Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 25966 |
| ensemblid | ENSG00000157617.17 |
| hgncid | 1266 |
| symbol | C2CD2 |
| name | C2 calcium dependent domain containing 2 |
| refseq_nuc | NM_015500.2 |
| refseq_prot | NP_056315.1 |
| ensembl_nuc | ENST00000380486.4 |
| ensembl_prot | ENSP00000369853.3 |
| mane_status | MANE Select |
| chr | chr21 |
| start | 41885112 |
| end | 41954018 |
| strand | - |
| ver | v1.2 |
| region | chr21:41885112-41954018 |
| region5000 | chr21:41880112-41959018 |
| regionname0 | C2CD2_chr21_41885112_41954018 |
| regionname5000 | C2CD2_chr21_41880112_41959018 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 696 | 343 | 73 | 64 | 149 | 18 | 37 | 111 | C2CD2_chr21_41880112_41959018 | C2CD2 | MAMAR others(691): Show |
chr21 | 41880112 | 41959018 |
| a0002 | 0/0 | 696 | 23 | 13 | 6 | 0 | 0 | 4 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | MAMAR others(691): Show |
chr21 | 41880112 | 41959018 |
| a0003 | 0/0 | 696 | 21 | 10 | 2 | 8 | 0 | 1 | 5 | C2CD2_chr21_41880112_41959018 | C2CD2 | MAMAR others(691): Show |
chr21 | 41880112 | 41959018 |
| a0004 | 0/0 | 696 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | MAMAR others(691): Show |
chr21 | 41880112 | 41959018 |
| a0005 | 0/0 | 696 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | C2CD2_chr21_41880112_41959018 | C2CD2 | MAMAR others(691): Show |
chr21 | 41880112 | 41959018 |
| a0006 | 0/0 | 696 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | MAMAR others(691): Show |
chr21 | 41880112 | 41959018 |
| a0007 | 0/0 | 696 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | MAMAR others(691): Show |
chr21 | 41880112 | 41959018 |
| a0008 | 0/0 | 696 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | MAMAR others(691): Show |
chr21 | 41880112 | 41959018 |
| a0009 | 0/0 | 696 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | MAMAR others(691): Show |
chr21 | 41880112 | 41959018 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 2088 | 106 | 4 | 22 | 44 | 12 | 23 | C2CD2_chr21_41880112_41959018 | C2CD2 | ATGGC others(2083): Show |
chr21 | 41880112 | 41959018 | ||
| a0001c0002 | 0/0 | 2088 | 90 | 4 | 28 | 49 | 2 | 7 | C2CD2_chr21_41880112_41959018 | C2CD2 | ATGGC others(2083): Show |
chr21 | 41880112 | 41959018 | ||
| a0001c0003 | 0/0 | 2088 | 80 | 18 | 6 | 50 | 3 | 3 | C2CD2_chr21_41880112_41959018 | C2CD2 | ATGGC others(2083): Show |
chr21 | 41880112 | 41959018 | ||
| a0001c0004 | 0/0 | 2088 | 15 | 15 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | ATGGC others(2083): Show |
chr21 | 41880112 | 41959018 | ||
| a0001c0005 | 0/0 | 2088 | 10 | 7 | 2 | 0 | 0 | 1 | C2CD2_chr21_41880112_41959018 | C2CD2 | ATGGC others(2083): Show |
chr21 | 41880112 | 41959018 | ||
| a0001c0006 | 1/0 | 2088 | 10 | 3 | 1 | 2 | 0 | 3 | C2CD2_chr21_41880112_41959018 | C2CD2 | ATGGC others(2083): Show |
chr21 | 41880112 | 41959018 | ||
| a0001c0007 | 0/0 | 2088 | 8 | 6 | 2 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | ATGGC others(2083): Show |
chr21 | 41880112 | 41959018 | ||
| a0001c0011 | 0/0 | 2088 | 5 | 5 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | ATGGC others(2083): Show |
chr21 | 41880112 | 41959018 | ||
| a0001c0013 | 0/0 | 2088 | 4 | 0 | 1 | 3 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | ATGGC others(2083): Show |
chr21 | 41880112 | 41959018 | ||
| a0001c0014 | 0/0 | 2088 | 4 | 4 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | ATGGC others(2083): Show |
chr21 | 41880112 | 41959018 | ||
| a0001c0021 | 0/0 | 2088 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | ATGGC others(2083): Show |
chr21 | 41880112 | 41959018 | ||
| a0001c0023 | 0/0 | 2088 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | ATGGC others(2083): Show |
chr21 | 41880112 | 41959018 | ||
| a0001c0024 | 0/0 | 2088 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | ATGGC others(2083): Show |
chr21 | 41880112 | 41959018 | ||
| a0001c0025 | 0/0 | 2088 | 1 | 0 | 0 | 0 | 1 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | ATGGC others(2083): Show |
chr21 | 41880112 | 41959018 | ||
| a0001c0028 | 0/0 | 2088 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | ATGGC others(2083): Show |
chr21 | 41880112 | 41959018 | ||
| a0001c0032 | 0/0 | 2088 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | ATGGC others(2083): Show |
chr21 | 41880112 | 41959018 | ||
| a0001c0033 | 0/0 | 2088 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | ATGGC others(2083): Show |
chr21 | 41880112 | 41959018 | ||
| a0001c0037 | 0/0 | 2088 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | ATGGC others(2083): Show |
chr21 | 41880112 | 41959018 | ||
| a0001c0039 | 0/0 | 2088 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | ATGGC others(2083): Show |
chr21 | 41880112 | 41959018 | ||
| a0001c0040 | 0/0 | 2088 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | ATGGC others(2083): Show |
chr21 | 41880112 | 41959018 | ||
| a0001c0042 | 0/0 | 2088 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | ATGGC others(2083): Show |
chr21 | 41880112 | 41959018 | ||
| a0002c0008 | 0/0 | 2088 | 7 | 7 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | ATGGC others(2083): Show |
chr21 | 41880112 | 41959018 | ||
| a0002c0010 | 0/0 | 2088 | 6 | 0 | 2 | 0 | 0 | 4 | C2CD2_chr21_41880112_41959018 | C2CD2 | ATGGC others(2083): Show |
chr21 | 41880112 | 41959018 | ||
| a0002c0012 | 0/0 | 2088 | 5 | 3 | 2 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | ATGGC others(2083): Show |
chr21 | 41880112 | 41959018 | ||
| a0002c0018 | 0/0 | 2088 | 3 | 2 | 1 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | ATGGC others(2083): Show |
chr21 | 41880112 | 41959018 | ||
| a0002c0027 | 0/0 | 2088 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | ATGGC others(2083): Show |
chr21 | 41880112 | 41959018 | ||
| a0002c0041 | 0/0 | 2088 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | ATGGC others(2083): Show |
chr21 | 41880112 | 41959018 | ||
| a0003c0009 | 0/0 | 2088 | 6 | 0 | 0 | 5 | 0 | 1 | C2CD2_chr21_41880112_41959018 | C2CD2 | ATGGC others(2083): Show |
chr21 | 41880112 | 41959018 | ||
| a0003c0015 | 0/0 | 2088 | 4 | 2 | 2 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | ATGGC others(2083): Show |
chr21 | 41880112 | 41959018 | ||
| a0003c0017 | 0/0 | 2088 | 3 | 3 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | ATGGC others(2083): Show |
chr21 | 41880112 | 41959018 | ||
| a0003c0020 | 0/0 | 2088 | 2 | 0 | 0 | 2 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | ATGGC others(2083): Show |
chr21 | 41880112 | 41959018 | ||
| a0003c0022 | 0/0 | 2088 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | ATGGC others(2083): Show |
chr21 | 41880112 | 41959018 | ||
| a0003c0029 | 0/0 | 2088 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | ATGGC others(2083): Show |
chr21 | 41880112 | 41959018 | ||
| a0003c0031 | 0/0 | 2088 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | ATGGC others(2083): Show |
chr21 | 41880112 | 41959018 | ||
| a0003c0034 | 0/0 | 2088 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | ATGGC others(2083): Show |
chr21 | 41880112 | 41959018 | ||
| a0003c0036 | 0/0 | 2088 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | ATGGC others(2083): Show |
chr21 | 41880112 | 41959018 | ||
| a0003c0038 | 0/0 | 2088 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | ATGGC others(2083): Show |
chr21 | 41880112 | 41959018 | ||
| a0004c0016 | 0/0 | 2088 | 3 | 0 | 3 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | ATGGC others(2083): Show |
chr21 | 41880112 | 41959018 | ||
| a0005c0019 | 0/0 | 2088 | 2 | 0 | 0 | 2 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | ATGGC others(2083): Show |
chr21 | 41880112 | 41959018 | ||
| a0006c0035 | 0/0 | 2088 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | ATGGC others(2083): Show |
chr21 | 41880112 | 41959018 | ||
| a0007c0030 | 0/0 | 2088 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | ATGGC others(2083): Show |
chr21 | 41880112 | 41959018 | ||
| a0008c0043 | 0/0 | 2088 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | ATGGC others(2083): Show |
chr21 | 41880112 | 41959018 | ||
| a0009c0026 | 0/0 | 2088 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | ATGGC others(2083): Show |
chr21 | 41880112 | 41959018 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 6472 | 14 | 0 | 1 | 9 | 0 | 4 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6467): Show |
chr21 | 41880112 | 41959018 |
| a0001c0001t0002 | 0/0 | 6473 | 28 | 0 | 8 | 11 | 3 | 6 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6468): Show |
chr21 | 41880112 | 41959018 |
| a0001c0001t0003 | 0/0 | 6472 | 16 | 0 | 3 | 9 | 1 | 3 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6467): Show |
chr21 | 41880112 | 41959018 |
| a0001c0001t0004 | 0/1 | 6472 | 16 | 0 | 6 | 6 | 2 | 1 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6467): Show |
chr21 | 41880112 | 41959018 |
| a0001c0001t0005 | 0/0 | 6472 | 4 | 1 | 0 | 0 | 0 | 3 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6467): Show |
chr21 | 41880112 | 41959018 |
| a0001c0001t0006 | 0/0 | 6472 | 5 | 0 | 3 | 2 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6467): Show |
chr21 | 41880112 | 41959018 |
| a0001c0001t0007 | 0/0 | 6472 | 3 | 1 | 0 | 0 | 2 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6467): Show |
chr21 | 41880112 | 41959018 |
| a0001c0001t0008 | 0/0 | 6470 | 2 | 0 | 0 | 0 | 1 | 1 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6465): Show |
chr21 | 41880112 | 41959018 |
| a0001c0001t0011 | 0/0 | 6472 | 2 | 0 | 0 | 2 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6467): Show |
chr21 | 41880112 | 41959018 |
| a0001c0001t0013 | 0/0 | 6472 | 2 | 1 | 0 | 0 | 1 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6467): Show |
chr21 | 41880112 | 41959018 |
| a0001c0001t0014 | 0/0 | 6472 | 3 | 0 | 0 | 3 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6467): Show |
chr21 | 41880112 | 41959018 |
| a0001c0001t0019 | 0/0 | 6472 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6467): Show |
chr21 | 41880112 | 41959018 |
| a0001c0001t0023 | 0/0 | 6473 | 2 | 0 | 0 | 0 | 2 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6468): Show |
chr21 | 41880112 | 41959018 |
| a0001c0001t0026 | 0/0 | 6473 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6468): Show |
chr21 | 41880112 | 41959018 |
| a0001c0001t0036 | 0/0 | 6473 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6468): Show |
chr21 | 41880112 | 41959018 |
| a0001c0001t0038 | 0/0 | 6473 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6468): Show |
chr21 | 41880112 | 41959018 |
| a0001c0001t0039 | 0/0 | 6472 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6467): Show |
chr21 | 41880112 | 41959018 |
| a0001c0001t0040 | 0/0 | 6472 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6467): Show |
chr21 | 41880112 | 41959018 |
| a0001c0001t0049 | 0/0 | 6469 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6464): Show |
chr21 | 41880112 | 41959018 |
| a0001c0001t0052 | 0/0 | 6472 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6467): Show |
chr21 | 41880112 | 41959018 |
| a0001c0001t0053 | 0/0 | 6472 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6467): Show |
chr21 | 41880112 | 41959018 |
| a0001c0002t0001 | 0/0 | 6472 | 19 | 0 | 12 | 4 | 0 | 3 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6467): Show |
chr21 | 41880112 | 41959018 |
| a0001c0002t0002 | 0/0 | 6473 | 24 | 0 | 8 | 15 | 0 | 1 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6468): Show |
chr21 | 41880112 | 41959018 |
| a0001c0002t0003 | 0/0 | 6472 | 13 | 1 | 3 | 8 | 0 | 1 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6467): Show |
chr21 | 41880112 | 41959018 |
| a0001c0002t0004 | 0/0 | 6472 | 13 | 0 | 0 | 12 | 0 | 1 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6467): Show |
chr21 | 41880112 | 41959018 |
| a0001c0002t0005 | 0/0 | 6472 | 3 | 2 | 1 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6467): Show |
chr21 | 41880112 | 41959018 |
| a0001c0002t0006 | 0/0 | 6472 | 5 | 0 | 0 | 5 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6467): Show |
chr21 | 41880112 | 41959018 |
| a0001c0002t0007 | 0/0 | 6472 | 3 | 0 | 1 | 0 | 2 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6467): Show |
chr21 | 41880112 | 41959018 |
| a0001c0002t0008 | 0/0 | 6470 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6465): Show |
chr21 | 41880112 | 41959018 |
| a0001c0002t0011 | 0/0 | 6472 | 2 | 0 | 0 | 2 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6467): Show |
chr21 | 41880112 | 41959018 |
| a0001c0002t0017 | 0/0 | 6471 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6466): Show |
chr21 | 41880112 | 41959018 |
| a0001c0002t0019 | 0/0 | 6472 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6467): Show |
chr21 | 41880112 | 41959018 |
| a0001c0002t0021 | 0/0 | 6473 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6468): Show |
chr21 | 41880112 | 41959018 |
| a0001c0002t0025 | 0/0 | 6473 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6468): Show |
chr21 | 41880112 | 41959018 |
| a0001c0002t0028 | 0/0 | 6473 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6468): Show |
chr21 | 41880112 | 41959018 |
| a0001c0002t0029 | 0/0 | 6472 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6467): Show |
chr21 | 41880112 | 41959018 |
| a0001c0002t0030 | 0/0 | 6472 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6467): Show |
chr21 | 41880112 | 41959018 |
| a0001c0003t0001 | 0/0 | 6472 | 22 | 5 | 1 | 16 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6467): Show |
chr21 | 41880112 | 41959018 |
| a0001c0003t0002 | 0/0 | 6473 | 2 | 0 | 0 | 2 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6468): Show |
chr21 | 41880112 | 41959018 |
| a0001c0003t0003 | 0/0 | 6472 | 17 | 0 | 2 | 14 | 0 | 1 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6467): Show |
chr21 | 41880112 | 41959018 |
| a0001c0003t0004 | 0/0 | 6472 | 7 | 0 | 0 | 7 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6467): Show |
chr21 | 41880112 | 41959018 |
| a0001c0003t0005 | 0/0 | 6472 | 6 | 4 | 2 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6467): Show |
chr21 | 41880112 | 41959018 |
| a0001c0003t0006 | 0/0 | 6472 | 6 | 0 | 0 | 5 | 0 | 1 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6467): Show |
chr21 | 41880112 | 41959018 |
| a0001c0003t0007 | 0/0 | 6472 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6467): Show |
chr21 | 41880112 | 41959018 |
| a0001c0003t0008 | 0/0 | 6470 | 3 | 0 | 1 | 0 | 2 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6465): Show |
chr21 | 41880112 | 41959018 |
| a0001c0003t0009 | 0/0 | 6473 | 2 | 2 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6468): Show |
chr21 | 41880112 | 41959018 |
| a0001c0003t0010 | 0/0 | 6472 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6467): Show |
chr21 | 41880112 | 41959018 |
| a0001c0003t0011 | 0/0 | 6472 | 3 | 0 | 0 | 3 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6467): Show |
chr21 | 41880112 | 41959018 |
| a0001c0003t0012 | 0/0 | 6472 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6467): Show |
chr21 | 41880112 | 41959018 |
| a0001c0003t0015 | 0/0 | 6472 | 3 | 3 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6467): Show |
chr21 | 41880112 | 41959018 |
| a0001c0003t0016 | 0/0 | 6469 | 1 | 0 | 0 | 0 | 1 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6464): Show |
chr21 | 41880112 | 41959018 |
| a0001c0003t0020 | 0/0 | 6472 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6467): Show |
chr21 | 41880112 | 41959018 |
| a0001c0003t0027 | 0/0 | 6471 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6466): Show |
chr21 | 41880112 | 41959018 |
| a0001c0003t0035 | 0/0 | 6474 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6469): Show |
chr21 | 41880112 | 41959018 |
| a0001c0003t0037 | 0/0 | 6472 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6467): Show |
chr21 | 41880112 | 41959018 |
| a0001c0003t0043 | 0/0 | 6472 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6467): Show |
chr21 | 41880112 | 41959018 |
| a0001c0004t0004 | 0/0 | 6472 | 2 | 2 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6467): Show |
chr21 | 41880112 | 41959018 |
| a0001c0004t0005 | 0/0 | 6472 | 4 | 4 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6467): Show |
chr21 | 41880112 | 41959018 |
| a0001c0004t0006 | 0/0 | 6472 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6467): Show |
chr21 | 41880112 | 41959018 |
| a0001c0004t0009 | 0/0 | 6473 | 3 | 3 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6468): Show |
chr21 | 41880112 | 41959018 |
| a0001c0004t0017 | 0/0 | 6471 | 2 | 2 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6466): Show |
chr21 | 41880112 | 41959018 |
| a0001c0004t0022 | 0/0 | 6473 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6468): Show |
chr21 | 41880112 | 41959018 |
| a0001c0004t0024 | 0/0 | 6472 | 2 | 2 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6467): Show |
chr21 | 41880112 | 41959018 |
| a0001c0005t0002 | 0/0 | 6473 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6468): Show |
chr21 | 41880112 | 41959018 |
| a0001c0005t0005 | 0/0 | 6472 | 6 | 6 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6467): Show |
chr21 | 41880112 | 41959018 |
| a0001c0005t0007 | 0/0 | 6472 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6467): Show |
chr21 | 41880112 | 41959018 |
| a0001c0005t0008 | 0/0 | 6470 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6465): Show |
chr21 | 41880112 | 41959018 |
| a0001c0005t0044 | 0/0 | 6472 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6467): Show |
chr21 | 41880112 | 41959018 |
| a0001c0006t0001 | 0/0 | 6472 | 2 | 0 | 0 | 2 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6467): Show |
chr21 | 41880112 | 41959018 |
| a0001c0006t0002 | 1/0 | 6473 | 1 | 0 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6468): Show |
chr21 | 41880112 | 41959018 |
| a0001c0006t0003 | 0/0 | 6472 | 2 | 0 | 0 | 0 | 0 | 2 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6467): Show |
chr21 | 41880112 | 41959018 |
| a0001c0006t0005 | 0/0 | 6472 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6467): Show |
chr21 | 41880112 | 41959018 |
| a0001c0006t0008 | 0/0 | 6470 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6465): Show |
chr21 | 41880112 | 41959018 |
| a0001c0006t0009 | 0/0 | 6473 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6468): Show |
chr21 | 41880112 | 41959018 |
| a0001c0006t0034 | 0/0 | 6473 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6468): Show |
chr21 | 41880112 | 41959018 |
| a0001c0006t0048 | 0/0 | 6472 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6467): Show |
chr21 | 41880112 | 41959018 |
| a0001c0007t0001 | 0/0 | 6472 | 3 | 2 | 1 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6467): Show |
chr21 | 41880112 | 41959018 |
| a0001c0007t0005 | 0/0 | 6472 | 3 | 2 | 1 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6467): Show |
chr21 | 41880112 | 41959018 |
| a0001c0007t0006 | 0/0 | 6472 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6467): Show |
chr21 | 41880112 | 41959018 |
| a0001c0007t0012 | 0/0 | 6472 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6467): Show |
chr21 | 41880112 | 41959018 |
| a0001c0011t0005 | 0/0 | 6472 | 2 | 2 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6467): Show |
chr21 | 41880112 | 41959018 |
| a0001c0011t0010 | 0/0 | 6472 | 3 | 3 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6467): Show |
chr21 | 41880112 | 41959018 |
| a0001c0013t0001 | 0/0 | 6472 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6467): Show |
chr21 | 41880112 | 41959018 |
| a0001c0013t0002 | 0/0 | 6473 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6468): Show |
chr21 | 41880112 | 41959018 |
| a0001c0013t0004 | 0/0 | 6472 | 2 | 0 | 0 | 2 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6467): Show |
chr21 | 41880112 | 41959018 |
| a0001c0014t0005 | 0/0 | 6472 | 2 | 2 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6467): Show |
chr21 | 41880112 | 41959018 |
| a0001c0014t0021 | 0/0 | 6473 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6468): Show |
chr21 | 41880112 | 41959018 |
| a0001c0014t0047 | 0/0 | 6472 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6467): Show |
chr21 | 41880112 | 41959018 |
| a0001c0021t0005 | 0/0 | 6472 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6467): Show |
chr21 | 41880112 | 41959018 |
| a0001c0023t0005 | 0/0 | 6472 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6467): Show |
chr21 | 41880112 | 41959018 |
| a0001c0024t0012 | 0/0 | 6472 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6467): Show |
chr21 | 41880112 | 41959018 |
| a0001c0025t0004 | 0/0 | 6472 | 1 | 0 | 0 | 0 | 1 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6467): Show |
chr21 | 41880112 | 41959018 |
| a0001c0028t0020 | 0/0 | 6472 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6467): Show |
chr21 | 41880112 | 41959018 |
| a0001c0032t0010 | 0/0 | 6472 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6467): Show |
chr21 | 41880112 | 41959018 |
| a0001c0033t0018 | 0/0 | 6468 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6463): Show |
chr21 | 41880112 | 41959018 |
| a0001c0037t0004 | 0/0 | 6472 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6467): Show |
chr21 | 41880112 | 41959018 |
| a0001c0039t0013 | 0/0 | 6472 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6467): Show |
chr21 | 41880112 | 41959018 |
| a0001c0040t0008 | 0/0 | 6470 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6465): Show |
chr21 | 41880112 | 41959018 |
| a0001c0042t0046 | 0/0 | 6472 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6467): Show |
chr21 | 41880112 | 41959018 |
| a0002c0008t0001 | 0/0 | 6472 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6467): Show |
chr21 | 41880112 | 41959018 |
| a0002c0008t0005 | 0/0 | 6472 | 4 | 4 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6467): Show |
chr21 | 41880112 | 41959018 |
| a0002c0008t0009 | 0/0 | 6473 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6468): Show |
chr21 | 41880112 | 41959018 |
| a0002c0008t0045 | 0/0 | 6472 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6467): Show |
chr21 | 41880112 | 41959018 |
| a0002c0010t0001 | 0/0 | 6472 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6467): Show |
chr21 | 41880112 | 41959018 |
| a0002c0010t0007 | 0/0 | 6472 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6467): Show |
chr21 | 41880112 | 41959018 |
| a0002c0010t0008 | 0/0 | 6470 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6465): Show |
chr21 | 41880112 | 41959018 |
| a0002c0010t0016 | 0/0 | 6469 | 2 | 0 | 2 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6464): Show |
chr21 | 41880112 | 41959018 |
| a0002c0010t0031 | 0/0 | 6472 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6467): Show |
chr21 | 41880112 | 41959018 |
| a0002c0012t0009 | 0/0 | 6473 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6468): Show |
chr21 | 41880112 | 41959018 |
| a0002c0012t0012 | 0/0 | 6472 | 3 | 3 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6467): Show |
chr21 | 41880112 | 41959018 |
| a0002c0012t0050 | 0/0 | 6474 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6469): Show |
chr21 | 41880112 | 41959018 |
| a0002c0018t0005 | 0/0 | 6472 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6467): Show |
chr21 | 41880112 | 41959018 |
| a0002c0018t0010 | 0/0 | 6472 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6467): Show |
chr21 | 41880112 | 41959018 |
| a0002c0018t0022 | 0/0 | 6473 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6468): Show |
chr21 | 41880112 | 41959018 |
| a0002c0027t0009 | 0/0 | 6473 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6468): Show |
chr21 | 41880112 | 41959018 |
| a0002c0041t0033 | 0/0 | 6470 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6465): Show |
chr21 | 41880112 | 41959018 |
| a0003c0009t0002 | 0/0 | 6473 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6468): Show |
chr21 | 41880112 | 41959018 |
| a0003c0009t0007 | 0/0 | 6472 | 4 | 0 | 0 | 3 | 0 | 1 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6467): Show |
chr21 | 41880112 | 41959018 |
| a0003c0009t0032 | 0/0 | 6472 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6467): Show |
chr21 | 41880112 | 41959018 |
| a0003c0015t0005 | 0/0 | 6472 | 3 | 1 | 2 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6467): Show |
chr21 | 41880112 | 41959018 |
| a0003c0015t0010 | 0/0 | 6472 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6467): Show |
chr21 | 41880112 | 41959018 |
| a0003c0017t0005 | 0/0 | 6472 | 2 | 2 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6467): Show |
chr21 | 41880112 | 41959018 |
| a0003c0017t0018 | 0/0 | 6468 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6463): Show |
chr21 | 41880112 | 41959018 |
| a0003c0020t0007 | 0/0 | 6472 | 2 | 0 | 0 | 2 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6467): Show |
chr21 | 41880112 | 41959018 |
| a0003c0022t0042 | 0/0 | 6473 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6468): Show |
chr21 | 41880112 | 41959018 |
| a0003c0029t0004 | 0/0 | 6472 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6467): Show |
chr21 | 41880112 | 41959018 |
| a0003c0031t0018 | 0/0 | 6468 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6463): Show |
chr21 | 41880112 | 41959018 |
| a0003c0034t0004 | 0/0 | 6472 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6467): Show |
chr21 | 41880112 | 41959018 |
| a0003c0036t0051 | 0/0 | 6473 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6468): Show |
chr21 | 41880112 | 41959018 |
| a0003c0038t0007 | 0/0 | 6472 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6467): Show |
chr21 | 41880112 | 41959018 |
| a0004c0016t0001 | 0/0 | 6472 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6467): Show |
chr21 | 41880112 | 41959018 |
| a0004c0016t0004 | 0/0 | 6472 | 2 | 0 | 2 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6467): Show |
chr21 | 41880112 | 41959018 |
| a0005c0019t0003 | 0/0 | 6472 | 2 | 0 | 0 | 2 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6467): Show |
chr21 | 41880112 | 41959018 |
| a0006c0035t0003 | 0/0 | 6472 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6467): Show |
chr21 | 41880112 | 41959018 |
| a0007c0030t0001 | 0/0 | 6472 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6467): Show |
chr21 | 41880112 | 41959018 |
| a0008c0043t0041 | 0/0 | 6472 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6467): Show |
chr21 | 41880112 | 41959018 |
| a0009c0026t0004 | 0/0 | 6472 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | AGAGC others(6467): Show |
