Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 1500 |
| ensemblid | ENSG00000198561.16 |
| hgncid | 2515 |
| symbol | CTNND1 |
| name | catenin delta 1 |
| refseq_nuc | NM_001085458.2 |
| refseq_prot | NP_001078927.1 |
| ensembl_nuc | ENST00000399050.10 |
| ensembl_prot | ENSP00000382004.5 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 57761802 |
| end | 57819540 |
| strand | + |
| ver | v1.2 |
| region | chr11:57761802-57819540 |
| region5000 | chr11:57756802-57824540 |
| regionname0 | CTNND1_chr11_57761802_57819540 |
| regionname5000 | CTNND1_chr11_57756802_57824540 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 968 | 262 | 58 | 63 | 89 | 14 | 36 | 63 | CTNND1_chr11_57756802_57824540 | CTNND1 | MDDSE others(963): Show |
chr11 | 57756802 | 57824540 |
| a0002 | 0/0 | 968 | 19 | 18 | 1 | 0 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | MDDSE others(963): Show |
chr11 | 57756802 | 57824540 |
| a0003 | 0/0 | 968 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | MDDSE others(963): Show |
chr11 | 57756802 | 57824540 |
| a0004 | 0/0 | 968 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | MDDSE others(963): Show |
chr11 | 57756802 | 57824540 |
| a0005 | 0/0 | 1004 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | MDDSE others(999): Show |
chr11 | 57756802 | 57824540 |
| a0006 | 0/0 | 968 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | MDDSE others(963): Show |
chr11 | 57756802 | 57824540 |
| a0007 | 0/0 | 968 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | MDDSE others(963): Show |
chr11 | 57756802 | 57824540 |
| a0008 | 0/0 | 968 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CTNND1_chr11_57756802_57824540 | CTNND1 | MDDSE others(963): Show |
chr11 | 57756802 | 57824540 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 2904 | 174 | 39 | 38 | 64 | 7 | 25 | CTNND1_chr11_57756802_57824540 | CTNND1 | ATGGA others(2899): Show |
chr11 | 57756802 | 57824540 | ||
| a0001c0002 | 0/0 | 2904 | 80 | 13 | 25 | 24 | 7 | 11 | CTNND1_chr11_57756802_57824540 | CTNND1 | ATGGA others(2899): Show |
chr11 | 57756802 | 57824540 | ||
| a0001c0004 | 0/0 | 2904 | 5 | 5 | 0 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | ATGGA others(2899): Show |
chr11 | 57756802 | 57824540 | ||
| a0001c0006 | 1/0 | 2904 | 2 | 1 | 0 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | ATGGA others(2899): Show |
chr11 | 57756802 | 57824540 | ||
| a0001c0010 | 0/0 | 2904 | 1 | 0 | 0 | 1 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | ATGGA others(2899): Show |
chr11 | 57756802 | 57824540 | ||
| a0002c0003 | 0/0 | 2904 | 15 | 14 | 1 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | ATGGA others(2899): Show |
chr11 | 57756802 | 57824540 | ||
| a0002c0005 | 0/0 | 2904 | 4 | 4 | 0 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | ATGGA others(2899): Show |
chr11 | 57756802 | 57824540 | ||
| a0003c0007 | 0/0 | 2904 | 2 | 0 | 0 | 2 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | ATGGA others(2899): Show |
chr11 | 57756802 | 57824540 | ||
| a0004c0012 | 0/0 | 2904 | 1 | 1 | 0 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | ATGGA others(2899): Show |
chr11 | 57756802 | 57824540 | ||
| a0005c0013 | 0/0 | 3012 | 1 | 1 | 0 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | ATGGA others(3007): Show |
chr11 | 57756802 | 57824540 | ||
| a0006c0009 | 0/0 | 2904 | 1 | 1 | 0 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | ATGGA others(2899): Show |
chr11 | 57756802 | 57824540 | ||
| a0007c0008 | 0/0 | 2904 | 1 | 1 | 0 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | ATGGA others(2899): Show |
chr11 | 57756802 | 57824540 | ||
| a0008c0011 | 0/0 | 2904 | 1 | 0 | 0 | 1 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | ATGGA others(2899): Show |
chr11 | 57756802 | 57824540 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 6670 | 107 | 28 | 21 | 41 | 3 | 13 | CTNND1_chr11_57756802_57824540 | CTNND1 | AGATC others(6665): Show |
chr11 | 57756802 | 57824540 |
| a0001c0001t0003 | 0/0 | 6670 | 49 | 1 | 14 | 19 | 4 | 11 | CTNND1_chr11_57756802_57824540 | CTNND1 | AGATC others(6665): Show |
chr11 | 57756802 | 57824540 |
| a0001c0001t0005 | 0/0 | 6670 | 6 | 6 | 0 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | AGATC others(6665): Show |
chr11 | 57756802 | 57824540 |
| a0001c0001t0006 | 0/0 | 6668 | 5 | 1 | 3 | 0 | 0 | 1 | CTNND1_chr11_57756802_57824540 | CTNND1 | AGATC others(6663): Show |
chr11 | 57756802 | 57824540 |
| a0001c0001t0007 | 0/0 | 6670 | 2 | 2 | 0 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | AGATC others(6665): Show |
chr11 | 57756802 | 57824540 |
| a0001c0001t0009 | 0/0 | 6670 | 2 | 0 | 0 | 2 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | AGATC others(6665): Show |
chr11 | 57756802 | 57824540 |
| a0001c0001t0011 | 0/0 | 6670 | 1 | 0 | 0 | 1 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | AGATC others(6665): Show |
chr11 | 57756802 | 57824540 |
| a0001c0001t0012 | 0/0 | 6670 | 1 | 1 | 0 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | AGATC others(6665): Show |
chr11 | 57756802 | 57824540 |
| a0001c0001t0013 | 0/0 | 6670 | 1 | 0 | 0 | 1 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | AGATC others(6665): Show |
chr11 | 57756802 | 57824540 |
| a0001c0002t0002 | 0/0 | 6670 | 77 | 12 | 23 | 24 | 7 | 11 | CTNND1_chr11_57756802_57824540 | CTNND1 | AGATC others(6665): Show |
chr11 | 57756802 | 57824540 |
| a0001c0002t0010 | 0/0 | 6670 | 2 | 0 | 2 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | AGATC others(6665): Show |
chr11 | 57756802 | 57824540 |
| a0001c0002t0014 | 0/0 | 6670 | 1 | 1 | 0 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | AGATC others(6665): Show |
chr11 | 57756802 | 57824540 |
| a0001c0004t0003 | 0/0 | 6670 | 5 | 5 | 0 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | AGATC others(6665): Show |
chr11 | 57756802 | 57824540 |
| a0001c0006t0001 | 1/0 | 6670 | 2 | 1 | 0 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | AGATC others(6665): Show |
chr11 | 57756802 | 57824540 |
| a0001c0010t0001 | 0/0 | 6670 | 1 | 0 | 0 | 1 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | AGATC others(6665): Show |
chr11 | 57756802 | 57824540 |
| a0002c0003t0004 | 0/0 | 6665 | 15 | 14 | 1 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | AGATC others(6660): Show |
chr11 | 57756802 | 57824540 |
| a0002c0005t0004 | 0/0 | 6665 | 4 | 4 | 0 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | AGATC others(6660): Show |
chr11 | 57756802 | 57824540 |
| a0003c0007t0008 | 0/0 | 6670 | 2 | 0 | 0 | 2 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | AGATC others(6665): Show |
chr11 | 57756802 | 57824540 |
| a0004c0012t0002 | 0/0 | 6670 | 1 | 1 | 0 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | AGATC others(6665): Show |
chr11 | 57756802 | 57824540 |
| a0005c0013t0003 | 0/0 | 6778 | 1 | 1 | 0 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | AGATC others(6773): Show |
chr11 | 57756802 | 57824540 |
| a0006c0009t0001 | 0/0 | 6670 | 1 | 1 | 0 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | AGATC others(6665): Show |
chr11 | 57756802 | 57824540 |
| a0007c0008t0005 | 0/0 | 6670 | 1 | 1 | 0 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | AGATC others(6665): Show |
chr11 | 57756802 | 57824540 |
| a0008c0011t0001 | 0/0 | 6670 | 1 | 0 | 0 | 1 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | AGATC others(6665): Show |
chr11 | 57756802 | 57824540 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0001g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0001g0141 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0003g0001 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0003g0002 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0003g0015 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0003g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0003g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0003g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0003g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0003g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0003g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0003g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0003g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0003g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0003g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0003g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0003g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0003g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0003g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0003g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0003g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0003g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0003g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0003g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0003g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0003g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0003g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0003g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0003g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0003g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0003g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0005g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0005g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0005g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0005g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0005g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0006g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0006g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0006g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0006g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0007g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0007g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0009g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0011g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0012g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0001t0013g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0002t0002g0003 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0002t0002g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0002t0002g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0002t0002g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0002t0002g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0002t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0002t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0002t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0002t0002g0022 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0002t0002g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0002t0002g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0002t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0002t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0002t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0002t0002g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0002t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0002t0002g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0002t0002g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0002t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0002t0002g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0002t0002g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0002t0002g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0002t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0002t0002g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0002t0002g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0002t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0002t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0002t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0002t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0002t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0002t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0002t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0002t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0002t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0002t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0002t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0002t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0002t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0002t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0002t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0002t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0002t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0002t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0002t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0002t0010g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0002t0010g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0002t0014g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0004t0003g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0004t0003g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0004t0003g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0006t0001g0012 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0001c0010t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0002c0003t0004g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0002c0003t0004g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0002c0003t0004g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0002c0003t0004g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0002c0003t0004g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0002c0003t0004g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0002c0003t0004g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0002c0003t0004g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0002c0003t0004g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0002c0003t0004g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0002c0003t0004g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0002c0003t0004g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0002c0003t0004g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0002c0003t0004g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0002c0003t0004g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0002c0005t0004g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0002c0005t0004g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0002c0005t0004g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0002c0005t0004g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0003c0007t0008g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0003c0007t0008g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0004c0012t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0005c0013t0003g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0006c0009t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0007c0008t0005g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| a0008c0011t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0002 | g0042 | EUR | GBR | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG00099 | hp2 | a0001 | c0002 | t0002 | g0022 | EUR | GBR | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG00140 | hp1 | a0001 | c0002 | t0002 | g0069 | EUR | GBR | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG00140 | hp2 | a0001 | c0001 | t0003 | g0002 | EUR | GBR | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG00323 | hp1 | a0001 | c0001 | t0003 | g0217 | EUR | FIN | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0138 | EUR | FIN | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG00408 | hp1 | a0001 | c0001 | t0003 | g0236 | EAS | CHS | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | CHS | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG00438 | hp1 | a0001 | c0001 | t0003 | g0219 | EAS | CHS | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | CHS | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | CHS | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG00544 | hp2 | a0003 | c0007 | t0008 | g0181 | EAS | CHS | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | CHS | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG00609 | hp2 | a0001 | c0002 | t0002 | g0021 | EAS | CHS | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | CHS | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG00621 | hp2 | a0001 | c0002 | t0002 | g0073 | EAS | CHS | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG00639 | hp2 | a0001 | c0002 | t0002 | g0054 | AMR | PUR | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG00642 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG00642 | hp2 | a0001 | c0002 | t0002 | g0035 | AMR | PUR | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG00673 | hp1 | a0001 | c0002 | t0002 | g0066 | EAS | CHS | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | CHS | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG00735 | hp1 | a0001 | c0002 | t0002 | g0003 | AMR | PUR | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG00738 | hp2 | a0001 | c0002 | t0002 | g0067 | AMR | PUR | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0238 | AMR | PUR | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG00741 | hp2 | a0001 | c0002 | t0002 | g0060 | AMR | PUR | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG01069 | hp1 | a0001 | c0002 | t0002 | g0047 | AMR | PUR | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG01069 | hp2 | a0001 | c0001 | t0003 | g0224 | AMR | PUR | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG01070 | hp1 | a0001 | c0002 | t0002 | g0084 | AMR | PUR | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG01070 | hp2 | a0001 | c0001 | t0003 | g0218 | AMR | PUR | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0223 | AMR | PUR | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG01071 | hp2 | a0001 | c0002 | t0002 | g0044 | AMR | PUR | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG01074 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG01081 | hp2 | a0001 | c0001 | t0003 | g0015 | AMR | PUR | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG01099 | hp2 | a0001 | c0002 | t0002 | g0003 | AMR | PUR | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG01106 | hp1 | a0001 | c0001 | t0003 | g0261 | AMR | PUR | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG01167 | hp1 | a0001 | c0002 | t0010 | g0023 | AMR | PUR | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG01167 | hp2 | a0001 | c0001 | t0003 | g0221 | AMR | PUR | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG01168 | hp2 | a0001 | c0002 | t0002 | g0034 | AMR | PUR | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG01169 | hp1 | a0001 | c0002 | t0010 | g0024 | AMR | PUR | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG01169 | hp2 | a0001 | c0002 | t0002 | g0033 | AMR | PUR | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG01175 | hp2 | a0001 | c0002 | t0002 | g0085 | AMR | PUR | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG01192 | hp1 | a0001 | c0002 | t0002 | g0089 | AMR | PUR | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG01255 | hp1 | a0001 | c0001 | t0003 | g0248 | AMR | CLM | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | CLM | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG01257 | hp1 | a0001 | c0001 | t0003 | g0260 | AMR | CLM | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG01258 | hp2 | a0001 | c0002 | t0002 | g0055 | AMR | CLM | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG01261 | hp1 | a0001 | c0001 | t0003 | g0237 | AMR | CLM | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG01261 | hp2 | a0002 | c0003 | t0004 | g0190 | AMR | CLM | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG01346 | hp1 | a0001 | c0001 | t0006 | g0011 | AMR | CLM | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG01346 | hp2 | a0001 | c0002 | t0002 | g0038 | AMR | CLM | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG01358 | hp1 | a0001 | c0001 | t0003 | g0258 | AMR | CLM | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG01358 | hp2 | a0001 | c0001 | t0006 | g0011 | AMR | CLM | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | CLM | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG01361 | hp2 | a0001 | c0002 | t0002 | g0064 | AMR | CLM | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG01496 | hp1 | a0001 | c0002 | t0002 | g0025 | AMR | CLM | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | CLM | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG01515 | hp1 | a0001 | c0002 | t0002 | g0080 | EUR | IBS | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG01515 | hp2 | a0001 | c0001 | t0003 | g0229 | EUR | IBS | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG01516 | hp1 | a0001 | c0001 | t0003 | g0245 | EUR | IBS | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG01516 | hp2 | a0001 | c0002 | t0002 | g0036 | EUR | IBS | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG01884 | hp1 | a0004 | c0012 | t0002 | g0075 | AFR | ACB | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | ACB | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG01891 | hp1 | a0001 | c0002 | t0002 | g0027 | AFR | ACB | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG01891 | hp2 | a0005 | c0013 | t0003 | g0222 | AFR | ACB | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PEL | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG01928 | hp2 | a0001 | c0002 | t0002 | g0041 | AMR | PEL | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG01934 | hp1 | a0001 | c0002 | t0002 | g0048 | AMR | PEL | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PEL | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PEL | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG01978 | hp2 | a0001 | c0002 | t0002 | g0083 | AMR | PEL | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG01993 | hp1 | a0001 | c0002 | t0002 | g0082 | AMR | PEL | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | PEL | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG02004 | hp1 | a0001 | c0002 | t0002 | g0051 | AMR | PEL | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG02004 | hp2 | a0001 | c0001 | t0006 | g0170 | AMR | PEL | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG02015 | hp1 | a0001 | c0001 | t0003 | g0185 | EAS | KHV | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG02015 | hp2 | a0001 | c0002 | t0002 | g0040 | EAS | KHV | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0235 | AFR | ACB | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG02055 | hp2 | a0001 | c0002 | t0002 | g0030 | AFR | ACB | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | KHV | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG02056 | hp2 | a0003 | c0007 | t0008 | g0214 | EAS | KHV | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG02071 | hp1 | a0001 | c0001 | t0003 | g0250 | EAS | KHV | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | KHV | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG02074 | hp1 | a0001 | c0002 | t0002 | g0068 | EAS | KHV | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | KHV | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | KHV | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | KHV | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG02129 | hp1 | a0001 | c0001 | t0003 | g0240 | EAS | KHV | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | KHV | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | KHV | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG02135 | hp2 | a0001 | c0001 | t0003 | g0231 | EAS | KHV | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG02145 | hp1 | a0002 | c0005 | t0004 | g0259 | AFR | ACB | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG02145 | hp2 | a0006 | c0009 | t0001 | g0213 | AFR | ACB | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | ACB | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG02257 | hp2 | a0001 | c0001 | t0006 | g0172 | AFR | ACB | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG02258 | hp1 | a0001 | c0002 | t0002 | g0079 | AFR | ACB | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | ACB | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | ACB | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | ACB | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PEL | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG02293 | hp2 | a0001 | c0001 | t0003 | g0242 | AMR | PEL | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PEL | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG02300 | hp2 | a0001 | c0002 | t0002 | g0037 | AMR | PEL | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0257 | AFR | ACB | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG02451 | hp2 | a0002 | c0003 | t0004 | g0201 | AFR | ACB | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG02572 | hp1 | a0001 | c0001 | t0005 | g0212 | AFR | GWD | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG02572 | hp2 | a0001 | c0002 | t0002 | g0058 | AFR | GWD | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG02602 | hp1 | a0001 | c0001 | t0003 | g0001 | SAS | PJL | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG02602 | hp2 | a0001 | c0002 | t0002 | g0031 | SAS | PJL | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG02615 | hp1 | a0001 | c0004 | t0003 | g0241 | AFR | GWD | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG02615 | hp2 | a0002 | c0003 | t0004 | g0197 | AFR | GWD | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | GWD | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG02622 | hp2 | a0001 | c0002 | t0002 | g0018 | AFR | GWD | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG02630 | hp1 | a0001 | c0002 | t0014 | g0028 | AFR | GWD | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | GWD | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | GWD | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | GWD | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG02683 | hp2 | a0001 | c0001 | t0003 | g0225 | SAS | PJL | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG02717 | hp1 | a0001 | c0002 | t0002 | g0059 | AFR | GWD | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG02717 | hp2 | a0001 | c0001 | t0005 | g0014 | AFR | GWD | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG02723 | hp1 | a0001 | c0002 | t0002 | g0019 | AFR | GWD | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | GWD | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG02735 | hp1 | a0001 | c0001 | t0003 | g0015 | SAS | PJL | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG02738 | hp1 | a0001 | c0002 | t0002 | g0061 | SAS | PJL | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG02738 | hp2 | a0001 | c0001 | t0003 | g0232 | SAS | PJL | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG02809 | hp1 | a0001 | c0002 | t0002 | g0029 | AFR | GWD | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG02809 | hp2 | a0001 | c0006 | t0001 | g0012 | AFR | GWD | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG02818 | hp1 | a0002 | c0003 | t0004 | g0204 | AFR | GWD | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG02895 | hp1 | a0001 | c0001 | t0007 | g0195 | AFR | GWD | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | GWD | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG02896 | hp1 | a0007 | c0008 | t0005 | g0210 | AFR | GWD | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | GWD | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | GWD | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG02897 | hp2 | a0001 | c0001 | t0007 | g0194 | AFR | GWD | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG02965 | hp1 | a0002 | c0005 | t0004 | g0199 | AFR | ESN | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG02965 | hp2 | a0002 | c0003 | t0004 | g0198 | AFR | ESN | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG02970 | hp1 | a0001 | c0001 | t0005 | g0209 | AFR | ESN | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | ESN | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG02976 | hp1 | a0002 | c0005 | t0004 | g0180 | AFR | ESN | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | ESN | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG03017 | hp2 | a0001 | c0001 | t0003 | g0243 | SAS | PJL | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | GWD | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG03041 | hp2 | a0002 | c0003 | t0004 | g0196 | AFR | GWD | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG03098 | hp1 | a0001 | c0002 | t0002 | g0020 | AFR | MSL | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG03098 | hp2 | a0001 | c0001 | t0005 | g0014 | AFR | MSL | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG03130 | hp2 | a0001 | c0004 | t0003 | g0001 | AFR | ESN | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG03139 | hp1 | a0002 | c0003 | t0004 | g0187 | AFR | ESN | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG03139 | hp2 | a0001 | c0004 | t0003 | g0001 | AFR | ESN | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG03209 | hp1 | a0002 | c0003 | t0004 | g0186 | AFR | MSL | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG03209 | hp2 | a0001 | c0001 | t0005 | g0211 | AFR | MSL | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG03225 | hp2 | a0002 | c0005 | t0004 | g0200 | AFR | MSL | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG03239 | hp1 | a0001 | c0001 | t0006 | g0171 | SAS | PJL | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG03239 | hp2 | a0001 | c0001 | t0003 | g0002 | SAS | PJL | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG03486 | hp1 | a0002 | c0003 | t0004 | g0189 | AFR | MSL | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | MSL | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG03491 | hp2 | a0001 | c0002 | t0002 | g0091 | SAS | PJL | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG03492 | hp1 | a0001 | c0002 | t0002 | g0057 | SAS | PJL | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG03516 | hp1 | a0002 | c0003 | t0004 | g0188 | AFR | ESN | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG03516 | hp2 | a0002 | c0003 | t0004 | g0253 | AFR | ESN | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | GWD | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0105 | SAS | STU | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG03688 | hp2 | a0001 | c0002 | t0002 | g0039 | SAS | STU | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | PJL | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG03704 | hp2 | a0001 | c0002 | t0002 | g0081 | SAS | PJL | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG03710 | hp1 | a0001 | c0002 | t0002 | g0045 | SAS | PJL | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG03710 | hp2 | a0001 | c0002 | t0002 | g0065 | SAS | PJL | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0145 | SAS | BEB | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0228 | SAS | BEB | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG03834 | hp1 | a0001 | c0001 | t0003 | g0226 | SAS | BEB | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0122 | SAS | BEB | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0129 | SAS | BEB | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG03927 | hp2 | a0001 | c0001 | t0003 | g0220 | SAS | BEB | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0158 | SAS | BEB | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG04184 | hp2 | a0001 | c0002 | t0002 | g0026 | SAS | BEB | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0177 | SAS | STU | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG04199 | hp2 | a0001 | c0002 | t0002 | g0052 | SAS | STU | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG04204 | hp1 | a0001 | c0001 | t0003 | g0216 | SAS | STU | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG04204 | hp2 | a0001 | c0002 | t0002 | g0017 | SAS | STU | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | YRI | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | YRI | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHB | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| NA18747 | hp2 | a0001 | c0002 | t0002 | g0078 | EAS | CHB | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| NA18906 | hp1 | a0002 | c0003 | t0004 | g0203 | AFR | YRI | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| NA18906 | hp2 | a0001 | c0001 | t0005 | g0254 | AFR | YRI | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| NA18943 | hp1 | a0001 | c0002 | t0002 | g0070 | EAS | JPT | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| NA18945 | hp2 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| NA18946 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| NA18947 | hp1 | a0001 | c0002 | t0002 | g0077 | EAS | JPT | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| NA18947 | hp2 | a0001 | c0001 | t0009 | g0004 | EAS | JPT | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| NA18950 | hp2 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| NA18954 | hp2 | a0001 | c0010 | t0001 | g0107 | EAS | JPT | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| NA18957 | hp1 | a0001 | c0002 | t0002 | g0086 | EAS | JPT | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| NA18961 | hp2 | a0001 | c0001 | t0003 | g0184 | EAS | JPT | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| NA18964 | hp2 | a0001 | c0002 | t0002 | g0032 | EAS | JPT | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| NA18971 | hp2 | a0008 | c0011 | t0001 | g0162 | EAS | JPT | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| NA18975 | hp1 | a0001 | c0001 | t0003 | g0246 | EAS | JPT | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| NA18977 | hp1 | a0001 | c0002 | t0002 | g0076 | EAS | JPT | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| NA18979 | hp1 | a0001 | c0001 | t0003 | g0233 | EAS | JPT | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| NA18983 | hp1 | a0001 | c0002 | t0002 | g0050 | EAS | JPT | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| NA18985 | hp2 | a0001 | c0002 | t0002 | g0074 | EAS | JPT | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| NA18991 | hp2 | a0001 | c0002 | t0002 | g0053 | EAS | JPT | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| NA18998 | hp1 | a0001 | c0001 | t0013 | g0124 | EAS | JPT | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| NA18998 | hp2 | a0001 | c0002 | t0002 | g0049 | EAS | JPT | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| NA19002 | hp2 | a0001 | c0001 | t0003 | g0215 | EAS | JPT | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| NA19003 | hp1 | a0001 | c0002 | t0002 | g0090 | EAS | JPT | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| NA19003 | hp2 | a0001 | c0001 | t0011 | g0154 | EAS | JPT | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| NA19007 | hp2 | a0001 | c0002 | t0002 | g0072 | EAS | JPT | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| NA19009 | hp2 | a0001 | c0002 | t0002 | g0088 | EAS | JPT | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| NA19010 | hp1 | a0001 | c0001 | t0003 | g0249 | EAS | JPT | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| NA19030 | hp1 | a0001 | c0002 | t0002 | g0016 | AFR | LWK | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | LWK | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| NA19043 | hp1 | a0001 | c0002 | t0002 | g0043 | AFR | LWK | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | LWK | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| NA19055 | hp1 | a0001 | c0001 | t0003 | g0234 | EAS | JPT | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| NA19055 | hp2 | a0001 | c0002 | t0002 | g0071 | EAS | JPT | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| NA19064 