Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 65981 |
| ensemblid | ENSG00000110888.19 |
| hgncid | 21259 |
| symbol | CAPRIN2 |
| name | caprin family member 2 |
| refseq_nuc | NM_001385503.1 |
| refseq_prot | NP_001372432.1 |
| ensembl_nuc | ENST00000695402.1 |
| ensembl_prot | ENSP00000511883.1 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 30709553 |
| end | 30754951 |
| strand | - |
| ver | v1.2 |
| region | chr12:30709553-30754951 |
| region5000 | chr12:30704553-30759951 |
| regionname0 | CAPRIN2_chr12_30709553_30754951 |
| regionname5000 | CAPRIN2_chr12_30704553_30759951 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 1045 | 155 | 13 | 27 | 98 | 3 | 13 | 82 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | MKSAK others(1040): Show |
chr12 | 30704553 | 30759951 |
| a0002 | 0/0 | 1045 | 118 | 71 | 16 | 11 | 2 | 18 | 5 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | MKSAK others(1040): Show |
chr12 | 30704553 | 30759951 |
| a0003 | 0/0 | 1045 | 90 | 6 | 13 | 63 | 3 | 5 | 53 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | MKSAK others(1040): Show |
chr12 | 30704553 | 30759951 |
| a0004 | 0/1 | 1045 | 5 | 0 | 2 | 0 | 0 | 2 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | MKSAK others(1040): Show |
chr12 | 30704553 | 30759951 |
| a0005 | 0/0 | 1045 | 4 | 0 | 3 | 0 | 0 | 1 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | MKSAK others(1040): Show |
chr12 | 30704553 | 30759951 |
| a0006 | 0/0 | 1045 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | MKSAK others(1040): Show |
chr12 | 30704553 | 30759951 |
| a0007 | 0/0 | 1045 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | MKSAK others(1040): Show |
chr12 | 30704553 | 30759951 |
| a0008 | 0/0 | 1045 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | MKSAK others(1040): Show |
chr12 | 30704553 | 30759951 |
| a0009 | 0/0 | 1045 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | MKSAK others(1040): Show |
chr12 | 30704553 | 30759951 |
| a0010 | 0/0 | 115 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | MKSAK others(110): Show |
chr12 | 30704553 | 30759951 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 3135 | 127 | 10 | 26 | 74 | 3 | 13 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | ATGAA others(3130): Show |
chr12 | 30704553 | 30759951 | ||
| a0001c0004 | 0/0 | 3135 | 23 | 0 | 0 | 23 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | ATGAA others(3130): Show |
chr12 | 30704553 | 30759951 | ||
| a0001c0009 | 0/0 | 3135 | 3 | 3 | 0 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | ATGAA others(3130): Show |
chr12 | 30704553 | 30759951 | ||
| a0001c0013 | 0/0 | 3135 | 1 | 0 | 1 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | ATGAA others(3130): Show |
chr12 | 30704553 | 30759951 | ||
| a0001c0014 | 0/0 | 3135 | 1 | 0 | 0 | 1 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | ATGAA others(3130): Show |
chr12 | 30704553 | 30759951 | ||
| a0002c0002 | 0/0 | 3135 | 103 | 58 | 16 | 9 | 2 | 18 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | ATGAA others(3130): Show |
chr12 | 30704553 | 30759951 | ||
| a0002c0005 | 0/0 | 3135 | 8 | 8 | 0 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | ATGAA others(3130): Show |
chr12 | 30704553 | 30759951 | ||
| a0002c0006 | 0/0 | 3135 | 5 | 5 | 0 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | ATGAA others(3130): Show |
chr12 | 30704553 | 30759951 | ||
| a0002c0011 | 0/0 | 3135 | 2 | 0 | 0 | 2 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | ATGAA others(3130): Show |
chr12 | 30704553 | 30759951 | ||
| a0003c0003 | 0/0 | 3135 | 89 | 6 | 13 | 62 | 3 | 5 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | ATGAA others(3130): Show |
chr12 | 30704553 | 30759951 | ||
| a0003c0016 | 0/0 | 3135 | 1 | 0 | 0 | 1 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | ATGAA others(3130): Show |
chr12 | 30704553 | 30759951 | ||
| a0004c0007 | 0/1 | 3135 | 5 | 0 | 2 | 0 | 0 | 2 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | ATGAA others(3130): Show |
chr12 | 30704553 | 30759951 | ||
| a0005c0008 | 0/0 | 3135 | 4 | 0 | 3 | 0 | 0 | 1 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | ATGAA others(3130): Show |
chr12 | 30704553 | 30759951 | ||
| a0006c0010 | 0/0 | 3135 | 2 | 2 | 0 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | ATGAA others(3130): Show |
chr12 | 30704553 | 30759951 | ||
| a0007c0015 | 0/0 | 3135 | 1 | 0 | 1 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | ATGAA others(3130): Show |
chr12 | 30704553 | 30759951 | ||
| a0008c0012 | 0/0 | 3135 | 1 | 0 | 0 | 0 | 0 | 1 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | ATGAA others(3130): Show |
chr12 | 30704553 | 30759951 | ||
| a0009c0017 | 0/0 | 3135 | 1 | 0 | 0 | 1 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | ATGAA others(3130): Show |
chr12 | 30704553 | 30759951 | ||
| a0010c0018 | 0/0 | 3135 | 1 | 0 | 0 | 1 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | ATGAA others(3130): Show |
chr12 | 30704553 | 30759951 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 3727 | 127 | 10 | 26 | 74 | 3 | 13 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | CTGGG others(3722): Show |
chr12 | 30704553 | 30759951 |
| a0001c0004t0001 | 0/0 | 3727 | 23 | 0 | 0 | 23 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | CTGGG others(3722): Show |
chr12 | 30704553 | 30759951 |
| a0001c0009t0001 | 0/0 | 3727 | 3 | 3 | 0 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | CTGGG others(3722): Show |
chr12 | 30704553 | 30759951 |
| a0001c0013t0001 | 0/0 | 3727 | 1 | 0 | 1 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | CTGGG others(3722): Show |
chr12 | 30704553 | 30759951 |
| a0001c0014t0001 | 0/0 | 3727 | 1 | 0 | 0 | 1 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | CTGGG others(3722): Show |
chr12 | 30704553 | 30759951 |
| a0002c0002t0001 | 0/0 | 3727 | 64 | 39 | 5 | 8 | 1 | 11 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | CTGGG others(3722): Show |
chr12 | 30704553 | 30759951 |
| a0002c0002t0002 | 0/0 | 3727 | 30 | 17 | 5 | 1 | 0 | 7 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | CTGGG others(3722): Show |
chr12 | 30704553 | 30759951 |
| a0002c0002t0003 | 0/0 | 3727 | 7 | 0 | 6 | 0 | 1 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | CTGGG others(3722): Show |
chr12 | 30704553 | 30759951 |
| a0002c0002t0004 | 0/0 | 3727 | 2 | 2 | 0 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | CTGGG others(3722): Show |
chr12 | 30704553 | 30759951 |
| a0002c0005t0001 | 0/0 | 3727 | 8 | 8 | 0 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | CTGGG others(3722): Show |
chr12 | 30704553 | 30759951 |
| a0002c0006t0001 | 0/0 | 3727 | 5 | 5 | 0 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | CTGGG others(3722): Show |
chr12 | 30704553 | 30759951 |
| a0002c0011t0001 | 0/0 | 3727 | 2 | 0 | 0 | 2 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | CTGGG others(3722): Show |
chr12 | 30704553 | 30759951 |
| a0003c0003t0001 | 0/0 | 3727 | 89 | 6 | 13 | 62 | 3 | 5 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | CTGGG others(3722): Show |
chr12 | 30704553 | 30759951 |
| a0003c0016t0001 | 0/0 | 3727 | 1 | 0 | 0 | 1 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | CTGGG others(3722): Show |
chr12 | 30704553 | 30759951 |
| a0004c0007t0001 | 0/0 | 3727 | 1 | 0 | 1 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | CTGGG others(3722): Show |
chr12 | 30704553 | 30759951 |
| a0004c0007t0002 | 0/1 | 3727 | 4 | 0 | 1 | 0 | 0 | 2 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | CTGGG others(3722): Show |
chr12 | 30704553 | 30759951 |
| a0005c0008t0002 | 0/0 | 3727 | 4 | 0 | 3 | 0 | 0 | 1 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | CTGGG others(3722): Show |
chr12 | 30704553 | 30759951 |
| a0006c0010t0001 | 0/0 | 3727 | 2 | 2 | 0 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | CTGGG others(3722): Show |
chr12 | 30704553 | 30759951 |
| a0007c0015t0001 | 0/0 | 3727 | 1 | 0 | 1 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | CTGGG others(3722): Show |
chr12 | 30704553 | 30759951 |
| a0008c0012t0001 | 0/0 | 3727 | 1 | 0 | 0 | 0 | 0 | 1 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | CTGGG others(3722): Show |
chr12 | 30704553 | 30759951 |
| a0009c0017t0001 | 0/0 | 3727 | 1 | 0 | 0 | 1 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | CTGGG others(3722): Show |
chr12 | 30704553 | 30759951 |
| a0010c0018t0001 | 0/0 | 3727 | 1 | 0 | 0 | 1 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | CTGGG others(3722): Show |
chr12 | 30704553 | 30759951 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 19 | 0 | 2 | 14 | 0 | 3 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0001c0001t0001g0006 | 0/0 | 5 | 0 | 4 | 1 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0001c0001t0001g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0001c0001t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0001c0001t0001g0073 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0001c0004t0001g0004 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0001c0004t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0001c0004t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0001c0004t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0001c0004t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0001c0004t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0001c0004t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0001c0004t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0001c0004t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0001c0004t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0001c0004t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0001c0004t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0001c0004t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0001c0004t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0001c0004t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0001c0009t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0001c0009t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0001c0009t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0001c0013t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0001c0014t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0002c0002t0001g0005 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0002c0002t0001g0007 | 0/0 | 5 | 0 | 0 | 2 | 0 | 3 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0002c0002t0001g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0002c0002t0001g0017 | 0/0 | 3 | 0 | 0 | 0 | 1 | 2 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0002c0002t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0002c0002t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0002c0002t0001g0023 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0002c0002t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0002c0002t0001g0039 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0002c0002t0001g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0002c0002t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0002c0002t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0002c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0002c0002t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0002c0002t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0002c0002t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0002c0002t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0002c0002t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0002c0002t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0002c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0002c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0002c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0002c0002t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0002c0002t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0002c0002t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0002c0002t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0002c0002t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0002c0002t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0002c0002t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0002c0002t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0002c0002t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0002c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0002c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0002c0002t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0002c0002t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0002c0002t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0002c0002t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0002c0002t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0002c0002t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0002c0002t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0002c0002t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0002c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0002c0002t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0002c0002t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0002c0002t0002g0012 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0002c0002t0002g0013 | 0/0 | 4 | 2 | 1 | 0 | 0 | 1 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0002c0002t0002g0044 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0002c0002t0002g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0002c0002t0002g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0002c0002t0002g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0002c0002t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0002c0002t0002g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0002c0002t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0002c0002t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0002c0002t0002g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0002c0002t0002g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0002c0002t0002g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0002c0002t0002g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0002c0002t0002g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0002c0002t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0002c0002t0002g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0002c0002t0002g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0002c0002t0002g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0002c0002t0002g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0002c0002t0003g0011 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0002c0002t0003g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0002c0002t0003g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0002c0002t0003g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0002c0002t0004g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0002c0002t0004g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0002c0005t0001g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0002c0005t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0002c0005t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0002c0005t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0002c0005t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0002c0005t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0002c0005t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0002c0006t0001g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0002c0006t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0002c0006t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0002c0011t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0002c0011t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0003c0003t0001g0002 | 0/0 | 16 | 2 | 2 | 11 | 1 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0003c0003t0001g0003 | 0/0 | 9 | 0 | 1 | 7 | 1 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0003c0003t0001g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0003c0003t0001g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0003c0003t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0003c0003t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0003c0003t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0003c0003t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0003c0003t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0003c0003t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0003c0003t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0003c0003t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0003c0003t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0003c0003t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0003c0003t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0003c0003t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0003c0003t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0003c0003t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0003c0003t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0003c0003t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0003c0003t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0003c0003t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0003c0003t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0003c0003t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0003c0003t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0003c0003t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0003c0003t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0003c0003t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0003c0003t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0003c0003t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0003c0003t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0003c0003t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0003c0003t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0003c0003t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0003c0003t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0003c0003t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0003c0003t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0003c0003t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0003c0003t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0003c0003t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0003c0003t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0003c0003t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0003c0003t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0003c0003t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0003c0003t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0003c0003t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0003c0003t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0003c0003t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0003c0003t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0003c0003t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0003c0003t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0003c0003t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0003c0003t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0003c0003t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0003c0003t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0003c0003t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0003c0003t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0003c0003t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0003c0016t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0004c0007t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0004c0007t0002g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0004c0007t0002g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0004c0007t0002g0247 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0004c0007t0002g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0005c0008t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0005c0008t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0005c0008t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0005c0008t0002g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0006c0010t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0006c0010t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0007c0015t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0008c0012t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0009c0017t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| a0010c0018t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0113 | EUR | FIN | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG00280 | hp2 | a0003 | c0003 | t0001 | g0146 | EUR | FIN | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG00408 | hp1 | a0001 | c0004 | t0001 | g0043 | EAS | CHS | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | CHS | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG00544 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | CHS | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG00544 | hp2 | a0001 | c0004 | t0001 | g0233 | EAS | CHS | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | CHS | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG00558 | hp2 | a0003 | c0003 | t0001 | g0009 | EAS | CHS | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG00621 | hp1 | a0002 | c0002 | t0001 | g0018 | EAS | CHS | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG00639 | hp2 | a0003 | c0003 | t0001 | g0147 | AMR | PUR | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | CHS | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG00673 | hp2 | a0003 | c0003 | t0001 | g0009 | EAS | CHS | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG00733 | hp2 | a0003 | c0003 | t0001 | g0103 | AMR | PUR | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG00735 | hp1 | a0003 | c0003 | t0001 | g0003 | AMR | PUR | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG00735 | hp2 | a0001 | c0013 | t0001 | g0060 | AMR | PUR | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG00738 | hp1 | a0002 | c0002 | t0001 | g0051 | AMR | PUR | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG00738 | hp2 | a0002 | c0002 | t0003 | g0204 | AMR | PUR | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG00741 | hp2 | a0002 | c0002 | t0003 | g0190 | AMR | PUR | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG01069 | hp1 | a0003 | c0003 | t0001 | g0050 | AMR | PUR | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG01070 | hp1 | a0004 | c0007 | t0002 | g0239 | AMR | PUR | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG01074 | hp2 | a0002 | c0002 | t0002 | g0256 | AMR | PUR | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG01081 | hp1 | a0005 | c0008 | t0002 | g0249 | AMR | PUR | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG01099 | hp1 | a0003 | c0003 | t0001 | g0150 | AMR | PUR | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG01099 | hp2 | a0002 | c0002 | t0003 | g0011 | AMR | PUR | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG01106 | hp2 | a0002 | c0002 | t0002 | g0240 | AMR | PUR | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG01167 | hp1 | a0002 | c0002 | t0001 | g0039 | AMR | PUR | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG01167 | hp2 | a0002 | c0002 | t0002 | g0253 | AMR | PUR | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG01168 | hp1 | a0002 | c0002 | t0002 | g0241 | AMR | PUR | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG01168 | hp2 | a0003 | c0003 | t0001 | g0152 | AMR | PUR | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG01169 | hp1 | a0002 | c0002 | t0001 | g0183 | AMR | PUR | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG01169 | hp2 | a0003 | c0003 | t0001 | g0126 | AMR | PUR | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG01192 | hp2 | a0002 | c0002 | t0001 | g0200 | AMR | PUR | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | CLM | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG01256 | hp2 | a0003 | c0003 | t0001 | g0002 | AMR | CLM | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG01257 | hp2 | a0003 | c0003 | t0001 | g0161 | AMR | CLM | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG01261 | hp2 | a0002 | c0002 | t0003 | g0201 | AMR | CLM | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG01346 | hp1 | a0003 | c0003 | t0001 | g0148 | AMR | CLM | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | CLM | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG01358 | hp1 | a0005 | c0008 | t0002 | g0248 | AMR | CLM | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG01358 | hp2 | a0003 | c0003 | t0001 | g0139 | AMR | CLM | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG01361 | hp1 | a0002 | c0002 | t0002 | g0013 | AMR | CLM | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG01433 | hp1 | a0005 | c0008 | t0002 | g0251 | AMR | CLM | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG01433 | hp2 | a0002 | c0002 | t0003 | g0011 | AMR | CLM | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG01496 | hp1 | a0002 | c0002 | t0001 | g0199 | AMR | CLM | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | CLM | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG01516 | hp1 | a0003 | c0003 | t0001 | g0002 | EUR | IBS | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0055 | EUR | IBS | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG01517 | hp1 | a0002 | c0002 | t0003 | g0011 | EUR | IBS | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0024 | EUR | IBS | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG01884 | hp1 | a0002 | c0002 | t0001 | g0038 | AFR | ACB | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG01884 | hp2 | a0001 | c0009 | t0001 | g0207 | AFR | ACB | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG01891 | hp1 | a0002 | c0002 | t0002 | g0047 | AFR | ACB | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG01891 | hp2 | a0002 | c0002 | t0001 | g0005 | AFR | ACB | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PEL | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PEL | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PEL | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG01934 | hp2 | a0003 | c0003 | t0001 | g0002 | AMR | PEL | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG01978 | hp1 | a0007 | c0015 | t0001 | g0099 | AMR | PEL | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PEL | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG01981 | hp1 | a0004 | c0007 | t0001 | g0213 | AMR | PEL | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | PEL | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG02015 | hp1 | a0003 | c0003 | t0001 | g0171 | EAS | KHV | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | KHV | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG02040 | hp1 | a0003 | c0003 | t0001 | g0003 | EAS | KHV | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | KHV | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG02071 | hp1 | a0001 | c0004 | t0001 | g0004 | EAS | KHV | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG02080 | hp1 | a0003 | c0003 | t0001 | g0009 | EAS | KHV | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG02080 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | KHV | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | KHV | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG02129 | hp2 | a0002 | c0002 | t0002 | g0242 | EAS | KHV | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG02135 | hp1 | a0003 | c0003 | t0001 | g0002 | EAS | KHV | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | KHV | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG02145 | hp2 | a0002 | c0002 | t0001 | g0049 | AFR | ACB | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG02165 | hp1 | a0003 | c0003 | t0001 | g0002 | EAS | CDX | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | CDX | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG02257 | hp1 | a0002 | c0002 | t0004 | g0260 | AFR | ACB | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG02257 | hp2 | a0002 | c0002 | t0001 | g0186 | AFR | ACB | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG02258 | hp1 | a0002 | c0002 | t0001 | g0193 | AFR | ACB | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG02258 | hp2 | a0002 | c0005 | t0001 | g0206 | AFR | ACB | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG02280 | hp1 | a0003 | c0003 | t0001 | g0155 | AFR | ACB | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PEL | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PEL | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG02300 | hp1 | a0002 | c0002 | t0003 | g0011 | AMR | PEL | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG02451 | hp1 | a0002 | c0002 | t0001 | g0039 | AFR | ACB | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG02451 | hp2 | a0002 | c0002 | t0001 | g0221 | AFR | ACB | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG02523 | hp1 | a0003 | c0003 | t0001 | g0168 | EAS | KHV | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG02523 | hp2 | a0002 | c0002 | t0001 | g0178 | EAS | KHV | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG02572 | hp1 | a0002 | c0002 | t0001 | g0041 | AFR | GWD | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG02572 | hp2 | a0002 | c0002 | t0001 | g0005 | AFR | GWD | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0067 | SAS | PJL | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG02602 | hp2 | a0004 | c0007 | t0002 | g0250 | SAS | PJL | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG02615 | hp1 | a0002 | c0002 | t0001 | g0005 | AFR | GWD | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG02615 | hp2 | a0002 | c0002 | t0002 | g0254 | AFR | GWD | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG02622 | hp1 | a0002 | c0006 | t0001 | g0194 | AFR | GWD | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG02622 | hp2 | a0002 | c0002 | t0002 | g0045 | AFR | GWD | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG02630 | hp1 | a0002 | c0002 | t0002 | g0013 | AFR | GWD | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG02630 | hp2 | a0002 | c0002 | t0002 | g0012 | AFR | GWD | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG02647 | hp1 | a0002 | c0002 | t0001 | g0133 | AFR | GWD | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG02647 | hp2 | a0002 | c0002 | t0001 | g0184 | AFR | GWD | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG02683 | hp1 | a0003 | c0003 | t0001 | g0157 | SAS | PJL | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG02698 | hp1 | a0008 | c0012 | t0001 | g0052 | SAS | PJL | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG02698 | hp2 | a0003 | c0003 | t0001 | g0175 | SAS | PJL | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG02723 | hp1 | a0002 | c0002 | t0001 | g0197 | AFR | GWD | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG02723 | hp2 | a0002 | c0002 | t0001 | g0181 | AFR | GWD | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG02735 | hp1 | a0003 | c0003 | t0001 | g0128 | SAS | PJL | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG02738 | hp1 | a0002 | c0002 | t0002 | g0257 | SAS | PJL | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG02809 | hp1 | a0003 | c0003 | t0001 | g0002 | AFR | GWD | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG02809 | hp2 | a0002 | c0006 | t0001 | g0019 | AFR | GWD | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG02818 | hp1 | a0002 | c0002 | t0001 | g0135 | AFR | GWD | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG02818 | hp2 | a0002 | c0002 | t0001 | g0195 | AFR | GWD | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG02886 | hp1 | a0002 | c0002 | t0001 | g0134 | AFR | GWD | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG02886 | hp2 | a0002 | c0002 | t0001 | g0005 | AFR | GWD | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG02895 | hp2 | a0002 | c0002 | t0002 | g0246 | AFR | GWD | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG02896 | hp1 | a0002 | c0002 | t0001 | g0021 | AFR | GWD | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | GWD | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG02897 | hp1 | a0002 | c0002 | t0001 | g0021 | AFR | GWD | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG02897 | hp2 | a0002 | c0002 | t0002 | g0245 | AFR | GWD | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG02922 | hp1 | a0002 | c0002 | t0002 | g0046 | AFR | ESN | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG02922 | hp2 | a0002 | c0002 | t0001 | g0132 | AFR | ESN | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG02965 | hp1 | a0002 | c0002 | t0001 | g0016 | AFR | ESN | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG02965 | hp2 | a0006 | c0010 | t0001 | g0217 | AFR | ESN | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | ESN | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG02970 | hp2 | a0002 | c0002 | t0001 | g0180 | AFR | ESN | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG02976 | hp1 | a0002 | c0002 | t0002 | g0258 | AFR | ESN | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | ESN | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG03041 | hp1 | a0002 | c0002 | t0002 | g0012 | AFR | GWD | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG03041 | hp2 | a0002 | c0002 | t0001 | g0185 | AFR | GWD | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG03098 | hp1 | a0002 | c0005 | t0001 | g0219 | AFR | MSL | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG03098 | hp2 | a0002 | c0005 | t0001 | g0040 | AFR | MSL | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG03130 | hp1 | a0002 | c0002 | t0001 | g0203 | AFR | ESN | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG03130 | hp2 | a0002 | c0002 | t0002 | g0013 | AFR | ESN | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG03139 | hp1 | a0002 | c0005 | t0001 | g0210 | AFR | ESN | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG03139 | hp2 | a0002 | c0002 | t0001 | g0005 | AFR | ESN | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG03195 | hp1 | a0002 | c0005 | t0001 | g0208 | AFR | ESN | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG03195 | hp2 | a0002 | c0002 | t0004 | g0259 | AFR | ESN | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG03209 | hp1 | a0002 | c0005 | t0001 | g0222 | AFR | MSL | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG03209 | hp2 | a0002 | c0006 | t0001 | g0019 | AFR | MSL | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG03225 | hp1 | a0003 | c0003 | t0001 | g0136 | AFR | MSL | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG03225 | hp2 | a0002 | c0002 | t0002 | g0012 | AFR | MSL | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG03239 | hp1 | a0002 | c0002 | t0002 | g0255 | SAS | PJL | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG03239 | hp2 | a0002 | c0002 | t0001 | g0177 | SAS | PJL | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG03453 | hp1 | a0006 | c0010 | t0001 | g0218 | AFR | MSL | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG03453 | hp2 | a0001 | c0009 | t0001 | g0209 | AFR | MSL | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG03486 | hp1 | a0002 | c0005 | t0001 | g0040 | AFR | MSL | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG03486 | hp2 | a0002 | c0002 | t0001 | g0179 | AFR | MSL | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG03491 | hp1 | a0002 | c0002 | t0001 | g0023 | SAS | PJL | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG03492 | hp2 | a0002 | c0002 | t0001 | g0023 | SAS | PJL | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG03516 | hp1 | a0002 | c0002 | t0001 | g0188 | AFR | ESN | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG03516 | hp2 | a0002 | c0002 | t0002 | g0237 | AFR | ESN | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG03540 | hp2 | a0002 | c0006 | t0001 | g0019 | AFR | GWD | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG03579 | hp1 | a0002 | c0002 | t0001 | g0041 | AFR | MSL | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG03579 | hp2 | a0001 | c0009 | t0001 | g0205 | AFR | MSL | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG03654 | hp1 | a0002 | c0002 | t0001 | g0007 | SAS | PJL | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG03654 | hp2 | a0002 | c0002 | t0002 | g0244 | SAS | PJL | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG03669 | hp1 | a0003 | c0003 | t0001 | g0156 | SAS | PJL | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG03669 | hp2 | a0002 | c0002 | t0002 | g0013 | SAS | PJL | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG03688 | hp1 | a0002 | c0002 | t0002 | g0243 | SAS | STU | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0077 | SAS | STU | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0058 | SAS | PJL | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG03704 | hp2 | a0002 | c0002 | t0001 | g0191 | SAS | PJL | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG03710 | hp1 | a0005 | c0008 | t0002 | g0252 | SAS | PJL | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0214 | SAS | BEB | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG03831 | hp2 | a0002 | c0002 | t0001 | g0007 | SAS | BEB | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG03834 | hp1 | a0002 | c0002 | t0001 | g0215 | SAS | BEB | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG03834 | hp2 | a0004 | c0007 | t0002 | g0238 | SAS | BEB | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0106 | SAS | BEB | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG03927 | hp2 | a0002 | c0002 | t0001 | g0017 | SAS | BEB | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0075 | SAS | BEB | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG03942 | hp2 | a0002 | c0002 | t0002 | g0044 | SAS | BEB | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG04199 | hp1 | a0002 | c0002 | t0002 | g0044 | SAS | STU | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG04199 | hp2 | a0002 | c0002 | t0001 | g0007 | SAS | STU | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG04228 | hp1 | a0002 | c0002 | t0001 | g0068 | SAS | STU | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA18522 | hp1 | a0002 | c0002 | t0001 | g0016 | AFR | YRI | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | YRI | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA18612 | hp2 | a0003 | c0003 | t0001 | g0123 | EAS | CHB | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA18747 | hp1 | a0003 | c0003 | t0001 | g0002 | EAS | CHB | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA18747 | hp2 | a0002 | c0002 | t0001 | g0176 | EAS | CHB | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA18906 | hp1 | a0002 | c0002 | t0001 | g0016 | AFR | YRI | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | YRI | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA18941 | hp2 | a0003 | c0003 | t0001 | g0165 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA18942 | hp1 | a0003 | c0003 | t0001 | g0002 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA18943 | hp1 | a0003 | c0003 | t0001 | g0145 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA18944 | hp1 | a0003 | c0003 | t0001 | g0160 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA18945 | hp1 | a0003 | c0003 | t0001 | g0037 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA18946 | hp1 | a0003 | c0003 | t0001 | g0140 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA18949 | hp2 | a0003 | c0003 | t0001 | g0036 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA18950 | hp1 | a0003 | c0003 | t0001 | g0010 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA18950 | hp2 | a0002 | c0011 | t0001 | g0182 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA18951 | hp2 | a0001 | c0004 | t0001 | g0223 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA18952 | hp1 | a0003 | c0003 | t0001 | g0002 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA18953 | hp2 | a0003 | c0003 | t0001 | g0144 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA18956 | hp1 | a0003 | c0003 | t0001 | g0125 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA18957 | hp2 | a0003 | c0003 | t0001 | g0129 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA18959 | hp1 | a0003 | c0003 | t0001 | g0159 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA18960 | hp1 | a0001 | c0004 | t0001 | g0004 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA18960 | hp2 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA18961 | hp2 | a0003 | c0003 | t0001 | g0130 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA18963 | hp1 | a0001 | c0004 | t0001 | g0004 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA18964 | hp1 | a0001 | c0004 | t0001 | g0004 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA18971 | hp2 | a0001 | c0004 | t0001 | g0004 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA18972 | hp1 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA18975 | hp2 | a0003 | c0003 | t0001 | g0009 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA18979 | hp2 | a0001 | c0004 | t0001 | g0227 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA18980 | hp1 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA18982 | hp1 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA18983 | hp1 | a0003 | c0003 | t0001 | g0127 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA18987 | hp2 | a0003 | c0003 | t0001 | g0138 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA18988 | hp2 | a0003 | c0003 | t0001 | g0010 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA18991 | hp1 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA18991 | hp2 | a0003 | c0003 | t0001 | g0048 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA18992 | hp1 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA18994 | hp2 | a0009 | c0017 | t0001 | g0163 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA18998 | hp1 | a0001 | c0004 | t0001 | g0225 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA18998 | hp2 | a0003 | c0003 | t0001 | g0037 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA18999 | hp2 | a0001 | c0004 | t0001 | g0043 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA19000 | hp1 | a0003 | c0003 | t0001 | g0151 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA19000 | hp2 | a0001 | c0004 | t0001 | g0228 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA19001 | hp1 | a0001 | c0004 | t0001 | g0229 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA19001 | hp2 | a0003 | c0003 | t0001 | g0002 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA19003 | hp1 | a0001 | c0004 | t0001 | g0042 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA19003 | hp2 | a0003 | c0003 | t0001 | g0172 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA19004 | hp1 | a0001 | c0004 | t0001 | g0042 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA19005 | hp1 | a0003 | c0003 | t0001 | g0169 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA19005 | hp2 | a0001 | c0014 | t0001 | g0083 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA19006 | hp1 | a0001 | c0004 | t0001 | g0236 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA19006 | hp2 | a0010 | c0018 | t0001 | g0115 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA19007 | hp1 | a0001 | c0004 | t0001 | g0231 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA19007 | hp2 | a0003 | c0003 | t0001 | g0174 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA19010 | hp1 | a0003 | c0003 | t0001 | g0158 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA19011 | hp2 | a0003 | c0016 | t0001 | g0154 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA19012 | hp2 | a0003 | c0003 | t0001 | g0002 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA19030 | hp1 | a0003 | c0003 | t0001 | g0149 | AFR | LWK | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA19030 | hp2 | a0002 | c0002 | t0001 | g0131 | AFR | LWK | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA19043 | hp1 | a0002 | c0002 | t0001 | g0187 | AFR | LWK | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA19043 | hp2 | a0002 | c0002 | t0001 | g0038 | AFR | LWK | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA19054 | hp1 | a0003 | c0003 | t0001 | g0002 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA19055 | hp2 | a0003 | c0003 | t0001 | g0124 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA19056 | hp2 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA19057 | hp1 | a0003 | c0003 | t0001 | g0143 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA19062 | hp1 | a0002 | c0002 | t0001 | g0189 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA19063 | hp2 | a0003 | c0003 | t0001 | g0166 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA19065 | hp2 | a0001 | c0004 | t0001 | g0004 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA19066 | hp1 | a0003 | c0003 | t0001 | g0036 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA19070 | hp1 | a0003 | c0003 | t0001 | g0170 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA19072 | hp1 | a0003 | c0003 | t0001 | g0164 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA19074 | hp1 | a0003 | c0003 | t0001 | g0010 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA19076 | hp2 | a0003 | c0003 | t0001 | g0122 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA19078 | hp1 | a0003 | c0003 | t0001 | g0167 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA19079 | hp1 | a0003 | c0003 | t0001 | g0162 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA19079 | hp2 | a0003 | c0003 | t0001 | g0232 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA19080 | hp1 | a0003 | c0003 | t0001 | g0142 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA19080 | hp2 | a0003 | c0003 | t0001 | g0173 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA19082 | hp1 | a0003 | c0003 | t0001 | g0002 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA19083 | hp2 | a0003 | c0003 | t0001 | g0002 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA19084 | hp1 | a0003 | c0003 | t0001 | g0002 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA19084 | hp2 | a0001 | c0004 | t0001 | g0230 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA19085 | hp1 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA19086 | hp1 | a0001 | c0004 | t0001 | g0226 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA19087 | hp2 | a0001 | c0004 | t0001 | g0235 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA19088 | hp1 | a0001 | c0004 | t0001 | g0224 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA19088 | hp2 | a0003 | c0003 | t0001 | g0010 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA19090 | hp1 | a0003 | c0003 | t0001 | g0141 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA19091 | hp1 | a0002 | c0011 | t0001 | g0202 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA20129 | hp1 | a0002 | c0002 | t0001 | g0005 | AFR | ASW | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA20129 | hp2 | a0002 | c0002 | t0002 | g0045 | AFR | ASW | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA20752 | hp1 | a0003 | c0003 | t0001 | g0003 | EUR | TSI | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA20752 | hp2 | a0002 | c0002 | t0001 | g0017 | EUR | TSI | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA20905 | hp1 | a0002 | c0002 | t0001 | g0017 | SAS | GIH | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA20905 | hp2 | a0003 | c0003 | t0001 | g0104 | SAS | GIH | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | CLM | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG01123 | hp2 | a0003 | c0003 | t0001 | g0153 | AMR | CLM | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG02109 | hp1 | a0002 | c0002 | t0001 | g0196 | AFR | ACB | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG02109 | hp2 | a0002 | c0002 | t0001 | g0220 | AFR | ACB | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG02486 | hp1 | a0002 | c0005 | t0001 | g0211 | AFR | ACB | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | ACB | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG02559 | hp1 | a0002 | c0002 | t0002 | g0012 | AFR | ACB | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG02559 | hp2 | a0003 | c0003 | t0001 | g0137 | AFR | ACB | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG03471 | hp1 | a0002 | c0002 | t0002 | g0047 | AFR | MSL | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG03471 | hp2 | a0002 | c0006 | t0001 | g0192 | AFR | MSL | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG06807 | hp1 | a0002 | c0002 | t0001 | g0121 | AFR | USA | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| HG06807 | hp2 | a0002 | c0002 | t0001 | g0198 | AFR | USA | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA18955 | hp2 | a0001 | c0004 | t0001 | g0004 | EAS | JPT | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA20300 | hp1 | a0002 | c0002 | t0002 | g0046 | AFR | USA | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| NA20300 | hp2 | a0003 | c0003 | t0001 | g0002 | AFR | USA | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| homoSapiens | chm13v2 | a0004 | c0007 | t0002 | g0247 | REF | REF | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0073 | REF | REF | CAPRIN2_chr12_30704553_30759951 | CAPRIN2 | chr12 | 30704553 | 30759951 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:30724393 | G | A | 1 | a0009 | 1 | NA18994.hp2 | missense_variant | MODERATE | c.1721C>T | p.Ser574Leu | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 11/19 | 1961/3727 | 1721/3138 | 574/1045 | chr12 | 30724393 | |||
| chr12:30726042 | G | C | 1 | a0005 | 4 | HG01081.hp1 HG01358.hp1 HG01433.hp1 others(1): Show |
missense_variant | MODERATE | c.1586C>G | p.Pro529Arg | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 10/19 | 1826/3727 | 1586/3138 | 529/1045 | chr12 | 30726042 | |||
| chr12:30728875 | T | C | 6 | a0002 a0003 a0004 others(3): Show |
219 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(216): Show |
missense_variant | MODERATE | c.1312A>G | p.Met438Val | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 9/19 | 1552/3727 | 1312/3138 | 438/1045 | chr12 | 30728875 | |||
| chr12:30729322 | G | A | 1 | a0007 | 1 | HG01978.hp1 | missense_variant | MODERATE | c.865C>T | p.Leu289Phe | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 9/19 | 1105/3727 | 865/3138 | 289/1045 | chr12 | 30729322 | |||
| chr12:30731402 | A | G | 1 | a0006 | 2 | HG02965.hp2 HG03453.hp1 |