chr21 | 41880112 | 41959018 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0001t0001g0353 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0001t0001g0380 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0001t0002g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0001t0002g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0001t0002g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0001t0002g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0001t0002g0367 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0001t0002g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0001t0002g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0001t0002g0386 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0001t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0001t0003g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0001t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0001t0003g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0001t0003g0351 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0001t0003g0366 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0001t0003g0383 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0001t0003g0384 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0001t0004g0039 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0001t0004g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0001t0004g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0001t0004g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0001t0004g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0001t0004g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0001t0004g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0001t0004g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0001t0004g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0001t0004g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0001t0004g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0001t0004g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0001t0004g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0001t0004g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0001t0004g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0001t0004g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0001t0005g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0001t0005g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0001t0005g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0001t0005g0379 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0001t0006g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0001t0006g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0001t0006g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0001t0006g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0001t0006g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0001t0007g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0001t0007g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0001t0007g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0001t0008g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0001t0008g0309 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0001t0011g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0001t0011g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0001t0013g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0001t0013g0371 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0001t0014g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0001t0014g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0001t0014g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0001t0019g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0001t0023g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0001t0023g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0001t0026g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0001t0036g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0001t0038g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0001t0039g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0001t0040g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0001t0049g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0001t0052g0394 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0001t0053g0395 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0002t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0002t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0002t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0002t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0002t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0002t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0002t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0002t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0002t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0002t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0002t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0002t0001g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0002t0001g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0002t0001g0362 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0002t0001g0393 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0002t0002g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0002t0002g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0002t0002g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0002t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0002t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0002t0002g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0002t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0002t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0002t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0002t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0002t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0002t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0002t0002g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0002t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0002t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0002t0002g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0002t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0002t0002g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0002t0002g0376 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0002t0002g0382 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0002t0002g0388 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0002t0003g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0002t0003g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0002t0003g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0002t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0002t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0002t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0002t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0002t0003g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0002t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0002t0003g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0002t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0002t0003g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0002t0003g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0002t0004g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0002t0004g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0002t0004g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0002t0004g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0002t0004g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0002t0004g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0002t0004g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0002t0004g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0002t0004g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0002t0004g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0002t0004g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0002t0004g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0002t0004g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0002t0005g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0002t0005g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0002t0005g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0002t0006g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0002t0006g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0002t0006g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0002t0006g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0002t0006g0381 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0002t0007g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0002t0007g0345 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0002t0007g0378 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0002t0008g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0002t0011g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0002t0011g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0002t0017g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0002t0019g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0002t0021g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0002t0025g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0002t0028g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0002t0029g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0002t0030g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0003t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0003t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0003t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0003t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0003t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0003t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0003t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0003t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0003t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0003t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0003t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0003t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0003t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0003t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0003t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0003t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0003t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0003t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0003t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0003t0001g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0003t0001g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0003t0001g0385 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0003t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0003t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0003t0003g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0003t0003g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0003t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0003t0003g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0003t0003g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0003t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0003t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0003t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0003t0003g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0003t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0003t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0003t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0003t0003g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0003t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0003t0003g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0003t0003g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0003t0003g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0003t0004g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0003t0004g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0003t0004g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0003t0004g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0003t0004g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0003t0004g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0003t0004g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0003t0005g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0003t0005g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0003t0005g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0003t0005g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0003t0005g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0003t0005g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0003t0006g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0003t0006g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0003t0006g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0003t0006g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0003t0006g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0003t0006g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0003t0007g0370 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0003t0008g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0003t0008g0341 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0003t0008g0347 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0003t0009g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0003t0009g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0003t0010g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0003t0011g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0003t0011g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0003t0011g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0003t0012g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0003t0015g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0003t0015g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0003t0015g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0003t0016g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0003t0020g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0003t0027g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0003t0035g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0003t0037g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0003t0043g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0004t0004g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0004t0004g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0004t0005g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0004t0005g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0004t0005g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0004t0005g0390 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0004t0006g0392 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0004t0009g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0004t0009g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0004t0009g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0004t0017g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0004t0017g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0004t0022g0391 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0004t0024g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0004t0024g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0005t0002g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0005t0005g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0005t0005g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0005t0005g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0005t0005g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0005t0005g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0005t0007g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0005t0008g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0005t0044g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0006t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0006t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0006t0002g0165 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0006t0003g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0006t0003g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0006t0005g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0006t0008g0387 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0006t0009g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0006t0034g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0006t0048g0357 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0007t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0007t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0007t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0007t0005g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0007t0005g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0007t0005g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0007t0006g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0007t0012g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0011t0005g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0011t0005g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0011t0010g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0011t0010g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0011t0010g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0013t0001g0389 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0013t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0013t0004g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0013t0004g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0014t0005g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0014t0005g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0014t0021g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0014t0047g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0021t0005g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0023t0005g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0024t0012g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0025t0004g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0028t0020g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0032t0010g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0033t0018g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0037t0004g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0039t0013g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0040t0008g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0001c0042t0046g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0002c0008t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0002c0008t0005g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0002c0008t0005g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0002c0008t0005g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0002c0008t0005g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0002c0008t0009g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0002c0008t0045g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0002c0010t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0002c0010t0007g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0002c0010t0008g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0002c0010t0016g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0002c0010t0016g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0002c0010t0031g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0002c0012t0009g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0002c0012t0012g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0002c0012t0012g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0002c0012t0012g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0002c0012t0050g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0002c0018t0005g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0002c0018t0010g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0002c0018t0022g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0002c0027t0009g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0002c0041t0033g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0003c0009t0002g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0003c0009t0007g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0003c0009t0007g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0003c0009t0007g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0003c0009t0007g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0003c0009t0032g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0003c0015t0005g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0003c0015t0005g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0003c0015t0005g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0003c0015t0010g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0003c0017t0005g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0003c0017t0005g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0003c0017t0018g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0003c0020t0007g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0003c0020t0007g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0003c0022t0042g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0003c0029t0004g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0003c0031t0018g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0003c0034t0004g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0003c0036t0051g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0003c0038t0007g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0004c0016t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0004c0016t0004g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0004c0016t0004g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0005c0019t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0005c0019t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0006c0035t0003g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0007c0030t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0008c0043t0041g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| a0009c0026t0004g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0007 | g0175 | EUR | GBR | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG00099 | hp2 | a0001 | c0003 | t0008 | g0347 | EUR | GBR | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0058 | EUR | GBR | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG00140 | hp2 | a0001 | c0003 | t0008 | g0341 | EUR | GBR | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG00280 | hp1 | a0001 | c0001 | t0013 | g0371 | EUR | FIN | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG00280 | hp2 | a0001 | c0001 | t0007 | g0159 | EUR | FIN | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG00323 | hp1 | a0001 | c0001 | t0004 | g0266 | EUR | FIN | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG00323 | hp2 | a0001 | c0001 | t0004 | g0152 | EUR | FIN | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0076 | EAS | CHS | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG00408 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | CHS | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG00438 | hp1 | a0001 | c0003 | t0003 | g0196 | EAS | CHS | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG00438 | hp2 | a0001 | c0003 | t0011 | g0108 | EAS | CHS | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG00597 | hp1 | a0001 | c0001 | t0003 | g0177 | EAS | CHS | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG00597 | hp2 | a0001 | c0002 | t0006 | g0071 | EAS | CHS | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG00609 | hp1 | a0001 | c0002 | t0004 | g0185 | EAS | CHS | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG00609 | hp2 | a0003 | c0009 | t0007 | g0352 | EAS | CHS | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG00621 | hp1 | a0001 | c0001 | t0004 | g0198 | EAS | CHS | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG00621 | hp2 | a0001 | c0003 | t0043 | g0201 | EAS | CHS | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG00639 | hp1 | a0002 | c0010 | t0016 | g0340 | AMR | PUR | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG00639 | hp2 | a0001 | c0001 | t0006 | g0276 | AMR | PUR | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG00642 | hp1 | a0001 | c0001 | t0006 | g0277 | AMR | PUR | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG00642 | hp2 | a0002 | c0010 | t0016 | g0292 | AMR | PUR | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG00673 | hp1 | a0003 | c0009 | t0002 | g0369 | EAS | CHS | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG00673 | hp2 | a0001 | c0002 | t0030 | g0106 | EAS | CHS | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG00735 | hp1 | a0001 | c0002 | t0002 | g0119 | AMR | PUR | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0046 | AMR | PUR | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG00738 | hp1 | a0001 | c0005 | t0008 | g0307 | AMR | PUR | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG00738 | hp2 | a0001 | c0002 | t0001 | g0393 | AMR | PUR | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG00741 | hp1 | a0004 | c0016 | t0004 | g0134 | AMR | PUR | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG00741 | hp2 | a0001 | c0007 | t0005 | g0059 | AMR | PUR | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG01069 | hp1 | a0001 | c0002 | t0002 | g0388 | AMR | PUR | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG01069 | hp2 | a0001 | c0002 | t0001 | g0275 | AMR | PUR | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG01070 | hp1 | a0001 | c0003 | t0005 | g0332 | AMR | PUR | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG01070 | hp2 | a0001 | c0040 | t0008 | g0305 | AMR | PUR | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG01071 | hp1 | a0001 | c0003 | t0005 | g0335 | AMR | PUR | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG01071 | hp2 | a0001 | c0002 | t0002 | g0274 | AMR | PUR | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG01074 | hp1 | a0001 | c0001 | t0004 | g0288 | AMR | PUR | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0154 | AMR | PUR | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG01099 | hp1 | a0001 | c0005 | t0007 | g0310 | AMR | PUR | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG01099 | hp2 | a0001 | c0001 | t0036 | g0356 | AMR | PUR | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG01106 | hp1 | a0001 | c0002 | t0021 | g0320 | AMR | PUR | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG01106 | hp2 | a0001 | c0001 | t0004 | g0149 | AMR | PUR | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG01109 | hp1 | a0001 | c0002 | t0005 | g0303 | AMR | PUR | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG01109 | hp2 | a0001 | c0002 | t0001 | g0359 | AMR | PUR | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG01167 | hp1 | a0002 | c0012 | t0050 | g0063 | AMR | PUR | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG01167 | hp2 | a0001 | c0007 | t0001 | g0253 | AMR | PUR | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG01168 | hp1 | a0002 | c0041 | t0033 | g0308 | AMR | PUR | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG01168 | hp2 | a0001 | c0001 | t0004 | g0297 | AMR | PUR | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG01169 | hp1 | a0002 | c0012 | t0009 | g0062 | AMR | PUR | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG01169 | hp2 | a0001 | c0001 | t0004 | g0298 | AMR | PUR | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG01175 | hp1 | a0001 | c0001 | t0004 | g0148 | AMR | PUR | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG01175 | hp2 | a0001 | c0002 | t0003 | g0365 | AMR | PUR | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG01192 | hp1 | a0004 | c0016 | t0004 | g0135 | AMR | PUR | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG01243 | hp1 | a0001 | c0002 | t0007 | g0318 | AMR | PUR | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG01243 | hp2 | a0002 | c0018 | t0010 | g0150 | AMR | PUR | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0342 | AMR | CLM | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0291 | AMR | CLM | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG01257 | hp1 | a0003 | c0015 | t0005 | g0329 | AMR | CLM | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG01257 | hp2 | a0001 | c0013 | t0002 | g0128 | AMR | CLM | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG01258 | hp1 | a0001 | c0002 | t0001 | g0319 | AMR | CLM | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG01258 | hp2 | a0003 | c0015 | t0005 | g0330 | AMR | CLM | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG01261 | hp1 | a0001 | c0002 | t0029 | g0363 | AMR | CLM | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0112 | AMR | CLM | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG01346 | hp1 | a0001 | c0003 | t0008 | g0155 | AMR | CLM | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG01346 | hp2 | a0001 | c0002 | t0002 | g0130 | AMR | CLM | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG01358 | hp1 | a0001 | c0002 | t0003 | g0182 | AMR | CLM | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG01358 | hp2 | a0001 | c0002 | t0002 | g0129 | AMR | CLM | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG01361 | hp1 | a0001 | c0002 | t0003 | g0299 | AMR | CLM | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG01361 | hp2 | a0001 | c0003 | t0001 | g0224 | AMR | CLM | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG01433 | hp1 | a0001 | c0001 | t0003 | g0290 | AMR | CLM | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG01433 | hp2 | a0001 | c0001 | t0003 | g0384 | AMR | CLM | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG01496 | hp1 | a0001 | c0003 | t0003 | g0065 | AMR | CLM | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG01496 | hp2 | a0001 | c0001 | t0004 | g0317 | AMR | CLM | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG01515 | hp1 | a0001 | c0001 | t0003 | g0366 | EUR | IBS | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG01515 | hp2 | a0001 | c0001 | t0023 | g0057 | EUR | IBS | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG01516 | hp1 | a0001 | c0025 | t0004 | g0273 | EUR | IBS | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0300 | EUR | IBS | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG01517 | hp1 | a0001 | c0001 | t0023 | g0052 | EUR | IBS | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0301 | EUR | IBS | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG01884 | hp1 | a0001 | c0004 | t0009 | g0223 | AFR | ACB | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG01884 | hp2 | a0002 | c0008 | t0045 | g0226 | AFR | ACB | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG01891 | hp1 | a0001 | c0011 | t0010 | g0245 | AFR | ACB | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG01891 | hp2 | a0001 | c0002 | t0003 | g0145 | AFR | ACB | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG01934 | hp1 | a0006 | c0035 | t0003 | g0116 | AMR | PEL | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG01934 | hp2 | a0001 | c0001 | t0006 | g0173 | AMR | PEL | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG01943 | hp1 | a0001 | c0002 | t0001 | g0127 | AMR | PEL | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG01943 | hp2 | a0001 | c0002 | t0002 | g0126 | AMR | PEL | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG01952 | hp1 | a0001 | c0003 | t0003 | g0268 | AMR | PEL | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0168 | AMR | PEL | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG01978 | hp1 | a0001 | c0002 | t0001 | g0120 | AMR | PEL | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0124 | AMR | PEL | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG01981 | hp1 | a0001 | c0039 | t0013 | g0302 | AMR | PEL | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG01981 | hp2 | a0001 | c0002 | t0001 | g0176 | AMR | PEL | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG01993 | hp1 | a0001 | c0002 | t0008 | g0311 | AMR | PEL | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG01993 | hp2 | a0001 | c0002 | t0002 | g0172 | AMR | PEL | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG02004 | hp1 | a0004 | c0016 | t0001 | g0191 | AMR | PEL | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG02004 | hp2 | a0001 | c0002 | t0002 | g0136 | AMR | PEL | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG02015 | hp1 | a0001 | c0001 | t0003 | g0081 | EAS | KHV | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG02015 | hp2 | a0001 | c0001 | t0004 | g0338 | EAS | KHV | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG02027 | hp1 | a0001 | c0002 | t0004 | g0114 | EAS | KHV | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG02027 | hp2 | a0001 | c0003 | t0001 | g0258 | EAS | KHV | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG02040 | hp1 | a0001 | c0003 | t0001 | g0385 | EAS | KHV | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG02040 | hp2 | a0001 | c0002 | t0006 | g0192 | EAS | KHV | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG02056 | hp1 | a0001 | c0003 | t0006 | g0215 | EAS | KHV | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG02056 | hp2 | a0001 | c0003 | t0037 | g0257 | EAS | KHV | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG02071 | hp1 | a0001 | c0003 | t0003 | g0019 | EAS | KHV | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG02071 | hp2 | a0001 | c0002 | t0006 | g0096 | EAS | KHV | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG02080 | hp1 | a0001 | c0002 | t0004 | g0115 | EAS | KHV | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG02080 | hp2 | a0001 | c0002 | t0004 | g0343 | EAS | KHV | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG02083 | hp1 | a0001 | c0003 | t0004 | g0213 | EAS | KHV | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG02083 | hp2 | a0001 | c0006 | t0001 | g0006 | EAS | KHV | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0386 | EAS | KHV | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG02129 | hp2 | a0001 | c0003 | t0004 | g0107 | EAS | KHV | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG02132 | hp1 | a0001 | c0001 | t0049 | g0220 | EAS | KHV | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG02132 | hp2 | a0001 | c0002 | t0004 | g0089 | EAS | KHV | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG02135 | hp1 | a0003 | c0009 | t0032 | g0026 | EAS | KHV | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG02135 | hp2 | a0001 | c0001 | t0006 | g0007 | EAS | KHV | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG02145 | hp1 | a0002 | c0018 | t0022 | g0285 | AFR | ACB | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG02145 | hp2 | a0001 | c0003 | t0001 | g0064 | AFR | ACB | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG02148 | hp1 | a0001 | c0002 | t0001 | g0122 | AMR | PEL | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG02148 | hp2 | a0001 | c0002 | t0001 | g0123 | AMR | PEL | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG02155 | hp1 | a0001 | c0003 | t0003 | g0105 | EAS | CDX | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG02155 | hp2 | a0001 | c0003 | t0001 | g0104 | EAS | CDX | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG02165 | hp1 | a0007 | c0030 | t0001 | g0118 | EAS | CDX | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG02165 | hp2 | a0001 | c0002 | t0025 | g0002 | EAS | CDX | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG02257 | hp1 | a0001 | c0003 | t0005 | g0246 | AFR | ACB | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG02257 | hp2 | a0002 | c0027 | t0009 | g0325 | AFR | ACB | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG02258 | hp1 | a0001 | c0003 | t0005 | g0263 | AFR | ACB | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG02258 | hp2 | a0003 | c0022 | t0042 | g0236 | AFR | ACB | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG02280 | hp1 | a0001 | c0003 | t0001 | g0294 | AFR | ACB | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG02280 | hp2 | a0001 | c0006 | t0005 | g0242 | AFR | ACB | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG02293 | hp1 | a0001 | c0002 | t0001 | g0265 | AMR | PEL | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0121 | AMR | PEL | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG02300 | hp1 | a0001 | c0002 | t0001 | g0095 | AMR | PEL | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0367 | AMR | PEL | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG02451 | hp1 | a0001 | c0004 | t0005 | g0390 | AFR | ACB | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG02451 | hp2 | a0003 | c0034 | t0004 | g0228 | AFR | ACB | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG02523 | hp1 | a0001 | c0001 | t0003 | g0184 | EAS | KHV | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG02523 | hp2 | a0001 | c0003 | t0003 | g0094 | EAS | KHV | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG02572 | hp1 | a0001 | c0004 | t0017 | g0028 | AFR | GWD | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG02572 | hp2 | a0008 | c0043 | t0041 | g0012 | AFR | GWD | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG02602 | hp1 | a0002 | c0010 | t0008 | g0023 | SAS | PJL | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG02602 | hp2 | a0001 | c0001 | t0019 | g0157 | SAS | PJL | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG02615 | hp1 | a0001 | c0005 | t0005 | g0156 | AFR | GWD | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG02615 | hp2 | a0001 | c0007 | t0006 | g0255 | AFR | GWD | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG02622 | hp1 | a0001 | c0006 | t0009 | g0256 | AFR | GWD | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG02622 | hp2 | a0002 | c0018 | t0005 | g0252 | AFR | GWD | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG02630 | hp1 | a0001 | c0004 | t0005 | g0358 | AFR | GWD | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG02630 | hp2 | a0001 | c0004 | t0006 | g0392 | AFR | GWD | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG02647 | hp1 | a0001 | c0004 | t0017 | g0232 | AFR | GWD | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG02647 | hp2 | a0001 | c0004 | t0009 | g0350 | AFR | GWD | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0296 | SAS | PJL | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0060 | SAS | PJL | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG02698 | hp1 | a0001 | c0002 | t0001 | g0339 | SAS | PJL | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG02698 | hp2 | a0001 | c0003 | t0007 | g0370 | SAS | PJL | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG02717 | hp1 | a0001 | c0024 | t0012 | g0233 | AFR | GWD | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG02717 | hp2 | a0001 | c0028 | t0020 | g0244 | AFR | GWD | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG02723 | hp1 | a0002 | c0008 | t0001 | g0225 | AFR | GWD | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG02723 | hp2 | a0001 | c0002 | t0017 | g0279 | AFR | GWD | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG02735 | hp1 | a0001 | c0005 | t0002 | g0327 | SAS | PJL | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG02735 | hp2 | a0001 | c0001 | t0003 | g0351 | SAS | PJL | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG02738 | hp1 | a0001 | c0001 | t0053 | g0395 | SAS | PJL | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG02738 | hp2 | a0001 | c0001 | t0003 | g0072 | SAS | PJL | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG02809 | hp1 | a0001 | c0005 | t0044 | g0254 | AFR | GWD | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG02809 | hp2 | a0001 | c0004 | t0004 | g0280 | AFR | GWD | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG02818 | hp1 | a0003 | c0017 | t0005 | g0314 | AFR | GWD | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG02818 | hp2 | a0003 | c0015 | t0010 | g0270 | AFR | GWD | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG02886 | hp1 | a0001 | c0005 | t0005 | g0221 | AFR | GWD | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG02886 | hp2 | a0001 | c0007 | t0012 | g0230 | AFR | GWD | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG02895 | hp1 | a0001 | c0004 | t0004 | g0281 | AFR | GWD | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG02895 | hp2 | a0001 | c0014 | t0005 | g0243 | AFR | GWD | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG02896 | hp1 | a0001 | c0003 | t0001 | g0272 | AFR | GWD | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG02896 | hp2 | a0002 | c0008 | t0005 | g0249 | AFR | GWD | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG02897 | hp1 | a0002 | c0008 | t0005 | g0251 | AFR | GWD | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG02897 | hp2 | a0001 | c0014 | t0005 | g0250 | AFR | GWD | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG02922 | hp1 | a0001 | c0014 | t0047 | g0261 | AFR | ESN | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG02922 | hp2 | a0003 | c0015 | t0005 | g0361 | AFR | ESN | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG02965 | hp1 | a0001 | c0003 | t0015 | g0328 | AFR | ESN | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG02965 | hp2 | a0001 | c0003 | t0009 | g0139 | AFR | ESN | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG02970 | hp1 | a0001 | c0003 | t0015 | g0312 | AFR | ESN | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG02970 | hp2 | a0001 | c0005 | t0005 | g0360 | AFR | ESN | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG02976 | hp1 | a0003 | c0017 | t0005 | g0238 | AFR | ESN | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG02976 | hp2 | a0001 | c0003 | t0005 | g0061 | AFR | ESN | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG03017 | hp1 | a0001 | c0002 | t0004 | g0321 | SAS | PJL | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG03017 | hp2 | a0001 | c0002 | t0001 | g0362 | SAS | PJL | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG03041 | hp1 | a0001 | c0005 | t0005 | g0348 | AFR | GWD | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG03041 | hp2 | a0003 | c0029 | t0004 | g0237 | AFR | GWD | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG03098 | hp1 | a0001 | c0011 | t0010 | g0222 | AFR | MSL | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG03098 | hp2 | a0001 | c0003 | t0009 | g0043 | AFR | MSL | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG03130 | hp1 | a0003 | c0031 | t0018 | g0158 | AFR | ESN | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG03130 | hp2 | a0002 | c0008 | t0009 | g0161 | AFR | ESN | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG03139 | hp1 | a0001 | c0033 | t0018 | g0229 | AFR | ESN | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG03139 | hp2 | a0001 | c0003 | t0001 | g0008 | AFR | ESN | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG03195 | hp1 | a0001 | c0003 | t0010 | g0153 | AFR | ESN | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG03195 | hp2 | a0001 | c0002 | t0005 | g0247 | AFR | ESN | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG03209 | hp1 | a0001 | c0005 | t0005 | g0001 | AFR | MSL | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG03209 | hp2 | a0001 | c0007 | t0001 | g0283 | AFR | MSL | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG03225 | hp1 | a0001 | c0003 | t0005 | g0024 | AFR | MSL | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG03225 | hp2 | a0002 | c0008 | t0005 | g0354 | AFR | MSL | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG03239 | hp1 | a0001 | c0001 | t0004 | g0125 | SAS | PJL | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG03239 | hp2 | a0001 | c0001 | t0039 | g0346 | SAS | PJL | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG03453 | hp1 | a0001 | c0005 | t0005 | g0001 | AFR | MSL | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG03453 | hp2 | a0001 | c0011 | t0010 | g0269 | AFR | MSL | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG03486 | hp1 | a0001 | c0004 | t0005 | g0313 | AFR | MSL | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG03486 | hp2 | a0001 | c0004 | t0009 | g0137 | AFR | MSL | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG03492 | hp1 | a0001 | c0003 | t0003 | g0151 | SAS | PJL | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG03492 | hp2 | a0001 | c0002 | t0019 | g0147 | SAS | PJL | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG03516 | hp1 | a0001 | c0003 | t0001 | g0349 | AFR | ESN | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG03516 | hp2 | a0001 | c0021 | t0005 | g0235 | AFR | ESN | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG03540 | hp1 | a0002 | c0012 | t0012 | g0262 | AFR | GWD | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG03540 | hp2 | a0001 | c0007 | t0001 | g0231 | AFR | GWD | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG03579 | hp1 | a0001 | c0004 | t0022 | g0391 | AFR | MSL | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG03579 | hp2 | a0001 | c0004 | t0005 | g0138 | AFR | MSL | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG03654 | hp1 | a0001 | c0006 | t0003 | g0344 | SAS | PJL | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG03654 | hp2 | a0001 | c0002 | t0002 | g0022 | SAS | PJL | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0353 | SAS | PJL | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG03669 | hp2 | a0001 | c0003 | t0006 | g0010 | SAS | PJL | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0146 | SAS | STU | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG03688 | hp2 | a0002 | c0010 | t0007 | g0111 | SAS | STU | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG03704 | hp1 | a0003 | c0009 | t0007 | g0293 | SAS | PJL | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG03704 | hp2 | a0001 | c0006 | t0048 | g0357 | SAS | PJL | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG03710 | hp1 | a0001 | c0001 | t0038 | g0110 | SAS | PJL | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0295 | SAS | PJL | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG03831 | hp1 | a0001 | c0001 | t0003 | g0383 | SAS | BEB | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG03831 | hp2 | a0001 | c0001 | t0005 | g0051 | SAS | BEB | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG03834 | hp1 | a0002 | c0010 | t0001 | g0131 | SAS | BEB | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0133 | SAS | BEB | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0316 | SAS | BEB | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG03942 | hp2 | a0001 | c0001 | t0005 | g0287 | SAS | BEB | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG04115 | hp1 | a0001 | c0001 | t0008 | g0267 | SAS | STU | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG04115 | hp2 | a0002 | c0010 | t0031 | g0278 | SAS | STU | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG04184 | hp1 | a0001 | c0006 | t0003 | g0324 | SAS | BEB | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG04184 | hp2 | a0001 | c0002 | t0003 | g0053 | SAS | BEB | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0085 | SAS | STU | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG04199 | hp2 | a0001 | c0001 | t0026 | g0322 | SAS | STU | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0042 | SAS | STU | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG04204 | hp2 | a0001 | c0002 | t0001 | g0073 | SAS | STU | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0380 | SAS | STU | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG04228 | hp2 | a0001 | c0001 | t0005 | g0379 | SAS | STU | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA18522 | hp1 | a0002 | c0012 | t0012 | g0241 | AFR | YRI | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA18522 | hp2 | a0001 | c0032 | t0010 | g0355 | AFR | YRI | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | CHB | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA18612 | hp2 | a0001 | c0002 | t0028 | g0080 | EAS | CHB | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA18747 | hp1 | a0001 | c0001 | t0003 | g0079 | EAS | CHB | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA18747 | hp2 | a0001 | c0002 | t0001 | g0078 | EAS | CHB | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA18906 | hp1 | a0001 | c0004 | t0024 | g0284 | AFR | YRI | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA18906 | hp2 | a0001 | c0002 | t0005 | g0248 | AFR | YRI | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA18939 | hp1 | a0001 | c0003 | t0003 | g0049 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA18939 | hp2 | a0001 | c0001 | t0003 | g0193 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA18940 | hp2 | a0001 | c0003 | t0003 | g0055 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA18943 | hp1 | a0001 | c0002 | t0003 | g0091 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA18943 | hp2 | a0001 | c0002 | t0004 | g0195 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA18944 | hp1 | a0001 | c0003 | t0001 | g0204 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA18944 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA18945 | hp1 | a0001 | c0002 | t0003 | g0217 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA18945 | hp2 | a0001 | c0003 | t0003 | g0334 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA18946 | hp2 | a0003 | c0020 | t0007 | g0075 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA18947 | hp1 | a0001 | c0002 | t0001 | g0194 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA18947 | hp2 | a0001 | c0006 | t0001 | g0082 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0264 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA18948 | hp2 | a0001 | c0002 | t0004 | g0181 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA18949 | hp1 | a0001 | c0002 | t0002 | g0102 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA18949 | hp2 | a0001 | c0001 | t0003 | g0044 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA18950 | hp2 | a0001 | c0001 | t0004 | g0199 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA18951 | hp1 | a0001 | c0003 | t0004 | g0170 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA18951 | hp2 | a0001 | c0002 | t0011 | g0336 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA18952 | hp1 | a0001 | c0003 | t0002 | g0200 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA18952 | hp2 | a0003 | c0038 | t0007 | g0099 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA18954 | hp1 | a0005 | c0019 | t0003 | g0040 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA18954 | hp2 | a0001 | c0003 | t0001 | g0187 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA18961 | hp1 | a0003 | c0009 | t0007 | g0169 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA18961 | hp2 | a0001 | c0003 | t0001 | g0103 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA18963 | hp1 | a0001 | c0002 | t0002 | g0013 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA18966 | hp1 | a0001 | c0003 | t0004 | g0219 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA18970 | hp1 | a0001 | c0002 | t0002 | g0364 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA18970 | hp2 | a0001 | c0003 | t0011 | g0166 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA18971 | hp1 | a0001 | c0003 | t0001 | g0218 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA18972 | hp2 | a0001 | c0001 | t0003 | g0163 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA18973 | hp1 | a0001 | c0002 | t0003 | g0090 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA18973 | hp2 | a0001 | c0002 | t0002 | g0216 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA18974 | hp1 | a0001 | c0001 | t0014 | g0032 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA18974 | hp2 | a0001 | c0002 | t0001 | g0202 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA18977 | hp1 | a0001 | c0001 | t0003 | g0092 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA18979 | hp2 | a0001 | c0003 | t0003 | g0036 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA18983 | hp1 | a0001 | c0002 | t0002 | g0083 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA18983 | hp2 | a0001 | c0001 | t0006 | g0375 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA18984 | hp1 | a0001 | c0003 | t0004 | g0084 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA18984 | hp2 | a0001 | c0003 | t0003 | g0029 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA18985 | hp1 | a0003 | c0009 | t0007 | g0208 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA18985 | hp2 | a0001 | c0013 | t0004 | g0171 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA18986 | hp1 | a0001 | c0003 | t0006 | g0048 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA18986 | hp2 | a0001 | c0003 | t0003 | g0056 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA18988 | hp1 | a0001 | c0001 | t0014 | g0034 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA18988 | hp2 | a0001 | c0002 | t0003 | g0016 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA18989 | hp1 | a0001 | c0002 | t0002 | g0015 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA18989 | hp2 | a0001 | c0001 | t0004 | g0113 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA18990 | hp1 | a0001 | c0003 | t0003 | g0031 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA18990 | hp2 | a0001 | c0002 | t0004 | g0326 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA18992 | hp1 | a0001 | c0002 | t0006 | g0381 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA18992 | hp2 | a0001 | c0003 | t0002 | g0030 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA18999 | hp1 | a0001 | c0002 | t0006 | g0100 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA18999 | hp2 | a0001 | c0013 | t0001 | g0389 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA19000 | hp1 | a0001 | c0001 | t0011 | g0210 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA19000 | hp2 | a0001 | c0002 | t0002 | g0086 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA19002 | hp1 | a0001 | c0001 | t0004 | g0098 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA19002 | hp2 | a0001 | c0002 | t0003 | g0014 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA19003 | hp1 | a0001 | c0002 | t0002 | g0020 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA19003 | hp2 | a0001 | c0003 | t0001 | g0209 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA19005 | hp2 | a0001 | c0003 | t0003 | g0069 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA19007 | hp1 | a0005 | c0019 | t0003 | g0074 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA19007 | hp2 | a0001 | c0003 | t0001 | g0377 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA19009 | hp1 | a0001 | c0002 | t0003 | g0068 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA19009 | hp2 | a0001 | c0003 | t0027 | g0179 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA19011 | hp1 | a0001 | c0002 | t0011 | g0337 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA19011 | hp2 | a0001 | c0003 | t0011 | g0186 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA19012 | hp1 | a0001 | c0002 | t0002 | g0376 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA19030 | hp1 | a0001 | c0023 | t0005 | g0234 | AFR | LWK | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA19030 | hp2 | a0001 | c0011 | t0005 | g0306 | AFR | LWK | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA19043 | hp1 | a0001 | c0006 | t0034 | g0289 | AFR | LWK | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA19043 | hp2 | a0001 | c0042 | t0046 | g0144 | AFR | LWK | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA19056 | hp2 | a0001 | c0002 | t0003 | g0160 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA19064 | hp1 | a0001 | c0003 | t0003 | g0372 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA19064 | hp2 | a0001 | c0003 | t0001 | g0189 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA19065 | hp1 | a0001 | c0003 | t0006 | g0174 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA19065 | hp2 | a0001 | c0002 | t0001 | g0315 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA19066 | hp1 | a0001 | c0003 | t0001 | g0045 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA19066 | hp2 | a0001 | c0003 | t0004 | g0109 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA19067 | hp1 | a0003 | c0020 | t0007 | g0167 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA19067 | hp2 | a0001 | c0002 | t0004 | g0067 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA19068 | hp1 | a0001 | c0013 | t0004 | g0097 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA19072 | hp1 | a0001 | c0001 | t0002 | g0373 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA19072 | hp2 | a0001 | c0003 | t0006 | g0214 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA19074 | hp1 | a0001 | c0002 | t0003 | g0101 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA19074 | hp2 | a0001 | c0001 | t0003 | g0093 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA19078 | hp1 | a0001 | c0003 | t0001 | g0333 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA19078 | hp2 | a0001 | c0002 | t0004 | g0087 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA19081 | hp1 | a0001 | c0001 | t0004 | g0190 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA19081 | hp2 | a0001 | c0001 | t0011 | g0077 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA19082 | hp1 | a0001 | c0002 | t0002 | g0304 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA19082 | hp2 | a0001 | c0002 | t0004 | g0368 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA19084 | hp1 | a0001 | c0003 | t0004 | g0162 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA19084 | hp2 | a0001 | c0003 | t0006 | g0070 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA19085 | hp1 | a0001 | c0003 | t0003 | g0033 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0374 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA19086 | hp2 | a0001 | c0002 | t0002 | g0205 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA19087 | hp1 | a0001 | c0002 | t0002 | g0382 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA19087 | hp2 | a0001 | c0003 | t0001 | g0180 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA19088 | hp1 | a0001 | c0037 | t0004 | g0021 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA19088 | hp2 | a0001 | c0003 | t0001 | g0188 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA19090 | hp1 | a0001 | c0003 | t0001 | g0047 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA19090 | hp2 | a0001 | c0002 | t0002 | g0164 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA19091 | hp1 | a0001 | c0002 | t0004 | g0206 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA19091 | hp2 | a0001 | c0001 | t0040 | g0018 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA19240 | hp1 | a0001 | c0007 | t0005 | g0041 | AFR | YRI | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA19240 | hp2 | a0001 | c0003 | t0015 | g0141 | AFR | YRI | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA20129 | hp1 | a0001 | c0001 | t0013 | g0142 | AFR | ASW | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA20129 | hp2 | a0002 | c0008 | t0005 | g0260 | AFR | ASW | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA20752 | hp1 | a0001 | c0002 | t0007 | g0345 | EUR | TSI | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA20752 | hp2 | a0001 | c0001 | t0008 | g0309 | EUR | TSI | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA20805 | hp1 | a0001 | c0002 | t0007 | g0378 | EUR | TSI | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA20805 | hp2 | a0001 | c0003 | t0016 | g0117 | EUR | TSI | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0197 | AMR | CLM | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG01123 | hp2 | a0001 | c0006 | t0008 | g0387 | AMR | CLM | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG02109 | hp1 | a0003 | c0017 | t0018 | g0331 | AFR | ACB | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG02109 | hp2 | a0001 | c0001 | t0052 | g0394 | AFR | ACB | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG02486 | hp1 | a0002 | c0012 | t0012 | g0282 | AFR | ACB | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG02486 | hp2 | a0001 | c0003 | t0020 | g0323 | AFR | ACB | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG02559 | hp1 | a0001 | c0011 | t0005 | g0140 | AFR | ACB | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG02559 | hp2 | a0001 | c0003 | t0035 | g0240 | AFR | ACB | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG03471 | hp1 | a0001 | c0007 | t0005 | g0009 | AFR | MSL | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG03471 | hp2 | a0009 | c0026 | t0004 | g0271 | AFR | MSL | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG06807 | hp1 | a0001 | c0003 | t0012 | g0239 | AFR | USA | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| HG06807 | hp2 | a0001 | c0004 | t0024 | g0286 | AFR | USA | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA18955 | hp1 | a0001 | c0001 | t0014 | g0054 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA18955 | hp2 | a0001 | c0003 | t0001 | g0203 | EAS | JPT | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA20300 | hp1 | a0001 | c0001 | t0005 | g0259 | AFR | USA | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA20300 | hp2 | a0001 | c0001 | t0007 | g0207 | AFR | USA | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA21309 | hp1 | a0001 | c0014 | t0021 | g0227 | AFR | LWK | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| NA21309 | hp2 | a0003 | c0036 | t0051 | g0143 | AFR | LWK | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0004 | g0039 | REF | REF | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| homoSapiens | grch38p0 | a0001 | c0006 | t0002 | g0165 | REF | REF | C2CD2_chr21_41880112_41959018 | C2CD2 | chr21 | 41880112 | 41959018 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr21:41899071 | T | C | 2 | a0003 a0009 |