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| NA19066 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| NA19067 | hp2 | a0001 | c0002 | t0002 | g0063 | EAS | JPT | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| NA19074 | hp1 | a0001 | c0001 | t0009 | g0004 | EAS | JPT | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| NA19078 | hp2 | a0001 | c0001 | t0003 | g0247 | EAS | JPT | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| NA19080 | hp1 | a0001 | c0002 | t0002 | g0087 | EAS | JPT | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| NA19086 | hp2 | a0001 | c0001 | t0003 | g0227 | EAS | JPT | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| NA19087 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| NA19087 | hp2 | a0001 | c0002 | t0002 | g0062 | EAS | JPT | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| NA19088 | hp2 | a0001 | c0001 | t0003 | g0239 | EAS | JPT | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0092 | EUR | TSI | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| NA20752 | hp2 | a0001 | c0002 | t0002 | g0003 | EUR | TSI | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| NA20805 | hp1 | a0001 | c0002 | t0002 | g0046 | EUR | TSI | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0126 | EUR | TSI | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0127 | SAS | GIH | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| NA20905 | hp2 | a0001 | c0001 | t0003 | g0244 | SAS | GIH | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG02486 | hp1 | a0002 | c0003 | t0004 | g0252 | AFR | ACB | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG02486 | hp2 | a0001 | c0004 | t0003 | g0001 | AFR | ACB | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG03471 | hp1 | a0001 | c0004 | t0003 | g0230 | AFR | MSL | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG03471 | hp2 | a0002 | c0003 | t0004 | g0263 | AFR | MSL | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | USA | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| HG06807 | hp2 | a0002 | c0003 | t0004 | g0202 | AFR | USA | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| NA21309 | hp1 | a0001 | c0001 | t0012 | g0251 | AFR | LWK | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| NA21309 | hp2 | a0001 | c0002 | t0002 | g0056 | AFR | LWK | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0141 | REF | REF | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| homoSapiens | grch38p0 | a0001 | c0006 | t0001 | g0012 | REF | REF | CTNND1_chr11_57756802_57824540 | CTNND1 | chr11 | 57756802 | 57824540 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:57796520 | G | A | 1 | a0007 | 1 | HG02896.hp1 | missense_variant | MODERATE | c.484G>A | p.Gly162Arg | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 6/21 | 1015/6670 | 484/2907 | 162/968 | chr11 | 57796520 | |||
| chr11:57802166 | C | T | 1 | a0004 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.1390C>T | p.Arg464Cys | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 7/21 | 1921/6670 | 1390/2907 | 464/968 | chr11 | 57802166 | |||
| chr11:57808168 | A | G | 1 | a0008 | 1 | NA18971.hp2 | missense_variant | MODERATE | c.1967A>G | p.Tyr656Cys | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 13/21 | 2498/6670 | 1967/2907 | 656/968 | chr11 | 57808168 | |||
| chr11:57814314 | A | C | 1 | a0006 | 1 | HG02145.hp2 | missense_variant | MODERATE | c.2642A>C | p.Lys881Thr | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 18/21 | 3173/6670 | 2642/2907 | 881/968 | chr11 | 57814314 | |||
| chr11:57814346 | A | G | 1 | a0003 | 2 | HG00544.hp2 HG02056.hp2 |
missense_variant | MODERATE | c.2674A>G | p.Asn892Asp | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 18/21 | 3205/6670 | 2674/2907 | 892/968 | chr11 | 57814346 | |||
| chr11:57815436 | G | A | 1 | a0002 | 19 | HG01261.hp2 HG02145.hp1 HG02451.hp2 others(16): Show |
missense_variant | MODERATE | c.2744G>A | p.Arg915Lys | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 19/21 | 3275/6670 | 2744/2907 | 915/968 | chr11 | 57815436 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:57796519 | C | T | 2 | a0001c0002 a0004c0012 |
81 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(78): Show |
synonymous_variant | LOW | c.483C>T | p.Asp161Asp | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 6/21 | 1014/6670 | 483/2907 | 161/968 | chr11 | 57796519 | |||
| chr11:57796774 | A | G | 1 | a0001c0004 | 5 | HG02486.hp2 HG02615.hp1 HG03130.hp2 others(2): Show |
synonymous_variant | LOW | c.738A>G | p.Glu246Glu | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 6/21 | 1269/6670 | 738/2907 | 246/968 | chr11 | 57796774 | |||
| chr11:57803760 | C | T | 12 | a0001c0001 a0001c0002 a0001c0004 others(9): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
synonymous_variant | LOW | c.1560C>T | p.His520His | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 8/21 | 2091/6670 | 1560/2907 | 520/968 | chr11 | 57803760 | |||
| chr11:57808238 | C | T | 1 | a0001c0010 | 1 | NA18954.hp2 | synonymous_variant | LOW | c.2037C>T | p.Ala679Ala | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 13/21 | 2568/6670 | 2037/2907 | 679/968 | chr11 | 57808238 | |||
| chr11:57815401 | C | T | 1 | a0002c0005 | 4 | HG02145.hp1 HG02965.hp1 HG02976.hp1 others(1): Show |
synonymous_variant | LOW | c.2709C>T | p.Asn903Asn | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 19/21 | 3240/6670 | 2709/2907 | 903/968 | chr11 | 57815401 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:57761957 | A | G | 4 | a0001c0002t0002 a0001c0002t0010 a0001c0002t0014 others(1): Show |
81 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(78): Show |
5_prime_UTR_variant | MODIFIER | c.-376A>G | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/21 | 29522 | chr11 | 57761957 | ||||||
| chr11:57816329 | C | T | 1 | a0001c0001t0013 | 1 | NA18998.hp1 | 3_prime_UTR_variant | MODIFIER | c.*21C>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 21/21 | 21 | chr11 | 57816329 | ||||||
| chr11:57816700 | A | G | 1 | a0001c0001t0012 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*392A>G | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 21/21 | 392 | chr11 | 57816700 | ||||||
| chr11:57817241 | G | A | 1 | a0001c0001t0007 | 2 | HG02895.hp1 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*933G>A | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 21/21 | 933 | chr11 | 57817241 | ||||||
| chr11:57817528 | C | A | 1 | a0001c0002t0010 | 2 | HG01167.hp1 HG01169.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1220C>A | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 21/21 | 1220 | chr11 | 57817528 | ||||||
| chr11:57817998 | C | G | 1 | a0001c0001t0009 | 2 | NA18947.hp2 NA19074.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1690C>G | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 21/21 | 1690 | chr11 | 57817998 | ||||||
| chr11:57818190 | C | T | 3 | a0001c0001t0003 a0001c0004t0003 a0005c0013t0003 |
55 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*1882C>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 21/21 | 1882 | chr11 | 57818190 | ||||||
| chr11:57818299 | A | G | 1 | a0003c0007t0008 | 2 | HG00544.hp2 HG02056.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1991A>G | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 21/21 | 1991 | chr11 | 57818299 | ||||||
| chr11:57818301 | T | A | 1 | a0001c0002t0014 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1993T>A | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 21/21 | 1993 | chr11 | 57818301 | ||||||
| chr11:57818369 | TTTCTC | T | 2 | a0002c0003t0004 a0002c0005t0004 |
19 | HG01261.hp2 HG02145.hp1 HG02451.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*2064_*2068delCTCT others(1): Show |
CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 21/21 | 2064 | INFO_REALIGN_3_PRIME | chr11 | 57818369 | |||||
| chr11:57818832 | G | A | 1 | a0001c0001t0011 | 1 | NA19003.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2524G>A | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 21/21 | 2524 | chr11 | 57818832 | ||||||
| chr11:57818970 | T | A | 2 | a0001c0001t0005 a0007c0008t0005 |
7 | HG02572.hp1 HG02717.hp2 HG02896.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2662T>A | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 21/21 | 2662 | chr11 | 57818970 | ||||||
| chr11:57819111 | CAA | C | 1 | a0001c0001t0006 | 5 | HG01346.hp1 HG01358.hp2 HG02004.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2804_*2805delAA | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 21/21 | 2804 | chr11 | 57819111 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:57762290 | A | AATACAGG others(23): Show |
1 | a0002c0003t0004g0263 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-214+173_-214+202d others(32): Show |
CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 57762290 | ||||||
| chr11:57762731 | A | G | 1 | a0001c0001t0001g0262 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-214+612A>G | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57762731 | |||||||
| chr11:57763056 | T | G | 78 | a0001c0002t0002g0003 a0001c0002t0002g0005 a0001c0002t0002g0016 others(75): Show |
81 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(78): Show |
intron_variant | MODIFIER | c.-214+937T>G | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57763056 | |||||||
| chr11:57763231 | C | A | 1 | a0001c0002t0002g0016 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-214+1112C>A | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57763231 | |||||||
| chr11:57763565 | G | A | 96 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(93): Show |
103 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.-214+1446G>A | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57763565 | |||||||
| chr11:57763687 | A | G | 1 | a0001c0002t0002g0091 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-214+1568A>G | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57763687 | |||||||
| chr11:57763787 | G | T | 1 | a0001c0001t0003g0261 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-214+1668G>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57763787 | |||||||
| chr11:57764072 | T | C | 1 | a0002c0005t0004g0180 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-214+1953T>C | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57764072 | |||||||
| chr11:57764238 | C | CG | 10 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0178 others(7): Show |
10 | HG01192.hp1 HG01257.hp1 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.-214+2126dupG | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 57764238 | ||||||
| chr11:57764239 | G | A | 1 | a0003c0007t0008g0181 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-214+2120G>A | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57764239 | |||||||
| chr11:57764292 | C | G | 1 | a0001c0001t0001g0175 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-214+2173C>G | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57764292 | |||||||
| chr11:57764415 | T | C | 1 | a0001c0001t0001g0092 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-214+2296T>C | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57764415 | |||||||
| chr11:57764621 | T | G | 1 | a0001c0001t0001g0093 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-214+2502T>G | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57764621 | |||||||
| chr11:57764944 | A | G | 3 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0001g0257 |
3 | HG02451.hp1 HG02647.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-214+2825A>G | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57764944 | |||||||
| chr11:57764951 | A | G | 1 | a0001c0001t0001g0179 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-214+2832A>G | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57764951 | |||||||
| chr11:57765254 | T | C | 2 | a0001c0001t0001g0094 a0001c0001t0001g0095 |
2 | NA18522.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-214+3135T>C | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57765254 | |||||||
| chr11:57765460 | A | AT | 87 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(84): Show |
93 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.-214+3364dupT | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 57765460 | ||||||
| chr11:57765460 | A | ATT | 8 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0178 others(5): Show |
9 | HG01192.hp2 HG01346.hp1 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.-214+3363_-214+336 others(6): Show |
CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 57765460 | ||||||
| chr11:57765460 | AT | A | 74 | a0001c0001t0001g0096 a0001c0001t0001g0182 a0001c0001t0001g0183 others(71): Show |
77 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(74): Show |
intron_variant | MODIFIER | c.-214+3364delT | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 57765460 | ||||||
| chr11:57765617 | C | T | 1 | a0001c0001t0001g0169 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-214+3498C>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57765617 | |||||||
| chr11:57765748 | G | A | 1 | a0001c0001t0003g0185 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-214+3629G>A | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57765748 | |||||||
| chr11:57765951 | G | A | 6 | a0002c0003t0004g0186 a0002c0003t0004g0187 a0002c0003t0004g0188 others(3): Show |
6 | HG01261.hp2 HG03139.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.-214+3832G>A | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57765951 | |||||||
| chr11:57766005 | C | T | 1 | a0001c0001t0012g0251 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-214+3886C>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57766005 | |||||||
| chr11:57766144 | G | T | 6 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0001t0001g0168 others(3): Show |
6 | HG01192.hp2 HG01993.hp2 NA18950.hp1 others(3): Show |
intron_variant | MODIFIER | c.-214+4025G>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57766144 | |||||||
| chr11:57766541 | C | G | 3 | a0001c0002t0002g0076 a0001c0002t0002g0077 a0001c0002t0002g0078 |
3 | NA18747.hp2 NA18947.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.-214+4422C>G | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57766541 | |||||||
| chr11:57766541 | C | T | 2 | a0001c0001t0003g0249 a0001c0001t0003g0250 |
2 | HG02071.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.-214+4422C>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57766541 | |||||||
| chr11:57766718 | A | G | 3 | a0001c0001t0003g0002 a0001c0001t0003g0248 a0001c0001t0003g0261 |
6 | HG00140.hp2 HG00642.hp1 HG01074.hp2 others(3): Show |
intron_variant | MODIFIER | c.-214+4599A>G | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57766718 | |||||||
| chr11:57766901 | G | A | 1 | a0001c0001t0012g0251 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-214+4782G>A | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57766901 | |||||||
| chr11:57766974 | C | CT | 17 | a0001c0001t0001g0010 a0001c0001t0001g0178 a0001c0001t0003g0246 others(14): Show |
18 | HG00140.hp1 HG00621.hp2 HG00673.hp1 others(15): Show |
intron_variant | MODIFIER | c.-214+4870dupT | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 57766974 | ||||||
| chr11:57767070 | C | G | 45 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0015 others(42): Show |
55 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(52): Show |
intron_variant | MODIFIER | c.-214+4951C>G | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57767070 | |||||||
| chr11:57767129 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-214+5010G>A | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57767129 | |||||||
| chr11:57767178 | G | T | 4 | a0001c0001t0001g0183 a0001c0001t0001g0255 a0001c0001t0001g0256 others(1): Show |
4 | HG02451.hp1 HG02647.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-214+5059G>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57767178 | |||||||
| chr11:57767187 | G | T | 1 | a0001c0001t0001g0165 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-214+5068G>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57767187 | |||||||
| chr11:57767254 | C | A | 4 | a0001c0001t0001g0182 a0001c0001t0001g0191 a0001c0001t0001g0192 others(1): Show |
4 | HG01496.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-214+5135C>A | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57767254 | |||||||
| chr11:57767290 | G | A | 1 | a0001c0002t0002g0065 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-214+5171G>A | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57767290 | |||||||
| chr11:57767308 | G | C | 1 | a0001c0001t0001g0103 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-214+5189G>C | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57767308 | |||||||
| chr11:57767327 | C | T | 78 | a0001c0002t0002g0003 a0001c0002t0002g0005 a0001c0002t0002g0016 others(75): Show |
81 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(78): Show |
intron_variant | MODIFIER | c.-214+5208C>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57767327 | |||||||
| chr11:57767393 | C | T | 2 | a0003c0007t0008g0181 a0003c0007t0008g0214 |
2 | HG00544.hp2 HG02056.hp2 |
intron_variant | MODIFIER | c.-214+5274C>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57767393 | |||||||
| chr11:57767693 | A | AG | 263 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(260): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.-214+5575dupG | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 57767693 | ||||||
| chr11:57767699 | T | C | 1 | a0001c0002t0002g0017 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-214+5580T>C | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57767699 | |||||||
| chr11:57767799 | C | T | 1 | a0001c0001t0001g0183 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-214+5680C>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57767799 | |||||||
