Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 83992 |
| ensemblid | ENSG00000077063.11 |
| hgncid | 15679 |
| symbol | CTTNBP2 |
| name | cortactin binding protein 2 |
| refseq_nuc | NM_033427.3 |
| refseq_prot | NP_219499.1 |
| ensembl_nuc | ENST00000160373.8 |
| ensembl_prot | ENSP00000160373.3 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 117710651 |
| end | 117873441 |
| strand | - |
| ver | v1.2 |
| region | chr7:117710651-117873441 |
| region5000 | chr7:117705651-117878441 |
| regionname0 | CTTNBP2_chr7_117710651_117873441 |
| regionname5000 | CTTNBP2_chr7_117705651_117878441 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1663 | 148 | 60 | 37 | 31 | 3 | 15 | 23 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | MATDG others(1658): Show |
chr7 | 117705651 | 117878441 |
| a0002 | 0/0 | 1663 | 4 | 2 | 2 | 0 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | MATDG others(1658): Show |
chr7 | 117705651 | 117878441 |
| a0003 | 0/0 | 1663 | 3 | 1 | 1 | 0 | 1 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | MATDG others(1658): Show |
chr7 | 117705651 | 117878441 |
| a0004 | 0/0 | 1663 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | MATDG others(1658): Show |
chr7 | 117705651 | 117878441 |
| a0005 | 0/0 | 1663 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | MATDG others(1658): Show |
chr7 | 117705651 | 117878441 |
| a0006 | 0/0 | 1663 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | MATDG others(1658): Show |
chr7 | 117705651 | 117878441 |
| a0007 | 0/0 | 1663 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | MATDG others(1658): Show |
chr7 | 117705651 | 117878441 |
| a0008 | 0/0 | 1663 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | MATDG others(1658): Show |
chr7 | 117705651 | 117878441 |
| a0009 | 0/0 | 1663 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | MATDG others(1658): Show |
chr7 | 117705651 | 117878441 |
| a0010 | 0/0 | 1663 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | MATDG others(1658): Show |
chr7 | 117705651 | 117878441 |
| a0011 | 0/0 | 1663 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | MATDG others(1658): Show |
chr7 | 117705651 | 117878441 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 4989 | 140 | 54 | 37 | 29 | 3 | 15 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | ATGGC others(4984): Show |
chr7 | 117705651 | 117878441 | ||
| a0001c0004 | 0/0 | 4989 | 2 | 2 | 0 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | ATGGC others(4984): Show |
chr7 | 117705651 | 117878441 | ||
| a0001c0006 | 0/0 | 4989 | 2 | 2 | 0 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | ATGGC others(4984): Show |
chr7 | 117705651 | 117878441 | ||
| a0001c0007 | 0/0 | 4989 | 1 | 1 | 0 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | ATGGC others(4984): Show |
chr7 | 117705651 | 117878441 | ||
| a0001c0015 | 0/0 | 4989 | 1 | 1 | 0 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | ATGGC others(4984): Show |
chr7 | 117705651 | 117878441 | ||
| a0001c0016 | 0/0 | 4989 | 1 | 0 | 0 | 1 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | ATGGC others(4984): Show |
chr7 | 117705651 | 117878441 | ||
| a0001c0017 | 0/0 | 4989 | 1 | 0 | 0 | 1 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | ATGGC others(4984): Show |
chr7 | 117705651 | 117878441 | ||
| a0002c0002 | 0/0 | 4989 | 4 | 2 | 2 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | ATGGC others(4984): Show |
chr7 | 117705651 | 117878441 | ||
| a0003c0003 | 0/0 | 4989 | 3 | 1 | 1 | 0 | 1 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | ATGGC others(4984): Show |
chr7 | 117705651 | 117878441 | ||
| a0004c0005 | 0/0 | 4989 | 2 | 1 | 1 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | ATGGC others(4984): Show |
chr7 | 117705651 | 117878441 | ||
| a0005c0009 | 0/0 | 4989 | 1 | 0 | 1 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | ATGGC others(4984): Show |
chr7 | 117705651 | 117878441 | ||
| a0006c0012 | 0/0 | 4989 | 1 | 1 | 0 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | ATGGC others(4984): Show |
chr7 | 117705651 | 117878441 | ||
| a0007c0011 | 0/0 | 4989 | 1 | 0 | 0 | 0 | 0 | 1 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | ATGGC others(4984): Show |
chr7 | 117705651 | 117878441 | ||
| a0008c0014 | 0/0 | 4989 | 1 | 0 | 0 | 0 | 0 | 1 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | ATGGC others(4984): Show |
chr7 | 117705651 | 117878441 | ||
| a0009c0008 | 0/0 | 4989 | 1 | 0 | 0 | 0 | 0 | 1 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | ATGGC others(4984): Show |
chr7 | 117705651 | 117878441 | ||
| a0010c0010 | 0/0 | 4989 | 1 | 1 | 0 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | ATGGC others(4984): Show |
chr7 | 117705651 | 117878441 | ||
| a0011c0013 | 0/0 | 4989 | 1 | 0 | 0 | 1 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | ATGGC others(4984): Show |
chr7 | 117705651 | 117878441 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 5904 | 110 | 42 | 25 | 27 | 3 | 12 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | GCATT others(5899): Show |
chr7 | 117705651 | 117878441 |
| a0001c0001t0002 | 0/0 | 5907 | 17 | 5 | 8 | 2 | 0 | 2 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | GCATT others(5902): Show |
chr7 | 117705651 | 117878441 |
| a0001c0001t0003 | 1/0 | 5904 | 7 | 2 | 3 | 0 | 0 | 1 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | GCATT others(5899): Show |
chr7 | 117705651 | 117878441 |
| a0001c0001t0004 | 0/0 | 5902 | 3 | 2 | 1 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | GCATT others(5897): Show |
chr7 | 117705651 | 117878441 |
| a0001c0001t0005 | 0/0 | 5901 | 3 | 3 | 0 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | GCATT others(5896): Show |
chr7 | 117705651 | 117878441 |
| a0001c0004t0001 | 0/0 | 5904 | 2 | 2 | 0 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | GCATT others(5899): Show |
chr7 | 117705651 | 117878441 |
| a0001c0006t0001 | 0/0 | 5904 | 1 | 1 | 0 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | GCATT others(5899): Show |
chr7 | 117705651 | 117878441 |
| a0001c0006t0002 | 0/0 | 5907 | 1 | 1 | 0 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | GCATT others(5902): Show |
chr7 | 117705651 | 117878441 |
| a0001c0007t0001 | 0/0 | 5904 | 1 | 1 | 0 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | GCATT others(5899): Show |
chr7 | 117705651 | 117878441 |
| a0001c0015t0001 | 0/0 | 5904 | 1 | 1 | 0 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | GCATT others(5899): Show |
chr7 | 117705651 | 117878441 |
| a0001c0016t0001 | 0/0 | 5904 | 1 | 0 | 0 | 1 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | GCATT others(5899): Show |
chr7 | 117705651 | 117878441 |
| a0001c0017t0001 | 0/0 | 5904 | 1 | 0 | 0 | 1 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | GCATT others(5899): Show |
chr7 | 117705651 | 117878441 |
| a0002c0002t0001 | 0/0 | 5904 | 2 | 0 | 2 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | GCATT others(5899): Show |
chr7 | 117705651 | 117878441 |
| a0002c0002t0002 | 0/0 | 5907 | 2 | 2 | 0 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | GCATT others(5902): Show |
chr7 | 117705651 | 117878441 |
| a0003c0003t0002 | 0/0 | 5907 | 3 | 1 | 1 | 0 | 1 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | GCATT others(5902): Show |
chr7 | 117705651 | 117878441 |
| a0004c0005t0001 | 0/0 | 5904 | 2 | 1 | 1 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | GCATT others(5899): Show |
chr7 | 117705651 | 117878441 |
| a0005c0009t0001 | 0/0 | 5904 | 1 | 0 | 1 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | GCATT others(5899): Show |
chr7 | 117705651 | 117878441 |
| a0006c0012t0002 | 0/0 | 5907 | 1 | 1 | 0 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | GCATT others(5902): Show |
chr7 | 117705651 | 117878441 |
| a0007c0011t0002 | 0/0 | 5907 | 1 | 0 | 0 | 0 | 0 | 1 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | GCATT others(5902): Show |
chr7 | 117705651 | 117878441 |
| a0008c0014t0001 | 0/0 | 5904 | 1 | 0 | 0 | 0 | 0 | 1 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | GCATT others(5899): Show |
chr7 | 117705651 | 117878441 |
| a0009c0008t0001 | 0/0 | 5904 | 1 | 0 | 0 | 0 | 0 | 1 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | GCATT others(5899): Show |
chr7 | 117705651 | 117878441 |
| a0010c0010t0001 | 0/0 | 5904 | 1 | 1 | 0 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | GCATT others(5899): Show |
chr7 | 117705651 | 117878441 |
| a0011c0013t0001 | 0/0 | 5904 | 1 | 0 | 0 | 1 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | GCATT others(5899): Show |
chr7 | 117705651 | 117878441 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0153 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0002g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0002g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0003g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0003g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0003g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0003g0134 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0003g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0003g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0004g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0004g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0004g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0005g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0005g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0001t0005g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0004t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0004t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0006t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0006t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0007t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0015t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0016t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0001c0017t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0002c0002t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0002c0002t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0002c0002t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0003c0003t0002g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0003c0003t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0003c0003t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0004c0005t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0004c0005t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0005c0009t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0006c0012t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0007c0011t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0008c0014t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0009c0008t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0010c0010t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| a0011c0013t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00323 | hp1 | a0003 | c0003 | t0002 | g0128 | EUR | FIN | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0161 | EUR | FIN | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | CHS | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG00609 | hp2 | a0001 | c0016 | t0001 | g0058 | EAS | CHS | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0130 | AMR | PUR | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0127 | AMR | PUR | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG01069 | hp1 | a0001 | c0001 | t0003 | g0137 | AMR | PUR | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG01074 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG01081 | hp2 | a0001 | c0001 | t0003 | g0075 | AMR | PUR | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG01109 | hp2 | a0003 | c0003 | t0002 | g0028 | AMR | PUR | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0121 | AMR | PUR | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG01192 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0144 | AMR | PUR | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | CLM | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0155 | AMR | CLM | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | CLM | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | CLM | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0156 | AMR | CLM | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | CLM | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0024 | AMR | CLM | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG01358 | hp2 | a0005 | c0009 | t0001 | g0102 | AMR | CLM | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | CLM | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG01433 | hp1 | a0001 | c0001 | t0004 | g0053 | AMR | CLM | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG01433 | hp2 | a0004 | c0005 | t0001 | g0029 | AMR | CLM | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0162 | AMR | CLM | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PEL | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PEL | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PEL | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PEL | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PEL | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PEL | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | KHV | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | KHV | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0032 | AFR | ACB | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0090 | AFR | ACB | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | CDX | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | CDX | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | ACB | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | ACB | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | ACB | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | ACB | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG02280 | hp2 | a0001 | c0001 | t0004 | g0039 | AFR | ACB | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG02451 | hp1 | a0006 | c0012 | t0002 | g0055 | AFR | ACB | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | ACB | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | KHV | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0131 | SAS | PJL | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | GWD | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | GWD | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | GWD | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | GWD | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | GWD | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | GWD | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG02723 | hp1 | a0001 | c0006 | t0002 | g0079 | AFR | GWD | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | GWD | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0047 | AFR | GWD | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG02818 | hp2 | a0002 | c0002 | t0002 | g0087 | AFR | GWD | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG02895 | hp1 | a0001 | c0006 | t0001 | g0078 | AFR | GWD | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG02895 | hp2 | a0001 | c0007 | t0001 | g0010 | AFR | GWD | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | GWD | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | GWD | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | ESN | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ESN | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | ESN | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG02965 | hp2 | a0001 | c0001 | t0005 | g0034 | AFR | ESN | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | ESN | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG02970 | hp2 | a0001 | c0004 | t0001 | g0008 | AFR | ESN | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | ESN | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG03017 | hp1 | a0007 | c0011 | t0002 | g0099 | SAS | PJL | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG03041 | hp1 | a0001 | c0001 | t0004 | g0033 | AFR | GWD | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | GWD | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | MSL | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0022 | AFR | MSL | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | MSL | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | MSL | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG03239 | hp1 | a0008 | c0014 | t0001 | g0083 | SAS | PJL | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG03491 | hp1 | a0009 | c0008 | t0001 | g0112 | SAS | PJL | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0143 | SAS | PJL | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG03540 | hp1 | a0001 | c0001 | t0005 | g0152 | AFR | GWD | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | GWD | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG03579 | hp1 | a0010 | c0010 | t0001 | g0120 | AFR | MSL | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | MSL | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | PJL | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | BEB | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0076 | SAS | BEB | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0035 | SAS | BEB | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0145 | SAS | BEB | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | STU | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0070 | SAS | STU | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | STU | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0154 | SAS | STU | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | YRI | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | YRI | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | YRI | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | YRI | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| NA19006 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| NA19011 | hp1 | a0011 | c0013 | t0001 | g0025 | EAS | JPT | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| NA19030 | hp1 | a0001 | c0015 | t0001 | g0160 | AFR | LWK | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| NA19030 | hp2 | a0002 | c0002 | t0002 | g0073 | AFR | LWK | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | LWK | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | LWK | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| NA19065 | hp2 | a0001 | c0017 | t0001 | g0043 | EAS | JPT | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | YRI | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| NA19240 | hp2 | a0001 | c0004 | t0001 | g0122 | AFR | YRI | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | ASW | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | ASW | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0139 | EUR | TSI | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0158 | EUR | TSI | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | ACB | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | ACB | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | ACB | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG02486 | hp2 | a0001 | c0001 | t0005 | g0048 | AFR | ACB | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | ACB | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0031 | AFR | ACB | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG06807 | hp1 | a0003 | c0003 | t0002 | g0138 | AFR | USA | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | USA | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | USA | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | USA | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| NA21309 | hp1 | a0004 | c0005 | t0001 | g0030 | AFR | LWK | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| NA21309 | hp2 | a0001 | c0001 | t0003 | g0147 | AFR | LWK | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0153 | REF | REF | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0134 | REF | REF | CTTNBP2_chr7_117705651_117878441 | CTTNBP2 | chr7 | 117705651 | 117878441 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:117711710 | A | G | 1 | a0006 | 1 | HG02451.hp1 | missense_variant | MODERATE | c.4819T>C | p.Ser1607Pro | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 23/23 | 4845/5904 | 4819/4992 | 1607/1663 | chr7 | 117711710 | |||
| chr7:117728198 | G | A | 1 | a0011 | 1 | NA19011.hp1 | missense_variant | MODERATE | c.3946C>T | p.Arg1316Cys | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 17/23 | 3972/5904 | 3946/4992 | 1316/1663 | chr7 | 117728198 | |||
| chr7:117728245 | G | C | 1 | a0008 | 1 | HG03239.hp1 | missense_variant | MODERATE | c.3899C>G | p.Pro1300Arg | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 17/23 | 3925/5904 | 3899/4992 | 1300/1663 | chr7 | 117728245 | |||
| chr7:117735276 | G | T | 1 | a0007 | 1 | HG03017.hp1 | missense_variant | MODERATE | c.3681C>A | p.Phe1227Leu | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 15/23 | 3707/5904 | 3681/4992 | 1227/1663 | chr7 | 117735276 | |||
| chr7:117735320 | A | C | 1 | a0003 | 3 | HG00323.hp1 HG01109.hp2 HG06807.hp1 |
missense_variant | MODERATE | c.3637T>G | p.Leu1213Val | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 15/23 | 3663/5904 | 3637/4992 | 1213/1663 | chr7 | 117735320 | |||
| chr7:117745924 | G | T | 1 | a0002 | 4 | HG01074.hp2 HG01192.hp1 HG02818.hp2 others(1): Show |
missense_variant | MODERATE | c.3442C>A | p.Gln1148Lys | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 14/23 | 3468/5904 | 3442/4992 | 1148/1663 | chr7 | 117745924 | |||
| chr7:117791649 | C | T | 1 | a0010 | 1 | HG03579.hp1 | missense_variant | MODERATE | c.1547G>A | p.Gly516Glu | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 4/23 | 1573/5904 | 1547/4992 | 516/1663 | chr7 | 117791649 | |||
| chr7:117791661 | A | G | 1 | a0005 | 1 | HG01358.hp2 | missense_variant | MODERATE | c.1535T>C | p.Val512Ala | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 4/23 | 1561/5904 | 1535/4992 | 512/1663 | chr7 | 117791661 | |||
| chr7:117791709 | A | T | 1 | a0009 | 1 | HG03491.hp1 | missense_variant | MODERATE | c.1487T>A | p.Leu496Gln | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 4/23 | 1513/5904 | 1487/4992 | 496/1663 | chr7 | 117791709 | |||
| chr7:117791917 | T | C | 1 | a0004 | 2 | HG01433.hp2 NA21309.hp1 |
missense_variant | MODERATE | c.1279A>G | p.Ser427Gly | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 4/23 | 1305/5904 | 1279/4992 | 427/1663 | chr7 | 117791917 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:117724617 | G | A | 1 | a0001c0007 | 1 | HG02895.hp2 | synonymous_variant | LOW | c.4377C>T | p.Asn1459Asn | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 19/23 | 4403/5904 | 4377/4992 | 1459/1663 | chr7 | 117724617 | |||
| chr7:117760535 | G | A | 1 | a0001c0004 | 2 | HG02970.hp2 NA19240.hp2 |
synonymous_variant | LOW | c.3072C>T | p.Ile1024Ile | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 10/23 | 3098/5904 | 3072/4992 | 1024/1663 | chr7 | 117760535 | |||
| chr7:117760595 | T | C | 1 | a0001c0015 | 1 | NA19030.hp1 | synonymous_variant | LOW | c.3012A>G | p.Thr1004Thr | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 10/23 | 3038/5904 | 3012/4992 | 1004/1663 | chr7 | 117760595 | |||
| chr7:117777565 | G | A | 1 | a0001c0016 | 1 | HG00609.hp2 | synonymous_variant | LOW | c.2724C>T | p.His908His | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/23 | 2750/5904 | 2724/4992 | 908/1663 | chr7 | 117777565 | |||
| chr7:117791771 | C | A | 1 | a0001c0017 | 1 | NA19065.hp2 | synonymous_variant | LOW | c.1425G>T | p.Ser475Ser | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 4/23 | 1451/5904 | 1425/4992 | 475/1663 | chr7 | 117791771 | |||
| chr7:117792593 | C | T | 1 | a0001c0007 | 1 | HG02895.hp2 | synonymous_variant | LOW | c.603G>A | p.Glu201Glu | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 4/23 | 629/5904 | 603/4992 | 201/1663 | chr7 | 117792593 | |||
| chr7:117861215 | G | A | 1 | a0001c0006 | 2 | HG02723.hp1 HG02895.hp1 |
synonymous_variant | LOW | c.183C>T | p.Ala61Ala | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/23 | 209/5904 | 183/4992 | 61/1663 | chr7 | 117861215 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:117710716 | CTG | C | 1 | a0001c0001t0004 | 3 | HG01433.hp1 HG02280.hp2 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*819_*820delCA | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 23/23 | 819 | chr7 | 117710716 | ||||||
| chr7:117710750 | CAAT | C | 1 | a0001c0001t0005 | 3 | HG02486.hp2 HG02965.hp2 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*784_*786delATT | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 23/23 | 784 | chr7 | 117710750 | ||||||
| chr7:117710774 | A | AAAT | 6 | a0001c0001t0002 a0001c0006t0002 a0002c0002t0002 others(3): Show |
25 | HG00323.hp1 HG00639.hp2 HG00642.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*760_*762dupATT | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 23/23 | 762 | chr7 | 117710774 | ||||||
| chr7:117711109 | C | T | 22 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(19): Show |
156 | HG00323.hp1 HG00323.hp2 HG00609.hp1 others(153): Show |
3_prime_UTR_variant | MODIFIER | c.*428G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 23/23 | 428 | chr7 | 117711109 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:117712087 | C | G | 6 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0089 others(3): Show |
6 | HG01346.hp1 HG02630.hp2 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.4747-305G>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 22/22 | chr7 | 117712087 | |||||||
| chr7:117712158 | T | C | 1 | a0001c0001t0002g0032 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.4747-376A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 22/22 | chr7 | 117712158 | |||||||
| chr7:117712482 | A | G | 25 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0022 others(22): Show |
25 | HG00323.hp1 HG00639.hp2 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.4747-700T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 22/22 | chr7 | 117712482 | |||||||
| chr7:117712544 | A | C | 1 | a0001c0001t0001g0101 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.4747-762T>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 22/22 | chr7 | 117712544 | |||||||
| chr7:117712850 | C | T | 1 | a0001c0001t0001g0044 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.4747-1068G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 22/22 | chr7 | 117712850 | |||||||
| chr7:117712974 | G | A | 1 | a0001c0001t0001g0159 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.4747-1192C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 22/22 | chr7 | 117712974 | |||||||
| chr7:117714003 | C | T | 1 | a0010c0010t0001g0120 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.4747-2221G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 22/22 | chr7 | 117714003 | |||||||
| chr7:117714017 | G | T | 1 | a0006c0012t0002g0055 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.4747-2235C>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 22/22 | chr7 | 117714017 | |||||||
| chr7:117714149 | G | C | 3 | a0001c0001t0004g0033 a0001c0001t0004g0039 a0001c0001t0004g0053 |
3 | HG01433.hp1 HG02280.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.4747-2367C>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 22/22 | chr7 | 117714149 | |||||||
| chr7:117714315 | C | T | 25 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0022 others(22): Show |
25 | HG00323.hp1 HG00639.hp2 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.4747-2533G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 22/22 | chr7 | 117714315 | |||||||
| chr7:117714513 | A | G | 1 | a0001c0001t0002g0047 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.4747-2731T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 22/22 | chr7 | 117714513 | |||||||
| chr7:117714812 | A | G | 105 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0009 others(102): Show |
106 | HG00323.hp1 HG00609.hp1 HG00639.hp2 others(103): Show |
intron_variant | MODIFIER | c.4747-3030T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 22/22 | chr7 | 117714812 | |||||||
| chr7:117714951 | A | G | 2 | a0001c0001t0001g0067 a0001c0001t0001g0068 |
2 | HG03225.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.4746+3067T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 22/22 | chr7 | 117714951 | |||||||
| chr7:117715213 | A | G | 11 | a0001c0001t0002g0002 a0001c0001t0002g0024 a0001c0001t0002g0090 others(8): Show |
11 | HG00323.hp1 HG00639.hp2 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.4746+2805T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 22/22 | chr7 | 117715213 | |||||||
| chr7:117715455 | T | C | 34 | a0001c0001t0001g0023 a0001c0001t0001g0056 a0001c0001t0001g0059 others(31): Show |
34 | HG00323.hp1 HG00639.hp2 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.4746+2563A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 22/22 | chr7 | 117715455 | |||||||
| chr7:117715475 | T | TAAA | 24 | a0001c0001t0001g0044 a0001c0001t0001g0158 a0001c0001t0002g0002 others(21): Show |
24 | HG00323.hp1 HG00639.hp2 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.4746+2540_4746+254 others(7): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 22/22 | chr7 | 117715475 | |||||||
| chr7:117715475 | T | TAAAAAA | 7 | a0001c0001t0001g0004 a0001c0001t0001g0061 a0001c0001t0001g0077 others(4): Show |
7 | HG01069.hp2 HG02896.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.4746+2537_4746+254 others(10): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 22/22 | chr7 | 117715475 | |||||||
| chr7:117715475 | T | TAAAAAAA | 52 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0014 others(49): Show |
53 | HG00609.hp1 HG00642.hp1 HG01071.hp1 others(50): Show |
intron_variant | MODIFIER | c.4746+2536_4746+254 others(11): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 22/22 | chr7 | 117715475 | |||||||
| chr7:117715475 | T | TAAAAAAA others(2): Show |
10 | a0001c0001t0001g0023 a0001c0001t0001g0056 a0001c0001t0001g0059 others(7): Show |
10 | HG01346.hp1 HG02723.hp2 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.4746+2534_4746+254 others(13): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 22/22 | chr7 | 117715475 | |||||||
| chr7:117715475 | T | TAAAAAAA others(3): Show |
2 | a0001c0001t0001g0072 a0001c0001t0001g0081 |
2 | NA18906.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.4746+2533_4746+254 others(14): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 22/22 | chr7 | 117715475 | |||||||
| chr7:117715475 | T | TAAAAAAA others(4): Show |
1 | a0001c0001t0001g0071 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.4746+2532_4746+254 others(15): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 22/22 | chr7 | 117715475 | |||||||
| chr7:117715475 | T | TAAAAAAA others(7): Show |
4 | a0001c0001t0001g0068 a0001c0001t0004g0033 a0001c0001t0004g0039 others(1): Show |
4 | HG01433.hp1 HG02280.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.4746+2529_4746+254 others(18): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 22/22 | chr7 | 117715475 | |||||||
| chr7:117715475 | T | TAAAAAAA others(8): Show |
1 | a0001c0001t0001g0067 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.4746+2528_4746+254 others(19): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 22/22 | chr7 | 117715475 | |||||||
| chr7:117716027 | T | TTGGGGAA others(9): Show |
6 | a0001c0001t0001g0044 a0001c0001t0001g0080 a0001c0001t0001g0082 others(3): Show |
6 | HG02258.hp1 HG02280.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.4746+1975_4746+199 others(20): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 22/22 | chr7 | 117716027 | |||||||
| chr7:117716052 | T | C | 9 | a0001c0001t0001g0077 a0001c0001t0001g0094 a0001c0001t0001g0095 others(6): Show |
10 | HG01074.hp2 HG01192.hp1 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.4746+1966A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 22/22 | chr7 | 117716052 | |||||||
| chr7:117716119 | A | T | 5 | a0001c0001t0001g0013 a0001c0001t0001g0038 a0001c0001t0001g0097 others(2): Show |
5 | HG01192.hp2 HG01255.hp2 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.4746+1899T>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 22/22 | chr7 | 117716119 | |||||||
| chr7:117716193 | A | AACTTTTT others(312): Show |
3 | a0001c0001t0002g0007 a0001c0001t0002g0022 a0001c0001t0002g0032 |
3 | HG02145.hp1 HG03041.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.4746+1824_4746+182 others(323): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 22/22 | chr7 | 117716193 | |||||||
| chr7:117716193 | A | AACTTTTT others(313): Show |
18 | a0001c0001t0002g0002 a0001c0001t0002g0024 a0001c0001t0002g0027 others(15): Show |
18 | HG00639.hp2 HG00642.hp2 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.4746+1824_4746+182 others(324): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 22/22 | chr7 | 117716193 | |||||||
| chr7:117716193 | A | AACTTTTT others(313): Show |
1 | a0001c0001t0002g0162 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.4746+1824_4746+182 others(324): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 22/22 | chr7 | 117716193 | |||||||
| chr7:117716193 | A | AACTTTTT others(313): Show |
1 | a0003c0003t0002g0128 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.4746+1824_4746+182 others(324): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 22/22 | chr7 | 117716193 | |||||||
| chr7:117716193 | A | AACTTTTT others(314): Show |
2 | a0002c0002t0002g0073 a0002c0002t0002g0087 |
2 | HG02818.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.4746+1824_4746+182 others(325): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 22/22 | chr7 | 117716193 | |||||||
| chr7:117716195 | C | T | 25 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0022 others(22): Show |
25 | HG00323.hp1 HG00639.hp2 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.4746+1823G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 22/22 | chr7 | 117716195 | |||||||
| chr7:117716242 | T | G | 2 | a0001c0001t0001g0080 a0001c0001t0001g0082 |
2 | HG02280.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.4746+1776A>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 22/22 | chr7 | 117716242 | |||||||
| chr7:117716429 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.4746+1589G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 22/22 | chr7 | 117716429 | |||||||
| chr7:117716481 | C | T | 52 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0009 others(49): Show |
52 | HG00609.hp1 HG00642.hp1 HG01069.hp2 others(49): Show |
intron_variant | MODIFIER | c.4746+1537G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 22/22 | chr7 | 117716481 | |||||||
| chr7:117716612 | T | C | 23 | a0001c0001t0002g0007 a0001c0001t0002g0022 a0001c0001t0002g0027 others(20): Show |
23 | HG00323.hp1 HG00639.hp2 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.4746+1406A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 22/22 | chr7 | 117716612 | |||||||
| chr7:117716778 | T | C | 1 | a0003c0003t0002g0138 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.4746+1240A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 22/22 | chr7 | 117716778 | |||||||
| chr7:117716839 | T | C | 102 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0009 others(99): Show |
103 | HG00323.hp1 HG00609.hp1 HG00639.hp2 others(100): Show |
intron_variant | MODIFIER | c.4746+1179A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 22/22 | chr7 | 117716839 | |||||||
| chr7:117716880 | C | T | 1 | a0001c0001t0001g0021 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.4746+1138G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 22/22 | chr7 | 117716880 | |||||||
| chr7:117717033 | T | C | 2 | a0001c0001t0001g0089 a0001c0001t0001g0106 |
2 | HG01346.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.4746+985A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 22/22 | chr7 | 117717033 | |||||||
| chr7:117717035 | A | AACAAACC others(313): Show |
1 | a0001c0001t0001g0084 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.4746+982_4746+983i others(322): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 22/22 | chr7 | 117717035 | |||||||
| chr7:117717321 | AT | A | 9 | a0001c0001t0001g0023 a0001c0001t0001g0056 a0001c0001t0001g0059 others(6): Show |
9 | HG02723.hp2 HG02922.hp2 HG03017.hp1 others(6): Show |
intron_variant | MODIFIER | c.4746+696delA | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 22/22 | chr7 | 117717321 | |||||||
| chr7:117717335 | C | A | 2 | a0001c0001t0001g0132 a0001c0017t0001g0043 |
2 | NA18969.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.4746+683G>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 22/22 | chr7 | 117717335 | |||||||
| chr7:117717356 | T | C | 1 | a0001c0001t0001g0006 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.4746+662A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 22/22 | chr7 | 117717356 | |||||||
| chr7:117717371 | TGTTTTGT others(57): Show |
T | 1 | a0001c0001t0001g0088 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.4746+583_4746+646d others(66): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 22/22 | chr7 | 117717371 | |||||||
| chr7:117717529 | T | C | 5 | a0001c0001t0001g0072 a0001c0001t0001g0089 a0001c0001t0001g0106 others(2): Show |
5 | HG01346.hp1 HG03540.hp2 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.4746+489A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 22/22 | chr7 | 117717529 | |||||||
| chr7:117717744 | G | GA | 16 | a0001c0001t0001g0023 a0001c0001t0001g0056 a0001c0001t0001g0059 others(13): Show |
16 | HG01433.hp1 HG01978.hp1 HG01978.hp2 others(13): Show |
intron_variant | MODIFIER | c.4746+273dupT | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 22/22 | chr7 | 117717744 | |||||||
| chr7:117717744 | GA | G | 14 | a0001c0001t0001g0077 a0001c0001t0001g0091 a0001c0001t0001g0094 others(11): Show |
15 | HG01074.hp2 HG01192.hp1 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.4746+273delT | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 22/22 | chr7 | 117717744 | |||||||
| chr7:117717855 | T | C | 103 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0009 others(100): Show |
104 | HG00323.hp1 HG00609.hp1 HG00639.hp2 others(101): Show |
intron_variant | MODIFIER | c.4746+163A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 22/22 | chr7 | 117717855 | |||||||
| chr7:117718344 | C | T | 1 | a0001c0001t0002g0130 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.4645-225G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 21/22 | chr7 | 117718344 | |||||||
| chr7:117718457 | A | G | 1 | a0001c0001t0001g0119 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.4645-338T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 21/22 | chr7 | 117718457 | |||||||
| chr7:117718806 | C | G | 1 | a0001c0001t0001g0157 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.4645-687G>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 21/22 | chr7 | 117718806 | |||||||
| chr7:117718974 | G | A | 20 | a0001c0001t0002g0007 a0001c0001t0002g0022 a0001c0001t0002g0027 others(17): Show |
20 | HG00323.hp1 HG00639.hp2 HG00642.hp2 others(17): Show |
intron_variant | MODIFIER | c.4644+530C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 21/22 | chr7 | 117718974 | |||||||
| chr7:117718984 | G | A | 2 | a0001c0001t0001g0089 a0001c0001t0001g0106 |
2 | HG01346.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.4644+520C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 21/22 | chr7 | 117718984 | |||||||
| chr7:117719018 | G | A | 3 | a0001c0001t0001g0023 a0001c0001t0001g0059 a0001c0001t0001g0117 |
3 | HG02922.hp2 HG06807.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.4644+486C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 21/22 | chr7 | 117719018 | |||||||
| chr7:117719091 | T | C | 1 | a0001c0001t0001g0003 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.4644+413A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 21/22 | chr7 | 117719091 | |||||||
| chr7:117719157 | C | T | 1 | a0001c0001t0001g0157 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.4644+347G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 21/22 | chr7 | 117719157 | |||||||
| chr7:117719158 | G | A | 1 | a0001c0001t0003g0131 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.4644+346C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 21/22 | chr7 | 117719158 | |||||||
| chr7:117719180 | G | A | 1 | a0008c0014t0001g0083 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.4644+324C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 21/22 | chr7 | 117719180 | |||||||
| chr7:117719189 | G | A | 1 | a0001c0001t0002g0037 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.4644+315C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 21/22 | chr7 | 117719189 | |||||||
| chr7:117719821 | A | G | 1 | a0001c0001t0001g0159 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.4512-185T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 20/22 | chr7 | 117719821 | |||||||
| chr7:117719997 | T | G | 1 | a0001c0001t0001g0005 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.4512-361A>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 20/22 | chr7 | 117719997 | |||||||
| chr7:117720185 | TTC | T | 17 | a0001c0001t0002g0027 a0001c0001t0002g0035 a0001c0001t0002g0037 others(14): Show |
17 | HG00323.hp1 HG00639.hp2 HG00642.hp2 others(14): Show |
intron_variant | MODIFIER | c.4512-551_4512-550d others(4): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 20/22 | chr7 | 117720185 | |||||||
| chr7:117720492 | G | A | 2 | a0001c0001t0001g0089 a0001c0001t0001g0106 |
2 | HG01346.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.4511+575C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 20/22 | chr7 | 117720492 | |||||||
| chr7:117720717 | G | A | 9 | a0001c0001t0001g0023 a0001c0001t0001g0056 a0001c0001t0001g0059 others(6): Show |
9 | HG02723.hp2 HG02922.hp2 HG03225.hp2 others(6): Show |
intron_variant | MODIFIER | c.4511+350C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 20/22 | chr7 | 117720717 | |||||||
| chr7:117720980 | A | ATAAT | 29 | a0001c0001t0001g0023 a0001c0001t0001g0056 a0001c0001t0001g0059 others(26): Show |
29 | HG00323.hp1 HG00639.hp2 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.4511+86_4511+87ins others(4): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 20/22 | chr7 | 117720980 | |||||||
| chr7:117721257 | TGAG | T | 3 | a0001c0001t0004g0033 a0001c0001t0004g0039 a0001c0001t0004g0053 |
3 | HG01433.hp1 HG02280.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.4448-130_4448-128d others(5): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 19/22 | chr7 | 117721257 | |||||||
| chr7:117721292 | T | C | 1 | a0001c0001t0001g0158 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.4448-162A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 19/22 | chr7 | 117721292 | |||||||
| chr7:117721413 | T | A | 1 | a0001c0001t0001g0126 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.4448-283A>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 19/22 | chr7 | 117721413 | |||||||
| chr7:117721530 | C | A | 3 | a0001c0001t0002g0027 a0001c0001t0002g0037 a0007c0011t0002g0099 |
3 | HG02040.hp1 HG03017.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.4448-400G>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 19/22 | chr7 | 117721530 | |||||||
| chr7:117721597 | T | C | 2 | a0001c0001t0002g0007 a0001c0001t0002g0022 |