missense_variant | MODERATE | c.758T>C | p.Met253Thr | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 7/19 | 998/3727 | 758/3138 | 253/1045 | chr12 | 30731402 | |||
| chr12:30734969 | T | A | 1 | a0010 | 1 | NA19006.hp2 | missense_variant&splice_region_variant | MODERATE | c.565A>T | p.Ser189Cys | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 5/19 | 805/3727 | 565/3138 | 189/1045 | chr12 | 30734969 | |||
| chr12:30734971 | A | C | 1 | a0010 | 1 | NA19006.hp2 | missense_variant | MODERATE | c.563T>G | p.Leu188Arg | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 5/19 | 803/3727 | 563/3138 | 188/1045 | chr12 | 30734971 | |||
| chr12:30734972 | G | T | 1 | a0010 | 1 | NA19006.hp2 | missense_variant | MODERATE | c.562C>A | p.Leu188Met | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 5/19 | 802/3727 | 562/3138 | 188/1045 | chr12 | 30734972 | |||
| chr12:30734990 | G | A | 1 | a0010 | 1 | NA19006.hp2 | missense_variant | MODERATE | c.544C>T | p.Pro182Ser | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 5/19 | 784/3727 | 544/3138 | 182/1045 | chr12 | 30734990 | |||
| chr12:30734993 | A | T | 1 | a0010 | 1 | NA19006.hp2 | missense_variant | MODERATE | c.541T>A | p.Cys181Ser | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 5/19 | 781/3727 | 541/3138 | 181/1045 | chr12 | 30734993 | |||
| chr12:30734995 | G | T | 1 | a0010 | 1 | NA19006.hp2 | missense_variant | MODERATE | c.539C>A | p.Thr180Asn | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 5/19 | 779/3727 | 539/3138 | 180/1045 | chr12 | 30734995 | |||
| chr12:30734996 | T | A | 1 | a0010 | 1 | NA19006.hp2 | missense_variant | MODERATE | c.538A>T | p.Thr180Ser | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 5/19 | 778/3727 | 538/3138 | 180/1045 | chr12 | 30734996 | |||
| chr12:30735007 | A | T | 1 | a0010 | 1 | NA19006.hp2 | missense_variant | MODERATE | c.527T>A | p.Phe176Tyr | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 5/19 | 767/3727 | 527/3138 | 176/1045 | chr12 | 30735007 | |||
| chr12:30735018 | G | T | 1 | a0010 | 1 | NA19006.hp2 | stop_gained | HIGH | c.516C>A | p.Tyr172* | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 5/19 | 756/3727 | 516/3138 | 172/1045 | chr12 | 30735018 | |||
| chr12:30735022 | T | A | 1 | a0010 | 1 | NA19006.hp2 | missense_variant | MODERATE | c.512A>T | p.Asp171Val | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 5/19 | 752/3727 | 512/3138 | 171/1045 | chr12 | 30735022 | |||
| chr12:30735043 | T | A | 1 | a0010 | 1 | NA19006.hp2 | missense_variant | MODERATE | c.491A>T | p.Tyr164Phe | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 5/19 | 731/3727 | 491/3138 | 164/1045 | chr12 | 30735043 | |||
| chr12:30735067 | T | C | 2 | a0003 a0009 |
91 | HG00280.hp2 HG00558.hp2 HG00639.hp2 others(88): Show |
missense_variant | MODERATE | c.467A>G | p.Lys156Arg | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 5/19 | 707/3727 | 467/3138 | 156/1045 | chr12 | 30735067 | |||
| chr12:30735121 | T | A | 1 | a0010 | 1 | NA19006.hp2 | missense_variant | MODERATE | c.413A>T | p.Gln138Leu | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 5/19 | 653/3727 | 413/3138 | 138/1045 | chr12 | 30735121 | |||
| chr12:30735160 | T | G | 1 | a0010 | 1 | NA19006.hp2 | missense_variant | MODERATE | c.374A>C | p.Lys125Thr | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 5/19 | 614/3727 | 374/3138 | 125/1045 | chr12 | 30735160 | |||
| chr12:30735188 | T | A | 1 | a0010 | 1 | NA19006.hp2 | stop_gained | HIGH | c.346A>T | p.Lys116* | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 5/19 | 586/3727 | 346/3138 | 116/1045 | chr12 | 30735188 | |||
| chr12:30735190 | T | C | 1 | a0010 | 1 | NA19006.hp2 | missense_variant | MODERATE | c.344A>G | p.Lys115Arg | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 5/19 | 584/3727 | 344/3138 | 115/1045 | chr12 | 30735190 | |||
| chr12:30753424 | G | A | 2 | a0004 a0005 |
8 | HG01070.hp1 HG01081.hp1 HG01358.hp1 others(5): Show |
missense_variant | MODERATE | c.97C>T | p.Pro33Ser | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 2/19 | 337/3727 | 97/3138 | 33/1045 | chr12 | 30753424 | |||
| chr12:30753459 | C | T | 1 | a0008 | 1 | HG02698.hp1 | missense_variant | MODERATE | c.62G>A | p.Ser21Asn | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 2/19 | 302/3727 | 62/3138 | 21/1045 | chr12 | 30753459 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:30710151 | G | A | 3 | a0001c0009 a0002c0005 a0006c0010 |
13 | HG01884.hp2 HG02258.hp2 HG02486.hp1 others(10): Show |
synonymous_variant | LOW | c.2889C>T | p.Tyr963Tyr | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 19/19 | 3129/3727 | 2889/3138 | 963/1045 | chr12 | 30710151 | |||
| chr12:30713839 | A | G | 1 | a0003c0016 | 1 | NA19011.hp2 | synonymous_variant | LOW | c.2451T>C | p.Tyr817Tyr | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 17/19 | 2691/3727 | 2451/3138 | 817/1045 | chr12 | 30713839 | |||
| chr12:30713872 | A | G | 2 | a0001c0014 a0002c0006 |
6 | HG02622.hp1 HG02809.hp2 HG03209.hp2 others(3): Show |
synonymous_variant | LOW | c.2418T>C | p.Tyr806Tyr | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 17/19 | 2658/3727 | 2418/3138 | 806/1045 | chr12 | 30713872 | |||
| chr12:30715068 | C | T | 12 | a0001c0004 a0001c0009 a0002c0002 others(9): Show |
245 | HG00280.hp2 HG00408.hp1 HG00544.hp1 others(242): Show |
synonymous_variant | LOW | c.2295G>A | p.Val765Val | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 16/19 | 2535/3727 | 2295/3138 | 765/1045 | chr12 | 30715068 | |||
| chr12:30715074 | C | T | 1 | a0001c0013 | 1 | HG00735.hp2 | synonymous_variant | LOW | c.2289G>A | p.Thr763Thr | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 16/19 | 2529/3727 | 2289/3138 | 763/1045 | chr12 | 30715074 | |||
| chr12:30719127 | A | G | 1 | a0006c0010 | 2 | HG02965.hp2 HG03453.hp1 |
synonymous_variant | LOW | c.2004T>C | p.Ser668Ser | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 14/19 | 2244/3727 | 2004/3138 | 668/1045 | chr12 | 30719127 | |||
| chr12:30735012 | A | T | 1 | a0010c0018 | 1 | NA19006.hp2 | synonymous_variant | LOW | c.522T>A | p.Ile174Ile | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 5/19 | 762/3727 | 522/3138 | 174/1045 | chr12 | 30735012 | |||
| chr12:30735189 | C | T | 1 | a0010c0018 | 1 | NA19006.hp2 | synonymous_variant | LOW | c.345G>A | p.Lys115Lys | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 5/19 | 585/3727 | 345/3138 | 115/1045 | chr12 | 30735189 | |||
| chr12:30741023 | T | C | 1 | a0002c0011 | 2 | NA18950.hp2 NA19091.hp1 |
synonymous_variant | LOW | c.324A>G | p.Leu108Leu | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 4/19 | 564/3727 | 324/3138 | 108/1045 | chr12 | 30741023 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:30709719 | T | A | 1 | a0002c0002t0003 | 7 | HG00738.hp2 HG00741.hp2 HG01099.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*183A>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 19/19 | 183 | chr12 | 30709719 | ||||||
| chr12:30709804 | A | G | 1 | a0002c0002t0004 | 2 | HG02257.hp1 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*98T>C | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 19/19 | 98 | chr12 | 30709804 | ||||||
| chr12:30754806 | T | G | 4 | a0002c0002t0002 a0002c0002t0004 a0004c0007t0002 others(1): Show |
39 | HG01070.hp1 HG01074.hp2 HG01081.hp1 others(36): Show |
5_prime_UTR_variant | MODIFIER | c.-95A>C | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 1/19 | 1286 | chr12 | 30754806 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:30710600 | T | C | 2 | a0006c0010t0001g0217 a0006c0010t0001g0218 |
2 | HG02965.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2570-130A>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 18/18 | chr12 | 30710600 | |||||||
| chr12:30710645 | C | T | 1 | a0002c0002t0001g0179 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2570-175G>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 18/18 | chr12 | 30710645 | |||||||
| chr12:30710668 | G | C | 16 | a0002c0002t0001g0023 a0002c0002t0001g0068 a0002c0002t0002g0044 others(13): Show |
18 | HG01070.hp1 HG01081.hp1 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.2570-198C>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 18/18 | chr12 | 30710668 | |||||||
| chr12:30710689 | C | T | 12 | a0001c0009t0001g0205 a0001c0009t0001g0207 a0001c0009t0001g0209 others(9): Show |
13 | HG01884.hp2 HG02258.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.2570-219G>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 18/18 | chr12 | 30710689 | |||||||
| chr12:30710761 | G | GTCTGAAC others(13): Show |
1 | a0001c0001t0001g0077 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2570-311_2570-292d others(22): Show |
CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 18/18 | chr12 | 30710761 | |||||||
| chr12:30710960 | C | G | 12 | a0001c0009t0001g0205 a0001c0009t0001g0207 a0001c0009t0001g0209 others(9): Show |
13 | HG01884.hp2 HG02258.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.2570-490G>C | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 18/18 | chr12 | 30710960 | |||||||
| chr12:30710975 | G | T | 150 | a0001c0004t0001g0004 a0001c0004t0001g0042 a0001c0004t0001g0043 others(147): Show |
222 | HG00280.hp2 HG00408.hp1 HG00544.hp1 others(219): Show |
intron_variant | MODIFIER | c.2570-505C>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 18/18 | chr12 | 30710975 | |||||||
| chr12:30711090 | G | A | 12 | a0001c0009t0001g0205 a0001c0009t0001g0207 a0001c0009t0001g0209 others(9): Show |
13 | HG01884.hp2 HG02258.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.2569+476C>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 18/18 | chr12 | 30711090 | |||||||
| chr12:30711164 | A | T | 12 | a0001c0009t0001g0205 a0001c0009t0001g0207 a0001c0009t0001g0209 others(9): Show |
13 | HG01884.hp2 HG02258.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.2569+402T>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 18/18 | chr12 | 30711164 | |||||||
| chr12:30711176 | C | T | 16 | a0002c0002t0001g0023 a0002c0002t0001g0068 a0002c0002t0002g0044 others(13): Show |
18 | HG01070.hp1 HG01081.hp1 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.2569+390G>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 18/18 | chr12 | 30711176 | |||||||
| chr12:30711231 | A | C | 1 | a0001c0004t0001g0225 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.2569+335T>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 18/18 | chr12 | 30711231 | |||||||
| chr12:30711232 | G | T | 1 | a0001c0004t0001g0225 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.2569+334C>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 18/18 | chr12 | 30711232 | |||||||
| chr12:30711233 | A | T | 1 | a0001c0004t0001g0225 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.2569+333T>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 18/18 | chr12 | 30711233 | |||||||
| chr12:30711234 | A | C | 1 | a0001c0004t0001g0225 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.2569+332T>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 18/18 | chr12 | 30711234 | |||||||
| chr12:30711235 | G | T | 1 | a0001c0004t0001g0225 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.2569+331C>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 18/18 | chr12 | 30711235 | |||||||
| chr12:30711240 | C | T | 1 | a0001c0004t0001g0225 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.2569+326G>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 18/18 | chr12 | 30711240 | |||||||
| chr12:30711241 | A | G | 1 | a0001c0004t0001g0225 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.2569+325T>C | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 18/18 | chr12 | 30711241 | |||||||
| chr12:30711295 | C | T | 1 | a0001c0001t0001g0212 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2569+271G>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 18/18 | chr12 | 30711295 | |||||||
| chr12:30711353 | C | G | 1 | a0002c0002t0001g0176 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2569+213G>C | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 18/18 | chr12 | 30711353 | |||||||
| chr12:30711413 | C | T | 34 | a0002c0002t0001g0005 a0002c0002t0001g0007 a0002c0002t0001g0017 others(31): Show |
53 | HG00544.hp1 HG00621.hp1 HG00738.hp2 others(50): Show |
intron_variant | MODIFIER | c.2569+153G>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 18/18 | chr12 | 30711413 | |||||||
| chr12:30711523 | G | A | 12 | a0001c0009t0001g0205 a0001c0009t0001g0207 a0001c0009t0001g0209 others(9): Show |
13 | HG01884.hp2 HG02258.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.2569+43C>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 18/18 | chr12 | 30711523 | |||||||
| chr12:30711662 | C | T | 12 | a0001c0009t0001g0205 a0001c0009t0001g0207 a0001c0009t0001g0209 others(9): Show |
13 | HG01884.hp2 HG02258.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.2506-33G>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 17/18 | chr12 | 30711662 | |||||||
| chr12:30711742 | G | A | 2 | a0004c0007t0002g0238 a0004c0007t0002g0239 |
2 | HG01070.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.2506-113C>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 17/18 | chr12 | 30711742 | |||||||
| chr12:30711791 | A | G | 8 | a0001c0009t0001g0205 a0001c0009t0001g0207 a0001c0009t0001g0209 others(5): Show |
9 | HG01884.hp2 HG02258.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.2506-162T>C | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 17/18 | chr12 | 30711791 | |||||||
| chr12:30711808 | A | T | 2 | a0002c0002t0002g0245 a0002c0002t0002g0246 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2506-179T>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 17/18 | chr12 | 30711808 | |||||||
| chr12:30711810 | T | A | 1 | a0003c0003t0001g0124 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.2506-181A>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 17/18 | chr12 | 30711810 | |||||||
| chr12:30711935 | A | C | 2 | a0002c0002t0001g0016 a0002c0002t0001g0049 |
4 | HG02145.hp2 HG02965.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.2506-306T>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 17/18 | chr12 | 30711935 | |||||||
| chr12:30711990 | A | G | 149 | a0001c0004t0001g0004 a0001c0004t0001g0042 a0001c0004t0001g0043 others(146): Show |
221 | HG00280.hp2 HG00408.hp1 HG00544.hp1 others(218): Show |
intron_variant | MODIFIER | c.2506-361T>C | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 17/18 | chr12 | 30711990 | |||||||
| chr12:30712231 | AGTG | A | 8 | a0001c0009t0001g0205 a0001c0009t0001g0207 a0001c0009t0001g0209 others(5): Show |
9 | HG01884.hp2 HG02258.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.2506-605_2506-603d others(5): Show |
CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 17/18 | chr12 | 30712231 | |||||||
| chr12:30712277 | G | A | 4 | a0001c0001t0001g0027 a0001c0001t0001g0071 a0001c0001t0001g0216 others(1): Show |
5 | HG02129.hp1 NA18980.hp2 NA18999.hp1 others(2): Show |
intron_variant | MODIFIER | c.2506-648C>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 17/18 | chr12 | 30712277 | |||||||
| chr12:30712408 | T | C | 1 | a0002c0002t0001g0191 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2506-779A>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 17/18 | chr12 | 30712408 | |||||||
| chr12:30712576 | A | C | 66 | a0002c0002t0001g0016 a0002c0002t0001g0021 a0002c0002t0001g0049 others(63): Show |
100 | HG00280.hp2 HG00558.hp2 HG00639.hp2 others(97): Show |
intron_variant | MODIFIER | c.2506-947T>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 17/18 | chr12 | 30712576 | |||||||
| chr12:30712673 | A | G | 1 | a0002c0002t0002g0253 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.2506-1044T>C | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 17/18 | chr12 | 30712673 | |||||||
| chr12:30712733 | C | CT | 123 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0015 others(120): Show |
193 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(190): Show |
intron_variant | MODIFIER | c.2505+1051dupA | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 17/18 | chr12 | 30712733 | |||||||
| chr12:30712733 | C | CTT | 18 | a0001c0001t0001g0008 a0001c0001t0001g0014 a0001c0001t0001g0031 others(15): Show |
24 | HG00438.hp1 HG00741.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.2505+1050_2505+105 others(6): Show |
CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 17/18 | chr12 | 30712733 | |||||||
| chr12:30712733 | C | T | 1 | a0002c0002t0001g0196 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2505+1052G>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 17/18 | chr12 | 30712733 | |||||||
| chr12:30712733 | CTTTTTTT others(2): Show |
C | 83 | a0002c0002t0001g0016 a0002c0002t0001g0021 a0002c0002t0001g0023 others(80): Show |
119 | HG00280.hp2 HG00558.hp2 HG00639.hp2 others(116): Show |
intron_variant | MODIFIER | c.2505+1043_2505+105 others(13): Show |
CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 17/18 | chr12 | 30712733 | |||||||
| chr12:30712733 | CTTTTTTT others(3): Show |
C | 9 | a0002c0002t0001g0041 a0002c0002t0001g0220 a0002c0002t0001g0221 others(6): Show |
10 | HG01167.hp2 HG01168.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.2505+1042_2505+105 others(14): Show |
CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 17/18 | chr12 | 30712733 | |||||||
| chr12:30712733 | CTTTTTTT others(8): Show |
C | 8 | a0002c0002t0001g0038 a0002c0002t0001g0051 a0002c0002t0001g0131 others(5): Show |
9 | HG00738.hp1 HG01884.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.2505+1037_2505+105 others(19): Show |
CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 17/18 | chr12 | 30712733 | |||||||
| chr12:30712912 | G | T | 1 | a0001c0001t0001g0084 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.2505+873C>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 17/18 | chr12 | 30712912 | |||||||
| chr12:30713033 | C | T | 1 | a0001c0004t0001g0043 | 2 | HG00408.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.2505+752G>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 17/18 | chr12 | 30713033 | |||||||
| chr12:30713155 | A | G | 1 | a0001c0001t0001g0076 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2505+630T>C | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 17/18 | chr12 | 30713155 | |||||||
| chr12:30713303 | G | A | 17 | a0002c0002t0001g0005 a0002c0002t0001g0039 a0002c0002t0001g0183 others(14): Show |
25 | HG01167.hp1 HG01169.hp1 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.2505+482C>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 17/18 | chr12 | 30713303 | |||||||
| chr12:30713320 | T | C | 256 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(253): Show |
373 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(370): Show |
intron_variant | MODIFIER | c.2505+465A>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 17/18 | chr12 | 30713320 | |||||||
| chr12:30713339 | TA | T | 101 | a0002c0002t0001g0016 a0002c0002t0001g0021 a0002c0002t0001g0023 others(98): Show |
139 | HG00280.hp2 HG00558.hp2 HG00639.hp2 others(136): Show |
intron_variant | MODIFIER | c.2505+445delT | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 17/18 | chr12 | 30713339 | |||||||
| chr12:30713342 | C | T | 1 | a0002c0006t0001g0194 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2505+443G>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 17/18 | chr12 | 30713342 | |||||||
| chr12:30713602 | T | C | 59 | a0003c0003t0001g0002 a0003c0003t0001g0003 a0003c0003t0001g0009 others(56): Show |
90 | HG00280.hp2 HG00558.hp2 HG00639.hp2 others(87): Show |
intron_variant | MODIFIER | c.2505+183A>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 17/18 | chr12 | 30713602 | |||||||
| chr12:30713918 | G | C | 2 | a0006c0010t0001g0217 a0006c0010t0001g0218 |
2 | HG02965.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2405-33C>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 16/18 | chr12 | 30713918 | |||||||
| chr12:30713954 | T | C | 46 | a0002c0002t0001g0005 a0002c0002t0001g0007 a0002c0002t0001g0017 others(43): Show |
74 | HG00544.hp1 HG00621.hp1 HG00738.hp2 others(71): Show |
intron_variant | MODIFIER | c.2405-69A>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 16/18 | chr12 | 30713954 | |||||||
| chr12:30713961 | C | T | 1 | a0002c0002t0001g0021 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2405-76G>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 16/18 | chr12 | 30713961 | |||||||
| chr12:30713970 | T | C | 10 | a0002c0002t0001g0038 a0002c0002t0001g0051 a0002c0002t0001g0131 others(7): Show |
11 | HG00738.hp1 HG01884.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.2405-85A>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 16/18 | chr12 | 30713970 | |||||||
| chr12:30714068 | T | C | 83 | a0002c0002t0001g0016 a0002c0002t0001g0021 a0002c0002t0001g0023 others(80): Show |
119 | HG00280.hp2 HG00558.hp2 HG00639.hp2 others(116): Show |
intron_variant | MODIFIER | c.2405-183A>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 16/18 | chr12 | 30714068 | |||||||
| chr12:30714200 | T | C | 83 | a0002c0002t0001g0016 a0002c0002t0001g0021 a0002c0002t0001g0023 others(80): Show |
119 | HG00280.hp2 HG00558.hp2 HG00639.hp2 others(116): Show |
intron_variant | MODIFIER | c.2405-315A>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 16/18 | chr12 | 30714200 | |||||||
| chr12:30714305 | C | T | 1 | a0001c0001t0001g0111 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.2405-420G>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 16/18 | chr12 | 30714305 | |||||||
| chr12:30714358 | A | G | 6 | a0002c0002t0001g0041 a0002c0002t0001g0220 a0002c0002t0001g0221 others(3): Show |
7 | HG01167.hp2 HG02109.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.2405-473T>C | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 16/18 | chr12 | 30714358 | |||||||
| chr12:30714385 | T | C | 1 | a0002c0002t0001g0135 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2405-500A>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 16/18 | chr12 | 30714385 | |||||||
| chr12:30714469 | C | T | 83 | a0002c0002t0001g0016 a0002c0002t0001g0021 a0002c0002t0001g0023 others(80): Show |
119 | HG00280.hp2 HG00558.hp2 HG00639.hp2 others(116): Show |
intron_variant | MODIFIER | c.2404+490G>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 16/18 | chr12 | 30714469 | |||||||
| chr12:30714472 | C | A | 2 | a0006c0010t0001g0217 a0006c0010t0001g0218 |
2 | HG02965.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2404+487G>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 16/18 | chr12 | 30714472 | |||||||
| chr12:30714581 | ATTC | A | 35 | a0002c0002t0001g0005 a0002c0002t0001g0007 a0002c0002t0001g0017 others(32): Show |
54 | HG00544.hp1 HG00621.hp1 HG00738.hp2 others(51): Show |
intron_variant | MODIFIER | c.2404+375_2404+377d others(5): Show |
CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 16/18 | chr12 | 30714581 | |||||||
| chr12:30714645 | T | TA | 5 | a0002c0002t0001g0041 a0002c0002t0001g0220 a0002c0002t0001g0221 others(2): Show |
6 | HG02109.hp2 HG02451.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.2404+313dupT | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 16/18 | chr12 | 30714645 | |||||||
| chr12:30714675 | C | T | 2 | a0002c0002t0004g0259 a0002c0002t0004g0260 |
2 | HG02257.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.2404+284G>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 16/18 | chr12 | 30714675 | |||||||
| chr12:30714832 | C | T | 1 | a0001c0013t0001g0060 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2404+127G>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 16/18 | chr12 | 30714832 | |||||||
| chr12:30714860 | C | T | 85 | a0002c0002t0001g0016 a0002c0002t0001g0021 a0002c0002t0001g0023 others(82): Show |
121 | HG00280.hp2 HG00558.hp2 HG00639.hp2 others(118): Show |
intron_variant | MODIFIER | c.2404+99G>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 16/18 | chr12 | 30714860 | |||||||
| chr12:30715294 | A | T | 11 | a0002c0002t0002g0012 a0002c0002t0002g0013 a0002c0002t0002g0045 others(8): Show |
20 | HG01074.hp2 HG01361.hp1 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.2222-153T>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 15/18 | chr12 | 30715294 | |||||||
| chr12:30715297 | C | T | 2 | a0001c0001t0001g0110 a0007c0015t0001g0099 |
2 | HG01928.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.2222-156G>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 15/18 | chr12 | 30715297 | |||||||
| chr12:30715391 | C | T | 1 | a0001c0001t0001g0117 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.2222-250G>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 15/18 | chr12 | 30715391 | |||||||
| chr12:30715729 | G | C | 1 | a0003c0003t0001g0037 | 2 | NA18945.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.2222-588C>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 15/18 | chr12 | 30715729 | |||||||
| chr12:30715764 | G | A | 1 | a0001c0009t0001g0205 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2222-623C>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 15/18 | chr12 | 30715764 | |||||||
| chr12:30715786 | T | C | 2 | a0006c0010t0001g0217 a0006c0010t0001g0218 |