| chr11:57767836 | C | CT | 49 | a0001c0001t0001g0164 a0001c0001t0003g0001 a0001c0001t0003g0002 others(46): Show |
59 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(56): Show |
intron_variant | MODIFIER | c.-214+5732dupT | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 57767836 | ||||||
| chr11:57768060 | C | T | 1 | a0001c0001t0001g0163 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-214+5941C>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57768060 | |||||||
| chr11:57768134 | C | T | 4 | a0001c0001t0003g0243 a0001c0001t0003g0244 a0001c0001t0003g0245 others(1): Show |
4 | HG01361.hp2 HG01516.hp1 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.-214+6015C>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57768134 | |||||||
| chr11:57768145 | T | TA | 96 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(93): Show |
103 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.-214+6030dupA | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 57768145 | ||||||
| chr11:57768386 | CT | C | 33 | a0001c0001t0001g0095 a0001c0001t0001g0155 a0001c0001t0001g0156 others(30): Show |
33 | HG00408.hp2 HG00621.hp1 HG00673.hp2 others(30): Show |
intron_variant | MODIFIER | c.-214+6293delT | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 57768386 | ||||||
| chr11:57768386 | CTT | C | 201 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(198): Show |
221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.-214+6292_-214+629 others(6): Show |
CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 57768386 | ||||||
| chr11:57768386 | CTTT | C | 15 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0182 others(12): Show |
15 | HG01496.hp2 HG02056.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.-214+6291_-214+629 others(7): Show |
CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 57768386 | ||||||
| chr11:57768494 | C | T | 103 | a0001c0001t0001g0183 a0001c0001t0001g0255 a0001c0001t0001g0256 others(100): Show |
106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.-214+6375C>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57768494 | |||||||
| chr11:57768550 | C | T | 5 | a0002c0003t0004g0201 a0002c0003t0004g0202 a0002c0003t0004g0203 others(2): Show |
5 | HG02451.hp2 HG02486.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.-214+6431C>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57768550 | |||||||
| chr11:57768583 | C | T | 1 | a0001c0001t0012g0251 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-214+6464C>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57768583 | |||||||
| chr11:57768586 | G | T | 1 | a0001c0002t0002g0058 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-214+6467G>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57768586 | |||||||
| chr11:57768829 | G | C | 8 | a0002c0003t0004g0196 a0002c0003t0004g0197 a0002c0003t0004g0198 others(5): Show |
8 | HG02451.hp2 HG02486.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.-214+6710G>C | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57768829 | |||||||
| chr11:57768874 | C | T | 101 | a0001c0001t0001g0183 a0001c0001t0001g0255 a0001c0001t0001g0256 others(98): Show |
104 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(101): Show |
intron_variant | MODIFIER | c.-214+6755C>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57768874 | |||||||
| chr11:57769035 | G | A | 3 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0002c0003t0004g0196 |
3 | HG03041.hp2 NA18522.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-214+6916G>A | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57769035 | |||||||
| chr11:57770056 | T | A | 2 | a0003c0007t0008g0181 a0003c0007t0008g0214 |
2 | HG00544.hp2 HG02056.hp2 |
intron_variant | MODIFIER | c.-214+7937T>A | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57770056 | |||||||
| chr11:57770141 | C | T | 2 | a0003c0007t0008g0181 a0003c0007t0008g0214 |
2 | HG00544.hp2 HG02056.hp2 |
intron_variant | MODIFIER | c.-214+8022C>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57770141 | |||||||
| chr11:57770202 | C | T | 4 | a0001c0001t0011g0154 a0001c0002t0002g0055 a0001c0002t0002g0056 others(1): Show |
4 | HG01258.hp2 HG03492.hp1 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.-214+8083C>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57770202 | |||||||
| chr11:57770206 | T | G | 1 | a0002c0003t0004g0253 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-214+8087T>G | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57770206 | |||||||
| chr11:57770273 | C | T | 262 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(259): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.-214+8154C>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57770273 | |||||||
| chr11:57770315 | G | A | 103 | a0001c0001t0001g0183 a0001c0001t0001g0255 a0001c0001t0001g0256 others(100): Show |
106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.-214+8196G>A | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57770315 | |||||||
| chr11:57770324 | C | T | 1 | a0001c0002t0002g0054 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-214+8205C>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57770324 | |||||||
| chr11:57770356 | A | G | 1 | a0002c0003t0004g0198 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-214+8237A>G | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57770356 | |||||||
| chr11:57770373 | G | T | 6 | a0002c0003t0004g0186 a0002c0003t0004g0187 a0002c0003t0004g0188 others(3): Show |
6 | HG01261.hp2 HG03139.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.-214+8254G>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57770373 | |||||||
| chr11:57770382 | C | T | 1 | a0001c0001t0001g0009 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.-214+8263C>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57770382 | |||||||
| chr11:57770385 | T | C | 1 | a0002c0003t0004g0186 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-214+8266T>C | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57770385 | |||||||
| chr11:57770478 | C | G | 2 | a0001c0001t0001g0008 a0001c0001t0001g0169 |
3 | HG02970.hp2 HG03130.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-214+8359C>G | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57770478 | |||||||
| chr11:57770668 | T | G | 5 | a0001c0001t0001g0009 a0001c0001t0001g0103 a0001c0001t0001g0105 others(2): Show |
6 | HG01257.hp2 HG01258.hp1 HG02129.hp2 others(3): Show |
intron_variant | MODIFIER | c.-214+8549T>G | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57770668 | |||||||
| chr11:57770724 | A | G | 1 | a0008c0011t0001g0162 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-214+8605A>G | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57770724 | |||||||
| chr11:57771026 | A | G | 1 | a0001c0001t0003g0236 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-214+8907A>G | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57771026 | |||||||
| chr11:57771141 | T | C | 1 | a0001c0001t0001g0255 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-214+9022T>C | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57771141 | |||||||
| chr11:57771146 | T | C | 1 | a0001c0002t0002g0066 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-214+9027T>C | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57771146 | |||||||
| chr11:57771270 | G | C | 4 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0110 others(1): Show |
4 | HG02280.hp2 HG02630.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.-214+9151G>C | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57771270 | |||||||
| chr11:57771315 | C | T | 4 | a0001c0001t0001g0182 a0001c0001t0001g0191 a0001c0001t0001g0192 others(1): Show |
4 | HG01496.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-214+9196C>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57771315 | |||||||
| chr11:57771336 | A | T | 1 | a0001c0001t0001g0153 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-214+9217A>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57771336 | |||||||
| chr11:57771405 | G | A | 4 | a0001c0001t0001g0097 a0001c0001t0001g0111 a0001c0001t0001g0153 others(1): Show |
4 | HG01081.hp1 HG01255.hp2 HG01928.hp1 others(1): Show |
intron_variant | MODIFIER | c.-214+9286G>A | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57771405 | |||||||
| chr11:57771422 | T | TTATATAG others(2): Show |
91 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(88): Show |
97 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.-214+9305_-214+931 others(13): Show |
CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 57771422 | ||||||
| chr11:57771483 | A | G | 1 | a0001c0002t0002g0016 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-214+9364A>G | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57771483 | |||||||
| chr11:57771704 | A | G | 1 | a0001c0001t0001g0152 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-214+9585A>G | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57771704 | |||||||
| chr11:57771895 | C | T | 4 | a0002c0005t0004g0180 a0002c0005t0004g0199 a0002c0005t0004g0200 others(1): Show |
4 | HG02145.hp1 HG02965.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-214+9776C>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57771895 | |||||||
| chr11:57771941 | T | G | 6 | a0002c0003t0004g0186 a0002c0003t0004g0187 a0002c0003t0004g0188 others(3): Show |
6 | HG01261.hp2 HG03139.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.-214+9822T>G | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57771941 | |||||||
| chr11:57772017 | G | A | 3 | a0001c0002t0002g0055 a0001c0002t0002g0056 a0001c0002t0002g0057 |
3 | HG01258.hp2 HG03492.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-214+9898G>A | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57772017 | |||||||
| chr11:57772096 | A | AT | 7 | a0001c0001t0003g0242 a0001c0002t0002g0051 a0001c0002t0002g0052 others(4): Show |
7 | HG02004.hp1 HG02145.hp1 HG02293.hp2 others(4): Show |
intron_variant | MODIFIER | c.-214+9993dupT | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 57772096 | ||||||
| chr11:57772096 | A | ATT | 82 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(79): Show |
88 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.-214+9992_-214+999 others(6): Show |
CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 57772096 | ||||||
| chr11:57772096 | A | ATTT | 10 | a0001c0001t0001g0009 a0001c0001t0001g0102 a0001c0001t0001g0148 others(7): Show |
11 | HG00621.hp1 HG00735.hp2 HG01257.hp2 others(8): Show |
intron_variant | MODIFIER | c.-214+9991_-214+999 others(7): Show |
CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 57772096 | ||||||
| chr11:57772564 | A | G | 5 | a0001c0002t0002g0049 a0001c0002t0002g0050 a0001c0002t0002g0073 others(2): Show |
5 | HG00621.hp2 NA18983.hp1 NA18998.hp2 others(2): Show |
intron_variant | MODIFIER | c.-214+10445A>G | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57772564 | |||||||
| chr11:57772611 | T | C | 2 | a0001c0001t0001g0112 a0001c0001t0001g0113 |
2 | HG00639.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.-214+10492T>C | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57772611 | |||||||
| chr11:57772846 | CCTCTTTC others(3): Show |
C | 1 | a0001c0001t0001g0152 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-214+10739_-214+10 others(16): Show |
CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 57772846 | ||||||
| chr11:57772986 | C | A | 45 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0015 others(42): Show |
55 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(52): Show |
intron_variant | MODIFIER | c.-214+10867C>A | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57772986 | |||||||
| chr11:57773027 | G | A | 1 | a0001c0001t0001g0114 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-214+10908G>A | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57773027 | |||||||
| chr11:57773044 | G | A | 96 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(93): Show |
103 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.-214+10925G>A | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57773044 | |||||||
| chr11:57773122 | ATTAC | A | 103 | a0001c0001t0001g0183 a0001c0001t0001g0255 a0001c0001t0001g0256 others(100): Show |
106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.-214+11006_-214+11 others(10): Show |
CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 57773122 | ||||||
| chr11:57773325 | G | C | 1 | a0001c0001t0001g0114 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-214+11206G>C | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57773325 | |||||||
| chr11:57773452 | G | GT | 9 | a0001c0001t0001g0110 a0001c0001t0001g0158 a0001c0001t0003g0235 others(6): Show |
9 | HG02055.hp1 HG02145.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.-214+11348dupT | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 57773452 | ||||||
| chr11:57773473 | G | A | 1 | a0001c0001t0001g0115 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-214+11354G>A | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57773473 | |||||||
| chr11:57773636 | T | A | 2 | a0001c0002t0002g0019 a0001c0002t0002g0020 |
2 | HG02723.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-214+11517T>A | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57773636 | |||||||
| chr11:57773637 | A | T | 5 | a0001c0001t0001g0183 a0001c0001t0001g0255 a0001c0001t0001g0256 others(2): Show |
5 | HG02451.hp1 HG02647.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.-214+11518A>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57773637 | |||||||
| chr11:57773645 | A | C | 1 | a0001c0002t0002g0048 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-214+11526A>C | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57773645 | |||||||
| chr11:57773648 | T | A | 92 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(89): Show |
99 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.-214+11529T>A | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57773648 | |||||||
| chr11:57774014 | A | G | 2 | a0001c0001t0003g0249 a0001c0001t0003g0250 |
2 | HG02071.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.-214+11895A>G | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57774014 | |||||||
| chr11:57774053 | G | A | 12 | a0002c0003t0004g0196 a0002c0003t0004g0197 a0002c0003t0004g0198 others(9): Show |
12 | HG02145.hp1 HG02451.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.-214+11934G>A | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57774053 | |||||||
| chr11:57774411 | A | T | 1 | a0001c0001t0001g0183 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-214+12292A>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57774411 | |||||||
| chr11:57774493 | C | T | 6 | a0002c0003t0004g0197 a0002c0003t0004g0201 a0002c0003t0004g0202 others(3): Show |
6 | HG02451.hp2 HG02486.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-214+12374C>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57774493 | |||||||
| chr11:57774531 | C | T | 2 | a0001c0001t0001g0147 a0008c0011t0001g0162 |
2 | NA18971.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.-214+12412C>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57774531 | |||||||
| chr11:57774691 | G | GTTTA | 12 | a0001c0001t0003g0216 a0001c0001t0003g0235 a0001c0001t0007g0194 others(9): Show |
12 | HG01261.hp2 HG02055.hp1 HG02056.hp2 others(9): Show |
intron_variant | MODIFIER | c.-214+12608_-214+12 others(10): Show |
CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 57774691 | ||||||
| chr11:57774691 | GTTTA | G | 86 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0110 others(83): Show |
89 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(86): Show |
intron_variant | MODIFIER | c.-214+12608_-214+12 others(10): Show |
CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 57774691 | ||||||
| chr11:57774691 | GTTTATTT others(1): Show |
G | 91 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(88): Show |
98 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.-214+12604_-214+12 others(14): Show |
CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 57774691 | ||||||
| chr11:57774800 | G | A | 2 | a0001c0001t0001g0116 a0001c0001t0001g0117 |
2 | NA19064.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.-214+12681G>A | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57774800 | |||||||
| chr11:57775020 | G | GT | 17 | a0001c0001t0001g0111 a0001c0001t0001g0177 a0001c0001t0001g0179 others(14): Show |
18 | HG00544.hp2 HG01069.hp1 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.-214+12916dupT | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 57775020 | ||||||
| chr11:57775332 | G | GA | 96 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(93): Show |
103 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.-214+13227dupA | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 57775332 | ||||||
| chr11:57775348 | A | AAC | 47 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0015 others(44): Show |
57 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(54): Show |
intron_variant | MODIFIER | c.-214+13249_-214+13 others(8): Show |
CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 57775348 | ||||||
| chr11:57775526 | G | C | 101 | a0001c0001t0001g0183 a0001c0001t0001g0255 a0001c0001t0001g0256 others(98): Show |
104 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(101): Show |
intron_variant | MODIFIER | c.-214+13407G>C | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57775526 | |||||||
| chr11:57775688 | G | T | 1 | a0001c0001t0003g0245 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-213-13349G>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57775688 | |||||||
| chr11:57775739 | G | T | 1 | a0002c0003t0004g0197 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-213-13298G>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57775739 | |||||||