22 | HG00609.hp2 HG00673.hp1 HG01257.hp1 others(19): Show |
missense_variant | MODERATE | c.1852A>G | p.Thr618Ala | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/14 | 2222/6473 | 1852/2091 | 618/696 | chr21 | 41899071 | |||
| chr21:41905754 | C | T | 1 | a0004 | 3 | HG00741.hp1 HG01192.hp1 HG02004.hp1 |
missense_variant | MODERATE | c.1402G>A | p.Val468Ile | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 11/14 | 1772/6473 | 1402/2091 | 468/696 | chr21 | 41905754 | |||
| chr21:41907058 | T | G | 1 | a0006 | 1 | HG01934.hp1 | missense_variant | MODERATE | c.1252A>C | p.Thr418Pro | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 10/14 | 1622/6473 | 1252/2091 | 418/696 | chr21 | 41907058 | |||
| chr21:41907088 | G | A | 1 | a0008 | 1 | HG02572.hp2 | missense_variant | MODERATE | c.1222C>T | p.Arg408Cys | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 10/14 | 1592/6473 | 1222/2091 | 408/696 | chr21 | 41907088 | |||
| chr21:41907099 | A | T | 1 | a0007 | 1 | HG02165.hp1 | missense_variant | MODERATE | c.1211T>A | p.Ile404Lys | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 10/14 | 1581/6473 | 1211/2091 | 404/696 | chr21 | 41907099 | |||
| chr21:41914628 | C | T | 1 | a0005 | 2 | NA18954.hp1 NA19007.hp1 |
missense_variant | MODERATE | c.814G>A | p.Val272Ile | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 6/14 | 1184/6473 | 814/2091 | 272/696 | chr21 | 41914628 | |||
| chr21:41918193 | A | G | 1 | a0002 | 23 | HG00639.hp1 HG00642.hp2 HG01167.hp1 others(20): Show |
missense_variant | MODERATE | c.632T>C | p.Val211Ala | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 5/14 | 1002/6473 | 632/2091 | 211/696 | chr21 | 41918193 | |||
| chr21:41942170 | C | T | 1 | a0009 | 1 | HG03471.hp2 | missense_variant | MODERATE | c.355G>A | p.Val119Met | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/14 | 725/6473 | 355/2091 | 119/696 | chr21 | 41942170 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr21:41899093 | G | A | 1 | a0001c0032 | 1 | NA18522.hp2 | synonymous_variant | LOW | c.1830C>T | p.Ser610Ser | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/14 | 2200/6473 | 1830/2091 | 610/696 | chr21 | 41899093 | |||
| chr21:41899105 | C | T | 11 | a0003c0009 a0003c0015 a0003c0017 others(8): Show |
22 | HG00609.hp2 HG00673.hp1 HG01257.hp1 others(19): Show |
synonymous_variant | LOW | c.1818G>A | p.Leu606Leu | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/14 | 2188/6473 | 1818/2091 | 606/696 | chr21 | 41899105 | |||
| chr21:41899234 | G | A | 1 | a0002c0012 | 5 | HG01167.hp1 HG01169.hp1 HG02486.hp1 others(2): Show |
synonymous_variant | LOW | c.1689C>T | p.Ala563Ala | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/14 | 2059/6473 | 1689/2091 | 563/696 | chr21 | 41899234 | |||
| chr21:41899315 | C | T | 3 | a0003c0009 a0003c0020 a0003c0038 |
9 | HG00609.hp2 HG00673.hp1 HG02135.hp1 others(6): Show |
synonymous_variant | LOW | c.1608G>A | p.Thr536Thr | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/14 | 1978/6473 | 1608/2091 | 536/696 | chr21 | 41899315 | |||
| chr21:41905800 | G | A | 1 | a0001c0033 | 1 | HG03139.hp1 | synonymous_variant | LOW | c.1356C>T | p.Ile452Ile | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 11/14 | 1726/6473 | 1356/2091 | 452/696 | chr21 | 41905800 | |||
| chr21:41905818 | G | T | 1 | a0002c0027 | 1 | HG02257.hp2 | synonymous_variant | LOW | c.1338C>A | p.Pro446Pro | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 11/14 | 1708/6473 | 1338/2091 | 446/696 | chr21 | 41905818 | |||
| chr21:41907008 | C | T | 21 | a0001c0003 a0001c0005 a0001c0011 others(18): Show |
136 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(133): Show |
synonymous_variant | LOW | c.1302G>A | p.Ala434Ala | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 10/14 | 1672/6473 | 1302/2091 | 434/696 | chr21 | 41907008 | |||
| chr21:41907023 | G | A | 1 | a0001c0021 | 1 | HG03516.hp2 | synonymous_variant | LOW | c.1287C>T | p.Val429Val | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 10/14 | 1657/6473 | 1287/2091 | 429/696 | chr21 | 41907023 | |||
| chr21:41907666 | C | T | 1 | a0001c0037 | 1 | NA19088.hp1 | synonymous_variant | LOW | c.1137G>A | p.Thr379Thr | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 9/14 | 1507/6473 | 1137/2091 | 379/696 | chr21 | 41907666 | |||
| chr21:41907684 | C | T | 20 | a0001c0002 a0001c0005 a0001c0011 others(17): Show |
146 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(143): Show |
synonymous_variant | LOW | c.1119G>A | p.Ser373Ser | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 9/14 | 1489/6473 | 1119/2091 | 373/696 | chr21 | 41907684 | |||
| chr21:41907705 | G | A | 3 | a0001c0013 a0001c0037 a0003c0038 |
6 | HG01257.hp2 NA18952.hp2 NA18985.hp2 others(3): Show |
synonymous_variant | LOW | c.1098C>T | p.Ser366Ser | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 9/14 | 1468/6473 | 1098/2091 | 366/696 | chr21 | 41907705 | |||
| chr21:41907747 | A | G | 25 | a0001c0001 a0001c0003 a0001c0007 others(22): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
synonymous_variant | LOW | c.1056T>C | p.Phe352Phe | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 9/14 | 1426/6473 | 1056/2091 | 352/696 | chr21 | 41907747 | |||
| chr21:41909463 | T | C | 4 | a0001c0039 a0001c0040 a0002c0010 others(1): Show |
9 | HG00639.hp1 HG00642.hp2 HG01070.hp2 others(6): Show |
synonymous_variant | LOW | c.1014A>G | p.Ser338Ser | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 8/14 | 1384/6473 | 1014/2091 | 338/696 | chr21 | 41909463 | |||
| chr21:41909471 | G | T | 2 | a0001c0021 a0001c0028 |
2 | HG02717.hp2 HG03516.hp2 |
synonymous_variant | LOW | c.1006C>A | p.Arg336Arg | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 8/14 | 1376/6473 | 1006/2091 | 336/696 | chr21 | 41909471 | |||
| chr21:41918219 | C | A | 4 | a0002c0010 a0002c0012 a0002c0018 others(1): Show |
15 | HG00639.hp1 HG00642.hp2 HG01167.hp1 others(12): Show |
synonymous_variant | LOW | c.606G>T | p.Val202Val | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 5/14 | 976/6473 | 606/2091 | 202/696 | chr21 | 41918219 | |||
| chr21:41922002 | G | A | 7 | a0001c0004 a0001c0007 a0001c0014 others(4): Show |
34 | HG00741.hp2 HG01167.hp2 HG01257.hp1 others(31): Show |
synonymous_variant | LOW | c.462C>T | p.Tyr154Tyr | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 3/14 | 832/6473 | 462/2091 | 154/696 | chr21 | 41922002 | |||
| chr21:41942186 | C | T | 1 | a0001c0025 | 1 | HG01516.hp1 | synonymous_variant | LOW | c.339G>A | p.Val113Val | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/14 | 709/6473 | 339/2091 | 113/696 | chr21 | 41942186 | |||
| chr21:41942213 | C | T | 4 | a0001c0021 a0001c0023 a0001c0024 others(1): Show |
4 | HG02258.hp2 HG02717.hp1 HG03516.hp2 others(1): Show |
synonymous_variant | LOW | c.312G>A | p.Pro104Pro | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/14 | 682/6473 | 312/2091 | 104/696 | chr21 | 41942213 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr21:41885326 | C | T | 122 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(119): Show |
326 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(323): Show |
3_prime_UTR_variant | MODIFIER | c.*3798G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 14/14 | 3798 | chr21 | 41885326 | ||||||
| chr21:41885354 | G | A | 30 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 others(27): Show |
78 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*3770C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 14/14 | 3770 | chr21 | 41885354 | ||||||
| chr21:41885458 | G | T | 1 | a0001c0005t0044 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3666C>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 14/14 | 3666 | chr21 | 41885458 | ||||||
| chr21:41885483 | T | G | 49 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0008 others(46): Show |
116 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(113): Show |
3_prime_UTR_variant | MODIFIER | c.*3641A>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 14/14 | 3641 | chr21 | 41885483 | ||||||
| chr21:41885501 | G | A | 1 | a0001c0001t0023 | 2 | HG01515.hp2 HG01517.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3623C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 14/14 | 3623 | chr21 | 41885501 | ||||||
| chr21:41885510 | C | T | 19 | a0001c0001t0003 a0001c0001t0006 a0001c0002t0003 others(16): Show |
77 | HG00438.hp1 HG00597.hp1 HG00597.hp2 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*3614G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 14/14 | 3614 | chr21 | 41885510 | ||||||
| chr21:41885637 | C | T | 4 | a0001c0003t0035 a0001c0004t0022 a0001c0006t0034 others(1): Show |
4 | HG02145.hp1 HG02559.hp2 HG03579.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3487G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 14/14 | 3487 | chr21 | 41885637 | ||||||
| chr21:41885669 | ACT | A | 3 | a0001c0001t0049 a0001c0003t0016 a0002c0010t0016 |
4 | HG00639.hp1 HG00642.hp2 HG02132.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3453_*3454delAG | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 14/14 | 3453 | chr21 | 41885669 | ||||||
| chr21:41885746 | T | G | 8 | a0001c0001t0008 a0001c0002t0008 a0001c0003t0008 others(5): Show |
11 | HG00099.hp2 HG00140.hp2 HG00738.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*3378A>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 14/14 | 3378 | chr21 | 41885746 | ||||||
| chr21:41885828 | G | A | 21 | a0001c0001t0004 a0001c0001t0011 a0001c0001t0013 others(18): Show |
61 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*3296C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 14/14 | 3296 | chr21 | 41885828 | ||||||
| chr21:41885961 | A | C | 8 | a0001c0003t0009 a0001c0004t0009 a0001c0006t0009 others(5): Show |
11 | HG01167.hp1 HG01169.hp1 HG01884.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*3163T>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 14/14 | 3163 | chr21 | 41885961 | ||||||
| chr21:41885966 | G | C | 34 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0014 others(31): Show |
120 | HG00738.hp2 HG00741.hp2 HG01069.hp2 others(117): Show |
3_prime_UTR_variant | MODIFIER | c.*3158C>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 14/14 | 3158 | chr21 | 41885966 | ||||||
| chr21:41885992 | A | G | 36 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0014 others(33): Show |
124 | HG00738.hp2 HG00741.hp2 HG01069.hp2 others(121): Show |
3_prime_UTR_variant | MODIFIER | c.*3132T>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 14/14 | 3132 | chr21 | 41885992 | ||||||
| chr21:41886063 | C | G | 1 | a0003c0036t0051 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3061G>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 14/14 | 3061 | chr21 | 41886063 | ||||||
| chr21:41886193 | T | C | 2 | a0001c0003t0016 a0002c0010t0016 |
3 | HG00639.hp1 HG00642.hp2 NA20805.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2931A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 14/14 | 2931 | chr21 | 41886193 | ||||||
| chr21:41886452 | C | T | 1 | a0001c0003t0043 | 1 | HG00621.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2672G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 14/14 | 2672 | chr21 | 41886452 | ||||||
| chr21:41886464 | C | T | 3 | a0001c0001t0049 a0001c0003t0016 a0002c0010t0016 |
4 | HG00639.hp1 HG00642.hp2 HG02132.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2660G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 14/14 | 2660 | chr21 | 41886464 | ||||||
| chr21:41886478 | G | A | 2 | a0001c0001t0013 a0001c0039t0013 |
3 | HG00280.hp1 HG01981.hp1 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2646C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 14/14 | 2646 | chr21 | 41886478 | ||||||
| chr21:41886481 | G | A | 1 | a0001c0014t0047 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2643C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 14/14 | 2643 | chr21 | 41886481 | ||||||
| chr21:41886522 | G | C | 2 | a0001c0004t0022 a0002c0018t0022 |
2 | HG02145.hp1 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2602C>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 14/14 | 2602 | chr21 | 41886522 | ||||||
| chr21:41886572 | G | A | 7 | a0001c0001t0008 a0001c0002t0008 a0001c0003t0008 others(4): Show |
10 | HG00099.hp2 HG00140.hp2 HG00738.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2552C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 14/14 | 2552 | chr21 | 41886572 | ||||||
| chr21:41886659 | CT | C | 120 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(117): Show |
326 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(323): Show |
3_prime_UTR_variant | MODIFIER | c.*2464delA | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 14/14 | 2464 | chr21 | 41886659 | ||||||
| chr21:41886707 | C | T | 1 | a0001c0001t0014 | 3 | NA18955.hp1 NA18974.hp1 NA18988.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2417G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 14/14 | 2417 | chr21 | 41886707 | ||||||
| chr21:41886740 | G | A | 1 | a0002c0008t0045 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2384C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 14/14 | 2384 | chr21 | 41886740 | ||||||
| chr21:41886761 | G | C | 1 | a0001c0003t0035 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2363C>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 14/14 | 2363 | chr21 | 41886761 | ||||||
| chr21:41886953 | A | C | 3 | a0001c0001t0049 a0001c0003t0016 a0002c0010t0016 |
4 | HG00639.hp1 HG00642.hp2 HG02132.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2171T>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 14/14 | 2171 | chr21 | 41886953 | ||||||
| chr21:41886980 | A | T | 13 | a0001c0003t0009 a0001c0003t0012 a0001c0004t0009 others(10): Show |
18 | HG01167.hp1 HG01169.hp1 HG01884.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*2144T>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 14/14 | 2144 | chr21 | 41886980 | ||||||
| chr21:41886981 | T | A | 8 | a0001c0001t0008 a0001c0002t0008 a0001c0003t0008 others(5): Show |
11 | HG00099.hp2 HG00140.hp2 HG00738.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2143A>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 14/14 | 2143 | chr21 | 41886981 | ||||||
| chr21:41887220 | A | G | 124 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(121): Show |
330 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(327): Show |
3_prime_UTR_variant | MODIFIER | c.*1904T>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 14/14 | 1904 | chr21 | 41887220 | ||||||
| chr21:41887288 | T | G | 1 | a0001c0042t0046 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1836A>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 14/14 | 1836 | chr21 | 41887288 | ||||||
| chr21:41887360 | T | C | 1 | a0001c0004t0024 | 2 | HG06807.hp2 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1764A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 14/14 | 1764 | chr21 | 41887360 | ||||||
| chr21:41887452 | GA | G | 17 | a0001c0001t0008 a0001c0001t0039 a0001c0001t0049 others(14): Show |
22 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*1671delT | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 14/14 | 1671 | chr21 | 41887452 | ||||||
| chr21:41887597 | G | GA | 14 | a0001c0002t0021 a0001c0003t0009 a0001c0003t0035 others(11): Show |
17 | HG01106.hp1 HG01167.hp1 HG01169.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1526dupT | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 14/14 | 1526 | chr21 | 41887597 | ||||||
| chr21:41887597 | GA | G | 9 | a0001c0001t0008 a0001c0002t0008 a0001c0003t0008 others(6): Show |
12 | HG00099.hp2 HG00140.hp2 HG00738.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1526delT | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 14/14 | 1526 | chr21 | 41887597 | ||||||
| chr21:41887628 | C | A | 122 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(119): Show |
326 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(323): Show |
3_prime_UTR_variant | MODIFIER | c.*1496G>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 14/14 | 1496 | chr21 | 41887628 | ||||||
| chr21:41887652 | T | C | 1 | a0001c0014t0047 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1472A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 14/14 | 1472 | chr21 | 41887652 | ||||||
| chr21:41887721 | T | A | 1 | a0001c0002t0029 | 1 | HG01261.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1403A>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 14/14 | 1403 | chr21 | 41887721 | ||||||
| chr21:41887780 | A | C | 1 | a0001c0003t0037 | 1 | HG02056.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1344T>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 14/14 | 1344 | chr21 | 41887780 | ||||||
| chr21:41887791 | C | T | 14 | a0001c0001t0001 a0001c0001t0014 a0001c0001t0038 others(11): Show |
71 | HG00738.hp2 HG01069.hp2 HG01109.hp2 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*1333G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 14/14 | 1333 | chr21 | 41887791 | ||||||
| chr21:41887816 | G | A | 8 | a0001c0001t0008 a0001c0002t0008 a0001c0003t0008 others(5): Show |
11 | HG00099.hp2 HG00140.hp2 HG00738.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1308C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 14/14 | 1308 | chr21 | 41887816 | ||||||
| chr21:41887988 | T | A | 1 | a0001c0002t0030 | 1 | HG00673.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1136A>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 14/14 | 1136 | chr21 | 41887988 | ||||||
| chr21:41888107 | C | A | 1 | a0001c0006t0048 | 1 | HG03704.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1017G>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 14/14 | 1017 | chr21 | 41888107 | ||||||
| chr21:41888216 | C | T | 12 | a0001c0003t0009 a0001c0003t0035 a0001c0004t0009 others(9): Show |
15 | HG01167.hp1 HG01169.hp1 HG01884.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*908G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 14/14 | 908 | chr21 | 41888216 | ||||||
| chr21:41888261 | G | A | 12 | a0001c0001t0007 a0001c0002t0007 a0001c0003t0007 others(9): Show |
20 | HG00099.hp1 HG00280.hp2 HG00609.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*863C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 14/14 | 863 | chr21 | 41888261 | ||||||
| chr21:41888378 | T | C | 3 | a0001c0001t0049 a0001c0003t0016 a0002c0010t0016 |
4 | HG00639.hp1 HG00642.hp2 HG02132.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*746A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 14/14 | 746 | chr21 | 41888378 | ||||||
| chr21:41888541 | T | C | 2 | a0001c0002t0017 a0001c0004t0017 |
3 | HG02572.hp1 HG02647.hp1 HG02723.hp2 |
3_prime_UTR_variant | MODIFIER | c.*583A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 14/14 | 583 | chr21 | 41888541 | ||||||
| chr21:41888552 | G | A | 18 | a0001c0002t0021 a0001c0003t0009 a0001c0003t0012 others(15): Show |
23 | HG01106.hp1 HG01167.hp1 HG01169.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*572C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 14/14 | 572 | chr21 | 41888552 | ||||||
| chr21:41888572 | T | C | 1 | a0003c0009t0032 | 1 | HG02135.hp1 | 3_prime_UTR_variant | MODIFIER | c.*552A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 14/14 | 552 | chr21 | 41888572 | ||||||
| chr21:41888598 | ATGT | A | 3 | a0001c0033t0018 a0003c0017t0018 a0003c0031t0018 |
3 | HG02109.hp1 HG03130.hp1 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*523_*525delACA | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 14/14 | 523 | chr21 | 41888598 | ||||||
| chr21:41888807 | G | A | 8 | a0001c0001t0008 a0001c0002t0008 a0001c0003t0008 others(5): Show |
11 | HG00099.hp2 HG00140.hp2 HG00738.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*317C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 14/14 | 317 | chr21 | 41888807 | ||||||
| chr21:41888862 | A | C | 2 | a0001c0001t0023 a0001c0001t0036 |
3 | HG01099.hp2 HG01515.hp2 HG01517.hp1 |
3_prime_UTR_variant | MODIFIER | c.*262T>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 14/14 | 262 | chr21 | 41888862 | ||||||
| chr21:41889081 | C | A | 4 | a0001c0003t0035 a0001c0004t0022 a0001c0006t0034 others(1): Show |
4 | HG02145.hp1 HG02559.hp2 HG03579.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*43G>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 14/14 | 43 | chr21 | 41889081 | ||||||
| chr21:41889082 | A | G | 56 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0007 others(53): Show |
150 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(147): Show |
3_prime_UTR_variant | MODIFIER | c.*42T>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 14/14 | 42 | chr21 | 41889082 | ||||||
| chr21:41953728 | G | A | 1 | a0001c0001t0052 | 1 | HG02109.hp2 | 5_prime_UTR_variant | MODIFIER | c.-80C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/14 | 80 | chr21 | 41953728 | ||||||
| chr21:41953788 | C | T | 1 | a0001c0002t0025 | 1 | HG02165.hp2 | 5_prime_UTR_variant | MODIFIER | c.-140G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/14 | 140 | chr21 | 41953788 | ||||||
| chr21:41953926 | G | C | 2 | a0001c0001t0052 a0001c0001t0053 |
2 | HG02109.hp2 HG02738.hp1 |
5_prime_UTR_variant | MODIFIER | c.-278C>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/14 | 278 | chr21 | 41953926 | ||||||
| chr21:41954011 | G | A | 1 | a0001c0001t0053 | 1 | HG02738.hp1 | 5_prime_UTR_variant | MODIFIER | c.-363C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/14 | 363 | chr21 | 41954011 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr21:41889499 | T | C | 119 | a0001c0001t0001g0353 a0001c0001t0003g0044 a0001c0001t0003g0046 others(116): Show |
119 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.1871-155A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41889499 | |||||||
| chr21:41889504 | G | A | 2 | a0004c0016t0004g0134 a0004c0016t0004g0135 |
2 | HG00741.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.1871-160C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41889504 | |||||||
| chr21:41889524 | C | T | 11 | a0001c0003t0009g0043 a0001c0003t0009g0139 a0001c0004t0009g0137 others(8): Show |
11 | HG01167.hp1 HG01169.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.1871-180G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41889524 | |||||||
| chr21:41889525 | G | T | 24 | a0001c0001t0007g0159 a0001c0001t0007g0175 a0001c0001t0007g0207 others(21): Show |
24 | HG00099.hp1 HG00280.hp2 HG00609.hp2 others(21): Show |
intron_variant | MODIFIER | c.1871-181C>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41889525 | |||||||
| chr21:41889597 | C | T | 4 | a0001c0001t0049g0220 a0001c0003t0016g0117 a0002c0010t0016g0292 others(1): Show |
4 | HG00639.hp1 HG00642.hp2 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.1871-253G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41889597 | |||||||
| chr21:41889637 | C | CT | 107 | a0001c0001t0001g0005 a0001c0001t0001g0025 a0001c0001t0001g0027 others(104): Show |
108 | HG00438.hp2 HG00738.hp2 HG00741.hp2 others(105): Show |
intron_variant | MODIFIER | c.1871-294dupA | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41889637 | |||||||
| chr21:41889637 | CT | C | 111 | a0001c0001t0001g0353 a0001c0001t0003g0044 a0001c0001t0003g0046 others(108): Show |
111 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.1871-294delA | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41889637 | |||||||
| chr21:41889672 | C | T | 40 | a0001c0001t0002g0017 a0001c0001t0002g0058 a0001c0001t0002g0076 others(37): Show |
40 | HG00140.hp1 HG00408.hp1 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.1871-328G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41889672 | |||||||
| chr21:41889879 | C | T | 34 | a0001c0001t0002g0017 a0001c0001t0002g0058 a0001c0001t0002g0076 others(31): Show |
34 | HG00140.hp1 HG00408.hp1 HG00673.hp1 others(31): Show |
intron_variant | MODIFIER | c.1871-535G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41889879 | |||||||
| chr21:41889921 | G | T | 5 | a0001c0003t0035g0240 a0001c0004t0022g0391 a0001c0006t0034g0289 others(2): Show |
5 | HG02145.hp1 HG02559.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1871-577C>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41889921 | |||||||
| chr21:41889923 | C | A | 5 | a0001c0003t0035g0240 a0001c0004t0022g0391 a0001c0006t0034g0289 others(2): Show |
5 | HG02145.hp1 HG02559.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1871-579G>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41889923 | |||||||
| chr21:41890068 | C | T | 4 | a0001c0001t0049g0220 a0001c0003t0016g0117 a0002c0010t0016g0292 others(1): Show |
4 | HG00639.hp1 HG00642.hp2 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.1871-724G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41890068 | |||||||
| chr21:41890085 | T | C | 12 | a0001c0001t0008g0267 a0001c0001t0008g0309 a0001c0002t0008g0311 others(9): Show |
12 | HG00099.hp2 HG00140.hp2 HG00738.hp1 others(9): Show |
intron_variant | MODIFIER | c.1871-741A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41890085 | |||||||
| chr21:41890130 | T | C | 5 | a0001c0003t0035g0240 a0001c0004t0022g0391 a0001c0006t0034g0289 others(2): Show |
5 | HG02145.hp1 HG02559.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1871-786A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41890130 | |||||||
| chr21:41890135 | T | C | 1 | a0001c0001t0005g0259 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1871-791A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41890135 | |||||||
| chr21:41890231 | GT | G | 3 | a0003c0015t0005g0329 a0003c0015t0005g0330 a0003c0015t0005g0361 |
3 | HG01257.hp1 HG01258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1871-888delA | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41890231 | |||||||
| chr21:41890264 | G | A | 5 | a0001c0002t0005g0248 a0001c0005t0005g0001 a0001c0005t0005g0360 others(2): Show |
6 | HG02970.hp2 HG03209.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.1871-920C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41890264 | |||||||
| chr21:41890282 | G | A | 1 | a0001c0002t0001g0339 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1871-938C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41890282 | |||||||
| chr21:41890363 | C | T | 112 | a0001c0001t0001g0353 a0001c0001t0003g0044 a0001c0001t0003g0046 others(109): Show |
112 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.1871-1019G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41890363 | |||||||
| chr21:41890390 | GCAA | G | 8 | a0001c0001t0006g0007 a0001c0001t0006g0375 a0001c0002t0006g0071 others(5): Show |
8 | HG00597.hp2 HG02056.hp1 HG02071.hp2 others(5): Show |
intron_variant | MODIFIER | c.1871-1049_1871-104 others(7): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41890390 | |||||||
| chr21:41890500 | A | T | 1 | a0001c0002t0002g0130 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1871-1156T>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41890500 | |||||||
| chr21:41890560 | C | T | 3 | a0001c0001t0003g0093 a0001c0002t0003g0160 a0001c0003t0003g0069 |
3 | NA19005.hp2 NA19056.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.1871-1216G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41890560 | |||||||
| chr21:41890640 | A | C | 2 | a0003c0017t0018g0331 a0003c0031t0018g0158 |
2 | HG02109.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1871-1296T>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41890640 | |||||||
| chr21:41890652 | T | C | 9 | a0001c0003t0005g0246 a0001c0003t0005g0332 a0001c0003t0005g0335 others(6): Show |
9 | HG01070.hp1 HG01071.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.1871-1308A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41890652 | |||||||
| chr21:41890688 | C | T | 114 | a0001c0001t0001g0353 a0001c0001t0003g0044 a0001c0001t0003g0046 others(111): Show |
114 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.1871-1344G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41890688 | |||||||
| chr21:41890743 | A | C | 1 | a0001c0002t0001g0275 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1871-1399T>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41890743 | |||||||
| chr21:41890745 | C | G | 1 | a0001c0003t0001g0218 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1871-1401G>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41890745 | |||||||
| chr21:41890848 | C | T | 38 | a0001c0001t0002g0017 a0001c0001t0002g0058 a0001c0001t0002g0076 others(35): Show |
38 | HG00140.hp1 HG00408.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.1871-1504G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41890848 | |||||||
| chr21:41890956 | G | A | 1 | a0001c0003t0001g0045 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1871-1612C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41890956 | |||||||
| chr21:41890958 | C | T | 1 | a0001c0001t0004g0190 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1871-1614G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41890958 | |||||||
| chr21:41890988 | C | T | 1 | a0001c0001t0002g0316 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1871-1644G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41890988 | |||||||