2 | HG02965.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2222-645A>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 15/18 | chr12 | 30715786 | |||||||
| chr12:30715872 | T | C | 2 | a0002c0002t0004g0259 a0002c0002t0004g0260 |
2 | HG02257.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.2221+636A>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 15/18 | chr12 | 30715872 | |||||||
| chr12:30715923 | C | T | 1 | a0001c0001t0001g0079 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2221+585G>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 15/18 | chr12 | 30715923 | |||||||
| chr12:30716016 | A | G | 1 | a0002c0002t0001g0193 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2221+492T>C | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 15/18 | chr12 | 30716016 | |||||||
| chr12:30716073 | T | A | 1 | a0003c0003t0001g0128 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2221+435A>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 15/18 | chr12 | 30716073 | |||||||
| chr12:30716152 | A | G | 5 | a0002c0002t0001g0041 a0002c0002t0001g0220 a0002c0002t0001g0221 others(2): Show |
6 | HG02109.hp2 HG02451.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.2221+356T>C | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 15/18 | chr12 | 30716152 | |||||||
| chr12:30716373 | G | A | 2 | a0002c0002t0004g0259 a0002c0002t0004g0260 |
2 | HG02257.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.2221+135C>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 15/18 | chr12 | 30716373 | |||||||
| chr12:30716390 | A | G | 1 | a0002c0002t0001g0221 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2221+118T>C | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 15/18 | chr12 | 30716390 | |||||||
| chr12:30716822 | A | T | 1 | a0001c0001t0001g0082 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2053-146T>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 14/18 | chr12 | 30716822 | |||||||
| chr12:30716931 | A | T | 1 | a0004c0007t0001g0213 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.2053-255T>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 14/18 | chr12 | 30716931 | |||||||
| chr12:30717108 | G | A | 1 | a0003c0003t0001g0157 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2053-432C>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 14/18 | chr12 | 30717108 | |||||||
| chr12:30717269 | A | G | 16 | a0001c0001t0001g0064 a0001c0004t0001g0004 a0001c0004t0001g0042 others(13): Show |
24 | HG00408.hp1 HG00544.hp2 HG02071.hp1 others(21): Show |
intron_variant | MODIFIER | c.2053-593T>C | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 14/18 | chr12 | 30717269 | |||||||
| chr12:30717487 | C | A | 18 | a0002c0002t0001g0023 a0002c0002t0001g0068 a0002c0002t0002g0044 others(15): Show |
20 | HG01070.hp1 HG01081.hp1 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.2053-811G>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 14/18 | chr12 | 30717487 | |||||||
| chr12:30717595 | TA | T | 9 | a0001c0009t0001g0205 a0001c0009t0001g0207 a0001c0009t0001g0209 others(6): Show |
10 | HG01884.hp2 HG02258.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.2053-920delT | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 14/18 | chr12 | 30717595 | |||||||
| chr12:30717729 | T | C | 1 | a0002c0002t0001g0181 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2053-1053A>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 14/18 | chr12 | 30717729 | |||||||
| chr12:30717780 | C | T | 18 | a0002c0002t0001g0023 a0002c0002t0001g0068 a0002c0002t0002g0044 others(15): Show |
20 | HG01070.hp1 HG01081.hp1 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.2053-1104G>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 14/18 | chr12 | 30717780 | |||||||
| chr12:30717935 | C | T | 18 | a0002c0002t0001g0023 a0002c0002t0001g0068 a0002c0002t0002g0044 others(15): Show |
20 | HG01070.hp1 HG01081.hp1 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.2052+1144G>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 14/18 | chr12 | 30717935 | |||||||
| chr12:30718048 | A | C | 2 | a0002c0002t0004g0259 a0002c0002t0004g0260 |
2 | HG02257.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.2052+1031T>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 14/18 | chr12 | 30718048 | |||||||
| chr12:30718061 | T | C | 1 | a0002c0002t0002g0047 | 2 | HG01891.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2052+1018A>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 14/18 | chr12 | 30718061 | |||||||
| chr12:30718199 | T | A | 2 | a0002c0002t0004g0259 a0002c0002t0004g0260 |
2 | HG02257.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.2052+880A>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 14/18 | chr12 | 30718199 | |||||||
| chr12:30718244 | A | G | 4 | a0003c0003t0001g0010 a0003c0003t0001g0142 a0003c0003t0001g0171 others(1): Show |
7 | HG02015.hp1 NA18950.hp1 NA18988.hp2 others(4): Show |
intron_variant | MODIFIER | c.2052+835T>C | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 14/18 | chr12 | 30718244 | |||||||
| chr12:30718248 | T | A | 2 | a0002c0002t0004g0259 a0002c0002t0004g0260 |
2 | HG02257.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.2052+831A>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 14/18 | chr12 | 30718248 | |||||||
| chr12:30718314 | C | A | 171 | a0001c0001t0001g0064 a0001c0004t0001g0004 a0001c0004t0001g0042 others(168): Show |
246 | HG00280.hp2 HG00408.hp1 HG00544.hp1 others(243): Show |
intron_variant | MODIFIER | c.2052+765G>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 14/18 | chr12 | 30718314 | |||||||
| chr12:30718349 | C | T | 1 | a0001c0009t0001g0209 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2052+730G>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 14/18 | chr12 | 30718349 | |||||||
| chr12:30718541 | G | T | 2 | a0002c0002t0001g0016 a0002c0002t0001g0049 |
4 | HG02145.hp2 HG02965.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.2052+538C>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 14/18 | chr12 | 30718541 | |||||||
| chr12:30718569 | T | C | 171 | a0001c0001t0001g0064 a0001c0004t0001g0004 a0001c0004t0001g0042 others(168): Show |
246 | HG00280.hp2 HG00408.hp1 HG00544.hp1 others(243): Show |
intron_variant | MODIFIER | c.2052+510A>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 14/18 | chr12 | 30718569 | |||||||
| chr12:30718578 | G | A | 1 | a0001c0001t0001g0057 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2052+501C>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 14/18 | chr12 | 30718578 | |||||||
| chr12:30718590 | G | A | 3 | a0001c0001t0001g0015 a0002c0002t0004g0259 a0002c0002t0004g0260 |
5 | HG02257.hp1 HG03195.hp2 NA18977.hp1 others(2): Show |
intron_variant | MODIFIER | c.2052+489C>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 14/18 | chr12 | 30718590 | |||||||
| chr12:30718654 | TA | T | 6 | a0002c0002t0001g0041 a0002c0002t0001g0220 a0002c0002t0001g0221 others(3): Show |
7 | HG01167.hp2 HG02109.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.2052+424delT | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 14/18 | chr12 | 30718654 | |||||||
| chr12:30718878 | C | T | 2 | a0002c0002t0004g0259 a0002c0002t0004g0260 |
2 | HG02257.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.2052+201G>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 14/18 | chr12 | 30718878 | |||||||
| chr12:30718932 | C | T | 147 | a0002c0002t0001g0005 a0002c0002t0001g0007 a0002c0002t0001g0016 others(144): Show |
213 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(210): Show |
intron_variant | MODIFIER | c.2052+147G>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 14/18 | chr12 | 30718932 | |||||||
| chr12:30719072 | T | C | 1 | a0001c0001t0001g0085 | 1 | HG00673.hp1 | splice_region_variant&intron_variant | LOW | c.2052+7A>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 14/18 | chr12 | 30719072 | |||||||
| chr12:30719244 | G | A | 16 | a0002c0002t0001g0023 a0002c0002t0001g0068 a0002c0002t0002g0044 others(13): Show |
18 | HG01070.hp1 HG01081.hp1 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.1906-19C>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 13/18 | chr12 | 30719244 | |||||||
| chr12:30719356 | T | C | 16 | a0002c0002t0001g0023 a0002c0002t0001g0068 a0002c0002t0002g0044 others(13): Show |
18 | HG01070.hp1 HG01081.hp1 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.1906-131A>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 13/18 | chr12 | 30719356 | |||||||
| chr12:30719409 | T | C | 1 | a0003c0003t0001g0156 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1906-184A>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 13/18 | chr12 | 30719409 | |||||||
| chr12:30719427 | G | A | 1 | a0003c0003t0001g0174 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1906-202C>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 13/18 | chr12 | 30719427 | |||||||
| chr12:30719436 | A | G | 2 | a0006c0010t0001g0217 a0006c0010t0001g0218 |
2 | HG02965.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1906-211T>C | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 13/18 | chr12 | 30719436 | |||||||
| chr12:30719441 | G | A | 1 | a0002c0002t0004g0260 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1906-216C>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 13/18 | chr12 | 30719441 | |||||||
| chr12:30719468 | G | A | 1 | a0002c0002t0002g0241 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1906-243C>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 13/18 | chr12 | 30719468 | |||||||
| chr12:30719596 | G | A | 18 | a0002c0002t0001g0023 a0002c0002t0001g0068 a0002c0002t0002g0044 others(15): Show |
20 | HG01070.hp1 HG01081.hp1 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.1906-371C>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 13/18 | chr12 | 30719596 | |||||||
| chr12:30719842 | T | G | 1 | a0005c0008t0002g0252 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1906-617A>C | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 13/18 | chr12 | 30719842 | |||||||
| chr12:30719878 | C | T | 2 | a0003c0003t0001g0050 a0003c0003t0001g0153 |
2 | HG01069.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.1906-653G>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 13/18 | chr12 | 30719878 | |||||||
| chr12:30720036 | A | T | 1 | a0001c0004t0001g0226 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1905+775T>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 13/18 | chr12 | 30720036 | |||||||
| chr12:30720038 | T | C | 1 | a0001c0004t0001g0233 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1905+773A>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 13/18 | chr12 | 30720038 | |||||||
| chr12:30720039 | G | A | 1 | a0001c0001t0001g0075 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1905+772C>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 13/18 | chr12 | 30720039 | |||||||
| chr12:30720087 | T | C | 256 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(253): Show |
373 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(370): Show |
intron_variant | MODIFIER | c.1905+724A>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 13/18 | chr12 | 30720087 | |||||||
| chr12:30720088 | TTTTA | T | 16 | a0002c0002t0001g0023 a0002c0002t0001g0068 a0002c0002t0002g0044 others(13): Show |
18 | HG01070.hp1 HG01081.hp1 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.1905+719_1905+722d others(6): Show |
CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 13/18 | chr12 | 30720088 | |||||||
| chr12:30720100 | A | T | 1 | a0001c0001t0001g0214 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1905+711T>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 13/18 | chr12 | 30720100 | |||||||
| chr12:30720115 | A | G | 155 | a0001c0009t0001g0205 a0001c0009t0001g0207 a0001c0009t0001g0209 others(152): Show |
222 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(219): Show |
intron_variant | MODIFIER | c.1905+696T>C | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 13/18 | chr12 | 30720115 | |||||||
| chr12:30720123 | C | CT | 5 | a0002c0002t0001g0041 a0002c0002t0001g0220 a0002c0002t0001g0221 others(2): Show |
6 | HG02109.hp2 HG02451.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1905+687dupA | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 13/18 | chr12 | 30720123 | |||||||
| chr12:30720124 | T | C | 1 | a0003c0003t0001g0160 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1905+687A>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 13/18 | chr12 | 30720124 | |||||||
| chr12:30720169 | C | T | 7 | a0003c0003t0001g0009 a0003c0003t0001g0162 a0003c0003t0001g0164 others(4): Show |
10 | HG00558.hp2 HG00673.hp2 HG02080.hp1 others(7): Show |
intron_variant | MODIFIER | c.1905+642G>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 13/18 | chr12 | 30720169 | |||||||
| chr12:30720182 | C | T | 18 | a0002c0002t0001g0023 a0002c0002t0001g0068 a0002c0002t0002g0044 others(15): Show |
20 | HG01070.hp1 HG01081.hp1 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.1905+629G>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 13/18 | chr12 | 30720182 | |||||||
| chr12:30720248 | T | A | 1 | a0001c0001t0001g0029 | 2 | HG02145.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1905+563A>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 13/18 | chr12 | 30720248 | |||||||
| chr12:30720377 | T | C | 18 | a0002c0002t0001g0023 a0002c0002t0001g0068 a0002c0002t0002g0044 others(15): Show |
20 | HG01070.hp1 HG01081.hp1 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.1905+434A>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 13/18 | chr12 | 30720377 | |||||||
| chr12:30720380 | G | A | 1 | a0001c0001t0001g0085 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1905+431C>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 13/18 | chr12 | 30720380 | |||||||
| chr12:30720391 | T | C | 1 | a0003c0003t0001g0151 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1905+420A>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 13/18 | chr12 | 30720391 | |||||||
| chr12:30720398 | C | T | 66 | a0002c0002t0001g0016 a0002c0002t0001g0021 a0002c0002t0001g0049 others(63): Show |
100 | HG00280.hp2 HG00558.hp2 HG00639.hp2 others(97): Show |
intron_variant | MODIFIER | c.1905+413G>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 13/18 | chr12 | 30720398 | |||||||
| chr12:30720729 | TAATCATG others(60): Show |
T | 2 | a0001c0001t0001g0118 a0001c0001t0001g0120 |
2 | NA19074.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.1905+15_1905+81del others(67): Show |
CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 13/18 | chr12 | 30720729 | |||||||
| chr12:30720732 | T | G | 1 | a0001c0001t0001g0015 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1905+79A>C | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 13/18 | chr12 | 30720732 | |||||||
| chr12:30721037 | T | C | 1 | a0001c0001t0001g0034 | 2 | NA18951.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.1801-122A>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 12/18 | chr12 | 30721037 | |||||||
| chr12:30721051 | G | A | 4 | a0002c0002t0002g0012 a0002c0002t0002g0045 a0002c0002t0002g0046 others(1): Show |
9 | HG02559.hp1 HG02615.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.1801-136C>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 12/18 | chr12 | 30721051 | |||||||
| chr12:30721286 | T | C | 2 | a0002c0002t0004g0259 a0002c0002t0004g0260 |
2 | HG02257.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1801-371A>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 12/18 | chr12 | 30721286 | |||||||
| chr12:30721288 | G | A | 2 | a0001c0004t0001g0227 a0001c0004t0001g0236 |
2 | NA18979.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.1801-373C>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 12/18 | chr12 | 30721288 | |||||||
| chr12:30721354 | GTA | G | 84 | a0002c0002t0001g0016 a0002c0002t0001g0021 a0002c0002t0001g0023 others(81): Show |
120 | HG00280.hp2 HG00558.hp2 HG00639.hp2 others(117): Show |
intron_variant | MODIFIER | c.1801-441_1801-440d others(4): Show |
CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 12/18 | chr12 | 30721354 | |||||||
| chr12:30721402 | G | A | 6 | a0002c0002t0001g0041 a0002c0002t0001g0220 a0002c0002t0001g0221 others(3): Show |
7 | HG01167.hp2 HG02109.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1801-487C>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 12/18 | chr12 | 30721402 | |||||||
| chr12:30721484 | A | G | 8 | a0002c0002t0001g0038 a0002c0002t0001g0051 a0002c0002t0001g0131 others(5): Show |
9 | HG00738.hp1 HG01884.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.1801-569T>C | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 12/18 | chr12 | 30721484 | |||||||
| chr12:30721582 | T | C | 5 | a0002c0005t0001g0040 a0002c0005t0001g0206 a0002c0005t0001g0208 others(2): Show |
6 | HG02258.hp2 HG02486.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1801-667A>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 12/18 | chr12 | 30721582 | |||||||
| chr12:30721583 | C | T | 1 | a0002c0006t0001g0192 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1801-668G>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 12/18 | chr12 | 30721583 | |||||||
| chr12:30721607 | C | T | 6 | a0002c0002t0001g0041 a0002c0002t0001g0220 a0002c0002t0001g0221 others(3): Show |
7 | HG01167.hp2 HG02109.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1801-692G>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 12/18 | chr12 | 30721607 | |||||||
| chr12:30721945 | C | T | 170 | a0001c0004t0001g0004 a0001c0004t0001g0042 a0001c0004t0001g0043 others(167): Show |
245 | HG00280.hp2 HG00408.hp1 HG00544.hp1 others(242): Show |
intron_variant | MODIFIER | c.1801-1030G>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 12/18 | chr12 | 30721945 | |||||||
| chr12:30721963 | G | T | 18 | a0001c0004t0001g0004 a0001c0004t0001g0042 a0001c0004t0001g0043 others(15): Show |
28 | HG00408.hp1 HG00544.hp2 HG00621.hp1 others(25): Show |
intron_variant | MODIFIER | c.1801-1048C>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 12/18 | chr12 | 30721963 | |||||||
| chr12:30722021 | C | T | 1 | a0004c0007t0002g0250 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1801-1106G>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 12/18 | chr12 | 30722021 | |||||||
| chr12:30722064 | A | G | 1 | a0006c0010t0001g0218 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1801-1149T>C | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 12/18 | chr12 | 30722064 | |||||||
| chr12:30722219 | T | C | 7 | a0002c0002t0001g0038 a0002c0002t0001g0051 a0002c0002t0001g0131 others(4): Show |
8 | HG00738.hp1 HG01884.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1800+1040A>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 12/18 | chr12 | 30722219 | |||||||
| chr12:30722393 | A | G | 3 | a0002c0002t0001g0038 a0002c0002t0001g0051 a0002c0002t0001g0180 |
4 | HG00738.hp1 HG01884.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1800+866T>C | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 12/18 | chr12 | 30722393 | |||||||
| chr12:30722411 | T | C | 2 | a0001c0004t0001g0043 a0001c0004t0001g0235 |
3 | HG00408.hp1 NA18999.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.1800+848A>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 12/18 | chr12 | 30722411 | |||||||
| chr12:30722439 | AACT | A | 11 | a0002c0002t0002g0012 a0002c0002t0002g0013 a0002c0002t0002g0045 others(8): Show |
20 | HG01074.hp2 HG01361.hp1 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.1800+817_1800+819d others(5): Show |
CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 12/18 | chr12 | 30722439 | |||||||
| chr12:30722540 | G | GTAAA | 86 | a0002c0002t0001g0016 a0002c0002t0001g0021 a0002c0002t0001g0023 others(83): Show |
122 | HG00280.hp2 HG00558.hp2 HG00639.hp2 others(119): Show |
intron_variant | MODIFIER | c.1800+715_1800+718d others(6): Show |
CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 12/18 | chr12 | 30722540 | |||||||
| chr12:30722619 | G | A | 2 | a0002c0002t0004g0259 a0002c0002t0004g0260 |
2 | HG02257.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1800+640C>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 12/18 | chr12 | 30722619 | |||||||
| chr12:30722670 | G | A | 1 | a0001c0001t0001g0029 | 2 | HG02145.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1800+589C>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 12/18 | chr12 | 30722670 | |||||||
| chr12:30722797 | G | A | 2 | a0002c0002t0002g0245 a0002c0002t0002g0246 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1800+462C>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 12/18 | chr12 | 30722797 | |||||||
| chr12:30722839 | C | T | 8 | a0002c0002t0001g0017 a0002c0002t0001g0191 a0002c0002t0001g0199 others(5): Show |
13 | HG00738.hp2 HG00741.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.1800+420G>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 12/18 | chr12 | 30722839 | |||||||
| chr12:30723035 | G | C | 150 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0117 others(147): Show |
218 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(215): Show |
intron_variant | MODIFIER | c.1800+224C>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 12/18 | chr12 | 30723035 | |||||||
| chr12:30723090 | G | A | 5 | a0002c0002t0001g0041 a0002c0002t0001g0220 a0002c0002t0001g0221 others(2): Show |
6 | HG02109.hp2 HG02451.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1800+169C>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 12/18 | chr12 | 30723090 | |||||||
| chr12:30723093 | G | A | 1 | a0002c0002t0001g0133 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1800+166C>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 12/18 | chr12 | 30723093 | |||||||
| chr12:30723254 | G | A | 6 | a0002c0002t0001g0041 a0002c0002t0001g0220 a0002c0002t0001g0221 others(3): Show |
7 | HG01167.hp2 HG02109.hp2 HG02451.hp2 others(4): Show |
splice_region_variant&intron_variant | LOW | c.1800+5C>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 12/18 | chr12 | 30723254 | |||||||
| chr12:30723363 | ACG | A | 15 | a0001c0004t0001g0004 a0001c0004t0001g0042 a0001c0004t0001g0043 others(12): Show |
23 | HG00408.hp1 HG00544.hp2 HG02071.hp1 others(20): Show |
intron_variant | MODIFIER | c.1745-51_1745-50del others(2): Show |
CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 11/18 | chr12 | 30723363 | |||||||
| chr12:30723429 | C | A | 1 | a0001c0001t0001g0081 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1745-115G>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 11/18 | chr12 | 30723429 | |||||||
| chr12:30723429 | C | T | 1 | a0001c0001t0001g0061 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1745-115G>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 11/18 | chr12 | 30723429 | |||||||
| chr12:30723458 | A | C | 1 | a0001c0001t0001g0088 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1745-144T>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 11/18 | chr12 | 30723458 | |||||||
| chr12:30723495 | A | T | 1 | a0006c0010t0001g0217 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1745-181T>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 11/18 | chr12 | 30723495 | |||||||
| chr12:30723631 | C | T | 34 | a0002c0002t0001g0005 a0002c0002t0001g0007 a0002c0002t0001g0017 others(31): Show |
53 | HG00544.hp1 HG00621.hp1 HG00738.hp2 others(50): Show |
intron_variant | MODIFIER | c.1745-317G>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 11/18 | chr12 | 30723631 | |||||||
| chr12:30723847 | G | A | 1 | a0001c0001t0001g0086 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1744+523C>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 11/18 | chr12 | 30723847 | |||||||
| chr12:30724101 | C | A | 84 | a0002c0002t0001g0016 a0002c0002t0001g0021 a0002c0002t0001g0023 others(81): Show |
120 | HG00280.hp2 HG00558.hp2 HG00639.hp2 others(117): Show |
intron_variant | MODIFIER | c.1744+269G>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 11/18 | chr12 | 30724101 | |||||||
| chr12:30724457 | G | T | 84 | a0002c0002t0001g0016 a0002c0002t0001g0021 a0002c0002t0001g0023 others(81): Show |
120 | HG00280.hp2 HG00558.hp2 HG00639.hp2 others(117): Show |
splice_region_variant&intron_variant | LOW | c.1663-6C>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 10/18 | chr12 | 30724457 | |||||||
| chr12:30724597 | T | C | 1 | a0003c0003t0001g0157 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1663-146A>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 10/18 | chr12 | 30724597 | |||||||
| chr12:30724782 | G | A | 1 | a0002c0002t0001g0197 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1663-331C>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 10/18 | chr12 | 30724782 | |||||||
| chr12:30724809 | G | C | 5 | a0002c0002t0001g0041 a0002c0002t0001g0220 a0002c0002t0001g0221 others(2): Show |
6 | HG02109.hp2 HG02451.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1663-358C>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 10/18 | chr12 | 30724809 | |||||||
| chr12:30725173 | G | A | 2 | a0002c0002t0002g0245 a0002c0002t0002g0246 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1663-722C>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 10/18 | chr12 | 30725173 | |||||||