| chr11:57775850 | T | TGCTCCTG others(5): Show |
1 | a0001c0001t0001g0146 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.-213-13186_-213-13 others(18): Show |
CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 57775850 | ||||||
| chr11:57776189 | A | G | 6 | a0001c0002t0002g0003 a0001c0002t0002g0044 a0001c0002t0002g0045 others(3): Show |
8 | HG00639.hp2 HG00735.hp1 HG01070.hp1 others(5): Show |
intron_variant | MODIFIER | c.-213-12848A>G | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57776189 | |||||||
| chr11:57776516 | A | G | 244 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(241): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.-213-12521A>G | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57776516 | |||||||
| chr11:57776867 | A | C | 1 | a0002c0003t0004g0186 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-213-12170A>C | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57776867 | |||||||
| chr11:57777012 | T | C | 78 | a0001c0002t0002g0003 a0001c0002t0002g0005 a0001c0002t0002g0016 others(75): Show |
81 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(78): Show |
intron_variant | MODIFIER | c.-213-12025T>C | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57777012 | |||||||
| chr11:57777697 | A | G | 19 | a0002c0003t0004g0186 a0002c0003t0004g0187 a0002c0003t0004g0188 others(16): Show |
19 | HG01261.hp2 HG02145.hp1 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.-213-11340A>G | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57777697 | |||||||
| chr11:57777980 | C | G | 1 | a0001c0004t0003g0241 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-213-11057C>G | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57777980 | |||||||
| chr11:57778476 | A | G | 96 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(93): Show |
103 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.-213-10561A>G | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57778476 | |||||||
| chr11:57778507 | T | C | 245 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(242): Show |
265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.-213-10530T>C | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57778507 | |||||||
| chr11:57778584 | G | A | 4 | a0001c0001t0001g0182 a0001c0001t0001g0191 a0001c0001t0001g0192 others(1): Show |
4 | HG01496.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-213-10453G>A | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57778584 | |||||||
| chr11:57778797 | G | C | 1 | a0001c0001t0001g0152 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-213-10240G>C | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57778797 | |||||||
| chr11:57778816 | C | T | 1 | a0001c0001t0001g0164 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-213-10221C>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57778816 | |||||||
| chr11:57779092 | A | G | 244 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(241): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.-213-9945A>G | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57779092 | |||||||
| chr11:57779180 | C | T | 1 | a0001c0001t0001g0009 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.-213-9857C>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57779180 | |||||||
| chr11:57779520 | G | A | 1 | a0001c0001t0001g0155 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-213-9517G>A | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57779520 | |||||||
| chr11:57779528 | T | C | 45 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0015 others(42): Show |
55 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(52): Show |
intron_variant | MODIFIER | c.-213-9509T>C | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57779528 | |||||||
| chr11:57779565 | A | G | 3 | a0001c0002t0002g0016 a0001c0002t0002g0018 a0001c0002t0002g0059 |
3 | HG02622.hp2 HG02717.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-213-9472A>G | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57779565 | |||||||
| chr11:57780071 | T | G | 1 | a0001c0001t0012g0251 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-213-8966T>G | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57780071 | |||||||
| chr11:57780071 | T | TTTTTG | 151 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(148): Show |
168 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.-213-8966_-213-896 others(9): Show |
CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57780071 | |||||||
| chr11:57780071 | T | TTTTTTG | 87 | a0001c0001t0001g0111 a0001c0001t0001g0115 a0001c0001t0001g0143 others(84): Show |
90 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(87): Show |
intron_variant | MODIFIER | c.-213-8966_-213-896 others(10): Show |
CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57780071 | |||||||
| chr11:57780132 | C | T | 1 | a0001c0002t0002g0043 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-213-8905C>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57780132 | |||||||
| chr11:57780286 | C | T | 1 | a0001c0001t0001g0142 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-213-8751C>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57780286 | |||||||
| chr11:57780353 | C | T | 2 | a0003c0007t0008g0181 a0003c0007t0008g0214 |
2 | HG00544.hp2 HG02056.hp2 |
intron_variant | MODIFIER | c.-213-8684C>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57780353 | |||||||
| chr11:57780778 | A | G | 1 | a0001c0001t0001g0167 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-213-8259A>G | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57780778 | |||||||
| chr11:57781037 | C | T | 1 | a0002c0003t0004g0198 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-213-8000C>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57781037 | |||||||
| chr11:57781072 | A | G | 1 | a0006c0009t0001g0213 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-213-7965A>G | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57781072 | |||||||
| chr11:57781095 | C | A | 1 | a0001c0001t0003g0231 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-213-7942C>A | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57781095 | |||||||
| chr11:57781161 | A | G | 1 | a0001c0001t0006g0172 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-213-7876A>G | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57781161 | |||||||
| chr11:57781191 | C | T | 1 | a0002c0005t0004g0199 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-213-7846C>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57781191 | |||||||
| chr11:57781409 | T | A | 256 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(253): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.-213-7628T>A | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57781409 | |||||||
| chr11:57781668 | C | T | 1 | a0001c0001t0003g0247 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.-213-7369C>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57781668 | |||||||
| chr11:57781797 | C | T | 1 | a0008c0011t0001g0162 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-213-7240C>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57781797 | |||||||
| chr11:57781869 | C | G | 1 | a0001c0002t0002g0042 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-213-7168C>G | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57781869 | |||||||
| chr11:57782081 | A | G | 1 | a0001c0001t0012g0251 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-213-6956A>G | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57782081 | |||||||
| chr11:57782133 | G | A | 3 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0001g0257 |
3 | HG02451.hp1 HG02647.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-213-6904G>A | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57782133 | |||||||
| chr11:57782136 | T | C | 1 | a0001c0002t0002g0022 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-213-6901T>C | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57782136 | |||||||
| chr11:57782469 | C | T | 4 | a0001c0002t0002g0041 a0001c0002t0002g0048 a0001c0002t0002g0082 others(1): Show |
4 | HG01928.hp2 HG01934.hp1 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.-213-6568C>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57782469 | |||||||
| chr11:57782499 | C | T | 2 | a0001c0002t0002g0047 a0001c0002t0002g0089 |
2 | HG01069.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.-213-6538C>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57782499 | |||||||
| chr11:57782547 | A | C | 2 | a0001c0001t0007g0194 a0001c0001t0007g0195 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-213-6490A>C | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57782547 | |||||||
| chr11:57782835 | A | G | 1 | a0001c0001t0001g0009 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.-213-6202A>G | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57782835 | |||||||
| chr11:57782863 | C | T | 1 | a0001c0001t0001g0193 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-213-6174C>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57782863 | |||||||
| chr11:57783004 | G | A | 4 | a0002c0005t0004g0180 a0002c0005t0004g0199 a0002c0005t0004g0200 others(1): Show |
4 | HG02145.hp1 HG02965.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-213-6033G>A | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57783004 | |||||||
| chr11:57783076 | G | A | 251 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(248): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.-213-5961G>A | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57783076 | |||||||
| chr11:57783242 | C | T | 1 | a0001c0002t0002g0083 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-213-5795C>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57783242 | |||||||
| chr11:57783313 | A | G | 46 | a0001c0002t0002g0003 a0001c0002t0002g0021 a0001c0002t0002g0022 others(43): Show |
48 | HG00099.hp2 HG00140.hp1 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.-213-5724A>G | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57783313 | |||||||
| chr11:57783574 | C | T | 7 | a0002c0003t0004g0196 a0002c0003t0004g0197 a0002c0003t0004g0201 others(4): Show |
7 | HG02451.hp2 HG02486.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.-213-5463C>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57783574 | |||||||
| chr11:57783613 | C | T | 2 | a0001c0001t0007g0194 a0001c0001t0007g0195 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-213-5424C>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57783613 | |||||||
| chr11:57783615 | C | T | 1 | a0001c0002t0002g0090 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-213-5422C>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57783615 | |||||||
| chr11:57783616 | G | A | 2 | a0003c0007t0008g0181 a0003c0007t0008g0214 |
2 | HG00544.hp2 HG02056.hp2 |
intron_variant | MODIFIER | c.-213-5421G>A | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57783616 | |||||||
| chr11:57783620 | C | T | 2 | a0003c0007t0008g0181 a0003c0007t0008g0214 |
2 | HG00544.hp2 HG02056.hp2 |
intron_variant | MODIFIER | c.-213-5417C>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57783620 | |||||||
| chr11:57783658 | C | CA | 7 | a0001c0001t0001g0095 a0001c0001t0003g0232 a0001c0002t0002g0016 others(4): Show |
7 | HG02074.hp1 HG02572.hp2 HG02602.hp2 others(4): Show |
intron_variant | MODIFIER | c.-213-5375dupA | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 57783658 | ||||||
| chr11:57783933 | A | G | 1 | a0001c0004t0003g0230 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-213-5104A>G | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57783933 | |||||||
| chr11:57784082 | T | C | 245 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(242): Show |
265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.-213-4955T>C | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57784082 | |||||||
| chr11:57784409 | C | CA | 65 | a0001c0001t0001g0105 a0001c0001t0001g0108 a0001c0001t0001g0148 others(62): Show |
68 | HG00099.hp2 HG00140.hp1 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.-213-4610dupA | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 57784409 | ||||||
| chr11:57784409 | C | CAA | 19 | a0001c0002t0002g0005 a0001c0002t0002g0017 a0001c0002t0002g0025 others(16): Show |
20 | HG00099.hp1 HG00738.hp2 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.-213-4611_-213-461 others(6): Show |
CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 57784409 | ||||||
| chr11:57784409 | CA | C | 6 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0160 others(3): Show |
6 | HG01099.hp1 HG01515.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.-213-4610delA | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 57784409 | ||||||
| chr11:57784454 | T | TGGCAAAA others(5): Show |
1 | a0001c0001t0001g0167 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-213-4583_-213-458 others(16): Show |
CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57784454 | |||||||
| chr11:57784458 | G | C | 1 | a0001c0001t0001g0167 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-213-4579G>C | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57784458 | |||||||
| chr11:57784460 | C | A | 1 | a0001c0001t0001g0167 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-213-4577C>A | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57784460 | |||||||
| chr11:57784465 | A | G | 1 | a0001c0001t0001g0167 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-213-4572A>G | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57784465 | |||||||
| chr11:57784468 | G | C | 1 | a0001c0001t0001g0167 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-213-4569G>C | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57784468 | |||||||
| chr11:57784477 | T | A | 1 | a0001c0001t0001g0167 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-213-4560T>A | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57784477 | |||||||
| chr11:57784493 | G | T | 1 | a0001c0001t0001g0167 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-213-4544G>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57784493 | |||||||
| chr11:57784495 | G | T | 1 | a0001c0001t0001g0167 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-213-4542G>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57784495 | |||||||
| chr11:57784498 | A | T | 1 | a0001c0001t0001g0167 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-213-4539A>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57784498 | |||||||
| chr11:57784502 | G | T | 1 | a0001c0001t0001g0167 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-213-4535G>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57784502 | |||||||
| chr11:57784504 | TTTG | T | 6 | a0002c0003t0004g0186 a0002c0003t0004g0187 a0002c0003t0004g0188 others(3): Show |
6 | HG01261.hp2 HG03139.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.-213-4521_-213-451 others(7): Show |
CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 57784504 | ||||||
| chr11:57784516 | G | T | 1 | a0001c0001t0001g0167 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-213-4521G>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57784516 | |||||||
| chr11:57784529 | A | G | 1 | a0001c0001t0001g0167 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-213-4508A>G | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57784529 | |||||||
| chr11:57784530 | G | A | 1 | a0001c0001t0001g0167 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-213-4507G>A | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57784530 | |||||||
| chr11:57784544 | T | G | 1 | a0001c0001t0001g0167 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-213-4493T>G | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57784544 | |||||||
| chr11:57784552 | G | A | 1 | a0001c0001t0001g0167 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-213-4485G>A | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57784552 | |||||||
| chr11:57784566 | C | T | 1 | a0001c0001t0001g0167 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-213-4471C>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57784566 | |||||||
| chr11:57784567 | A | G | 1 | a0001c0001t0001g0167 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-213-4470A>G | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57784567 | |||||||
| chr11:57784573 | G | A | 1 | a0001c0001t0001g0167 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-213-4464G>A | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57784573 | |||||||
| chr11:57784576 | A | T | 1 | a0001c0001t0001g0167 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-213-4461A>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57784576 | |||||||
| chr11:57784581 | G | A | 1 | a0001c0001t0001g0167 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-213-4456G>A | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57784581 | |||||||
| chr11:57784582 | A | C | 1 | a0001c0001t0001g0167 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-213-4455A>C | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57784582 | |||||||
| chr11:57784584 | A | G | 1 | a0001c0001t0001g0167 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-213-4453A>G | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57784584 | |||||||
| chr11:57784586 | T | A | 1 | a0001c0001t0001g0167 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-213-4451T>A | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57784586 | |||||||
| chr11:57784589 | T | G | 1 | a0001c0001t0001g0167 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-213-4448T>G | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57784589 | |||||||
| chr11:57784596 | T | G | 1 | a0001c0001t0001g0167 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-213-4441T>G | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57784596 | |||||||