| chr21:41891046 | G | A | 1 | a0002c0010t0008g0023 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1871-1702C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41891046 | |||||||
| chr21:41891048 | G | A | 5 | a0001c0003t0035g0240 a0001c0004t0022g0391 a0001c0006t0034g0289 others(2): Show |
5 | HG02145.hp1 HG02559.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1871-1704C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41891048 | |||||||
| chr21:41891105 | G | A | 4 | a0001c0001t0002g0060 a0001c0002t0017g0279 a0001c0004t0017g0028 others(1): Show |
4 | HG02572.hp1 HG02647.hp1 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.1871-1761C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41891105 | |||||||
| chr21:41891107 | GGACTGCT others(83): Show |
G | 57 | a0001c0001t0004g0098 a0001c0001t0004g0113 a0001c0001t0004g0125 others(54): Show |
57 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(54): Show |
intron_variant | MODIFIER | c.1871-1853_1871-176 others(94): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41891107 | |||||||
| chr21:41891126 | G | A | 1 | a0001c0003t0005g0263 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1871-1782C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41891126 | |||||||
| chr21:41891287 | T | TG | 11 | a0001c0002t0005g0303 a0001c0003t0005g0024 a0001c0004t0005g0138 others(8): Show |
11 | HG01109.hp1 HG01257.hp1 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1871-1944dupC | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41891287 | |||||||
| chr21:41891308 | T | C | 5 | a0001c0003t0035g0240 a0001c0004t0022g0391 a0001c0006t0034g0289 others(2): Show |
5 | HG02145.hp1 HG02559.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1871-1964A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41891308 | |||||||
| chr21:41891334 | G | A | 52 | a0001c0001t0004g0098 a0001c0001t0004g0113 a0001c0001t0004g0125 others(49): Show |
52 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.1871-1990C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41891334 | |||||||
| chr21:41891343 | C | T | 1 | a0001c0001t0002g0088 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1871-1999G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41891343 | |||||||
| chr21:41891442 | G | A | 2 | a0003c0017t0018g0331 a0003c0031t0018g0158 |
2 | HG02109.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1871-2098C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41891442 | |||||||
| chr21:41891465 | G | A | 1 | a0001c0032t0010g0355 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1871-2121C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41891465 | |||||||
| chr21:41891657 | T | C | 5 | a0001c0003t0035g0240 a0001c0004t0022g0391 a0001c0006t0034g0289 others(2): Show |
5 | HG02145.hp1 HG02559.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1871-2313A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41891657 | |||||||
| chr21:41891749 | A | G | 43 | a0001c0001t0002g0017 a0001c0001t0002g0058 a0001c0001t0002g0076 others(40): Show |
43 | HG00140.hp1 HG00408.hp1 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.1871-2405T>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41891749 | |||||||
| chr21:41891876 | C | T | 76 | a0001c0001t0002g0017 a0001c0001t0002g0058 a0001c0001t0002g0076 others(73): Show |
76 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(73): Show |
intron_variant | MODIFIER | c.1871-2532G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41891876 | |||||||
| chr21:41891924 | G | A | 11 | a0001c0002t0005g0303 a0001c0003t0005g0024 a0001c0004t0005g0138 others(8): Show |
11 | HG01109.hp1 HG01257.hp1 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1871-2580C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41891924 | |||||||
| chr21:41891987 | C | T | 5 | a0001c0003t0035g0240 a0001c0004t0022g0391 a0001c0006t0034g0289 others(2): Show |
5 | HG02145.hp1 HG02559.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1871-2643G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41891987 | |||||||
| chr21:41892072 | T | C | 5 | a0001c0003t0035g0240 a0001c0004t0022g0391 a0001c0006t0034g0289 others(2): Show |
5 | HG02145.hp1 HG02559.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1871-2728A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41892072 | |||||||
| chr21:41892140 | G | A | 5 | a0001c0003t0035g0240 a0001c0004t0022g0391 a0001c0006t0034g0289 others(2): Show |
5 | HG02145.hp1 HG02559.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1871-2796C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41892140 | |||||||
| chr21:41892165 | C | T | 9 | a0001c0003t0005g0246 a0001c0003t0005g0332 a0001c0003t0005g0335 others(6): Show |
9 | HG01070.hp1 HG01071.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.1871-2821G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41892165 | |||||||
| chr21:41892503 | A | G | 1 | a0001c0001t0004g0098 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1871-3159T>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41892503 | |||||||
| chr21:41892631 | T | G | 49 | a0001c0001t0004g0098 a0001c0001t0004g0113 a0001c0001t0004g0125 others(46): Show |
49 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(46): Show |
intron_variant | MODIFIER | c.1871-3287A>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41892631 | |||||||
| chr21:41892642 | T | C | 282 | a0001c0001t0001g0005 a0001c0001t0001g0025 a0001c0001t0001g0027 others(279): Show |
283 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(280): Show |
intron_variant | MODIFIER | c.1871-3298A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41892642 | |||||||
| chr21:41892667 | TC | T | 49 | a0001c0001t0004g0098 a0001c0001t0004g0113 a0001c0001t0004g0125 others(46): Show |
49 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(46): Show |
intron_variant | MODIFIER | c.1871-3324delG | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41892667 | |||||||
| chr21:41892674 | T | G | 1 | a0001c0003t0004g0170 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1871-3330A>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41892674 | |||||||
| chr21:41892756 | T | C | 68 | a0001c0001t0004g0098 a0001c0001t0004g0113 a0001c0001t0004g0125 others(65): Show |
68 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.1871-3412A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41892756 | |||||||
| chr21:41892884 | G | A | 64 | a0001c0001t0004g0098 a0001c0001t0004g0113 a0001c0001t0004g0125 others(61): Show |
64 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(61): Show |
intron_variant | MODIFIER | c.1871-3540C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41892884 | |||||||
| chr21:41892924 | T | C | 49 | a0001c0001t0004g0098 a0001c0001t0004g0113 a0001c0001t0004g0125 others(46): Show |
49 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(46): Show |
intron_variant | MODIFIER | c.1871-3580A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41892924 | |||||||
| chr21:41892941 | G | A | 106 | a0001c0001t0001g0005 a0001c0001t0001g0025 a0001c0001t0001g0027 others(103): Show |
107 | HG00438.hp2 HG00738.hp2 HG00741.hp2 others(104): Show |
intron_variant | MODIFIER | c.1871-3597C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41892941 | |||||||
| chr21:41892947 | C | T | 49 | a0001c0001t0004g0098 a0001c0001t0004g0113 a0001c0001t0004g0125 others(46): Show |
49 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(46): Show |
intron_variant | MODIFIER | c.1871-3603G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41892947 | |||||||
| chr21:41893019 | A | T | 66 | a0001c0001t0004g0098 a0001c0001t0004g0113 a0001c0001t0004g0125 others(63): Show |
66 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(63): Show |
intron_variant | MODIFIER | c.1871-3675T>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41893019 | |||||||
| chr21:41893058 | G | C | 1 | a0001c0002t0002g0216 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1871-3714C>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41893058 | |||||||
| chr21:41893134 | C | T | 5 | a0001c0002t0005g0303 a0001c0003t0005g0024 a0001c0005t0005g0156 others(2): Show |
5 | HG01109.hp1 HG02615.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1871-3790G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41893134 | |||||||
| chr21:41893136 | C | T | 1 | a0001c0001t0004g0338 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1871-3792G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41893136 | |||||||
| chr21:41893138 | T | C | 93 | a0001c0001t0001g0353 a0001c0001t0002g0168 a0001c0001t0003g0044 others(90): Show |
93 | HG00438.hp1 HG00597.hp1 HG00597.hp2 others(90): Show |
intron_variant | MODIFIER | c.1871-3794A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41893138 | |||||||
| chr21:41893173 | T | C | 2 | a0001c0002t0021g0320 a0001c0014t0021g0227 |
2 | HG01106.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1871-3829A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41893173 | |||||||
| chr21:41893392 | T | C | 10 | a0001c0001t0008g0267 a0001c0001t0008g0309 a0001c0002t0008g0311 others(7): Show |
10 | HG00099.hp2 HG00140.hp2 HG00738.hp1 others(7): Show |
intron_variant | MODIFIER | c.1871-4048A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41893392 | |||||||
| chr21:41893445 | T | C | 13 | a0001c0003t0009g0043 a0001c0003t0009g0139 a0001c0004t0009g0137 others(10): Show |
13 | HG01167.hp1 HG01169.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.1871-4101A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41893445 | |||||||
| chr21:41893460 | A | G | 1 | a0001c0006t0034g0289 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1871-4116T>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41893460 | |||||||
| chr21:41893574 | T | C | 73 | a0001c0001t0004g0098 a0001c0001t0004g0113 a0001c0001t0004g0125 others(70): Show |
73 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.1871-4230A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41893574 | |||||||
| chr21:41893585 | GA | G | 72 | a0001c0001t0004g0098 a0001c0001t0004g0113 a0001c0001t0004g0125 others(69): Show |
72 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(69): Show |
intron_variant | MODIFIER | c.1871-4242delT | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41893585 | |||||||
| chr21:41893698 | C | CCT | 12 | a0001c0002t0005g0303 a0001c0003t0005g0024 a0001c0004t0005g0138 others(9): Show |
12 | HG01109.hp1 HG01257.hp1 HG01258.hp2 others(9): Show |
intron_variant | MODIFIER | c.1871-4355_1871-435 others(6): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41893698 | |||||||
| chr21:41893698 | C | CT | 34 | a0001c0001t0001g0050 a0001c0001t0002g0374 a0001c0001t0003g0092 others(31): Show |
34 | HG00673.hp1 HG01070.hp1 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.1871-4355dupA | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41893698 | |||||||
| chr21:41893698 | C | CTT | 45 | a0001c0001t0004g0098 a0001c0001t0004g0113 a0001c0001t0004g0125 others(42): Show |
45 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(42): Show |
intron_variant | MODIFIER | c.1871-4356_1871-435 others(6): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41893698 | |||||||
| chr21:41893698 | C | CTTT | 8 | a0001c0003t0010g0153 a0001c0003t0027g0179 a0001c0011t0010g0222 others(5): Show |
8 | HG01243.hp2 HG01891.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.1871-4357_1871-435 others(7): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41893698 | |||||||
| chr21:41893698 | CTTTTTTT | C | 28 | a0001c0001t0008g0267 a0001c0001t0008g0309 a0001c0001t0049g0220 others(25): Show |
28 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.1871-4361_1871-435 others(11): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41893698 | |||||||
| chr21:41893706 | T | G | 5 | a0001c0001t0002g0112 a0001c0001t0002g0154 a0001c0001t0013g0142 others(2): Show |
5 | HG01069.hp1 HG01071.hp2 HG01074.hp2 others(2): Show |
intron_variant | MODIFIER | c.1871-4362A>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41893706 | |||||||
| chr21:41893719 | T | C | 23 | a0001c0001t0008g0267 a0001c0001t0008g0309 a0001c0001t0049g0220 others(20): Show |
23 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(20): Show |
intron_variant | MODIFIER | c.1871-4375A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41893719 | |||||||
| chr21:41893772 | GCTCACTG others(4): Show |
G | 1 | a0001c0007t0005g0041 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1871-4439_1871-442 others(15): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41893772 | |||||||
| chr21:41893863 | C | T | 15 | a0001c0001t0008g0267 a0001c0001t0008g0309 a0001c0001t0049g0220 others(12): Show |
15 | HG00099.hp2 HG00140.hp2 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.1871-4519G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41893863 | |||||||
| chr21:41893921 | G | A | 1 | a0001c0006t0003g0324 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1871-4577C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41893921 | |||||||
| chr21:41894175 | G | T | 23 | a0001c0001t0008g0267 a0001c0001t0008g0309 a0001c0001t0049g0220 others(20): Show |
23 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(20): Show |
intron_variant | MODIFIER | c.1871-4831C>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41894175 | |||||||
| chr21:41894236 | C | A | 1 | a0001c0004t0009g0223 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1870+4817G>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41894236 | |||||||
| chr21:41894305 | T | C | 23 | a0001c0001t0008g0267 a0001c0001t0008g0309 a0001c0001t0049g0220 others(20): Show |
23 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(20): Show |
intron_variant | MODIFIER | c.1870+4748A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41894305 | |||||||
| chr21:41894397 | G | T | 354 | a0001c0001t0001g0005 a0001c0001t0001g0025 a0001c0001t0001g0027 others(351): Show |
355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.1870+4656C>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41894397 | |||||||
| chr21:41894405 | C | T | 1 | a0001c0001t0049g0220 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1870+4648G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41894405 | |||||||
| chr21:41894421 | G | A | 3 | a0001c0001t0002g0373 a0001c0001t0002g0374 a0001c0003t0001g0189 |
3 | NA19064.hp2 NA19072.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.1870+4632C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41894421 | |||||||
| chr21:41894495 | G | A | 109 | a0001c0001t0001g0005 a0001c0001t0001g0025 a0001c0001t0001g0027 others(106): Show |
110 | HG00438.hp2 HG00738.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.1870+4558C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41894495 | |||||||
| chr21:41894565 | G | A | 4 | a0001c0002t0007g0318 a0001c0002t0007g0345 a0001c0003t0003g0268 others(1): Show |
4 | HG01243.hp1 HG01952.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.1870+4488C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41894565 | |||||||
| chr21:41894756 | T | C | 23 | a0001c0001t0008g0267 a0001c0001t0008g0309 a0001c0001t0049g0220 others(20): Show |
23 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(20): Show |
intron_variant | MODIFIER | c.1870+4297A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41894756 | |||||||
| chr21:41894759 | G | C | 3 | a0001c0001t0003g0081 a0001c0001t0004g0198 a0001c0003t0003g0105 |
3 | HG00621.hp1 HG02015.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.1870+4294C>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41894759 | |||||||
| chr21:41894854 | C | T | 1 | a0001c0003t0001g0064 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1870+4199G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41894854 | |||||||
| chr21:41894934 | T | C | 1 | a0001c0004t0017g0232 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1870+4119A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41894934 | |||||||
| chr21:41894948 | C | T | 285 | a0001c0001t0001g0005 a0001c0001t0001g0025 a0001c0001t0001g0027 others(282): Show |
286 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(283): Show |
intron_variant | MODIFIER | c.1870+4105G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41894948 | |||||||
| chr21:41894972 | T | C | 1 | a0001c0002t0002g0136 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1870+4081A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41894972 | |||||||
| chr21:41895204 | C | T | 9 | a0001c0003t0009g0043 a0001c0003t0009g0139 a0001c0004t0009g0137 others(6): Show |
9 | HG01884.hp1 HG02257.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1870+3849G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41895204 | |||||||
| chr21:41895336 | A | T | 1 | a0001c0001t0003g0046 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1870+3717T>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41895336 | |||||||
| chr21:41895371 | G | C | 2 | a0001c0002t0001g0359 a0001c0003t0001g0224 |
2 | HG01109.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.1870+3682C>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41895371 | |||||||
| chr21:41895383 | C | A | 1 | a0002c0012t0012g0241 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1870+3670G>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41895383 | |||||||
| chr21:41895432 | G | A | 5 | a0001c0001t0052g0394 a0001c0003t0015g0141 a0001c0003t0015g0312 others(2): Show |
5 | HG02109.hp2 HG02886.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1870+3621C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41895432 | |||||||
| chr21:41895660 | C | G | 3 | a0001c0002t0005g0247 a0001c0003t0020g0323 a0001c0028t0020g0244 |
3 | HG02486.hp2 HG02717.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1870+3393G>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41895660 | |||||||
| chr21:41895969 | G | A | 39 | a0001c0001t0008g0267 a0001c0001t0008g0309 a0001c0001t0049g0220 others(36): Show |
39 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.1870+3084C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41895969 | |||||||
| chr21:41895976 | C | T | 52 | a0001c0001t0003g0081 a0001c0001t0004g0098 a0001c0001t0004g0113 others(49): Show |
52 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.1870+3077G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41895976 | |||||||
| chr21:41896097 | C | T | 1 | a0001c0001t0049g0220 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1870+2956G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41896097 | |||||||
| chr21:41896106 | G | C | 150 | a0001c0001t0001g0353 a0001c0001t0002g0017 a0001c0001t0002g0058 others(147): Show |
150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
intron_variant | MODIFIER | c.1870+2947C>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41896106 | |||||||
| chr21:41896127 | G | A | 1 | a0001c0002t0029g0363 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1870+2926C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41896127 | |||||||
| chr21:41896312 | A | G | 3 | a0001c0004t0009g0137 a0001c0004t0009g0350 a0001c0006t0009g0256 |
3 | HG02622.hp1 HG02647.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1870+2741T>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41896312 | |||||||
| chr21:41896372 | G | A | 2 | a0001c0001t0002g0076 a0001c0001t0002g0088 |
2 | HG00408.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.1870+2681C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41896372 | |||||||
| chr21:41896374 | C | T | 2 | a0001c0002t0021g0320 a0001c0014t0021g0227 |
2 | HG01106.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1870+2679G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41896374 | |||||||
| chr21:41896397 | G | A | 21 | a0001c0001t0003g0177 a0001c0001t0003g0184 a0001c0001t0003g0290 others(18): Show |
21 | HG00438.hp1 HG00597.hp1 HG01433.hp1 others(18): Show |
intron_variant | MODIFIER | c.1870+2656C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41896397 | |||||||
| chr21:41896502 | A | T | 3 | a0001c0002t0005g0247 a0001c0003t0020g0323 a0001c0028t0020g0244 |
3 | HG02486.hp2 HG02717.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1870+2551T>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41896502 | |||||||
| chr21:41896580 | G | A | 2 | a0001c0006t0034g0289 a0001c0033t0018g0229 |
2 | HG03139.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1870+2473C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41896580 | |||||||
| chr21:41896634 | G | A | 3 | a0001c0001t0003g0092 a0001c0001t0003g0163 a0001c0001t0003g0193 |
3 | NA18939.hp2 NA18972.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.1870+2419C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41896634 | |||||||
| chr21:41896707 | C | CA | 88 | a0001c0001t0001g0042 a0001c0001t0001g0066 a0001c0001t0001g0353 others(85): Show |
88 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(85): Show |
intron_variant | MODIFIER | c.1870+2345dupT | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41896707 | |||||||
| chr21:41896707 | C | CAA | 34 | a0001c0001t0002g0146 a0001c0001t0006g0007 a0001c0001t0006g0276 others(31): Show |
34 | HG00597.hp2 HG00639.hp2 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.1870+2344_1870+234 others(6): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41896707 | |||||||
| chr21:41896707 | C | CAAA | 6 | a0001c0003t0035g0240 a0001c0004t0009g0137 a0001c0004t0024g0284 others(3): Show |
6 | HG02559.hp2 HG02602.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.1870+2343_1870+234 others(7): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41896707 | |||||||
| chr21:41896707 | C | CAAAA | 18 | a0001c0001t0005g0051 a0001c0001t0008g0267 a0001c0001t0008g0309 others(15): Show |
18 | HG00099.hp2 HG00140.hp2 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.1870+2342_1870+234 others(8): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41896707 | |||||||
| chr21:41896707 | CA | C | 15 | a0001c0001t0001g0005 a0001c0001t0011g0077 a0001c0002t0001g0078 others(12): Show |
15 | HG01257.hp1 HG02572.hp1 HG02647.hp1 others(12): Show |
intron_variant | MODIFIER | c.1870+2345delT | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41896707 | |||||||
| chr21:41896707 | CAA | C | 7 | a0001c0001t0052g0394 a0001c0003t0015g0141 a0001c0003t0015g0312 others(4): Show |
7 | HG02109.hp2 HG02145.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1870+2344_1870+234 others(6): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41896707 | |||||||
| chr21:41896971 | C | A | 8 | a0001c0003t0005g0246 a0001c0003t0005g0332 a0001c0003t0005g0335 others(5): Show |
8 | HG01070.hp1 HG01071.hp1 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.1870+2082G>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41896971 | |||||||
| chr21:41896997 | T | C | 1 | a0001c0002t0003g0101 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1870+2056A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41896997 | |||||||
| chr21:41897032 | T | A | 2 | a0001c0006t0034g0289 a0001c0033t0018g0229 |
2 | HG03139.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1870+2021A>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41897032 | |||||||
| chr21:41897042 | G | A | 161 | a0001c0001t0001g0353 a0001c0001t0002g0168 a0001c0001t0003g0046 others(158): Show |
161 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.1870+2011C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41897042 | |||||||
| chr21:41897073 | C | T | 1 | a0001c0011t0005g0140 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1870+1980G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41897073 | |||||||
| chr21:41897124 | G | C | 79 | a0001c0001t0002g0168 a0001c0001t0003g0046 a0001c0001t0003g0081 others(76): Show |
79 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.1870+1929C>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41897124 | |||||||
| chr21:41897290 | C | T | 1 | a0001c0003t0005g0061 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1870+1763G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41897290 | |||||||
| chr21:41897296 | G | A | 1 | a0001c0003t0003g0049 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1870+1757C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41897296 | |||||||
| chr21:41897332 | C | G | 79 | a0001c0001t0001g0353 a0001c0001t0003g0177 a0001c0001t0003g0184 others(76): Show |
79 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.1870+1721G>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41897332 | |||||||
| chr21:41897340 | T | A | 1 | a0001c0006t0008g0387 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1870+1713A>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41897340 | |||||||
| chr21:41897345 | G | C | 1 | a0001c0001t0005g0259 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1870+1708C>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41897345 | |||||||
| chr21:41897473 | G | A | 7 | a0001c0001t0003g0384 a0001c0001t0004g0266 a0001c0001t0004g0288 others(4): Show |
7 | HG00323.hp1 HG01074.hp1 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.1870+1580C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41897473 | |||||||
| chr21:41897533 | C | T | 2 | a0001c0002t0001g0359 a0001c0003t0001g0224 |
2 | HG01109.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.1870+1520G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41897533 | |||||||
| chr21:41897562 | T | A | 1 | a0001c0001t0002g0296 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1870+1491A>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41897562 | |||||||
| chr21:41897607 | C | T | 1 | a0001c0003t0001g0064 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1870+1446G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41897607 | |||||||
| chr21:41897671 | C | G | 1 | a0001c0003t0003g0065 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1870+1382G>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41897671 | |||||||
| chr21:41897728 | C | T | 1 | a0001c0003t0001g0064 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1870+1325G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41897728 | |||||||
| chr21:41897731 | C | T | 1 | a0002c0008t0009g0161 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1870+1322G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41897731 | |||||||
| chr21:41897805 | T | C | 93 | a0001c0001t0001g0353 a0001c0001t0002g0264 a0001c0001t0003g0177 others(90): Show |
93 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.1870+1248A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41897805 | |||||||
| chr21:41897864 | G | A | 1 | a0001c0033t0018g0229 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1870+1189C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41897864 | |||||||
| chr21:41897901 | C | T | 1 | a0001c0001t0004g0098 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1870+1152G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41897901 | |||||||
| chr21:41897914 | C | A | 16 | a0001c0001t0006g0276 a0001c0001t0006g0277 a0001c0002t0001g0275 others(13): Show |
16 | HG00639.hp2 HG00642.hp1 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.1870+1139G>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41897914 | |||||||
| chr21:41897946 | C | T | 3 | a0002c0012t0012g0241 a0002c0012t0012g0262 a0002c0012t0012g0282 |
3 | HG02486.hp1 HG03540.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1870+1107G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41897946 | |||||||
| chr21:41898150 | C | T | 15 | a0001c0001t0005g0051 a0001c0001t0008g0267 a0001c0001t0008g0309 others(12): Show |
15 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(12): Show |
intron_variant | MODIFIER | c.1870+903G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41898150 | |||||||
| chr21:41898229 | T | C | 1 | a0001c0003t0003g0334 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1870+824A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41898229 | |||||||
| chr21:41898243 | T | C | 1 | a0001c0003t0003g0268 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1870+810A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41898243 | |||||||
| chr21:41898272 | G | A | 11 | a0001c0001t0002g0017 a0001c0001t0004g0113 a0001c0001t0040g0018 others(8): Show |
11 | HG02027.hp1 HG02080.hp2 HG02132.hp2 others(8): Show |
intron_variant | MODIFIER | c.1870+781C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41898272 | |||||||
| chr21:41898273 | T | G | 99 | a0001c0001t0001g0353 a0001c0001t0003g0177 a0001c0001t0003g0184 others(96): Show |
99 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.1870+780A>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41898273 | |||||||
| chr21:41898349 | G | C | 1 | a0001c0005t0005g0221 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1870+704C>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41898349 | |||||||
| chr21:41898361 | A | G | 7 | a0001c0001t0052g0394 a0001c0003t0015g0141 a0001c0003t0015g0312 others(4): Show |
7 | HG02109.hp2 HG02622.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1870+692T>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41898361 | |||||||
| chr21:41898364 | T | G | 1 | a0001c0003t0008g0341 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1870+689A>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41898364 | |||||||
| chr21:41898369 | C | CG | 3 | a0001c0002t0005g0303 a0001c0003t0005g0024 a0001c0005t0005g0348 |