| chr12:30725202 | G | A | 1 | a0002c0002t0001g0198 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1663-751C>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 10/18 | chr12 | 30725202 | |||||||
| chr12:30725247 | A | G | 34 | a0002c0002t0001g0005 a0002c0002t0001g0007 a0002c0002t0001g0017 others(31): Show |
53 | HG00544.hp1 HG00621.hp1 HG00738.hp2 others(50): Show |
intron_variant | MODIFIER | c.1662+719T>C | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 10/18 | chr12 | 30725247 | |||||||
| chr12:30725565 | T | C | 1 | a0001c0001t0001g0070 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1662+401A>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 10/18 | chr12 | 30725565 | |||||||
| chr12:30725574 | G | A | 1 | a0001c0001t0001g0087 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1662+392C>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 10/18 | chr12 | 30725574 | |||||||
| chr12:30725575 | G | C | 1 | a0001c0001t0001g0087 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1662+391C>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 10/18 | chr12 | 30725575 | |||||||
| chr12:30725615 | G | A | 1 | a0002c0002t0001g0188 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1662+351C>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 10/18 | chr12 | 30725615 | |||||||
| chr12:30725630 | T | C | 34 | a0002c0002t0001g0005 a0002c0002t0001g0007 a0002c0002t0001g0017 others(31): Show |
53 | HG00544.hp1 HG00621.hp1 HG00738.hp2 others(50): Show |
intron_variant | MODIFIER | c.1662+336A>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 10/18 | chr12 | 30725630 | |||||||
| chr12:30725738 | AT | A | 17 | a0001c0004t0001g0004 a0001c0004t0001g0042 a0001c0004t0001g0043 others(14): Show |
25 | HG00408.hp1 HG00544.hp2 HG02071.hp1 others(22): Show |
intron_variant | MODIFIER | c.1662+227delA | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 10/18 | chr12 | 30725738 | |||||||
| chr12:30725795 | T | C | 84 | a0002c0002t0001g0016 a0002c0002t0001g0021 a0002c0002t0001g0023 others(81): Show |
120 | HG00280.hp2 HG00558.hp2 HG00639.hp2 others(117): Show |
intron_variant | MODIFIER | c.1662+171A>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 10/18 | chr12 | 30725795 | |||||||
| chr12:30725925 | G | C | 170 | a0001c0004t0001g0004 a0001c0004t0001g0042 a0001c0004t0001g0043 others(167): Show |
245 | HG00280.hp2 HG00408.hp1 HG00544.hp1 others(242): Show |
intron_variant | MODIFIER | c.1662+41C>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 10/18 | chr12 | 30725925 | |||||||
| chr12:30725940 | T | C | 2 | a0002c0002t0004g0259 a0002c0002t0004g0260 |
2 | HG02257.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1662+26A>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 10/18 | chr12 | 30725940 | |||||||
| chr12:30726098 | A | G | 4 | a0002c0002t0001g0021 a0002c0002t0001g0121 a0002c0002t0001g0134 others(1): Show |
5 | HG02818.hp1 HG02886.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1540-10T>C | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 9/18 | chr12 | 30726098 | |||||||
| chr12:30726154 | T | C | 84 | a0002c0002t0001g0016 a0002c0002t0001g0021 a0002c0002t0001g0023 others(81): Show |
120 | HG00280.hp2 HG00558.hp2 HG00639.hp2 others(117): Show |
intron_variant | MODIFIER | c.1540-66A>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 9/18 | chr12 | 30726154 | |||||||
| chr12:30726424 | AT | A | 84 | a0002c0002t0001g0016 a0002c0002t0001g0021 a0002c0002t0001g0023 others(81): Show |
120 | HG00280.hp2 HG00558.hp2 HG00639.hp2 others(117): Show |
intron_variant | MODIFIER | c.1540-337delA | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 9/18 | chr12 | 30726424 | |||||||
| chr12:30726486 | G | A | 1 | a0003c0003t0001g0169 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1540-398C>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 9/18 | chr12 | 30726486 | |||||||
| chr12:30726557 | G | T | 34 | a0002c0002t0001g0005 a0002c0002t0001g0007 a0002c0002t0001g0017 others(31): Show |
53 | HG00544.hp1 HG00621.hp1 HG00738.hp2 others(50): Show |
intron_variant | MODIFIER | c.1540-469C>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 9/18 | chr12 | 30726557 | |||||||
| chr12:30726634 | T | C | 1 | a0002c0002t0001g0199 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1540-546A>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 9/18 | chr12 | 30726634 | |||||||
| chr12:30726666 | CT | C | 5 | a0002c0002t0001g0041 a0002c0002t0001g0220 a0002c0002t0001g0221 others(2): Show |
6 | HG02109.hp2 HG02451.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1540-579delA | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 9/18 | chr12 | 30726666 | |||||||
| chr12:30726672 | A | G | 5 | a0002c0002t0001g0041 a0002c0002t0001g0220 a0002c0002t0001g0221 others(2): Show |
6 | HG02109.hp2 HG02451.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1540-584T>C | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 9/18 | chr12 | 30726672 | |||||||
| chr12:30726958 | T | A | 1 | a0002c0002t0001g0021 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1540-870A>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 9/18 | chr12 | 30726958 | |||||||
| chr12:30726971 | CAGTAACT | C | 3 | a0002c0002t0001g0121 a0002c0002t0001g0134 a0002c0002t0001g0135 |
3 | HG02818.hp1 HG02886.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1540-890_1540-884d others(9): Show |
CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 9/18 | chr12 | 30726971 | |||||||
| chr12:30727171 | G | A | 84 | a0002c0002t0001g0016 a0002c0002t0001g0021 a0002c0002t0001g0023 others(81): Show |
120 | HG00280.hp2 HG00558.hp2 HG00639.hp2 others(117): Show |
intron_variant | MODIFIER | c.1540-1083C>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 9/18 | chr12 | 30727171 | |||||||
| chr12:30727201 | T | C | 2 | a0001c0001t0001g0028 a0001c0001t0001g0088 |
3 | HG00642.hp1 HG03492.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.1540-1113A>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 9/18 | chr12 | 30727201 | |||||||
| chr12:30727229 | G | T | 1 | a0002c0002t0002g0046 | 2 | HG02922.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1540-1141C>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 9/18 | chr12 | 30727229 | |||||||
| chr12:30727298 | T | C | 2 | a0002c0002t0002g0245 a0002c0002t0002g0246 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1540-1210A>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 9/18 | chr12 | 30727298 | |||||||
| chr12:30727324 | C | A | 2 | a0002c0002t0004g0259 a0002c0002t0004g0260 |
2 | HG02257.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1540-1236G>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 9/18 | chr12 | 30727324 | |||||||
| chr12:30727584 | ATAG | A | 2 | a0002c0002t0001g0016 a0002c0002t0001g0049 |
4 | HG02145.hp2 HG02965.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1539+1061_1539+106 others(7): Show |
CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 9/18 | chr12 | 30727584 | |||||||
| chr12:30727816 | A | C | 13 | a0001c0001t0001g0026 a0001c0001t0001g0033 a0001c0001t0001g0034 others(10): Show |
17 | HG01261.hp1 HG02135.hp2 HG02293.hp2 others(14): Show |
intron_variant | MODIFIER | c.1539+832T>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 9/18 | chr12 | 30727816 | |||||||
| chr12:30727847 | T | A | 1 | a0001c0001t0001g0029 | 2 | HG02145.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1539+801A>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 9/18 | chr12 | 30727847 | |||||||
| chr12:30728038 | G | C | 1 | a0001c0001t0001g0089 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1539+610C>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 9/18 | chr12 | 30728038 | |||||||
| chr12:30728256 | G | C | 1 | a0001c0009t0001g0207 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1539+392C>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 9/18 | chr12 | 30728256 | |||||||
| chr12:30728278 | G | A | 2 | a0002c0002t0002g0245 a0002c0002t0002g0246 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1539+370C>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 9/18 | chr12 | 30728278 | |||||||
| chr12:30728362 | G | A | 84 | a0002c0002t0001g0016 a0002c0002t0001g0021 a0002c0002t0001g0023 others(81): Show |
120 | HG00280.hp2 HG00558.hp2 HG00639.hp2 others(117): Show |
intron_variant | MODIFIER | c.1539+286C>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 9/18 | chr12 | 30728362 | |||||||
| chr12:30728415 | T | C | 84 | a0002c0002t0001g0016 a0002c0002t0001g0021 a0002c0002t0001g0023 others(81): Show |
120 | HG00280.hp2 HG00558.hp2 HG00639.hp2 others(117): Show |
intron_variant | MODIFIER | c.1539+233A>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 9/18 | chr12 | 30728415 | |||||||
| chr12:30728416 | G | A | 84 | a0002c0002t0001g0016 a0002c0002t0001g0021 a0002c0002t0001g0023 others(81): Show |
120 | HG00280.hp2 HG00558.hp2 HG00639.hp2 others(117): Show |
intron_variant | MODIFIER | c.1539+232C>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 9/18 | chr12 | 30728416 | |||||||
| chr12:30728472 | T | C | 1 | a0001c0001t0001g0212 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1539+176A>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 9/18 | chr12 | 30728472 | |||||||
| chr12:30728526 | G | A | 6 | a0002c0002t0001g0041 a0002c0002t0001g0220 a0002c0002t0001g0221 others(3): Show |
7 | HG01167.hp2 HG02109.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1539+122C>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 9/18 | chr12 | 30728526 | |||||||
| chr12:30728554 | C | CA | 141 | a0001c0001t0001g0064 a0002c0002t0001g0005 a0002c0002t0001g0007 others(138): Show |
206 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(203): Show |
intron_variant | MODIFIER | c.1539+93dupT | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 9/18 | chr12 | 30728554 | |||||||
| chr12:30729440 | A | G | 2 | a0002c0002t0004g0259 a0002c0002t0004g0260 |
2 | HG02257.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.862-115T>C | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 8/18 | chr12 | 30729440 | |||||||
| chr12:30729474 | C | T | 6 | a0002c0002t0001g0041 a0002c0002t0001g0220 a0002c0002t0001g0221 others(3): Show |
7 | HG01167.hp2 HG02109.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.862-149G>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 8/18 | chr12 | 30729474 | |||||||
| chr12:30729491 | T | C | 1 | a0001c0001t0001g0090 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.862-166A>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 8/18 | chr12 | 30729491 | |||||||
| chr12:30729505 | G | A | 82 | a0002c0002t0001g0016 a0002c0002t0001g0021 a0002c0002t0001g0023 others(79): Show |
118 | HG00280.hp2 HG00558.hp2 HG00639.hp2 others(115): Show |
intron_variant | MODIFIER | c.862-180C>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 8/18 | chr12 | 30729505 | |||||||
| chr12:30729548 | A | C | 3 | a0003c0003t0001g0126 a0003c0003t0001g0152 a0003c0003t0001g0161 |
3 | HG01168.hp2 HG01169.hp2 HG01257.hp2 |
intron_variant | MODIFIER | c.862-223T>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 8/18 | chr12 | 30729548 | |||||||
| chr12:30729801 | C | A | 1 | a0002c0002t0001g0179 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.861+438G>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 8/18 | chr12 | 30729801 | |||||||
| chr12:30729883 | TTC | T | 3 | a0001c0009t0001g0205 a0001c0009t0001g0207 a0001c0009t0001g0209 |
3 | HG01884.hp2 HG03453.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.861+354_861+355del others(2): Show |
CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 8/18 | chr12 | 30729883 | |||||||
| chr12:30729905 | C | T | 1 | a0002c0002t0002g0044 | 2 | HG03942.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.861+334G>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 8/18 | chr12 | 30729905 | |||||||
| chr12:30730066 | G | T | 1 | a0001c0001t0001g0096 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.861+173C>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 8/18 | chr12 | 30730066 | |||||||
| chr12:30730149 | C | A | 5 | a0002c0002t0001g0041 a0002c0002t0001g0220 a0002c0002t0001g0221 others(2): Show |
6 | HG02109.hp2 HG02451.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.861+90G>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 8/18 | chr12 | 30730149 | |||||||
| chr12:30730380 | C | T | 6 | a0002c0002t0001g0041 a0002c0002t0001g0220 a0002c0002t0001g0221 others(3): Show |
7 | HG01167.hp2 HG02109.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.818-98G>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 7/18 | chr12 | 30730380 | |||||||
| chr12:30730407 | C | T | 3 | a0001c0001t0001g0078 a0001c0001t0001g0097 a0008c0012t0001g0052 |
3 | HG02486.hp2 HG02698.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.818-125G>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 7/18 | chr12 | 30730407 | |||||||
| chr12:30730529 | A | C | 1 | a0003c0003t0001g0139 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.818-247T>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 7/18 | chr12 | 30730529 | |||||||
| chr12:30730962 | C | G | 1 | a0003c0003t0001g0151 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.817+381G>C | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 7/18 | chr12 | 30730962 | |||||||
| chr12:30731130 | C | A | 2 | a0003c0003t0001g0164 a0003c0003t0001g0165 |
2 | NA18941.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.817+213G>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 7/18 | chr12 | 30731130 | |||||||
| chr12:30731146 | A | G | 1 | a0003c0003t0001g0122 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.817+197T>C | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 7/18 | chr12 | 30731146 | |||||||
| chr12:30731158 | C | T | 17 | a0001c0001t0001g0108 a0002c0002t0001g0023 a0002c0002t0001g0068 others(14): Show |
19 | HG01070.hp1 HG01081.hp1 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.817+185G>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 7/18 | chr12 | 30731158 | |||||||
| chr12:30731579 | A | C | 2 | a0006c0010t0001g0217 a0006c0010t0001g0218 |
2 | HG02965.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.650-69T>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 6/18 | chr12 | 30731579 | |||||||
| chr12:30731637 | T | G | 1 | a0001c0001t0001g0093 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.650-127A>C | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 6/18 | chr12 | 30731637 | |||||||
| chr12:30731696 | T | C | 2 | a0001c0004t0001g0043 a0001c0004t0001g0235 |
3 | HG00408.hp1 NA18999.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.650-186A>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 6/18 | chr12 | 30731696 | |||||||
| chr12:30731714 | T | C | 8 | a0002c0002t0001g0038 a0002c0002t0001g0051 a0002c0002t0001g0131 others(5): Show |
9 | HG00738.hp1 HG01884.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.650-204A>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 6/18 | chr12 | 30731714 | |||||||
| chr12:30731735 | G | A | 1 | a0001c0001t0001g0093 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.650-225C>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 6/18 | chr12 | 30731735 | |||||||
| chr12:30731753 | TTAATGAG others(11): Show |
T | 1 | a0002c0002t0001g0189 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.650-261_650-244del others(18): Show |
CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 6/18 | chr12 | 30731753 | |||||||
| chr12:30732000 | T | C | 1 | a0002c0005t0001g0208 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.650-490A>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 6/18 | chr12 | 30732000 | |||||||
| chr12:30732049 | T | G | 84 | a0002c0002t0001g0016 a0002c0002t0001g0021 a0002c0002t0001g0023 others(81): Show |
120 | HG00280.hp2 HG00558.hp2 HG00639.hp2 others(117): Show |
intron_variant | MODIFIER | c.650-539A>C | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 6/18 | chr12 | 30732049 | |||||||
| chr12:30732084 | CT | C | 10 | a0002c0002t0001g0038 a0002c0002t0001g0051 a0002c0002t0001g0131 others(7): Show |
11 | HG00738.hp1 HG01884.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.650-575delA | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 6/18 | chr12 | 30732084 | |||||||
| chr12:30732333 | C | T | 1 | a0002c0002t0002g0253 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.650-823G>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 6/18 | chr12 | 30732333 | |||||||
| chr12:30732339 | C | T | 1 | a0002c0002t0001g0131 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.650-829G>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 6/18 | chr12 | 30732339 | |||||||
| chr12:30732396 | TA | T | 7 | a0002c0002t0001g0039 a0002c0002t0001g0041 a0002c0002t0001g0183 others(4): Show |
9 | HG01167.hp1 HG01169.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.650-887delT | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 6/18 | chr12 | 30732396 | |||||||
| chr12:30732445 | T | A | 1 | a0001c0001t0001g0102 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.650-935A>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 6/18 | chr12 | 30732445 | |||||||
| chr12:30732532 | T | C | 86 | a0002c0002t0001g0016 a0002c0002t0001g0021 a0002c0002t0001g0023 others(83): Show |
122 | HG00280.hp2 HG00558.hp2 HG00639.hp2 others(119): Show |
intron_variant | MODIFIER | c.650-1022A>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 6/18 | chr12 | 30732532 | |||||||
| chr12:30732554 | T | C | 5 | a0002c0002t0001g0041 a0002c0002t0001g0220 a0002c0002t0001g0221 others(2): Show |
6 | HG02109.hp2 HG02451.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.650-1044A>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 6/18 | chr12 | 30732554 | |||||||
| chr12:30732769 | C | G | 2 | a0002c0005t0001g0219 a0002c0005t0001g0222 |
2 | HG03098.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.649+860G>C | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 6/18 | chr12 | 30732769 | |||||||
| chr12:30732817 | G | A | 1 | a0002c0002t0002g0253 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.649+812C>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 6/18 | chr12 | 30732817 | |||||||
| chr12:30732958 | T | G | 1 | a0002c0002t0002g0241 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.649+671A>C | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 6/18 | chr12 | 30732958 | |||||||
| chr12:30733029 | T | A | 2 | a0001c0001t0001g0026 a0001c0001t0001g0091 |
3 | HG01261.hp1 HG02293.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.649+600A>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 6/18 | chr12 | 30733029 | |||||||
| chr12:30733469 | T | C | 1 | a0003c0003t0001g0125 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.649+160A>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 6/18 | chr12 | 30733469 | |||||||
| chr12:30733501 | G | A | 37 | a0001c0001t0001g0064 a0001c0004t0001g0004 a0001c0004t0001g0042 others(34): Show |
48 | HG00408.hp1 HG00544.hp2 HG01070.hp1 others(45): Show |
intron_variant | MODIFIER | c.649+128C>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 6/18 | chr12 | 30733501 | |||||||
| chr12:30733582 | A | G | 1 | a0005c0008t0002g0249 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.649+47T>C | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 6/18 | chr12 | 30733582 | |||||||
| chr12:30733806 | G | A | 5 | a0002c0002t0001g0041 a0002c0002t0001g0220 a0002c0002t0001g0221 others(2): Show |
6 | HG02109.hp2 HG02451.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.567-95C>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 5/18 | chr12 | 30733806 | |||||||
| chr12:30733943 | A | G | 16 | a0001c0001t0001g0064 a0001c0004t0001g0004 a0001c0004t0001g0042 others(13): Show |
24 | HG00408.hp1 HG00544.hp2 HG02071.hp1 others(21): Show |
intron_variant | MODIFIER | c.567-232T>C | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 5/18 | chr12 | 30733943 | |||||||
| chr12:30734180 | A | G | 1 | a0005c0008t0002g0248 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.567-469T>C | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 5/18 | chr12 | 30734180 | |||||||
| chr12:30734216 | A | G | 2 | a0002c0002t0004g0259 a0002c0002t0004g0260 |
2 | HG02257.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.567-505T>C | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 5/18 | chr12 | 30734216 | |||||||
| chr12:30734217 | T | C | 5 | a0003c0003t0001g0144 a0003c0003t0001g0151 a0003c0003t0001g0158 others(2): Show |
5 | NA18944.hp1 NA18953.hp2 NA18959.hp1 others(2): Show |
intron_variant | MODIFIER | c.567-506A>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 5/18 | chr12 | 30734217 | |||||||
| chr12:30734453 | G | C | 2 | a0002c0002t0001g0016 a0002c0002t0001g0049 |
4 | HG02145.hp2 HG02965.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.566+515C>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 5/18 | chr12 | 30734453 | |||||||
| chr12:30734725 | T | TTTATTTT others(46): Show |
1 | a0010c0018t0001g0115 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.566+242_566+243ins others(53): Show |
CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 5/18 | chr12 | 30734725 | |||||||
| chr12:30734729 | G | A | 1 | a0010c0018t0001g0115 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.566+239C>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 5/18 | chr12 | 30734729 | |||||||
| chr12:30734731 | G | T | 1 | a0010c0018t0001g0115 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.566+237C>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 5/18 | chr12 | 30734731 | |||||||
| chr12:30734734 | C | A | 1 | a0010c0018t0001g0115 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.566+234G>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 5/18 | chr12 | 30734734 | |||||||
| chr12:30734736 | T | A | 1 | a0010c0018t0001g0115 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.566+232A>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 5/18 | chr12 | 30734736 | |||||||
| chr12:30734744 | C | A | 1 | a0010c0018t0001g0115 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.566+224G>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 5/18 | chr12 | 30734744 | |||||||
| chr12:30734746 | C | A | 1 | a0010c0018t0001g0115 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.566+222G>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 5/18 | chr12 | 30734746 | |||||||
| chr12:30734751 | C | G | 1 | a0010c0018t0001g0115 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.566+217G>C | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 5/18 | chr12 | 30734751 | |||||||
| chr12:30734754 | C | T | 1 | a0010c0018t0001g0115 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.566+214G>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 5/18 | chr12 | 30734754 | |||||||
| chr12:30734755 | C | A | 1 | a0010c0018t0001g0115 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.566+213G>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 5/18 | chr12 | 30734755 | |||||||
| chr12:30734757 | G | T | 1 | a0010c0018t0001g0115 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.566+211C>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 5/18 | chr12 | 30734757 | |||||||
| chr12:30734759 | C | T | 1 | a0010c0018t0001g0115 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.566+209G>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 5/18 | chr12 | 30734759 | |||||||
| chr12:30734761 | A | G | 1 | a0010c0018t0001g0115 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.566+207T>C | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 5/18 | chr12 | 30734761 | |||||||
| chr12:30734762 | TCTGTCAA others(5): Show |
T | 1 | a0010c0018t0001g0115 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.566+194_566+205del others(12): Show |
CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 5/18 | chr12 | 30734762 | |||||||
| chr12:30734776 | C | A | 1 | a0010c0018t0001g0115 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.566+192G>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 5/18 | chr12 | 30734776 | |||||||
| chr12:30734787 | C | A | 1 | a0010c0018t0001g0115 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.566+181G>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 5/18 | chr12 | 30734787 | |||||||
| chr12:30734789 | A | T | 1 | a0010c0018t0001g0115 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.566+179T>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 5/18 | chr12 | 30734789 | |||||||
| chr12:30734792 | C | T | 1 | a0010c0018t0001g0115 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.566+176G>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 5/18 | chr12 | 30734792 | |||||||
| chr12:30734800 | C | G | 1 | a0010c0018t0001g0115 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.566+168G>C | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 5/18 | chr12 | 30734800 | |||||||
| chr12:30734806 | T | A | 1 | a0010c0018t0001g0115 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.566+162A>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 5/18 | chr12 | 30734806 | |||||||