| chr11:57784610 | T | C | 1 | a0001c0001t0001g0167 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-213-4427T>C | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57784610 | |||||||
| chr11:57784747 | C | T | 1 | a0001c0010t0001g0107 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-213-4290C>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57784747 | |||||||
| chr11:57784793 | G | A | 102 | a0001c0001t0001g0167 a0001c0001t0001g0183 a0001c0001t0001g0255 others(99): Show |
105 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(102): Show |
intron_variant | MODIFIER | c.-213-4244G>A | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57784793 | |||||||
| chr11:57785277 | A | G | 1 | a0002c0003t0004g0253 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-213-3760A>G | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57785277 | |||||||
| chr11:57785550 | G | T | 242 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(239): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.-213-3487G>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57785550 | |||||||
| chr11:57785554 | G | A | 1 | a0001c0001t0001g0193 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-213-3483G>A | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57785554 | |||||||
| chr11:57785565 | T | G | 3 | a0001c0001t0001g0118 a0001c0002t0010g0023 a0001c0002t0010g0024 |
3 | HG01167.hp1 HG01169.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.-213-3472T>G | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57785565 | |||||||
| chr11:57785789 | C | T | 2 | a0001c0001t0001g0106 a0001c0010t0001g0107 |
2 | HG02129.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.-213-3248C>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57785789 | |||||||
| chr11:57785884 | G | GT | 4 | a0001c0001t0001g0013 a0001c0001t0001g0206 a0001c0001t0001g0207 others(1): Show |
5 | HG02257.hp1 HG02258.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.-213-3151dupT | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 57785884 | ||||||
| chr11:57785927 | A | C | 1 | a0001c0001t0001g0092 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-213-3110A>C | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57785927 | |||||||
| chr11:57786188 | T | C | 1 | a0001c0001t0001g0152 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-213-2849T>C | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57786188 | |||||||
| chr11:57786190 | AT | A | 221 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(218): Show |
241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.-213-2829delT | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 57786190 | ||||||
| chr11:57786190 | ATT | A | 8 | a0001c0002t0002g0032 a0001c0004t0003g0241 a0002c0003t0004g0197 others(5): Show |
8 | HG02451.hp2 HG02486.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.-213-2830_-213-282 others(6): Show |
CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 57786190 | ||||||
| chr11:57786330 | G | A | 1 | a0001c0001t0001g0119 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-213-2707G>A | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57786330 | |||||||
| chr11:57786343 | C | T | 2 | a0001c0001t0001g0096 a0001c0001t0001g0177 |
2 | HG03704.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-213-2694C>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57786343 | |||||||
| chr11:57786349 | C | T | 5 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0138 others(2): Show |
5 | HG00323.hp2 HG00639.hp1 HG01106.hp2 others(2): Show |
intron_variant | MODIFIER | c.-213-2688C>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57786349 | |||||||
| chr11:57786448 | G | T | 1 | a0001c0001t0011g0154 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-213-2589G>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57786448 | |||||||
| chr11:57786494 | C | T | 1 | a0001c0002t0002g0058 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-213-2543C>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57786494 | |||||||
| chr11:57786524 | C | T | 6 | a0002c0003t0004g0197 a0002c0003t0004g0201 a0002c0003t0004g0202 others(3): Show |
6 | HG02451.hp2 HG02486.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-213-2513C>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57786524 | |||||||
| chr11:57786556 | G | A | 6 | a0001c0001t0003g0219 a0001c0001t0003g0233 a0001c0001t0003g0234 others(3): Show |
6 | HG00408.hp1 HG00438.hp1 NA18975.hp1 others(3): Show |
intron_variant | MODIFIER | c.-213-2481G>A | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57786556 | |||||||
| chr11:57786601 | G | A | 1 | a0001c0001t0003g0243 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-213-2436G>A | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57786601 | |||||||
| chr11:57786994 | T | C | 3 | a0001c0001t0001g0103 a0001c0001t0001g0106 a0001c0010t0001g0107 |
3 | HG02129.hp2 NA18954.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.-213-2043T>C | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57786994 | |||||||
| chr11:57787186 | A | G | 1 | a0002c0003t0004g0190 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-213-1851A>G | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57787186 | |||||||
| chr11:57787544 | C | G | 1 | a0001c0001t0001g0093 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-213-1493C>G | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57787544 | |||||||
| chr11:57787594 | G | A | 1 | a0001c0001t0001g0114 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-213-1443G>A | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57787594 | |||||||
| chr11:57787636 | G | A | 1 | a0002c0003t0004g0198 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-213-1401G>A | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57787636 | |||||||
| chr11:57788298 | T | C | 79 | a0001c0001t0001g0167 a0001c0002t0002g0003 a0001c0002t0002g0005 others(76): Show |
82 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(79): Show |
intron_variant | MODIFIER | c.-213-739T>C | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57788298 | |||||||
| chr11:57788563 | G | T | 1 | a0001c0002t0002g0076 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-213-474G>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57788563 | |||||||
| chr11:57788808 | G | A | 1 | a0002c0003t0004g0253 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-213-229G>A | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57788808 | |||||||
| chr11:57788988 | A | G | 2 | a0003c0007t0008g0181 a0003c0007t0008g0214 |
2 | HG00544.hp2 HG02056.hp2 |
intron_variant | MODIFIER | c.-213-49A>G | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 1/20 | chr11 | 57788988 | |||||||
| chr11:57789201 | T | A | 19 | a0001c0002t0002g0005 a0001c0002t0002g0017 a0001c0002t0002g0025 others(16): Show |
20 | HG00099.hp1 HG01167.hp1 HG01169.hp1 others(17): Show |
intron_variant | MODIFIER | c.-95+46T>A | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 2/20 | chr11 | 57789201 | |||||||
| chr11:57789399 | C | T | 1 | a0001c0001t0003g0226 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-95+244C>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 2/20 | chr11 | 57789399 | |||||||
| chr11:57789526 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-95+371C>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 2/20 | chr11 | 57789526 | |||||||
| chr11:57789841 | C | T | 1 | a0001c0001t0001g0105 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-95+686C>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 2/20 | chr11 | 57789841 | |||||||
| chr11:57789921 | G | T | 1 | a0003c0007t0008g0214 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-95+766G>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 2/20 | chr11 | 57789921 | |||||||
| chr11:57790164 | C | T | 1 | a0001c0001t0001g0136 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-95+1009C>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 2/20 | chr11 | 57790164 | |||||||
| chr11:57790186 | A | G | 12 | a0002c0003t0004g0196 a0002c0003t0004g0197 a0002c0003t0004g0198 others(9): Show |
12 | HG02145.hp1 HG02451.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.-95+1031A>G | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 2/20 | chr11 | 57790186 | |||||||
| chr11:57790196 | C | T | 99 | a0001c0001t0001g0167 a0001c0001t0001g0183 a0001c0002t0002g0003 others(96): Show |
102 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(99): Show |
intron_variant | MODIFIER | c.-95+1041C>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 2/20 | chr11 | 57790196 | |||||||
| chr11:57790333 | C | T | 1 | a0001c0001t0012g0251 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-94-1052C>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 2/20 | chr11 | 57790333 | |||||||
| chr11:57790385 | C | CT | 8 | a0001c0001t0001g0101 a0001c0001t0001g0139 a0001c0001t0001g0140 others(5): Show |
8 | HG01099.hp1 HG03831.hp1 HG03831.hp2 others(5): Show |
intron_variant | MODIFIER | c.-94-984dupT | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr11 | 57790385 | ||||||
| chr11:57790385 | CT | C | 6 | a0001c0001t0001g0191 a0001c0001t0012g0251 a0001c0002t0002g0032 others(3): Show |
6 | HG01070.hp1 HG01169.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.-94-984delT | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr11 | 57790385 | ||||||
| chr11:57790422 | C | T | 4 | a0001c0001t0001g0182 a0001c0001t0001g0191 a0001c0001t0001g0192 others(1): Show |
4 | HG01496.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-94-963C>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 2/20 | chr11 | 57790422 | |||||||
| chr11:57790468 | C | CCGCCTCC others(8): Show |
45 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0015 others(42): Show |
55 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(52): Show |
intron_variant | MODIFIER | c.-94-914_-94-913ins others(15): Show |
CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr11 | 57790468 | ||||||
| chr11:57790542 | C | CTG | 82 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(79): Show |
89 | HG00323.hp2 HG00544.hp1 HG00639.hp1 others(86): Show |
intron_variant | MODIFIER | c.-94-833_-94-832dup others(2): Show |
CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr11 | 57790542 | ||||||
| chr11:57790550 | G | GT | 15 | a0001c0002t0002g0020 a0001c0002t0002g0026 a0001c0002t0002g0029 others(12): Show |
15 | HG01169.hp2 HG01192.hp1 HG01346.hp2 others(12): Show |
intron_variant | MODIFIER | c.-94-834dupT | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr11 | 57790550 | ||||||
| chr11:57790552 | G | GT | 8 | a0001c0001t0001g0013 a0001c0001t0001g0183 a0001c0001t0005g0212 others(5): Show |
8 | HG02145.hp1 HG02145.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.-94-810dupT | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr11 | 57790552 | ||||||
| chr11:57790552 | G | GTGT | 10 | a0001c0001t0001g0093 a0001c0001t0001g0095 a0001c0001t0001g0100 others(7): Show |
10 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(7): Show |
intron_variant | MODIFIER | c.-94-832_-94-831ins others(3): Show |
CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr11 | 57790552 | ||||||
| chr11:57790552 | G | T | 77 | a0001c0001t0001g0167 a0001c0002t0002g0003 a0001c0002t0002g0005 others(74): Show |
80 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(77): Show |
intron_variant | MODIFIER | c.-94-833G>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 2/20 | chr11 | 57790552 | |||||||
| chr11:57790552 | GT | G | 39 | a0001c0001t0001g0206 a0001c0001t0003g0001 a0001c0001t0003g0002 others(36): Show |
48 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(45): Show |
intron_variant | MODIFIER | c.-94-810delT | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr11 | 57790552 | ||||||
| chr11:57790552 | GTTT | G | 6 | a0002c0003t0004g0197 a0002c0003t0004g0201 a0002c0003t0004g0202 others(3): Show |
6 | HG02451.hp2 HG02486.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-94-812_-94-810del others(3): Show |
CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr11 | 57790552 | ||||||
| chr11:57790553 | T | TG | 6 | a0001c0001t0001g0114 a0001c0001t0001g0120 a0001c0001t0001g0121 others(3): Show |
6 | HG02056.hp1 HG02735.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-94-832_-94-831ins others(1): Show |
CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 2/20 | chr11 | 57790553 | |||||||
| chr11:57790554 | T | G | 1 | a0001c0001t0001g0152 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-94-831T>G | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 2/20 | chr11 | 57790554 | |||||||
| chr11:57790732 | A | AT | 95 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(92): Show |
102 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.-94-646dupT | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr11 | 57790732 | ||||||
| chr11:57790917 | C | T | 3 | a0001c0002t0002g0042 a0001c0002t0010g0023 a0001c0002t0010g0024 |
3 | HG00099.hp1 HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-94-468C>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 2/20 | chr11 | 57790917 | |||||||
| chr11:57791084 | A | G | 2 | a0001c0001t0001g0116 a0001c0001t0001g0117 |
2 | NA19064.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.-94-301A>G | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 2/20 | chr11 | 57791084 | |||||||
| chr11:57791293 | C | T | 1 | a0002c0003t0004g0196 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-94-92C>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 2/20 | chr11 | 57791293 | |||||||
| chr11:57791377 | C | G | 4 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0151 others(1): Show |
4 | HG02647.hp1 HG02895.hp2 HG03540.hp2 others(1): Show |
splice_region_variant&intron_variant | LOW | c.-94-8C>G | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 2/20 | chr11 | 57791377 | |||||||
| chr11:57791797 | A | G | 1 | a0001c0001t0001g0158 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.195+124A>G | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 3/20 | chr11 | 57791797 | |||||||
| chr11:57791980 | ACTTTT | A | 7 | a0002c0003t0004g0196 a0002c0003t0004g0197 a0002c0003t0004g0201 others(4): Show |
7 | HG02451.hp2 HG02486.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.195+315_195+319del others(5): Show |
CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr11 | 57791980 | ||||||
| chr11:57791998 | T | C | 2 | a0001c0001t0001g0119 a0001c0001t0001g0122 |
2 | HG02683.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.195+325T>C | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 3/20 | chr11 | 57791998 | |||||||
| chr11:57792044 | G | T | 7 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0143 others(4): Show |
7 | HG00735.hp2 HG01074.hp1 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.195+371G>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 3/20 | chr11 | 57792044 | |||||||
| chr11:57792409 | C | T | 3 | a0001c0001t0001g0007 a0001c0001t0001g0133 a0001c0001t0001g0159 |
4 | HG00621.hp1 NA18945.hp1 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.195+736C>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 3/20 | chr11 | 57792409 | |||||||
| chr11:57792448 | C | T | 1 | a0001c0001t0001g0183 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.195+775C>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 3/20 | chr11 | 57792448 | |||||||
| chr11:57792521 | A | G | 2 | a0001c0001t0001g0207 a0001c0001t0001g0208 |
2 | HG02257.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.195+848A>G | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 3/20 | chr11 | 57792521 | |||||||
| chr11:57792540 | T | C | 1 | a0001c0001t0012g0251 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.195+867T>C | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 3/20 | chr11 | 57792540 | |||||||
| chr11:57792750 | C | T | 1 | a0001c0001t0001g0164 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.195+1077C>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 3/20 | chr11 | 57792750 | |||||||
| chr11:57792832 | AT | A | 205 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(202): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.196-1159delT | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr11 | 57792832 | ||||||
| chr11:57792832 | ATT | A | 24 | a0001c0001t0001g0098 a0001c0001t0001g0183 a0001c0001t0003g0185 others(21): Show |
24 | HG00544.hp2 HG01167.hp2 HG01168.hp2 others(21): Show |
intron_variant | MODIFIER | c.196-1160_196-1159d others(4): Show |
CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr11 | 57792832 | ||||||
| chr11:57792980 | A | C | 45 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0015 others(42): Show |
55 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(52): Show |
intron_variant | MODIFIER | c.196-1030A>C | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 3/20 | chr11 | 57792980 | |||||||
| chr11:57793014 | A | G | 245 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(242): Show |
265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.196-996A>G | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 3/20 | chr11 | 57793014 | |||||||
| chr11:57793206 | A | G | 2 | a0001c0001t0007g0194 a0001c0001t0007g0195 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.196-804A>G | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 3/20 | chr11 | 57793206 | |||||||
| chr11:57793300 | CAG | C | 45 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0015 others(42): Show |
55 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(52): Show |
intron_variant | MODIFIER | c.196-707_196-706del others(2): Show |
CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr11 | 57793300 | ||||||
| chr11:57793542 | C | A | 2 | a0001c0002t0002g0047 a0001c0002t0002g0089 |