2 | HG03041.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.4448-467A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 19/22 | chr7 | 117721597 | |||||||
| chr7:117721923 | A | G | 9 | a0001c0001t0001g0077 a0001c0001t0001g0094 a0001c0001t0001g0095 others(6): Show |
10 | HG01074.hp2 HG01192.hp1 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.4448-793T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 19/22 | chr7 | 117721923 | |||||||
| chr7:117722113 | C | T | 20 | a0001c0001t0002g0007 a0001c0001t0002g0022 a0001c0001t0002g0027 others(17): Show |
20 | HG00323.hp1 HG00639.hp2 HG00642.hp2 others(17): Show |
intron_variant | MODIFIER | c.4448-983G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 19/22 | chr7 | 117722113 | |||||||
| chr7:117722257 | G | GT | 9 | a0001c0001t0001g0003 a0001c0001t0001g0066 a0001c0001t0001g0084 others(6): Show |
9 | HG01109.hp1 HG02486.hp2 HG02602.hp2 others(6): Show |
intron_variant | MODIFIER | c.4448-1128dupA | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 19/22 | chr7 | 117722257 | |||||||
| chr7:117722257 | GT | G | 54 | a0001c0001t0001g0023 a0001c0001t0001g0044 a0001c0001t0001g0056 others(51): Show |
55 | HG00323.hp1 HG00639.hp2 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.4448-1128delA | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 19/22 | chr7 | 117722257 | |||||||
| chr7:117722584 | G | A | 1 | a0001c0001t0001g0049 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.4448-1454C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 19/22 | chr7 | 117722584 | |||||||
| chr7:117722801 | G | A | 1 | a0001c0001t0001g0054 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.4448-1671C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 19/22 | chr7 | 117722801 | |||||||
| chr7:117722868 | A | T | 1 | a0001c0001t0001g0114 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.4447+1679T>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 19/22 | chr7 | 117722868 | |||||||
| chr7:117723332 | A | G | 2 | a0001c0001t0001g0072 a0001c0001t0001g0110 |
2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.4447+1215T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 19/22 | chr7 | 117723332 | |||||||
| chr7:117723419 | C | T | 1 | a0001c0001t0001g0077 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.4447+1128G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 19/22 | chr7 | 117723419 | |||||||
| chr7:117723433 | T | C | 1 | a0011c0013t0001g0025 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.4447+1114A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 19/22 | chr7 | 117723433 | |||||||
| chr7:117723741 | G | C | 18 | a0001c0001t0002g0027 a0001c0001t0002g0035 a0001c0001t0002g0037 others(15): Show |
18 | HG00323.hp1 HG00639.hp2 HG00642.hp2 others(15): Show |
intron_variant | MODIFIER | c.4447+806C>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 19/22 | chr7 | 117723741 | |||||||
| chr7:117723752 | C | CTT | 6 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0109 others(3): Show |
6 | HG01433.hp2 HG02622.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.4447+793_4447+794d others(4): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 19/22 | chr7 | 117723752 | |||||||
| chr7:117723752 | CT | C | 23 | a0001c0001t0001g0023 a0001c0001t0001g0044 a0001c0001t0001g0056 others(20): Show |
23 | HG01257.hp2 HG01258.hp1 HG01433.hp1 others(20): Show |
intron_variant | MODIFIER | c.4447+794delA | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 19/22 | chr7 | 117723752 | |||||||
| chr7:117723752 | CTT | C | 21 | a0001c0001t0001g0082 a0001c0001t0002g0007 a0001c0001t0002g0022 others(18): Show |
21 | HG00323.hp1 HG00639.hp2 HG00642.hp2 others(18): Show |
intron_variant | MODIFIER | c.4447+793_4447+794d others(4): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 19/22 | chr7 | 117723752 | |||||||
| chr7:117724094 | C | T | 1 | a0001c0001t0001g0019 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.4447+453G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 19/22 | chr7 | 117724094 | |||||||
| chr7:117724448 | C | T | 1 | a0001c0001t0001g0148 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.4447+99G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 19/22 | chr7 | 117724448 | |||||||
| chr7:117724536 | C | T | 3 | a0001c0001t0005g0034 a0001c0001t0005g0048 a0001c0001t0005g0152 |
3 | HG02486.hp2 HG02965.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.4447+11G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 19/22 | chr7 | 117724536 | |||||||
| chr7:117724944 | G | A | 56 | a0001c0001t0001g0023 a0001c0001t0001g0044 a0001c0001t0001g0056 others(53): Show |
57 | HG00323.hp1 HG00639.hp2 HG00642.hp2 others(54): Show |
intron_variant | MODIFIER | c.4261+108C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 18/22 | chr7 | 117724944 | |||||||
| chr7:117725294 | G | A | 1 | a0001c0001t0003g0075 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.4056-37C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 17/22 | chr7 | 117725294 | |||||||
| chr7:117725390 | G | C | 1 | a0001c0001t0001g0093 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.4056-133C>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 17/22 | chr7 | 117725390 | |||||||
| chr7:117725700 | C | CT | 20 | a0001c0001t0002g0007 a0001c0001t0002g0022 a0001c0001t0002g0027 others(17): Show |
20 | HG00323.hp1 HG00639.hp2 HG00642.hp2 others(17): Show |
intron_variant | MODIFIER | c.4056-444dupA | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 17/22 | chr7 | 117725700 | |||||||
| chr7:117725757 | G | A | 3 | a0001c0001t0001g0023 a0001c0001t0001g0059 a0001c0001t0001g0117 |
3 | HG02922.hp2 HG06807.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.4056-500C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 17/22 | chr7 | 117725757 | |||||||
| chr7:117725832 | C | T | 8 | a0001c0001t0001g0023 a0001c0001t0001g0056 a0001c0001t0001g0059 others(5): Show |
8 | HG02723.hp2 HG02922.hp2 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.4056-575G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 17/22 | chr7 | 117725832 | |||||||
| chr7:117726042 | G | C | 6 | a0001c0001t0001g0066 a0001c0001t0001g0084 a0001c0001t0001g0123 others(3): Show |
6 | HG02486.hp2 HG02615.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.4056-785C>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 17/22 | chr7 | 117726042 | |||||||
| chr7:117726191 | T | C | 8 | a0001c0001t0001g0077 a0001c0001t0001g0094 a0001c0001t0001g0095 others(5): Show |
8 | HG01433.hp2 HG02257.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.4056-934A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 17/22 | chr7 | 117726191 | |||||||
| chr7:117726430 | C | T | 1 | a0008c0014t0001g0083 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.4056-1173G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 17/22 | chr7 | 117726430 | |||||||
| chr7:117726538 | A | G | 20 | a0001c0001t0002g0007 a0001c0001t0002g0022 a0001c0001t0002g0027 others(17): Show |
20 | HG00323.hp1 HG00639.hp2 HG00642.hp2 others(17): Show |
intron_variant | MODIFIER | c.4056-1281T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 17/22 | chr7 | 117726538 | |||||||
| chr7:117727038 | CTTTAA | C | 4 | a0001c0001t0001g0011 a0001c0001t0001g0103 a0001c0001t0001g0105 others(1): Show |
4 | NA18954.hp2 NA18962.hp1 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.4055+1046_4055+105 others(9): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 17/22 | chr7 | 117727038 | |||||||
| chr7:117727160 | T | C | 2 | a0002c0002t0002g0073 a0002c0002t0002g0087 |
2 | HG02818.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.4055+929A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 17/22 | chr7 | 117727160 | |||||||
| chr7:117727224 | C | G | 7 | a0001c0001t0001g0044 a0001c0001t0001g0080 a0001c0001t0001g0082 others(4): Show |
7 | HG02145.hp1 HG02258.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.4055+865G>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 17/22 | chr7 | 117727224 | |||||||
| chr7:117727373 | T | A | 3 | a0001c0001t0004g0033 a0001c0001t0004g0039 a0001c0001t0004g0053 |
3 | HG01433.hp1 HG02280.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.4055+716A>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 17/22 | chr7 | 117727373 | |||||||
| chr7:117727805 | T | C | 1 | a0001c0001t0001g0081 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.4055+284A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 17/22 | chr7 | 117727805 | |||||||
| chr7:117727876 | A | G | 24 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0019 others(21): Show |
24 | HG00609.hp1 HG00642.hp1 HG01258.hp1 others(21): Show |
intron_variant | MODIFIER | c.4055+213T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 17/22 | chr7 | 117727876 | |||||||
| chr7:117727885 | C | T | 1 | a0001c0001t0002g0037 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.4055+204G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 17/22 | chr7 | 117727885 | |||||||
| chr7:117728069 | T | C | 3 | a0001c0001t0004g0033 a0001c0001t0004g0039 a0001c0001t0004g0053 |
3 | HG01433.hp1 HG02280.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.4055+20A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 17/22 | chr7 | 117728069 | |||||||
| chr7:117728533 | G | A | 17 | a0001c0001t0001g0021 a0001c0001t0002g0027 a0001c0001t0002g0037 others(14): Show |
17 | HG00323.hp1 HG00639.hp2 HG00642.hp2 others(14): Show |
intron_variant | MODIFIER | c.3877-266C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 16/22 | chr7 | 117728533 | |||||||
| chr7:117729096 | G | A | 1 | a0001c0001t0001g0042 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.3877-829C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 16/22 | chr7 | 117729096 | |||||||
| chr7:117729584 | G | T | 1 | a0001c0001t0001g0119 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.3877-1317C>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 16/22 | chr7 | 117729584 | |||||||
| chr7:117729597 | A | G | 1 | a0001c0001t0001g0042 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.3877-1330T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 16/22 | chr7 | 117729597 | |||||||
| chr7:117729678 | T | G | 2 | a0001c0001t0002g0007 a0001c0001t0002g0022 |
2 | HG03041.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.3877-1411A>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 16/22 | chr7 | 117729678 | |||||||
| chr7:117730050 | CAAGGTGC others(4): Show |
C | 1 | a0001c0001t0001g0072 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.3877-1794_3877-178 others(15): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 16/22 | chr7 | 117730050 | |||||||
| chr7:117730210 | T | C | 9 | a0001c0001t0001g0023 a0001c0001t0001g0056 a0001c0001t0001g0059 others(6): Show |
9 | HG02630.hp2 HG02723.hp2 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.3877-1943A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 16/22 | chr7 | 117730210 | |||||||
| chr7:117730278 | A | G | 6 | a0001c0001t0002g0035 a0001c0001t0004g0033 a0001c0001t0004g0039 others(3): Show |
6 | HG01433.hp1 HG02280.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.3877-2011T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 16/22 | chr7 | 117730278 | |||||||
| chr7:117730429 | G | A | 1 | a0001c0001t0001g0157 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.3877-2162C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 16/22 | chr7 | 117730429 | |||||||
| chr7:117730637 | C | T | 2 | a0001c0001t0002g0155 a0001c0001t0002g0156 |
2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.3877-2370G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 16/22 | chr7 | 117730637 | |||||||
| chr7:117730753 | G | T | 1 | a0001c0001t0002g0032 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3877-2486C>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 16/22 | chr7 | 117730753 | |||||||
| chr7:117730866 | AT | A | 29 | a0001c0001t0001g0021 a0001c0001t0001g0072 a0001c0001t0001g0089 others(26): Show |
29 | HG00323.hp1 HG00639.hp2 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.3877-2600delA | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 16/22 | chr7 | 117730866 | |||||||
| chr7:117731515 | AC | A | 3 | a0001c0001t0001g0023 a0001c0001t0001g0059 a0001c0001t0001g0117 |
3 | HG02922.hp2 HG06807.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.3877-3249delG | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 16/22 | chr7 | 117731515 | |||||||
| chr7:117731689 | C | T | 7 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0093 others(4): Show |
7 | HG00609.hp1 HG01952.hp1 HG02523.hp2 others(4): Show |
intron_variant | MODIFIER | c.3876+3224G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 16/22 | chr7 | 117731689 | |||||||
| chr7:117732013 | A | G | 40 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0056 others(37): Show |
40 | HG00323.hp1 HG00639.hp2 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.3876+2900T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 16/22 | chr7 | 117732013 | |||||||
| chr7:117732106 | A | C | 1 | a0001c0001t0002g0032 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3876+2807T>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 16/22 | chr7 | 117732106 | |||||||
| chr7:117732149 | G | A | 38 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0056 others(35): Show |
38 | HG00323.hp1 HG00639.hp2 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.3876+2764C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 16/22 | chr7 | 117732149 | |||||||
| chr7:117732217 | A | G | 3 | a0001c0001t0003g0031 a0001c0001t0003g0121 a0001c0001t0003g0131 |
3 | HG01168.hp2 HG02559.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.3876+2696T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 16/22 | chr7 | 117732217 | |||||||
| chr7:117732409 | G | T | 17 | a0001c0001t0001g0021 a0001c0001t0002g0027 a0001c0001t0002g0037 others(14): Show |
17 | HG00323.hp1 HG00639.hp2 HG00642.hp2 others(14): Show |
intron_variant | MODIFIER | c.3876+2504C>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 16/22 | chr7 | 117732409 | |||||||
| chr7:117732447 | G | A | 1 | a0001c0001t0001g0140 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.3876+2466C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 16/22 | chr7 | 117732447 | |||||||
| chr7:117732467 | GGTGAAAC others(3): Show |
G | 9 | a0001c0001t0001g0040 a0001c0001t0001g0046 a0001c0001t0001g0049 others(6): Show |
9 | HG02109.hp2 HG02258.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.3876+2436_3876+244 others(14): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 16/22 | chr7 | 117732467 | |||||||
| chr7:117732519 | G | C | 1 | a0001c0001t0002g0032 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3876+2394C>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 16/22 | chr7 | 117732519 | |||||||
| chr7:117732541 | T | C | 1 | a0001c0001t0001g0088 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.3876+2372A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 16/22 | chr7 | 117732541 | |||||||
| chr7:117732581 | C | T | 1 | a0001c0001t0002g0035 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.3876+2332G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 16/22 | chr7 | 117732581 | |||||||
| chr7:117732644 | C | T | 1 | a0002c0002t0002g0073 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3876+2269G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 16/22 | chr7 | 117732644 | |||||||
| chr7:117732826 | A | C | 1 | a0001c0001t0001g0123 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.3876+2087T>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 16/22 | chr7 | 117732826 | |||||||
| chr7:117732944 | T | C | 41 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0056 others(38): Show |
41 | HG00323.hp1 HG00639.hp2 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.3876+1969A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 16/22 | chr7 | 117732944 | |||||||
| chr7:117733060 | T | G | 9 | a0001c0001t0001g0077 a0001c0001t0001g0094 a0001c0001t0001g0095 others(6): Show |
10 | HG01074.hp2 HG01192.hp1 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.3876+1853A>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 16/22 | chr7 | 117733060 | |||||||
| chr7:117733106 | G | A | 3 | a0001c0001t0001g0009 a0001c0001t0001g0060 a0001c0001t0001g0069 |
3 | HG01243.hp1 HG02615.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.3876+1807C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 16/22 | chr7 | 117733106 | |||||||
| chr7:117733207 | CT | C | 9 | a0001c0001t0001g0077 a0001c0001t0001g0094 a0001c0001t0001g0095 others(6): Show |
10 | HG01074.hp2 HG01192.hp1 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.3876+1705delA | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 16/22 | chr7 | 117733207 | |||||||
| chr7:117733329 | G | GA | 3 | a0001c0001t0001g0056 a0001c0001t0001g0085 a0010c0010t0001g0120 |
3 | HG02723.hp2 HG03579.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.3876+1583dupT | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 16/22 | chr7 | 117733329 | |||||||
| chr7:117733480 | A | T | 1 | a0003c0003t0002g0128 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.3876+1433T>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 16/22 | chr7 | 117733480 | |||||||
| chr7:117733534 | C | T | 1 | a0001c0001t0003g0075 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.3876+1379G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 16/22 | chr7 | 117733534 | |||||||
| chr7:117733602 | T | C | 2 | a0001c0001t0001g0089 a0001c0001t0002g0090 |
2 | HG01346.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.3876+1311A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 16/22 | chr7 | 117733602 | |||||||
| chr7:117733635 | T | C | 1 | a0001c0001t0001g0076 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.3876+1278A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 16/22 | chr7 | 117733635 | |||||||
| chr7:117733779 | G | A | 1 | a0001c0001t0001g0111 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3876+1134C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 16/22 | chr7 | 117733779 | |||||||
| chr7:117733871 | A | G | 7 | a0001c0001t0001g0044 a0001c0001t0001g0080 a0001c0001t0001g0081 others(4): Show |
7 | HG02258.hp1 HG02280.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.3876+1042T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 16/22 | chr7 | 117733871 | |||||||
| chr7:117734096 | C | T | 1 | a0001c0001t0002g0032 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3876+817G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 16/22 | chr7 | 117734096 | |||||||
| chr7:117734380 | T | C | 9 | a0001c0001t0001g0023 a0001c0001t0001g0056 a0001c0001t0001g0059 others(6): Show |
9 | HG02630.hp2 HG02723.hp2 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.3876+533A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 16/22 | chr7 | 117734380 | |||||||
| chr7:117734487 | A | G | 1 | a0001c0001t0002g0032 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3876+426T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 16/22 | chr7 | 117734487 | |||||||
| chr7:117734705 | G | A | 1 | a0001c0001t0001g0060 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3876+208C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 16/22 | chr7 | 117734705 | |||||||
| chr7:117734765 | C | T | 9 | a0001c0001t0001g0023 a0001c0001t0001g0056 a0001c0001t0001g0059 others(6): Show |
9 | HG02630.hp2 HG02723.hp2 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.3876+148G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 16/22 | chr7 | 117734765 | |||||||
| chr7:117736055 | C | T | 3 | a0001c0001t0001g0089 a0001c0001t0001g0106 a0001c0001t0002g0090 |
3 | HG01346.hp1 HG02145.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.3536-634G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 14/22 | chr7 | 117736055 | |||||||
| chr7:117736057 | G | A | 1 | a0001c0001t0001g0111 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3536-636C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 14/22 | chr7 | 117736057 | |||||||
| chr7:117736181 | G | A | 1 | a0006c0012t0002g0055 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3536-760C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 14/22 | chr7 | 117736181 | |||||||
| chr7:117736270 | C | T | 2 | a0002c0002t0002g0073 a0002c0002t0002g0087 |
2 | HG02818.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.3536-849G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 14/22 | chr7 | 117736270 | |||||||
| chr7:117736274 | G | A | 1 | a0001c0001t0001g0066 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.3536-853C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 14/22 | chr7 | 117736274 | |||||||
| chr7:117736306 | A | G | 3 | a0001c0001t0004g0033 a0001c0001t0004g0039 a0001c0001t0004g0053 |
3 | HG01433.hp1 HG02280.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.3536-885T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 14/22 | chr7 | 117736306 | |||||||
| chr7:117736336 | T | C | 1 | a0001c0001t0001g0057 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3536-915A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 14/22 | chr7 | 117736336 | |||||||
| chr7:117736418 | C | T | 18 | a0001c0001t0001g0044 a0001c0001t0001g0077 a0001c0001t0001g0080 others(15): Show |
19 | HG01074.hp2 HG01192.hp1 HG01433.hp2 others(16): Show |
intron_variant | MODIFIER | c.3536-997G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 14/22 | chr7 | 117736418 | |||||||
| chr7:117736440 | GA | G | 10 | a0001c0001t0001g0023 a0001c0001t0001g0056 a0001c0001t0001g0059 others(7): Show |
10 | HG02451.hp1 HG02630.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.3536-1020delT | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 14/22 | chr7 | 117736440 | |||||||
| chr7:117736645 | G | A | 22 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0020 others(19): Show |
22 | HG01069.hp2 HG01071.hp1 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.3536-1224C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 14/22 | chr7 | 117736645 | |||||||
| chr7:117736975 | T | C | 1 | a0001c0001t0002g0035 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.3536-1554A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 14/22 | chr7 | 117736975 | |||||||
| chr7:117737038 | C | A | 1 | a0001c0001t0001g0020 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.3536-1617G>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 14/22 | chr7 | 117737038 | |||||||
| chr7:117737092 | C | A | 6 | a0001c0001t0001g0044 a0001c0001t0001g0080 a0001c0001t0001g0082 others(3): Show |
6 | HG02258.hp1 HG02280.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.3536-1671G>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 14/22 | chr7 | 117737092 | |||||||
| chr7:117737525 | G | A | 3 | a0001c0001t0001g0070 a0001c0001t0001g0086 a0009c0008t0001g0112 |
3 | HG02602.hp1 HG03491.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.3536-2104C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 14/22 | chr7 | 117737525 | |||||||
| chr7:117737591 | G | T | 78 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0020 others(75): Show |
79 | HG00323.hp1 HG00639.hp2 HG00642.hp2 others(76): Show |
intron_variant | MODIFIER | c.3536-2170C>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 14/22 | chr7 | 117737591 | |||||||
| chr7:117737722 | C | T | 1 | a0001c0001t0001g0016 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.3536-2301G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 14/22 | chr7 | 117737722 | |||||||
| chr7:117737743 | A | T | 3 | a0001c0001t0004g0033 a0001c0001t0004g0039 a0001c0001t0004g0053 |
3 | HG01433.hp1 HG02280.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.3536-2322T>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 14/22 | chr7 | 117737743 | |||||||
| chr7:117737913 | C | T | 1 | a0001c0001t0002g0035 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.3536-2492G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 14/22 | chr7 | 117737913 | |||||||
| chr7:117737928 | G | A | 1 | a0001c0001t0001g0038 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.3536-2507C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 14/22 | chr7 | 117737928 | |||||||
| chr7:117737990 | G | A | 1 | a0001c0001t0001g0125 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.3536-2569C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 14/22 | chr7 | 117737990 | |||||||
| chr7:117738008 | A | C | 1 | a0001c0001t0001g0065 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3536-2587T>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 14/22 | chr7 | 117738008 | |||||||
| chr7:117738073 | G | A | 1 | a0007c0011t0002g0099 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.3536-2652C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 14/22 | chr7 | 117738073 | |||||||
| chr7:117738179 | A | G | 6 | a0001c0001t0001g0044 a0001c0001t0001g0080 a0001c0001t0001g0082 others(3): Show |
6 | HG02258.hp1 HG02280.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.3536-2758T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 14/22 | chr7 | 117738179 | |||||||
| chr7:117738302 | T | C | 81 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0020 others(78): Show |
82 | HG00323.hp1 HG00639.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.3536-2881A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 14/22 | chr7 | 117738302 | |||||||
| chr7:117738449 | C | A | 1 | a0001c0001t0002g0127 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.3536-3028G>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 14/22 | chr7 | 117738449 | |||||||
| chr7:117738508 | C | T | 2 | a0001c0001t0001g0021 a0001c0001t0002g0154 |
2 | HG01358.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3536-3087G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 14/22 | chr7 | 117738508 | |||||||
| chr7:117738890 | T | C | 1 | a0001c0001t0001g0057 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3536-3469A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 14/22 | chr7 | 117738890 | |||||||
| chr7:117739074 | C | T | 26 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0020 others(23): Show |
26 | HG01069.hp2 HG01071.hp1 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.3536-3653G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 14/22 | chr7 | 117739074 | |||||||
| chr7:117739183 | G | C | 3 | a0001c0001t0002g0035 a0002c0002t0002g0073 a0002c0002t0002g0087 |
3 | HG02818.hp2 HG04184.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.3536-3762C>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 14/22 | chr7 | 117739183 | |||||||
| chr7:117739192 | C | T | 31 | a0001c0001t0001g0021 a0001c0001t0001g0044 a0001c0001t0001g0072 others(28): Show |
31 | HG00323.hp1 HG00639.hp2 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.3536-3771G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 14/22 | chr7 | 117739192 | |||||||
| chr7:117739558 | T | A | 2 | a0001c0001t0002g0155 a0001c0001t0002g0156 |
2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.3536-4137A>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 14/22 | chr7 | 117739558 | |||||||
| chr7:117739767 | A | G | 1 | a0001c0001t0001g0054 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.3536-4346T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 14/22 | chr7 | 117739767 | |||||||
| chr7:117739849 | T | C | 3 | a0001c0001t0002g0035 a0002c0002t0002g0073 a0002c0002t0002g0087 |
3 | HG02818.hp2 HG04184.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.3536-4428A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 14/22 | chr7 | 117739849 | |||||||
| chr7:117739881 | A | G | 3 | a0001c0001t0002g0035 a0002c0002t0002g0073 a0002c0002t0002g0087 |
3 | HG02818.hp2 HG04184.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.3536-4460T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 14/22 | chr7 | 117739881 | |||||||
| chr7:117740134 | A | C | 1 | a0002c0002t0002g0073 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3536-4713T>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 14/22 | chr7 | 117740134 | |||||||
| chr7:117740145 | A | G | 27 | a0001c0001t0001g0021 a0001c0001t0001g0044 a0001c0001t0001g0072 others(24): Show |
27 | HG00323.hp1 HG00639.hp2 HG00642.hp2 others(24): Show |
intron_variant | MODIFIER | c.3536-4724T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 14/22 | chr7 | 117740145 | |||||||
| chr7:117740247 | C | T | 3 | a0001c0001t0004g0033 a0001c0001t0004g0039 a0001c0001t0004g0053 |
3 | HG01433.hp1 HG02280.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.3536-4826G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 14/22 | chr7 | 117740247 | |||||||
| chr7:117740266 | T | TAAGTTTT others(329): Show |
1 | a0001c0001t0001g0052 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3536-4846_3536-484 others(340): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 14/22 | chr7 | 117740266 | |||||||
| chr7:117740266 | T | TAAGTTTT others(330): Show |
8 | a0001c0001t0001g0062 a0001c0001t0001g0066 a0001c0001t0001g0084 others(5): Show |
8 | HG01069.hp2 HG01071.hp1 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.3536-4846_3536-484 others(341): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 14/22 | chr7 | 117740266 | |||||||
| chr7:117740266 | T | TAAGTTTT others(330): Show |
2 | a0001c0001t0001g0046 a0001c0001t0001g0074 |
2 | HG02258.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.3536-4846_3536-484 others(341): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 14/22 | chr7 | 117740266 | |||||||
| chr7:117740266 | T | TAAGTTTT others(331): Show |
3 | a0001c0001t0001g0040 a0001c0001t0001g0057 a0001c0001t0005g0152 |
3 | HG02451.hp2 HG03209.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.3536-4846_3536-484 others(342): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 14/22 | chr7 | 117740266 | |||||||
| chr7:117740266 | T | TAAGTTTT others(331): Show |
4 | a0001c0001t0001g0051 a0001c0001t0001g0061 a0001c0001t0001g0107 others(1): Show |
4 | HG02486.hp1 HG02622.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.3536-4846_3536-484 others(342): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 14/22 | chr7 | 117740266 | |||||||
| chr7:117740266 | T | TAAGTTTT others(332): Show |
3 | a0001c0001t0001g0049 a0001c0001t0001g0139 a0001c0001t0005g0048 |
3 | HG02109.hp2 HG02486.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.3536-4846_3536-484 others(343): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 14/22 | chr7 | 117740266 | |||||||
| chr7:117740266 | T | TAAGTTTT others(333): Show |
2 | a0001c0001t0001g0006 a0001c0001t0001g0020 |
2 | HG01361.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.3536-4846_3536-484 others(344): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 14/22 | chr7 | 117740266 | |||||||
| chr7:117740266 | T | TAAGTTTT others(334): Show |
1 | a0001c0001t0001g0009 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.3536-4846_3536-484 others(345): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 14/22 | chr7 | 117740266 | |||||||
| chr7:117740266 | T | TAAGTTTT others(335): Show |
1 | a0001c0001t0001g0069 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3536-4846_3536-484 others(346): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 14/22 | chr7 | 117740266 | |||||||
| chr7:117740266 | T | TAAGTTTT others(341): Show |
1 | a0001c0001t0001g0060 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3536-4846_3536-484 others(352): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 14/22 | chr7 | 117740266 | |||||||
| chr7:117740568 | T | C | 30 | a0001c0001t0001g0021 a0001c0001t0001g0044 a0001c0001t0001g0072 others(27): Show |
30 | HG00323.hp1 HG00639.hp2 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.3536-5147A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 14/22 | chr7 | 117740568 | |||||||
| chr7:117740675 | C | T | 1 | a0001c0001t0001g0072 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.3535+5156G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 14/22 | chr7 | 117740675 | |||||||
| chr7:117740721 | G | A | 13 | a0001c0001t0001g0023 a0001c0001t0001g0056 a0001c0001t0001g0059 others(10): Show |
13 | HG02145.hp1 HG02451.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.3535+5110C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 14/22 | chr7 | 117740721 | |||||||
| chr7:117740972 | G | A | 2 | a0001c0001t0001g0066 a0001c0001t0001g0084 |
2 | NA18522.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.3535+4859C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 14/22 | chr7 | 117740972 | |||||||
| chr7:117741271 | A | G | 1 | a0001c0001t0001g0110 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.3535+4560T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 14/22 | chr7 | 117741271 | |||||||
| chr7:117741339 | C | T | 28 | a0001c0001t0001g0021 a0001c0001t0001g0044 a0001c0001t0001g0072 others(25): Show |
28 | HG00323.hp1 HG00639.hp2 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.3535+4492G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 14/22 | chr7 | 117741339 | |||||||
| chr7:117741419 | A | G | 1 | a0001c0001t0001g0072 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.3535+4412T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 14/22 | chr7 | 117741419 | |||||||
| chr7:117741490 | AT | A | 16 | a0001c0001t0001g0021 a0001c0001t0001g0126 a0001c0001t0001g0157 others(13): Show |
16 | HG00323.hp1 HG00639.hp2 HG00642.hp2 others(13): Show |
intron_variant | MODIFIER | c.3535+4340delA | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 14/22 | chr7 | 117741490 | |||||||
| chr7:117741752 | A | T | 81 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0020 others(78): Show |
82 | HG00323.hp1 HG00639.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.3535+4079T>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 14/22 | chr7 | 117741752 | |||||||
| chr7:117741789 | T | C | 1 | a0001c0007t0001g0010 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.3535+4042A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 14/22 | chr7 | 117741789 | |||||||
| chr7:117742207 | A | G | 75 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0020 others(72): Show |
76 | HG00323.hp1 HG00639.hp2 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.3535+3624T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 14/22 | chr7 | 117742207 | |||||||
| chr7:117742231 | C | T | 12 | a0001c0001t0001g0077 a0001c0001t0001g0094 a0001c0001t0001g0095 others(9): Show |
13 | HG01074.hp2 HG01192.hp1 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.3535+3600G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 14/22 | chr7 | 117742231 | |||||||
| chr7:117742446 | T | G | 3 | a0001c0001t0002g0035 a0002c0002t0002g0073 a0002c0002t0002g0087 |
3 | HG02818.hp2 HG04184.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.3535+3385A>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 14/22 | chr7 | 117742446 | |||||||
| chr7:117742703 | C | T | 22 | a0001c0001t0001g0023 a0001c0001t0001g0044 a0001c0001t0001g0056 others(19): Show |
22 | HG02145.hp1 HG02258.hp1 HG02280.hp1 others(19): Show |
intron_variant | MODIFIER | c.3535+3128G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 14/22 | chr7 | 117742703 | |||||||
| chr7:117742875 | C | T | 7 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0103 others(4): Show |
7 | HG00323.hp2 HG01952.hp1 NA18954.hp2 others(4): Show |
intron_variant | MODIFIER | c.3535+2956G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 14/22 | chr7 | 117742875 | |||||||
| chr7:117742956 | C | A | 20 | a0001c0001t0001g0044 a0001c0001t0001g0077 a0001c0001t0001g0080 others(17): Show |
20 | HG01433.hp1 HG01433.hp2 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.3535+2875G>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 14/22 | chr7 | 117742956 | |||||||
| chr7:117743122 | G | T | 26 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0020 others(23): Show |
26 | HG01069.hp2 HG01071.hp1 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.3535+2709C>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 14/22 | chr7 | 117743122 | |||||||
| chr7:117743141 | A | C | 1 | a0001c0001t0002g0035 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.3535+2690T>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 14/22 | chr7 | 117743141 | |||||||
| chr7:117743169 | C | T | 2 | a0001c0001t0002g0047 a0001c0006t0002g0079 |
2 | HG02723.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.3535+2662G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 14/22 | chr7 | 117743169 | |||||||
| chr7:117743258 | A | G | 61 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0020 others(58): Show |
61 | HG01069.hp2 HG01071.hp1 HG01074.hp1 others(58): Show |
intron_variant | MODIFIER | c.3535+2573T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 14/22 | chr7 | 117743258 | |||||||
| chr7:117743395 | G | T | 35 | a0001c0001t0001g0023 a0001c0001t0001g0044 a0001c0001t0001g0056 others(32): Show |
35 | HG01433.hp1 HG01433.hp2 HG02145.hp1 others(32): Show |
intron_variant | MODIFIER | c.3535+2436C>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 14/22 | chr7 | 117743395 | |||||||
| chr7:117743688 | C | T | 26 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0020 others(23): Show |
26 | HG01069.hp2 HG01071.hp1 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.3535+2143G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 14/22 | chr7 | 117743688 | |||||||
| chr7:117743761 | C | CA | 34 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0014 others(31): Show |
34 | HG01192.hp2 HG01243.hp2 HG01346.hp1 others(31): Show |
intron_variant | MODIFIER | c.3535+2069dupT | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 14/22 | chr7 | 117743761 | |||||||
| chr7:117743761 | C | CAA | 10 | a0001c0001t0001g0071 a0001c0001t0001g0082 a0001c0001t0001g0110 others(7): Show |
10 | HG01433.hp1 HG02145.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.3535+2068_3535+206 others(6): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 14/22 | chr7 | 117743761 | |||||||
| chr7:117743761 | CA | C | 31 | a0001c0001t0001g0006 a0001c0001t0001g0020 a0001c0001t0001g0021 others(28): Show |
31 | HG00323.hp1 HG00642.hp2 HG01071.hp1 others(28): Show |
intron_variant | MODIFIER | c.3535+2069delT | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 14/22 | chr7 | 117743761 | |||||||
| chr7:117743761 | CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0001g0081 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3535+2059_3535+206 others(15): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 14/22 | chr7 | 117743761 | |||||||
| chr7:117744023 | A | T | 15 | a0001c0001t0001g0023 a0001c0001t0001g0056 a0001c0001t0001g0059 others(12): Show |
15 | HG02145.hp1 HG02451.hp1 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.3535+1808T>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 14/22 | chr7 | 117744023 | |||||||
| chr7:117744162 | C | A | 1 | a0001c0001t0001g0114 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.3535+1669G>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 14/22 | chr7 | 117744162 | |||||||
| chr7:117744284 | AT | A | 15 | a0001c0001t0001g0023 a0001c0001t0001g0056 a0001c0001t0001g0059 others(12): Show |
15 | HG02145.hp1 HG02451.hp1 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.3535+1546delA | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 14/22 | chr7 | 117744284 | |||||||
| chr7:117744498 | T | C | 1 | a0001c0001t0001g0157 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.3535+1333A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 14/22 | chr7 | 117744498 | |||||||
| chr7:117744728 | TAC | T | 79 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0020 others(76): Show |
79 | HG00323.hp1 HG00642.hp2 HG01069.hp2 others(76): Show |
intron_variant | MODIFIER | c.3535+1101_3535+110 others(6): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 14/22 | chr7 | 117744728 | |||||||
| chr7:117745224 | G | A | 15 | a0001c0001t0001g0023 a0001c0001t0001g0056 a0001c0001t0001g0059 others(12): Show |
15 | HG02145.hp1 HG02451.hp1 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.3535+607C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 14/22 | chr7 | 117745224 | |||||||
| chr7:117745383 | A | G | 1 | a0001c0001t0001g0064 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.3535+448T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 14/22 | chr7 | 117745383 | |||||||
| chr7:117745535 | A | G | 1 | a0001c0001t0002g0162 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.3535+296T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 14/22 | chr7 | 117745535 | |||||||
| chr7:117745620 | A | AATAACAA others(3): Show |
80 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0020 others(77): Show |
81 | HG00323.hp1 HG00642.hp2 HG01069.hp2 others(78): Show |
intron_variant | MODIFIER | c.3535+210_3535+211i others(12): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 14/22 | chr7 | 117745620 | |||||||
| chr7:117745743 | C | T | 1 | a0001c0001t0001g0072 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.3535+88G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 14/22 | chr7 | 117745743 | |||||||
| chr7:117745752 | A | G | 3 | a0001c0001t0001g0009 a0001c0001t0001g0060 a0001c0001t0001g0069 |
3 | HG01243.hp1 HG02615.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.3535+79T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 14/22 | chr7 | 117745752 | |||||||
| chr7:117746147 | G | T | 1 | a0001c0001t0001g0044 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3349-48C>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 12/22 | chr7 | 117746147 | |||||||
| chr7:117746300 | G | A | 1 | a0003c0003t0002g0028 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.3349-201C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 12/22 | chr7 | 117746300 | |||||||
| chr7:117746323 | A | AT | 3 | a0001c0001t0001g0089 a0001c0001t0001g0106 a0001c0001t0002g0090 |
3 | HG01346.hp1 HG02145.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.3349-225dupA | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 12/22 | chr7 | 117746323 | |||||||
| chr7:117746351 | G | A | 8 | a0001c0001t0001g0077 a0001c0001t0001g0094 a0001c0001t0001g0095 others(5): Show |
8 | HG01433.hp2 HG02257.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.3349-252C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 12/22 | chr7 | 117746351 | |||||||
| chr7:117746522 | G | A | 1 | a0001c0001t0001g0161 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.3349-423C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 12/22 | chr7 | 117746522 | |||||||
| chr7:117746635 | G | T | 15 | a0001c0001t0001g0023 a0001c0001t0001g0056 a0001c0001t0001g0059 others(12): Show |
15 | HG02145.hp1 HG02451.hp1 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.3349-536C>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 12/22 | chr7 | 117746635 | |||||||
| chr7:117746676 | T | C | 1 | a0001c0001t0001g0140 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.3349-577A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 12/22 | chr7 | 117746676 | |||||||
| chr7:117746879 | G | T | 2 | a0001c0001t0001g0066 a0001c0001t0001g0084 |
2 | NA18522.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.3349-780C>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 12/22 | chr7 | 117746879 | |||||||
| chr7:117746922 | C | T | 2 | a0001c0001t0002g0047 a0001c0006t0002g0079 |
2 | HG02723.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.3349-823G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 12/22 | chr7 | 117746922 | |||||||