3 | HG01109.hp1 HG03041.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1870+683dupC | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41898369 | |||||||
| chr21:41898497 | T | C | 1 | a0001c0002t0001g0095 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1870+556A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41898497 | |||||||
| chr21:41898747 | A | G | 177 | a0001c0001t0001g0353 a0001c0001t0001g0380 a0001c0001t0002g0017 others(174): Show |
177 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.1870+306T>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41898747 | |||||||
| chr21:41898762 | G | C | 91 | a0001c0001t0001g0353 a0001c0001t0003g0177 a0001c0001t0003g0184 others(88): Show |
91 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.1870+291C>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41898762 | |||||||
| chr21:41898775 | G | A | 1 | a0001c0003t0035g0240 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1870+278C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41898775 | |||||||
| chr21:41898782 | A | G | 177 | a0001c0001t0001g0353 a0001c0001t0001g0380 a0001c0001t0002g0017 others(174): Show |
177 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.1870+271T>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41898782 | |||||||
| chr21:41898885 | C | T | 92 | a0001c0001t0001g0353 a0001c0001t0003g0177 a0001c0001t0003g0184 others(89): Show |
92 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.1870+168G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41898885 | |||||||
| chr21:41898888 | G | A | 2 | a0001c0003t0005g0061 a0001c0003t0009g0139 |
2 | HG02965.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1870+165C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41898888 | |||||||
| chr21:41898897 | T | C | 5 | a0002c0012t0009g0062 a0002c0012t0012g0241 a0002c0012t0012g0262 others(2): Show |
5 | HG01167.hp1 HG01169.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1870+156A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41898897 | |||||||
| chr21:41898934 | C | T | 92 | a0001c0001t0001g0353 a0001c0001t0003g0177 a0001c0001t0003g0184 others(89): Show |
92 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.1870+119G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41898934 | |||||||
| chr21:41898951 | G | A | 2 | a0001c0001t0004g0297 a0001c0001t0004g0298 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1870+102C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41898951 | |||||||
| chr21:41898970 | G | GCAGATGA others(15): Show |
10 | a0001c0004t0009g0137 a0001c0004t0009g0223 a0001c0004t0009g0350 others(7): Show |
10 | HG01257.hp1 HG01258.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.1870+61_1870+82dup others(22): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41898970 | |||||||
| chr21:41899013 | C | G | 3 | a0003c0009t0002g0369 a0003c0009t0007g0208 a0003c0009t0007g0352 |
3 | HG00609.hp2 HG00673.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.1870+40G>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41899013 | |||||||
| chr21:41899014 | A | C | 1 | a0001c0003t0001g0224 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1870+39T>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41899014 | |||||||
| chr21:41899027 | G | A | 1 | a0001c0003t0005g0263 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1870+26C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41899027 | |||||||
| chr21:41899045 | G | A | 5 | a0001c0011t0005g0140 a0001c0021t0005g0235 a0002c0008t0005g0260 others(2): Show |
5 | HG01884.hp2 HG02559.hp1 HG03225.hp2 others(2): Show |
splice_region_variant&intron_variant | LOW | c.1870+8C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 13/13 | chr21 | 41899045 | |||||||
| chr21:41899412 | G | A | 3 | a0001c0002t0017g0279 a0001c0004t0017g0028 a0001c0004t0017g0232 |
3 | HG02572.hp1 HG02647.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1561-50C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 12/13 | chr21 | 41899412 | |||||||
| chr21:41899425 | A | C | 198 | a0001c0001t0001g0353 a0001c0001t0001g0380 a0001c0001t0002g0017 others(195): Show |
198 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.1561-63T>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 12/13 | chr21 | 41899425 | |||||||
| chr21:41899447 | A | C | 11 | a0001c0003t0001g0008 a0001c0003t0001g0272 a0001c0003t0005g0246 others(8): Show |
11 | HG01070.hp1 HG01071.hp1 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.1561-85T>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 12/13 | chr21 | 41899447 | |||||||
| chr21:41899496 | T | G | 138 | a0001c0001t0001g0353 a0001c0001t0001g0380 a0001c0001t0002g0017 others(135): Show |
138 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.1561-134A>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 12/13 | chr21 | 41899496 | |||||||
| chr21:41899504 | G | A | 13 | a0001c0003t0005g0263 a0001c0003t0012g0239 a0001c0004t0005g0313 others(10): Show |
13 | HG00741.hp2 HG02258.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.1561-142C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 12/13 | chr21 | 41899504 | |||||||
| chr21:41899522 | T | C | 1 | a0001c0001t0001g0042 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1561-160A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 12/13 | chr21 | 41899522 | |||||||
| chr21:41899628 | A | G | 130 | a0001c0001t0001g0353 a0001c0001t0001g0380 a0001c0001t0002g0017 others(127): Show |
130 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.1561-266T>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 12/13 | chr21 | 41899628 | |||||||
| chr21:41899675 | A | G | 85 | a0001c0001t0001g0380 a0001c0001t0002g0017 a0001c0001t0002g0168 others(82): Show |
85 | HG00323.hp1 HG00597.hp2 HG00621.hp1 others(82): Show |
intron_variant | MODIFIER | c.1561-313T>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 12/13 | chr21 | 41899675 | |||||||
| chr21:41899689 | G | T | 11 | a0001c0003t0005g0263 a0001c0003t0012g0239 a0001c0004t0005g0313 others(8): Show |
11 | HG00741.hp2 HG02258.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.1561-327C>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 12/13 | chr21 | 41899689 | |||||||
| chr21:41899695 | G | A | 1 | a0001c0001t0001g0178 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1561-333C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 12/13 | chr21 | 41899695 | |||||||
| chr21:41899710 | C | T | 4 | a0001c0003t0001g0008 a0001c0003t0005g0246 a0001c0003t0005g0332 others(1): Show |
4 | HG01070.hp1 HG01071.hp1 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.1561-348G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 12/13 | chr21 | 41899710 | |||||||
| chr21:41899726 | A | G | 52 | a0001c0001t0001g0353 a0001c0001t0003g0177 a0001c0001t0003g0184 others(49): Show |
52 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.1561-364T>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 12/13 | chr21 | 41899726 | |||||||
| chr21:41899743 | G | A | 1 | a0001c0002t0002g0129 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1561-381C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 12/13 | chr21 | 41899743 | |||||||
| chr21:41899774 | T | C | 2 | a0003c0017t0018g0331 a0003c0031t0018g0158 |
2 | HG02109.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1561-412A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 12/13 | chr21 | 41899774 | |||||||
| chr21:41899847 | A | G | 2 | a0001c0001t0023g0052 a0001c0001t0023g0057 |
2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1561-485T>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 12/13 | chr21 | 41899847 | |||||||
| chr21:41899865 | C | T | 52 | a0001c0001t0001g0353 a0001c0001t0003g0177 a0001c0001t0003g0184 others(49): Show |
52 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.1561-503G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 12/13 | chr21 | 41899865 | |||||||
| chr21:41899875 | C | A | 52 | a0001c0001t0001g0353 a0001c0001t0003g0177 a0001c0001t0003g0184 others(49): Show |
52 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.1561-513G>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 12/13 | chr21 | 41899875 | |||||||
| chr21:41899892 | A | C | 1 | a0003c0015t0005g0361 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1561-530T>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 12/13 | chr21 | 41899892 | |||||||
| chr21:41899892 | A | G | 5 | a0001c0001t0004g0190 a0001c0001t0004g0199 a0001c0002t0004g0087 others(2): Show |
5 | NA18950.hp2 NA18951.hp1 NA18999.hp2 others(2): Show |
intron_variant | MODIFIER | c.1561-530T>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 12/13 | chr21 | 41899892 | |||||||
| chr21:41899996 | G | A | 51 | a0001c0001t0001g0353 a0001c0001t0003g0177 a0001c0001t0003g0184 others(48): Show |
51 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.1561-634C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 12/13 | chr21 | 41899996 | |||||||
| chr21:41900015 | G | A | 2 | a0001c0003t0020g0323 a0002c0008t0009g0161 |
2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1561-653C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 12/13 | chr21 | 41900015 | |||||||
| chr21:41900090 | A | C | 7 | a0001c0003t0020g0323 a0002c0008t0009g0161 a0002c0012t0009g0062 others(4): Show |
7 | HG01167.hp1 HG01169.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1561-728T>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 12/13 | chr21 | 41900090 | |||||||
| chr21:41900108 | T | A | 60 | a0001c0001t0001g0353 a0001c0001t0003g0177 a0001c0001t0003g0184 others(57): Show |
60 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.1561-746A>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 12/13 | chr21 | 41900108 | |||||||
| chr21:41900147 | G | A | 1 | a0002c0010t0001g0131 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1561-785C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 12/13 | chr21 | 41900147 | |||||||
| chr21:41900229 | A | G | 61 | a0001c0001t0001g0353 a0001c0001t0003g0177 a0001c0001t0003g0184 others(58): Show |
61 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.1561-867T>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 12/13 | chr21 | 41900229 | |||||||
| chr21:41900231 | G | C | 3 | a0002c0012t0012g0241 a0002c0012t0012g0262 a0002c0012t0012g0282 |
3 | HG02486.hp1 HG03540.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1561-869C>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 12/13 | chr21 | 41900231 | |||||||
| chr21:41900259 | G | C | 1 | a0001c0002t0007g0345 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1561-897C>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 12/13 | chr21 | 41900259 | |||||||
| chr21:41900281 | T | A | 60 | a0001c0001t0001g0353 a0001c0001t0003g0177 a0001c0001t0003g0184 others(57): Show |
60 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.1561-919A>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 12/13 | chr21 | 41900281 | |||||||
| chr21:41900283 | A | T | 60 | a0001c0001t0001g0353 a0001c0001t0003g0177 a0001c0001t0003g0184 others(57): Show |
60 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.1561-921T>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 12/13 | chr21 | 41900283 | |||||||
| chr21:41900338 | G | A | 4 | a0001c0002t0005g0303 a0001c0003t0005g0024 a0001c0005t0005g0156 others(1): Show |
4 | HG01109.hp1 HG02615.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1561-976C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 12/13 | chr21 | 41900338 | |||||||
| chr21:41900411 | T | C | 15 | a0001c0001t0005g0051 a0001c0001t0008g0267 a0001c0001t0008g0309 others(12): Show |
15 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(12): Show |
intron_variant | MODIFIER | c.1561-1049A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 12/13 | chr21 | 41900411 | |||||||
| chr21:41900483 | C | A | 60 | a0001c0001t0001g0353 a0001c0001t0003g0177 a0001c0001t0003g0184 others(57): Show |
60 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.1561-1121G>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 12/13 | chr21 | 41900483 | |||||||
| chr21:41900488 | C | T | 12 | a0001c0003t0005g0061 a0001c0003t0009g0139 a0003c0015t0005g0329 others(9): Show |
12 | HG01257.hp1 HG01258.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.1561-1126G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 12/13 | chr21 | 41900488 | |||||||
| chr21:41900491 | C | T | 1 | a0003c0034t0004g0228 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1561-1129G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 12/13 | chr21 | 41900491 | |||||||
| chr21:41900641 | A | G | 176 | a0001c0001t0001g0353 a0001c0001t0001g0380 a0001c0001t0002g0017 others(173): Show |
176 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.1560+981T>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 12/13 | chr21 | 41900641 | |||||||
| chr21:41900669 | C | T | 1 | a0001c0001t0001g0025 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1560+953G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 12/13 | chr21 | 41900669 | |||||||
| chr21:41900738 | TC | T | 4 | a0001c0004t0009g0137 a0001c0004t0009g0350 a0001c0006t0009g0256 others(1): Show |
4 | HG02622.hp1 HG02647.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1560+883delG | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 12/13 | chr21 | 41900738 | |||||||
| chr21:41900842 | A | G | 7 | a0001c0002t0017g0279 a0001c0004t0004g0280 a0001c0004t0004g0281 others(4): Show |
7 | HG02572.hp1 HG02647.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1560+780T>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 12/13 | chr21 | 41900842 | |||||||
| chr21:41900868 | G | C | 62 | a0001c0001t0001g0050 a0001c0001t0001g0353 a0001c0001t0001g0380 others(59): Show |
62 | HG00438.hp1 HG00597.hp1 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.1560+754C>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 12/13 | chr21 | 41900868 | |||||||
| chr21:41900890 | A | G | 1 | a0001c0003t0012g0239 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1560+732T>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 12/13 | chr21 | 41900890 | |||||||
| chr21:41900988 | T | C | 1 | a0001c0002t0007g0318 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1560+634A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 12/13 | chr21 | 41900988 | |||||||
| chr21:41901028 | T | G | 1 | a0001c0001t0007g0175 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1560+594A>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 12/13 | chr21 | 41901028 | |||||||
| chr21:41901077 | T | C | 1 | a0001c0001t0006g0007 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1560+545A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 12/13 | chr21 | 41901077 | |||||||
| chr21:41901151 | G | A | 1 | a0002c0010t0007g0111 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1560+471C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 12/13 | chr21 | 41901151 | |||||||
| chr21:41901174 | G | A | 63 | a0001c0001t0005g0259 a0001c0001t0006g0276 a0001c0001t0006g0277 others(60): Show |
64 | HG00609.hp2 HG00639.hp2 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.1560+448C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 12/13 | chr21 | 41901174 | |||||||
| chr21:41901262 | G | T | 15 | a0001c0001t0005g0287 a0001c0003t0008g0155 a0001c0005t0005g0001 others(12): Show |
16 | HG00609.hp2 HG00673.hp1 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.1560+360C>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 12/13 | chr21 | 41901262 | |||||||
| chr21:41901317 | C | A | 91 | a0001c0001t0001g0005 a0001c0001t0001g0037 a0001c0001t0003g0081 others(88): Show |
91 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(88): Show |
intron_variant | MODIFIER | c.1560+305G>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 12/13 | chr21 | 41901317 | |||||||
| chr21:41901332 | C | T | 1 | a0001c0001t0002g0154 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1560+290G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 12/13 | chr21 | 41901332 | |||||||
| chr21:41901419 | A | G | 203 | a0001c0001t0001g0380 a0001c0001t0002g0211 a0001c0001t0003g0081 others(200): Show |
204 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.1560+203T>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 12/13 | chr21 | 41901419 | |||||||
| chr21:41901533 | T | C | 2 | a0002c0012t0009g0062 a0002c0012t0050g0063 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1560+89A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 12/13 | chr21 | 41901533 | |||||||
| chr21:41901768 | T | C | 1 | a0001c0001t0003g0177 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1433-19A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 11/13 | chr21 | 41901768 | |||||||
| chr21:41901837 | G | A | 24 | a0001c0002t0005g0303 a0001c0003t0005g0024 a0001c0005t0005g0001 others(21): Show |
25 | HG01109.hp1 HG01257.hp1 HG01258.hp2 others(22): Show |
intron_variant | MODIFIER | c.1433-88C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 11/13 | chr21 | 41901837 | |||||||
| chr21:41901895 | T | A | 25 | a0001c0002t0005g0303 a0001c0003t0005g0024 a0001c0003t0035g0240 others(22): Show |
26 | HG01109.hp1 HG01257.hp1 HG01258.hp2 others(23): Show |
intron_variant | MODIFIER | c.1433-146A>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 11/13 | chr21 | 41901895 | |||||||
| chr21:41901924 | A | C | 1 | a0001c0033t0018g0229 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1433-175T>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 11/13 | chr21 | 41901924 | |||||||
| chr21:41902015 | C | T | 11 | a0001c0003t0005g0061 a0001c0003t0009g0139 a0001c0003t0012g0239 others(8): Show |
11 | HG02280.hp2 HG02451.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.1433-266G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 11/13 | chr21 | 41902015 | |||||||
| chr21:41902195 | A | C | 292 | a0001c0001t0001g0005 a0001c0001t0001g0025 a0001c0001t0001g0027 others(289): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.1433-446T>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 11/13 | chr21 | 41902195 | |||||||
| chr21:41902338 | G | A | 26 | a0001c0001t0013g0371 a0001c0001t0036g0356 a0001c0003t0001g0047 others(23): Show |
26 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(23): Show |
intron_variant | MODIFIER | c.1433-589C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 11/13 | chr21 | 41902338 | |||||||
| chr21:41902380 | C | T | 176 | a0001c0001t0001g0005 a0001c0001t0001g0025 a0001c0001t0001g0027 others(173): Show |
176 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(173): Show |
intron_variant | MODIFIER | c.1433-631G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 11/13 | chr21 | 41902380 | |||||||
| chr21:41902416 | G | A | 1 | a0001c0003t0003g0069 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1433-667C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 11/13 | chr21 | 41902416 | |||||||
| chr21:41902757 | T | C | 114 | a0001c0001t0001g0066 a0001c0001t0013g0371 a0001c0001t0036g0356 others(111): Show |
115 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.1433-1008A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 11/13 | chr21 | 41902757 | |||||||
| chr21:41902793 | CA | C | 68 | a0001c0001t0001g0066 a0001c0003t0001g0045 a0001c0003t0001g0047 others(65): Show |
68 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.1433-1045delT | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 11/13 | chr21 | 41902793 | |||||||
| chr21:41902854 | T | C | 10 | a0001c0003t0001g0272 a0001c0003t0009g0043 a0001c0003t0010g0153 others(7): Show |
10 | HG01243.hp2 HG02622.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.1433-1105A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 11/13 | chr21 | 41902854 | |||||||
| chr21:41902881 | T | C | 278 | a0001c0001t0001g0005 a0001c0001t0001g0025 a0001c0001t0001g0027 others(275): Show |
279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.1433-1132A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 11/13 | chr21 | 41902881 | |||||||
| chr21:41902957 | C | T | 1 | a0001c0033t0018g0229 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1433-1208G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 11/13 | chr21 | 41902957 | |||||||
| chr21:41902994 | C | A | 9 | a0001c0003t0005g0024 a0001c0005t0005g0001 a0001c0005t0005g0156 others(6): Show |
10 | HG01257.hp1 HG01258.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1433-1245G>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 11/13 | chr21 | 41902994 | |||||||
| chr21:41903137 | C | T | 6 | a0001c0011t0005g0140 a0001c0011t0005g0306 a0001c0011t0010g0222 others(3): Show |
6 | HG01891.hp1 HG02559.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1433-1388G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 11/13 | chr21 | 41903137 | |||||||
| chr21:41903153 | C | T | 6 | a0001c0011t0005g0140 a0001c0011t0005g0306 a0001c0011t0010g0222 others(3): Show |
6 | HG01891.hp1 HG02559.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1433-1404G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 11/13 | chr21 | 41903153 | |||||||
| chr21:41903184 | A | C | 155 | a0001c0001t0001g0005 a0001c0001t0001g0025 a0001c0001t0001g0027 others(152): Show |
155 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.1433-1435T>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 11/13 | chr21 | 41903184 | |||||||
| chr21:41903507 | T | C | 1 | a0001c0002t0004g0067 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1433-1758A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 11/13 | chr21 | 41903507 | |||||||
| chr21:41903595 | G | A | 1 | a0001c0007t0005g0009 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1433-1846C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 11/13 | chr21 | 41903595 | |||||||
| chr21:41903670 | G | T | 1 | a0001c0002t0005g0247 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1433-1921C>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 11/13 | chr21 | 41903670 | |||||||
| chr21:41903674 | C | A | 1 | a0001c0002t0006g0100 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1433-1925G>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 11/13 | chr21 | 41903674 | |||||||
| chr21:41903711 | T | C | 2 | a0001c0014t0005g0243 a0001c0014t0005g0250 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1433-1962A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 11/13 | chr21 | 41903711 | |||||||
| chr21:41903782 | G | A | 2 | a0002c0008t0005g0354 a0002c0008t0045g0226 |
2 | HG01884.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1432+1942C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 11/13 | chr21 | 41903782 | |||||||
| chr21:41903816 | G | C | 2 | a0001c0003t0012g0239 a0009c0026t0004g0271 |
2 | HG03471.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1432+1908C>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 11/13 | chr21 | 41903816 | |||||||
| chr21:41903822 | C | G | 27 | a0001c0003t0001g0272 a0001c0003t0001g0349 a0001c0003t0005g0263 others(24): Show |
27 | HG00639.hp1 HG00642.hp2 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.1432+1902G>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 11/13 | chr21 | 41903822 | |||||||
| chr21:41903853 | A | C | 1 | a0001c0003t0003g0019 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1432+1871T>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 11/13 | chr21 | 41903853 | |||||||
| chr21:41903915 | G | A | 158 | a0001c0001t0001g0005 a0001c0001t0001g0025 a0001c0001t0001g0027 others(155): Show |
158 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.1432+1809C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 11/13 | chr21 | 41903915 | |||||||
| chr21:41903929 | C | T | 10 | a0001c0005t0002g0327 a0001c0005t0007g0310 a0001c0005t0008g0307 others(7): Show |
10 | HG00639.hp1 HG00642.hp2 HG00738.hp1 others(7): Show |
intron_variant | MODIFIER | c.1432+1795G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 11/13 | chr21 | 41903929 | |||||||
| chr21:41903946 | G | C | 1 | a0003c0036t0051g0143 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1432+1778C>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 11/13 | chr21 | 41903946 | |||||||
| chr21:41903967 | C | T | 8 | a0001c0003t0001g0272 a0001c0003t0009g0043 a0001c0003t0010g0153 others(5): Show |
8 | HG01243.hp2 HG02622.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.1432+1757G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 11/13 | chr21 | 41903967 | |||||||
| chr21:41904008 | T | G | 2 | a0002c0008t0009g0161 a0002c0027t0009g0325 |
2 | HG02257.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1432+1716A>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 11/13 | chr21 | 41904008 | |||||||
| chr21:41904146 | C | T | 286 | a0001c0001t0001g0005 a0001c0001t0001g0025 a0001c0001t0001g0027 others(283): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.1432+1578G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 11/13 | chr21 | 41904146 | |||||||
| chr21:41904168 | C | T | 1 | a0001c0003t0001g0187 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1432+1556G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 11/13 | chr21 | 41904168 | |||||||
| chr21:41904331 | C | CTG | 286 | a0001c0001t0001g0005 a0001c0001t0001g0025 a0001c0001t0001g0027 others(283): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.1432+1392_1432+139 others(6): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 11/13 | chr21 | 41904331 | |||||||
| chr21:41904446 | T | C | 5 | a0001c0040t0008g0305 a0002c0010t0007g0111 a0002c0010t0016g0292 others(2): Show |
5 | HG00639.hp1 HG00642.hp2 HG01070.hp2 others(2): Show |
intron_variant | MODIFIER | c.1432+1278A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 11/13 | chr21 | 41904446 | |||||||
| chr21:41904532 | C | T | 1 | a0001c0014t0021g0227 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1432+1192G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 11/13 | chr21 | 41904532 | |||||||
| chr21:41904617 | C | CG | 5 | a0001c0001t0003g0044 a0001c0002t0002g0164 a0001c0002t0002g0205 others(2): Show |
5 | HG00741.hp2 NA18949.hp2 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.1432+1106dupC | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 11/13 | chr21 | 41904617 | |||||||
| chr21:41904618 | G | A | 5 | a0001c0001t0006g0007 a0001c0002t0001g0123 a0001c0002t0001g0124 others(2): Show |
5 | HG01943.hp1 HG01978.hp2 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.1432+1106C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 11/13 | chr21 | 41904618 | |||||||
| chr21:41904634 | A | C | 1 | a0001c0023t0005g0234 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1432+1090T>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 11/13 | chr21 | 41904634 | |||||||
| chr21:41904689 | G | A | 19 | a0001c0003t0001g0272 a0001c0003t0009g0043 a0001c0003t0010g0153 others(16): Show |
19 | HG01243.hp2 HG01891.hp1 HG02486.hp2 others(16): Show |
intron_variant | MODIFIER | c.1432+1035C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 11/13 | chr21 | 41904689 | |||||||
| chr21:41904834 | A | G | 1 | a0001c0028t0020g0244 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1432+890T>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 11/13 | chr21 | 41904834 | |||||||
| chr21:41904859 | G | A | 4 | a0001c0002t0002g0015 a0001c0002t0002g0376 a0001c0002t0002g0382 others(1): Show |
4 | HG02040.hp2 NA18989.hp1 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.1432+865C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 11/13 | chr21 | 41904859 | |||||||
| chr21:41904897 | C | T | 1 | a0001c0004t0005g0358 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1432+827G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 11/13 | chr21 | 41904897 | |||||||
| chr21:41904936 | A | AT | 285 | a0001c0001t0001g0005 a0001c0001t0001g0025 a0001c0001t0001g0027 others(282): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.1432+787_1432+788i others(3): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 11/13 | chr21 | 41904936 | |||||||
| chr21:41904936 | A | T | 1 | a0001c0001t0005g0287 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1432+788T>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 11/13 | chr21 | 41904936 | |||||||
| chr21:41905036 | G | C | 86 | a0001c0003t0001g0008 a0001c0003t0001g0045 a0001c0003t0001g0047 others(83): Show |
86 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.1432+688C>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 11/13 | chr21 | 41905036 | |||||||
| chr21:41905102 | GC | G | 19 | a0001c0003t0001g0272 a0001c0003t0009g0043 a0001c0003t0010g0153 others(16): Show |
19 | HG01243.hp2 HG01891.hp1 HG02486.hp2 others(16): Show |
intron_variant | MODIFIER | c.1432+621delG | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 11/13 | chr21 | 41905102 | |||||||
| chr21:41905110 | T | C | 200 | a0001c0001t0001g0005 a0001c0001t0001g0025 a0001c0001t0001g0027 others(197): Show |
201 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.1432+614A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 11/13 | chr21 | 41905110 | |||||||
| chr21:41905310 | C | CT | 6 | a0001c0001t0003g0046 a0001c0002t0001g0073 a0001c0002t0002g0129 others(3): Show |
6 | HG00735.hp2 HG01175.hp2 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.1432+413dupA | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 11/13 | chr21 | 41905310 | |||||||
| chr21:41905310 | CT | C | 8 | a0001c0001t0001g0085 a0001c0001t0003g0044 a0001c0001t0036g0356 others(5): Show |