| chr12:30734807 | G | C | 1 | a0010c0018t0001g0115 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.566+161C>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 5/18 | chr12 | 30734807 | |||||||
| chr12:30734815 | T | C | 1 | a0010c0018t0001g0115 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.566+153A>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 5/18 | chr12 | 30734815 | |||||||
| chr12:30734816 | T | A | 2 | a0001c0004t0001g0223 a0001c0004t0001g0228 |
2 | NA18951.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.566+152A>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 5/18 | chr12 | 30734816 | |||||||
| chr12:30734817 | A | C | 1 | a0010c0018t0001g0115 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.566+151T>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 5/18 | chr12 | 30734817 | |||||||
| chr12:30734830 | G | A | 1 | a0010c0018t0001g0115 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.566+138C>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 5/18 | chr12 | 30734830 | |||||||
| chr12:30734833 | C | A | 1 | a0010c0018t0001g0115 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.566+135G>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 5/18 | chr12 | 30734833 | |||||||
| chr12:30734843 | C | A | 1 | a0010c0018t0001g0115 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.566+125G>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 5/18 | chr12 | 30734843 | |||||||
| chr12:30734849 | A | AAC | 17 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0020 others(14): Show |
27 | HG00639.hp1 HG01069.hp2 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.566+117_566+118dup others(2): Show |
CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 5/18 | chr12 | 30734849 | |||||||
| chr12:30734849 | A | AACAC | 3 | a0001c0001t0001g0026 a0001c0001t0001g0075 a0001c0001t0001g0098 |
4 | HG01261.hp1 HG01928.hp1 HG02293.hp2 others(1): Show |
intron_variant | MODIFIER | c.566+115_566+118dup others(4): Show |
CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 5/18 | chr12 | 30734849 | |||||||
| chr12:30734849 | AAC | A | 6 | a0001c0001t0001g0092 a0001c0001t0001g0116 a0001c0001t0001g0120 others(3): Show |
6 | HG00738.hp1 HG01192.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.566+117_566+118del others(2): Show |
CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 5/18 | chr12 | 30734849 | |||||||
| chr12:30734849 | AACACAC | A | 15 | a0001c0001t0001g0093 a0001c0004t0001g0223 a0001c0009t0001g0207 others(12): Show |
17 | HG01884.hp1 HG01884.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.566+113_566+118del others(6): Show |
CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 5/18 | chr12 | 30734849 | |||||||
| chr12:30734849 | AACACACA others(1): Show |
A | 19 | a0001c0001t0001g0064 a0001c0004t0001g0004 a0001c0004t0001g0042 others(16): Show |
27 | HG00544.hp2 HG01167.hp2 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.566+111_566+118del others(8): Show |
CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 5/18 | chr12 | 30734849 | |||||||
| chr12:30734849 | AACACACA others(3): Show |
A | 3 | a0001c0004t0001g0043 a0001c0004t0001g0235 a0001c0009t0001g0209 |
4 | HG00408.hp1 HG03453.hp2 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.566+109_566+118del others(10): Show |
CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 5/18 | chr12 | 30734849 | |||||||
| chr12:30734849 | AACACACA others(5): Show |
A | 14 | a0002c0002t0002g0012 a0002c0002t0002g0013 a0002c0002t0002g0045 others(11): Show |
23 | HG01074.hp2 HG01361.hp1 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.566+107_566+118del others(12): Show |
CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 5/18 | chr12 | 30734849 | |||||||
| chr12:30734849 | AACACACA others(7): Show |
A | 17 | a0002c0002t0001g0023 a0002c0002t0001g0068 a0002c0002t0002g0044 others(14): Show |
19 | HG01070.hp1 HG01081.hp1 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.566+105_566+118del others(14): Show |
CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 5/18 | chr12 | 30734849 | |||||||
| chr12:30734849 | AACACACA others(9): Show |
A | 1 | a0002c0002t0001g0180 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.566+103_566+118del others(16): Show |
CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 5/18 | chr12 | 30734849 | |||||||
| chr12:30734849 | AACACACA others(13): Show |
A | 1 | a0001c0009t0001g0205 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.566+99_566+118delG others(19): Show |
CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 5/18 | chr12 | 30734849 | |||||||
| chr12:30734852 | A | T | 1 | a0010c0018t0001g0115 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.566+116T>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 5/18 | chr12 | 30734852 | |||||||
| chr12:30734853 | C | A | 1 | a0010c0018t0001g0115 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.566+115G>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 5/18 | chr12 | 30734853 | |||||||
| chr12:30734854 | A | T | 1 | a0010c0018t0001g0115 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.566+114T>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 5/18 | chr12 | 30734854 | |||||||
| chr12:30734857 | C | A | 1 | a0010c0018t0001g0115 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.566+111G>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 5/18 | chr12 | 30734857 | |||||||
| chr12:30734858 | A | T | 1 | a0010c0018t0001g0115 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.566+110T>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 5/18 | chr12 | 30734858 | |||||||
| chr12:30734861 | C | A | 1 | a0010c0018t0001g0115 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.566+107G>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 5/18 | chr12 | 30734861 | |||||||
| chr12:30734875 | C | A | 1 | a0010c0018t0001g0115 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.566+93G>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 5/18 | chr12 | 30734875 | |||||||
| chr12:30734877 | C | A | 1 | a0010c0018t0001g0115 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.566+91G>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 5/18 | chr12 | 30734877 | |||||||
| chr12:30734877 | C | T | 11 | a0002c0002t0002g0012 a0002c0002t0002g0013 a0002c0002t0002g0045 others(8): Show |
20 | HG01074.hp2 HG01361.hp1 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.566+91G>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 5/18 | chr12 | 30734877 | |||||||
| chr12:30734878 | A | T | 1 | a0010c0018t0001g0115 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.566+90T>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 5/18 | chr12 | 30734878 | |||||||
| chr12:30734878 | ACACACAC others(3): Show |
A | 6 | a0002c0002t0001g0016 a0002c0002t0001g0021 a0002c0002t0001g0049 others(3): Show |
9 | HG02145.hp2 HG02818.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.566+80_566+89delAG others(8): Show |
CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 5/18 | chr12 | 30734878 | |||||||
| chr12:30734880 | ACACACAC others(1): Show |
A | 7 | a0002c0005t0001g0219 a0003c0003t0001g0002 a0003c0003t0001g0003 others(4): Show |
7 | HG01168.hp2 HG01169.hp2 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.566+80_566+87delAG others(6): Show |
CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 5/18 | chr12 | 30734880 | |||||||
| chr12:30734882 | ACACACT | A | 52 | a0003c0003t0001g0002 a0003c0003t0001g0003 a0003c0003t0001g0009 others(49): Show |
77 | HG00280.hp2 HG00558.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.566+80_566+85delAG others(4): Show |
CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 5/18 | chr12 | 30734882 | |||||||
| chr12:30734884 | A | C | 1 | a0010c0018t0001g0115 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.566+84T>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 5/18 | chr12 | 30734884 | |||||||
| chr12:30734884 | A | T | 2 | a0002c0002t0001g0068 a0002c0002t0002g0240 |
2 | HG01106.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.566+84T>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 5/18 | chr12 | 30734884 | |||||||
| chr12:30734884 | ACACT | A | 5 | a0003c0003t0001g0002 a0003c0003t0001g0009 a0003c0003t0001g0142 others(2): Show |
7 | HG02080.hp1 HG02165.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.566+80_566+83delAG others(2): Show |
CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 5/18 | chr12 | 30734884 | |||||||
| chr12:30734885 | C | T | 1 | a0010c0018t0001g0115 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.566+83G>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 5/18 | chr12 | 30734885 | |||||||
| chr12:30734886 | A | ACT | 4 | a0001c0001t0001g0100 a0002c0002t0001g0005 a0002c0002t0001g0007 others(1): Show |
5 | HG01891.hp2 HG02809.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.566+80_566+81dupAG | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 5/18 | chr12 | 30734886 | |||||||
| chr12:30734886 | A | T | 55 | a0001c0001t0001g0065 a0001c0001t0001g0087 a0001c0009t0001g0209 others(52): Show |
72 | HG00544.hp1 HG00621.hp1 HG00738.hp2 others(69): Show |
intron_variant | MODIFIER | c.566+82T>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 5/18 | chr12 | 30734886 | |||||||
| chr12:30734888 | T | A | 2 | a0001c0001t0001g0101 a0001c0001t0001g0102 |
2 | HG00558.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.566+80A>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 5/18 | chr12 | 30734888 | |||||||
| chr12:30734889 | C | A | 1 | a0010c0018t0001g0115 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.566+79G>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 5/18 | chr12 | 30734889 | |||||||
| chr12:30734896 | T | A | 1 | a0010c0018t0001g0115 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.566+72A>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 5/18 | chr12 | 30734896 | |||||||
| chr12:30734899 | C | T | 1 | a0010c0018t0001g0115 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.566+69G>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 5/18 | chr12 | 30734899 | |||||||
| chr12:30734912 | C | T | 2 | a0002c0002t0002g0245 a0002c0002t0002g0246 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.566+56G>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 5/18 | chr12 | 30734912 | |||||||
| chr12:30734917 | A | C | 1 | a0010c0018t0001g0115 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.566+51T>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 5/18 | chr12 | 30734917 | |||||||
| chr12:30734921 | T | C | 1 | a0010c0018t0001g0115 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.566+47A>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 5/18 | chr12 | 30734921 | |||||||
| chr12:30734930 | A | T | 1 | a0010c0018t0001g0115 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.566+38T>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 5/18 | chr12 | 30734930 | |||||||
| chr12:30734955 | T | G | 1 | a0010c0018t0001g0115 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.566+13A>C | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 5/18 | chr12 | 30734955 | |||||||
| chr12:30735393 | A | G | 1 | a0003c0003t0001g0141 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.328-187T>C | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 4/18 | chr12 | 30735393 | |||||||
| chr12:30735405 | C | A | 55 | a0002c0002t0001g0005 a0002c0002t0001g0007 a0002c0002t0001g0017 others(52): Show |
84 | HG00544.hp1 HG00621.hp1 HG00738.hp1 others(81): Show |
intron_variant | MODIFIER | c.328-199G>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 4/18 | chr12 | 30735405 | |||||||
| chr12:30735448 | A | G | 1 | a0010c0018t0001g0115 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.328-242T>C | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 4/18 | chr12 | 30735448 | |||||||
| chr12:30735449 | G | A | 1 | a0010c0018t0001g0115 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.328-243C>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 4/18 | chr12 | 30735449 | |||||||
| chr12:30735583 | T | C | 1 | a0001c0001t0001g0094 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.328-377A>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 4/18 | chr12 | 30735583 | |||||||
| chr12:30735641 | G | A | 1 | a0003c0003t0001g0166 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.328-435C>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 4/18 | chr12 | 30735641 | |||||||
| chr12:30735953 | C | A | 1 | a0001c0013t0001g0060 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.328-747G>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 4/18 | chr12 | 30735953 | |||||||
| chr12:30736008 | G | T | 1 | a0010c0018t0001g0115 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.328-802C>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 4/18 | chr12 | 30736008 | |||||||
| chr12:30736009 | T | G | 1 | a0010c0018t0001g0115 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.328-803A>C | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 4/18 | chr12 | 30736009 | |||||||
| chr12:30736054 | T | G | 7 | a0003c0003t0001g0009 a0003c0003t0001g0162 a0003c0003t0001g0164 others(4): Show |
10 | HG00558.hp2 HG00673.hp2 HG02080.hp1 others(7): Show |
intron_variant | MODIFIER | c.328-848A>C | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 4/18 | chr12 | 30736054 | |||||||
| chr12:30736056 | G | T | 1 | a0003c0003t0001g0150 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.328-850C>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 4/18 | chr12 | 30736056 | |||||||
| chr12:30736140 | C | CA | 16 | a0001c0001t0001g0015 a0001c0001t0001g0063 a0001c0001t0001g0106 others(13): Show |
20 | HG00408.hp1 HG01884.hp2 HG02135.hp2 others(17): Show |
intron_variant | MODIFIER | c.328-935dupT | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 4/18 | chr12 | 30736140 | |||||||
| chr12:30736298 | C | T | 34 | a0002c0002t0001g0005 a0002c0002t0001g0007 a0002c0002t0001g0017 others(31): Show |
53 | HG00544.hp1 HG00621.hp1 HG00738.hp2 others(50): Show |
intron_variant | MODIFIER | c.328-1092G>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 4/18 | chr12 | 30736298 | |||||||
| chr12:30736359 | T | C | 79 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(76): Show |
119 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.328-1153A>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 4/18 | chr12 | 30736359 | |||||||
| chr12:30736361 | A | G | 2 | a0002c0002t0002g0245 a0002c0002t0002g0246 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.328-1155T>C | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 4/18 | chr12 | 30736361 | |||||||
| chr12:30736375 | G | A | 1 | a0001c0001t0001g0095 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.328-1169C>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 4/18 | chr12 | 30736375 | |||||||
| chr12:30736397 | C | CA | 58 | a0001c0001t0001g0035 a0001c0001t0001g0117 a0002c0002t0001g0005 others(55): Show |
88 | HG00544.hp1 HG00621.hp1 HG00738.hp1 others(85): Show |
intron_variant | MODIFIER | c.328-1192dupT | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 4/18 | chr12 | 30736397 | |||||||
| chr12:30736397 | CA | C | 17 | a0001c0001t0001g0064 a0001c0001t0001g0071 a0001c0004t0001g0004 others(14): Show |
25 | HG00408.hp1 HG00544.hp2 HG02071.hp1 others(22): Show |
intron_variant | MODIFIER | c.328-1192delT | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 4/18 | chr12 | 30736397 | |||||||
| chr12:30736476 | T | C | 1 | a0002c0002t0002g0244 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.328-1270A>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 4/18 | chr12 | 30736476 | |||||||
| chr12:30736784 | T | C | 1 | a0001c0001t0001g0096 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.328-1578A>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 4/18 | chr12 | 30736784 | |||||||
| chr12:30736893 | C | A | 5 | a0002c0002t0001g0068 a0002c0002t0002g0044 a0002c0002t0002g0242 others(2): Show |
6 | HG02129.hp2 HG03654.hp2 HG03688.hp1 others(3): Show |
intron_variant | MODIFIER | c.328-1687G>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 4/18 | chr12 | 30736893 | |||||||
| chr12:30737069 | G | A | 102 | a0001c0001t0001g0064 a0001c0004t0001g0004 a0001c0004t0001g0042 others(99): Show |
146 | HG00280.hp2 HG00408.hp1 HG00544.hp2 others(143): Show |
intron_variant | MODIFIER | c.328-1863C>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 4/18 | chr12 | 30737069 | |||||||
| chr12:30737221 | C | T | 16 | a0001c0001t0001g0064 a0001c0004t0001g0004 a0001c0004t0001g0042 others(13): Show |
24 | HG00408.hp1 HG00544.hp2 HG02071.hp1 others(21): Show |
intron_variant | MODIFIER | c.328-2015G>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 4/18 | chr12 | 30737221 | |||||||
| chr12:30737243 | A | G | 16 | a0001c0001t0001g0064 a0001c0004t0001g0004 a0001c0004t0001g0042 others(13): Show |
24 | HG00408.hp1 HG00544.hp2 HG02071.hp1 others(21): Show |
intron_variant | MODIFIER | c.328-2037T>C | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 4/18 | chr12 | 30737243 | |||||||
| chr12:30737300 | T | C | 60 | a0003c0003t0001g0002 a0003c0003t0001g0003 a0003c0003t0001g0009 others(57): Show |
91 | HG00280.hp2 HG00558.hp2 HG00639.hp2 others(88): Show |
intron_variant | MODIFIER | c.328-2094A>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 4/18 | chr12 | 30737300 | |||||||
| chr12:30737368 | A | G | 1 | a0002c0002t0001g0021 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.328-2162T>C | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 4/18 | chr12 | 30737368 | |||||||
| chr12:30737443 | T | C | 1 | a0001c0004t0001g0231 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.328-2237A>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 4/18 | chr12 | 30737443 | |||||||
| chr12:30737489 | T | C | 1 | a0002c0002t0001g0179 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.328-2283A>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 4/18 | chr12 | 30737489 | |||||||
| chr12:30737575 | T | G | 8 | a0002c0002t0001g0038 a0002c0002t0001g0051 a0002c0002t0001g0131 others(5): Show |
9 | HG00738.hp1 HG01884.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.328-2369A>C | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 4/18 | chr12 | 30737575 | |||||||
| chr12:30737598 | C | CT | 22 | a0001c0001t0001g0064 a0001c0001t0001g0097 a0001c0004t0001g0004 others(19): Show |
30 | HG00408.hp1 HG00544.hp2 HG02071.hp1 others(27): Show |
intron_variant | MODIFIER | c.328-2393dupA | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 4/18 | chr12 | 30737598 | |||||||
| chr12:30737598 | C | CTT | 59 | a0002c0002t0001g0016 a0002c0002t0001g0121 a0002c0002t0001g0134 others(56): Show |
92 | HG00280.hp2 HG00558.hp2 HG00639.hp2 others(89): Show |
intron_variant | MODIFIER | c.328-2394_328-2393d others(4): Show |
CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 4/18 | chr12 | 30737598 | |||||||
| chr12:30737598 | C | CTTT | 22 | a0002c0002t0001g0021 a0002c0002t0001g0023 a0002c0002t0001g0049 others(19): Show |
25 | HG01070.hp1 HG01081.hp1 HG01099.hp1 others(22): Show |
intron_variant | MODIFIER | c.328-2395_328-2393d others(5): Show |
CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 4/18 | chr12 | 30737598 | |||||||
| chr12:30737598 | CT | C | 31 | a0002c0002t0001g0005 a0002c0002t0001g0007 a0002c0002t0001g0017 others(28): Show |
50 | HG00544.hp1 HG00621.hp1 HG00738.hp2 others(47): Show |
intron_variant | MODIFIER | c.328-2393delA | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 4/18 | chr12 | 30737598 | |||||||
| chr12:30737621 | G | A | 2 | a0002c0002t0004g0259 a0002c0002t0004g0260 |
2 | HG02257.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.328-2415C>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 4/18 | chr12 | 30737621 | |||||||
| chr12:30737637 | G | A | 1 | a0001c0001t0001g0065 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.328-2431C>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 4/18 | chr12 | 30737637 | |||||||
| chr12:30737666 | C | T | 2 | a0004c0007t0002g0238 a0004c0007t0002g0239 |
2 | HG01070.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.328-2460G>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 4/18 | chr12 | 30737666 | |||||||
| chr12:30737690 | C | T | 8 | a0001c0009t0001g0205 a0001c0009t0001g0207 a0001c0009t0001g0209 others(5): Show |
9 | HG01884.hp2 HG02258.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.328-2484G>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 4/18 | chr12 | 30737690 | |||||||
| chr12:30737723 | G | A | 1 | a0001c0001t0001g0097 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.328-2517C>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 4/18 | chr12 | 30737723 | |||||||
| chr12:30737742 | C | T | 1 | a0002c0002t0002g0240 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.328-2536G>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 4/18 | chr12 | 30737742 | |||||||
| chr12:30737821 | T | C | 1 | a0003c0003t0001g0129 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.328-2615A>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 4/18 | chr12 | 30737821 | |||||||
| chr12:30737977 | G | C | 3 | a0002c0002t0002g0012 a0002c0002t0002g0046 a0002c0002t0002g0254 |
7 | HG02559.hp1 HG02615.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.328-2771C>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 4/18 | chr12 | 30737977 | |||||||
| chr12:30738060 | A | G | 1 | a0002c0002t0002g0258 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.328-2854T>C | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 4/18 | chr12 | 30738060 | |||||||
| chr12:30738180 | C | G | 1 | a0002c0005t0001g0211 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.327+2840G>C | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 4/18 | chr12 | 30738180 | |||||||
| chr12:30738306 | G | GA | 12 | a0001c0001t0001g0113 a0002c0002t0002g0012 a0002c0002t0002g0013 others(9): Show |
21 | HG00280.hp1 HG01074.hp2 HG01361.hp1 others(18): Show |
intron_variant | MODIFIER | c.327+2713dupT | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 4/18 | chr12 | 30738306 | |||||||
| chr12:30738313 | A | C | 1 | a0001c0001t0001g0216 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.327+2707T>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 4/18 | chr12 | 30738313 | |||||||
| chr12:30738344 | G | A | 84 | a0002c0002t0001g0016 a0002c0002t0001g0021 a0002c0002t0001g0023 others(81): Show |
120 | HG00280.hp2 HG00558.hp2 HG00639.hp2 others(117): Show |
intron_variant | MODIFIER | c.327+2676C>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 4/18 | chr12 | 30738344 | |||||||
| chr12:30738346 | T | A | 2 | a0002c0002t0002g0245 a0002c0002t0002g0246 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.327+2674A>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 4/18 | chr12 | 30738346 | |||||||
| chr12:30738346 | T | C | 1 | a0001c0009t0001g0209 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.327+2674A>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 4/18 | chr12 | 30738346 | |||||||
| chr12:30738368 | C | T | 1 | a0001c0001t0001g0029 | 2 | HG02145.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.327+2652G>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 4/18 | chr12 | 30738368 | |||||||
| chr12:30738589 | G | A | 2 | a0001c0001t0001g0098 a0007c0015t0001g0099 |
2 | HG01928.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.327+2431C>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 4/18 | chr12 | 30738589 | |||||||
| chr12:30738706 | T | C | 1 | a0004c0007t0002g0239 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.327+2314A>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 4/18 | chr12 | 30738706 | |||||||
| chr12:30738727 | A | C | 1 | a0001c0001t0001g0212 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.327+2293T>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 4/18 | chr12 | 30738727 | |||||||
| chr12:30738738 | A | C | 2 | a0002c0002t0004g0259 a0002c0002t0004g0260 |
2 | HG02257.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.327+2282T>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 4/18 | chr12 | 30738738 | |||||||
| chr12:30739149 | A | C | 1 | a0001c0004t0001g0229 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.327+1871T>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 4/18 | chr12 | 30739149 | |||||||
| chr12:30739189 | G | A | 8 | a0001c0009t0001g0205 a0001c0009t0001g0207 a0001c0009t0001g0209 others(5): Show |
9 | HG01884.hp2 HG02258.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.327+1831C>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 4/18 | chr12 | 30739189 | |||||||
| chr12:30739268 | T | C | 6 | a0002c0002t0001g0041 a0002c0002t0001g0220 a0002c0002t0001g0221 others(3): Show |
7 | HG01167.hp2 HG02109.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.327+1752A>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 4/18 | chr12 | 30739268 | |||||||
| chr12:30739271 | C | G | 84 | a0002c0002t0001g0016 a0002c0002t0001g0021 a0002c0002t0001g0023 others(81): Show |
120 | HG00280.hp2 HG00558.hp2 HG00639.hp2 others(117): Show |