| chr7:117747054 | C | T | 26 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0020 others(23): Show |
26 | HG01069.hp2 HG01071.hp1 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.3349-955G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 12/22 | chr7 | 117747054 | |||||||
| chr7:117747352 | A | AAGAT | 3 | a0001c0001t0001g0009 a0001c0001t0001g0060 a0001c0001t0001g0069 |
3 | HG01243.hp1 HG02615.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.3349-1257_3349-125 others(8): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 12/22 | chr7 | 117747352 | |||||||
| chr7:117747598 | C | T | 1 | a0001c0001t0001g0136 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.3349-1499G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 12/22 | chr7 | 117747598 | |||||||
| chr7:117748035 | AGGCTTAC | A | 13 | a0001c0001t0001g0023 a0001c0001t0001g0056 a0001c0001t0001g0059 others(10): Show |
13 | HG02145.hp1 HG02451.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.3349-1943_3349-193 others(11): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 12/22 | chr7 | 117748035 | |||||||
| chr7:117748050 | GTGCA | G | 3 | a0001c0001t0001g0089 a0001c0001t0001g0106 a0001c0001t0002g0090 |
3 | HG01346.hp1 HG02145.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.3349-1955_3349-195 others(8): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 12/22 | chr7 | 117748050 | |||||||
| chr7:117748055 | G | A | 3 | a0001c0001t0001g0089 a0001c0001t0001g0106 a0001c0001t0002g0090 |
3 | HG01346.hp1 HG02145.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.3349-1956C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 12/22 | chr7 | 117748055 | |||||||
| chr7:117748205 | G | T | 3 | a0001c0001t0001g0089 a0001c0001t0001g0106 a0001c0001t0002g0090 |
3 | HG01346.hp1 HG02145.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.3349-2106C>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 12/22 | chr7 | 117748205 | |||||||
| chr7:117748264 | C | G | 13 | a0001c0001t0001g0023 a0001c0001t0001g0056 a0001c0001t0001g0059 others(10): Show |
13 | HG02145.hp1 HG02451.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.3349-2165G>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 12/22 | chr7 | 117748264 | |||||||
| chr7:117748299 | T | G | 1 | a0001c0001t0001g0133 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.3349-2200A>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 12/22 | chr7 | 117748299 | |||||||
| chr7:117748417 | A | T | 35 | a0001c0001t0001g0023 a0001c0001t0001g0044 a0001c0001t0001g0056 others(32): Show |
35 | HG01433.hp1 HG01433.hp2 HG02145.hp1 others(32): Show |
intron_variant | MODIFIER | c.3349-2318T>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 12/22 | chr7 | 117748417 | |||||||
| chr7:117748569 | C | T | 34 | a0001c0001t0001g0023 a0001c0001t0001g0044 a0001c0001t0001g0056 others(31): Show |
34 | HG01433.hp1 HG01433.hp2 HG02145.hp1 others(31): Show |
intron_variant | MODIFIER | c.3349-2470G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 12/22 | chr7 | 117748569 | |||||||
| chr7:117748694 | T | C | 19 | a0001c0001t0001g0021 a0001c0001t0001g0072 a0001c0001t0001g0126 others(16): Show |
20 | HG00323.hp1 HG00642.hp2 HG01074.hp2 others(17): Show |
intron_variant | MODIFIER | c.3349-2595A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 12/22 | chr7 | 117748694 | |||||||
| chr7:117748742 | C | A | 1 | a0009c0008t0001g0112 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.3349-2643G>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 12/22 | chr7 | 117748742 | |||||||
| chr7:117748869 | G | A | 1 | a0001c0001t0001g0116 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.3349-2770C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 12/22 | chr7 | 117748869 | |||||||
| chr7:117749215 | C | T | 3 | a0001c0001t0004g0033 a0001c0001t0004g0039 a0001c0001t0004g0053 |
3 | HG01433.hp1 HG02280.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.3349-3116G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 12/22 | chr7 | 117749215 | |||||||
| chr7:117749257 | C | G | 61 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0020 others(58): Show |
61 | HG01069.hp2 HG01071.hp1 HG01074.hp1 others(58): Show |
intron_variant | MODIFIER | c.3349-3158G>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 12/22 | chr7 | 117749257 | |||||||
| chr7:117749479 | C | T | 1 | a0001c0001t0003g0121 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.3349-3380G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 12/22 | chr7 | 117749479 | |||||||
| chr7:117749582 | C | T | 1 | a0001c0001t0002g0022 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3349-3483G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 12/22 | chr7 | 117749582 | |||||||
| chr7:117749701 | CTTTT | C | 3 | a0001c0001t0001g0089 a0001c0001t0001g0106 a0001c0001t0002g0090 |
3 | HG01346.hp1 HG02145.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.3349-3606_3349-360 others(8): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 12/22 | chr7 | 117749701 | |||||||
| chr7:117749918 | T | C | 16 | a0001c0001t0001g0021 a0001c0001t0001g0072 a0001c0001t0001g0126 others(13): Show |
16 | HG00323.hp1 HG00642.hp2 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.3349-3819A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 12/22 | chr7 | 117749918 | |||||||
| chr7:117750008 | A | G | 2 | a0001c0001t0001g0132 a0001c0017t0001g0043 |
2 | NA18969.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.3349-3909T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 12/22 | chr7 | 117750008 | |||||||
| chr7:117750610 | T | G | 1 | a0001c0001t0001g0163 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.3349-4511A>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 12/22 | chr7 | 117750610 | |||||||
| chr7:117750643 | A | C | 1 | a0001c0007t0001g0010 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.3349-4544T>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 12/22 | chr7 | 117750643 | |||||||
| chr7:117750699 | T | C | 1 | a0001c0001t0001g0086 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.3349-4600A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 12/22 | chr7 | 117750699 | |||||||
| chr7:117750849 | A | G | 9 | a0001c0001t0001g0044 a0001c0001t0001g0080 a0001c0001t0001g0081 others(6): Show |
9 | HG02258.hp1 HG02280.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.3349-4750T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 12/22 | chr7 | 117750849 | |||||||
| chr7:117750965 | T | A | 35 | a0001c0001t0001g0023 a0001c0001t0001g0044 a0001c0001t0001g0056 others(32): Show |
35 | HG01433.hp1 HG01433.hp2 HG02145.hp1 others(32): Show |
intron_variant | MODIFIER | c.3349-4866A>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 12/22 | chr7 | 117750965 | |||||||
| chr7:117751249 | C | T | 3 | a0001c0001t0001g0089 a0001c0001t0001g0106 a0001c0001t0002g0090 |
3 | HG01346.hp1 HG02145.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.3349-5150G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 12/22 | chr7 | 117751249 | |||||||
| chr7:117751309 | G | A | 1 | a0001c0001t0001g0038 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.3349-5210C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 12/22 | chr7 | 117751309 | |||||||
| chr7:117751374 | C | T | 15 | a0001c0001t0001g0023 a0001c0001t0001g0056 a0001c0001t0001g0059 others(12): Show |
15 | HG02145.hp1 HG02451.hp1 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.3348+5181G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 12/22 | chr7 | 117751374 | |||||||
| chr7:117751524 | C | T | 3 | a0001c0001t0001g0023 a0001c0001t0001g0059 a0001c0001t0001g0117 |
3 | HG02922.hp2 HG06807.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.3348+5031G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 12/22 | chr7 | 117751524 | |||||||
| chr7:117751755 | A | G | 1 | a0001c0001t0001g0072 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.3348+4800T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 12/22 | chr7 | 117751755 | |||||||
| chr7:117751973 | G | A | 1 | a0002c0002t0002g0087 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3348+4582C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 12/22 | chr7 | 117751973 | |||||||
| chr7:117752359 | C | T | 35 | a0001c0001t0001g0023 a0001c0001t0001g0044 a0001c0001t0001g0056 others(32): Show |
35 | HG01433.hp1 HG01433.hp2 HG02145.hp1 others(32): Show |
intron_variant | MODIFIER | c.3348+4196G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 12/22 | chr7 | 117752359 | |||||||
| chr7:117752387 | G | C | 1 | a0001c0001t0001g0057 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3348+4168C>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 12/22 | chr7 | 117752387 | |||||||
| chr7:117752719 | A | G | 26 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0020 others(23): Show |
26 | HG01069.hp2 HG01071.hp1 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.3348+3836T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 12/22 | chr7 | 117752719 | |||||||
| chr7:117753455 | G | A | 2 | a0001c0001t0001g0094 a0001c0001t0001g0095 |
2 | HG02970.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.3348+3100C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 12/22 | chr7 | 117753455 | |||||||
| chr7:117753462 | T | C | 61 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0020 others(58): Show |
61 | HG01069.hp2 HG01071.hp1 HG01074.hp1 others(58): Show |
intron_variant | MODIFIER | c.3348+3093A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 12/22 | chr7 | 117753462 | |||||||
| chr7:117753549 | A | T | 1 | a0001c0001t0001g0136 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.3348+3006T>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 12/22 | chr7 | 117753549 | |||||||
| chr7:117753557 | T | C | 16 | a0001c0001t0001g0021 a0001c0001t0001g0072 a0001c0001t0001g0126 others(13): Show |
16 | HG00323.hp1 HG00642.hp2 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.3348+2998A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 12/22 | chr7 | 117753557 | |||||||
| chr7:117753764 | TG | T | 16 | a0001c0001t0001g0021 a0001c0001t0001g0072 a0001c0001t0001g0126 others(13): Show |
16 | HG00323.hp1 HG00642.hp2 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.3348+2790delC | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 12/22 | chr7 | 117753764 | |||||||
| chr7:117754150 | C | T | 61 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0020 others(58): Show |
61 | HG01069.hp2 HG01071.hp1 HG01074.hp1 others(58): Show |
intron_variant | MODIFIER | c.3348+2405G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 12/22 | chr7 | 117754150 | |||||||
| chr7:117754164 | C | T | 61 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0020 others(58): Show |
61 | HG01069.hp2 HG01071.hp1 HG01074.hp1 others(58): Show |
intron_variant | MODIFIER | c.3348+2391G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 12/22 | chr7 | 117754164 | |||||||
| chr7:117754256 | G | A | 1 | a0001c0001t0004g0039 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.3348+2299C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 12/22 | chr7 | 117754256 | |||||||
| chr7:117754539 | C | A | 8 | a0001c0001t0001g0077 a0001c0001t0001g0094 a0001c0001t0001g0095 others(5): Show |
8 | HG01433.hp2 HG02257.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.3348+2016G>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 12/22 | chr7 | 117754539 | |||||||
| chr7:117754590 | T | C | 10 | a0001c0001t0001g0021 a0001c0001t0001g0126 a0001c0001t0001g0157 others(7): Show |
10 | HG00323.hp1 HG00642.hp2 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.3348+1965A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 12/22 | chr7 | 117754590 | |||||||
| chr7:117754970 | C | T | 1 | a0001c0001t0001g0101 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.3348+1585G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 12/22 | chr7 | 117754970 | |||||||
| chr7:117755106 | C | G | 77 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0020 others(74): Show |
77 | HG00323.hp1 HG00642.hp2 HG01069.hp2 others(74): Show |
intron_variant | MODIFIER | c.3348+1449G>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 12/22 | chr7 | 117755106 | |||||||
| chr7:117755173 | G | A | 1 | a0001c0001t0002g0027 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.3348+1382C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 12/22 | chr7 | 117755173 | |||||||
| chr7:117755224 | G | A | 3 | a0001c0001t0002g0027 a0001c0001t0002g0037 a0007c0011t0002g0099 |
3 | HG02040.hp1 HG03017.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.3348+1331C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 12/22 | chr7 | 117755224 | |||||||
| chr7:117755413 | T | C | 1 | a0001c0001t0001g0140 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.3348+1142A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 12/22 | chr7 | 117755413 | |||||||
| chr7:117755471 | TCA | T | 13 | a0001c0001t0001g0023 a0001c0001t0001g0056 a0001c0001t0001g0059 others(10): Show |
13 | HG02145.hp1 HG02451.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.3348+1082_3348+108 others(6): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 12/22 | chr7 | 117755471 | |||||||
| chr7:117755548 | T | C | 3 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0082 |
3 | HG02280.hp1 HG03579.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.3348+1007A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 12/22 | chr7 | 117755548 | |||||||
| chr7:117755610 | T | G | 3 | a0001c0001t0001g0089 a0001c0001t0001g0106 a0001c0001t0002g0090 |
3 | HG01346.hp1 HG02145.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.3348+945A>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 12/22 | chr7 | 117755610 | |||||||
| chr7:117755834 | T | C | 83 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0020 others(80): Show |
84 | HG00323.hp1 HG00642.hp2 HG01069.hp2 others(81): Show |
intron_variant | MODIFIER | c.3348+721A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 12/22 | chr7 | 117755834 | |||||||
| chr7:117755941 | A | G | 83 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0020 others(80): Show |
84 | HG00323.hp1 HG00642.hp2 HG01069.hp2 others(81): Show |
intron_variant | MODIFIER | c.3348+614T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 12/22 | chr7 | 117755941 | |||||||
| chr7:117756139 | G | A | 19 | a0001c0001t0001g0021 a0001c0001t0001g0072 a0001c0001t0001g0126 others(16): Show |
20 | HG00323.hp1 HG00642.hp2 HG01074.hp2 others(17): Show |
intron_variant | MODIFIER | c.3348+416C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 12/22 | chr7 | 117756139 | |||||||
| chr7:117756186 | C | G | 1 | a0001c0001t0001g0076 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.3348+369G>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 12/22 | chr7 | 117756186 | |||||||
| chr7:117756250 | T | C | 3 | a0001c0001t0001g0089 a0001c0001t0001g0106 a0001c0001t0002g0090 |
3 | HG01346.hp1 HG02145.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.3348+305A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 12/22 | chr7 | 117756250 | |||||||
| chr7:117756330 | A | T | 1 | a0001c0001t0001g0157 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.3348+225T>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 12/22 | chr7 | 117756330 | |||||||
| chr7:117756342 | T | C | 13 | a0001c0001t0001g0023 a0001c0001t0001g0056 a0001c0001t0001g0059 others(10): Show |
13 | HG02145.hp1 HG02451.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.3348+213A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 12/22 | chr7 | 117756342 | |||||||
| chr7:117756437 | G | A | 4 | a0001c0001t0001g0056 a0001c0001t0001g0085 a0001c0001t0002g0032 others(1): Show |
4 | HG02145.hp1 HG02723.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.3348+118C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 12/22 | chr7 | 117756437 | |||||||
| chr7:117756652 | C | T | 1 | a0001c0001t0001g0163 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.3269-18G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 11/22 | chr7 | 117756652 | |||||||
| chr7:117756923 | C | T | 11 | a0001c0001t0001g0077 a0001c0001t0001g0094 a0001c0001t0001g0095 others(8): Show |
11 | HG01433.hp1 HG01433.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.3269-289G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 11/22 | chr7 | 117756923 | |||||||
| chr7:117757000 | T | C | 1 | a0001c0001t0003g0137 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.3269-366A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 11/22 | chr7 | 117757000 | |||||||
| chr7:117757010 | T | C | 1 | a0001c0001t0001g0126 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3269-376A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 11/22 | chr7 | 117757010 | |||||||
| chr7:117757198 | G | C | 1 | a0010c0010t0001g0120 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3269-564C>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 11/22 | chr7 | 117757198 | |||||||
| chr7:117757267 | C | T | 1 | a0001c0001t0001g0062 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3268+608G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 11/22 | chr7 | 117757267 | |||||||
| chr7:117757435 | T | G | 5 | a0001c0001t0001g0066 a0001c0001t0001g0084 a0001c0001t0005g0034 others(2): Show |
5 | HG02486.hp2 HG02965.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.3268+440A>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 11/22 | chr7 | 117757435 | |||||||
| chr7:117757528 | T | TA | 27 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0041 others(24): Show |
27 | HG00323.hp1 HG00642.hp2 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.3268+346dupT | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 11/22 | chr7 | 117757528 | |||||||
| chr7:117757528 | TA | T | 22 | a0001c0001t0001g0011 a0001c0001t0001g0023 a0001c0001t0001g0044 others(19): Show |
22 | HG01346.hp1 HG02145.hp2 HG02258.hp1 others(19): Show |
intron_variant | MODIFIER | c.3268+346delT | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 11/22 | chr7 | 117757528 | |||||||
| chr7:117757677 | T | C | 3 | a0001c0001t0001g0089 a0001c0001t0001g0106 a0001c0001t0002g0090 |
3 | HG01346.hp1 HG02145.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.3268+198A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 11/22 | chr7 | 117757677 | |||||||
| chr7:117758184 | T | G | 1 | a0001c0001t0001g0146 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.3173-214A>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 10/22 | chr7 | 117758184 | |||||||
| chr7:117758188 | C | A | 1 | a0001c0001t0001g0064 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.3173-218G>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 10/22 | chr7 | 117758188 | |||||||
| chr7:117758424 | A | G | 1 | a0001c0001t0001g0011 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.3173-454T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 10/22 | chr7 | 117758424 | |||||||
| chr7:117758550 | T | G | 83 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0020 others(80): Show |
84 | HG00323.hp1 HG00642.hp2 HG01069.hp2 others(81): Show |
intron_variant | MODIFIER | c.3173-580A>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 10/22 | chr7 | 117758550 | |||||||
| chr7:117758800 | T | C | 1 | a0001c0001t0001g0017 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.3173-830A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 10/22 | chr7 | 117758800 | |||||||
| chr7:117759094 | A | G | 1 | a0001c0001t0003g0075 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.3173-1124T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 10/22 | chr7 | 117759094 | |||||||
| chr7:117759212 | G | A | 1 | a0001c0001t0001g0148 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.3172+1223C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 10/22 | chr7 | 117759212 | |||||||
| chr7:117759880 | T | C | 11 | a0001c0001t0001g0077 a0001c0001t0001g0094 a0001c0001t0001g0095 others(8): Show |
11 | HG01433.hp1 HG01433.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.3172+555A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 10/22 | chr7 | 117759880 | |||||||
| chr7:117760027 | C | T | 1 | a0001c0001t0001g0045 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.3172+408G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 10/22 | chr7 | 117760027 | |||||||
| chr7:117760259 | A | G | 2 | a0001c0001t0001g0021 a0001c0001t0002g0154 |
2 | HG01358.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3172+176T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 10/22 | chr7 | 117760259 | |||||||
| chr7:117760916 | C | A | 16 | a0001c0001t0001g0021 a0001c0001t0001g0072 a0001c0001t0001g0126 others(13): Show |
16 | HG00323.hp1 HG00642.hp2 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.2897-206G>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 9/22 | chr7 | 117760916 | |||||||
| chr7:117761167 | T | A | 1 | a0001c0001t0001g0124 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2897-457A>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 9/22 | chr7 | 117761167 | |||||||
| chr7:117761344 | G | A | 80 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0020 others(77): Show |
80 | HG00323.hp1 HG00642.hp2 HG01069.hp2 others(77): Show |
intron_variant | MODIFIER | c.2897-634C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 9/22 | chr7 | 117761344 | |||||||
| chr7:117761353 | G | C | 2 | a0001c0001t0001g0066 a0001c0001t0001g0084 |
2 | NA18522.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2897-643C>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 9/22 | chr7 | 117761353 | |||||||
| chr7:117761744 | A | C | 1 | a0001c0001t0002g0090 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2897-1034T>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 9/22 | chr7 | 117761744 | |||||||
| chr7:117761871 | C | A | 26 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0020 others(23): Show |
26 | HG01069.hp2 HG01071.hp1 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.2897-1161G>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 9/22 | chr7 | 117761871 | |||||||
| chr7:117762014 | C | T | 34 | a0001c0001t0001g0023 a0001c0001t0001g0044 a0001c0001t0001g0056 others(31): Show |
34 | HG01433.hp1 HG01433.hp2 HG02145.hp1 others(31): Show |
intron_variant | MODIFIER | c.2897-1304G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 9/22 | chr7 | 117762014 | |||||||
| chr7:117762112 | A | G | 1 | a0001c0001t0002g0130 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2897-1402T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 9/22 | chr7 | 117762112 | |||||||
| chr7:117762299 | T | C | 1 | a0001c0001t0001g0063 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.2897-1589A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 9/22 | chr7 | 117762299 | |||||||
| chr7:117762711 | G | A | 1 | a0001c0001t0001g0089 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2897-2001C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 9/22 | chr7 | 117762711 | |||||||
| chr7:117762775 | G | A | 8 | a0001c0001t0001g0044 a0001c0001t0001g0080 a0001c0001t0001g0082 others(5): Show |
8 | HG02258.hp1 HG02280.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.2897-2065C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 9/22 | chr7 | 117762775 | |||||||
| chr7:117763248 | A | C | 1 | a0001c0001t0001g0140 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2897-2538T>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 9/22 | chr7 | 117763248 | |||||||
| chr7:117763439 | G | A | 1 | a0001c0001t0001g0072 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2897-2729C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 9/22 | chr7 | 117763439 | |||||||
| chr7:117763555 | CT | C | 13 | a0001c0001t0001g0016 a0001c0001t0001g0077 a0001c0001t0001g0094 others(10): Show |
13 | HG01258.hp1 HG01433.hp2 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.2897-2846delA | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 9/22 | chr7 | 117763555 | |||||||
| chr7:117763555 | CTT | C | 38 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0044 others(35): Show |
38 | HG00323.hp1 HG00642.hp2 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.2897-2847_2897-284 others(6): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 9/22 | chr7 | 117763555 | |||||||
| chr7:117763555 | CTTTTTTT others(1): Show |
C | 25 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0020 others(22): Show |
25 | HG01069.hp2 HG01071.hp1 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.2897-2853_2897-284 others(12): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 9/22 | chr7 | 117763555 | |||||||
| chr7:117763717 | G | A | 1 | a0001c0001t0001g0074 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2897-3007C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 9/22 | chr7 | 117763717 | |||||||
| chr7:117763876 | A | C | 61 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0020 others(58): Show |
61 | HG01069.hp2 HG01071.hp1 HG01074.hp1 others(58): Show |
intron_variant | MODIFIER | c.2897-3166T>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 9/22 | chr7 | 117763876 | |||||||
| chr7:117764031 | C | G | 3 | a0001c0001t0004g0033 a0001c0001t0004g0039 a0001c0001t0004g0053 |
3 | HG01433.hp1 HG02280.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.2896+3028G>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 9/22 | chr7 | 117764031 | |||||||
| chr7:117764417 | G | C | 1 | a0001c0001t0005g0034 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2896+2642C>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 9/22 | chr7 | 117764417 | |||||||
| chr7:117765064 | C | T | 66 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0020 others(63): Show |
66 | HG01069.hp2 HG01071.hp1 HG01074.hp1 others(63): Show |
intron_variant | MODIFIER | c.2896+1995G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 9/22 | chr7 | 117765064 | |||||||
| chr7:117765093 | G | A | 3 | a0001c0001t0001g0089 a0001c0001t0001g0106 a0001c0001t0002g0090 |
3 | HG01346.hp1 HG02145.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.2896+1966C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 9/22 | chr7 | 117765093 | |||||||
| chr7:117765216 | G | A | 2 | a0001c0001t0002g0047 a0001c0006t0002g0079 |
2 | HG02723.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.2896+1843C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 9/22 | chr7 | 117765216 | |||||||
| chr7:117765266 | G | A | 8 | a0001c0001t0001g0077 a0001c0001t0001g0094 a0001c0001t0001g0095 others(5): Show |
8 | HG01433.hp2 HG02257.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.2896+1793C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 9/22 | chr7 | 117765266 | |||||||
| chr7:117765845 | T | C | 1 | a0001c0001t0001g0111 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2896+1214A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 9/22 | chr7 | 117765845 | |||||||
| chr7:117765955 | C | T | 2 | a0001c0001t0001g0041 a0001c0016t0001g0058 |
2 | HG00609.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.2896+1104G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 9/22 | chr7 | 117765955 | |||||||
| chr7:117766035 | C | T | 66 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0020 others(63): Show |
66 | HG01069.hp2 HG01071.hp1 HG01074.hp1 others(63): Show |
intron_variant | MODIFIER | c.2896+1024G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 9/22 | chr7 | 117766035 | |||||||
| chr7:117766150 | G | A | 8 | a0001c0001t0001g0077 a0001c0001t0001g0094 a0001c0001t0001g0095 others(5): Show |
8 | HG01433.hp2 HG02257.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.2896+909C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 9/22 | chr7 | 117766150 | |||||||
| chr7:117766184 | G | A | 83 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0020 others(80): Show |
84 | HG00323.hp1 HG00642.hp2 HG01069.hp2 others(81): Show |
intron_variant | MODIFIER | c.2896+875C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 9/22 | chr7 | 117766184 | |||||||
| chr7:117766235 | C | T | 1 | a0001c0001t0001g0132 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.2896+824G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 9/22 | chr7 | 117766235 | |||||||
| chr7:117766284 | C | A | 2 | a0001c0001t0001g0072 a0001c0001t0002g0035 |
2 | HG04184.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2896+775G>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 9/22 | chr7 | 117766284 | |||||||
| chr7:117766290 | C | T | 1 | a0001c0001t0001g0126 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2896+769G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 9/22 | chr7 | 117766290 | |||||||
| chr7:117767556 | C | A | 8 | a0001c0001t0001g0072 a0001c0001t0001g0089 a0001c0001t0001g0106 others(5): Show |
9 | HG01074.hp2 HG01192.hp1 HG01346.hp1 others(6): Show |
intron_variant | MODIFIER | c.2779-380G>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/22 | chr7 | 117767556 | |||||||
| chr7:117767779 | T | C | 26 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0020 others(23): Show |
26 | HG01069.hp2 HG01071.hp1 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.2779-603A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/22 | chr7 | 117767779 | |||||||
| chr7:117767827 | C | A | 1 | a0001c0001t0001g0148 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.2779-651G>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/22 | chr7 | 117767827 | |||||||
| chr7:117767828 | G | A | 1 | a0001c0001t0001g0135 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.2779-652C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/22 | chr7 | 117767828 | |||||||
| chr7:117767870 | G | C | 7 | a0001c0001t0001g0046 a0001c0001t0001g0051 a0001c0001t0001g0052 others(4): Show |
7 | HG02258.hp2 HG02486.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.2779-694C>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/22 | chr7 | 117767870 | |||||||
| chr7:117768091 | G | GCA | 13 | a0001c0001t0001g0021 a0001c0001t0001g0126 a0001c0001t0001g0157 others(10): Show |
13 | HG00323.hp1 HG00642.hp2 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.2779-917_2779-916d others(4): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/22 | chr7 | 117768091 | |||||||
| chr7:117768091 | GCA | G | 137 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(134): Show |
138 | HG00323.hp2 HG00609.hp1 HG00609.hp2 others(135): Show |
intron_variant | MODIFIER | c.2779-917_2779-916d others(4): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/22 | chr7 | 117768091 | |||||||
| chr7:117768117 | C | A | 1 | a0001c0001t0001g0157 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2779-941G>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/22 | chr7 | 117768117 | |||||||
| chr7:117768182 | CCTTTT | C | 3 | a0001c0001t0001g0089 a0001c0001t0001g0106 a0001c0001t0002g0090 |
3 | HG01346.hp1 HG02145.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.2779-1011_2779-100 others(9): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/22 | chr7 | 117768182 | |||||||
| chr7:117768227 | A | G | 6 | a0001c0001t0001g0072 a0001c0001t0001g0081 a0001c0001t0002g0035 others(3): Show |
7 | HG01074.hp2 HG01192.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.2779-1051T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/22 | chr7 | 117768227 | |||||||
| chr7:117768581 | A | AAAAAAAA others(3): Show |
23 | a0001c0001t0001g0006 a0001c0001t0001g0020 a0001c0001t0001g0040 others(20): Show |
23 | HG01069.hp2 HG01071.hp1 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.2779-1406_2779-140 others(14): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/22 | chr7 | 117768581 | |||||||
| chr7:117768581 | A | AAAAAAAG | 4 | a0001c0001t0002g0035 a0002c0002t0001g0001 a0002c0002t0002g0073 others(1): Show |
5 | HG01074.hp2 HG01192.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.2779-1406_2779-140 others(11): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/22 | chr7 | 117768581 | |||||||
| chr7:117768581 | A | AAAAAGAA others(2): Show |
11 | a0001c0001t0001g0011 a0001c0001t0001g0077 a0001c0001t0001g0094 others(8): Show |
11 | HG00642.hp1 HG01433.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.2779-1406_2779-140 others(13): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/22 | chr7 | 117768581 | |||||||
| chr7:117768581 | A | AAAAAGAA others(6): Show |
3 | a0001c0001t0004g0033 a0001c0001t0004g0039 a0001c0001t0004g0053 |
3 | HG01433.hp1 HG02280.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.2779-1406_2779-140 others(17): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/22 | chr7 | 117768581 | |||||||
| chr7:117768581 | A | AAAAG | 17 | a0001c0001t0001g0056 a0001c0001t0001g0067 a0001c0001t0001g0068 others(14): Show |
17 | HG01081.hp2 HG01346.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.2779-1409_2779-140 others(8): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/22 | chr7 | 117768581 | |||||||
| chr7:117768581 | A | AAAAGAAA others(1): Show |
80 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(77): Show |
80 | HG00323.hp1 HG00323.hp2 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.2779-1413_2779-140 others(12): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/22 | chr7 | 117768581 | |||||||
| chr7:117768581 | A | AAAAGAAA others(5): Show |
3 | a0001c0001t0002g0002 a0001c0001t0002g0024 a0001c0001t0002g0162 |
3 | HG01071.hp2 HG01346.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.2779-1417_2779-140 others(16): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/22 | chr7 | 117768581 | |||||||
| chr7:117769124 | G | C | 2 | a0001c0001t0001g0054 a0001c0001t0001g0091 |
2 | HG02165.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.2779-1948C>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/22 | chr7 | 117769124 | |||||||
| chr7:117769174 | G | A | 8 | a0001c0001t0001g0077 a0001c0001t0001g0094 a0001c0001t0001g0095 others(5): Show |
8 | HG01433.hp2 HG02257.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.2779-1998C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/22 | chr7 | 117769174 | |||||||
| chr7:117769627 | C | T | 1 | a0001c0001t0001g0140 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2779-2451G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/22 | chr7 | 117769627 | |||||||
| chr7:117770180 | T | C | 1 | a0001c0001t0002g0090 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2779-3004A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/22 | chr7 | 117770180 | |||||||
| chr7:117770245 | G | C | 8 | a0001c0001t0001g0077 a0001c0001t0001g0094 a0001c0001t0001g0095 others(5): Show |
8 | HG01433.hp2 HG02257.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.2779-3069C>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/22 | chr7 | 117770245 | |||||||
| chr7:117770367 | G | T | 31 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0020 others(28): Show |
31 | HG01069.hp2 HG01071.hp1 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.2779-3191C>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/22 | chr7 | 117770367 | |||||||
| chr7:117770442 | G | C | 9 | a0001c0001t0001g0044 a0001c0001t0001g0080 a0001c0001t0001g0081 others(6): Show |
9 | HG02258.hp1 HG02280.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.2779-3266C>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/22 | chr7 | 117770442 | |||||||
| chr7:117770578 | G | A | 6 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0050 others(3): Show |
6 | HG00639.hp1 HG01168.hp1 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.2779-3402C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/22 | chr7 | 117770578 | |||||||
| chr7:117770613 | A | G | 1 | a0001c0001t0001g0140 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2779-3437T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/22 | chr7 | 117770613 | |||||||
| chr7:117770935 | C | T | 1 | a0001c0001t0001g0004 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.2779-3759G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/22 | chr7 | 117770935 | |||||||
| chr7:117771475 | A | G | 9 | a0001c0001t0001g0072 a0001c0001t0001g0081 a0001c0001t0001g0089 others(6): Show |
10 | HG01074.hp2 HG01192.hp1 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.2779-4299T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/22 | chr7 | 117771475 | |||||||
| chr7:117771617 | C | G | 1 | a0001c0007t0001g0010 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2779-4441G>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/22 | chr7 | 117771617 | |||||||
| chr7:117771742 | A | G | 35 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0020 others(32): Show |
36 | HG01069.hp2 HG01071.hp1 HG01074.hp1 others(33): Show |
intron_variant | MODIFIER | c.2779-4566T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/22 | chr7 | 117771742 | |||||||
| chr7:117771988 | A | G | 35 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0020 others(32): Show |
36 | HG01069.hp2 HG01071.hp1 HG01074.hp1 others(33): Show |
intron_variant | MODIFIER | c.2779-4812T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/22 | chr7 | 117771988 | |||||||
| chr7:117772008 | G | A | 13 | a0001c0001t0001g0023 a0001c0001t0001g0056 a0001c0001t0001g0059 others(10): Show |
13 | HG02145.hp1 HG02451.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.2779-4832C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/22 | chr7 | 117772008 | |||||||
| chr7:117772034 | C | T | 3 | a0001c0001t0001g0089 a0001c0001t0001g0106 a0001c0001t0002g0090 |
3 | HG01346.hp1 HG02145.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.2779-4858G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/22 | chr7 | 117772034 | |||||||
| chr7:117772067 | G | A | 1 | a0001c0001t0001g0159 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2779-4891C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/22 | chr7 | 117772067 | |||||||
| chr7:117772168 | C | G | 2 | a0001c0001t0001g0044 a0001c0007t0001g0010 |
2 | HG02258.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.2779-4992G>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/22 | chr7 | 117772168 | |||||||
| chr7:117772199 | G | T | 3 | a0001c0001t0001g0141 a0001c0001t0001g0158 a0001c0001t0003g0147 |
3 | HG01258.hp1 NA20805.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2779-5023C>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/22 | chr7 | 117772199 | |||||||
| chr7:117772428 | C | A | 2 | a0001c0001t0001g0054 a0001c0001t0001g0091 |
2 | HG02165.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.2778+5083G>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/22 | chr7 | 117772428 | |||||||
| chr7:117772535 | T | C | 1 | a0001c0016t0001g0058 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2778+4976A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/22 | chr7 | 117772535 | |||||||
| chr7:117772581 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2778+4930C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/22 | chr7 | 117772581 | |||||||
| chr7:117772738 | A | T | 1 | a0001c0001t0001g0015 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2778+4773T>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/22 | chr7 | 117772738 | |||||||
| chr7:117773079 | C | G | 3 | a0001c0001t0001g0072 a0001c0001t0001g0081 a0001c0001t0002g0035 |
3 | HG04184.hp1 NA18906.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2778+4432G>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/22 | chr7 | 117773079 | |||||||
| chr7:117773263 | G | C | 1 | a0001c0001t0004g0039 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2778+4248C>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/22 | chr7 | 117773263 | |||||||
| chr7:117773494 | T | C | 1 | a0001c0001t0001g0141 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.2778+4017A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/22 | chr7 | 117773494 | |||||||
| chr7:117773500 | T | C | 1 | a0001c0001t0001g0100 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2778+4011A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/22 | chr7 | 117773500 | |||||||
| chr7:117773648 | A | AAC | 13 | a0001c0001t0001g0017 a0001c0001t0001g0045 a0001c0001t0001g0050 others(10): Show |
13 | HG00642.hp1 HG00642.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.2778+3861_2778+386 others(6): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/22 | chr7 | 117773648 | |||||||
| chr7:117773648 | A | AACAC | 10 | a0001c0001t0001g0012 a0001c0001t0001g0108 a0001c0001t0001g0111 others(7): Show |
10 | HG00609.hp1 HG01168.hp2 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.2778+3859_2778+386 others(8): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/22 | chr7 | 117773648 | |||||||
| chr7:117773648 | A | AACACAC | 6 | a0001c0001t0001g0013 a0001c0001t0001g0021 a0001c0001t0001g0041 others(3): Show |
6 | HG01109.hp1 HG01255.hp2 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.2778+3857_2778+386 others(10): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/22 | chr7 | 117773648 | |||||||
| chr7:117773648 | A | AACACACA others(1): Show |
3 | a0001c0001t0001g0125 a0001c0001t0002g0027 a0001c0001t0005g0048 |
3 | HG01255.hp1 HG02040.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.2778+3855_2778+386 others(12): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/22 | chr7 | 117773648 | |||||||
| chr7:117773648 | A | AACACACA others(3): Show |
3 | a0001c0001t0001g0019 a0001c0001t0001g0070 a0001c0001t0001g0089 |
3 | HG01346.hp1 HG04199.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.2778+3853_2778+386 others(14): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/22 | chr7 | 117773648 | |||||||
| chr7:117773648 | A | AACACACA others(5): Show |
2 | a0001c0001t0001g0124 a0001c0001t0005g0152 |
2 | HG02040.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2778+3851_2778+386 others(16): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/22 | chr7 | 117773648 | |||||||
| chr7:117773648 | A | AACACACA others(11): Show |
1 | a0001c0001t0002g0090 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2778+3845_2778+386 others(22): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/22 | chr7 | 117773648 | |||||||
| chr7:117773648 | A | AACACACA others(15): Show |
1 | a0003c0003t0002g0128 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2778+3841_2778+386 others(26): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/22 | chr7 | 117773648 | |||||||
| chr7:117773648 | A | AACACACA others(47): Show |
1 | a0001c0001t0004g0053 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2778+3809_2778+386 others(58): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/22 | chr7 | 117773648 | |||||||
| chr7:117773648 | A | AACACACA others(53): Show |
1 | a0001c0001t0001g0095 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2778+3803_2778+386 others(64): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/22 | chr7 | 117773648 | |||||||
| chr7:117773648 | A | AACACACA others(57): Show |
1 | a0001c0001t0004g0033 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2778+3862_2778+386 others(68): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/22 | chr7 | 117773648 | |||||||
| chr7:117773648 | A | AACACACA others(71): Show |
1 | a0001c0001t0001g0104 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2778+3862_2778+386 others(82): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/22 | chr7 | 117773648 | |||||||
| chr7:117773648 | A | AACACACA others(73): Show |
2 | a0001c0001t0001g0094 a0004c0005t0001g0030 |
2 | HG02970.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2778+3862_2778+386 others(84): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/22 | chr7 | 117773648 | |||||||