8 | HG00741.hp2 HG01099.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1432+413delA | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 11/13 | chr21 | 41905310 | |||||||
| chr21:41905310 | CTT | C | 153 | a0001c0001t0001g0005 a0001c0001t0001g0025 a0001c0001t0001g0027 others(150): Show |
153 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.1432+412_1432+413d others(4): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 11/13 | chr21 | 41905310 | |||||||
| chr21:41905310 | CTTT | C | 79 | a0001c0001t0001g0035 a0001c0001t0002g0300 a0001c0001t0003g0093 others(76): Show |
79 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.1432+411_1432+413d others(5): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 11/13 | chr21 | 41905310 | |||||||
| chr21:41905310 | CTTTT | C | 16 | a0001c0003t0001g0209 a0001c0003t0001g0272 a0001c0003t0009g0043 others(13): Show |
16 | HG01243.hp2 HG01891.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.1432+410_1432+413d others(6): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 11/13 | chr21 | 41905310 | |||||||
| chr21:41905312 | TTTTTTTT others(31): Show |
T | 31 | a0001c0003t0001g0349 a0001c0003t0005g0024 a0001c0003t0005g0263 others(28): Show |
32 | HG01257.hp1 HG01258.hp2 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.1432+374_1432+411d others(40): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 11/13 | chr21 | 41905312 | |||||||
| chr21:41905315 | T | C | 2 | a0001c0005t0002g0327 a0001c0005t0007g0310 |
2 | HG01099.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.1432+409A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 11/13 | chr21 | 41905315 | |||||||
| chr21:41905406 | C | T | 2 | a0001c0004t0005g0138 a0003c0036t0051g0143 |
2 | HG03579.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1432+318G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 11/13 | chr21 | 41905406 | |||||||
| chr21:41905412 | G | A | 2 | a0001c0003t0020g0323 a0003c0031t0018g0158 |
2 | HG02486.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1432+312C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 11/13 | chr21 | 41905412 | |||||||
| chr21:41905515 | G | C | 1 | a0001c0001t0001g0132 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1432+209C>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 11/13 | chr21 | 41905515 | |||||||
| chr21:41905523 | G | A | 2 | a0001c0002t0001g0362 a0001c0002t0002g0022 |
2 | HG03017.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.1432+201C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 11/13 | chr21 | 41905523 | |||||||
| chr21:41905594 | G | A | 1 | a0003c0017t0018g0331 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1432+130C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 11/13 | chr21 | 41905594 | |||||||
| chr21:41905633 | CA | C | 151 | a0001c0001t0001g0005 a0001c0001t0001g0025 a0001c0001t0001g0027 others(148): Show |
151 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.1432+90delT | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 11/13 | chr21 | 41905633 | |||||||
| chr21:41905694 | G | A | 1 | a0001c0001t0002g0386 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1432+30C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 11/13 | chr21 | 41905694 | |||||||
| chr21:41905864 | A | G | 125 | a0001c0003t0001g0008 a0001c0003t0001g0045 a0001c0003t0001g0047 others(122): Show |
126 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.1319-27T>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 10/13 | chr21 | 41905864 | |||||||
| chr21:41905899 | G | A | 3 | a0001c0011t0010g0222 a0001c0011t0010g0245 a0001c0011t0010g0269 |
3 | HG01891.hp1 HG03098.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1319-62C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 10/13 | chr21 | 41905899 | |||||||
| chr21:41905963 | C | T | 2 | a0001c0040t0008g0305 a0002c0010t0007g0111 |
2 | HG01070.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.1319-126G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 10/13 | chr21 | 41905963 | |||||||
| chr21:41905964 | G | A | 1 | a0001c0003t0005g0061 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1319-127C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 10/13 | chr21 | 41905964 | |||||||
| chr21:41905970 | T | C | 136 | a0001c0002t0001g0359 a0001c0003t0001g0008 a0001c0003t0001g0045 others(133): Show |
137 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.1319-133A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 10/13 | chr21 | 41905970 | |||||||
| chr21:41906099 | C | T | 1 | a0001c0003t0001g0104 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1319-262G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 10/13 | chr21 | 41906099 | |||||||
| chr21:41906221 | C | G | 125 | a0001c0003t0001g0008 a0001c0003t0001g0045 a0001c0003t0001g0047 others(122): Show |
126 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.1319-384G>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 10/13 | chr21 | 41906221 | |||||||
| chr21:41906415 | T | G | 276 | a0001c0001t0001g0005 a0001c0001t0001g0025 a0001c0001t0001g0027 others(273): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.1318+577A>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 10/13 | chr21 | 41906415 | |||||||
| chr21:41906487 | T | C | 6 | a0001c0005t0002g0327 a0001c0005t0007g0310 a0001c0005t0008g0307 others(3): Show |
6 | HG00738.hp1 HG01099.hp1 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.1318+505A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 10/13 | chr21 | 41906487 | |||||||
| chr21:41906501 | G | C | 1 | a0001c0024t0012g0233 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1318+491C>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 10/13 | chr21 | 41906501 | |||||||
| chr21:41906505 | C | A | 125 | a0001c0003t0001g0008 a0001c0003t0001g0045 a0001c0003t0001g0047 others(122): Show |
126 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.1318+487G>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 10/13 | chr21 | 41906505 | |||||||
| chr21:41906508 | C | T | 125 | a0001c0003t0001g0008 a0001c0003t0001g0045 a0001c0003t0001g0047 others(122): Show |
126 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.1318+484G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 10/13 | chr21 | 41906508 | |||||||
| chr21:41906512 | C | T | 125 | a0001c0003t0001g0008 a0001c0003t0001g0045 a0001c0003t0001g0047 others(122): Show |
126 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.1318+480G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 10/13 | chr21 | 41906512 | |||||||
| chr21:41906537 | G | C | 1 | a0001c0002t0002g0004 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1318+455C>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 10/13 | chr21 | 41906537 | |||||||
| chr21:41906566 | C | T | 125 | a0001c0003t0001g0008 a0001c0003t0001g0045 a0001c0003t0001g0047 others(122): Show |
126 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.1318+426G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 10/13 | chr21 | 41906566 | |||||||
| chr21:41906617 | G | A | 1 | a0003c0034t0004g0228 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1318+375C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 10/13 | chr21 | 41906617 | |||||||
| chr21:41906688 | C | T | 1 | a0001c0003t0009g0043 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1318+304G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 10/13 | chr21 | 41906688 | |||||||
| chr21:41906727 | T | C | 1 | a0001c0033t0018g0229 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1318+265A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 10/13 | chr21 | 41906727 | |||||||
| chr21:41906739 | C | T | 38 | a0001c0003t0001g0045 a0001c0003t0001g0064 a0001c0003t0001g0103 others(35): Show |
38 | HG00140.hp2 HG00438.hp2 HG01361.hp2 others(35): Show |
intron_variant | MODIFIER | c.1318+253G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 10/13 | chr21 | 41906739 | |||||||
| chr21:41907341 | G | A | 2 | a0001c0002t0002g0274 a0001c0002t0002g0388 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1144-175C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 9/13 | chr21 | 41907341 | |||||||
| chr21:41907470 | C | T | 1 | a0001c0003t0001g0047 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1143+190G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 9/13 | chr21 | 41907470 | |||||||
| chr21:41907522 | G | A | 89 | a0001c0003t0001g0008 a0001c0003t0001g0045 a0001c0003t0001g0047 others(86): Show |
89 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.1143+138C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 9/13 | chr21 | 41907522 | |||||||
| chr21:41907567 | G | A | 50 | a0001c0001t0001g0066 a0001c0001t0001g0085 a0001c0001t0004g0113 others(47): Show |
50 | HG00609.hp2 HG00621.hp1 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.1143+93C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 9/13 | chr21 | 41907567 | |||||||
| chr21:41907602 | G | A | 52 | a0001c0001t0001g0066 a0001c0001t0001g0085 a0001c0001t0002g0291 others(49): Show |
52 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.1143+58C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 9/13 | chr21 | 41907602 | |||||||
| chr21:41907640 | G | A | 1 | a0001c0003t0016g0117 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1143+20C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 9/13 | chr21 | 41907640 | |||||||
| chr21:41907642 | C | T | 3 | a0001c0003t0035g0240 a0001c0032t0010g0355 a0001c0033t0018g0229 |
3 | HG02559.hp2 HG03139.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1143+18G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 9/13 | chr21 | 41907642 | |||||||
| chr21:41907816 | G | A | 19 | a0001c0005t0002g0327 a0001c0005t0007g0310 a0001c0005t0008g0307 others(16): Show |
19 | HG00639.hp1 HG00642.hp2 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.1019-32C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 8/13 | chr21 | 41907816 | |||||||
| chr21:41907828 | C | T | 1 | a0002c0008t0005g0260 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1019-44G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 8/13 | chr21 | 41907828 | |||||||
| chr21:41907841 | G | A | 1 | a0001c0002t0003g0160 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1019-57C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 8/13 | chr21 | 41907841 | |||||||
| chr21:41907858 | C | T | 37 | a0001c0001t0052g0394 a0001c0003t0035g0240 a0001c0004t0004g0280 others(34): Show |
37 | HG00741.hp2 HG01123.hp2 HG01167.hp2 others(34): Show |
intron_variant | MODIFIER | c.1019-74G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 8/13 | chr21 | 41907858 | |||||||
| chr21:41907886 | G | A | 10 | a0001c0011t0005g0140 a0001c0011t0005g0306 a0001c0011t0010g0222 others(7): Show |
10 | HG01891.hp1 HG02486.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.1019-102C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 8/13 | chr21 | 41907886 | |||||||
| chr21:41907962 | G | A | 263 | a0001c0001t0001g0005 a0001c0001t0001g0025 a0001c0001t0001g0027 others(260): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.1019-178C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 8/13 | chr21 | 41907962 | |||||||
| chr21:41907973 | G | A | 59 | a0001c0001t0001g0027 a0001c0001t0001g0035 a0001c0001t0001g0066 others(56): Show |
59 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.1019-189C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 8/13 | chr21 | 41907973 | |||||||
| chr21:41908072 | G | A | 3 | a0001c0003t0005g0024 a0001c0014t0005g0243 a0001c0014t0005g0250 |
3 | HG02895.hp2 HG02897.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1019-288C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 8/13 | chr21 | 41908072 | |||||||
| chr21:41908128 | T | A | 11 | a0001c0005t0002g0327 a0001c0005t0007g0310 a0001c0005t0008g0307 others(8): Show |
11 | HG00639.hp1 HG00642.hp2 HG00738.hp1 others(8): Show |
intron_variant | MODIFIER | c.1019-344A>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 8/13 | chr21 | 41908128 | |||||||
| chr21:41908168 | T | C | 1 | a0003c0017t0005g0238 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1019-384A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 8/13 | chr21 | 41908168 | |||||||
| chr21:41908190 | C | G | 16 | a0001c0005t0002g0327 a0001c0005t0007g0310 a0001c0005t0008g0307 others(13): Show |
16 | HG00639.hp1 HG00642.hp2 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.1019-406G>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 8/13 | chr21 | 41908190 | |||||||
| chr21:41908243 | T | TTG | 19 | a0001c0002t0004g0114 a0001c0003t0035g0240 a0001c0005t0005g0001 others(16): Show |
20 | HG01257.hp1 HG01258.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.1019-461_1019-460d others(4): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 8/13 | chr21 | 41908243 | |||||||
| chr21:41908243 | T | TTGTGTGT others(3): Show |
9 | a0001c0005t0002g0327 a0001c0005t0007g0310 a0001c0005t0008g0307 others(6): Show |
9 | HG00639.hp1 HG00642.hp2 HG00738.hp1 others(6): Show |
intron_variant | MODIFIER | c.1019-469_1019-460d others(12): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 8/13 | chr21 | 41908243 | |||||||
| chr21:41908243 | T | TTGTGTGT others(5): Show |
7 | a0001c0003t0005g0061 a0001c0006t0003g0344 a0001c0021t0005g0235 others(4): Show |
7 | HG01981.hp1 HG02602.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.1019-471_1019-460d others(14): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 8/13 | chr21 | 41908243 | |||||||
| chr21:41908243 | T | TTGTGTGT others(7): Show |
84 | a0001c0003t0001g0045 a0001c0003t0001g0047 a0001c0003t0001g0064 others(81): Show |
84 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.1019-473_1019-460d others(16): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 8/13 | chr21 | 41908243 | |||||||
| chr21:41908243 | T | TTGTGTGT others(9): Show |
17 | a0001c0003t0004g0109 a0001c0004t0004g0280 a0001c0004t0004g0281 others(14): Show |
17 | HG01123.hp2 HG02083.hp2 HG02622.hp1 others(14): Show |
intron_variant | MODIFIER | c.1019-475_1019-460d others(18): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 8/13 | chr21 | 41908243 | |||||||
| chr21:41908243 | T | TTGTGTGT others(11): Show |
4 | a0001c0001t0002g0154 a0001c0001t0013g0371 a0001c0001t0019g0157 others(1): Show |
4 | HG00280.hp1 HG01074.hp2 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.1019-477_1019-460d others(20): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 8/13 | chr21 | 41908243 | |||||||
| chr21:41908243 | T | TTGTGTGT others(13): Show |
8 | a0001c0001t0002g0133 a0001c0001t0002g0316 a0001c0001t0004g0198 others(5): Show |
8 | HG00621.hp1 HG01074.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.1019-460_1019-459i others(22): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 8/13 | chr21 | 41908243 | |||||||
| chr21:41908243 | T | TTGTGTGT others(15): Show |
84 | a0001c0001t0001g0005 a0001c0001t0001g0037 a0001c0001t0001g0038 others(81): Show |
84 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.1019-460_1019-459i others(24): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 8/13 | chr21 | 41908243 | |||||||
| chr21:41908243 | T | TTGTGTGT others(17): Show |
15 | a0001c0001t0001g0025 a0001c0001t0002g0011 a0001c0001t0002g0342 others(12): Show |
15 | HG00099.hp1 HG01255.hp1 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.1019-460_1019-459i others(26): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 8/13 | chr21 | 41908243 | |||||||
| chr21:41908243 | T | TTGTGTGT others(19): Show |
19 | a0001c0001t0001g0027 a0001c0001t0001g0035 a0001c0001t0001g0066 others(16): Show |
19 | HG00639.hp2 HG00735.hp2 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.1019-460_1019-459i others(28): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 8/13 | chr21 | 41908243 | |||||||
| chr21:41908243 | T | TTGTGTGT others(21): Show |
7 | a0001c0001t0004g0113 a0001c0001t0006g0277 a0003c0009t0002g0369 others(4): Show |
7 | HG00642.hp1 HG00673.hp1 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1019-460_1019-459i others(30): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 8/13 | chr21 | 41908243 | |||||||
| chr21:41908243 | T | TTGTGTGT others(23): Show |
3 | a0001c0003t0009g0043 a0002c0012t0012g0282 a0003c0031t0018g0158 |
3 | HG02486.hp1 HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1019-460_1019-459i others(32): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 8/13 | chr21 | 41908243 | |||||||
| chr21:41908243 | T | TTGTGTGT others(25): Show |
1 | a0003c0009t0007g0352 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1019-460_1019-459i others(34): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 8/13 | chr21 | 41908243 | |||||||
| chr21:41908243 | T | TTGTGTGT others(31): Show |
1 | a0001c0003t0020g0323 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1019-460_1019-459i others(40): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 8/13 | chr21 | 41908243 | |||||||
| chr21:41908276 | T | G | 13 | a0001c0005t0002g0327 a0001c0005t0007g0310 a0001c0005t0008g0307 others(10): Show |
13 | HG00639.hp1 HG00642.hp2 HG00738.hp1 others(10): Show |
intron_variant | MODIFIER | c.1019-492A>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 8/13 | chr21 | 41908276 | |||||||
| chr21:41908300 | G | C | 1 | a0002c0018t0005g0252 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1019-516C>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 8/13 | chr21 | 41908300 | |||||||
| chr21:41908411 | G | T | 1 | a0001c0002t0003g0145 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1019-627C>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 8/13 | chr21 | 41908411 | |||||||
| chr21:41908511 | C | G | 1 | a0001c0006t0034g0289 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1019-727G>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 8/13 | chr21 | 41908511 | |||||||
| chr21:41908514 | C | T | 3 | a0001c0003t0005g0024 a0001c0014t0005g0243 a0001c0014t0005g0250 |
3 | HG02895.hp2 HG02897.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1019-730G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 8/13 | chr21 | 41908514 | |||||||
| chr21:41908547 | T | C | 11 | a0001c0005t0002g0327 a0001c0005t0007g0310 a0001c0005t0008g0307 others(8): Show |
11 | HG00639.hp1 HG00642.hp2 HG00738.hp1 others(8): Show |
intron_variant | MODIFIER | c.1019-763A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 8/13 | chr21 | 41908547 | |||||||
| chr21:41908559 | A | C | 1 | a0001c0003t0001g0294 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1019-775T>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 8/13 | chr21 | 41908559 | |||||||
| chr21:41908829 | T | TAC | 3 | a0001c0001t0002g0197 a0001c0001t0008g0309 a0001c0003t0006g0010 |
3 | HG01123.hp1 HG03669.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1018+628_1018+629d others(4): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 8/13 | chr21 | 41908829 | |||||||
| chr21:41908923 | G | T | 36 | a0001c0001t0001g0027 a0001c0001t0001g0035 a0001c0001t0001g0066 others(33): Show |
36 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.1018+536C>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 8/13 | chr21 | 41908923 | |||||||
| chr21:41908972 | C | T | 3 | a0001c0003t0005g0024 a0001c0014t0005g0243 a0001c0014t0005g0250 |
3 | HG02895.hp2 HG02897.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1018+487G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 8/13 | chr21 | 41908972 | |||||||
| chr21:41908991 | GA | G | 36 | a0001c0001t0001g0027 a0001c0001t0001g0035 a0001c0001t0001g0066 others(33): Show |
36 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.1018+467delT | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 8/13 | chr21 | 41908991 | |||||||
| chr21:41909133 | T | C | 1 | a0001c0002t0002g0083 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1018+326A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 8/13 | chr21 | 41909133 | |||||||
| chr21:41909222 | T | C | 3 | a0001c0003t0001g0103 a0001c0003t0004g0109 a0001c0003t0011g0186 |
3 | NA18961.hp2 NA19011.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.1018+237A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 8/13 | chr21 | 41909222 | |||||||
| chr21:41909268 | C | A | 3 | a0001c0005t0002g0327 a0001c0005t0007g0310 a0001c0005t0008g0307 |
3 | HG00738.hp1 HG01099.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.1018+191G>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 8/13 | chr21 | 41909268 | |||||||
| chr21:41909429 | G | A | 1 | a0001c0003t0016g0117 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1018+30C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 8/13 | chr21 | 41909429 | |||||||
| chr21:41909675 | T | A | 71 | a0001c0001t0002g0300 a0001c0001t0002g0301 a0001c0001t0003g0072 others(68): Show |
71 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.954-152A>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 7/13 | chr21 | 41909675 | |||||||
| chr21:41909685 | C | T | 2 | a0001c0021t0005g0235 a0001c0028t0020g0244 |
2 | HG02717.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.954-162G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 7/13 | chr21 | 41909685 | |||||||
| chr21:41909846 | A | T | 173 | a0001c0001t0001g0005 a0001c0001t0001g0025 a0001c0001t0001g0027 others(170): Show |
173 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.954-323T>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 7/13 | chr21 | 41909846 | |||||||
| chr21:41909917 | A | G | 1 | a0001c0001t0011g0210 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.954-394T>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 7/13 | chr21 | 41909917 | |||||||
| chr21:41909939 | C | T | 39 | a0001c0003t0001g0045 a0001c0003t0001g0064 a0001c0003t0001g0104 others(36): Show |
39 | HG00140.hp2 HG00438.hp2 HG01361.hp2 others(36): Show |
intron_variant | MODIFIER | c.954-416G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 7/13 | chr21 | 41909939 | |||||||
| chr21:41909967 | C | T | 135 | a0001c0001t0001g0005 a0001c0001t0001g0025 a0001c0001t0001g0027 others(132): Show |
135 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.954-444G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 7/13 | chr21 | 41909967 | |||||||
| chr21:41909998 | TA | T | 111 | a0001c0001t0002g0300 a0001c0001t0002g0301 a0001c0001t0003g0072 others(108): Show |
111 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.954-476delT | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 7/13 | chr21 | 41909998 | |||||||
| chr21:41909998 | TAA | T | 151 | a0001c0001t0001g0005 a0001c0001t0001g0025 a0001c0001t0001g0027 others(148): Show |
151 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.954-477_954-476del others(2): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 7/13 | chr21 | 41909998 | |||||||
| chr21:41910049 | G | C | 4 | a0001c0003t0001g0008 a0001c0003t0005g0246 a0001c0003t0005g0332 others(1): Show |
4 | HG01070.hp1 HG01071.hp1 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.954-526C>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 7/13 | chr21 | 41910049 | |||||||
| chr21:41910090 | C | T | 388 | a0001c0001t0001g0005 a0001c0001t0001g0025 a0001c0001t0001g0027 others(385): Show |
389 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(386): Show |
intron_variant | MODIFIER | c.954-567G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 7/13 | chr21 | 41910090 | |||||||
| chr21:41910104 | G | C | 164 | a0001c0001t0001g0005 a0001c0001t0001g0025 a0001c0001t0001g0027 others(161): Show |
164 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.954-581C>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 7/13 | chr21 | 41910104 | |||||||
| chr21:41910123 | C | T | 349 | a0001c0001t0001g0005 a0001c0001t0001g0025 a0001c0001t0001g0027 others(346): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.954-600G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 7/13 | chr21 | 41910123 | |||||||
| chr21:41910125 | C | T | 7 | a0001c0011t0005g0140 a0001c0011t0005g0306 a0001c0011t0010g0222 others(4): Show |
7 | HG01891.hp1 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.954-602G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 7/13 | chr21 | 41910125 | |||||||
| chr21:41910163 | G | C | 3 | a0001c0005t0002g0327 a0001c0005t0007g0310 a0001c0005t0008g0307 |
3 | HG00738.hp1 HG01099.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.954-640C>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 7/13 | chr21 | 41910163 | |||||||
| chr21:41910214 | T | C | 7 | a0001c0011t0005g0140 a0001c0011t0005g0306 a0001c0011t0010g0222 others(4): Show |
7 | HG01891.hp1 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.954-691A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 7/13 | chr21 | 41910214 | |||||||
| chr21:41910233 | C | CT | 7 | a0001c0011t0005g0140 a0001c0011t0005g0306 a0001c0011t0010g0222 others(4): Show |
7 | HG01891.hp1 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.954-711dupA | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 7/13 | chr21 | 41910233 | |||||||
| chr21:41910257 | T | C | 1 | a0001c0006t0034g0289 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.954-734A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 7/13 | chr21 | 41910257 | |||||||
| chr21:41910435 | C | T | 1 | a0001c0001t0005g0287 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.954-912G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 7/13 | chr21 | 41910435 | |||||||
| chr21:41910436 | G | A | 7 | a0001c0001t0004g0125 a0001c0001t0004g0148 a0001c0001t0004g0149 others(4): Show |
7 | HG00741.hp1 HG01106.hp2 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.954-913C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 7/13 | chr21 | 41910436 | |||||||
| chr21:41910460 | T | C | 6 | a0001c0002t0001g0194 a0001c0002t0002g0304 a0001c0002t0003g0068 others(3): Show |
6 | NA18947.hp1 NA18990.hp2 NA19009.hp1 others(3): Show |
intron_variant | MODIFIER | c.954-937A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 7/13 | chr21 | 41910460 | |||||||
| chr21:41910489 | A | G | 138 | a0001c0001t0001g0005 a0001c0001t0001g0025 a0001c0001t0001g0037 others(135): Show |
138 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.954-966T>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 7/13 | chr21 | 41910489 | |||||||
| chr21:41910530 | C | T | 1 | a0001c0001t0003g0351 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.954-1007G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 7/13 | chr21 | 41910530 | |||||||
| chr21:41910691 | T | TAC | 4 | a0001c0001t0002g0060 a0001c0001t0002g0296 a0001c0003t0001g0272 others(1): Show |
4 | HG01243.hp2 HG02683.hp1 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.954-1170_954-1169d others(4): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 7/13 | chr21 | 41910691 | |||||||
| chr21:41910691 | T | TACAC | 11 | a0001c0003t0010g0153 a0001c0011t0005g0140 a0001c0011t0005g0306 others(8): Show |
11 | HG01891.hp1 HG02486.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.954-1172_954-1169d others(6): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 7/13 | chr21 | 41910691 | |||||||
| chr21:41910691 | TAC | T | 10 | a0001c0001t0002g0300 a0001c0001t0002g0301 a0001c0001t0003g0072 others(7): Show |
10 | HG01070.hp1 HG01071.hp1 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.954-1170_954-1169d others(4): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 7/13 | chr21 | 41910691 | |||||||
| chr21:41910707 | C | T | 64 | a0001c0003t0001g0045 a0001c0003t0001g0047 a0001c0003t0001g0064 others(61): Show |
64 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.954-1184G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 7/13 | chr21 | 41910707 | |||||||
| chr21:41910745 | T | C | 9 | a0001c0001t0004g0125 a0001c0001t0004g0148 a0001c0001t0004g0149 others(6): Show |
9 | HG00741.hp1 HG01106.hp2 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.954-1222A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 7/13 | chr21 | 41910745 | |||||||
| chr21:41910960 | T | C | 6 | a0001c0004t0005g0313 a0001c0004t0005g0358 a0001c0004t0005g0390 others(3): Show |
6 | HG02280.hp2 HG02451.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.953+1372A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 7/13 | chr21 | 41910960 | |||||||
| chr21:41911005 | T | C | 288 | a0001c0001t0001g0005 a0001c0001t0001g0025 a0001c0001t0001g0027 others(285): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.953+1327A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 7/13 | chr21 | 41911005 | |||||||
| chr21:41911007 | A | AAAC | 266 | a0001c0001t0001g0005 a0001c0001t0001g0025 a0001c0001t0001g0027 others(263): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.953+1324_953+1325i others(5): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 7/13 | chr21 | 41911007 | |||||||
| chr21:41911184 | A | G | 1 | a0001c0002t0001g0315 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.953+1148T>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 7/13 | chr21 | 41911184 | |||||||
| chr21:41911248 | C | T | 1 | a0001c0002t0006g0096 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.953+1084G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 7/13 | chr21 | 41911248 | |||||||
| chr21:41911253 | A | G | 187 | a0001c0001t0001g0005 a0001c0001t0001g0025 a0001c0001t0001g0027 others(184): Show |
187 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.953+1079T>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 7/13 | chr21 | 41911253 | |||||||