2 | HG01069.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.196-468C>A | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 3/20 | chr11 | 57793542 | |||||||
| chr11:57793634 | G | T | 95 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(92): Show |
102 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.196-376G>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 3/20 | chr11 | 57793634 | |||||||
| chr11:57793945 | G | A | 1 | a0002c0003t0004g0253 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.196-65G>A | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 3/20 | chr11 | 57793945 | |||||||
| chr11:57793989 | T | C | 2 | a0003c0007t0008g0181 a0003c0007t0008g0214 |
2 | HG00544.hp2 HG02056.hp2 |
intron_variant | MODIFIER | c.196-21T>C | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 3/20 | chr11 | 57793989 | |||||||
| chr11:57794018 | G | GTTTGTGG others(101): Show |
1 | a0005c0013t0003g0222 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.206_267+46dupTTGTG others(103): Show |
CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr11 | 57794018 | ||||||
| chr11:57794237 | A | G | 1 | a0001c0001t0012g0251 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.267+156A>G | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 4/20 | chr11 | 57794237 | |||||||
| chr11:57794464 | A | G | 2 | a0003c0007t0008g0181 a0003c0007t0008g0214 |
2 | HG00544.hp2 HG02056.hp2 |
intron_variant | MODIFIER | c.267+383A>G | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 4/20 | chr11 | 57794464 | |||||||
| chr11:57794614 | C | T | 1 | a0001c0002t0002g0051 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.267+533C>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 4/20 | chr11 | 57794614 | |||||||
| chr11:57794697 | A | G | 45 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0015 others(42): Show |
55 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(52): Show |
intron_variant | MODIFIER | c.267+616A>G | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 4/20 | chr11 | 57794697 | |||||||
| chr11:57794785 | CA | C | 10 | a0001c0001t0001g0104 a0001c0001t0001g0183 a0001c0002t0002g0046 others(7): Show |
10 | HG02451.hp2 HG02486.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.267+719delA | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr11 | 57794785 | ||||||
| chr11:57794878 | C | T | 1 | a0001c0001t0001g0132 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.268-699C>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 4/20 | chr11 | 57794878 | |||||||
| chr11:57794883 | C | CA | 20 | a0001c0001t0001g0096 a0001c0001t0001g0134 a0001c0001t0001g0152 others(17): Show |
20 | HG00323.hp1 HG00741.hp1 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.268-678dupA | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr11 | 57794883 | ||||||
| chr11:57794980 | C | T | 1 | a0001c0001t0003g0260 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.268-597C>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 4/20 | chr11 | 57794980 | |||||||
| chr11:57795053 | G | A | 45 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0015 others(42): Show |
55 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(52): Show |
intron_variant | MODIFIER | c.268-524G>A | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 4/20 | chr11 | 57795053 | |||||||
| chr11:57795153 | C | G | 1 | a0002c0003t0004g0253 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.268-424C>G | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 4/20 | chr11 | 57795153 | |||||||
| chr11:57795308 | T | A | 1 | a0001c0001t0001g0123 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.268-269T>A | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 4/20 | chr11 | 57795308 | |||||||
| chr11:57795824 | A | G | 1 | a0002c0003t0004g0253 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.420+95A>G | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 5/20 | chr11 | 57795824 | |||||||
| chr11:57795848 | A | C | 3 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0001g0257 |
3 | HG02451.hp1 HG02647.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.420+119A>C | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 5/20 | chr11 | 57795848 | |||||||
| chr11:57795914 | A | G | 2 | a0002c0003t0004g0189 a0002c0003t0004g0263 |
2 | HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.420+185A>G | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 5/20 | chr11 | 57795914 | |||||||
| chr11:57795919 | G | T | 1 | a0001c0001t0001g0131 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.420+190G>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 5/20 | chr11 | 57795919 | |||||||
| chr11:57796033 | A | C | 1 | a0001c0001t0003g0240 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.420+304A>C | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 5/20 | chr11 | 57796033 | |||||||
| chr11:57796057 | A | T | 2 | a0001c0001t0003g0223 a0001c0001t0003g0224 |
2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.420+328A>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 5/20 | chr11 | 57796057 | |||||||
| chr11:57796161 | C | T | 6 | a0002c0003t0004g0197 a0002c0003t0004g0201 a0002c0003t0004g0202 others(3): Show |
6 | HG02451.hp2 HG02486.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.421-296C>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 5/20 | chr11 | 57796161 | |||||||
| chr11:57796247 | G | T | 1 | a0001c0001t0001g0183 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.421-210G>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 5/20 | chr11 | 57796247 | |||||||
| chr11:57796359 | C | G | 1 | a0002c0003t0004g0187 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.421-98C>G | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 5/20 | chr11 | 57796359 | |||||||
| chr11:57797041 | A | G | 1 | a0001c0002t0002g0016 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.956+49A>G | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 6/20 | chr11 | 57797041 | |||||||
| chr11:57797061 | A | G | 3 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0001g0257 |
3 | HG02451.hp1 HG02647.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.956+69A>G | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 6/20 | chr11 | 57797061 | |||||||
| chr11:57797124 | G | T | 3 | a0001c0001t0006g0170 a0001c0001t0006g0171 a0001c0001t0006g0172 |
3 | HG02004.hp2 HG02257.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.956+132G>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 6/20 | chr11 | 57797124 | |||||||
| chr11:57797325 | G | A | 96 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(93): Show |
103 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.956+333G>A | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 6/20 | chr11 | 57797325 | |||||||
| chr11:57797364 | G | A | 98 | a0001c0001t0001g0183 a0001c0002t0002g0003 a0001c0002t0002g0005 others(95): Show |
101 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(98): Show |
intron_variant | MODIFIER | c.956+372G>A | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 6/20 | chr11 | 57797364 | |||||||
| chr11:57797437 | G | A | 1 | a0001c0001t0001g0146 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.956+445G>A | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 6/20 | chr11 | 57797437 | |||||||
| chr11:57797527 | G | C | 1 | a0001c0001t0001g0109 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.956+535G>C | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 6/20 | chr11 | 57797527 | |||||||
| chr11:57797842 | C | CA | 167 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(164): Show |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.956+871dupA | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr11 | 57797842 | ||||||
| chr11:57797842 | C | CAA | 24 | a0001c0001t0001g0111 a0001c0001t0001g0116 a0001c0001t0001g0120 others(21): Show |
24 | HG00544.hp1 HG01175.hp2 HG01261.hp2 others(21): Show |
intron_variant | MODIFIER | c.956+870_956+871dup others(2): Show |
CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr11 | 57797842 | ||||||
| chr11:57798050 | G | A | 1 | a0005c0013t0003g0222 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.956+1058G>A | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 6/20 | chr11 | 57798050 | |||||||
| chr11:57798114 | C | T | 1 | a0001c0001t0003g0231 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.956+1122C>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 6/20 | chr11 | 57798114 | |||||||
| chr11:57798226 | A | C | 2 | a0001c0001t0001g0008 a0001c0001t0001g0169 |
3 | HG02970.hp2 HG03130.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.956+1234A>C | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 6/20 | chr11 | 57798226 | |||||||
| chr11:57798328 | C | T | 45 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0015 others(42): Show |
55 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(52): Show |
intron_variant | MODIFIER | c.956+1336C>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 6/20 | chr11 | 57798328 | |||||||
| chr11:57798344 | CA | C | 226 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(223): Show |
246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.956+1370delA | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr11 | 57798344 | ||||||
| chr11:57798347 | A | T | 1 | a0001c0001t0003g0215 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.956+1355A>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 6/20 | chr11 | 57798347 | |||||||
| chr11:57798348 | A | T | 44 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0015 others(41): Show |
54 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.956+1356A>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 6/20 | chr11 | 57798348 | |||||||
| chr11:57798362 | A | G | 1 | a0001c0001t0001g0120 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.956+1370A>G | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 6/20 | chr11 | 57798362 | |||||||
| chr11:57798363 | G | C | 1 | a0001c0001t0001g0120 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.956+1371G>C | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 6/20 | chr11 | 57798363 | |||||||
| chr11:57798365 | C | A | 1 | a0001c0001t0001g0120 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.956+1373C>A | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 6/20 | chr11 | 57798365 | |||||||
| chr11:57798511 | A | G | 242 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(239): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.956+1519A>G | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 6/20 | chr11 | 57798511 | |||||||
| chr11:57798722 | A | G | 1 | a0001c0002t0002g0016 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.956+1730A>G | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 6/20 | chr11 | 57798722 | |||||||
| chr11:57798855 | A | T | 96 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(93): Show |
103 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.956+1863A>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 6/20 | chr11 | 57798855 | |||||||
| chr11:57798979 | A | G | 4 | a0001c0001t0001g0013 a0001c0001t0001g0206 a0001c0001t0001g0207 others(1): Show |
5 | HG02257.hp1 HG02258.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.956+1987A>G | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 6/20 | chr11 | 57798979 | |||||||
| chr11:57799378 | A | G | 96 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(93): Show |
103 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.957-2355A>G | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 6/20 | chr11 | 57799378 | |||||||
| chr11:57799451 | C | G | 2 | a0003c0007t0008g0181 a0003c0007t0008g0214 |
2 | HG00544.hp2 HG02056.hp2 |
intron_variant | MODIFIER | c.957-2282C>G | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 6/20 | chr11 | 57799451 | |||||||
| chr11:57799737 | G | T | 1 | a0001c0001t0001g0109 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.957-1996G>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 6/20 | chr11 | 57799737 | |||||||
| chr11:57799933 | T | C | 242 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(239): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.957-1800T>C | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 6/20 | chr11 | 57799933 | |||||||
| chr11:57799979 | G | GT | 17 | a0001c0001t0005g0212 a0001c0002t0002g0020 a0001c0002t0002g0030 others(14): Show |
17 | HG02055.hp2 HG02145.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.957-1728dupT | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr11 | 57799979 | ||||||
| chr11:57799979 | G | GTT | 32 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0003g0001 others(29): Show |
42 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(39): Show |
intron_variant | MODIFIER | c.957-1729_957-1728d others(4): Show |
CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr11 | 57799979 | ||||||
| chr11:57799979 | G | GTTT | 15 | a0001c0001t0001g0182 a0001c0001t0001g0193 a0001c0001t0003g0184 others(12): Show |
15 | HG00738.hp2 HG01167.hp2 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.957-1730_957-1728d others(5): Show |
CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr11 | 57799979 | ||||||
| chr11:57799979 | GT | G | 19 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0095 others(16): Show |
21 | HG00741.hp2 HG01167.hp1 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.957-1728delT | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr11 | 57799979 | ||||||
| chr11:57799979 | GTT | G | 71 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0009 others(68): Show |
76 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.957-1729_957-1728d others(4): Show |
CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr11 | 57799979 | ||||||
| chr11:57799979 | GTTT | G | 10 | a0001c0001t0001g0104 a0001c0001t0001g0121 a0001c0001t0001g0125 others(7): Show |
10 | HG00544.hp1 HG00544.hp2 HG02056.hp2 others(7): Show |
intron_variant | MODIFIER | c.957-1730_957-1728d others(5): Show |
CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr11 | 57799979 | ||||||
| chr11:57799981 | T | A | 1 | a0001c0001t0001g0183 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.957-1752T>A | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 6/20 | chr11 | 57799981 | |||||||
| chr11:57800083 | C | A | 2 | a0003c0007t0008g0181 a0003c0007t0008g0214 |
2 | HG00544.hp2 HG02056.hp2 |
intron_variant | MODIFIER | c.957-1650C>A | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 6/20 | chr11 | 57800083 | |||||||
| chr11:57800232 | G | A | 1 | a0001c0002t0002g0027 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.957-1501G>A | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 6/20 | chr11 | 57800232 | |||||||
| chr11:57800299 | G | A | 1 | a0001c0001t0001g0010 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.957-1434G>A | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 6/20 | chr11 | 57800299 | |||||||
| chr11:57800533 | G | T | 1 | a0002c0003t0004g0263 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.957-1200G>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 6/20 | chr11 | 57800533 | |||||||
| chr11:57800775 | G | A | 1 | a0001c0002t0002g0026 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.957-958G>A | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 6/20 | chr11 | 57800775 | |||||||
| chr11:57801533 | G | T | 1 | a0001c0001t0003g0231 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.957-200G>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 6/20 | chr11 | 57801533 | |||||||
| chr11:57802356 | A | T | 262 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(259): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.1420+160A>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 7/20 | chr11 | 57802356 | |||||||
| chr11:57802526 | C | T | 1 | a0001c0001t0001g0105 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1420+330C>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 7/20 | chr11 | 57802526 | |||||||
| chr11:57802674 | A | G | 2 | a0001c0002t0002g0044 a0001c0002t0002g0084 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1420+478A>G | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 7/20 | chr11 | 57802674 | |||||||
| chr11:57802756 | G | A | 3 | a0001c0001t0001g0092 a0001c0001t0001g0099 a0001c0001t0001g0126 |
3 | HG01168.hp1 NA20752.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1420+560G>A | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 7/20 | chr11 | 57802756 | |||||||
| chr11:57802958 | A | G | 77 | a0001c0002t0002g0003 a0001c0002t0002g0005 a0001c0002t0002g0016 others(74): Show |
80 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(77): Show |
intron_variant | MODIFIER | c.1421-663A>G | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 7/20 | chr11 | 57802958 | |||||||
| chr11:57803193 | C | T | 2 | a0001c0001t0001g0102 a0001c0001t0001g0128 |
2 | NA18975.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.1421-428C>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 7/20 | chr11 | 57803193 | |||||||
| chr11:57803208 | C | T | 40 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0184 others(37): Show |
49 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(46): Show |
intron_variant | MODIFIER | c.1421-413C>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 7/20 | chr11 | 57803208 | |||||||
| chr11:57803265 | G | A | 1 | a0001c0001t0003g0185 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1421-356G>A | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 7/20 | chr11 | 57803265 | |||||||
| chr11:57803321 | C | T | 2 | a0001c0001t0003g0221 a0001c0001t0003g0238 |
2 | HG00741.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.1421-300C>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 7/20 | chr11 | 57803321 | |||||||
| chr11:57803378 | A | G | 6 | a0001c0002t0002g0003 a0001c0002t0002g0044 a0001c0002t0002g0046 others(3): Show |