| chr7:117773648 | A | AACACACA others(75): Show |
1 | a0001c0001t0004g0039 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2778+3862_2778+386 others(86): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/22 | chr7 | 117773648 | |||||||
| chr7:117773648 | A | AACACACA others(77): Show |
1 | a0004c0005t0001g0029 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2778+3862_2778+386 others(88): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/22 | chr7 | 117773648 | |||||||
| chr7:117773648 | A | AACACACA others(83): Show |
1 | a0001c0001t0001g0077 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2778+3862_2778+386 others(94): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/22 | chr7 | 117773648 | |||||||
| chr7:117773648 | A | AACACACA others(85): Show |
1 | a0001c0001t0001g0113 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2778+3862_2778+386 others(96): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/22 | chr7 | 117773648 | |||||||
| chr7:117773648 | AAC | A | 16 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(13): Show |
16 | HG01081.hp2 HG01192.hp2 HG01258.hp2 others(13): Show |
intron_variant | MODIFIER | c.2778+3861_2778+386 others(6): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/22 | chr7 | 117773648 | |||||||
| chr7:117773648 | AACAC | A | 7 | a0001c0001t0001g0064 a0001c0001t0001g0100 a0001c0001t0001g0101 others(4): Show |
7 | HG01952.hp1 HG02523.hp1 HG02523.hp2 others(4): Show |
intron_variant | MODIFIER | c.2778+3859_2778+386 others(8): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/22 | chr7 | 117773648 | |||||||
| chr7:117773648 | AACACAC | A | 18 | a0001c0001t0001g0026 a0001c0001t0001g0054 a0001c0001t0001g0057 others(15): Show |
19 | HG00323.hp2 HG01069.hp2 HG01074.hp2 others(16): Show |
intron_variant | MODIFIER | c.2778+3857_2778+386 others(10): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/22 | chr7 | 117773648 | |||||||
| chr7:117773648 | AACACACA others(1): Show |
A | 8 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0060 others(5): Show |
8 | HG01071.hp1 HG01074.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.2778+3855_2778+386 others(12): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/22 | chr7 | 117773648 | |||||||
| chr7:117773648 | AACACACA others(3): Show |
A | 7 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0052 others(4): Show |
7 | HG02258.hp1 HG02258.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.2778+3853_2778+386 others(14): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/22 | chr7 | 117773648 | |||||||
| chr7:117773648 | AACACACA others(5): Show |
A | 11 | a0001c0001t0001g0006 a0001c0001t0001g0020 a0001c0001t0001g0040 others(8): Show |
11 | HG01361.hp1 HG02109.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.2778+3851_2778+386 others(16): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/22 | chr7 | 117773648 | |||||||
| chr7:117773648 | AACACACA others(7): Show |
A | 6 | a0001c0001t0001g0051 a0001c0001t0001g0067 a0001c0001t0001g0068 others(3): Show |
6 | HG02622.hp2 HG02630.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.2778+3849_2778+386 others(18): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/22 | chr7 | 117773648 | |||||||
| chr7:117773648 | AACACACA others(9): Show |
A | 2 | a0001c0001t0001g0163 a0001c0001t0002g0032 |
2 | HG02145.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.2778+3847_2778+386 others(20): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/22 | chr7 | 117773648 | |||||||
| chr7:117773648 | AACACACA others(11): Show |
A | 7 | a0001c0001t0001g0023 a0001c0001t0001g0056 a0001c0001t0001g0059 others(4): Show |
7 | HG02723.hp2 HG02922.hp2 HG03540.hp2 others(4): Show |
intron_variant | MODIFIER | c.2778+3845_2778+386 others(22): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/22 | chr7 | 117773648 | |||||||
| chr7:117773648 | AACACACA others(15): Show |
A | 1 | a0006c0012t0002g0055 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2778+3841_2778+386 others(26): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/22 | chr7 | 117773648 | |||||||
| chr7:117773666 | C | T | 1 | a0001c0001t0001g0026 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.2778+3845G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/22 | chr7 | 117773666 | |||||||
| chr7:117773702 | C | T | 1 | a0001c0001t0001g0103 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.2778+3809G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/22 | chr7 | 117773702 | |||||||
| chr7:117773703 | A | C | 7 | a0001c0001t0001g0020 a0001c0001t0001g0107 a0001c0001t0001g0139 others(4): Show |
7 | HG01069.hp2 HG01071.hp1 HG01074.hp1 others(4): Show |
intron_variant | MODIFIER | c.2778+3808T>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/22 | chr7 | 117773703 | |||||||
| chr7:117773705 | A | C | 7 | a0001c0001t0001g0044 a0001c0001t0001g0080 a0001c0001t0001g0082 others(4): Show |
7 | HG02258.hp1 HG02280.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.2778+3806T>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/22 | chr7 | 117773705 | |||||||
| chr7:117773707 | A | ACACACAC others(5): Show |
1 | a0003c0003t0002g0028 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2778+3803_2778+380 others(16): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/22 | chr7 | 117773707 | |||||||
| chr7:117773707 | A | C | 27 | a0001c0001t0001g0009 a0001c0001t0001g0020 a0001c0001t0001g0044 others(24): Show |
27 | HG01069.hp2 HG01071.hp1 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.2778+3804T>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/22 | chr7 | 117773707 | |||||||
| chr7:117773708 | C | CA | 2 | a0001c0001t0001g0018 a0001c0001t0001g0106 |
2 | HG03654.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.2778+3802_2778+380 others(5): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/22 | chr7 | 117773708 | |||||||
| chr7:117773708 | C | CACACA | 2 | a0001c0001t0001g0145 a0001c0016t0001g0058 |
2 | HG00609.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.2778+3802_2778+380 others(9): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/22 | chr7 | 117773708 | |||||||
| chr7:117773708 | C | CACACACA others(80): Show |
1 | a0001c0001t0001g0109 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2778+3802_2778+380 others(91): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/22 | chr7 | 117773708 | |||||||
| chr7:117773709 | C | A | 1 | a0001c0001t0002g0027 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2778+3802G>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/22 | chr7 | 117773709 | |||||||
| chr7:117773898 | T | G | 1 | a0001c0001t0005g0048 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2778+3613A>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/22 | chr7 | 117773898 | |||||||
| chr7:117774026 | A | G | 50 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0020 others(47): Show |
51 | HG01069.hp2 HG01071.hp1 HG01074.hp1 others(48): Show |
intron_variant | MODIFIER | c.2778+3485T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/22 | chr7 | 117774026 | |||||||
| chr7:117774632 | C | T | 3 | a0001c0001t0001g0089 a0001c0001t0001g0106 a0001c0001t0002g0090 |
3 | HG01346.hp1 HG02145.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.2778+2879G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/22 | chr7 | 117774632 | |||||||
| chr7:117774646 | T | C | 9 | a0001c0001t0001g0044 a0001c0001t0001g0080 a0001c0001t0001g0081 others(6): Show |
9 | HG02258.hp1 HG02280.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.2778+2865A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/22 | chr7 | 117774646 | |||||||
| chr7:117774686 | G | A | 3 | a0001c0001t0004g0033 a0001c0001t0004g0039 a0001c0001t0004g0053 |
3 | HG01433.hp1 HG02280.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.2778+2825C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/22 | chr7 | 117774686 | |||||||
| chr7:117774845 | T | G | 1 | a0006c0012t0002g0055 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2778+2666A>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/22 | chr7 | 117774845 | |||||||
| chr7:117774890 | A | G | 1 | a0001c0001t0001g0072 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2778+2621T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/22 | chr7 | 117774890 | |||||||
| chr7:117775227 | G | T | 31 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0020 others(28): Show |
31 | HG01069.hp2 HG01071.hp1 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.2778+2284C>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/22 | chr7 | 117775227 | |||||||
| chr7:117775584 | CT | C | 29 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0020 others(26): Show |
29 | HG01069.hp2 HG01071.hp1 HG01074.hp1 others(26): Show |
intron_variant | MODIFIER | c.2778+1926delA | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/22 | chr7 | 117775584 | |||||||
| chr7:117775785 | C | G | 1 | a0001c0001t0001g0098 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.2778+1726G>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/22 | chr7 | 117775785 | |||||||
| chr7:117775857 | C | A | 2 | a0001c0001t0001g0041 a0001c0016t0001g0058 |
2 | HG00609.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.2778+1654G>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/22 | chr7 | 117775857 | |||||||
| chr7:117775946 | T | C | 2 | a0001c0001t0002g0047 a0001c0006t0002g0079 |
2 | HG02723.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.2778+1565A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/22 | chr7 | 117775946 | |||||||
| chr7:117776016 | A | G | 7 | a0001c0001t0001g0044 a0001c0001t0001g0080 a0001c0001t0001g0081 others(4): Show |
7 | HG02258.hp1 HG02280.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.2778+1495T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/22 | chr7 | 117776016 | |||||||
| chr7:117776033 | A | G | 1 | a0001c0001t0004g0039 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2778+1478T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/22 | chr7 | 117776033 | |||||||
| chr7:117776116 | T | C | 1 | a0001c0001t0001g0086 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2778+1395A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/22 | chr7 | 117776116 | |||||||
| chr7:117776227 | C | A | 3 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0082 |
3 | HG02280.hp1 HG03579.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2778+1284G>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/22 | chr7 | 117776227 | |||||||
| chr7:117776403 | G | A | 2 | a0001c0001t0001g0072 a0001c0001t0002g0035 |
2 | HG04184.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2778+1108C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/22 | chr7 | 117776403 | |||||||
| chr7:117776476 | C | T | 1 | a0001c0001t0002g0037 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.2778+1035G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/22 | chr7 | 117776476 | |||||||
| chr7:117776570 | T | C | 1 | a0001c0001t0001g0139 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2778+941A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/22 | chr7 | 117776570 | |||||||
| chr7:117776583 | T | G | 3 | a0001c0001t0001g0141 a0001c0001t0001g0158 a0001c0001t0003g0147 |
3 | HG01258.hp1 NA20805.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2778+928A>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/22 | chr7 | 117776583 | |||||||
| chr7:117776594 | C | T | 15 | a0001c0001t0001g0023 a0001c0001t0001g0056 a0001c0001t0001g0059 others(12): Show |
15 | HG02145.hp1 HG02451.hp1 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.2778+917G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/22 | chr7 | 117776594 | |||||||
| chr7:117776623 | T | C | 66 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0020 others(63): Show |
66 | HG01069.hp2 HG01071.hp1 HG01074.hp1 others(63): Show |
intron_variant | MODIFIER | c.2778+888A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/22 | chr7 | 117776623 | |||||||
| chr7:117776679 | C | T | 1 | a0006c0012t0002g0055 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2778+832G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/22 | chr7 | 117776679 | |||||||
| chr7:117776878 | A | C | 1 | a0001c0015t0001g0160 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2778+633T>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/22 | chr7 | 117776878 | |||||||
| chr7:117776882 | G | A | 1 | a0001c0015t0001g0160 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2778+629C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/22 | chr7 | 117776882 | |||||||
| chr7:117777011 | G | A | 156 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(153): Show |
157 | HG00323.hp1 HG00323.hp2 HG00609.hp1 others(154): Show |
intron_variant | MODIFIER | c.2778+500C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/22 | chr7 | 117777011 | |||||||
| chr7:117777422 | T | C | 26 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0020 others(23): Show |
26 | HG01069.hp2 HG01071.hp1 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.2778+89A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 8/22 | chr7 | 117777422 | |||||||
| chr7:117778056 | T | C | 6 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0038 others(3): Show |
6 | HG01192.hp2 HG01255.hp2 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.2524-291A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 7/22 | chr7 | 117778056 | |||||||
| chr7:117778084 | T | C | 1 | a0001c0001t0001g0021 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2524-319A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 7/22 | chr7 | 117778084 | |||||||
| chr7:117778217 | T | C | 1 | a0001c0001t0002g0037 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.2524-452A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 7/22 | chr7 | 117778217 | |||||||
| chr7:117778329 | T | C | 1 | a0001c0001t0002g0022 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2524-564A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 7/22 | chr7 | 117778329 | |||||||
| chr7:117778400 | T | G | 69 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0020 others(66): Show |
70 | HG01069.hp2 HG01071.hp1 HG01074.hp1 others(67): Show |
intron_variant | MODIFIER | c.2524-635A>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 7/22 | chr7 | 117778400 | |||||||
| chr7:117778563 | T | C | 1 | a0001c0001t0001g0098 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.2524-798A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 7/22 | chr7 | 117778563 | |||||||
| chr7:117779055 | C | T | 1 | a0001c0001t0002g0037 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.2524-1290G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 7/22 | chr7 | 117779055 | |||||||
| chr7:117779138 | A | C | 26 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0020 others(23): Show |
26 | HG01069.hp2 HG01071.hp1 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.2523+1303T>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 7/22 | chr7 | 117779138 | |||||||
| chr7:117779181 | G | A | 8 | a0001c0001t0001g0044 a0001c0001t0001g0080 a0001c0001t0001g0082 others(5): Show |
8 | HG02258.hp1 HG02280.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.2523+1260C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 7/22 | chr7 | 117779181 | |||||||
| chr7:117779305 | A | T | 1 | a0001c0001t0001g0066 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2523+1136T>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 7/22 | chr7 | 117779305 | |||||||
| chr7:117779387 | T | C | 1 | a0001c0001t0001g0088 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.2523+1054A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 7/22 | chr7 | 117779387 | |||||||
| chr7:117779452 | T | C | 3 | a0003c0003t0002g0028 a0003c0003t0002g0128 a0003c0003t0002g0138 |
3 | HG00323.hp1 HG01109.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2523+989A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 7/22 | chr7 | 117779452 | |||||||
| chr7:117779456 | T | G | 1 | a0001c0001t0001g0148 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.2523+985A>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 7/22 | chr7 | 117779456 | |||||||
| chr7:117779532 | AAATT | A | 13 | a0001c0001t0001g0023 a0001c0001t0001g0056 a0001c0001t0001g0059 others(10): Show |
13 | HG02145.hp1 HG02451.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.2523+905_2523+908d others(6): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 7/22 | chr7 | 117779532 | |||||||
| chr7:117779571 | G | A | 47 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0020 others(44): Show |
47 | HG01069.hp2 HG01071.hp1 HG01074.hp1 others(44): Show |
intron_variant | MODIFIER | c.2523+870C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 7/22 | chr7 | 117779571 | |||||||
| chr7:117779729 | C | CAT | 2 | a0001c0001t0001g0036 a0001c0001t0001g0072 |
2 | NA18906.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.2523+710_2523+711d others(4): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 7/22 | chr7 | 117779729 | |||||||
| chr7:117780004 | C | T | 18 | a0001c0001t0001g0018 a0001c0001t0001g0026 a0001c0001t0001g0036 others(15): Show |
18 | HG00609.hp1 HG00642.hp1 HG01952.hp2 others(15): Show |
intron_variant | MODIFIER | c.2523+437G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 7/22 | chr7 | 117780004 | |||||||
| chr7:117780033 | T | G | 1 | a0001c0001t0001g0014 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.2523+408A>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 7/22 | chr7 | 117780033 | |||||||
| chr7:117780039 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2523+402G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 7/22 | chr7 | 117780039 | |||||||
| chr7:117780150 | T | C | 3 | a0001c0001t0001g0009 a0001c0001t0001g0060 a0001c0001t0001g0069 |
3 | HG01243.hp1 HG02615.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.2523+291A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 7/22 | chr7 | 117780150 | |||||||
| chr7:117780166 | G | T | 8 | a0001c0001t0001g0077 a0001c0001t0001g0094 a0001c0001t0001g0095 others(5): Show |
8 | HG01433.hp2 HG02257.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.2523+275C>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 7/22 | chr7 | 117780166 | |||||||
| chr7:117780396 | T | C | 1 | a0001c0001t0001g0076 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2523+45A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 7/22 | chr7 | 117780396 | |||||||
| chr7:117780730 | T | C | 26 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0020 others(23): Show |
26 | HG01069.hp2 HG01071.hp1 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.2373-139A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 6/22 | chr7 | 117780730 | |||||||
| chr7:117780753 | C | A | 44 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0020 others(41): Show |
44 | HG01069.hp2 HG01071.hp1 HG01074.hp1 others(41): Show |
intron_variant | MODIFIER | c.2373-162G>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 6/22 | chr7 | 117780753 | |||||||
| chr7:117781035 | G | A | 1 | a0001c0001t0001g0012 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.2373-444C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 6/22 | chr7 | 117781035 | |||||||
| chr7:117781490 | C | T | 3 | a0001c0001t0001g0089 a0001c0001t0001g0106 a0001c0001t0002g0090 |
3 | HG01346.hp1 HG02145.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.2373-899G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 6/22 | chr7 | 117781490 | |||||||
| chr7:117781794 | A | G | 58 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0020 others(55): Show |
59 | HG01069.hp2 HG01071.hp1 HG01074.hp1 others(56): Show |
intron_variant | MODIFIER | c.2372+1068T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 6/22 | chr7 | 117781794 | |||||||
| chr7:117781860 | G | A | 1 | a0001c0001t0001g0126 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2372+1002C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 6/22 | chr7 | 117781860 | |||||||
| chr7:117782366 | C | G | 2 | a0001c0001t0001g0072 a0001c0001t0002g0035 |
2 | HG04184.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2372+496G>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 6/22 | chr7 | 117782366 | |||||||
| chr7:117782539 | A | C | 3 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0082 |
3 | HG02280.hp1 HG03579.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2372+323T>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 6/22 | chr7 | 117782539 | |||||||
| chr7:117782786 | G | A | 1 | a0001c0001t0002g0002 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.2372+76C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 6/22 | chr7 | 117782786 | |||||||
| chr7:117782814 | A | C | 1 | a0001c0001t0002g0035 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2372+48T>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 6/22 | chr7 | 117782814 | |||||||
| chr7:117783139 | A | C | 2 | a0001c0001t0001g0054 a0001c0001t0001g0091 |
2 | HG02165.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.2273-178T>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 5/22 | chr7 | 117783139 | |||||||
| chr7:117783180 | C | CGT | 26 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0020 others(23): Show |
26 | HG01069.hp2 HG01071.hp1 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.2273-221_2273-220d others(4): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 5/22 | chr7 | 117783180 | |||||||
| chr7:117783181 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2273-220C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 5/22 | chr7 | 117783181 | |||||||
| chr7:117783201 | A | G | 1 | a0001c0001t0001g0092 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2273-240T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 5/22 | chr7 | 117783201 | |||||||
| chr7:117783475 | G | A | 2 | a0001c0001t0002g0007 a0001c0001t0002g0022 |
2 | HG03041.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2273-514C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 5/22 | chr7 | 117783475 | |||||||
| chr7:117783806 | C | T | 26 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0020 others(23): Show |
26 | HG01069.hp2 HG01071.hp1 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.2272+445G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 5/22 | chr7 | 117783806 | |||||||
| chr7:117784223 | G | A | 2 | a0001c0001t0002g0007 a0001c0001t0002g0022 |
2 | HG03041.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2272+28C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 5/22 | chr7 | 117784223 | |||||||
| chr7:117784237 | C | G | 2 | a0001c0001t0001g0072 a0001c0001t0001g0081 |
2 | NA18906.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2272+14G>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 5/22 | chr7 | 117784237 | |||||||
| chr7:117784240 | G | A | 13 | a0001c0001t0001g0023 a0001c0001t0001g0056 a0001c0001t0001g0059 others(10): Show |
13 | HG02145.hp1 HG02451.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.2272+11C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 5/22 | chr7 | 117784240 | |||||||
| chr7:117784564 | G | A | 1 | a0001c0001t0002g0130 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2069-110C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 4/22 | chr7 | 117784564 | |||||||
| chr7:117784982 | G | A | 3 | a0001c0001t0004g0033 a0001c0001t0004g0039 a0001c0001t0004g0053 |
3 | HG01433.hp1 HG02280.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.2069-528C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 4/22 | chr7 | 117784982 | |||||||
| chr7:117785351 | C | G | 7 | a0001c0001t0001g0046 a0001c0001t0001g0051 a0001c0001t0001g0052 others(4): Show |
7 | HG02258.hp2 HG02486.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.2069-897G>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 4/22 | chr7 | 117785351 | |||||||
| chr7:117785697 | C | A | 1 | a0001c0001t0001g0060 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2069-1243G>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 4/22 | chr7 | 117785697 | |||||||
| chr7:117785798 | T | C | 26 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0020 others(23): Show |
26 | HG01069.hp2 HG01071.hp1 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.2069-1344A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 4/22 | chr7 | 117785798 | |||||||
| chr7:117786085 | C | T | 66 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0020 others(63): Show |
66 | HG01069.hp2 HG01071.hp1 HG01074.hp1 others(63): Show |
intron_variant | MODIFIER | c.2069-1631G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 4/22 | chr7 | 117786085 | |||||||
| chr7:117786212 | C | A | 26 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0020 others(23): Show |
26 | HG01069.hp2 HG01071.hp1 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.2069-1758G>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 4/22 | chr7 | 117786212 | |||||||
| chr7:117786430 | AAAAC | A | 26 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0020 others(23): Show |
26 | HG01069.hp2 HG01071.hp1 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.2069-1980_2069-197 others(8): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 4/22 | chr7 | 117786430 | |||||||
| chr7:117786592 | G | A | 1 | a0001c0001t0001g0109 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2069-2138C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 4/22 | chr7 | 117786592 | |||||||
| chr7:117786623 | A | G | 1 | a0001c0001t0001g0057 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2069-2169T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 4/22 | chr7 | 117786623 | |||||||
| chr7:117786695 | G | A | 1 | a0001c0001t0001g0072 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2069-2241C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 4/22 | chr7 | 117786695 | |||||||
| chr7:117787317 | A | C | 26 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0020 others(23): Show |
26 | HG01069.hp2 HG01071.hp1 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.2069-2863T>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 4/22 | chr7 | 117787317 | |||||||
| chr7:117787377 | C | T | 1 | a0001c0001t0001g0146 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.2069-2923G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 4/22 | chr7 | 117787377 | |||||||
| chr7:117787471 | T | C | 3 | a0001c0001t0004g0033 a0001c0001t0004g0039 a0001c0001t0004g0053 |
3 | HG01433.hp1 HG02280.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.2069-3017A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 4/22 | chr7 | 117787471 | |||||||
| chr7:117787709 | A | T | 15 | a0001c0001t0001g0023 a0001c0001t0001g0056 a0001c0001t0001g0059 others(12): Show |
15 | HG02145.hp1 HG02451.hp1 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.2069-3255T>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 4/22 | chr7 | 117787709 | |||||||
| chr7:117787773 | A | G | 1 | a0001c0001t0001g0017 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2069-3319T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 4/22 | chr7 | 117787773 | |||||||
| chr7:117787957 | C | T | 66 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0020 others(63): Show |
66 | HG01069.hp2 HG01071.hp1 HG01074.hp1 others(63): Show |
intron_variant | MODIFIER | c.2068+3171G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 4/22 | chr7 | 117787957 | |||||||
| chr7:117788007 | C | T | 5 | a0001c0001t0001g0072 a0001c0001t0001g0089 a0001c0001t0001g0106 others(2): Show |
5 | HG01346.hp1 HG02145.hp2 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.2068+3121G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 4/22 | chr7 | 117788007 | |||||||
| chr7:117788715 | G | A | 1 | a0003c0003t0002g0128 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2068+2413C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 4/22 | chr7 | 117788715 | |||||||
| chr7:117788810 | C | T | 1 | a0001c0001t0001g0014 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.2068+2318G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 4/22 | chr7 | 117788810 | |||||||
| chr7:117788983 | AT | A | 38 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0020 others(35): Show |
38 | HG01069.hp2 HG01071.hp1 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.2068+2144delA | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 4/22 | chr7 | 117788983 | |||||||
| chr7:117789245 | A | G | 154 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(151): Show |
155 | HG00323.hp1 HG00323.hp2 HG00609.hp1 others(152): Show |
intron_variant | MODIFIER | c.2068+1883T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 4/22 | chr7 | 117789245 | |||||||
| chr7:117789264 | C | G | 1 | a0001c0001t0001g0136 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2068+1864G>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 4/22 | chr7 | 117789264 | |||||||
| chr7:117789493 | A | G | 1 | a0001c0001t0001g0129 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2068+1635T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 4/22 | chr7 | 117789493 | |||||||
| chr7:117789745 | CA | C | 28 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0020 others(25): Show |
28 | HG01069.hp2 HG01071.hp1 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.2068+1382delT | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 4/22 | chr7 | 117789745 | |||||||
| chr7:117789806 | A | T | 10 | a0001c0001t0001g0044 a0001c0001t0001g0080 a0001c0001t0001g0081 others(7): Show |
10 | HG01346.hp1 HG02145.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.2068+1322T>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 4/22 | chr7 | 117789806 | |||||||
| chr7:117789902 | C | T | 1 | a0001c0001t0002g0022 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2068+1226G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 4/22 | chr7 | 117789902 | |||||||
| chr7:117789963 | T | C | 1 | a0001c0001t0002g0035 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2068+1165A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 4/22 | chr7 | 117789963 | |||||||
| chr7:117790050 | G | C | 2 | a0001c0001t0001g0054 a0001c0001t0001g0091 |
2 | HG02165.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.2068+1078C>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 4/22 | chr7 | 117790050 | |||||||
| chr7:117790059 | A | G | 1 | a0001c0001t0002g0027 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2068+1069T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 4/22 | chr7 | 117790059 | |||||||
| chr7:117790125 | C | G | 1 | a0001c0015t0001g0160 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2068+1003G>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 4/22 | chr7 | 117790125 | |||||||
| chr7:117790310 | C | T | 10 | a0001c0001t0001g0044 a0001c0001t0001g0080 a0001c0001t0001g0081 others(7): Show |
10 | HG01346.hp1 HG02145.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.2068+818G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 4/22 | chr7 | 117790310 | |||||||
| chr7:117790499 | C | T | 2 | a0001c0001t0001g0072 a0001c0001t0002g0035 |
2 | HG04184.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2068+629G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 4/22 | chr7 | 117790499 | |||||||
| chr7:117790527 | AG | A | 11 | a0001c0001t0001g0077 a0001c0001t0001g0094 a0001c0001t0001g0095 others(8): Show |
11 | HG01433.hp1 HG01433.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.2068+600delC | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 4/22 | chr7 | 117790527 | |||||||
| chr7:117790598 | T | TA | 13 | a0001c0001t0001g0044 a0001c0001t0001g0076 a0001c0001t0001g0080 others(10): Show |
13 | HG01346.hp1 HG02145.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.2068+529dupT | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 4/22 | chr7 | 117790598 | |||||||
| chr7:117790598 | TA | T | 12 | a0001c0001t0001g0023 a0001c0001t0001g0056 a0001c0001t0001g0059 others(9): Show |
12 | HG02451.hp1 HG02615.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.2068+529delT | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 4/22 | chr7 | 117790598 | |||||||
| chr7:117790823 | C | T | 1 | a0001c0001t0001g0077 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2068+305G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 4/22 | chr7 | 117790823 | |||||||
| chr7:117790855 | T | C | 2 | a0001c0001t0001g0018 a0001c0001t0001g0096 |
2 | HG00642.hp1 NA18951.hp2 |
intron_variant | MODIFIER | c.2068+273A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 4/22 | chr7 | 117790855 | |||||||
| chr7:117790857 | G | T | 1 | a0001c0001t0001g0064 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.2068+271C>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 4/22 | chr7 | 117790857 | |||||||
| chr7:117790973 | A | C | 1 | a0001c0001t0001g0101 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2068+155T>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 4/22 | chr7 | 117790973 | |||||||
| chr7:117791041 | A | T | 2 | a0001c0001t0002g0047 a0001c0006t0002g0079 |
2 | HG02723.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.2068+87T>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 4/22 | chr7 | 117791041 | |||||||
| chr7:117791059 | A | G | 10 | a0001c0001t0001g0044 a0001c0001t0001g0080 a0001c0001t0001g0081 others(7): Show |
10 | HG01346.hp1 HG02145.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.2068+69T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 4/22 | chr7 | 117791059 | |||||||
| chr7:117791105 | G | A | 1 | a0001c0001t0001g0111 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2068+23C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 4/22 | chr7 | 117791105 | |||||||
| chr7:117792831 | T | C | 1 | a0001c0001t0004g0033 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.415-50A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117792831 | |||||||
| chr7:117793325 | T | C | 1 | a0001c0001t0001g0011 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.415-544A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117793325 | |||||||
| chr7:117793402 | T | C | 54 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0020 others(51): Show |
55 | HG01069.hp2 HG01071.hp1 HG01074.hp1 others(52): Show |
intron_variant | MODIFIER | c.415-621A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117793402 | |||||||
| chr7:117793433 | T | C | 12 | a0001c0001t0001g0072 a0001c0001t0001g0077 a0001c0001t0001g0094 others(9): Show |
12 | HG01433.hp1 HG01433.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.415-652A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117793433 | |||||||
| chr7:117793442 | C | T | 26 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0020 others(23): Show |
26 | HG01069.hp2 HG01071.hp1 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.415-661G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117793442 | |||||||
| chr7:117793451 | C | T | 3 | a0001c0001t0001g0089 a0001c0001t0001g0106 a0001c0001t0002g0090 |
3 | HG01346.hp1 HG02145.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.415-670G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117793451 | |||||||
| chr7:117793462 | C | A | 3 | a0001c0001t0001g0089 a0001c0001t0001g0106 a0001c0001t0002g0090 |
3 | HG01346.hp1 HG02145.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.415-681G>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117793462 | |||||||
| chr7:117793567 | T | C | 40 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0020 others(37): Show |
41 | HG01069.hp2 HG01071.hp1 HG01074.hp1 others(38): Show |
intron_variant | MODIFIER | c.415-786A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117793567 | |||||||
| chr7:117793726 | C | G | 1 | a0001c0001t0001g0110 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.415-945G>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117793726 | |||||||
| chr7:117794154 | G | A | 3 | a0001c0001t0001g0089 a0001c0001t0001g0106 a0001c0001t0002g0090 |
3 | HG01346.hp1 HG02145.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.415-1373C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117794154 | |||||||
| chr7:117794159 | T | A | 1 | a0001c0001t0001g0136 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.415-1378A>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117794159 | |||||||
| chr7:117794600 | G | A | 25 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0020 others(22): Show |
25 | HG01069.hp2 HG01071.hp1 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.415-1819C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117794600 | |||||||
| chr7:117794871 | G | C | 2 | a0001c0001t0001g0106 a0001c0001t0002g0090 |
2 | HG02145.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.415-2090C>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117794871 | |||||||
| chr7:117794872 | TATATC | T | 2 | a0001c0001t0001g0106 a0001c0001t0002g0090 |
2 | HG02145.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.415-2096_415-2092d others(7): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117794872 | |||||||
| chr7:117794877 | C | CT | 13 | a0001c0001t0001g0041 a0001c0001t0001g0076 a0001c0001t0001g0081 others(10): Show |
13 | HG01074.hp2 HG01109.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.415-2097dupA | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117794877 | |||||||
| chr7:117794877 | C | CTT | 19 | a0001c0001t0001g0023 a0001c0001t0001g0056 a0001c0001t0001g0059 others(16): Show |
19 | HG00642.hp1 HG02451.hp1 HG02615.hp2 others(16): Show |
intron_variant | MODIFIER | c.415-2098_415-2097d others(4): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117794877 | |||||||
| chr7:117794877 | CT | C | 21 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0020 others(18): Show |
21 | HG00609.hp1 HG00609.hp2 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.415-2097delA | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117794877 | |||||||
| chr7:117794877 | CTT | C | 9 | a0001c0001t0001g0062 a0001c0001t0001g0072 a0001c0001t0001g0077 others(6): Show |
9 | HG01433.hp2 HG02257.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.415-2098_415-2097d others(4): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117794877 | |||||||
| chr7:117794927 | G | A | 6 | a0001c0001t0001g0044 a0001c0001t0001g0080 a0001c0001t0001g0082 others(3): Show |
6 | HG02258.hp1 HG02280.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.415-2146C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117794927 | |||||||
| chr7:117794955 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.415-2174G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117794955 | |||||||
| chr7:117794963 | C | T | 6 | a0001c0001t0001g0046 a0001c0001t0001g0051 a0001c0001t0001g0052 others(3): Show |
6 | HG02258.hp2 HG02486.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.415-2182G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117794963 | |||||||
| chr7:117794981 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.415-2200C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117794981 | |||||||
| chr7:117795056 | G | A | 1 | a0001c0001t0001g0163 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.415-2275C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117795056 | |||||||
| chr7:117795186 | C | T | 13 | a0001c0001t0001g0023 a0001c0001t0001g0056 a0001c0001t0001g0059 others(10): Show |
13 | HG02145.hp1 HG02451.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.415-2405G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117795186 | |||||||
| chr7:117795229 | A | T | 69 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0020 others(66): Show |
70 | HG01069.hp2 HG01071.hp1 HG01074.hp1 others(67): Show |
intron_variant | MODIFIER | c.415-2448T>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117795229 | |||||||
| chr7:117795350 | C | T | 3 | a0001c0001t0001g0089 a0001c0001t0001g0106 a0001c0001t0002g0090 |
3 | HG01346.hp1 HG02145.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.415-2569G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117795350 | |||||||
| chr7:117795828 | C | T | 2 | a0001c0001t0002g0007 a0001c0001t0002g0022 |
2 | HG03041.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.415-3047G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117795828 | |||||||
| chr7:117795910 | T | C | 69 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0020 others(66): Show |
70 | HG01069.hp2 HG01071.hp1 HG01074.hp1 others(67): Show |
intron_variant | MODIFIER | c.415-3129A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117795910 | |||||||
| chr7:117795984 | T | C | 25 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0020 others(22): Show |
25 | HG01069.hp2 HG01071.hp1 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.415-3203A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117795984 | |||||||
| chr7:117796043 | T | A | 1 | a0001c0001t0001g0081 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.415-3262A>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117796043 | |||||||
| chr7:117796048 | A | G | 1 | a0003c0003t0002g0028 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.415-3267T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117796048 | |||||||
| chr7:117796200 | C | T | 3 | a0001c0001t0001g0089 a0001c0001t0001g0106 a0001c0001t0002g0090 |
3 | HG01346.hp1 HG02145.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.415-3419G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117796200 | |||||||
| chr7:117796384 | G | T | 20 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0020 others(17): Show |
20 | HG01069.hp2 HG01071.hp1 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.415-3603C>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117796384 | |||||||
| chr7:117796515 | T | G | 6 | a0001c0001t0001g0044 a0001c0001t0001g0080 a0001c0001t0001g0082 others(3): Show |
6 | HG02258.hp1 HG02280.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.415-3734A>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117796515 | |||||||
| chr7:117796682 | C | T | 3 | a0001c0001t0001g0089 a0001c0001t0001g0106 a0001c0001t0002g0090 |
3 | HG01346.hp1 HG02145.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.415-3901G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117796682 | |||||||
| chr7:117796801 | T | C | 1 | a0001c0001t0001g0081 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.415-4020A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117796801 | |||||||
| chr7:117796823 | G | T | 1 | a0001c0001t0001g0118 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.415-4042C>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117796823 | |||||||
| chr7:117796926 | C | G | 25 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0020 others(22): Show |
25 | HG01069.hp2 HG01071.hp1 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.415-4145G>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117796926 | |||||||
| chr7:117797306 | A | G | 1 | a0001c0001t0002g0032 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.415-4525T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117797306 | |||||||
| chr7:117797415 | A | G | 2 | a0001c0001t0002g0007 a0001c0001t0002g0022 |
2 | HG03041.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.415-4634T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117797415 | |||||||
| chr7:117797730 | T | TAAAGC | 6 | a0001c0001t0001g0074 a0001c0001t0001g0081 a0001c0001t0002g0035 others(3): Show |
7 | HG01074.hp2 HG01192.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.415-4954_415-4950d others(7): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117797730 | |||||||
