0001t0002g0131 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2137+442G>C | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 14/14 | chr3 | 41238518 | |||||||
| chr3:41238528 | A | T | 1 | a0001c0001t0002g0131 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2137+452A>T | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 14/14 | chr3 | 41238528 | |||||||
| chr3:41238529 | T | G | 1 | a0001c0001t0002g0131 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2137+453T>G | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 14/14 | chr3 | 41238529 | |||||||
| chr3:41238536 | C | G | 1 | a0001c0001t0002g0131 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2137+460C>G | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 14/14 | chr3 | 41238536 | |||||||
| chr3:41238537 | T | A | 1 | a0001c0001t0002g0131 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2137+461T>A | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 14/14 | chr3 | 41238537 | |||||||
| chr3:41238542 | A | G | 17 | a0001c0001t0001g0034 a0001c0001t0001g0179 a0001c0001t0001g0187 others(14): Show |
19 | HG00558.hp2 HG02015.hp2 HG02071.hp1 others(16): Show |
intron_variant | MODIFIER | c.2137+466A>G | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 14/14 | chr3 | 41238542 | |||||||
| chr3:41238545 | A | T | 1 | a0001c0001t0002g0131 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2137+469A>T | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 14/14 | chr3 | 41238545 | |||||||
| chr3:41238548 | A | C | 1 | a0001c0001t0002g0131 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2137+472A>C | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 14/14 | chr3 | 41238548 | |||||||
| chr3:41238551 | G | A | 1 | a0001c0001t0002g0131 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2137+475G>A | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 14/14 | chr3 | 41238551 | |||||||
| chr3:41238556 | A | C | 1 | a0001c0001t0002g0131 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2137+480A>C | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 14/14 | chr3 | 41238556 | |||||||
| chr3:41238558 | A | T | 1 | a0001c0001t0002g0131 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2137+482A>T | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 14/14 | chr3 | 41238558 | |||||||
| chr3:41238560 | T | G | 1 | a0001c0001t0002g0131 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2137+484T>G | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 14/14 | chr3 | 41238560 | |||||||
| chr3:41238561 | T | G | 1 | a0001c0001t0002g0131 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2137+485T>G | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 14/14 | chr3 | 41238561 | |||||||
| chr3:41238562 | A | G | 1 | a0001c0001t0002g0131 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2137+486A>G | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 14/14 | chr3 | 41238562 | |||||||
| chr3:41238563 | T | C | 1 | a0001c0001t0002g0131 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2137+487T>C | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 14/14 | chr3 | 41238563 | |||||||
| chr3:41238564 | A | T | 1 | a0001c0001t0002g0131 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2137+488A>T | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 14/14 | chr3 | 41238564 | |||||||
| chr3:41238566 | C | G | 1 | a0001c0001t0002g0131 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2137+490C>G | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 14/14 | chr3 | 41238566 | |||||||
| chr3:41238572 | C | T | 1 | a0001c0001t0002g0131 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2137+496C>T | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 14/14 | chr3 | 41238572 | |||||||
| chr3:41238577 | T | A | 1 | a0001c0001t0002g0131 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2137+501T>A | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 14/14 | chr3 | 41238577 | |||||||
| chr3:41238579 | T | A | 1 | a0001c0001t0002g0131 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2137+503T>A | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 14/14 | chr3 | 41238579 | |||||||
| chr3:41238581 | C | A | 1 | a0001c0001t0002g0131 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2137+505C>A | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 14/14 | chr3 | 41238581 | |||||||
| chr3:41238582 | C | G | 1 | a0001c0001t0002g0131 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2137+506C>G | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 14/14 | chr3 | 41238582 | |||||||
| chr3:41238583 | T | G | 1 | a0001c0001t0002g0131 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2137+507T>G | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 14/14 | chr3 | 41238583 | |||||||
| chr3:41238584 | A | T | 1 | a0001c0001t0002g0131 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2137+508A>T | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 14/14 | chr3 | 41238584 | |||||||
| chr3:41238654 | T | G | 1 | a0001c0001t0002g0120 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2138-480T>G | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 14/14 | chr3 | 41238654 | |||||||
| chr3:41238811 | T | G | 5 | a0001c0001t0002g0015 a0001c0001t0002g0122 a0001c0001t0002g0135 others(2): Show |
6 | HG00733.hp2 HG01123.hp2 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.2138-323T>G | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 14/14 | chr3 | 41238811 | |||||||
| chr3:41238820 | C | T | 2 | a0001c0006t0010g0040 a0001c0006t0010g0041 |
2 | NA18956.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.2138-314C>T | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 14/14 | chr3 | 41238820 | |||||||
| chr3:41238901 | G | T | 3 | a0001c0001t0001g0192 a0001c0001t0001g0194 a0001c0001t0001g0214 |
3 | NA18747.hp1 NA18946.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.2138-233G>T | CTNNB1 | ENSG00000168036.18 | transcript | ENST00000349496.11 | protein_coding | 14/14 | chr3 | 41238901 |