8 | HG00639.hp2 HG00735.hp1 HG01070.hp1 others(5): Show |
intron_variant | MODIFIER | c.1421-243A>G | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 7/20 | chr11 | 57803378 | |||||||
| chr11:57803562 | G | A | 1 | a0001c0001t0001g0129 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1421-59G>A | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 7/20 | chr11 | 57803562 | |||||||
| chr11:57804411 | C | T | 44 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0015 others(41): Show |
54 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.1605-252C>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 8/20 | chr11 | 57804411 | |||||||
| chr11:57804421 | A | C | 1 | a0006c0009t0001g0213 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1605-242A>C | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 8/20 | chr11 | 57804421 | |||||||
| chr11:57804604 | G | T | 5 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0001g0257 others(2): Show |
5 | HG02451.hp1 HG02647.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1605-59G>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 8/20 | chr11 | 57804604 | |||||||
| chr11:57804904 | A | G | 1 | a0001c0002t0002g0054 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1722+124A>G | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 9/20 | chr11 | 57804904 | |||||||
| chr11:57805260 | T | C | 1 | a0003c0007t0008g0181 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1722+480T>C | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 9/20 | chr11 | 57805260 | |||||||
| chr11:57805272 | G | A | 2 | a0003c0007t0008g0181 a0003c0007t0008g0214 |
2 | HG00544.hp2 HG02056.hp2 |
intron_variant | MODIFIER | c.1722+492G>A | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 9/20 | chr11 | 57805272 | |||||||
| chr11:57805307 | G | A | 1 | a0002c0003t0004g0252 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1722+527G>A | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 9/20 | chr11 | 57805307 | |||||||
| chr11:57805331 | T | G | 1 | a0001c0001t0012g0251 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1722+551T>G | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 9/20 | chr11 | 57805331 | |||||||
| chr11:57805334 | C | G | 1 | a0002c0005t0004g0200 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1723-548C>G | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 9/20 | chr11 | 57805334 | |||||||
| chr11:57805350 | A | G | 7 | a0002c0003t0004g0196 a0002c0003t0004g0197 a0002c0003t0004g0201 others(4): Show |
7 | HG02451.hp2 HG02486.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1723-532A>G | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 9/20 | chr11 | 57805350 | |||||||
| chr11:57805401 | G | A | 1 | a0001c0001t0001g0129 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1723-481G>A | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 9/20 | chr11 | 57805401 | |||||||
| chr11:57805550 | CT | C | 240 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(237): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.1723-322delT | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chr11 | 57805550 | ||||||
| chr11:57805601 | T | G | 2 | a0001c0001t0001g0116 a0001c0001t0001g0117 |
2 | NA19064.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.1723-281T>G | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 9/20 | chr11 | 57805601 | |||||||
| chr11:57805714 | A | C | 1 | a0001c0001t0003g0244 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1723-168A>C | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 9/20 | chr11 | 57805714 | |||||||
| chr11:57805747 | G | A | 1 | a0001c0002t0002g0069 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1723-135G>A | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 9/20 | chr11 | 57805747 | |||||||
| chr11:57806227 | TTGG | T | 249 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(246): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.1877-205_1877-203d others(5): Show |
CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr11 | 57806227 | ||||||
| chr11:57806677 | G | A | 1 | a0001c0001t0003g0247 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1894+199G>A | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 11/20 | chr11 | 57806677 | |||||||
| chr11:57806678 | A | G | 1 | a0001c0001t0003g0247 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1894+200A>G | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 11/20 | chr11 | 57806678 | |||||||
| chr11:57806805 | G | A | 1 | a0001c0001t0001g0148 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1895-110G>A | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 11/20 | chr11 | 57806805 | |||||||
| chr11:57806842 | A | G | 1 | a0001c0002t0002g0081 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1895-73A>G | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 11/20 | chr11 | 57806842 | |||||||
| chr11:57807156 | T | A | 1 | a0001c0001t0001g0183 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1963+173T>A | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 12/20 | chr11 | 57807156 | |||||||
| chr11:57807313 | G | T | 3 | a0001c0001t0001g0182 a0001c0001t0001g0191 a0007c0008t0005g0210 |
3 | HG02896.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1963+330G>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 12/20 | chr11 | 57807313 | |||||||
| chr11:57807314 | A | T | 3 | a0001c0001t0001g0182 a0001c0001t0001g0191 a0007c0008t0005g0210 |
3 | HG02896.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1963+331A>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 12/20 | chr11 | 57807314 | |||||||
| chr11:57807605 | C | CA | 44 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0148 others(41): Show |
54 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.1964-534dupA | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chr11 | 57807605 | ||||||
| chr11:57807605 | CA | C | 25 | a0001c0001t0001g0099 a0001c0001t0001g0108 a0001c0001t0001g0123 others(22): Show |
25 | HG01168.hp1 HG01993.hp2 HG02015.hp2 others(22): Show |
intron_variant | MODIFIER | c.1964-534delA | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chr11 | 57807605 | ||||||
| chr11:57807627 | A | AG | 8 | a0001c0002t0002g0025 a0001c0002t0002g0061 a0001c0002t0002g0064 others(5): Show |
8 | HG01175.hp2 HG01361.hp2 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.1964-538_1964-537i others(3): Show |
CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 12/20 | chr11 | 57807627 | |||||||
| chr11:57807627 | A | G | 70 | a0001c0002t0002g0003 a0001c0002t0002g0005 a0001c0002t0002g0016 others(67): Show |
73 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(70): Show |
intron_variant | MODIFIER | c.1964-538A>G | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 12/20 | chr11 | 57807627 | |||||||
| chr11:57807791 | G | A | 1 | a0002c0003t0004g0189 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1964-374G>A | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 12/20 | chr11 | 57807791 | |||||||
| chr11:57807918 | G | A | 1 | a0001c0002t0002g0064 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1964-247G>A | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 12/20 | chr11 | 57807918 | |||||||
| chr11:57807979 | A | G | 1 | a0001c0001t0003g0248 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1964-186A>G | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 12/20 | chr11 | 57807979 | |||||||
| chr11:57809143 | C | T | 2 | a0003c0007t0008g0181 a0003c0007t0008g0214 |
2 | HG00544.hp2 HG02056.hp2 |
intron_variant | MODIFIER | c.2243-131C>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 14/20 | chr11 | 57809143 | |||||||
| chr11:57809154 | A | G | 7 | a0001c0001t0003g0217 a0001c0001t0003g0221 a0001c0001t0003g0229 others(4): Show |
7 | HG00323.hp1 HG00741.hp1 HG01167.hp2 others(4): Show |
intron_variant | MODIFIER | c.2243-120A>G | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 14/20 | chr11 | 57809154 | |||||||
| chr11:57809526 | C | T | 5 | a0001c0001t0001g0123 a0001c0001t0001g0149 a0001c0001t0001g0150 others(2): Show |
5 | HG02647.hp1 HG02895.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.2435+60C>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 15/20 | chr11 | 57809526 | |||||||
| chr11:57809538 | C | T | 1 | a0001c0010t0001g0107 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.2435+72C>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 15/20 | chr11 | 57809538 | |||||||
| chr11:57809565 | C | T | 1 | a0001c0001t0001g0183 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2435+99C>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 15/20 | chr11 | 57809565 | |||||||
| chr11:57809620 | A | G | 2 | a0002c0003t0004g0186 a0002c0003t0004g0187 |
2 | HG03139.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2435+154A>G | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 15/20 | chr11 | 57809620 | |||||||
| chr11:57809624 | A | G | 96 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(93): Show |
103 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.2435+158A>G | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 15/20 | chr11 | 57809624 | |||||||
| chr11:57809803 | G | A | 1 | a0002c0003t0004g0197 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2436-306G>A | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 15/20 | chr11 | 57809803 | |||||||
| chr11:57810040 | G | A | 3 | a0001c0002t0002g0049 a0001c0002t0002g0087 a0001c0002t0002g0090 |
3 | NA18998.hp2 NA19003.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.2436-69G>A | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 15/20 | chr11 | 57810040 | |||||||
| chr11:57810327 | T | A | 1 | a0006c0009t0001g0213 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2550+104T>A | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 16/20 | chr11 | 57810327 | |||||||
| chr11:57810343 | T | A | 1 | a0001c0001t0001g0108 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2550+120T>A | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 16/20 | chr11 | 57810343 | |||||||
| chr11:57810345 | C | T | 2 | a0001c0001t0001g0112 a0001c0001t0001g0113 |
2 | HG00639.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.2550+122C>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 16/20 | chr11 | 57810345 | |||||||
| chr11:57810418 | T | A | 1 | a0001c0002t0002g0078 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2550+195T>A | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 16/20 | chr11 | 57810418 | |||||||
| chr11:57810422 | G | A | 1 | a0001c0001t0001g0193 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2550+199G>A | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 16/20 | chr11 | 57810422 | |||||||
| chr11:57810542 | T | C | 242 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(239): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.2550+319T>C | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 16/20 | chr11 | 57810542 | |||||||
| chr11:57810580 | C | G | 1 | a0001c0001t0001g0114 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2550+357C>G | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 16/20 | chr11 | 57810580 | |||||||
| chr11:57810905 | C | T | 22 | a0001c0001t0001g0092 a0001c0001t0001g0099 a0001c0001t0001g0126 others(19): Show |
22 | HG01168.hp1 HG01261.hp2 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.2551-494C>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 16/20 | chr11 | 57810905 | |||||||
| chr11:57810940 | T | C | 96 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(93): Show |
103 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.2551-459T>C | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 16/20 | chr11 | 57810940 | |||||||
| chr11:57810975 | A | T | 1 | a0002c0003t0004g0253 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2551-424A>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 16/20 | chr11 | 57810975 | |||||||
| chr11:57811124 | G | A | 1 | a0002c0003t0004g0202 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2551-275G>A | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 16/20 | chr11 | 57811124 | |||||||
| chr11:57811177 | A | G | 1 | a0001c0004t0003g0230 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2551-222A>G | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 16/20 | chr11 | 57811177 | |||||||
| chr11:57811352 | G | T | 1 | a0001c0001t0001g0208 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2551-47G>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 16/20 | chr11 | 57811352 | |||||||
| chr11:57811502 | G | A | 2 | a0003c0007t0008g0181 a0003c0007t0008g0214 |
2 | HG00544.hp2 HG02056.hp2 |
intron_variant | MODIFIER | c.2638+16G>A | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 17/20 | chr11 | 57811502 | |||||||
| chr11:57811694 | T | C | 98 | a0001c0001t0001g0183 a0001c0002t0002g0003 a0001c0002t0002g0005 others(95): Show |
101 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(98): Show |
intron_variant | MODIFIER | c.2638+208T>C | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 17/20 | chr11 | 57811694 | |||||||
| chr11:57811796 | A | AATAG | 242 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(239): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.2638+311_2638+314d others(6): Show |
CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr11 | 57811796 | ||||||
| chr11:57811996 | A | G | 5 | a0001c0001t0001g0123 a0001c0001t0001g0149 a0001c0001t0001g0150 others(2): Show |
5 | HG02647.hp1 HG02895.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.2638+510A>G | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 17/20 | chr11 | 57811996 | |||||||
| chr11:57812116 | G | C | 3 | a0001c0002t0002g0042 a0001c0002t0010g0023 a0001c0002t0010g0024 |
3 | HG00099.hp1 HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.2638+630G>C | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 17/20 | chr11 | 57812116 | |||||||
| chr11:57812461 | A | G | 1 | a0001c0002t0002g0046 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2638+975A>G | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 17/20 | chr11 | 57812461 | |||||||
| chr11:57812537 | C | G | 2 | a0001c0001t0003g0229 a0001c0001t0003g0242 |
2 | HG01515.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.2638+1051C>G | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 17/20 | chr11 | 57812537 | |||||||
| chr11:57812794 | G | A | 19 | a0002c0003t0004g0186 a0002c0003t0004g0187 a0002c0003t0004g0188 others(16): Show |
19 | HG01261.hp2 HG02145.hp1 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.2638+1308G>A | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 17/20 | chr11 | 57812794 | |||||||
| chr11:57812915 | C | T | 1 | a0001c0001t0001g0256 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2639-1396C>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 17/20 | chr11 | 57812915 | |||||||
| chr11:57812988 | G | A | 1 | a0006c0009t0001g0213 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2639-1323G>A | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 17/20 | chr11 | 57812988 | |||||||
| chr11:57813088 | T | G | 141 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(138): Show |
158 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(155): Show |
intron_variant | MODIFIER | c.2639-1223T>G | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 17/20 | chr11 | 57813088 | |||||||
| chr11:57813507 | G | A | 2 | a0003c0007t0008g0181 a0003c0007t0008g0214 |
2 | HG00544.hp2 HG02056.hp2 |
intron_variant | MODIFIER | c.2639-804G>A | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 17/20 | chr11 | 57813507 | |||||||
| chr11:57813896 | A | G | 1 | a0008c0011t0001g0162 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.2639-415A>G | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 17/20 | chr11 | 57813896 | |||||||
| chr11:57814048 | C | G | 1 | a0001c0001t0001g0193 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2639-263C>G | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 17/20 | chr11 | 57814048 | |||||||
| chr11:57814054 | C | T | 1 | a0001c0001t0001g0127 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2639-257C>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 17/20 | chr11 | 57814054 | |||||||
| chr11:57814141 | C | A | 141 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(138): Show |
158 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(155): Show |
intron_variant | MODIFIER | c.2639-170C>A | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 17/20 | chr11 | 57814141 | |||||||
| chr11:57814544 | C | T | 3 | a0001c0001t0001g0103 a0001c0001t0001g0106 a0001c0010t0001g0107 |
3 | HG02129.hp2 NA18954.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.2701+171C>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 18/20 | chr11 | 57814544 | |||||||
| chr11:57815230 | A | G | 1 | a0001c0001t0001g0165 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.2702-164A>G | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 18/20 | chr11 | 57815230 | |||||||
| chr11:57815537 | T | C | 1 | a0002c0003t0004g0198 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2808+37T>C | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 19/20 | chr11 | 57815537 | |||||||
| chr11:57815884 | A | G | 1 | a0001c0001t0001g0256 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2809-31A>G | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 19/20 | chr11 | 57815884 | |||||||
| chr11:57816074 | C | T | 7 | a0002c0003t0004g0196 a0002c0003t0004g0197 a0002c0003t0004g0201 others(4): Show |
7 | HG02451.hp2 HG02486.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.2895+73C>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 20/20 | chr11 | 57816074 | |||||||
| chr11:57816242 | G | T | 1 | a0001c0002t0002g0021 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2896-55G>T | CTNND1 | ENSG00000198561.16 | transcript | ENST00000399050.10 | protein_coding | 20/20 | chr11 | 57816242 |