| chr7:117797741 | C | A | 54 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0020 others(51): Show |
55 | HG01069.hp2 HG01071.hp1 HG01074.hp1 others(52): Show |
intron_variant | MODIFIER | c.415-4960G>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117797741 | |||||||
| chr7:117798111 | T | C | 1 | a0001c0001t0001g0041 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.415-5330A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117798111 | |||||||
| chr7:117798477 | A | T | 2 | a0001c0001t0002g0047 a0001c0006t0002g0079 |
2 | HG02723.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.415-5696T>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117798477 | |||||||
| chr7:117798479 | T | C | 1 | a0001c0001t0002g0037 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.415-5698A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117798479 | |||||||
| chr7:117798642 | C | A | 1 | a0001c0001t0001g0071 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.415-5861G>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117798642 | |||||||
| chr7:117799203 | A | T | 1 | a0001c0001t0002g0035 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.415-6422T>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117799203 | |||||||
| chr7:117799929 | T | A | 2 | a0001c0001t0001g0044 a0001c0007t0001g0010 |
2 | HG02258.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.415-7148A>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117799929 | |||||||
| chr7:117799930 | G | A | 1 | a0001c0001t0001g0106 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.415-7149C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117799930 | |||||||
| chr7:117800141 | A | AT | 9 | a0001c0001t0001g0072 a0001c0001t0001g0077 a0001c0001t0001g0094 others(6): Show |
9 | HG01433.hp2 HG02257.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.415-7361dupA | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117800141 | |||||||
| chr7:117800164 | C | G | 20 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0020 others(17): Show |
20 | HG01069.hp2 HG01071.hp1 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.415-7383G>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117800164 | |||||||
| chr7:117800174 | A | G | 3 | a0001c0001t0001g0089 a0001c0001t0001g0106 a0001c0001t0002g0090 |
3 | HG01346.hp1 HG02145.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.415-7393T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117800174 | |||||||
| chr7:117800333 | C | A | 3 | a0001c0001t0001g0089 a0001c0001t0001g0106 a0001c0001t0002g0090 |
3 | HG01346.hp1 HG02145.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.415-7552G>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117800333 | |||||||
| chr7:117800529 | A | G | 1 | a0001c0001t0001g0005 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.415-7748T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117800529 | |||||||
| chr7:117800576 | G | A | 2 | a0001c0001t0002g0047 a0001c0006t0002g0079 |
2 | HG02723.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.415-7795C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117800576 | |||||||
| chr7:117800613 | C | T | 4 | a0001c0001t0001g0044 a0001c0004t0001g0008 a0001c0004t0001g0122 others(1): Show |
4 | HG02258.hp1 HG02895.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.415-7832G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117800613 | |||||||
| chr7:117800918 | T | C | 6 | a0001c0001t0001g0074 a0001c0001t0001g0081 a0001c0001t0002g0035 others(3): Show |
7 | HG01074.hp2 HG01192.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.415-8137A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117800918 | |||||||
| chr7:117800967 | C | T | 2 | a0001c0001t0001g0036 a0001c0001t0001g0093 |
2 | NA18969.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.415-8186G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117800967 | |||||||
| chr7:117801178 | A | G | 3 | a0001c0001t0001g0089 a0001c0001t0001g0106 a0001c0001t0002g0090 |
3 | HG01346.hp1 HG02145.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.415-8397T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117801178 | |||||||
| chr7:117801344 | T | C | 21 | a0001c0001t0001g0044 a0001c0001t0001g0072 a0001c0001t0001g0077 others(18): Show |
21 | HG01433.hp1 HG01433.hp2 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.415-8563A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117801344 | |||||||
| chr7:117801611 | T | C | 2 | a0001c0001t0002g0047 a0001c0006t0002g0079 |
2 | HG02723.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.415-8830A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117801611 | |||||||
| chr7:117801673 | A | G | 2 | a0001c0001t0002g0047 a0001c0006t0002g0079 |
2 | HG02723.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.415-8892T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117801673 | |||||||
| chr7:117801868 | A | C | 3 | a0001c0001t0001g0089 a0001c0001t0001g0106 a0001c0001t0002g0090 |
3 | HG01346.hp1 HG02145.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.414+8897T>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117801868 | |||||||
| chr7:117802064 | C | G | 25 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0020 others(22): Show |
25 | HG01069.hp2 HG01071.hp1 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.414+8701G>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117802064 | |||||||
| chr7:117802102 | A | C | 25 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0020 others(22): Show |
25 | HG01069.hp2 HG01071.hp1 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.414+8663T>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117802102 | |||||||
| chr7:117802206 | C | G | 65 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0020 others(62): Show |
65 | HG01069.hp2 HG01071.hp1 HG01074.hp1 others(62): Show |
intron_variant | MODIFIER | c.414+8559G>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117802206 | |||||||
| chr7:117802328 | C | T | 2 | a0001c0001t0002g0007 a0001c0001t0002g0022 |
2 | HG03041.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.414+8437G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117802328 | |||||||
| chr7:117802352 | G | T | 3 | a0001c0001t0001g0089 a0001c0001t0001g0106 a0001c0001t0002g0090 |
3 | HG01346.hp1 HG02145.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.414+8413C>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117802352 | |||||||
| chr7:117802437 | CA | C | 30 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0020 others(27): Show |
30 | HG01069.hp2 HG01071.hp1 HG01074.hp1 others(27): Show |
intron_variant | MODIFIER | c.414+8327delT | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117802437 | |||||||
| chr7:117802444 | AAAAAAAA others(7): Show |
A | 3 | a0001c0001t0001g0089 a0001c0001t0001g0106 a0001c0001t0002g0090 |
3 | HG01346.hp1 HG02145.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.414+8307_414+8320d others(16): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117802444 | |||||||
| chr7:117802452 | A | AAC | 5 | a0001c0001t0001g0056 a0001c0001t0001g0085 a0001c0001t0001g0110 others(2): Show |
5 | HG02451.hp1 HG02723.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.414+8312_414+8313i others(4): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117802452 | |||||||
| chr7:117802452 | A | AC | 10 | a0001c0001t0001g0023 a0001c0001t0001g0059 a0001c0001t0001g0067 others(7): Show |
10 | HG02615.hp2 HG02630.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.414+8312_414+8313i others(3): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117802452 | |||||||
| chr7:117802452 | A | C | 89 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0018 others(86): Show |
90 | HG00323.hp1 HG00609.hp1 HG00642.hp1 others(87): Show |
intron_variant | MODIFIER | c.414+8313T>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117802452 | |||||||
| chr7:117802489 | A | T | 7 | a0001c0001t0001g0044 a0001c0001t0001g0080 a0001c0001t0001g0081 others(4): Show |
7 | HG02258.hp1 HG02280.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.414+8276T>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117802489 | |||||||
| chr7:117802490 | G | A | 12 | a0001c0001t0001g0072 a0001c0001t0001g0077 a0001c0001t0001g0094 others(9): Show |
12 | HG01433.hp1 HG01433.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.414+8275C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117802490 | |||||||
| chr7:117802511 | G | A | 3 | a0001c0001t0001g0089 a0001c0001t0001g0106 a0001c0001t0002g0090 |
3 | HG01346.hp1 HG02145.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.414+8254C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117802511 | |||||||
| chr7:117802586 | C | T | 3 | a0001c0001t0001g0089 a0001c0001t0001g0106 a0001c0001t0002g0090 |
3 | HG01346.hp1 HG02145.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.414+8179G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117802586 | |||||||
| chr7:117802627 | T | C | 25 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0020 others(22): Show |
25 | HG01069.hp2 HG01071.hp1 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.414+8138A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117802627 | |||||||
| chr7:117802758 | C | T | 2 | a0001c0001t0002g0007 a0001c0001t0002g0022 |
2 | HG03041.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.414+8007G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117802758 | |||||||
| chr7:117802815 | A | G | 3 | a0001c0001t0001g0089 a0001c0001t0001g0106 a0001c0001t0002g0090 |
3 | HG01346.hp1 HG02145.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.414+7950T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117802815 | |||||||
| chr7:117803186 | C | T | 15 | a0001c0001t0001g0023 a0001c0001t0001g0059 a0001c0001t0001g0072 others(12): Show |
15 | HG01433.hp1 HG01433.hp2 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.414+7579G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117803186 | |||||||
| chr7:117803485 | C | T | 8 | a0001c0001t0001g0044 a0001c0001t0001g0070 a0001c0001t0001g0080 others(5): Show |
8 | HG02258.hp1 HG02280.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.414+7280G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117803485 | |||||||
| chr7:117803516 | A | C | 3 | a0001c0001t0001g0089 a0001c0001t0001g0106 a0001c0001t0002g0090 |
3 | HG01346.hp1 HG02145.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.414+7249T>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117803516 | |||||||
| chr7:117803729 | T | C | 3 | a0001c0001t0001g0089 a0001c0001t0001g0106 a0001c0001t0002g0090 |
3 | HG01346.hp1 HG02145.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.414+7036A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117803729 | |||||||
| chr7:117803760 | A | G | 1 | a0003c0003t0002g0138 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.414+7005T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117803760 | |||||||
| chr7:117804009 | C | T | 2 | a0001c0001t0001g0094 a0001c0001t0001g0095 |
2 | HG02970.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.414+6756G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117804009 | |||||||
| chr7:117804048 | T | G | 1 | a0001c0001t0001g0042 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.414+6717A>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117804048 | |||||||
| chr7:117804111 | C | T | 25 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0020 others(22): Show |
25 | HG01069.hp2 HG01071.hp1 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.414+6654G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117804111 | |||||||
| chr7:117804276 | A | G | 25 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0020 others(22): Show |
25 | HG01069.hp2 HG01071.hp1 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.414+6489T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117804276 | |||||||
| chr7:117804348 | G | T | 3 | a0001c0001t0001g0089 a0001c0001t0001g0106 a0001c0001t0002g0090 |
3 | HG01346.hp1 HG02145.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.414+6417C>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117804348 | |||||||
| chr7:117804510 | A | G | 56 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0020 others(53): Show |
57 | HG01069.hp2 HG01071.hp1 HG01074.hp1 others(54): Show |
intron_variant | MODIFIER | c.414+6255T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117804510 | |||||||
| chr7:117804546 | T | G | 13 | a0001c0001t0001g0023 a0001c0001t0001g0056 a0001c0001t0001g0059 others(10): Show |
13 | HG02145.hp1 HG02451.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.414+6219A>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117804546 | |||||||
| chr7:117804621 | A | G | 3 | a0001c0001t0001g0089 a0001c0001t0001g0106 a0001c0001t0002g0090 |
3 | HG01346.hp1 HG02145.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.414+6144T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117804621 | |||||||
| chr7:117804738 | G | C | 3 | a0001c0001t0001g0089 a0001c0001t0001g0106 a0001c0001t0002g0090 |
3 | HG01346.hp1 HG02145.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.414+6027C>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117804738 | |||||||
| chr7:117804994 | T | C | 66 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0020 others(63): Show |
67 | HG01069.hp2 HG01071.hp1 HG01074.hp1 others(64): Show |
intron_variant | MODIFIER | c.414+5771A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117804994 | |||||||
| chr7:117805178 | T | G | 5 | a0001c0001t0001g0074 a0001c0001t0002g0035 a0002c0002t0001g0001 others(2): Show |
6 | HG01074.hp2 HG01192.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.414+5587A>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117805178 | |||||||
| chr7:117805259 | T | A | 5 | a0001c0001t0002g0035 a0002c0002t0001g0001 a0002c0002t0002g0073 others(2): Show |
6 | HG01074.hp2 HG01192.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.414+5506A>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117805259 | |||||||
| chr7:117805516 | A | G | 34 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0023 others(31): Show |
35 | HG00323.hp1 HG00609.hp1 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.414+5249T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117805516 | |||||||
| chr7:117805610 | A | G | 138 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(135): Show |
139 | HG00323.hp2 HG00609.hp2 HG00639.hp1 others(136): Show |
intron_variant | MODIFIER | c.414+5155T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117805610 | |||||||
| chr7:117806038 | C | T | 78 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(75): Show |
78 | HG00323.hp2 HG00609.hp2 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.414+4727G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117806038 | |||||||
| chr7:117806073 | G | A | 1 | a0001c0001t0002g0035 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.414+4692C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117806073 | |||||||
| chr7:117806110 | T | A | 6 | a0001c0001t0001g0044 a0001c0001t0001g0080 a0001c0001t0001g0081 others(3): Show |
6 | HG02258.hp1 HG02280.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.414+4655A>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117806110 | |||||||
| chr7:117806296 | A | G | 1 | a0001c0001t0002g0024 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.414+4469T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117806296 | |||||||
| chr7:117806321 | A | G | 1 | a0001c0001t0002g0002 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.414+4444T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117806321 | |||||||
| chr7:117806428 | C | T | 3 | a0001c0001t0001g0089 a0001c0001t0001g0106 a0001c0001t0003g0121 |
3 | HG01168.hp2 HG01346.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.414+4337G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117806428 | |||||||
| chr7:117806509 | C | T | 10 | a0001c0001t0001g0072 a0001c0001t0001g0074 a0001c0001t0001g0077 others(7): Show |
10 | HG01433.hp2 HG02257.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.414+4256G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117806509 | |||||||
| chr7:117806514 | A | C | 1 | a0001c0001t0002g0035 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.414+4251T>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117806514 | |||||||
| chr7:117806522 | G | A | 1 | a0001c0001t0001g0065 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.414+4243C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117806522 | |||||||
| chr7:117806696 | G | A | 1 | a0001c0001t0002g0037 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.414+4069C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117806696 | |||||||
| chr7:117806744 | AT | A | 27 | a0001c0001t0001g0004 a0001c0001t0001g0068 a0001c0001t0001g0085 others(24): Show |
28 | HG00609.hp1 HG01069.hp1 HG01074.hp2 others(25): Show |
intron_variant | MODIFIER | c.414+4020delA | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117806744 | |||||||
| chr7:117806744 | ATT | A | 118 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(115): Show |
118 | HG00323.hp2 HG00609.hp2 HG00639.hp1 others(115): Show |
intron_variant | MODIFIER | c.414+4019_414+4020d others(4): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117806744 | |||||||
| chr7:117806744 | ATTT | A | 8 | a0001c0001t0001g0016 a0001c0001t0001g0065 a0001c0001t0001g0080 others(5): Show |
8 | HG01496.hp1 HG01496.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.414+4018_414+4020d others(5): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117806744 | |||||||
| chr7:117806756 | T | G | 7 | a0001c0001t0002g0035 a0001c0001t0002g0047 a0001c0006t0002g0079 others(4): Show |
8 | HG01074.hp2 HG01192.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.414+4009A>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117806756 | |||||||
| chr7:117806757 | T | G | 10 | a0001c0001t0001g0004 a0001c0001t0001g0085 a0001c0001t0001g0116 others(7): Show |
10 | HG00609.hp1 HG01952.hp1 HG01952.hp2 others(7): Show |
intron_variant | MODIFIER | c.414+4008A>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117806757 | |||||||
| chr7:117806758 | T | G | 119 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(116): Show |
119 | HG00323.hp2 HG00609.hp2 HG00639.hp1 others(116): Show |
intron_variant | MODIFIER | c.414+4007A>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117806758 | |||||||
| chr7:117806759 | T | G | 6 | a0001c0001t0001g0044 a0001c0001t0001g0080 a0001c0001t0001g0081 others(3): Show |
6 | HG02258.hp1 HG02280.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.414+4006A>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117806759 | |||||||
| chr7:117806760 | T | G | 1 | a0008c0014t0001g0083 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.414+4005A>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117806760 | |||||||
| chr7:117806789 | C | T | 1 | a0001c0001t0002g0130 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.414+3976G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117806789 | |||||||
| chr7:117806813 | C | A | 91 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(88): Show |
91 | HG00323.hp2 HG00609.hp2 HG00639.hp1 others(88): Show |
intron_variant | MODIFIER | c.414+3952G>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117806813 | |||||||
| chr7:117806852 | A | G | 97 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(94): Show |
98 | HG00323.hp2 HG00609.hp2 HG00639.hp1 others(95): Show |
intron_variant | MODIFIER | c.414+3913T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117806852 | |||||||
| chr7:117807003 | C | T | 1 | a0001c0001t0001g0092 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.414+3762G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117807003 | |||||||
| chr7:117807113 | C | T | 1 | a0001c0001t0001g0146 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.414+3652G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117807113 | |||||||
| chr7:117807262 | C | A | 1 | a0002c0002t0002g0073 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.414+3503G>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117807262 | |||||||
| chr7:117807351 | A | G | 1 | a0001c0001t0002g0032 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.414+3414T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117807351 | |||||||
| chr7:117807450 | A | T | 91 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(88): Show |
91 | HG00323.hp2 HG00609.hp2 HG00639.hp1 others(88): Show |
intron_variant | MODIFIER | c.414+3315T>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117807450 | |||||||
| chr7:117807575 | T | C | 1 | a0001c0001t0001g0042 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.414+3190A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117807575 | |||||||
| chr7:117807577 | T | C | 1 | a0001c0001t0003g0131 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.414+3188A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117807577 | |||||||
| chr7:117808176 | C | T | 141 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(138): Show |
142 | HG00323.hp2 HG00609.hp2 HG00639.hp1 others(139): Show |
intron_variant | MODIFIER | c.414+2589G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117808176 | |||||||
| chr7:117808299 | A | C | 2 | a0001c0001t0001g0109 a0001c0001t0001g0113 |
2 | HG02622.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.414+2466T>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117808299 | |||||||
| chr7:117808509 | C | T | 3 | a0001c0001t0002g0007 a0001c0004t0001g0008 a0006c0012t0002g0055 |
3 | HG02451.hp1 HG02970.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.414+2256G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117808509 | |||||||
| chr7:117808640 | G | A | 1 | a0001c0001t0001g0113 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.414+2125C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117808640 | |||||||
| chr7:117808751 | T | C | 2 | a0001c0001t0001g0098 a0001c0016t0001g0058 |
2 | HG00609.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.414+2014A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117808751 | |||||||
| chr7:117808926 | A | G | 1 | a0001c0001t0001g0076 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.414+1839T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117808926 | |||||||
| chr7:117809070 | C | T | 1 | a0001c0001t0002g0047 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.414+1695G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117809070 | |||||||
| chr7:117809152 | C | A | 1 | a0001c0001t0002g0035 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.414+1613G>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117809152 | |||||||
| chr7:117809188 | TA | T | 102 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(99): Show |
103 | HG00323.hp2 HG00609.hp2 HG00639.hp1 others(100): Show |
intron_variant | MODIFIER | c.414+1576delT | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117809188 | |||||||
| chr7:117809482 | T | C | 1 | a0001c0001t0001g0065 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.414+1283A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117809482 | |||||||
| chr7:117809790 | T | C | 78 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(75): Show |
79 | HG00323.hp2 HG00609.hp2 HG00639.hp1 others(76): Show |
intron_variant | MODIFIER | c.414+975A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117809790 | |||||||
| chr7:117810044 | C | T | 1 | a0001c0001t0002g0127 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.414+721G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117810044 | |||||||
| chr7:117810375 | A | G | 6 | a0001c0001t0001g0044 a0001c0001t0001g0080 a0001c0001t0001g0081 others(3): Show |
6 | HG02258.hp1 HG02280.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.414+390T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117810375 | |||||||
| chr7:117810379 | A | G | 1 | a0001c0001t0001g0065 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.414+386T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117810379 | |||||||
| chr7:117810738 | A | C | 91 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(88): Show |
92 | HG00323.hp2 HG00609.hp2 HG00639.hp1 others(89): Show |
intron_variant | MODIFIER | c.414+27T>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117810738 | |||||||
| chr7:117810756 | C | T | 6 | a0001c0001t0001g0044 a0001c0001t0001g0080 a0001c0001t0001g0081 others(3): Show |
6 | HG02258.hp1 HG02280.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.414+9G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 3/22 | chr7 | 117810756 | |||||||
| chr7:117811070 | T | C | 69 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(66): Show |
69 | HG00323.hp2 HG00609.hp1 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.190-81A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117811070 | |||||||
| chr7:117811216 | A | G | 2 | a0001c0001t0001g0006 a0001c0001t0001g0049 |
2 | HG02109.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.190-227T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117811216 | |||||||
| chr7:117811648 | C | T | 22 | a0001c0001t0001g0044 a0001c0001t0001g0065 a0001c0001t0001g0077 others(19): Show |
22 | HG01433.hp2 HG02145.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.190-659G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117811648 | |||||||
| chr7:117811680 | G | A | 1 | a0001c0001t0001g0044 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.190-691C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117811680 | |||||||
| chr7:117811733 | C | T | 1 | a0002c0002t0002g0087 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.190-744G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117811733 | |||||||
| chr7:117811825 | A | T | 1 | a0001c0001t0001g0163 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.190-836T>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117811825 | |||||||
| chr7:117811829 | T | TAAAATTT others(24): Show |
1 | a0001c0001t0001g0101 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.190-871_190-841dup others(31): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117811829 | |||||||
| chr7:117811829 | TAAAATTT others(24): Show |
T | 99 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(96): Show |
100 | HG00323.hp2 HG00609.hp1 HG00639.hp2 others(97): Show |
intron_variant | MODIFIER | c.190-871_190-841del others(31): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117811829 | |||||||
| chr7:117811829 | TAAAATTT others(55): Show |
T | 18 | a0001c0001t0001g0023 a0001c0001t0001g0040 a0001c0001t0001g0044 others(15): Show |
18 | HG01168.hp2 HG01346.hp1 HG01433.hp1 others(15): Show |
intron_variant | MODIFIER | c.190-902_190-841del others(62): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117811829 | |||||||
| chr7:117811977 | C | T | 3 | a0001c0001t0002g0007 a0001c0004t0001g0008 a0006c0012t0002g0055 |
3 | HG02451.hp1 HG02970.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.190-988G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117811977 | |||||||
| chr7:117812111 | A | G | 5 | a0001c0001t0001g0044 a0001c0001t0001g0080 a0001c0001t0001g0081 others(2): Show |
5 | HG02258.hp1 HG02280.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.190-1122T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117812111 | |||||||
| chr7:117812117 | G | A | 1 | a0001c0001t0001g0074 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.190-1128C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117812117 | |||||||
| chr7:117812161 | C | A | 69 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(66): Show |
69 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(66): Show |
intron_variant | MODIFIER | c.190-1172G>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117812161 | |||||||
| chr7:117812168 | A | G | 6 | a0001c0001t0001g0045 a0001c0001t0002g0144 a0001c0001t0003g0075 others(3): Show |
7 | HG01074.hp2 HG01081.hp1 HG01081.hp2 others(4): Show |
intron_variant | MODIFIER | c.190-1179T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117812168 | |||||||
| chr7:117812227 | G | A | 8 | a0001c0001t0001g0077 a0001c0001t0001g0094 a0001c0001t0001g0095 others(5): Show |
8 | HG01433.hp2 HG02257.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.190-1238C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117812227 | |||||||
| chr7:117812589 | T | C | 1 | a0001c0001t0001g0089 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.190-1600A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117812589 | |||||||
| chr7:117812651 | T | C | 4 | a0001c0001t0001g0065 a0001c0001t0002g0007 a0001c0004t0001g0008 others(1): Show |
4 | HG02451.hp1 HG02965.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.190-1662A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117812651 | |||||||
| chr7:117812820 | C | T | 82 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(79): Show |
82 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.190-1831G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117812820 | |||||||
| chr7:117812850 | C | T | 82 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(79): Show |
82 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.190-1861G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117812850 | |||||||
| chr7:117813103 | G | A | 82 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(79): Show |
82 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.190-2114C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117813103 | |||||||
| chr7:117813212 | C | G | 82 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(79): Show |
82 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.190-2223G>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117813212 | |||||||
| chr7:117813698 | C | T | 5 | a0001c0001t0001g0023 a0001c0001t0002g0022 a0001c0001t0004g0033 others(2): Show |
5 | HG01433.hp1 HG02280.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.190-2709G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117813698 | |||||||
| chr7:117813947 | T | A | 1 | a0001c0001t0001g0003 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.190-2958A>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117813947 | |||||||
| chr7:117814212 | A | G | 1 | a0002c0002t0002g0087 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.190-3223T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117814212 | |||||||
| chr7:117814277 | T | G | 4 | a0001c0001t0001g0065 a0001c0001t0002g0007 a0001c0004t0001g0008 others(1): Show |
4 | HG02451.hp1 HG02965.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.190-3288A>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117814277 | |||||||
| chr7:117814487 | G | A | 4 | a0001c0001t0001g0044 a0001c0001t0001g0080 a0001c0001t0001g0082 others(1): Show |
4 | HG02258.hp1 HG02280.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.190-3498C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117814487 | |||||||
| chr7:117814521 | G | A | 82 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(79): Show |
82 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.190-3532C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117814521 | |||||||
| chr7:117814565 | C | T | 82 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(79): Show |
82 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.190-3576G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117814565 | |||||||
| chr7:117814813 | G | C | 6 | a0001c0001t0001g0045 a0001c0001t0002g0144 a0001c0001t0003g0075 others(3): Show |
7 | HG01074.hp2 HG01081.hp1 HG01081.hp2 others(4): Show |
intron_variant | MODIFIER | c.190-3824C>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117814813 | |||||||
| chr7:117815320 | T | C | 1 | a0001c0001t0001g0114 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.190-4331A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117815320 | |||||||
| chr7:117815322 | A | T | 82 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(79): Show |
82 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.190-4333T>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117815322 | |||||||
| chr7:117815328 | G | C | 82 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(79): Show |
82 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.190-4339C>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117815328 | |||||||
| chr7:117815358 | T | A | 82 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(79): Show |
82 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.190-4369A>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117815358 | |||||||
| chr7:117815929 | G | A | 82 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(79): Show |
82 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.190-4940C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117815929 | |||||||
| chr7:117815938 | C | A | 1 | a0001c0001t0001g0026 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.190-4949G>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117815938 | |||||||
| chr7:117816163 | A | G | 1 | a0001c0001t0001g0003 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.190-5174T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117816163 | |||||||
| chr7:117816251 | G | A | 7 | a0001c0001t0001g0114 a0001c0001t0001g0159 a0001c0001t0002g0154 others(4): Show |
7 | HG00323.hp1 HG01109.hp2 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.190-5262C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117816251 | |||||||
| chr7:117816364 | C | T | 1 | a0001c0001t0001g0111 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.190-5375G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117816364 | |||||||
| chr7:117816385 | T | C | 92 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(89): Show |
93 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(90): Show |
intron_variant | MODIFIER | c.190-5396A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117816385 | |||||||
| chr7:117816386 | G | A | 1 | a0001c0001t0001g0069 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.190-5397C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117816386 | |||||||
| chr7:117816643 | T | C | 1 | a0001c0001t0001g0159 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.190-5654A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117816643 | |||||||
| chr7:117816847 | T | C | 4 | a0001c0001t0001g0065 a0001c0001t0002g0007 a0001c0004t0001g0008 others(1): Show |
4 | HG02451.hp1 HG02965.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.190-5858A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117816847 | |||||||
| chr7:117816850 | C | T | 87 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(84): Show |
88 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(85): Show |
intron_variant | MODIFIER | c.190-5861G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117816850 | |||||||
| chr7:117816968 | T | C | 1 | a0001c0001t0001g0003 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.190-5979A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117816968 | |||||||
| chr7:117817087 | G | C | 91 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(88): Show |
92 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(89): Show |
intron_variant | MODIFIER | c.190-6098C>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117817087 | |||||||
| chr7:117817203 | G | A | 1 | a0001c0001t0002g0127 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.190-6214C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117817203 | |||||||
| chr7:117817344 | A | T | 86 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(83): Show |
87 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(84): Show |
intron_variant | MODIFIER | c.190-6355T>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117817344 | |||||||
| chr7:117817345 | A | T | 1 | a0011c0013t0001g0025 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.190-6356T>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117817345 | |||||||
| chr7:117817347 | A | T | 1 | a0001c0001t0001g0111 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.190-6358T>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117817347 | |||||||
| chr7:117817349 | A | T | 87 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(84): Show |
88 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(85): Show |
intron_variant | MODIFIER | c.190-6360T>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117817349 | |||||||
| chr7:117817350 | A | T | 1 | a0011c0013t0001g0025 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.190-6361T>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117817350 | |||||||
| chr7:117817350 | AAAAAAAA others(6): Show |
A | 1 | a0001c0001t0003g0075 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.190-6374_190-6362d others(15): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117817350 | |||||||
| chr7:117817352 | A | T | 1 | a0001c0001t0001g0111 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.190-6363T>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117817352 | |||||||
| chr7:117817353 | A | T | 3 | a0001c0001t0001g0006 a0001c0001t0001g0049 a0001c0006t0001g0078 |
3 | HG02109.hp2 HG02895.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.190-6364T>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117817353 | |||||||
| chr7:117817354 | A | T | 86 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(83): Show |
87 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(84): Show |
intron_variant | MODIFIER | c.190-6365T>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117817354 | |||||||
| chr7:117817355 | A | T | 1 | a0011c0013t0001g0025 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.190-6366T>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117817355 | |||||||
| chr7:117817357 | A | ATAATATA others(13): Show |
2 | a0001c0001t0002g0127 a0001c0006t0002g0079 |
2 | HG00642.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.190-6369_190-6368i others(22): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117817357 | |||||||
| chr7:117817357 | A | ATATATAT others(2): Show |
3 | a0001c0001t0001g0052 a0001c0001t0001g0056 a0001c0001t0001g0061 |
3 | HG02723.hp2 HG02896.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.190-6369_190-6368i others(11): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117817357 | |||||||
| chr7:117817357 | A | ATATATAT others(4): Show |
2 | a0001c0001t0001g0046 a0001c0001t0001g0107 |
2 | HG02258.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.190-6369_190-6368i others(13): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117817357 | |||||||
| chr7:117817357 | A | ATATATAT others(6): Show |
2 | a0001c0001t0001g0062 a0001c0001t0001g0126 |
2 | HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.190-6369_190-6368i others(15): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117817357 | |||||||
| chr7:117817357 | A | ATATATAT others(8): Show |
1 | a0001c0001t0001g0074 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.190-6369_190-6368i others(17): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117817357 | |||||||
| chr7:117817357 | A | ATATATAT others(10): Show |
1 | a0001c0001t0001g0015 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.190-6369_190-6368i others(19): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117817357 | |||||||
| chr7:117817357 | A | ATATATAT others(14): Show |
1 | a0001c0001t0001g0072 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.190-6369_190-6368i others(23): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117817357 | |||||||
| chr7:117817357 | A | T | 4 | a0001c0001t0001g0081 a0001c0001t0001g0111 a0001c0004t0001g0122 others(1): Show |
4 | HG02109.hp1 HG02895.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.190-6368T>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117817357 | |||||||
| chr7:117817357 | AAAAAAT | A | 6 | a0001c0001t0001g0077 a0001c0001t0001g0094 a0001c0001t0001g0095 others(3): Show |
6 | HG01433.hp2 HG02257.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.190-6374_190-6369d others(8): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117817357 | |||||||
| chr7:117817358 | A | T | 74 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(71): Show |
75 | HG00323.hp2 HG00639.hp2 HG01069.hp2 others(72): Show |
intron_variant | MODIFIER | c.190-6369T>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117817358 | |||||||
| chr7:117817359 | A | AATATATA others(19): Show |
1 | a0001c0006t0001g0078 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.190-6371_190-6370i others(28): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117817359 | |||||||
| chr7:117817359 | A | AT | 4 | a0001c0001t0001g0059 a0001c0001t0001g0117 a0003c0003t0002g0138 others(1): Show |
4 | HG03579.hp1 HG06807.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.190-6371_190-6370i others(3): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117817359 | |||||||
| chr7:117817359 | A | T | 17 | a0001c0001t0001g0015 a0001c0001t0001g0046 a0001c0001t0001g0052 others(14): Show |
17 | HG00642.hp2 HG02258.hp2 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.190-6370T>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117817359 | |||||||
| chr7:117817361 | A | ATAAATAA others(26): Show |
1 | a0001c0001t0003g0121 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.190-6373_190-6372i others(35): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117817361 | |||||||
| chr7:117817361 | A | ATAAATAA others(24): Show |
1 | a0001c0001t0001g0106 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.190-6373_190-6372i others(33): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117817361 | |||||||
| chr7:117817361 | A | ATAAATAA others(8): Show |
1 | a0001c0001t0001g0161 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.190-6373_190-6372i others(17): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117817361 | |||||||
| chr7:117817361 | A | ATAAATAA others(16): Show |
1 | a0001c0001t0001g0071 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.190-6373_190-6372i others(25): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117817361 | |||||||
| chr7:117817361 | A | ATAAATAA others(18): Show |
2 | a0001c0001t0001g0067 a0008c0014t0001g0083 |
2 | HG03225.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.190-6373_190-6372i others(27): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117817361 | |||||||
| chr7:117817361 | A | ATAAATAA others(20): Show |
1 | a0001c0001t0001g0068 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.190-6373_190-6372i others(29): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117817361 | |||||||
| chr7:117817361 | A | ATAAATAA others(22): Show |
2 | a0001c0001t0001g0057 a0001c0001t0002g0144 |
2 | HG01243.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.190-6373_190-6372i others(31): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117817361 | |||||||
| chr7:117817361 | A | ATAAATAA others(24): Show |
1 | a0001c0001t0001g0045 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.190-6373_190-6372i others(33): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117817361 | |||||||
| chr7:117817361 | A | ATAAATAA others(26): Show |
2 | a0002c0002t0001g0001 a0002c0002t0002g0073 |
3 | HG01074.hp2 HG01192.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.190-6373_190-6372i others(35): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117817361 | |||||||
| chr7:117817361 | A | ATAAATAT others(6): Show |