intron_variant | MODIFIER | c.327+1749G>C | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 4/18 | chr12 | 30739271 | |||||||
| chr12:30739323 | G | A | 2 | a0002c0002t0001g0016 a0002c0002t0001g0049 |
4 | HG02145.hp2 HG02965.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.327+1697C>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 4/18 | chr12 | 30739323 | |||||||
| chr12:30739338 | T | TG | 11 | a0002c0002t0002g0012 a0002c0002t0002g0013 a0002c0002t0002g0045 others(8): Show |
20 | HG01074.hp2 HG01361.hp1 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.327+1681dupC | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 4/18 | chr12 | 30739338 | |||||||
| chr12:30739451 | T | G | 1 | a0003c0003t0001g0136 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.327+1569A>C | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 4/18 | chr12 | 30739451 | |||||||
| chr12:30739465 | A | C | 84 | a0002c0002t0001g0016 a0002c0002t0001g0021 a0002c0002t0001g0023 others(81): Show |
120 | HG00280.hp2 HG00558.hp2 HG00639.hp2 others(117): Show |
intron_variant | MODIFIER | c.327+1555T>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 4/18 | chr12 | 30739465 | |||||||
| chr12:30739528 | C | A | 2 | a0003c0003t0001g0168 a0003c0003t0001g0169 |
2 | HG02523.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.327+1492G>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 4/18 | chr12 | 30739528 | |||||||
| chr12:30739585 | C | T | 1 | a0002c0002t0001g0185 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.327+1435G>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 4/18 | chr12 | 30739585 | |||||||
| chr12:30739632 | G | A | 86 | a0002c0002t0001g0016 a0002c0002t0001g0021 a0002c0002t0001g0023 others(83): Show |
122 | HG00280.hp2 HG00558.hp2 HG00639.hp2 others(119): Show |
intron_variant | MODIFIER | c.327+1388C>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 4/18 | chr12 | 30739632 | |||||||
| chr12:30739647 | G | A | 15 | a0001c0004t0001g0004 a0001c0004t0001g0042 a0001c0004t0001g0043 others(12): Show |
23 | HG00408.hp1 HG00544.hp2 HG02071.hp1 others(20): Show |
intron_variant | MODIFIER | c.327+1373C>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 4/18 | chr12 | 30739647 | |||||||
| chr12:30739658 | T | C | 1 | a0001c0009t0001g0207 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.327+1362A>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 4/18 | chr12 | 30739658 | |||||||
| chr12:30739697 | A | T | 2 | a0002c0002t0002g0245 a0002c0002t0002g0246 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.327+1323T>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 4/18 | chr12 | 30739697 | |||||||
| chr12:30739707 | T | C | 1 | a0001c0009t0001g0207 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.327+1313A>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 4/18 | chr12 | 30739707 | |||||||
| chr12:30739714 | C | CA | 43 | a0001c0001t0001g0100 a0001c0009t0001g0209 a0002c0002t0001g0005 others(40): Show |
63 | HG00544.hp1 HG00621.hp1 HG00738.hp1 others(60): Show |
intron_variant | MODIFIER | c.327+1305dupT | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 4/18 | chr12 | 30739714 | |||||||
| chr12:30739789 | T | C | 8 | a0002c0002t0001g0038 a0002c0002t0001g0051 a0002c0002t0001g0131 others(5): Show |
9 | HG00738.hp1 HG01884.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.327+1231A>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 4/18 | chr12 | 30739789 | |||||||
| chr12:30739968 | C | A | 2 | a0006c0010t0001g0217 a0006c0010t0001g0218 |
2 | HG02965.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.327+1052G>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 4/18 | chr12 | 30739968 | |||||||
| chr12:30740154 | A | G | 2 | a0001c0004t0001g0043 a0001c0004t0001g0235 |
3 | HG00408.hp1 NA18999.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.327+866T>C | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 4/18 | chr12 | 30740154 | |||||||
| chr12:30740162 | G | A | 84 | a0002c0002t0001g0016 a0002c0002t0001g0021 a0002c0002t0001g0023 others(81): Show |
120 | HG00280.hp2 HG00558.hp2 HG00639.hp2 others(117): Show |
intron_variant | MODIFIER | c.327+858C>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 4/18 | chr12 | 30740162 | |||||||
| chr12:30740173 | G | A | 84 | a0002c0002t0001g0016 a0002c0002t0001g0021 a0002c0002t0001g0023 others(81): Show |
120 | HG00280.hp2 HG00558.hp2 HG00639.hp2 others(117): Show |
intron_variant | MODIFIER | c.327+847C>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 4/18 | chr12 | 30740173 | |||||||
| chr12:30740217 | T | G | 2 | a0006c0010t0001g0217 a0006c0010t0001g0218 |
2 | HG02965.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.327+803A>C | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 4/18 | chr12 | 30740217 | |||||||
| chr12:30740256 | G | A | 2 | a0002c0002t0004g0259 a0002c0002t0004g0260 |
2 | HG02257.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.327+764C>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 4/18 | chr12 | 30740256 | |||||||
| chr12:30740279 | T | TA | 24 | a0002c0002t0001g0016 a0002c0002t0001g0021 a0002c0002t0001g0023 others(21): Show |
29 | HG01070.hp1 HG01081.hp1 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.327+740dupT | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 4/18 | chr12 | 30740279 | |||||||
| chr12:30740285 | A | AT | 60 | a0003c0003t0001g0002 a0003c0003t0001g0003 a0003c0003t0001g0009 others(57): Show |
91 | HG00280.hp2 HG00558.hp2 HG00639.hp2 others(88): Show |
intron_variant | MODIFIER | c.327+734_327+735ins others(1): Show |
CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 4/18 | chr12 | 30740285 | |||||||
| chr12:30740347 | T | G | 5 | a0002c0002t0001g0041 a0002c0002t0001g0220 a0002c0002t0001g0221 others(2): Show |
6 | HG02109.hp2 HG02451.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.327+673A>C | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 4/18 | chr12 | 30740347 | |||||||
| chr12:30740387 | T | C | 1 | a0002c0002t0001g0177 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.327+633A>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 4/18 | chr12 | 30740387 | |||||||
| chr12:30740433 | AAAAGT | A | 8 | a0002c0002t0001g0038 a0002c0002t0001g0051 a0002c0002t0001g0131 others(5): Show |
9 | HG00738.hp1 HG01884.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.327+582_327+586del others(5): Show |
CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 4/18 | chr12 | 30740433 | |||||||
| chr12:30740540 | G | T | 1 | a0003c0003t0001g0172 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.327+480C>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 4/18 | chr12 | 30740540 | |||||||
| chr12:30740566 | T | C | 84 | a0002c0002t0001g0016 a0002c0002t0001g0021 a0002c0002t0001g0023 others(81): Show |
120 | HG00280.hp2 HG00558.hp2 HG00639.hp2 others(117): Show |
intron_variant | MODIFIER | c.327+454A>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 4/18 | chr12 | 30740566 | |||||||
| chr12:30740895 | T | C | 1 | a0002c0002t0001g0178 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.327+125A>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 4/18 | chr12 | 30740895 | |||||||
| chr12:30740941 | T | C | 60 | a0003c0003t0001g0002 a0003c0003t0001g0003 a0003c0003t0001g0009 others(57): Show |
91 | HG00280.hp2 HG00558.hp2 HG00639.hp2 others(88): Show |
intron_variant | MODIFIER | c.327+79A>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 4/18 | chr12 | 30740941 | |||||||
| chr12:30741304 | A | T | 2 | a0002c0002t0004g0259 a0002c0002t0004g0260 |
2 | HG02257.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.241-198T>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 3/18 | chr12 | 30741304 | |||||||
| chr12:30741482 | G | A | 84 | a0002c0002t0001g0016 a0002c0002t0001g0021 a0002c0002t0001g0023 others(81): Show |
120 | HG00280.hp2 HG00558.hp2 HG00639.hp2 others(117): Show |
intron_variant | MODIFIER | c.241-376C>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 3/18 | chr12 | 30741482 | |||||||
| chr12:30741655 | G | A | 1 | a0003c0003t0001g0147 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.241-549C>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 3/18 | chr12 | 30741655 | |||||||
| chr12:30741660 | G | T | 1 | a0003c0003t0001g0149 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.241-554C>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 3/18 | chr12 | 30741660 | |||||||
| chr12:30741682 | A | G | 1 | a0001c0001t0001g0054 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.241-576T>C | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 3/18 | chr12 | 30741682 | |||||||
| chr12:30741744 | G | A | 2 | a0002c0002t0004g0259 a0002c0002t0004g0260 |
2 | HG02257.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.241-638C>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 3/18 | chr12 | 30741744 | |||||||
| chr12:30741793 | C | T | 2 | a0002c0002t0004g0259 a0002c0002t0004g0260 |
2 | HG02257.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.241-687G>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 3/18 | chr12 | 30741793 | |||||||
| chr12:30741794 | A | G | 7 | a0002c0002t0002g0013 a0002c0002t0002g0047 a0002c0002t0002g0237 others(4): Show |
11 | HG01074.hp2 HG01361.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.241-688T>C | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 3/18 | chr12 | 30741794 | |||||||
| chr12:30741905 | A | G | 16 | a0002c0002t0001g0023 a0002c0002t0001g0068 a0002c0002t0002g0044 others(13): Show |
18 | HG01070.hp1 HG01081.hp1 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.241-799T>C | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 3/18 | chr12 | 30741905 | |||||||
| chr12:30742028 | A | G | 8 | a0002c0002t0001g0038 a0002c0002t0001g0051 a0002c0002t0001g0131 others(5): Show |
9 | HG00738.hp1 HG01884.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.241-922T>C | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 3/18 | chr12 | 30742028 | |||||||
| chr12:30742132 | T | C | 4 | a0002c0002t0002g0012 a0002c0002t0002g0045 a0002c0002t0002g0046 others(1): Show |
9 | HG02559.hp1 HG02615.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.241-1026A>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 3/18 | chr12 | 30742132 | |||||||
| chr12:30742158 | C | T | 3 | a0001c0001t0001g0022 a0001c0001t0001g0062 a0001c0001t0001g0063 |
4 | HG02040.hp2 NA18941.hp1 NA18952.hp2 others(1): Show |
intron_variant | MODIFIER | c.241-1052G>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 3/18 | chr12 | 30742158 | |||||||
| chr12:30742235 | T | C | 1 | a0001c0004t0001g0228 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.241-1129A>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 3/18 | chr12 | 30742235 | |||||||
| chr12:30742286 | G | C | 2 | a0002c0002t0004g0259 a0002c0002t0004g0260 |
2 | HG02257.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.241-1180C>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 3/18 | chr12 | 30742286 | |||||||
| chr12:30742317 | T | C | 84 | a0002c0002t0001g0016 a0002c0002t0001g0021 a0002c0002t0001g0023 others(81): Show |
120 | HG00280.hp2 HG00558.hp2 HG00639.hp2 others(117): Show |
intron_variant | MODIFIER | c.241-1211A>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 3/18 | chr12 | 30742317 | |||||||
| chr12:30742411 | G | A | 2 | a0002c0002t0001g0016 a0002c0002t0001g0049 |
4 | HG02145.hp2 HG02965.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.241-1305C>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 3/18 | chr12 | 30742411 | |||||||
| chr12:30742423 | C | T | 1 | a0003c0003t0001g0104 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.241-1317G>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 3/18 | chr12 | 30742423 | |||||||
| chr12:30742460 | C | G | 2 | a0002c0002t0002g0245 a0002c0002t0002g0246 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.241-1354G>C | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 3/18 | chr12 | 30742460 | |||||||
| chr12:30742504 | A | C | 2 | a0002c0002t0002g0245 a0002c0002t0002g0246 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.241-1398T>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 3/18 | chr12 | 30742504 | |||||||
| chr12:30742532 | C | T | 86 | a0002c0002t0001g0016 a0002c0002t0001g0021 a0002c0002t0001g0023 others(83): Show |
122 | HG00280.hp2 HG00558.hp2 HG00639.hp2 others(119): Show |
intron_variant | MODIFIER | c.241-1426G>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 3/18 | chr12 | 30742532 | |||||||
| chr12:30742550 | A | G | 2 | a0002c0002t0004g0259 a0002c0002t0004g0260 |
2 | HG02257.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.241-1444T>C | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 3/18 | chr12 | 30742550 | |||||||
| chr12:30742685 | C | CA | 95 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0004t0001g0043 others(92): Show |
131 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(128): Show |
intron_variant | MODIFIER | c.241-1580dupT | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 3/18 | chr12 | 30742685 | |||||||
| chr12:30742783 | G | A | 66 | a0002c0002t0001g0016 a0002c0002t0001g0021 a0002c0002t0001g0049 others(63): Show |
100 | HG00280.hp2 HG00558.hp2 HG00639.hp2 others(97): Show |
intron_variant | MODIFIER | c.241-1677C>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 3/18 | chr12 | 30742783 | |||||||
| chr12:30742927 | A | G | 1 | a0003c0003t0001g0148 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.241-1821T>C | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 3/18 | chr12 | 30742927 | |||||||
| chr12:30743346 | T | C | 171 | a0001c0001t0001g0064 a0001c0004t0001g0004 a0001c0004t0001g0042 others(168): Show |
246 | HG00280.hp2 HG00408.hp1 HG00544.hp1 others(243): Show |
intron_variant | MODIFIER | c.241-2240A>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 3/18 | chr12 | 30743346 | |||||||
| chr12:30743441 | A | G | 84 | a0002c0002t0001g0016 a0002c0002t0001g0021 a0002c0002t0001g0023 others(81): Show |
120 | HG00280.hp2 HG00558.hp2 HG00639.hp2 others(117): Show |
intron_variant | MODIFIER | c.241-2335T>C | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 3/18 | chr12 | 30743441 | |||||||
| chr12:30743737 | A | T | 71 | a0001c0001t0001g0064 a0001c0004t0001g0004 a0001c0004t0001g0042 others(68): Show |
108 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(105): Show |
intron_variant | MODIFIER | c.241-2631T>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 3/18 | chr12 | 30743737 | |||||||
| chr12:30743772 | A | G | 1 | a0001c0001t0001g0070 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.241-2666T>C | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 3/18 | chr12 | 30743772 | |||||||
| chr12:30743833 | C | T | 1 | a0002c0002t0002g0256 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.241-2727G>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 3/18 | chr12 | 30743833 | |||||||
| chr12:30743984 | G | A | 169 | a0001c0001t0001g0064 a0001c0004t0001g0004 a0001c0004t0001g0042 others(166): Show |
244 | HG00280.hp2 HG00408.hp1 HG00544.hp1 others(241): Show |
intron_variant | MODIFIER | c.241-2878C>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 3/18 | chr12 | 30743984 | |||||||
| chr12:30744071 | C | A | 65 | a0002c0002t0001g0016 a0002c0002t0001g0049 a0002c0002t0001g0121 others(62): Show |
98 | HG00280.hp2 HG00558.hp2 HG00639.hp2 others(95): Show |
intron_variant | MODIFIER | c.241-2965G>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 3/18 | chr12 | 30744071 | |||||||
| chr12:30744110 | C | A | 2 | a0002c0002t0001g0016 a0002c0002t0001g0049 |
4 | HG02145.hp2 HG02965.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.241-3004G>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 3/18 | chr12 | 30744110 | |||||||
| chr12:30744154 | T | C | 1 | a0004c0007t0002g0239 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.241-3048A>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 3/18 | chr12 | 30744154 | |||||||
| chr12:30744280 | C | T | 7 | a0001c0009t0001g0205 a0001c0009t0001g0207 a0001c0009t0001g0209 others(4): Show |
8 | HG01884.hp2 HG02258.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.241-3174G>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 3/18 | chr12 | 30744280 | |||||||
| chr12:30744422 | G | C | 1 | a0003c0003t0001g0050 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.241-3316C>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 3/18 | chr12 | 30744422 | |||||||
| chr12:30744491 | C | G | 1 | a0001c0001t0001g0069 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.241-3385G>C | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 3/18 | chr12 | 30744491 | |||||||
| chr12:30744524 | A | T | 21 | a0001c0001t0001g0022 a0001c0001t0001g0062 a0001c0001t0001g0063 others(18): Show |
30 | HG00408.hp1 HG00544.hp2 HG02015.hp1 others(27): Show |
intron_variant | MODIFIER | c.241-3418T>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 3/18 | chr12 | 30744524 | |||||||
| chr12:30744831 | T | C | 111 | a0002c0002t0001g0005 a0002c0002t0001g0007 a0002c0002t0001g0016 others(108): Show |
165 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(162): Show |
intron_variant | MODIFIER | c.241-3725A>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 3/18 | chr12 | 30744831 | |||||||
| chr12:30744852 | T | C | 3 | a0002c0002t0001g0038 a0002c0002t0001g0051 a0002c0002t0001g0180 |
4 | HG00738.hp1 HG01884.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.241-3746A>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 3/18 | chr12 | 30744852 | |||||||
| chr12:30744896 | G | C | 109 | a0002c0002t0001g0005 a0002c0002t0001g0007 a0002c0002t0001g0016 others(106): Show |
162 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(159): Show |
intron_variant | MODIFIER | c.241-3790C>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 3/18 | chr12 | 30744896 | |||||||
| chr12:30745066 | G | A | 162 | a0001c0001t0001g0022 a0001c0001t0001g0062 a0001c0001t0001g0063 others(159): Show |
235 | HG00280.hp2 HG00408.hp1 HG00544.hp1 others(232): Show |
intron_variant | MODIFIER | c.241-3960C>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 3/18 | chr12 | 30745066 | |||||||
| chr12:30745075 | G | A | 1 | a0002c0011t0001g0202 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.241-3969C>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 3/18 | chr12 | 30745075 | |||||||
| chr12:30745082 | C | T | 106 | a0002c0002t0001g0005 a0002c0002t0001g0007 a0002c0002t0001g0016 others(103): Show |
159 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(156): Show |
intron_variant | MODIFIER | c.241-3976G>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 3/18 | chr12 | 30745082 | |||||||
| chr12:30745488 | T | G | 27 | a0002c0002t0002g0012 a0002c0002t0002g0013 a0002c0002t0002g0044 others(24): Show |
37 | HG01070.hp1 HG01074.hp2 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.241-4382A>C | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 3/18 | chr12 | 30745488 | |||||||
| chr12:30745579 | A | C | 2 | a0001c0001t0001g0024 a0001c0001t0001g0055 |
3 | HG00642.hp2 HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.241-4473T>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 3/18 | chr12 | 30745579 | |||||||
| chr12:30745658 | T | C | 1 | a0002c0002t0002g0253 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.241-4552A>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 3/18 | chr12 | 30745658 | |||||||
| chr12:30746012 | T | G | 27 | a0002c0002t0002g0012 a0002c0002t0002g0013 a0002c0002t0002g0044 others(24): Show |
37 | HG01070.hp1 HG01074.hp2 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.241-4906A>C | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 3/18 | chr12 | 30746012 | |||||||
| chr12:30746131 | AAAC | A | 111 | a0002c0002t0001g0005 a0002c0002t0001g0007 a0002c0002t0001g0016 others(108): Show |
165 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(162): Show |
intron_variant | MODIFIER | c.240+4937_240+4939d others(5): Show |
CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 3/18 | chr12 | 30746131 | |||||||
| chr12:30746216 | T | C | 1 | a0002c0002t0002g0254 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.240+4855A>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 3/18 | chr12 | 30746216 | |||||||
| chr12:30746217 | G | T | 1 | a0002c0002t0002g0255 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.240+4854C>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 3/18 | chr12 | 30746217 | |||||||
| chr12:30746244 | C | T | 4 | a0002c0002t0002g0012 a0002c0002t0002g0045 a0002c0002t0002g0046 others(1): Show |
9 | HG02559.hp1 HG02615.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.240+4827G>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 3/18 | chr12 | 30746244 | |||||||
| chr12:30746294 | G | A | 1 | a0003c0003t0001g0170 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.240+4777C>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 3/18 | chr12 | 30746294 | |||||||
| chr12:30746300 | G | A | 1 | a0003c0003t0001g0104 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.240+4771C>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 3/18 | chr12 | 30746300 | |||||||
| chr12:30746342 | T | C | 3 | a0001c0001t0001g0234 a0001c0004t0001g0043 a0001c0004t0001g0235 |
4 | HG00408.hp1 NA18962.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.240+4729A>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 3/18 | chr12 | 30746342 | |||||||
| chr12:30746410 | G | A | 21 | a0001c0001t0001g0022 a0001c0001t0001g0062 a0001c0001t0001g0063 others(18): Show |
30 | HG00408.hp1 HG00544.hp2 HG02040.hp2 others(27): Show |
intron_variant | MODIFIER | c.240+4661C>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 3/18 | chr12 | 30746410 | |||||||
| chr12:30746546 | T | C | 112 | a0001c0001t0001g0105 a0002c0002t0001g0005 a0002c0002t0001g0007 others(109): Show |
166 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(163): Show |
intron_variant | MODIFIER | c.240+4525A>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 3/18 | chr12 | 30746546 | |||||||
| chr12:30746584 | AC | A | 14 | a0002c0002t0002g0044 a0002c0002t0002g0240 a0002c0002t0002g0241 others(11): Show |
15 | HG01070.hp1 HG01081.hp1 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.240+4486delG | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 3/18 | chr12 | 30746584 | |||||||
| chr12:30746599 | T | C | 3 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0117 |
5 | NA18951.hp1 NA18986.hp1 NA18988.hp1 others(2): Show |
intron_variant | MODIFIER | c.240+4472A>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 3/18 | chr12 | 30746599 | |||||||
| chr12:30746663 | C | T | 2 | a0006c0010t0001g0217 a0006c0010t0001g0218 |
2 | HG02965.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.240+4408G>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 3/18 | chr12 | 30746663 | |||||||
| chr12:30746886 | T | G | 1 | a0003c0003t0001g0048 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.240+4185A>C | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 3/18 | chr12 | 30746886 | |||||||
| chr12:30746913 | T | C | 1 | a0002c0002t0004g0260 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.240+4158A>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 3/18 | chr12 | 30746913 | |||||||
| chr12:30747049 | T | A | 2 | a0002c0002t0002g0245 a0002c0002t0002g0246 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.240+4022A>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 3/18 | chr12 | 30747049 | |||||||
| chr12:30747377 | C | T | 1 | a0002c0002t0001g0131 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.240+3694G>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 3/18 | chr12 | 30747377 | |||||||
| chr12:30747400 | G | A | 1 | a0003c0003t0001g0125 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.240+3671C>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 3/18 | chr12 | 30747400 | |||||||
| chr12:30747434 | T | C | 1 | a0002c0002t0001g0215 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.240+3637A>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 3/18 | chr12 | 30747434 | |||||||
| chr12:30747452 | C | T | 111 | a0002c0002t0001g0005 a0002c0002t0001g0007 a0002c0002t0001g0016 others(108): Show |
165 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(162): Show |
intron_variant | MODIFIER | c.240+3619G>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 3/18 | chr12 | 30747452 | |||||||
| chr12:30747453 | A | G | 113 | a0002c0002t0001g0005 a0002c0002t0001g0007 a0002c0002t0001g0016 others(110): Show |
167 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(164): Show |
intron_variant | MODIFIER | c.240+3618T>C | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 3/18 | chr12 | 30747453 | |||||||
| chr12:30747570 | A | T | 2 | a0006c0010t0001g0217 a0006c0010t0001g0218 |
2 | HG02965.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.240+3501T>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 3/18 | chr12 | 30747570 | |||||||
| chr12:30747592 | G | A | 2 | a0006c0010t0001g0217 a0006c0010t0001g0218 |
2 | HG02965.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.240+3479C>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 3/18 | chr12 | 30747592 | |||||||