1 | a0001c0001t0002g0002 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.190-6373_190-6372i others(15): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117817361 | |||||||
| chr7:117817361 | A | ATAAATAT others(8): Show |
1 | a0001c0001t0001g0076 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.190-6373_190-6372i others(17): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117817361 | |||||||
| chr7:117817361 | A | ATAAATAT others(10): Show |
1 | a0001c0001t0001g0020 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.190-6373_190-6372i others(19): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117817361 | |||||||
| chr7:117817361 | A | ATAAATAT others(12): Show |
2 | a0001c0001t0001g0103 a0001c0001t0001g0105 |
2 | NA18954.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.190-6373_190-6372i others(21): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117817361 | |||||||
| chr7:117817361 | A | ATAAATAT others(14): Show |
1 | a0001c0001t0002g0022 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.190-6373_190-6372i others(23): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117817361 | |||||||
| chr7:117817361 | A | ATAAATAT others(16): Show |
1 | a0001c0001t0001g0088 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.190-6373_190-6372i others(25): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117817361 | |||||||
| chr7:117817361 | A | ATAAATAT others(18): Show |
2 | a0001c0001t0001g0040 a0001c0001t0001g0089 |
2 | HG01346.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.190-6373_190-6372i others(27): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117817361 | |||||||
| chr7:117817361 | A | ATAAATAT others(22): Show |
1 | a0001c0001t0004g0033 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.190-6373_190-6372i others(31): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117817361 | |||||||
| chr7:117817361 | A | ATAAATAT others(24): Show |
1 | a0001c0001t0001g0023 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.190-6373_190-6372i others(33): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117817361 | |||||||
| chr7:117817361 | A | ATAAATAT others(26): Show |
1 | a0001c0001t0004g0039 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.190-6373_190-6372i others(35): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117817361 | |||||||
| chr7:117817361 | A | ATAATATA others(9): Show |
1 | a0001c0001t0001g0019 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.190-6373_190-6372i others(18): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117817361 | |||||||
| chr7:117817361 | A | ATAATATA others(19): Show |
1 | a0001c0001t0004g0053 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.190-6373_190-6372i others(28): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117817361 | |||||||
| chr7:117817361 | A | ATATATAT others(6): Show |
1 | a0001c0001t0001g0069 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.190-6373_190-6372i others(15): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117817361 | |||||||
| chr7:117817361 | A | ATATATAT others(8): Show |
6 | a0001c0001t0001g0009 a0001c0001t0001g0086 a0001c0001t0001g0140 others(3): Show |
6 | HG00639.hp2 HG01346.hp2 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.190-6373_190-6372i others(17): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117817361 | |||||||
| chr7:117817361 | A | ATATATAT others(10): Show |
5 | a0001c0001t0001g0060 a0001c0001t0001g0063 a0001c0001t0001g0092 others(2): Show |
5 | HG01168.hp1 HG02486.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.190-6373_190-6372i others(19): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117817361 | |||||||
| chr7:117817361 | A | ATATATAT others(12): Show |
4 | a0001c0001t0001g0051 a0001c0001t0001g0141 a0001c0001t0001g0148 others(1): Show |
4 | HG01258.hp1 HG01952.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.190-6373_190-6372i others(21): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117817361 | |||||||
| chr7:117817361 | A | ATATATAT others(14): Show |
8 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(5): Show |
8 | HG01952.hp1 HG02040.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.190-6373_190-6372i others(23): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117817361 | |||||||
| chr7:117817361 | A | ATATATAT others(16): Show |
6 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0050 others(3): Show |
6 | HG01255.hp2 HG01993.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.190-6373_190-6372i others(25): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117817361 | |||||||
| chr7:117817361 | A | ATATATAT others(18): Show |
8 | a0001c0001t0001g0011 a0001c0001t0001g0084 a0001c0001t0001g0132 others(5): Show |
8 | HG01069.hp2 HG01071.hp1 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.190-6373_190-6372i others(27): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117817361 | |||||||
| chr7:117817361 | A | ATATATAT others(20): Show |
2 | a0001c0001t0001g0041 a0001c0001t0001g0119 |
2 | HG02523.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.190-6373_190-6372i others(29): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117817361 | |||||||
| chr7:117817361 | A | ATATATAT others(22): Show |
2 | a0001c0001t0001g0012 a0001c0001t0001g0042 |
2 | NA18960.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.190-6373_190-6372i others(31): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117817361 | |||||||
| chr7:117817361 | A | T | 23 | a0001c0001t0001g0015 a0001c0001t0001g0046 a0001c0001t0001g0052 others(20): Show |
23 | HG00642.hp2 HG02109.hp1 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.190-6372T>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117817361 | |||||||
| chr7:117817362 | AT | A | 26 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0026 others(23): Show |
26 | HG00323.hp1 HG00609.hp1 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.190-6374delA | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117817362 | |||||||
| chr7:117817363 | T | A | 16 | a0001c0001t0001g0021 a0001c0001t0001g0038 a0001c0001t0001g0070 others(13): Show |
16 | HG01192.hp2 HG01255.hp1 HG01358.hp1 others(13): Show |
intron_variant | MODIFIER | c.190-6374A>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117817363 | |||||||
| chr7:117817365 | T | A | 14 | a0001c0001t0001g0006 a0001c0001t0001g0021 a0001c0001t0001g0036 others(11): Show |
14 | HG01192.hp2 HG01358.hp1 HG01358.hp2 others(11): Show |
intron_variant | MODIFIER | c.190-6376A>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117817365 | |||||||
| chr7:117817367 | T | A | 5 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0002g0007 others(2): Show |
5 | HG02451.hp1 HG02965.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.190-6378A>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117817367 | |||||||
| chr7:117817368 | A | G | 1 | a0001c0001t0001g0057 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.190-6379T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117817368 | |||||||
| chr7:117817369 | T | A | 2 | a0001c0001t0001g0006 a0001c0001t0001g0049 |
2 | HG02109.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.190-6380A>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117817369 | |||||||
| chr7:117817387 | T | A | 1 | a0001c0001t0001g0005 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.190-6398A>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117817387 | |||||||
| chr7:117817471 | G | T | 1 | a0001c0001t0002g0027 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.190-6482C>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117817471 | |||||||
| chr7:117817844 | T | G | 1 | a0001c0001t0001g0077 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.190-6855A>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117817844 | |||||||
| chr7:117818290 | A | T | 86 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(83): Show |
86 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(83): Show |
intron_variant | MODIFIER | c.190-7301T>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117818290 | |||||||
| chr7:117818361 | C | T | 6 | a0001c0001t0001g0060 a0001c0001t0001g0066 a0001c0001t0001g0084 others(3): Show |
6 | HG02486.hp2 HG02615.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.190-7372G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117818361 | |||||||
| chr7:117818436 | A | C | 134 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(131): Show |
135 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(132): Show |
intron_variant | MODIFIER | c.190-7447T>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117818436 | |||||||
| chr7:117818459 | C | T | 2 | a0001c0001t0001g0115 a0001c0001t0001g0118 |
2 | NA18951.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.190-7470G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117818459 | |||||||
| chr7:117818632 | G | A | 1 | a0001c0004t0001g0122 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.190-7643C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117818632 | |||||||
| chr7:117818969 | A | G | 110 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(107): Show |
111 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(108): Show |
intron_variant | MODIFIER | c.190-7980T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117818969 | |||||||
| chr7:117818973 | C | T | 86 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(83): Show |
86 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(83): Show |
intron_variant | MODIFIER | c.190-7984G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117818973 | |||||||
| chr7:117818989 | G | C | 6 | a0001c0001t0001g0045 a0001c0001t0002g0144 a0001c0001t0003g0075 others(3): Show |
7 | HG01074.hp2 HG01081.hp1 HG01081.hp2 others(4): Show |
intron_variant | MODIFIER | c.190-8000C>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117818989 | |||||||
| chr7:117819135 | T | C | 4 | a0001c0001t0001g0085 a0001c0001t0001g0110 a0001c0001t0002g0032 others(1): Show |
4 | HG02145.hp1 HG03540.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.190-8146A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117819135 | |||||||
| chr7:117819318 | G | A | 1 | a0008c0014t0001g0083 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.190-8329C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117819318 | |||||||
| chr7:117819356 | T | TTC | 27 | a0001c0001t0001g0006 a0001c0001t0001g0020 a0001c0001t0001g0046 others(24): Show |
27 | HG00642.hp2 HG01069.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.190-8369_190-8368d others(4): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117819356 | |||||||
| chr7:117819356 | T | TTCTC | 36 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(33): Show |
36 | HG00323.hp2 HG00639.hp2 HG01071.hp2 others(33): Show |
intron_variant | MODIFIER | c.190-8371_190-8368d others(6): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117819356 | |||||||
| chr7:117819356 | T | TTCTCTC | 18 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0023 others(15): Show |
18 | HG01168.hp2 HG01255.hp2 HG01433.hp1 others(15): Show |
intron_variant | MODIFIER | c.190-8373_190-8368d others(8): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117819356 | |||||||
| chr7:117819356 | TTC | T | 9 | a0001c0001t0001g0026 a0001c0001t0001g0054 a0001c0001t0001g0064 others(6): Show |
9 | HG02145.hp2 HG02165.hp1 HG02165.hp2 others(6): Show |
intron_variant | MODIFIER | c.190-8369_190-8368d others(4): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117819356 | |||||||
| chr7:117819365 | T | TCA | 4 | a0001c0001t0001g0036 a0001c0001t0001g0158 a0001c0001t0002g0027 others(1): Show |
4 | HG02040.hp1 NA18969.hp2 NA20805.hp2 others(1): Show |
intron_variant | MODIFIER | c.190-8377_190-8376i others(4): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117819365 | |||||||
| chr7:117819365 | TCTCACA | T | 4 | a0001c0001t0001g0038 a0001c0001t0001g0097 a0001c0001t0001g0108 others(1): Show |
4 | HG01192.hp2 HG01358.hp2 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.190-8382_190-8377d others(8): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117819365 | |||||||
| chr7:117819365 | TCTCACAC others(1): Show |
T | 2 | a0001c0001t0001g0125 a0001c0015t0001g0160 |
2 | HG01255.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.190-8384_190-8377d others(10): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117819365 | |||||||
| chr7:117819367 | T | A | 6 | a0001c0001t0001g0036 a0001c0001t0001g0059 a0001c0001t0001g0093 others(3): Show |
6 | HG02040.hp1 HG06807.hp2 NA18969.hp2 others(3): Show |
intron_variant | MODIFIER | c.190-8378A>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117819367 | |||||||
| chr7:117819367 | T | TCA | 2 | a0004c0005t0001g0029 a0004c0005t0001g0030 |
2 | HG01433.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.190-8380_190-8379d others(4): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117819367 | |||||||
| chr7:117819367 | TCA | T | 25 | a0001c0001t0001g0014 a0001c0001t0001g0018 a0001c0001t0001g0021 others(22): Show |
26 | HG00323.hp1 HG00609.hp2 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.190-8380_190-8379d others(4): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117819367 | |||||||
| chr7:117819367 | TCACA | T | 2 | a0001c0001t0001g0065 a0001c0001t0001g0081 |
2 | HG02965.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.190-8382_190-8379d others(6): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117819367 | |||||||
| chr7:117819367 | TCACACA | T | 9 | a0001c0001t0001g0044 a0001c0001t0001g0085 a0001c0001t0001g0110 others(6): Show |
9 | HG01109.hp1 HG02145.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.190-8384_190-8379d others(8): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117819367 | |||||||
| chr7:117819367 | TCACACAC others(1): Show |
T | 2 | a0001c0001t0001g0080 a0001c0001t0001g0082 |
2 | HG02280.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.190-8386_190-8379d others(10): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117819367 | |||||||
| chr7:117819367 | TCACACAC others(3): Show |
T | 3 | a0001c0001t0002g0007 a0001c0004t0001g0008 a0006c0012t0002g0055 |
3 | HG02451.hp1 HG02970.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.190-8388_190-8379d others(12): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117819367 | |||||||
| chr7:117819367 | TCACACAC others(13): Show |
T | 1 | a0001c0007t0001g0010 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.190-8398_190-8379d others(22): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117819367 | |||||||
| chr7:117819369 | A | T | 86 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(83): Show |
86 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(83): Show |
intron_variant | MODIFIER | c.190-8380T>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117819369 | |||||||
| chr7:117819371 | A | T | 90 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(87): Show |
91 | HG00323.hp2 HG00639.hp1 HG00639.hp2 others(88): Show |
intron_variant | MODIFIER | c.190-8382T>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117819371 | |||||||
| chr7:117819373 | A | T | 86 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(83): Show |
87 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(84): Show |
intron_variant | MODIFIER | c.190-8384T>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117819373 | |||||||
| chr7:117819375 | A | T | 80 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(77): Show |
80 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(77): Show |
intron_variant | MODIFIER | c.190-8386T>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117819375 | |||||||
| chr7:117819377 | A | T | 40 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0020 others(37): Show |
40 | HG00642.hp2 HG01069.hp2 HG01071.hp1 others(37): Show |
intron_variant | MODIFIER | c.190-8388T>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117819377 | |||||||
| chr7:117819379 | A | T | 19 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0049 others(16): Show |
19 | HG01433.hp1 HG02109.hp2 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.190-8390T>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117819379 | |||||||
| chr7:117819381 | A | T | 6 | a0001c0001t0001g0006 a0001c0001t0001g0049 a0001c0001t0001g0065 others(3): Show |
6 | HG02109.hp2 HG02451.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.190-8392T>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117819381 | |||||||
| chr7:117819383 | A | T | 4 | a0001c0001t0001g0065 a0001c0001t0002g0007 a0001c0004t0001g0008 others(1): Show |
4 | HG02451.hp1 HG02965.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.190-8394T>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117819383 | |||||||
| chr7:117819385 | A | T | 4 | a0001c0001t0001g0065 a0001c0001t0002g0007 a0001c0004t0001g0008 others(1): Show |
4 | HG02451.hp1 HG02965.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.190-8396T>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117819385 | |||||||
| chr7:117819387 | A | T | 4 | a0001c0001t0001g0065 a0001c0001t0002g0007 a0001c0004t0001g0008 others(1): Show |
4 | HG02451.hp1 HG02965.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.190-8398T>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117819387 | |||||||
| chr7:117819389 | A | T | 3 | a0001c0001t0002g0007 a0001c0004t0001g0008 a0006c0012t0002g0055 |
3 | HG02451.hp1 HG02970.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.190-8400T>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117819389 | |||||||
| chr7:117819517 | T | C | 3 | a0001c0001t0002g0047 a0001c0006t0001g0078 a0001c0006t0002g0079 |
3 | HG02723.hp1 HG02818.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.190-8528A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117819517 | |||||||
| chr7:117820077 | C | G | 8 | a0001c0001t0001g0077 a0001c0001t0001g0094 a0001c0001t0001g0095 others(5): Show |
8 | HG01433.hp2 HG02257.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.190-9088G>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117820077 | |||||||
| chr7:117820200 | G | A | 86 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(83): Show |
86 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(83): Show |
intron_variant | MODIFIER | c.190-9211C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117820200 | |||||||
| chr7:117820796 | T | A | 2 | a0001c0001t0001g0021 a0001c0001t0001g0129 |
2 | HG00639.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.190-9807A>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117820796 | |||||||
| chr7:117820870 | G | A | 5 | a0001c0001t0001g0085 a0001c0001t0001g0110 a0001c0001t0002g0032 others(2): Show |
5 | HG02145.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.190-9881C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117820870 | |||||||
| chr7:117820902 | C | T | 13 | a0001c0001t0001g0023 a0001c0001t0001g0040 a0001c0001t0001g0057 others(10): Show |
13 | HG01168.hp2 HG01346.hp1 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.190-9913G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117820902 | |||||||
| chr7:117820903 | A | G | 86 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(83): Show |
86 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(83): Show |
intron_variant | MODIFIER | c.190-9914T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117820903 | |||||||
| chr7:117821156 | C | A | 86 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(83): Show |
86 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(83): Show |
intron_variant | MODIFIER | c.190-10167G>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117821156 | |||||||
| chr7:117821197 | G | A | 1 | a0001c0001t0001g0005 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.190-10208C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117821197 | |||||||
| chr7:117821231 | G | T | 1 | a0001c0001t0001g0003 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.190-10242C>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117821231 | |||||||
| chr7:117821326 | T | TG | 5 | a0001c0001t0001g0040 a0001c0001t0001g0057 a0001c0001t0001g0067 others(2): Show |
5 | HG02451.hp2 HG02630.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.190-10338dupC | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117821326 | |||||||
| chr7:117821329 | T | G | 81 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(78): Show |
81 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(78): Show |
intron_variant | MODIFIER | c.190-10340A>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117821329 | |||||||
| chr7:117821336 | TTTG | T | 8 | a0001c0001t0001g0077 a0001c0001t0001g0094 a0001c0001t0001g0095 others(5): Show |
8 | HG01433.hp2 HG02257.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.190-10350_190-1034 others(7): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117821336 | |||||||
| chr7:117821588 | A | AT | 23 | a0001c0001t0001g0017 a0001c0001t0001g0038 a0001c0001t0001g0046 others(20): Show |
23 | HG01069.hp1 HG01109.hp1 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.190-10600dupA | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117821588 | |||||||
| chr7:117821648 | G | C | 1 | a0001c0001t0003g0075 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.190-10659C>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117821648 | |||||||
| chr7:117822017 | C | A | 8 | a0001c0001t0001g0077 a0001c0001t0001g0094 a0001c0001t0001g0095 others(5): Show |
8 | HG01433.hp2 HG02257.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.190-11028G>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117822017 | |||||||
| chr7:117822231 | TC | T | 110 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(107): Show |
111 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(108): Show |
intron_variant | MODIFIER | c.190-11243delG | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117822231 | |||||||
| chr7:117822242 | C | T | 8 | a0001c0001t0001g0077 a0001c0001t0001g0094 a0001c0001t0001g0095 others(5): Show |
8 | HG01433.hp2 HG02257.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.190-11253G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117822242 | |||||||
| chr7:117822315 | C | A | 69 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(66): Show |
69 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(66): Show |
intron_variant | MODIFIER | c.190-11326G>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117822315 | |||||||
| chr7:117822381 | T | G | 86 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(83): Show |
86 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(83): Show |
intron_variant | MODIFIER | c.190-11392A>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117822381 | |||||||
| chr7:117822393 | CAA | C | 6 | a0001c0001t0001g0045 a0001c0001t0002g0144 a0001c0001t0003g0075 others(3): Show |
7 | HG01074.hp2 HG01081.hp1 HG01081.hp2 others(4): Show |
intron_variant | MODIFIER | c.190-11406_190-1140 others(6): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117822393 | |||||||
| chr7:117822562 | G | A | 82 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(79): Show |
82 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.190-11573C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117822562 | |||||||
| chr7:117822669 | C | T | 5 | a0001c0001t0001g0085 a0001c0001t0001g0110 a0001c0001t0002g0032 others(2): Show |
5 | HG02145.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.190-11680G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117822669 | |||||||
| chr7:117822767 | T | C | 1 | a0003c0003t0002g0128 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.190-11778A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117822767 | |||||||
| chr7:117822797 | A | G | 110 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(107): Show |
111 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(108): Show |
intron_variant | MODIFIER | c.190-11808T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117822797 | |||||||
| chr7:117822920 | TGA | T | 13 | a0001c0001t0001g0040 a0001c0001t0001g0045 a0001c0001t0001g0057 others(10): Show |
14 | HG01074.hp2 HG01081.hp1 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.190-11933_190-1193 others(6): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117822920 | |||||||
| chr7:117823140 | C | A | 114 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(111): Show |
115 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(112): Show |
intron_variant | MODIFIER | c.190-12151G>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117823140 | |||||||
| chr7:117823313 | C | T | 110 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(107): Show |
111 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(108): Show |
intron_variant | MODIFIER | c.190-12324G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117823313 | |||||||
| chr7:117823530 | T | C | 3 | a0001c0001t0001g0060 a0001c0001t0001g0066 a0001c0001t0001g0084 |
3 | HG02615.hp1 NA18522.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.190-12541A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117823530 | |||||||
| chr7:117823533 | C | T | 1 | a0001c0001t0002g0022 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.190-12544G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117823533 | |||||||
| chr7:117823721 | C | T | 1 | a0001c0001t0001g0003 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.190-12732G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117823721 | |||||||
| chr7:117823740 | C | A | 1 | a0001c0001t0001g0062 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.190-12751G>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117823740 | |||||||
| chr7:117823741 | C | A | 1 | a0001c0001t0001g0062 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.190-12752G>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117823741 | |||||||
| chr7:117823951 | C | CT | 105 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(102): Show |
106 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(103): Show |
intron_variant | MODIFIER | c.190-12963dupA | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117823951 | |||||||
| chr7:117824180 | G | GT | 98 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(95): Show |
99 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(96): Show |
intron_variant | MODIFIER | c.190-13192dupA | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117824180 | |||||||
| chr7:117824210 | T | C | 2 | a0001c0001t0001g0004 a0001c0001t0001g0133 |
2 | HG01952.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.190-13221A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117824210 | |||||||
| chr7:117824661 | T | C | 6 | a0001c0001t0001g0081 a0001c0001t0001g0085 a0001c0001t0001g0110 others(3): Show |
6 | HG02145.hp1 HG03540.hp2 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.190-13672A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117824661 | |||||||
| chr7:117825061 | G | A | 1 | a0008c0014t0001g0083 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.190-14072C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117825061 | |||||||
| chr7:117825085 | T | C | 1 | a0001c0004t0001g0122 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.190-14096A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117825085 | |||||||
| chr7:117825245 | G | C | 1 | a0001c0001t0003g0137 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.190-14256C>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117825245 | |||||||
| chr7:117825321 | G | T | 1 | a0002c0002t0002g0073 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.190-14332C>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117825321 | |||||||
| chr7:117825409 | A | C | 1 | a0002c0002t0002g0087 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.190-14420T>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117825409 | |||||||
| chr7:117825606 | G | T | 1 | a0001c0001t0005g0152 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.190-14617C>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117825606 | |||||||
| chr7:117825646 | G | GCTTCAAA others(28): Show |
1 | a0001c0001t0002g0154 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.190-14692_190-1465 others(39): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117825646 | |||||||
| chr7:117825664 | C | A | 2 | a0001c0001t0001g0044 a0001c0007t0001g0010 |
2 | HG02258.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.190-14675G>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117825664 | |||||||
| chr7:117826005 | C | A | 1 | a0001c0001t0002g0154 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.190-15016G>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117826005 | |||||||
| chr7:117826398 | T | A | 1 | a0001c0001t0001g0101 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.190-15409A>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117826398 | |||||||
| chr7:117826712 | ATAT | A | 5 | a0001c0001t0001g0085 a0001c0001t0001g0110 a0001c0001t0002g0032 others(2): Show |
5 | HG02145.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.190-15726_190-1572 others(7): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117826712 | |||||||
| chr7:117826713 | T | C | 102 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(99): Show |
103 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(100): Show |
intron_variant | MODIFIER | c.190-15724A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117826713 | |||||||
| chr7:117826716 | T | C | 5 | a0001c0001t0001g0085 a0001c0001t0001g0110 a0001c0001t0002g0032 others(2): Show |
5 | HG02145.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.190-15727A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117826716 | |||||||
| chr7:117826785 | T | C | 2 | a0001c0001t0001g0135 a0001c0001t0002g0130 |
2 | HG00639.hp2 HG01257.hp2 |
intron_variant | MODIFIER | c.190-15796A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117826785 | |||||||
| chr7:117826826 | C | CATT | 2 | a0001c0001t0001g0094 a0011c0013t0001g0025 |
2 | HG02970.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.190-15840_190-1583 others(7): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117826826 | |||||||
| chr7:117826826 | CATT | C | 23 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0016 others(20): Show |
23 | HG00609.hp1 HG01257.hp1 HG01258.hp1 others(20): Show |
intron_variant | MODIFIER | c.190-15840_190-1583 others(7): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117826826 | |||||||
| chr7:117826826 | CATTATT | C | 67 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(64): Show |
68 | HG00323.hp1 HG00323.hp2 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.190-15843_190-1583 others(10): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117826826 | |||||||
| chr7:117826826 | CATTATTA others(2): Show |
C | 22 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0019 others(19): Show |
22 | HG01109.hp1 HG02280.hp1 HG02451.hp2 others(19): Show |
intron_variant | MODIFIER | c.190-15846_190-1583 others(13): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117826826 | |||||||
| chr7:117826826 | CATTATTA others(5): Show |
C | 28 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0020 others(25): Show |
28 | HG00642.hp2 HG01069.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.190-15849_190-1583 others(16): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117826826 | |||||||
| chr7:117826826 | CATTATTA others(8): Show |
C | 2 | a0001c0001t0003g0075 a0001c0001t0005g0152 |
2 | HG01081.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.190-15852_190-1583 others(19): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117826826 | |||||||
| chr7:117826826 | CATTATTA others(11): Show |
C | 1 | a0001c0001t0001g0136 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.190-15855_190-1583 others(22): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117826826 | |||||||
| chr7:117826894 | C | T | 13 | a0001c0001t0001g0040 a0001c0001t0001g0045 a0001c0001t0001g0057 others(10): Show |
14 | HG01074.hp2 HG01081.hp1 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.190-15905G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117826894 | |||||||
| chr7:117826949 | T | A | 102 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(99): Show |
103 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(100): Show |
intron_variant | MODIFIER | c.190-15960A>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117826949 | |||||||
| chr7:117827494 | C | T | 5 | a0001c0001t0001g0085 a0001c0001t0001g0110 a0001c0001t0002g0032 others(2): Show |
5 | HG02145.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.190-16505G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117827494 | |||||||
| chr7:117827511 | C | G | 8 | a0001c0001t0001g0040 a0001c0001t0001g0057 a0001c0001t0001g0067 others(5): Show |
8 | HG01168.hp2 HG01346.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.190-16522G>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117827511 | |||||||
| chr7:117827610 | G | A | 1 | a0001c0001t0002g0035 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.190-16621C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117827610 | |||||||
| chr7:117828002 | C | T | 68 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(65): Show |
68 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.190-17013G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117828002 | |||||||
| chr7:117828280 | T | C | 110 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(107): Show |
111 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(108): Show |
intron_variant | MODIFIER | c.190-17291A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117828280 | |||||||
| chr7:117829142 | C | A | 1 | a0001c0001t0005g0034 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.190-18153G>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117829142 | |||||||
| chr7:117829208 | A | G | 8 | a0001c0001t0001g0077 a0001c0001t0001g0094 a0001c0001t0001g0095 others(5): Show |
8 | HG01433.hp2 HG02257.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.190-18219T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117829208 | |||||||
| chr7:117829466 | A | G | 1 | a0001c0004t0001g0122 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.190-18477T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117829466 | |||||||
| chr7:117829607 | G | A | 1 | a0001c0001t0001g0111 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.190-18618C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117829607 | |||||||
| chr7:117829617 | T | G | 1 | a0001c0001t0002g0035 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.190-18628A>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117829617 | |||||||
| chr7:117829688 | T | C | 1 | a0002c0002t0002g0087 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.190-18699A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117829688 | |||||||
| chr7:117829709 | G | A | 1 | a0001c0001t0001g0013 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.190-18720C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117829709 | |||||||
| chr7:117830007 | C | T | 1 | a0001c0001t0001g0142 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.190-19018G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117830007 | |||||||
| chr7:117830639 | C | G | 111 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(108): Show |
112 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(109): Show |
intron_variant | MODIFIER | c.190-19650G>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117830639 | |||||||
| chr7:117830896 | T | C | 2 | a0001c0001t0001g0004 a0001c0001t0001g0133 |
2 | HG01952.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.190-19907A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117830896 | |||||||
| chr7:117830958 | T | C | 1 | a0001c0001t0001g0015 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.190-19969A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117830958 | |||||||
| chr7:117831057 | C | T | 1 | a0001c0004t0001g0122 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.190-20068G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117831057 | |||||||
| chr7:117831495 | C | T | 83 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(80): Show |
83 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(80): Show |
intron_variant | MODIFIER | c.190-20506G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117831495 | |||||||
| chr7:117831683 | TAGA | T | 68 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(65): Show |
68 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.190-20697_190-2069 others(7): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117831683 | |||||||
| chr7:117831966 | A | C | 8 | a0001c0001t0001g0077 a0001c0001t0001g0094 a0001c0001t0001g0095 others(5): Show |
8 | HG01433.hp2 HG02257.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.190-20977T>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117831966 | |||||||
| chr7:117832187 | A | G | 5 | a0001c0001t0001g0081 a0001c0001t0001g0085 a0001c0001t0001g0110 others(2): Show |
5 | HG02145.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.190-21198T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117832187 | |||||||
| chr7:117832279 | A | G | 1 | a0001c0001t0001g0077 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.190-21290T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117832279 | |||||||
| chr7:117832535 | A | AT | 20 | a0001c0001t0001g0023 a0001c0001t0001g0040 a0001c0001t0001g0045 others(17): Show |
21 | HG01074.hp2 HG01081.hp1 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.190-21547dupA | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117832535 | |||||||
| chr7:117832626 | C | T | 4 | a0001c0001t0001g0065 a0001c0001t0002g0007 a0001c0004t0001g0008 others(1): Show |
4 | HG02451.hp1 HG02965.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.190-21637G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117832626 | |||||||
| chr7:117832737 | C | CT | 14 | a0001c0001t0001g0044 a0001c0001t0001g0065 a0001c0001t0001g0076 others(11): Show |
14 | HG00323.hp2 HG01361.hp2 HG01993.hp1 others(11): Show |
intron_variant | MODIFIER | c.190-21749dupA | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117832737 | |||||||
| chr7:117832737 | CT | C | 14 | a0001c0001t0001g0026 a0001c0001t0001g0054 a0001c0001t0001g0059 others(11): Show |
15 | HG01074.hp2 HG01192.hp1 HG01993.hp2 others(12): Show |
intron_variant | MODIFIER | c.190-21749delA | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117832737 | |||||||
| chr7:117832919 | CT | C | 103 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(100): Show |
104 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(101): Show |
intron_variant | MODIFIER | c.190-21931delA | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117832919 | |||||||
| chr7:117833007 | G | A | 4 | a0001c0001t0001g0085 a0001c0001t0001g0110 a0001c0001t0002g0032 others(1): Show |
4 | HG02145.hp1 HG03540.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.190-22018C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117833007 | |||||||
| chr7:117833034 | C | T | 4 | a0001c0001t0001g0085 a0001c0001t0001g0110 a0001c0001t0002g0032 others(1): Show |
4 | HG02145.hp1 HG03540.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.190-22045G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117833034 | |||||||
| chr7:117833038 | A | G | 19 | a0001c0001t0001g0023 a0001c0001t0001g0040 a0001c0001t0001g0045 others(16): Show |
20 | HG01074.hp2 HG01081.hp1 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.190-22049T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117833038 | |||||||
| chr7:117833045 | G | A | 2 | a0001c0001t0001g0158 a0001c0001t0003g0147 |
2 | NA20805.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.190-22056C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117833045 | |||||||
| chr7:117833372 | C | T | 1 | a0001c0001t0001g0111 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.190-22383G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117833372 | |||||||
| chr7:117833417 | G | A | 1 | a0001c0004t0001g0122 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.190-22428C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117833417 | |||||||
| chr7:117833536 | C | T | 3 | a0001c0001t0001g0014 a0001c0001t0001g0115 a0001c0001t0001g0118 |
3 | NA18951.hp1 NA18960.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.190-22547G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117833536 | |||||||
| chr7:117833632 | C | T | 1 | a0001c0001t0003g0075 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.190-22643G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117833632 | |||||||
| chr7:117833802 | T | C | 5 | a0001c0001t0001g0044 a0001c0001t0001g0080 a0001c0001t0001g0081 others(2): Show |
5 | HG02258.hp1 HG02280.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.190-22813A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117833802 | |||||||
| chr7:117833970 | A | T | 1 | a0001c0017t0001g0043 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.190-22981T>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117833970 | |||||||
| chr7:117833980 | T | C | 2 | a0001c0001t0001g0006 a0001c0001t0001g0049 |
2 | HG02109.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.190-22991A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117833980 | |||||||
| chr7:117834046 | T | C | 1 | a0002c0002t0002g0087 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.190-23057A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117834046 | |||||||
| chr7:117834057 | C | CT | 95 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(92): Show |
96 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(93): Show |
intron_variant | MODIFIER | c.190-23069dupA | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117834057 | |||||||
| chr7:117834057 | C | CTT | 6 | a0001c0001t0001g0013 a0001c0001t0001g0017 a0001c0001t0001g0050 others(3): Show |
6 | HG01168.hp1 HG01255.hp2 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.190-23070_190-2306 others(6): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117834057 | |||||||
| chr7:117834213 | C | T | 15 | a0001c0001t0001g0026 a0001c0001t0001g0036 a0001c0001t0001g0038 others(12): Show |
15 | HG01192.hp2 HG01255.hp1 HG01358.hp2 others(12): Show |
intron_variant | MODIFIER | c.190-23224G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117834213 | |||||||
| chr7:117834471 | G | A | 2 | a0001c0001t0001g0045 a0001c0001t0002g0144 |
2 | HG01081.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.190-23482C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117834471 | |||||||
| chr7:117834666 | T | A | 112 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(109): Show |
113 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(110): Show |
intron_variant | MODIFIER | c.190-23677A>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117834666 | |||||||
| chr7:117834990 | G | T | 3 | a0001c0001t0002g0047 a0001c0006t0001g0078 a0001c0006t0002g0079 |
3 | HG02723.hp1 HG02818.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.190-24001C>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117834990 | |||||||
| chr7:117835039 | T | C | 1 | a0005c0009t0001g0102 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.190-24050A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117835039 | |||||||
| chr7:117835076 | G | A | 1 | a0001c0001t0001g0049 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.190-24087C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117835076 | |||||||
| chr7:117835129 | C | G | 4 | a0001c0001t0001g0059 a0001c0001t0001g0085 a0001c0001t0001g0110 others(1): Show |
4 | HG03540.hp2 HG03579.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.190-24140G>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117835129 | |||||||
| chr7:117835270 | C | G | 94 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(91): Show |
94 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(91): Show |
intron_variant | MODIFIER | c.190-24281G>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117835270 | |||||||
| chr7:117835274 | T | C | 113 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(110): Show |
114 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(111): Show |
intron_variant | MODIFIER | c.190-24285A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117835274 | |||||||
| chr7:117835699 | A | G | 114 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(111): Show |
115 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(112): Show |
intron_variant | MODIFIER | c.190-24710T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117835699 | |||||||
| chr7:117835730 | C | T | 4 | a0001c0001t0001g0065 a0001c0001t0002g0007 a0001c0004t0001g0008 others(1): Show |
4 | HG02451.hp1 HG02965.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.190-24741G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117835730 | |||||||
| chr7:117835756 | T | G | 4 | a0001c0001t0001g0070 a0001c0001t0001g0089 a0001c0001t0001g0106 others(1): Show |
4 | HG01168.hp2 HG01346.hp1 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.190-24767A>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117835756 | |||||||
| chr7:117835955 | C | T | 6 | a0001c0001t0001g0011 a0001c0001t0001g0036 a0001c0001t0001g0124 others(3): Show |
6 | HG02040.hp2 HG04184.hp2 NA18969.hp2 others(3): Show |
intron_variant | MODIFIER | c.190-24966G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117835955 | |||||||
| chr7:117836323 | G | A | 1 | a0001c0001t0001g0092 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.189+24886C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117836323 | |||||||
| chr7:117836380 | C | G | 2 | a0001c0001t0001g0045 a0001c0001t0002g0144 |
2 | HG01081.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.189+24829G>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117836380 | |||||||
| chr7:117836437 | G | A | 1 | a0001c0001t0001g0060 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.189+24772C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117836437 | |||||||
| chr7:117836481 | A | G | 2 | a0001c0001t0001g0021 a0001c0001t0001g0129 |
2 | HG00639.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.189+24728T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117836481 | |||||||
| chr7:117836517 | C | T | 1 | a0001c0001t0001g0038 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.189+24692G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117836517 | |||||||
| chr7:117836703 | T | C | 1 | a0001c0001t0001g0065 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.189+24506A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117836703 | |||||||
| chr7:117836709 | G | A | 32 | a0001c0001t0001g0038 a0001c0001t0001g0044 a0001c0001t0001g0046 others(29): Show |
32 | HG00609.hp1 HG01192.hp2 HG01433.hp2 others(29): Show |
intron_variant | MODIFIER | c.189+24500C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117836709 | |||||||
| chr7:117836966 | T | C | 6 | a0001c0001t0001g0044 a0001c0001t0001g0080 a0001c0001t0001g0081 others(3): Show |
6 | HG02258.hp1 HG02280.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.189+24243A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117836966 | |||||||
| chr7:117837001 | A | G | 3 | a0001c0001t0001g0004 a0001c0001t0001g0092 a0001c0001t0001g0119 |
3 | HG02523.hp1 NA19011.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.189+24208T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117837001 | |||||||
| chr7:117837084 | A | G | 60 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0019 others(57): Show |
60 | HG00609.hp1 HG00639.hp1 HG00642.hp1 others(57): Show |
intron_variant | MODIFIER | c.189+24125T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117837084 | |||||||
| chr7:117837245 | T | C | 39 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0009 others(36): Show |
39 | HG00639.hp2 HG01069.hp1 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.189+23964A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117837245 | |||||||
| chr7:117837853 | C | T | 3 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0077 |
3 | HG02630.hp2 HG02896.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.189+23356G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117837853 | |||||||
| chr7:117837935 | G | C | 3 | a0001c0001t0001g0006 a0001c0001t0001g0110 a0001c0001t0001g0111 |
3 | HG02109.hp1 HG03540.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.189+23274C>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117837935 | |||||||
| chr7:117837955 | C | CATAG | 3 | a0001c0001t0002g0047 a0001c0006t0001g0078 a0001c0006t0002g0079 |
3 | HG02723.hp1 HG02818.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.189+23253_189+2325 others(8): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117837955 | |||||||
| chr7:117837974 | T | C | 117 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(114): Show |
117 | HG00323.hp2 HG00609.hp1 HG00639.hp2 others(114): Show |
intron_variant | MODIFIER | c.189+23235A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117837974 | |||||||
| chr7:117838285 | C | T | 3 | a0001c0001t0002g0047 a0001c0006t0001g0078 a0001c0006t0002g0079 |
3 | HG02723.hp1 HG02818.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.189+22924G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117838285 | |||||||
| chr7:117838417 | G | T | 1 | a0003c0003t0002g0138 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.189+22792C>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117838417 | |||||||
| chr7:117838752 | G | T | 1 | a0001c0001t0001g0084 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.189+22457C>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117838752 | |||||||
| chr7:117838962 | G | A | 1 | a0006c0012t0002g0055 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.189+22247C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117838962 | |||||||
| chr7:117838967 | C | CG | 20 | a0001c0001t0001g0012 a0001c0001t0001g0036 a0001c0001t0001g0044 others(17): Show |
20 | HG00323.hp2 HG00609.hp1 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.189+22241dupC | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117838967 | |||||||
| chr7:117838967 | C | CGG | 12 | a0001c0001t0001g0038 a0001c0001t0001g0040 a0001c0001t0001g0041 others(9): Show |
12 | HG01071.hp2 HG01192.hp2 HG01952.hp1 others(9): Show |
intron_variant | MODIFIER | c.189+22240_189+2224 others(6): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117838967 | |||||||
| chr7:117838967 | CG | C | 57 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0009 others(54): Show |
58 | HG00639.hp2 HG00642.hp1 HG01069.hp1 others(55): Show |
intron_variant | MODIFIER | c.189+22241delC | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117838967 | |||||||
| chr7:117838968 | G | C | 3 | a0001c0001t0001g0006 a0001c0001t0001g0110 a0001c0001t0001g0111 |
3 | HG02109.hp1 HG03540.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.189+22241C>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117838968 | |||||||
| chr7:117839009 | T | A | 1 | a0001c0001t0005g0152 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.189+22200A>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117839009 | |||||||
| chr7:117839010 | A | T | 1 | a0001c0001t0001g0070 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.189+22199T>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117839010 | |||||||
| chr7:117839082 | C | G | 2 | a0001c0001t0001g0158 a0001c0001t0001g0159 |
2 | HG03831.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.189+22127G>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117839082 | |||||||
| chr7:117839254 | T | C | 2 | a0001c0001t0001g0081 a0001c0001t0002g0022 |
2 | HG03209.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.189+21955A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117839254 | |||||||
| chr7:117839469 | TA | T | 46 | a0001c0001t0001g0036 a0001c0001t0001g0041 a0001c0001t0001g0042 others(43): Show |
46 | HG00609.hp1 HG00642.hp1 HG01069.hp2 others(43): Show |
intron_variant | MODIFIER | c.189+21739delT | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117839469 | |||||||
| chr7:117839507 | T | C | 2 | a0001c0001t0001g0074 a0001c0004t0001g0122 |
2 | HG02922.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.189+21702A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117839507 | |||||||
| chr7:117839745 | G | A | 1 | a0001c0001t0002g0022 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.189+21464C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117839745 | |||||||
| chr7:117839943 | G | T | 1 | a0001c0001t0001g0135 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.189+21266C>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117839943 | |||||||
| chr7:117840080 | T | C | 1 | a0001c0001t0001g0009 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.189+21129A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117840080 | |||||||
| chr7:117840289 | T | C | 1 | a0001c0001t0002g0022 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.189+20920A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117840289 | |||||||
| chr7:117840339 | C | T | 3 | a0001c0001t0002g0047 a0001c0006t0001g0078 a0001c0006t0002g0079 |
3 | HG02723.hp1 HG02818.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.189+20870G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117840339 | |||||||
| chr7:117840342 | G | A | 27 | a0001c0001t0001g0023 a0001c0001t0001g0038 a0001c0001t0001g0044 others(24): Show |
27 | HG00323.hp2 HG01192.hp2 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.189+20867C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117840342 | |||||||
| chr7:117840384 | C | T | 78 | a0001c0001t0001g0023 a0001c0001t0001g0036 a0001c0001t0001g0038 others(75): Show |
78 | HG00323.hp2 HG00609.hp1 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.189+20825G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117840384 | |||||||
| chr7:117841043 | T | G | 1 | a0001c0001t0001g0141 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.189+20166A>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117841043 | |||||||
| chr7:117841179 | C | A | 2 | a0001c0001t0001g0062 a0001c0001t0001g0065 |
2 | HG02965.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.189+20030G>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117841179 | |||||||
| chr7:117841338 | A | G | 1 | a0011c0013t0001g0025 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.189+19871T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117841338 | |||||||
| chr7:117841416 | C | CT | 11 | a0001c0001t0001g0023 a0001c0001t0001g0060 a0001c0001t0001g0066 others(8): Show |
11 | HG01433.hp1 HG02280.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.189+19792dupA | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117841416 | |||||||
| chr7:117841640 | T | C | 5 | a0001c0001t0001g0060 a0001c0001t0001g0066 a0001c0001t0002g0007 others(2): Show |
5 | HG02451.hp1 HG02615.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.189+19569A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117841640 | |||||||
| chr7:117841749 | G | A | 1 | a0001c0001t0001g0081 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.189+19460C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117841749 | |||||||
| chr7:117842125 | G | A | 1 | a0001c0001t0001g0084 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.189+19084C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117842125 | |||||||
| chr7:117842264 | G | A | 1 | a0001c0001t0001g0092 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.189+18945C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117842264 | |||||||
| chr7:117842269 | C | T | 1 | a0001c0001t0002g0022 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.189+18940G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117842269 | |||||||
| chr7:117842417 | G | A | 11 | a0001c0001t0001g0023 a0001c0001t0001g0060 a0001c0001t0001g0066 others(8): Show |
11 | HG01433.hp1 HG02280.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.189+18792C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117842417 | |||||||
| chr7:117842463 | A | G | 4 | a0001c0001t0001g0062 a0001c0001t0001g0065 a0001c0001t0001g0158 others(1): Show |
4 | HG02965.hp1 HG03225.hp1 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.189+18746T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117842463 | |||||||
| chr7:117842566 | C | G | 1 | a0001c0001t0001g0159 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.189+18643G>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117842566 | |||||||
| chr7:117842751 | TTC | T | 11 | a0001c0001t0001g0023 a0001c0001t0001g0060 a0001c0001t0001g0066 others(8): Show |
11 | HG01433.hp1 HG02280.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.189+18456_189+1845 others(6): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117842751 | |||||||
| chr7:117842763 | A | G | 10 | a0001c0001t0001g0023 a0001c0001t0001g0060 a0001c0001t0001g0066 others(7): Show |
10 | HG01433.hp1 HG02280.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.189+18446T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117842763 | |||||||
| chr7:117842816 | A | C | 81 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(78): Show |
81 | HG00609.hp1 HG00639.hp2 HG00642.hp1 others(78): Show |
intron_variant | MODIFIER | c.189+18393T>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117842816 | |||||||
| chr7:117842985 | T | C | 11 | a0001c0001t0001g0023 a0001c0001t0001g0060 a0001c0001t0001g0066 others(8): Show |
11 | HG01433.hp1 HG02280.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.189+18224A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117842985 | |||||||
| chr7:117843020 | C | G | 7 | a0001c0001t0001g0046 a0001c0001t0001g0051 a0001c0001t0001g0052 others(4): Show |
7 | HG02258.hp2 HG02486.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.189+18189G>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117843020 | |||||||
| chr7:117843062 | G | A | 1 | a0001c0001t0003g0137 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.189+18147C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117843062 | |||||||
| chr7:117843083 | C | T | 46 | a0001c0001t0001g0036 a0001c0001t0001g0041 a0001c0001t0001g0042 others(43): Show |
46 | HG00609.hp1 HG00642.hp1 HG01069.hp2 others(43): Show |
intron_variant | MODIFIER | c.189+18126G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117843083 | |||||||
| chr7:117843088 | A | T | 81 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(78): Show |
81 | HG00609.hp1 HG00639.hp2 HG00642.hp1 others(78): Show |
intron_variant | MODIFIER | c.189+18121T>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117843088 | |||||||
| chr7:117843206 | A | G | 1 | a0001c0001t0001g0084 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.189+18003T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117843206 | |||||||
| chr7:117843543 | C | G | 2 | a0001c0001t0001g0135 a0001c0001t0002g0130 |
2 | HG00639.hp2 HG01257.hp2 |
intron_variant | MODIFIER | c.189+17666G>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117843543 | |||||||
| chr7:117843796 | C | T | 57 | a0001c0001t0001g0023 a0001c0001t0001g0036 a0001c0001t0001g0041 others(54): Show |
57 | HG00609.hp1 HG00642.hp1 HG01069.hp2 others(54): Show |
intron_variant | MODIFIER | c.189+17413G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117843796 | |||||||
| chr7:117843864 | C | T | 1 | a0001c0001t0001g0081 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.189+17345G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117843864 | |||||||
| chr7:117843867 | C | T | 1 | a0001c0001t0001g0081 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.189+17342G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117843867 | |||||||
| chr7:117843868 | G | A | 5 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0077 others(2): Show |
5 | HG01433.hp2 HG02630.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.189+17341C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117843868 | |||||||
| chr7:117843914 | T | A | 1 | a0001c0001t0002g0162 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.189+17295A>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117843914 | |||||||
| chr7:117843940 | G | A | 4 | a0001c0001t0001g0062 a0001c0001t0001g0065 a0001c0001t0001g0158 others(1): Show |
4 | HG02965.hp1 HG03225.hp1 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.189+17269C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117843940 | |||||||
| chr7:117844049 | GA | G | 66 | a0001c0001t0001g0023 a0001c0001t0001g0036 a0001c0001t0001g0038 others(63): Show |
66 | HG00323.hp2 HG00609.hp1 HG00642.hp1 others(63): Show |
intron_variant | MODIFIER | c.189+17159delT | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117844049 | |||||||
| chr7:117844106 | T | C | 4 | a0001c0001t0001g0044 a0001c0001t0001g0080 a0001c0001t0001g0082 others(1): Show |
4 | HG02258.hp1 HG02280.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.189+17103A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117844106 | |||||||
| chr7:117844224 | G | A | 2 | a0001c0001t0001g0124 a0001c0001t0001g0145 |
2 | HG02040.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.189+16985C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117844224 | |||||||
| chr7:117844450 | A | G | 1 | a0001c0001t0001g0057 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.189+16759T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117844450 | |||||||
| chr7:117844496 | A | G | 1 | a0001c0001t0002g0022 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.189+16713T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117844496 | |||||||
| chr7:117844953 | T | C | 60 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0036 others(57): Show |
61 | HG00323.hp1 HG00609.hp1 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.189+16256A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117844953 | |||||||
| chr7:117845131 | ATTT | A | 5 | a0001c0001t0001g0040 a0001c0001t0001g0049 a0001c0001t0001g0057 others(2): Show |
5 | HG02109.hp2 HG02451.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.189+16075_189+1607 others(7): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117845131 | |||||||
| chr7:117845393 | A | G | 4 | a0001c0001t0001g0038 a0001c0001t0001g0069 a0001c0001t0001g0161 others(1): Show |
4 | HG00323.hp2 HG01192.hp2 HG01243.hp1 others(1): Show |
intron_variant | MODIFIER | c.189+15816T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117845393 | |||||||
| chr7:117845607 | C | T | 19 | a0001c0001t0001g0044 a0001c0001t0001g0062 a0001c0001t0001g0065 others(16): Show |
19 | HG01433.hp2 HG02258.hp1 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.189+15602G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117845607 | |||||||
| chr7:117845854 | T | G | 3 | a0001c0001t0002g0047 a0001c0006t0001g0078 a0001c0006t0002g0079 |
3 | HG02723.hp1 HG02818.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.189+15355A>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117845854 | |||||||
| chr7:117845889 | C | T | 1 | a0001c0001t0001g0006 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.189+15320G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117845889 | |||||||
| chr7:117845944 | G | A | 4 | a0001c0001t0001g0044 a0001c0001t0001g0080 a0001c0001t0001g0082 others(1): Show |
4 | HG02258.hp1 HG02280.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.189+15265C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117845944 | |||||||
| chr7:117845946 | G | A | 48 | a0001c0001t0001g0005 a0001c0001t0001g0036 a0001c0001t0001g0041 others(45): Show |
48 | HG00609.hp1 HG00642.hp1 HG01069.hp2 others(45): Show |
intron_variant | MODIFIER | c.189+15263C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117845946 | |||||||
| chr7:117845995 | C | T | 3 | a0001c0001t0002g0047 a0001c0006t0001g0078 a0001c0006t0002g0079 |
3 | HG02723.hp1 HG02818.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.189+15214G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117845995 | |||||||
| chr7:117846041 | CAG | C | 48 | a0001c0001t0001g0005 a0001c0001t0001g0036 a0001c0001t0001g0041 others(45): Show |
48 | HG00609.hp1 HG00642.hp1 HG01069.hp2 others(45): Show |
intron_variant | MODIFIER | c.189+15166_189+1516 others(6): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117846041 | |||||||
| chr7:117846098 | G | A | 18 | a0001c0001t0001g0044 a0001c0001t0001g0062 a0001c0001t0001g0065 others(15): Show |
18 | HG01433.hp2 HG02258.hp1 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.189+15111C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117846098 | |||||||
| chr7:117846220 | G | T | 33 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0009 others(30): Show |
33 | HG00639.hp2 HG01069.hp1 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.189+14989C>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117846220 | |||||||
| chr7:117846258 | T | C | 78 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0011 others(75): Show |
79 | HG00323.hp1 HG00323.hp2 HG00609.hp1 others(76): Show |
intron_variant | MODIFIER | c.189+14951A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117846258 | |||||||
| chr7:117846358 | C | T | 19 | a0001c0001t0001g0044 a0001c0001t0001g0062 a0001c0001t0001g0065 others(16): Show |
19 | HG01433.hp2 HG02258.hp1 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.189+14851G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117846358 | |||||||
| chr7:117846361 | T | C | 1 | a0001c0001t0001g0084 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.189+14848A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117846361 | |||||||
| chr7:117846426 | G | T | 1 | a0001c0001t0001g0081 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.189+14783C>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117846426 | |||||||
| chr7:117846565 | GAAAAAAG others(3): Show |
G | 1 | a0001c0001t0001g0116 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.189+14634_189+1464 others(14): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117846565 | |||||||
| chr7:117846880 | A | T | 130 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(127): Show |
131 | HG00323.hp1 HG00323.hp2 HG00609.hp1 others(128): Show |
intron_variant | MODIFIER | c.189+14329T>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117846880 | |||||||
| chr7:117846956 | A | T | 2 | a0001c0001t0001g0124 a0001c0001t0001g0145 |
2 | HG02040.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.189+14253T>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117846956 | |||||||
| chr7:117846978 | C | T | 1 | a0001c0001t0001g0126 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.189+14231G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117846978 | |||||||
| chr7:117847171 | A | G | 10 | a0001c0001t0001g0023 a0001c0001t0001g0060 a0001c0001t0001g0066 others(7): Show |
10 | HG01433.hp1 HG02280.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.189+14038T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117847171 | |||||||
| chr7:117847175 | A | G | 3 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0077 |
3 | HG02630.hp2 HG02896.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.189+14034T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117847175 | |||||||
| chr7:117847263 | T | C | 4 | a0001c0001t0001g0044 a0001c0001t0001g0080 a0001c0001t0001g0082 others(1): Show |
4 | HG02258.hp1 HG02280.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.189+13946A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117847263 | |||||||
| chr7:117847372 | C | T | 1 | a0001c0001t0001g0110 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.189+13837G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117847372 | |||||||
| chr7:117847397 | G | A | 1 | a0001c0001t0001g0088 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.189+13812C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117847397 | |||||||
| chr7:117847800 | T | C | 1 | a0001c0001t0001g0116 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.189+13409A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117847800 | |||||||
| chr7:117847819 | C | CT | 21 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0019 others(18): Show |
21 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(18): Show |
intron_variant | MODIFIER | c.189+13389dupA | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117847819 | |||||||
| chr7:117847819 | C | CTTT | 5 | a0001c0001t0001g0006 a0001c0001t0001g0050 a0001c0001t0001g0066 others(2): Show |
5 | HG01109.hp1 HG02257.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.189+13387_189+1338 others(7): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117847819 | |||||||
| chr7:117847819 | C | CTTTT | 5 | a0001c0001t0001g0060 a0001c0001t0001g0069 a0001c0001t0001g0110 others(2): Show |
5 | HG01243.hp1 HG02615.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.189+13386_189+1338 others(8): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117847819 | |||||||
| chr7:117847819 | C | CTTTTTTT others(4): Show |
1 | a0001c0001t0001g0084 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.189+13379_189+1338 others(15): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117847819 | |||||||
| chr7:117847819 | C | CTTTTTTT others(10): Show |
2 | a0001c0001t0001g0044 a0001c0007t0001g0010 |
2 | HG02258.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.189+13373_189+1338 others(21): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117847819 | |||||||
| chr7:117847819 | CTTTTTTT others(3): Show |
C | 5 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0077 others(2): Show |
5 | HG01433.hp2 HG02630.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.189+13380_189+1338 others(14): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117847819 | |||||||
| chr7:117847819 | CTTTTTTT others(7): Show |
C | 3 | a0001c0001t0001g0092 a0001c0001t0001g0098 a0001c0001t0002g0037 |
3 | NA18947.hp2 NA19006.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.189+13376_189+1338 others(18): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117847819 | |||||||
| chr7:117847819 | CTTTTTTT others(8): Show |
C | 57 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0011 others(54): Show |
58 | HG00323.hp1 HG00609.hp1 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.189+13375_189+1338 others(19): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117847819 | |||||||
| chr7:117847819 | CTTTTTTT others(9): Show |
C | 2 | a0001c0001t0001g0091 a0001c0001t0001g0105 |
2 | HG02165.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.189+13374_189+1338 others(20): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117847819 | |||||||
| chr7:117848028 | A | G | 1 | a0001c0001t0001g0074 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.189+13181T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117848028 | |||||||
| chr7:117848124 | C | T | 1 | a0001c0001t0002g0022 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.189+13085G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117848124 | |||||||
| chr7:117848186 | T | C | 2 | a0001c0001t0001g0021 a0001c0001t0001g0129 |
2 | HG00639.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.189+13023A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117848186 | |||||||
| chr7:117848201 | G | C | 1 | a0001c0001t0002g0032 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.189+13008C>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117848201 | |||||||
| chr7:117848561 | G | C | 4 | a0001c0001t0001g0038 a0001c0001t0001g0069 a0001c0001t0001g0161 others(1): Show |
4 | HG00323.hp2 HG01192.hp2 HG01243.hp1 others(1): Show |
intron_variant | MODIFIER | c.189+12648C>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117848561 | |||||||
| chr7:117848612 | T | C | 1 | a0001c0001t0001g0084 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.189+12597A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117848612 | |||||||
| chr7:117848625 | C | T | 10 | a0001c0001t0001g0023 a0001c0001t0001g0060 a0001c0001t0001g0066 others(7): Show |
10 | HG01433.hp1 HG02280.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.189+12584G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117848625 | |||||||
| chr7:117848881 | C | T | 3 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0077 |
3 | HG02630.hp2 HG02896.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.189+12328G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117848881 | |||||||
| chr7:117849285 | T | C | 1 | a0001c0001t0001g0163 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.189+11924A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117849285 | |||||||
| chr7:117849368 | T | C | 5 | a0001c0001t0001g0060 a0001c0001t0001g0066 a0001c0001t0002g0007 others(2): Show |
5 | HG02451.hp1 HG02615.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.189+11841A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117849368 | |||||||
| chr7:117849529 | A | G | 4 | a0001c0001t0001g0038 a0001c0001t0001g0069 a0001c0001t0001g0161 others(1): Show |
4 | HG00323.hp2 HG01192.hp2 HG01243.hp1 others(1): Show |
intron_variant | MODIFIER | c.189+11680T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117849529 | |||||||
| chr7:117849651 | C | T | 2 | a0004c0005t0001g0029 a0004c0005t0001g0030 |
2 | HG01433.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.189+11558G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117849651 | |||||||
| chr7:117850082 | A | C | 1 | a0001c0001t0002g0022 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.189+11127T>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117850082 | |||||||
| chr7:117850131 | A | ATT | 4 | a0001c0001t0001g0038 a0001c0001t0001g0069 a0001c0001t0001g0161 others(1): Show |
4 | HG00323.hp2 HG01192.hp2 HG01243.hp1 others(1): Show |
intron_variant | MODIFIER | c.189+11076_189+1107 others(6): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117850131 | |||||||
| chr7:117850280 | G | A | 117 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(114): Show |
117 | HG00323.hp2 HG00609.hp1 HG00639.hp2 others(114): Show |
intron_variant | MODIFIER | c.189+10929C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117850280 | |||||||
| chr7:117850543 | T | C | 1 | a0001c0001t0001g0076 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.189+10666A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117850543 | |||||||
| chr7:117850855 | C | T | 2 | a0001c0001t0001g0103 a0001c0001t0001g0105 |
2 | NA18954.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.189+10354G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117850855 | |||||||
| chr7:117850876 | C | T | 1 | a0002c0002t0001g0001 | 2 | HG01074.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.189+10333G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117850876 | |||||||
| chr7:117851092 | G | C | 11 | a0001c0001t0001g0023 a0001c0001t0001g0060 a0001c0001t0001g0066 others(8): Show |
11 | HG01433.hp1 HG02280.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.189+10117C>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117851092 | |||||||
| chr7:117851585 | G | T | 3 | a0001c0001t0001g0084 a0001c0001t0001g0110 a0001c0001t0001g0111 |
3 | HG02109.hp1 HG03540.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.189+9624C>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117851585 | |||||||
| chr7:117851630 | T | C | 1 | a0001c0016t0001g0058 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.189+9579A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117851630 | |||||||
| chr7:117851656 | C | A | 3 | a0001c0001t0002g0047 a0001c0006t0001g0078 a0001c0006t0002g0079 |
3 | HG02723.hp1 HG02818.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.189+9553G>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117851656 | |||||||
| chr7:117851846 | G | A | 1 | a0001c0001t0001g0044 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.189+9363C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117851846 | |||||||
| chr7:117851851 | A | T | 3 | a0001c0001t0001g0084 a0001c0001t0001g0110 a0001c0001t0001g0111 |
3 | HG02109.hp1 HG03540.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.189+9358T>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117851851 | |||||||
| chr7:117852004 | G | A | 4 | a0001c0001t0001g0012 a0001c0001t0001g0018 a0001c0001t0002g0027 others(1): Show |
4 | HG00609.hp2 HG02040.hp1 NA18951.hp2 others(1): Show |
intron_variant | MODIFIER | c.189+9205C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117852004 | |||||||
| chr7:117852063 | G | A | 6 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0104 others(3): Show |
6 | HG02257.hp1 HG02615.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.189+9146C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117852063 | |||||||
| chr7:117852232 | A | G | 2 | a0001c0001t0001g0142 a0001c0001t0001g0143 |
2 | HG01993.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.189+8977T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117852232 | |||||||
| chr7:117852252 | T | G | 1 | a0001c0001t0001g0104 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.189+8957A>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117852252 | |||||||
| chr7:117852303 | A | G | 6 | a0001c0001t0001g0038 a0001c0001t0001g0103 a0001c0001t0001g0105 others(3): Show |
6 | HG00323.hp2 HG01192.hp2 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.189+8906T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117852303 | |||||||
| chr7:117852331 | A | G | 1 | a0001c0001t0001g0107 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.189+8878T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117852331 | |||||||
| chr7:117853241 | A | C | 1 | a0001c0001t0001g0107 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.189+7968T>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117853241 | |||||||
| chr7:117853359 | A | G | 3 | a0001c0001t0001g0060 a0001c0001t0001g0066 a0006c0012t0002g0055 |
3 | HG02451.hp1 HG02615.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.189+7850T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117853359 | |||||||
| chr7:117853456 | C | T | 27 | a0001c0001t0001g0005 a0001c0001t0001g0084 a0001c0001t0001g0085 others(24): Show |
27 | HG00642.hp1 HG01168.hp2 HG01952.hp2 others(24): Show |
intron_variant | MODIFIER | c.189+7753G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117853456 | |||||||
| chr7:117853756 | C | T | 2 | a0001c0001t0002g0007 a0001c0004t0001g0008 |
2 | HG02970.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.189+7453G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117853756 | |||||||
| chr7:117853820 | C | T | 3 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0082 |
3 | HG02280.hp1 HG03579.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.189+7389G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117853820 | |||||||
| chr7:117854589 | T | C | 1 | a0001c0001t0002g0022 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.189+6620A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117854589 | |||||||
| chr7:117854771 | A | AATTT | 8 | a0001c0001t0001g0046 a0001c0001t0001g0051 a0001c0001t0001g0052 others(5): Show |
8 | HG02258.hp2 HG02280.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.189+6437_189+6438i others(6): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117854771 | |||||||
| chr7:117854775 | A | T | 38 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(35): Show |
39 | HG01074.hp2 HG01109.hp2 HG01192.hp1 others(36): Show |
intron_variant | MODIFIER | c.189+6434T>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117854775 | |||||||
| chr7:117854779 | A | T | 82 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(79): Show |
83 | HG00609.hp1 HG01069.hp2 HG01071.hp1 others(80): Show |
intron_variant | MODIFIER | c.189+6430T>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117854779 | |||||||
| chr7:117854783 | A | T | 130 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(127): Show |
131 | HG00323.hp2 HG00609.hp1 HG00642.hp1 others(128): Show |
intron_variant | MODIFIER | c.189+6426T>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117854783 | |||||||
| chr7:117854787 | T | A | 5 | a0001c0001t0001g0106 a0001c0001t0001g0139 a0001c0001t0001g0140 others(2): Show |
5 | HG01258.hp1 HG01978.hp2 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.189+6422A>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117854787 | |||||||
| chr7:117854855 | G | A | 13 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0151 others(10): Show |
13 | HG00323.hp2 HG01069.hp2 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.189+6354C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117854855 | |||||||
| chr7:117855003 | T | G | 2 | a0001c0006t0001g0078 a0001c0006t0002g0079 |
2 | HG02723.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.189+6206A>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117855003 | |||||||
| chr7:117855004 | C | A | 2 | a0001c0006t0001g0078 a0001c0006t0002g0079 |
2 | HG02723.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.189+6205G>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117855004 | |||||||
| chr7:117855178 | G | C | 2 | a0004c0005t0001g0029 a0004c0005t0001g0030 |
2 | HG01433.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.189+6031C>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117855178 | |||||||
| chr7:117855240 | G | A | 35 | a0001c0001t0001g0005 a0001c0001t0001g0084 a0001c0001t0001g0085 others(32): Show |
35 | HG00609.hp1 HG00642.hp1 HG01168.hp2 others(32): Show |
intron_variant | MODIFIER | c.189+5969C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117855240 | |||||||
| chr7:117855336 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.189+5873G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117855336 | |||||||
| chr7:117855337 | G | A | 35 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0038 others(32): Show |
35 | HG00323.hp2 HG00609.hp2 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.189+5872C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117855337 | |||||||
| chr7:117855543 | G | C | 3 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0002g0130 |
3 | HG00639.hp2 HG01993.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.189+5666C>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117855543 | |||||||
| chr7:117855613 | C | A | 18 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0014 others(15): Show |
18 | HG01109.hp2 HG01346.hp2 HG01358.hp1 others(15): Show |
intron_variant | MODIFIER | c.189+5596G>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117855613 | |||||||
| chr7:117855660 | G | C | 1 | a0001c0017t0001g0043 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.189+5549C>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117855660 | |||||||
| chr7:117855973 | G | A | 5 | a0001c0001t0001g0060 a0001c0001t0001g0066 a0001c0006t0001g0078 others(2): Show |
5 | HG02451.hp1 HG02615.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.189+5236C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117855973 | |||||||
| chr7:117856090 | C | T | 73 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0011 others(70): Show |
74 | HG00609.hp1 HG00642.hp1 HG01074.hp2 others(71): Show |
intron_variant | MODIFIER | c.189+5119G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117856090 | |||||||
| chr7:117856117 | C | T | 2 | a0001c0001t0001g0097 a0001c0001t0001g0108 |
2 | HG01361.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.189+5092G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117856117 | |||||||
| chr7:117856265 | C | T | 33 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(30): Show |
34 | HG01074.hp2 HG01109.hp2 HG01192.hp1 others(31): Show |
intron_variant | MODIFIER | c.189+4944G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117856265 | |||||||
| chr7:117856836 | T | G | 38 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(35): Show |
39 | HG01074.hp2 HG01109.hp2 HG01192.hp1 others(36): Show |
intron_variant | MODIFIER | c.189+4373A>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117856836 | |||||||
| chr7:117856940 | C | T | 1 | a0001c0001t0001g0085 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.189+4269G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117856940 | |||||||
| chr7:117857110 | A | C | 3 | a0001c0001t0001g0044 a0001c0001t0001g0059 a0001c0001t0002g0047 |
3 | HG02258.hp1 HG02818.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.189+4099T>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117857110 | |||||||
| chr7:117857140 | CTGTT | C | 3 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0082 |
3 | HG02280.hp1 HG03579.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.189+4065_189+4068d others(6): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117857140 | |||||||
| chr7:117857501 | T | C | 1 | a0001c0001t0001g0076 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.189+3708A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117857501 | |||||||
| chr7:117857568 | T | C | 12 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0038 others(9): Show |
12 | HG00609.hp2 HG01192.hp2 HG02165.hp2 others(9): Show |
intron_variant | MODIFIER | c.189+3641A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117857568 | |||||||
| chr7:117857757 | A | G | 136 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(133): Show |
137 | HG00323.hp2 HG00609.hp1 HG00609.hp2 others(134): Show |
intron_variant | MODIFIER | c.189+3452T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117857757 | |||||||
| chr7:117858013 | G | A | 1 | a0001c0001t0001g0020 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.189+3196C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117858013 | |||||||
| chr7:117858093 | G | A | 3 | a0001c0001t0004g0033 a0001c0001t0004g0039 a0001c0001t0004g0053 |
3 | HG01433.hp1 HG02280.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.189+3116C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117858093 | |||||||
| chr7:117858118 | C | T | 1 | a0001c0004t0001g0122 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.189+3091G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117858118 | |||||||
| chr7:117858228 | G | A | 1 | a0001c0001t0001g0018 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.189+2981C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117858228 | |||||||
| chr7:117858351 | CAGAGTGA others(18): Show |
C | 1 | a0001c0004t0001g0122 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.189+2833_189+2857d others(27): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117858351 | |||||||
| chr7:117858407 | C | T | 135 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(132): Show |
136 | HG00323.hp2 HG00609.hp1 HG00609.hp2 others(133): Show |
intron_variant | MODIFIER | c.189+2802G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117858407 | |||||||
| chr7:117858737 | A | G | 1 | a0001c0001t0001g0114 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.189+2472T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117858737 | |||||||