| chr12:30747672 | C | T | 2 | a0006c0010t0001g0217 a0006c0010t0001g0218 |
2 | HG02965.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.240+3399G>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 3/18 | chr12 | 30747672 | |||||||
| chr12:30747673 | G | A | 5 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0058 others(2): Show |
7 | HG02145.hp1 HG02896.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.240+3398C>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 3/18 | chr12 | 30747673 | |||||||
| chr12:30747748 | G | A | 111 | a0002c0002t0001g0005 a0002c0002t0001g0007 a0002c0002t0001g0016 others(108): Show |
165 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(162): Show |
intron_variant | MODIFIER | c.240+3323C>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 3/18 | chr12 | 30747748 | |||||||
| chr12:30747753 | G | A | 2 | a0002c0002t0002g0245 a0002c0002t0002g0246 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.240+3318C>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 3/18 | chr12 | 30747753 | |||||||
| chr12:30747767 | G | C | 2 | a0002c0002t0002g0047 a0002c0002t0002g0237 |
3 | HG01891.hp1 HG03471.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.240+3304C>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 3/18 | chr12 | 30747767 | |||||||
| chr12:30747798 | T | C | 2 | a0002c0002t0002g0245 a0002c0002t0002g0246 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.240+3273A>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 3/18 | chr12 | 30747798 | |||||||
| chr12:30747917 | A | G | 1 | a0002c0002t0002g0044 | 2 | HG03942.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.240+3154T>C | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 3/18 | chr12 | 30747917 | |||||||
| chr12:30748178 | C | T | 62 | a0002c0002t0001g0016 a0002c0002t0001g0049 a0002c0002t0001g0121 others(59): Show |
95 | HG00280.hp2 HG00558.hp2 HG00639.hp2 others(92): Show |
intron_variant | MODIFIER | c.240+2893G>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 3/18 | chr12 | 30748178 | |||||||
| chr12:30748294 | T | C | 2 | a0002c0002t0004g0259 a0002c0002t0004g0260 |
2 | HG02257.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.240+2777A>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 3/18 | chr12 | 30748294 | |||||||
| chr12:30748333 | C | T | 3 | a0001c0004t0001g0042 a0001c0004t0001g0225 a0001c0004t0001g0233 |
4 | HG00544.hp2 NA18998.hp1 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.240+2738G>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 3/18 | chr12 | 30748333 | |||||||
| chr12:30748533 | C | T | 3 | a0003c0003t0001g0137 a0003c0003t0001g0146 a0003c0003t0001g0147 |
3 | HG00280.hp2 HG00639.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.240+2538G>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 3/18 | chr12 | 30748533 | |||||||
| chr12:30748559 | G | A | 1 | a0001c0001t0001g0107 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.240+2512C>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 3/18 | chr12 | 30748559 | |||||||
| chr12:30748625 | AG | A | 5 | a0001c0004t0001g0224 a0001c0004t0001g0229 a0001c0004t0001g0230 others(2): Show |
5 | NA19001.hp1 NA19007.hp1 NA19079.hp2 others(2): Show |
intron_variant | MODIFIER | c.240+2445delC | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 3/18 | chr12 | 30748625 | |||||||
| chr12:30748664 | T | C | 1 | a0001c0001t0001g0108 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.240+2407A>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 3/18 | chr12 | 30748664 | |||||||
| chr12:30748821 | A | G | 111 | a0002c0002t0001g0005 a0002c0002t0001g0007 a0002c0002t0001g0016 others(108): Show |
165 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(162): Show |
intron_variant | MODIFIER | c.240+2250T>C | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 3/18 | chr12 | 30748821 | |||||||
| chr12:30749055 | C | T | 2 | a0002c0002t0004g0259 a0002c0002t0004g0260 |
2 | HG02257.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.240+2016G>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 3/18 | chr12 | 30749055 | |||||||
| chr12:30749102 | G | A | 27 | a0002c0002t0002g0012 a0002c0002t0002g0013 a0002c0002t0002g0044 others(24): Show |
37 | HG01070.hp1 HG01074.hp2 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.240+1969C>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 3/18 | chr12 | 30749102 | |||||||
| chr12:30749109 | A | C | 1 | a0002c0002t0001g0068 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.240+1962T>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 3/18 | chr12 | 30749109 | |||||||
| chr12:30749176 | C | T | 14 | a0002c0002t0002g0044 a0002c0002t0002g0240 a0002c0002t0002g0241 others(11): Show |
15 | HG01070.hp1 HG01081.hp1 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.240+1895G>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 3/18 | chr12 | 30749176 | |||||||
| chr12:30749214 | C | G | 111 | a0002c0002t0001g0005 a0002c0002t0001g0007 a0002c0002t0001g0016 others(108): Show |
165 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(162): Show |
intron_variant | MODIFIER | c.240+1857G>C | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 3/18 | chr12 | 30749214 | |||||||
| chr12:30749230 | G | A | 8 | a0001c0009t0001g0205 a0001c0009t0001g0207 a0001c0009t0001g0209 others(5): Show |
9 | HG01884.hp2 HG02258.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.240+1841C>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 3/18 | chr12 | 30749230 | |||||||
| chr12:30749304 | C | T | 111 | a0002c0002t0001g0005 a0002c0002t0001g0007 a0002c0002t0001g0016 others(108): Show |
165 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(162): Show |
intron_variant | MODIFIER | c.240+1767G>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 3/18 | chr12 | 30749304 | |||||||
| chr12:30749372 | G | A | 21 | a0001c0001t0001g0022 a0001c0001t0001g0062 a0001c0001t0001g0063 others(18): Show |
30 | HG00408.hp1 HG00544.hp2 HG02040.hp2 others(27): Show |
intron_variant | MODIFIER | c.240+1699C>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 3/18 | chr12 | 30749372 | |||||||
| chr12:30749378 | C | T | 2 | a0006c0010t0001g0217 a0006c0010t0001g0218 |
2 | HG02965.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.240+1693G>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 3/18 | chr12 | 30749378 | |||||||
| chr12:30749406 | C | T | 1 | a0001c0001t0001g0054 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.240+1665G>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 3/18 | chr12 | 30749406 | |||||||
| chr12:30749497 | T | C | 7 | a0002c0002t0002g0013 a0002c0002t0002g0047 a0002c0002t0002g0237 others(4): Show |
11 | HG01074.hp2 HG01361.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.240+1574A>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 3/18 | chr12 | 30749497 | |||||||
| chr12:30749512 | T | C | 1 | a0002c0002t0002g0253 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.240+1559A>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 3/18 | chr12 | 30749512 | |||||||
| chr12:30749929 | G | C | 1 | a0001c0001t0001g0109 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.240+1142C>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 3/18 | chr12 | 30749929 | |||||||
| chr12:30749958 | C | A | 21 | a0001c0001t0001g0022 a0001c0001t0001g0062 a0001c0001t0001g0063 others(18): Show |
30 | HG00408.hp1 HG00544.hp2 HG02040.hp2 others(27): Show |
intron_variant | MODIFIER | c.240+1113G>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 3/18 | chr12 | 30749958 | |||||||
| chr12:30750080 | A | T | 1 | a0001c0001t0001g0067 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.240+991T>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 3/18 | chr12 | 30750080 | |||||||
| chr12:30750297 | T | G | 27 | a0002c0002t0002g0012 a0002c0002t0002g0013 a0002c0002t0002g0044 others(24): Show |
37 | HG01070.hp1 HG01074.hp2 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.240+774A>C | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 3/18 | chr12 | 30750297 | |||||||
| chr12:30750484 | G | A | 6 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0110 others(3): Show |
8 | HG00280.hp1 HG00733.hp1 HG01069.hp2 others(5): Show |
intron_variant | MODIFIER | c.240+587C>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 3/18 | chr12 | 30750484 | |||||||
| chr12:30750500 | G | GA | 7 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(4): Show |
10 | HG02135.hp2 NA18951.hp1 NA18956.hp2 others(7): Show |
intron_variant | MODIFIER | c.240+570dupT | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 3/18 | chr12 | 30750500 | |||||||
| chr12:30750535 | C | CT | 10 | a0001c0001t0001g0014 a0001c0001t0001g0066 a0002c0002t0001g0038 others(7): Show |
13 | HG00738.hp1 HG01884.hp1 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.240+535dupA | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 3/18 | chr12 | 30750535 | |||||||
| chr12:30750595 | G | A | 1 | a0002c0002t0001g0181 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.240+476C>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 3/18 | chr12 | 30750595 | |||||||
| chr12:30750643 | T | C | 111 | a0002c0002t0001g0005 a0002c0002t0001g0007 a0002c0002t0001g0016 others(108): Show |
165 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(162): Show |
intron_variant | MODIFIER | c.240+428A>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 3/18 | chr12 | 30750643 | |||||||
| chr12:30750867 | G | A | 111 | a0002c0002t0001g0005 a0002c0002t0001g0007 a0002c0002t0001g0016 others(108): Show |
165 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(162): Show |
intron_variant | MODIFIER | c.240+204C>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 3/18 | chr12 | 30750867 | |||||||
| chr12:30751151 | G | C | 4 | a0003c0003t0001g0010 a0003c0003t0001g0171 a0003c0003t0001g0172 others(1): Show |
7 | HG02015.hp1 NA18950.hp1 NA18988.hp2 others(4): Show |
intron_variant | MODIFIER | c.178-18C>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 2/18 | chr12 | 30751151 | |||||||
| chr12:30751354 | C | A | 11 | a0002c0002t0002g0012 a0002c0002t0002g0013 a0002c0002t0002g0045 others(8): Show |
20 | HG01074.hp2 HG01361.hp1 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.178-221G>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 2/18 | chr12 | 30751354 | |||||||
| chr12:30751374 | C | T | 104 | a0002c0002t0001g0005 a0002c0002t0001g0007 a0002c0002t0001g0016 others(101): Show |
157 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(154): Show |
intron_variant | MODIFIER | c.178-241G>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 2/18 | chr12 | 30751374 | |||||||
| chr12:30751474 | G | C | 1 | a0001c0004t0001g0233 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.178-341C>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 2/18 | chr12 | 30751474 | |||||||
| chr12:30751475 | T | A | 1 | a0002c0005t0001g0211 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.178-342A>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 2/18 | chr12 | 30751475 | |||||||
| chr12:30751531 | G | A | 1 | a0001c0001t0001g0061 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.178-398C>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 2/18 | chr12 | 30751531 | |||||||
| chr12:30751756 | G | A | 2 | a0003c0003t0001g0130 a0003c0003t0001g0174 |
2 | NA18961.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.178-623C>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 2/18 | chr12 | 30751756 | |||||||
| chr12:30751771 | CAAGA | C | 2 | a0001c0001t0001g0065 a0002c0002t0001g0023 |
3 | HG01123.hp1 HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.178-642_178-639del others(4): Show |
CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 2/18 | chr12 | 30751771 | |||||||
| chr12:30751790 | TTATCA | T | 170 | a0001c0001t0001g0022 a0001c0001t0001g0062 a0001c0001t0001g0063 others(167): Show |
244 | HG00280.hp2 HG00408.hp1 HG00544.hp1 others(241): Show |
intron_variant | MODIFIER | c.178-662_178-658del others(5): Show |
CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 2/18 | chr12 | 30751790 | |||||||
| chr12:30751796 | T | C | 1 | a0002c0002t0001g0203 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.178-663A>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 2/18 | chr12 | 30751796 | |||||||
| chr12:30751907 | GTATTTTT | G | 15 | a0003c0003t0001g0003 a0003c0003t0001g0048 a0003c0003t0001g0122 others(12): Show |
23 | HG00735.hp1 HG01358.hp2 HG02040.hp1 others(20): Show |
intron_variant | MODIFIER | c.178-781_178-775del others(7): Show |
CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 2/18 | chr12 | 30751907 | |||||||
| chr12:30751907 | GTATTTTT others(1): Show |
G | 39 | a0003c0003t0001g0002 a0003c0003t0001g0009 a0003c0003t0001g0010 others(36): Show |
61 | HG00280.hp2 HG00558.hp2 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.178-782_178-775del others(8): Show |
CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 2/18 | chr12 | 30751907 | |||||||
| chr12:30751907 | GTATTTTT others(3): Show |
G | 1 | a0003c0003t0001g0175 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.178-784_178-775del others(10): Show |
CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 2/18 | chr12 | 30751907 | |||||||
| chr12:30751909 | A | AT | 17 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0020 others(14): Show |
19 | HG00673.hp1 HG00733.hp1 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.178-777dupA | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 2/18 | chr12 | 30751909 | |||||||
| chr12:30751909 | AT | A | 35 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(32): Show |
39 | HG00408.hp2 HG01070.hp1 HG01070.hp2 others(36): Show |
intron_variant | MODIFIER | c.178-777delA | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 2/18 | chr12 | 30751909 | |||||||
| chr12:30751909 | ATT | A | 25 | a0001c0001t0001g0022 a0001c0001t0001g0062 a0001c0001t0001g0066 others(22): Show |
33 | HG00408.hp1 HG00544.hp2 HG01884.hp2 others(30): Show |
intron_variant | MODIFIER | c.178-778_178-777del others(2): Show |
CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 2/18 | chr12 | 30751909 | |||||||
| chr12:30751909 | ATTT | A | 6 | a0002c0002t0002g0012 a0002c0005t0001g0040 a0002c0005t0001g0206 others(3): Show |
6 | HG02258.hp2 HG02486.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.178-779_178-777del others(3): Show |
CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 2/18 | chr12 | 30751909 | |||||||
| chr12:30751909 | ATTTTTTT | A | 8 | a0002c0002t0001g0179 a0002c0002t0001g0180 a0002c0002t0001g0220 others(5): Show |
8 | HG02109.hp2 HG02451.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.178-783_178-777del others(7): Show |
CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 2/18 | chr12 | 30751909 | |||||||
| chr12:30751909 | ATTTTTTT others(1): Show |
A | 12 | a0002c0002t0001g0038 a0002c0002t0001g0041 a0002c0002t0001g0051 others(9): Show |
14 | HG00738.hp1 HG01884.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.178-784_178-777del others(8): Show |
CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 2/18 | chr12 | 30751909 | |||||||
| chr12:30751909 | ATTTTTTT others(2): Show |
A | 34 | a0002c0002t0001g0005 a0002c0002t0001g0007 a0002c0002t0001g0016 others(31): Show |
54 | HG00544.hp1 HG00621.hp1 HG00738.hp2 others(51): Show |
intron_variant | MODIFIER | c.178-785_178-777del others(9): Show |
CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 2/18 | chr12 | 30751909 | |||||||
| chr12:30751909 | ATTTTTTT others(3): Show |
A | 2 | a0002c0002t0001g0187 a0002c0006t0001g0019 |
2 | HG02809.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.178-786_178-777del others(10): Show |
CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 2/18 | chr12 | 30751909 | |||||||
| chr12:30751955 | G | A | 27 | a0002c0002t0002g0012 a0002c0002t0002g0013 a0002c0002t0002g0044 others(24): Show |
37 | HG01070.hp1 HG01074.hp2 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.178-822C>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 2/18 | chr12 | 30751955 | |||||||
| chr12:30752132 | G | A | 1 | a0002c0002t0003g0204 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.178-999C>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 2/18 | chr12 | 30752132 | |||||||
| chr12:30752218 | G | A | 34 | a0002c0002t0001g0005 a0002c0002t0001g0007 a0002c0002t0001g0017 others(31): Show |
53 | HG00544.hp1 HG00621.hp1 HG00738.hp2 others(50): Show |
intron_variant | MODIFIER | c.178-1085C>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 2/18 | chr12 | 30752218 | |||||||
| chr12:30752322 | T | A | 113 | a0002c0002t0001g0005 a0002c0002t0001g0007 a0002c0002t0001g0016 others(110): Show |
167 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(164): Show |
intron_variant | MODIFIER | c.177+1022A>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 2/18 | chr12 | 30752322 | |||||||
| chr12:30752428 | T | C | 113 | a0002c0002t0001g0005 a0002c0002t0001g0007 a0002c0002t0001g0016 others(110): Show |
167 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(164): Show |
intron_variant | MODIFIER | c.177+916A>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 2/18 | chr12 | 30752428 | |||||||
| chr12:30752445 | G | C | 111 | a0002c0002t0001g0005 a0002c0002t0001g0007 a0002c0002t0001g0016 others(108): Show |
165 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(162): Show |
intron_variant | MODIFIER | c.177+899C>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 2/18 | chr12 | 30752445 | |||||||
| chr12:30752502 | C | T | 3 | a0001c0001t0001g0059 a0001c0001t0001g0061 a0001c0013t0001g0060 |
3 | HG00735.hp2 HG01106.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.177+842G>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 2/18 | chr12 | 30752502 | |||||||
| chr12:30752503 | G | A | 111 | a0002c0002t0001g0005 a0002c0002t0001g0007 a0002c0002t0001g0016 others(108): Show |
165 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(162): Show |
intron_variant | MODIFIER | c.177+841C>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 2/18 | chr12 | 30752503 | |||||||
| chr12:30752572 | T | TA | 79 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0001g0120 others(76): Show |
115 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(112): Show |
intron_variant | MODIFIER | c.177+771dupT | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 2/18 | chr12 | 30752572 | |||||||
| chr12:30752572 | T | TAA | 35 | a0002c0002t0001g0005 a0002c0002t0001g0007 a0002c0002t0001g0017 others(32): Show |
55 | HG00544.hp1 HG00621.hp1 HG00738.hp2 others(52): Show |
intron_variant | MODIFIER | c.177+770_177+771dup others(2): Show |
CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 2/18 | chr12 | 30752572 | |||||||
| chr12:30752572 | TA | T | 10 | a0001c0001t0001g0020 a0001c0001t0001g0054 a0001c0001t0001g0055 others(7): Show |
12 | HG01070.hp2 HG01516.hp2 HG02165.hp2 others(9): Show |
intron_variant | MODIFIER | c.177+771delT | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 2/18 | chr12 | 30752572 | |||||||
| chr12:30752652 | A | C | 1 | a0001c0009t0001g0205 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.177+692T>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 2/18 | chr12 | 30752652 | |||||||
| chr12:30752770 | C | A | 104 | a0002c0002t0001g0005 a0002c0002t0001g0007 a0002c0002t0001g0016 others(101): Show |
157 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(154): Show |
intron_variant | MODIFIER | c.177+574G>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 2/18 | chr12 | 30752770 | |||||||
| chr12:30752773 | GC | G | 104 | a0002c0002t0001g0005 a0002c0002t0001g0007 a0002c0002t0001g0016 others(101): Show |
157 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(154): Show |
intron_variant | MODIFIER | c.177+570delG | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 2/18 | chr12 | 30752773 | |||||||
| chr12:30752916 | G | A | 111 | a0002c0002t0001g0005 a0002c0002t0001g0007 a0002c0002t0001g0016 others(108): Show |
165 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(162): Show |
intron_variant | MODIFIER | c.177+428C>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 2/18 | chr12 | 30752916 | |||||||
| chr12:30752920 | G | A | 1 | a0001c0004t0001g0235 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.177+424C>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 2/18 | chr12 | 30752920 | |||||||
| chr12:30752936 | T | C | 2 | a0002c0002t0004g0259 a0002c0002t0004g0260 |
2 | HG02257.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.177+408A>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 2/18 | chr12 | 30752936 | |||||||
| chr12:30752947 | CG | C | 8 | a0001c0009t0001g0205 a0001c0009t0001g0207 a0001c0009t0001g0209 others(5): Show |
9 | HG01884.hp2 HG02258.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.177+396delC | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 2/18 | chr12 | 30752947 | |||||||
| chr12:30753066 | C | G | 1 | a0001c0001t0001g0053 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.177+278G>C | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 2/18 | chr12 | 30753066 | |||||||
| chr12:30753133 | T | C | 1 | a0002c0002t0002g0258 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.177+211A>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 2/18 | chr12 | 30753133 | |||||||
| chr12:30753150 | T | A | 1 | a0001c0001t0001g0212 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.177+194A>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 2/18 | chr12 | 30753150 | |||||||
| chr12:30753655 | G | A | 1 | a0001c0004t0001g0236 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-39-96C>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 1/18 | chr12 | 30753655 | |||||||
| chr12:30754074 | CACA | C | 15 | a0002c0002t0002g0044 a0002c0002t0002g0240 a0002c0002t0002g0241 others(12): Show |
16 | HG01070.hp1 HG01081.hp1 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.-39-518_-39-516del others(3): Show |
CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 1/18 | chr12 | 30754074 | |||||||
| chr12:30754076 | CAACATTC others(12): Show |
C | 11 | a0002c0002t0002g0012 a0002c0002t0002g0013 a0002c0002t0002g0045 others(8): Show |
20 | HG01074.hp2 HG01361.hp1 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.-39-536_-39-518del others(19): Show |
CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 1/18 | chr12 | 30754076 | |||||||
| chr12:30754176 | G | C | 1 | a0001c0001t0001g0214 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-40+575C>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 1/18 | chr12 | 30754176 | |||||||
| chr12:30754184 | C | T | 1 | a0002c0002t0001g0051 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-40+567G>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 1/18 | chr12 | 30754184 | |||||||
| chr12:30754194 | C | T | 1 | a0003c0003t0001g0050 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-40+557G>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 1/18 | chr12 | 30754194 | |||||||
| chr12:30754365 | G | A | 1 | a0002c0002t0001g0215 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-40+386C>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 1/18 | chr12 | 30754365 | |||||||
| chr12:30754373 | T | C | 1 | a0001c0001t0001g0216 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-40+378A>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 1/18 | chr12 | 30754373 | |||||||
| chr12:30754382 | C | G | 2 | a0006c0010t0001g0217 a0006c0010t0001g0218 |
2 | HG02965.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-40+369G>C | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 1/18 | chr12 | 30754382 | |||||||
| chr12:30754383 | C | T | 2 | a0004c0007t0002g0238 a0004c0007t0002g0239 |
2 | HG01070.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.-40+368G>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 1/18 | chr12 | 30754383 | |||||||
| chr12:30754453 | G | C | 7 | a0002c0002t0001g0041 a0002c0002t0001g0220 a0002c0002t0001g0221 others(4): Show |
8 | HG02109.hp2 HG02451.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.-40+298C>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 1/18 | chr12 | 30754453 | |||||||
| chr12:30754486 | C | T | 1 | a0002c0002t0002g0237 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-40+265G>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 1/18 | chr12 | 30754486 | |||||||
| chr12:30754493 | G | A | 17 | a0001c0001t0001g0234 a0001c0004t0001g0004 a0001c0004t0001g0042 others(14): Show |
25 | HG00408.hp1 HG00544.hp2 HG02071.hp1 others(22): Show |
intron_variant | MODIFIER | c.-40+258C>T | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 1/18 | chr12 | 30754493 | |||||||
| chr12:30754660 | A | C | 28 | a0002c0002t0001g0049 a0002c0002t0002g0012 a0002c0002t0002g0013 others(25): Show |
38 | HG01070.hp1 HG01074.hp2 HG01081.hp1 others(35): Show |
intron_variant | MODIFIER | c.-40+91T>G | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 1/18 | chr12 | 30754660 | |||||||
| chr12:30754674 | C | T | 1 | a0003c0003t0001g0048 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.-40+77G>A | CAPRIN2 | ENSG00000110888.19 | transcript | ENST00000695402.1 | protein_coding | 1/18 | chr12 | 30754674 |