| chr7:117858835 | C | T | 2 | a0001c0006t0001g0078 a0001c0006t0002g0079 |
2 | HG02723.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.189+2374G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117858835 | |||||||
| chr7:117858998 | CGT | C | 3 | a0001c0001t0001g0006 a0001c0001t0002g0022 a0001c0007t0001g0010 |
3 | HG02895.hp2 HG03209.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.189+2209_189+2210d others(4): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117858998 | |||||||
| chr7:117859854 | G | A | 1 | a0001c0001t0001g0077 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.189+1355C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117859854 | |||||||
| chr7:117860034 | C | T | 4 | a0001c0001t0001g0013 a0001c0001t0001g0045 a0001c0001t0001g0050 others(1): Show |
4 | HG01081.hp1 HG01168.hp1 HG01255.hp2 others(1): Show |
intron_variant | MODIFIER | c.189+1175G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117860034 | |||||||
| chr7:117860059 | C | A | 45 | a0001c0001t0001g0005 a0001c0001t0001g0084 a0001c0001t0001g0085 others(42): Show |
45 | HG00609.hp1 HG00642.hp1 HG01168.hp2 others(42): Show |
intron_variant | MODIFIER | c.189+1150G>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117860059 | |||||||
| chr7:117860255 | G | C | 1 | a0001c0001t0001g0062 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.189+954C>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117860255 | |||||||
| chr7:117860325 | T | G | 1 | a0001c0001t0001g0126 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.189+884A>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117860325 | |||||||
| chr7:117860395 | T | C | 1 | a0001c0001t0001g0126 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.189+814A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117860395 | |||||||
| chr7:117860552 | C | T | 15 | a0001c0001t0001g0040 a0001c0001t0001g0046 a0001c0001t0001g0049 others(12): Show |
15 | HG01243.hp1 HG02109.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.189+657G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117860552 | |||||||
| chr7:117860600 | C | T | 2 | a0001c0001t0001g0006 a0001c0007t0001g0010 |
2 | HG02895.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.189+609G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117860600 | |||||||
| chr7:117860998 | G | A | 4 | a0001c0001t0001g0084 a0001c0001t0001g0110 a0001c0001t0001g0111 others(1): Show |
4 | HG02109.hp1 HG03540.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.189+211C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117860998 | |||||||
| chr7:117861059 | G | C | 3 | a0001c0001t0004g0033 a0001c0001t0004g0039 a0001c0001t0004g0053 |
3 | HG01433.hp1 HG02280.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.189+150C>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 2/22 | chr7 | 117861059 | |||||||
| chr7:117861443 | A | G | 1 | a0001c0001t0005g0152 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.82-127T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117861443 | |||||||
| chr7:117862056 | T | TAC | 4 | a0001c0001t0001g0076 a0001c0001t0003g0075 a0001c0006t0001g0078 others(1): Show |
4 | HG01081.hp2 HG02723.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.82-742_82-741dupGT | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117862056 | |||||||
| chr7:117862076 | T | C | 2 | a0001c0006t0001g0078 a0001c0006t0002g0079 |
2 | HG02723.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.82-760A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117862076 | |||||||
| chr7:117862488 | T | C | 4 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0082 others(1): Show |
4 | HG02280.hp1 HG02630.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.82-1172A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117862488 | |||||||
| chr7:117862520 | C | T | 90 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(87): Show |
91 | HG00323.hp2 HG00609.hp2 HG01069.hp2 others(88): Show |
intron_variant | MODIFIER | c.82-1204G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117862520 | |||||||
| chr7:117862874 | C | G | 1 | a0001c0001t0001g0004 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.82-1558G>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117862874 | |||||||
| chr7:117863175 | G | A | 2 | a0004c0005t0001g0029 a0004c0005t0001g0030 |
2 | HG01433.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.82-1859C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117863175 | |||||||
| chr7:117863596 | G | A | 1 | a0009c0008t0001g0112 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.82-2280C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117863596 | |||||||
| chr7:117863636 | T | C | 1 | a0001c0001t0002g0047 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.82-2320A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117863636 | |||||||
| chr7:117863928 | T | G | 23 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(20): Show |
24 | HG01074.hp2 HG01109.hp2 HG01192.hp1 others(21): Show |
intron_variant | MODIFIER | c.82-2612A>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117863928 | |||||||
| chr7:117864326 | C | A | 1 | a0001c0001t0001g0126 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.82-3010G>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117864326 | |||||||
| chr7:117864493 | G | A | 3 | a0001c0001t0004g0033 a0001c0001t0004g0039 a0001c0001t0004g0053 |
3 | HG01433.hp1 HG02280.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.82-3177C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117864493 | |||||||
| chr7:117864527 | G | T | 1 | a0001c0001t0001g0126 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.82-3211C>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117864527 | |||||||
| chr7:117864629 | A | AGAATATA others(23): Show |
1 | a0001c0001t0001g0019 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.82-3314_82-3313ins others(30): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117864629 | |||||||
| chr7:117864629 | A | AGAATATA others(23): Show |
18 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(15): Show |
19 | HG01074.hp2 HG01109.hp2 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.82-3343_82-3314dup others(30): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117864629 | |||||||
| chr7:117864629 | A | AGAATATA others(53): Show |
4 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0002g0024 others(1): Show |
4 | HG01346.hp2 HG01496.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.82-3314_82-3313ins others(60): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117864629 | |||||||
| chr7:117864637 | T | C | 1 | a0001c0001t0001g0038 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.82-3321A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117864637 | |||||||
| chr7:117864679 | T | TATATATA others(21): Show |
1 | a0001c0001t0002g0162 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.82-3391_82-3364dup others(28): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117864679 | |||||||
| chr7:117864681 | TATATATT others(11): Show |
T | 1 | a0001c0001t0001g0056 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.82-3383_82-3366del others(18): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117864681 | |||||||
| chr7:117864723 | T | TATTCATA others(120): Show |
1 | a0001c0001t0003g0031 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.82-3408_82-3407ins others(127): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117864723 | |||||||
| chr7:117864725 | C | CATATATT others(18): Show |
7 | a0001c0001t0001g0044 a0001c0001t0001g0059 a0001c0001t0001g0060 others(4): Show |
7 | HG01109.hp2 HG02258.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.82-3434_82-3410dup others(25): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117864725 | |||||||
| chr7:117864725 | C | CATATATT others(43): Show |
2 | a0001c0001t0001g0014 a0001c0001t0001g0020 |
2 | HG01361.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.82-3459_82-3410dup others(50): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117864725 | |||||||
| chr7:117864725 | C | CATATATT others(68): Show |
15 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0017 others(12): Show |
16 | HG01074.hp2 HG01192.hp1 HG01358.hp1 others(13): Show |
intron_variant | MODIFIER | c.82-3410_82-3409ins others(75): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117864725 | |||||||
| chr7:117864725 | C | CATATATT others(93): Show |
3 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0002g0024 |
3 | HG01346.hp2 HG01496.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.82-3410_82-3409ins others(100): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117864725 | |||||||
| chr7:117864725 | C | T | 1 | a0001c0001t0003g0031 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.82-3409G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117864725 | |||||||
| chr7:117864751 | A | ATATATTC others(35): Show |
1 | a0001c0001t0001g0074 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.82-3436_82-3435ins others(42): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117864751 | |||||||
| chr7:117864797 | C | CAATA | 2 | a0001c0001t0001g0011 a0001c0001t0001g0126 |
2 | HG02630.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.82-3482_82-3481ins others(4): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117864797 | |||||||
| chr7:117864800 | T | C | 3 | a0001c0001t0001g0060 a0001c0001t0001g0066 a0006c0012t0002g0055 |
3 | HG02451.hp1 HG02615.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.82-3484A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117864800 | |||||||
| chr7:117864819 | A | T | 1 | a0001c0001t0001g0126 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.82-3503T>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117864819 | |||||||
| chr7:117864822 | A | ATTCATAT others(35): Show |
1 | a0001c0001t0001g0126 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.82-3507_82-3506ins others(42): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117864822 | |||||||
| chr7:117864843 | C | CAATA | 4 | a0001c0001t0001g0011 a0001c0001t0001g0074 a0001c0001t0001g0123 others(1): Show |
4 | HG02615.hp2 HG02630.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.82-3528_82-3527ins others(4): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117864843 | |||||||
| chr7:117864843 | C | CTATATTC others(18): Show |
18 | a0001c0001t0001g0021 a0001c0001t0001g0069 a0001c0001t0001g0071 others(15): Show |
18 | HG01243.hp1 HG01358.hp1 HG01952.hp2 others(15): Show |
intron_variant | MODIFIER | c.82-3552_82-3528dup others(25): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117864843 | |||||||
| chr7:117864843 | C | CTATATTC others(43): Show |
7 | a0001c0001t0001g0050 a0001c0001t0001g0063 a0001c0001t0001g0077 others(4): Show |
7 | HG01168.hp1 HG01433.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.82-3577_82-3528dup others(50): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117864843 | |||||||
| chr7:117864843 | C | CTATATTC others(68): Show |
1 | a0001c0001t0001g0013 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.82-3602_82-3528dup others(75): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117864843 | |||||||
| chr7:117864843 | C | CTATATTC others(89): Show |
1 | a0001c0001t0001g0045 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.82-3528_82-3527ins others(96): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117864843 | |||||||
| chr7:117864843 | CTATATTC others(43): Show |
C | 2 | a0001c0006t0001g0078 a0001c0006t0002g0079 |
2 | HG02723.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.82-3577_82-3528del others(50): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117864843 | |||||||
| chr7:117864843 | CTATATTC others(68): Show |
C | 1 | a0001c0017t0001g0043 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.82-3602_82-3528del others(75): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117864843 | |||||||
| chr7:117864865 | A | T | 1 | a0001c0001t0001g0011 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.82-3549T>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117864865 | |||||||
| chr7:117864868 | A | ATTCATAT others(35): Show |
1 | a0001c0001t0001g0011 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.82-3553_82-3552ins others(42): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117864868 | |||||||
| chr7:117865433 | G | A | 93 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(90): Show |
94 | HG00323.hp2 HG00609.hp2 HG01069.hp2 others(91): Show |
intron_variant | MODIFIER | c.82-4117C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117865433 | |||||||
| chr7:117865490 | G | A | 2 | a0004c0005t0001g0029 a0004c0005t0001g0030 |
2 | HG01433.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.82-4174C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117865490 | |||||||
| chr7:117865544 | C | T | 3 | a0001c0001t0004g0033 a0001c0001t0004g0039 a0001c0001t0004g0053 |
3 | HG01433.hp1 HG02280.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.82-4228G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117865544 | |||||||
| chr7:117865632 | G | A | 17 | a0001c0001t0001g0086 a0001c0001t0001g0089 a0001c0001t0001g0091 others(14): Show |
17 | HG00642.hp1 HG01168.hp2 HG01346.hp1 others(14): Show |
intron_variant | MODIFIER | c.82-4316C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117865632 | |||||||
| chr7:117865671 | C | CA | 6 | a0001c0001t0001g0021 a0001c0001t0001g0045 a0001c0001t0001g0060 others(3): Show |
6 | HG01081.hp1 HG01358.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.82-4356dupT | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117865671 | |||||||
| chr7:117865671 | C | CAAA | 39 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0088 others(36): Show |
39 | HG00609.hp1 HG00642.hp1 HG01168.hp2 others(36): Show |
intron_variant | MODIFIER | c.82-4358_82-4356dup others(3): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117865671 | |||||||
| chr7:117865671 | CA | C | 19 | a0001c0001t0001g0129 a0001c0001t0001g0149 a0001c0001t0001g0150 others(16): Show |
19 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(16): Show |
intron_variant | MODIFIER | c.82-4356delT | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117865671 | |||||||
| chr7:117865671 | CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0001g0126 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.82-4365_82-4356del others(10): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117865671 | |||||||
| chr7:117865885 | T | C | 3 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0002c0002t0002g0073 |
3 | HG02630.hp2 NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.82-4569A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117865885 | |||||||
| chr7:117865899 | T | C | 3 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0002c0002t0002g0073 |
3 | HG02630.hp2 NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.82-4583A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117865899 | |||||||
| chr7:117866159 | G | A | 2 | a0004c0005t0001g0029 a0004c0005t0001g0030 |
2 | HG01433.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.82-4843C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117866159 | |||||||
| chr7:117866195 | C | T | 2 | a0001c0006t0001g0078 a0001c0006t0002g0079 |
2 | HG02723.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.82-4879G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117866195 | |||||||
| chr7:117866297 | T | G | 26 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(23): Show |
27 | HG01074.hp2 HG01109.hp2 HG01192.hp1 others(24): Show |
intron_variant | MODIFIER | c.82-4981A>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117866297 | |||||||
| chr7:117866416 | C | G | 90 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(87): Show |
91 | HG00323.hp2 HG00609.hp2 HG01069.hp2 others(88): Show |
intron_variant | MODIFIER | c.82-5100G>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117866416 | |||||||
| chr7:117866427 | G | T | 1 | a0001c0001t0001g0014 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.82-5111C>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117866427 | |||||||
| chr7:117866538 | T | C | 13 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(10): Show |
13 | HG00609.hp2 HG01192.hp2 HG02165.hp2 others(10): Show |
intron_variant | MODIFIER | c.82-5222A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117866538 | |||||||
| chr7:117866707 | C | A | 4 | a0001c0001t0001g0091 a0001c0001t0001g0100 a0001c0001t0001g0119 others(1): Show |
4 | HG01952.hp2 HG02165.hp1 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.82-5391G>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117866707 | |||||||
| chr7:117866709 | C | T | 141 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(138): Show |
142 | HG00323.hp2 HG00609.hp1 HG00609.hp2 others(139): Show |
intron_variant | MODIFIER | c.82-5393G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117866709 | |||||||
| chr7:117866756 | T | A | 29 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(26): Show |
30 | HG01074.hp2 HG01109.hp2 HG01192.hp1 others(27): Show |
intron_variant | MODIFIER | c.82-5440A>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117866756 | |||||||
| chr7:117866804 | G | C | 141 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(138): Show |
142 | HG00323.hp2 HG00609.hp1 HG00609.hp2 others(139): Show |
intron_variant | MODIFIER | c.82-5488C>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117866804 | |||||||
| chr7:117867203 | A | G | 3 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0082 |
3 | HG02280.hp1 HG03579.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.82-5887T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117867203 | |||||||
| chr7:117867264 | C | T | 3 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0082 |
3 | HG02280.hp1 HG03579.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.82-5948G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117867264 | |||||||
| chr7:117867484 | T | C | 1 | a0001c0001t0001g0041 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.81+5851A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117867484 | |||||||
| chr7:117867667 | G | C | 1 | a0001c0001t0001g0042 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.81+5668C>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117867667 | |||||||
| chr7:117868452 | T | C | 141 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(138): Show |
142 | HG00323.hp2 HG00609.hp1 HG00609.hp2 others(139): Show |
intron_variant | MODIFIER | c.81+4883A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117868452 | |||||||
| chr7:117868568 | A | G | 13 | a0001c0001t0001g0088 a0001c0001t0001g0092 a0001c0001t0001g0093 others(10): Show |
13 | HG00609.hp1 HG01255.hp1 HG01358.hp2 others(10): Show |
intron_variant | MODIFIER | c.81+4767T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117868568 | |||||||
| chr7:117868909 | A | G | 1 | a0001c0001t0005g0048 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.81+4426T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117868909 | |||||||
| chr7:117869140 | T | C | 47 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 others(44): Show |
47 | HG00609.hp1 HG00642.hp1 HG01168.hp2 others(44): Show |
intron_variant | MODIFIER | c.81+4195A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117869140 | |||||||
| chr7:117869158 | G | T | 3 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0082 |
3 | HG02280.hp1 HG03579.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.81+4177C>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117869158 | |||||||
| chr7:117869796 | GA | G | 30 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0011 others(27): Show |
31 | HG01074.hp2 HG01109.hp2 HG01192.hp1 others(28): Show |
intron_variant | MODIFIER | c.81+3538delT | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117869796 | |||||||
| chr7:117869912 | A | C | 2 | a0001c0001t0001g0011 a0001c0001t0001g0012 |
2 | NA19003.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.81+3423T>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117869912 | |||||||
| chr7:117870214 | T | C | 47 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 others(44): Show |
47 | HG00609.hp1 HG00642.hp1 HG01168.hp2 others(44): Show |
intron_variant | MODIFIER | c.81+3121A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117870214 | |||||||
| chr7:117870415 | T | C | 1 | a0001c0001t0001g0126 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.81+2920A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117870415 | |||||||
| chr7:117870433 | T | C | 1 | a0001c0017t0001g0043 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.81+2902A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117870433 | |||||||
| chr7:117870567 | C | T | 18 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(15): Show |
18 | HG01109.hp2 HG01255.hp2 HG01346.hp2 others(15): Show |
intron_variant | MODIFIER | c.81+2768G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117870567 | |||||||
| chr7:117870787 | G | A | 1 | a0001c0001t0001g0041 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.81+2548C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117870787 | |||||||
| chr7:117871012 | A | T | 1 | a0001c0001t0002g0162 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.81+2323T>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117871012 | |||||||
| chr7:117871087 | A | G | 4 | a0001c0001t0001g0161 a0001c0001t0002g0154 a0001c0001t0002g0155 others(1): Show |
4 | HG00323.hp2 HG01257.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.81+2248T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117871087 | |||||||
| chr7:117871339 | A | G | 3 | a0001c0001t0001g0023 a0004c0005t0001g0029 a0004c0005t0001g0030 |
3 | HG01433.hp2 HG02922.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.81+1996T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117871339 | |||||||
| chr7:117871507 | C | T | 1 | a0001c0001t0001g0126 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.81+1828G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117871507 | |||||||
| chr7:117871527 | C | G | 7 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0074 others(4): Show |
7 | HG01081.hp2 HG02630.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.81+1808G>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117871527 | |||||||
| chr7:117871604 | A | T | 3 | a0001c0001t0001g0006 a0001c0001t0002g0022 a0001c0007t0001g0010 |
3 | HG02895.hp2 HG03209.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.81+1731T>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117871604 | |||||||
| chr7:117871793 | C | CCA | 3 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0082 |
3 | HG02280.hp1 HG03579.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.81+1540_81+1541dup others(2): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117871793 | |||||||
| chr7:117871793 | CCA | C | 129 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(126): Show |
130 | HG00323.hp2 HG00609.hp1 HG00609.hp2 others(127): Show |
intron_variant | MODIFIER | c.81+1540_81+1541del others(2): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117871793 | |||||||
| chr7:117871793 | CCACA | C | 2 | a0001c0006t0001g0078 a0001c0006t0002g0079 |
2 | HG02723.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.81+1538_81+1541del others(4): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117871793 | |||||||
| chr7:117871843 | T | TACACACA others(15): Show |
1 | a0001c0001t0001g0107 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.81+1491_81+1492ins others(22): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117871843 | |||||||
| chr7:117871844 | T | A | 1 | a0001c0001t0001g0107 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.81+1491A>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117871844 | |||||||
| chr7:117871844 | T | TCA | 6 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0149 others(3): Show |
6 | HG01069.hp2 HG01071.hp1 HG01074.hp1 others(3): Show |
intron_variant | MODIFIER | c.81+1489_81+1490dup others(2): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117871844 | |||||||
| chr7:117871844 | T | TCACA | 6 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0002g0007 others(3): Show |
7 | HG01074.hp2 HG01192.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.81+1487_81+1490dup others(4): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117871844 | |||||||
| chr7:117871844 | T | TCACACAC others(1): Show |
13 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(10): Show |
13 | HG01255.hp2 HG01358.hp1 HG01361.hp1 others(10): Show |
intron_variant | MODIFIER | c.81+1483_81+1490dup others(8): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117871844 | |||||||
| chr7:117871844 | T | TCACACAC others(3): Show |
8 | a0001c0001t0001g0023 a0001c0001t0001g0026 a0001c0001t0001g0085 others(5): Show |
8 | HG01109.hp2 HG01346.hp2 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.81+1481_81+1490dup others(10): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117871844 | |||||||
| chr7:117871844 | T | TCACACAC others(5): Show |
10 | a0001c0001t0001g0072 a0001c0001t0001g0077 a0001c0001t0002g0032 others(7): Show |
10 | HG01433.hp2 HG02145.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.81+1479_81+1490dup others(12): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117871844 | |||||||
| chr7:117871844 | T | TCACACAC others(7): Show |
7 | a0001c0001t0001g0036 a0001c0001t0001g0038 a0001c0001t0001g0086 others(4): Show |
7 | HG01192.hp2 HG02602.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.81+1477_81+1490dup others(14): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117871844 | |||||||
| chr7:117871844 | T | TCACACAC others(9): Show |
6 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0091 others(3): Show |
6 | HG01257.hp1 HG01258.hp2 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.81+1475_81+1490dup others(16): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117871844 | |||||||
| chr7:117871844 | T | TCACACAC others(11): Show |
13 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0076 others(10): Show |
13 | HG00642.hp1 HG01081.hp2 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.81+1473_81+1490dup others(18): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117871844 | |||||||
| chr7:117871844 | T | TCACACAC others(13): Show |
8 | a0001c0001t0001g0042 a0001c0001t0001g0097 a0001c0001t0001g0098 others(5): Show |
8 | HG01361.hp2 HG03017.hp1 HG03017.hp2 others(5): Show |
intron_variant | MODIFIER | c.81+1471_81+1490dup others(20): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117871844 | |||||||
| chr7:117871844 | T | TCACACAC others(15): Show |
11 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0046 others(8): Show |
11 | HG00323.hp2 HG01081.hp1 HG01358.hp2 others(8): Show |
intron_variant | MODIFIER | c.81+1469_81+1490dup others(22): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117871844 | |||||||
| chr7:117871844 | T | TCACACAC others(17): Show |
11 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0080 others(8): Show |
11 | HG01993.hp2 HG02109.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.81+1467_81+1490dup others(24): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117871844 | |||||||
| chr7:117871844 | T | TCACACAC others(19): Show |
6 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0054 others(3): Show |
6 | HG01433.hp1 HG01978.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.81+1465_81+1490dup others(26): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117871844 | |||||||
| chr7:117871844 | T | TCACACAC others(21): Show |
9 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0081 others(6): Show |
9 | HG00609.hp1 HG00609.hp2 HG01952.hp2 others(6): Show |
intron_variant | MODIFIER | c.81+1463_81+1490dup others(28): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117871844 | |||||||
| chr7:117871844 | T | TCACACAC others(23): Show |
3 | a0001c0001t0001g0059 a0001c0001t0001g0118 a0001c0001t0001g0119 |
3 | HG02523.hp1 HG06807.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.81+1461_81+1490dup others(30): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117871844 | |||||||
| chr7:117871844 | T | TCACACAC others(25): Show |
4 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 others(1): Show |
4 | HG01168.hp1 HG02615.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.81+1490_81+1491ins others(32): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117871844 | |||||||
| chr7:117871844 | T | TCACACAC others(27): Show |
3 | a0001c0001t0001g0082 a0001c0001t0003g0121 a0010c0010t0001g0120 |
3 | HG01168.hp2 HG03579.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.81+1490_81+1491ins others(34): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117871844 | |||||||
| chr7:117871844 | T | TCACACAC others(33): Show |
1 | a0001c0001t0001g0064 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.81+1490_81+1491ins others(40): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117871844 | |||||||
| chr7:117871844 | TCA | T | 2 | a0001c0006t0001g0078 a0001c0006t0002g0079 |
2 | HG02723.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.81+1489_81+1490del others(2): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117871844 | |||||||
| chr7:117871844 | TCACACAC others(7): Show |
T | 1 | a0001c0001t0001g0074 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.81+1477_81+1490del others(14): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117871844 | |||||||
| chr7:117871871 | C | CACACACA others(10): Show |
1 | a0001c0001t0001g0005 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.81+1463_81+1464ins others(17): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117871871 | |||||||
| chr7:117871874 | A | ACACAACA others(24): Show |
1 | a0001c0001t0001g0004 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.81+1460_81+1461ins others(31): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117871874 | |||||||
| chr7:117871874 | A | ACACACAC others(23): Show |
1 | a0001c0001t0001g0084 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.81+1460_81+1461ins others(30): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117871874 | |||||||
| chr7:117871874 | A | ACACACAC others(17): Show |
2 | a0001c0001t0001g0003 a0008c0014t0001g0083 |
2 | HG03239.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.81+1460_81+1461ins others(24): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117871874 | |||||||
| chr7:117871875 | C | CACACACA others(6): Show |
1 | a0001c0001t0001g0065 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.81+1459_81+1460ins others(13): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117871875 | |||||||
| chr7:117871875 | C | CACACACA others(12): Show |
3 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0004t0001g0122 |
3 | HG03225.hp2 NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.81+1459_81+1460ins others(19): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117871875 | |||||||
| chr7:117871875 | C | CACACACA others(14): Show |
2 | a0001c0001t0001g0068 a0001c0001t0001g0123 |
2 | HG02615.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.81+1459_81+1460ins others(21): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117871875 | |||||||
| chr7:117871875 | C | CACACACA others(16): Show |
1 | a0001c0001t0001g0069 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.81+1459_81+1460ins others(23): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117871875 | |||||||
| chr7:117871875 | C | CACACACA others(22): Show |
2 | a0001c0001t0001g0124 a0001c0001t0001g0125 |
2 | HG01255.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.81+1459_81+1460ins others(29): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117871875 | |||||||
| chr7:117871875 | C | CACACACA others(28): Show |
1 | a0001c0001t0001g0070 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.81+1459_81+1460ins others(35): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117871875 | |||||||
| chr7:117872333 | C | T | 3 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0002c0002t0002g0073 |
3 | HG02630.hp2 NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.81+1002G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117872333 | |||||||
| chr7:117872367 | CG | C | 7 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0074 others(4): Show |
7 | HG01081.hp2 HG02630.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.81+967delC | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117872367 | |||||||
| chr7:117872384 | G | C | 45 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 others(42): Show |
45 | HG00609.hp1 HG00642.hp1 HG01168.hp2 others(42): Show |
intron_variant | MODIFIER | c.81+951C>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117872384 | |||||||
| chr7:117872547 | A | G | 140 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(137): Show |
141 | HG00323.hp2 HG00609.hp1 HG00609.hp2 others(138): Show |
intron_variant | MODIFIER | c.81+788T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117872547 | |||||||
| chr7:117872558 | G | C | 1 | a0001c0001t0001g0077 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.81+777C>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117872558 | |||||||
| chr7:117872599 | C | T | 141 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(138): Show |
142 | HG00323.hp2 HG00609.hp1 HG00609.hp2 others(139): Show |
intron_variant | MODIFIER | c.81+736G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117872599 | |||||||
| chr7:117872878 | A | G | 90 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(87): Show |
91 | HG00323.hp2 HG00609.hp2 HG01069.hp2 others(88): Show |
intron_variant | MODIFIER | c.81+457T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117872878 | |||||||
| chr7:117872931 | G | T | 141 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(138): Show |
142 | HG00323.hp2 HG00609.hp1 HG00609.hp2 others(139): Show |
intron_variant | MODIFIER | c.81+404C>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117872931 | |||||||
| chr7:117872949 | G | A | 1 | a0001c0001t0003g0147 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.81+386C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117872949 | |||||||
| chr7:117873000 | C | G | 1 | a0001c0001t0002g0002 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.81+335G>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117873000 | |||||||
| chr7:117873001 | T | A | 1 | a0001c0001t0002g0002 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.81+334A>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117873001 | |||||||
| chr7:117873008 | G | T | 1 | a0001c0001t0002g0002 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.81+327C>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117873008 | |||||||
| chr7:117873009 | C | T | 1 | a0001c0001t0002g0002 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.81+326G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117873009 | |||||||
| chr7:117873013 | A | C | 1 | a0001c0001t0002g0002 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.81+322T>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117873013 | |||||||
| chr7:117873014 | A | T | 1 | a0001c0001t0002g0002 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.81+321T>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117873014 | |||||||
| chr7:117873018 | A | C | 1 | a0001c0001t0002g0002 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.81+317T>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117873018 | |||||||
| chr7:117873019 | C | G | 1 | a0001c0001t0002g0002 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.81+316G>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117873019 | |||||||
| chr7:117873025 | C | T | 1 | a0001c0001t0002g0002 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.81+310G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117873025 | |||||||
| chr7:117873028 | A | T | 1 | a0001c0001t0002g0002 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.81+307T>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117873028 | |||||||
| chr7:117873029 | G | T | 1 | a0001c0001t0002g0002 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.81+306C>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117873029 | |||||||
| chr7:117873032 | A | C | 1 | a0001c0001t0002g0002 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.81+303T>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117873032 | |||||||
| chr7:117873034 | T | C | 1 | a0001c0001t0002g0002 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.81+301A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117873034 | |||||||
| chr7:117873036 | G | T | 1 | a0001c0001t0002g0002 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.81+299C>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117873036 | |||||||
| chr7:117873038 | C | T | 1 | a0001c0001t0002g0002 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.81+297G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117873038 | |||||||
| chr7:117873039 | A | C | 1 | a0001c0001t0002g0002 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.81+296T>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117873039 | |||||||
| chr7:117873041 | A | C | 1 | a0001c0001t0002g0002 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.81+294T>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117873041 | |||||||
| chr7:117873046 | T | G | 1 | a0001c0001t0002g0002 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.81+289A>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117873046 | |||||||
| chr7:117873047 | C | T | 1 | a0001c0001t0002g0002 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.81+288G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117873047 | |||||||
| chr7:117873055 | A | C | 1 | a0001c0001t0002g0002 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.81+280T>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117873055 | |||||||
| chr7:117873059 | A | T | 1 | a0001c0001t0002g0002 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.81+276T>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117873059 | |||||||
| chr7:117873060 | G | C | 1 | a0001c0001t0002g0002 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.81+275C>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117873060 | |||||||
| chr7:117873062 | C | G | 1 | a0001c0001t0002g0002 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.81+273G>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117873062 | |||||||
| chr7:117873063 | A | C | 1 | a0001c0001t0002g0002 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.81+272T>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117873063 | |||||||
| chr7:117873066 | G | A | 1 | a0001c0001t0002g0002 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.81+269C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117873066 | |||||||
| chr7:117873067 | A | C | 1 | a0001c0001t0002g0002 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.81+268T>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117873067 | |||||||
| chr7:117873068 | G | C | 1 | a0001c0001t0002g0002 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.81+267C>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117873068 | |||||||
| chr7:117873070 | T | G | 1 | a0001c0001t0002g0002 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.81+265A>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117873070 | |||||||
| chr7:117873077 | A | G | 1 | a0001c0001t0002g0002 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.81+258T>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117873077 | |||||||
| chr7:117873079 | C | T | 1 | a0001c0001t0002g0002 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.81+256G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117873079 | |||||||
| chr7:117873083 | C | G | 1 | a0001c0001t0002g0002 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.81+252G>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117873083 | |||||||
| chr7:117873086 | C | G | 1 | a0001c0001t0002g0002 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.81+249G>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117873086 | |||||||
| chr7:117873087 | C | G | 1 | a0001c0001t0002g0002 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.81+248G>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117873087 | |||||||
| chr7:117873088 | C | T | 1 | a0001c0001t0002g0002 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.81+247G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117873088 | |||||||
| chr7:117873092 | G | C | 1 | a0001c0001t0002g0002 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.81+243C>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117873092 | |||||||
| chr7:117873094 | C | A | 1 | a0001c0001t0002g0002 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.81+241G>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117873094 | |||||||
| chr7:117873095 | G | T | 1 | a0001c0001t0002g0002 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.81+240C>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117873095 | |||||||
| chr7:117873097 | T | G | 1 | a0001c0001t0002g0002 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.81+238A>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117873097 | |||||||
| chr7:117873098 | T | C | 1 | a0001c0001t0002g0002 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.81+237A>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117873098 | |||||||
| chr7:117873102 | G | A | 1 | a0001c0001t0002g0002 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.81+233C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117873102 | |||||||
| chr7:117873103 | T | G | 1 | a0001c0001t0002g0002 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.81+232A>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117873103 | |||||||
| chr7:117873104 | G | C | 1 | a0001c0001t0002g0002 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.81+231C>G | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117873104 | |||||||
| chr7:117873105 | G | A | 1 | a0001c0001t0002g0002 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.81+230C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117873105 | |||||||
| chr7:117873108 | C | T | 1 | a0001c0001t0002g0002 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.81+227G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117873108 | |||||||
| chr7:117873110 | C | T | 1 | a0001c0001t0002g0002 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.81+225G>A | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117873110 | |||||||
| chr7:117873112 | GAAGGGAC others(4): Show |
G | 1 | a0001c0001t0002g0002 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.81+212_81+222delTC others(9): Show |
CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117873112 | |||||||
| chr7:117873129 | C | G | 1 | a0001c0001t0002g0002 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.81+206G>C | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117873129 | |||||||
| chr7:117873140 | G | A | 1 | a0001c0001t0001g0148 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.81+195C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117873140 | |||||||
| chr7:117873146 | G | A | 14 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0151 others(11): Show |
14 | HG00323.hp2 HG01069.hp2 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.81+189C>T | CTTNBP2 | ENSG00000077063.11 | transcript | ENST00000160373.8 | protein_coding | 1/22 | chr7 | 117873146 |