| chr21:41911322 | T | A | 1 | a0001c0001t0011g0077 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.953+1010A>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 7/13 | chr21 | 41911322 | |||||||
| chr21:41911378 | T | G | 2 | a0001c0001t0005g0051 a0001c0001t0026g0322 |
2 | HG03831.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.953+954A>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 7/13 | chr21 | 41911378 | |||||||
| chr21:41911388 | C | CT | 22 | a0001c0001t0003g0177 a0001c0003t0010g0153 a0001c0004t0005g0358 others(19): Show |
22 | HG00597.hp1 HG00639.hp1 HG00642.hp2 others(19): Show |
intron_variant | MODIFIER | c.953+943dupA | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 7/13 | chr21 | 41911388 | |||||||
| chr21:41911388 | C | CTTTTTTT others(15): Show |
1 | a0001c0005t0044g0254 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.953+943_953+944ins others(22): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 7/13 | chr21 | 41911388 | |||||||
| chr21:41911388 | C | CTTTTTTT others(16): Show |
1 | a0001c0005t0005g0221 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.953+943_953+944ins others(23): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 7/13 | chr21 | 41911388 | |||||||
| chr21:41911388 | CT | C | 7 | a0001c0001t0003g0351 a0001c0002t0001g0339 a0001c0002t0002g0004 others(4): Show |
7 | HG00408.hp2 HG02698.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.953+943delA | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 7/13 | chr21 | 41911388 | |||||||
| chr21:41911388 | CTT | C | 67 | a0001c0001t0004g0338 a0001c0003t0001g0045 a0001c0003t0001g0047 others(64): Show |
67 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.953+942_953+943del others(2): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 7/13 | chr21 | 41911388 | |||||||
| chr21:41911388 | CTTTT | C | 6 | a0001c0003t0005g0024 a0001c0003t0009g0043 a0001c0003t0020g0323 others(3): Show |
6 | HG02486.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.953+940_953+943del others(4): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 7/13 | chr21 | 41911388 | |||||||
| chr21:41911504 | G | A | 1 | a0001c0003t0003g0029 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.953+828C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 7/13 | chr21 | 41911504 | |||||||
| chr21:41911548 | T | C | 1 | a0003c0017t0018g0331 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.953+784A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 7/13 | chr21 | 41911548 | |||||||
| chr21:41911685 | G | T | 2 | a0001c0002t0004g0321 a0001c0003t0006g0010 |
2 | HG03017.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.953+647C>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 7/13 | chr21 | 41911685 | |||||||
| chr21:41911767 | T | G | 6 | a0001c0003t0005g0024 a0001c0003t0009g0043 a0001c0003t0020g0323 others(3): Show |
6 | HG02486.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.953+565A>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 7/13 | chr21 | 41911767 | |||||||
| chr21:41911776 | G | A | 1 | a0001c0003t0003g0019 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.953+556C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 7/13 | chr21 | 41911776 | |||||||
| chr21:41911804 | C | T | 1 | a0001c0003t0001g0209 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.953+528G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 7/13 | chr21 | 41911804 | |||||||
| chr21:41911842 | G | C | 11 | a0001c0003t0010g0153 a0001c0011t0005g0140 a0001c0011t0005g0306 others(8): Show |
11 | HG01891.hp1 HG02486.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.953+490C>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 7/13 | chr21 | 41911842 | |||||||
| chr21:41911899 | G | A | 1 | a0001c0003t0003g0065 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.953+433C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 7/13 | chr21 | 41911899 | |||||||
| chr21:41912000 | C | T | 80 | a0001c0001t0004g0338 a0001c0003t0001g0045 a0001c0003t0001g0047 others(77): Show |
80 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.953+332G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 7/13 | chr21 | 41912000 | |||||||
| chr21:41912075 | G | A | 11 | a0001c0003t0015g0141 a0001c0003t0035g0240 a0001c0005t0005g0001 others(8): Show |
12 | HG01257.hp1 HG01258.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.953+257C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 7/13 | chr21 | 41912075 | |||||||
| chr21:41912199 | A | G | 4 | a0001c0004t0006g0392 a0001c0004t0009g0137 a0001c0004t0009g0350 others(1): Show |
4 | HG02622.hp1 HG02630.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.953+133T>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 7/13 | chr21 | 41912199 | |||||||
| chr21:41912493 | A | AT | 7 | a0001c0002t0002g0205 a0001c0004t0005g0138 a0001c0011t0005g0306 others(4): Show |
7 | HG01891.hp1 HG03041.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.845-54dupA | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 6/13 | chr21 | 41912493 | |||||||
| chr21:41912493 | A | T | 5 | a0001c0003t0001g0103 a0003c0009t0002g0369 a0003c0009t0007g0169 others(2): Show |
5 | HG00609.hp2 HG00673.hp1 HG02135.hp1 others(2): Show |
intron_variant | MODIFIER | c.845-53T>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 6/13 | chr21 | 41912493 | |||||||
| chr21:41912493 | AT | A | 11 | a0001c0003t0009g0043 a0001c0003t0020g0323 a0002c0008t0001g0225 others(8): Show |
11 | HG01168.hp1 HG01884.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.845-54delA | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 6/13 | chr21 | 41912493 | |||||||
| chr21:41912494 | T | TTTA | 137 | a0001c0001t0001g0005 a0001c0001t0001g0025 a0001c0001t0001g0037 others(134): Show |
137 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.845-55_845-54insTA others(1): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 6/13 | chr21 | 41912494 | |||||||
| chr21:41912496 | T | TA | 6 | a0001c0003t0010g0153 a0001c0011t0005g0140 a0002c0012t0012g0241 others(3): Show |
6 | HG02486.hp1 HG02559.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.845-57_845-56insT | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 6/13 | chr21 | 41912496 | |||||||
| chr21:41912497 | T | A | 39 | a0001c0001t0001g0027 a0001c0001t0001g0035 a0001c0001t0001g0066 others(36): Show |
39 | HG00735.hp2 HG00738.hp1 HG01070.hp2 others(36): Show |
intron_variant | MODIFIER | c.845-57A>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 6/13 | chr21 | 41912497 | |||||||
| chr21:41912498 | T | A | 139 | a0001c0001t0001g0005 a0001c0001t0001g0025 a0001c0001t0001g0037 others(136): Show |
139 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.845-58A>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 6/13 | chr21 | 41912498 | |||||||
| chr21:41912501 | T | A | 1 | a0001c0003t0003g0029 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.845-61A>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 6/13 | chr21 | 41912501 | |||||||
| chr21:41912502 | T | A | 139 | a0001c0001t0001g0005 a0001c0001t0001g0025 a0001c0001t0001g0037 others(136): Show |
139 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.845-62A>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 6/13 | chr21 | 41912502 | |||||||
| chr21:41912514 | A | G | 139 | a0001c0001t0001g0005 a0001c0001t0001g0025 a0001c0001t0001g0037 others(136): Show |
139 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.845-74T>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 6/13 | chr21 | 41912514 | |||||||
| chr21:41912640 | G | A | 6 | a0001c0003t0015g0312 a0001c0003t0015g0328 a0002c0012t0009g0062 others(3): Show |
6 | HG01167.hp1 HG01169.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.845-200C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 6/13 | chr21 | 41912640 | |||||||
| chr21:41912642 | C | T | 6 | a0002c0008t0001g0225 a0002c0008t0005g0249 a0002c0008t0005g0251 others(3): Show |
6 | HG01884.hp2 HG02723.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.845-202G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 6/13 | chr21 | 41912642 | |||||||
| chr21:41912667 | A | T | 127 | a0001c0001t0001g0027 a0001c0001t0001g0035 a0001c0001t0001g0066 others(124): Show |
127 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(124): Show |
intron_variant | MODIFIER | c.845-227T>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 6/13 | chr21 | 41912667 | |||||||
| chr21:41912727 | G | A | 38 | a0001c0001t0052g0394 a0001c0003t0001g0349 a0001c0003t0005g0263 others(35): Show |
38 | HG00741.hp2 HG01123.hp2 HG01167.hp2 others(35): Show |
intron_variant | MODIFIER | c.845-287C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 6/13 | chr21 | 41912727 | |||||||
| chr21:41912831 | G | GA | 11 | a0001c0003t0010g0153 a0001c0011t0005g0140 a0001c0011t0005g0306 others(8): Show |
11 | HG01891.hp1 HG02486.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.845-392dupT | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 6/13 | chr21 | 41912831 | |||||||
| chr21:41912896 | G | T | 46 | a0001c0001t0001g0027 a0001c0001t0001g0035 a0001c0001t0001g0066 others(43): Show |
46 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.845-456C>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 6/13 | chr21 | 41912896 | |||||||
| chr21:41912944 | A | G | 7 | a0001c0001t0001g0027 a0001c0001t0001g0035 a0001c0001t0001g0066 others(4): Show |
7 | HG00735.hp2 HG04199.hp1 NA18946.hp1 others(4): Show |
intron_variant | MODIFIER | c.845-504T>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 6/13 | chr21 | 41912944 | |||||||
| chr21:41912969 | C | T | 1 | a0003c0017t0018g0331 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.845-529G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 6/13 | chr21 | 41912969 | |||||||
| chr21:41913029 | C | T | 2 | a0002c0008t0009g0161 a0002c0027t0009g0325 |
2 | HG02257.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.845-589G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 6/13 | chr21 | 41913029 | |||||||
| chr21:41913037 | C | T | 135 | a0001c0001t0001g0005 a0001c0001t0001g0025 a0001c0001t0001g0037 others(132): Show |
135 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.845-597G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 6/13 | chr21 | 41913037 | |||||||
| chr21:41913054 | C | T | 2 | a0001c0001t0001g0027 a0001c0001t0001g0035 |
2 | NA18946.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.845-614G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 6/13 | chr21 | 41913054 | |||||||
| chr21:41913129 | C | T | 2 | a0001c0021t0005g0235 a0001c0028t0020g0244 |
2 | HG02717.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.845-689G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 6/13 | chr21 | 41913129 | |||||||
| chr21:41913191 | TACACCAG others(4): Show |
T | 80 | a0001c0001t0004g0338 a0001c0003t0001g0045 a0001c0003t0001g0047 others(77): Show |
80 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.845-762_845-752del others(11): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 6/13 | chr21 | 41913191 | |||||||
| chr21:41913213 | T | C | 1 | a0001c0002t0001g0359 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.845-773A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 6/13 | chr21 | 41913213 | |||||||
| chr21:41913227 | G | T | 11 | a0001c0003t0010g0153 a0001c0011t0005g0140 a0001c0011t0005g0306 others(8): Show |
11 | HG01891.hp1 HG02486.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.845-787C>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 6/13 | chr21 | 41913227 | |||||||
| chr21:41913353 | G | A | 1 | a0001c0001t0052g0394 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.845-913C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 6/13 | chr21 | 41913353 | |||||||
| chr21:41913395 | C | T | 21 | a0001c0001t0001g0027 a0001c0001t0001g0035 a0001c0001t0001g0066 others(18): Show |
21 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(18): Show |
intron_variant | MODIFIER | c.845-955G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 6/13 | chr21 | 41913395 | |||||||
| chr21:41913519 | C | T | 1 | a0001c0003t0003g0334 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.844+1079G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 6/13 | chr21 | 41913519 | |||||||
| chr21:41913759 | G | A | 2 | a0001c0001t0001g0027 a0001c0002t0007g0318 |
2 | HG01243.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.844+839C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 6/13 | chr21 | 41913759 | |||||||
| chr21:41913859 | T | C | 64 | a0001c0001t0052g0394 a0001c0002t0001g0073 a0001c0002t0001g0123 others(61): Show |
64 | HG00408.hp2 HG00738.hp2 HG00741.hp2 others(61): Show |
intron_variant | MODIFIER | c.844+739A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 6/13 | chr21 | 41913859 | |||||||
| chr21:41913910 | G | A | 3 | a0001c0002t0001g0194 a0001c0002t0003g0068 a0003c0020t0007g0167 |
3 | NA18947.hp1 NA19009.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.844+688C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 6/13 | chr21 | 41913910 | |||||||
| chr21:41913943 | C | A | 9 | a0001c0003t0001g0272 a0001c0003t0015g0312 a0001c0003t0015g0328 others(6): Show |
9 | HG01167.hp1 HG01169.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.844+655G>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 6/13 | chr21 | 41913943 | |||||||
| chr21:41913958 | T | A | 103 | a0001c0001t0001g0027 a0001c0001t0001g0035 a0001c0001t0001g0066 others(100): Show |
103 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.844+640A>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 6/13 | chr21 | 41913958 | |||||||
| chr21:41913998 | C | T | 3 | a0002c0010t0001g0131 a0002c0010t0008g0023 a0002c0010t0031g0278 |
3 | HG02602.hp1 HG03834.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.844+600G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 6/13 | chr21 | 41913998 | |||||||
| chr21:41914002 | C | T | 8 | a0001c0039t0013g0302 a0001c0040t0008g0305 a0002c0010t0001g0131 others(5): Show |
8 | HG00639.hp1 HG00642.hp2 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.844+596G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 6/13 | chr21 | 41914002 | |||||||
| chr21:41914061 | G | C | 113 | a0001c0001t0001g0005 a0001c0001t0001g0025 a0001c0001t0001g0037 others(110): Show |
113 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.844+537C>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 6/13 | chr21 | 41914061 | |||||||
| chr21:41914151 | A | G | 152 | a0001c0001t0002g0300 a0001c0001t0002g0301 a0001c0001t0003g0072 others(149): Show |
152 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(149): Show |
intron_variant | MODIFIER | c.844+447T>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 6/13 | chr21 | 41914151 | |||||||
| chr21:41914181 | G | A | 106 | a0001c0001t0001g0005 a0001c0001t0001g0025 a0001c0001t0001g0037 others(103): Show |
106 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.844+417C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 6/13 | chr21 | 41914181 | |||||||
| chr21:41914194 | T | C | 5 | a0001c0005t0002g0327 a0001c0005t0007g0310 a0002c0010t0001g0131 others(2): Show |
5 | HG01099.hp1 HG02602.hp1 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.844+404A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 6/13 | chr21 | 41914194 | |||||||
| chr21:41914207 | C | T | 40 | a0001c0001t0004g0338 a0001c0002t0002g0216 a0001c0002t0003g0217 others(37): Show |
40 | HG00140.hp2 HG00438.hp2 HG00673.hp1 others(37): Show |
intron_variant | MODIFIER | c.844+391G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 6/13 | chr21 | 41914207 | |||||||
| chr21:41914219 | T | C | 10 | a0001c0005t0002g0327 a0001c0005t0007g0310 a0001c0039t0013g0302 others(7): Show |
10 | HG00639.hp1 HG00642.hp2 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.844+379A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 6/13 | chr21 | 41914219 | |||||||
| chr21:41914254 | T | G | 1 | a0001c0002t0002g0102 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.844+344A>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 6/13 | chr21 | 41914254 | |||||||
| chr21:41914287 | C | A | 1 | a0001c0001t0004g0198 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.844+311G>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 6/13 | chr21 | 41914287 | |||||||
| chr21:41914292 | G | GT | 3 | a0001c0003t0035g0240 a0001c0032t0010g0355 a0001c0033t0018g0229 |
3 | HG02559.hp2 HG03139.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.844+305dupA | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 6/13 | chr21 | 41914292 | |||||||
| chr21:41914294 | TA | T | 206 | a0001c0001t0001g0005 a0001c0001t0001g0025 a0001c0001t0001g0027 others(203): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.844+303delT | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 6/13 | chr21 | 41914294 | |||||||
| chr21:41914294 | TAA | T | 10 | a0001c0001t0004g0098 a0001c0003t0003g0049 a0001c0003t0005g0061 others(7): Show |
10 | HG02486.hp1 HG02486.hp2 HG02976.hp2 others(7): Show |
intron_variant | MODIFIER | c.844+302_844+303del others(2): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 6/13 | chr21 | 41914294 | |||||||
| chr21:41914295 | A | T | 90 | a0001c0001t0052g0394 a0001c0002t0001g0073 a0001c0002t0001g0123 others(87): Show |
91 | HG00408.hp2 HG00738.hp2 HG00741.hp2 others(88): Show |
intron_variant | MODIFIER | c.844+303T>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 6/13 | chr21 | 41914295 | |||||||
| chr21:41914296 | A | T | 1 | a0002c0008t0045g0226 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.844+302T>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 6/13 | chr21 | 41914296 | |||||||
| chr21:41914319 | A | AAAGAT | 8 | a0001c0003t0001g0272 a0001c0003t0015g0312 a0001c0003t0015g0328 others(5): Show |
8 | HG01167.hp1 HG01169.hp1 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.844+274_844+278dup others(5): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 6/13 | chr21 | 41914319 | |||||||
| chr21:41914324 | T | A | 57 | a0001c0001t0052g0394 a0001c0002t0001g0073 a0001c0002t0001g0123 others(54): Show |
57 | HG00408.hp2 HG00738.hp2 HG00741.hp2 others(54): Show |
intron_variant | MODIFIER | c.844+274A>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 6/13 | chr21 | 41914324 | |||||||
| chr21:41914376 | T | C | 36 | a0001c0002t0001g0073 a0001c0002t0001g0123 a0001c0002t0001g0124 others(33): Show |
36 | HG00408.hp2 HG00738.hp2 HG01106.hp1 others(33): Show |
intron_variant | MODIFIER | c.844+222A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 6/13 | chr21 | 41914376 | |||||||
| chr21:41914399 | A | G | 1 | a0003c0034t0004g0228 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.844+199T>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 6/13 | chr21 | 41914399 | |||||||
| chr21:41914401 | G | A | 2 | a0001c0002t0011g0336 a0001c0002t0011g0337 |
2 | NA18951.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.844+197C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 6/13 | chr21 | 41914401 | |||||||
| chr21:41914425 | T | C | 1 | a0001c0001t0001g0085 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.844+173A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 6/13 | chr21 | 41914425 | |||||||
| chr21:41914469 | C | G | 1 | a0001c0002t0001g0176 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.844+129G>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 6/13 | chr21 | 41914469 | |||||||
| chr21:41914560 | G | C | 140 | a0001c0001t0001g0005 a0001c0001t0001g0025 a0001c0001t0001g0037 others(137): Show |
141 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.844+38C>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 6/13 | chr21 | 41914560 | |||||||
| chr21:41914787 | A | G | 315 | a0001c0001t0001g0005 a0001c0001t0001g0025 a0001c0001t0001g0027 others(312): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.721-66T>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 5/13 | chr21 | 41914787 | |||||||
| chr21:41914813 | G | A | 6 | a0002c0008t0001g0225 a0002c0008t0005g0249 a0002c0008t0005g0251 others(3): Show |
6 | HG01884.hp2 HG02723.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.721-92C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 5/13 | chr21 | 41914813 | |||||||
| chr21:41914918 | C | T | 1 | a0003c0031t0018g0158 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.721-197G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 5/13 | chr21 | 41914918 | |||||||
| chr21:41914948 | C | T | 2 | a0002c0012t0012g0262 a0002c0012t0012g0282 |
2 | HG02486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.721-227G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 5/13 | chr21 | 41914948 | |||||||
| chr21:41915003 | C | A | 188 | a0001c0001t0001g0025 a0001c0001t0001g0037 a0001c0001t0001g0038 others(185): Show |
188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.721-282G>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 5/13 | chr21 | 41915003 | |||||||
| chr21:41915017 | C | T | 1 | a0001c0003t0009g0043 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.721-296G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 5/13 | chr21 | 41915017 | |||||||
| chr21:41915048 | T | C | 25 | a0001c0003t0001g0349 a0001c0003t0005g0024 a0001c0003t0005g0263 others(22): Show |
26 | HG01884.hp2 HG02257.hp2 HG02258.hp1 others(23): Show |
intron_variant | MODIFIER | c.721-327A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 5/13 | chr21 | 41915048 | |||||||
| chr21:41915097 | C | T | 74 | a0001c0001t0001g0027 a0001c0001t0001g0035 a0001c0001t0001g0066 others(71): Show |
75 | HG00609.hp2 HG00621.hp1 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.721-376G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 5/13 | chr21 | 41915097 | |||||||
| chr21:41915143 | A | G | 24 | a0001c0004t0005g0313 a0001c0004t0005g0358 a0001c0004t0005g0390 others(21): Show |
24 | HG00741.hp2 HG01167.hp2 HG01257.hp1 others(21): Show |
intron_variant | MODIFIER | c.721-422T>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 5/13 | chr21 | 41915143 | |||||||
| chr21:41915308 | T | C | 7 | a0001c0004t0004g0281 a0002c0010t0001g0131 a0002c0010t0007g0111 others(4): Show |
7 | HG00639.hp1 HG00642.hp2 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.721-587A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 5/13 | chr21 | 41915308 | |||||||
| chr21:41915353 | C | G | 1 | a0003c0017t0018g0331 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.721-632G>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 5/13 | chr21 | 41915353 | |||||||
| chr21:41915401 | CCCAAACC others(5): Show |
C | 2 | a0001c0003t0020g0323 a0003c0031t0018g0158 |
2 | HG02486.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.721-692_721-681del others(12): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 5/13 | chr21 | 41915401 | |||||||
| chr21:41915442 | C | CT | 13 | a0001c0003t0009g0043 a0001c0003t0020g0323 a0002c0010t0001g0131 others(10): Show |
13 | HG00639.hp1 HG00642.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.721-722dupA | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 5/13 | chr21 | 41915442 | |||||||
| chr21:41915480 | G | A | 300 | a0001c0001t0001g0005 a0001c0001t0001g0025 a0001c0001t0001g0027 others(297): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.721-759C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 5/13 | chr21 | 41915480 | |||||||
| chr21:41915598 | G | A | 3 | a0001c0001t0004g0098 a0001c0003t0001g0258 a0003c0034t0004g0228 |
3 | HG02027.hp2 HG02451.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.721-877C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 5/13 | chr21 | 41915598 | |||||||
| chr21:41915603 | A | G | 1 | a0001c0001t0004g0098 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.721-882T>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 5/13 | chr21 | 41915603 | |||||||
| chr21:41915682 | C | T | 7 | a0002c0010t0001g0131 a0002c0010t0007g0111 a0002c0010t0008g0023 others(4): Show |
7 | HG00639.hp1 HG00642.hp2 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.721-961G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 5/13 | chr21 | 41915682 | |||||||
| chr21:41915683 | G | A | 2 | a0001c0021t0005g0235 a0001c0028t0020g0244 |
2 | HG02717.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.721-962C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 5/13 | chr21 | 41915683 | |||||||
| chr21:41915801 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.721-1080G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 5/13 | chr21 | 41915801 | |||||||
| chr21:41915828 | G | C | 2 | a0002c0018t0005g0252 a0002c0018t0022g0285 |
2 | HG02145.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.721-1107C>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 5/13 | chr21 | 41915828 | |||||||
| chr21:41915867 | C | T | 1 | a0003c0034t0004g0228 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.721-1146G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 5/13 | chr21 | 41915867 | |||||||
| chr21:41915893 | G | A | 5 | a0001c0011t0005g0140 a0001c0011t0010g0222 a0001c0011t0010g0245 others(2): Show |
5 | HG01891.hp1 HG02559.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.721-1172C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 5/13 | chr21 | 41915893 | |||||||
| chr21:41915901 | C | T | 2 | a0001c0001t0002g0373 a0001c0001t0002g0374 |
2 | NA19072.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.721-1180G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 5/13 | chr21 | 41915901 | |||||||
| chr21:41916125 | A | G | 26 | a0001c0003t0001g0349 a0001c0003t0005g0024 a0001c0003t0005g0263 others(23): Show |
27 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(24): Show |
intron_variant | MODIFIER | c.721-1404T>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 5/13 | chr21 | 41916125 | |||||||
| chr21:41916207 | G | C | 2 | a0002c0008t0009g0161 a0002c0027t0009g0325 |
2 | HG02257.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.721-1486C>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 5/13 | chr21 | 41916207 | |||||||
| chr21:41916297 | C | G | 25 | a0002c0008t0001g0225 a0002c0008t0005g0249 a0002c0008t0005g0251 others(22): Show |
25 | HG00639.hp1 HG00642.hp2 HG01167.hp1 others(22): Show |
intron_variant | MODIFIER | c.721-1576G>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 5/13 | chr21 | 41916297 | |||||||
| chr21:41916365 | G | A | 2 | a0001c0007t0001g0253 a0001c0007t0006g0255 |
2 | HG01167.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.721-1644C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 5/13 | chr21 | 41916365 | |||||||
| chr21:41916405 | G | A | 7 | a0002c0008t0001g0225 a0002c0008t0005g0249 a0002c0008t0005g0251 others(4): Show |
7 | HG01884.hp2 HG02723.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.721-1684C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 5/13 | chr21 | 41916405 | |||||||
| chr21:41916428 | C | CCTCTT | 96 | a0001c0001t0001g0027 a0001c0001t0001g0035 a0001c0001t0001g0066 others(93): Show |
97 | HG00280.hp2 HG00609.hp2 HG00621.hp1 others(94): Show |
intron_variant | MODIFIER | c.720+1676_720+1677i others(7): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 5/13 | chr21 | 41916428 | |||||||
| chr21:41916433 | A | G | 13 | a0001c0003t0010g0153 a0002c0010t0001g0131 a0002c0010t0007g0111 others(10): Show |
13 | HG00639.hp1 HG00642.hp2 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.720+1672T>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 5/13 | chr21 | 41916433 | |||||||
| chr21:41916444 | C | T | 1 | a0001c0003t0004g0162 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.720+1661G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 5/13 | chr21 | 41916444 | |||||||
| chr21:41916574 | A | G | 13 | a0001c0003t0010g0153 a0002c0010t0001g0131 a0002c0010t0007g0111 others(10): Show |
13 | HG00639.hp1 HG00642.hp2 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.720+1531T>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 5/13 | chr21 | 41916574 | |||||||
| chr21:41916664 | T | TAC | 14 | a0001c0001t0002g0121 a0001c0001t0004g0297 a0001c0001t0004g0298 others(11): Show |
14 | HG01168.hp2 HG01169.hp2 HG02056.hp1 others(11): Show |
intron_variant | MODIFIER | c.720+1439_720+1440d others(4): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 5/13 | chr21 | 41916664 | |||||||
| chr21:41916664 | T | TACAC | 3 | a0001c0002t0003g0090 a0001c0003t0003g0268 a0003c0022t0042g0236 |
3 | HG01952.hp1 HG02258.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.720+1437_720+1440d others(6): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 5/13 | chr21 | 41916664 | |||||||
| chr21:41916664 | TAC | T | 77 | a0001c0001t0001g0038 a0001c0001t0001g0178 a0001c0001t0002g0300 others(74): Show |
77 | HG00099.hp2 HG00408.hp2 HG00741.hp1 others(74): Show |
intron_variant | MODIFIER | c.720+1439_720+1440d others(4): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 5/13 | chr21 | 41916664 | |||||||
| chr21:41916664 | TACAC | T | 56 | a0001c0001t0002g0112 a0001c0001t0002g0296 a0001c0001t0007g0175 others(53): Show |
56 | HG00099.hp1 HG00621.hp2 HG00741.hp2 others(53): Show |
intron_variant | MODIFIER | c.720+1437_720+1440d others(6): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 5/13 | chr21 | 41916664 | |||||||
| chr21:41916664 | TACACAC | T | 103 | a0001c0001t0001g0005 a0001c0001t0001g0025 a0001c0001t0001g0037 others(100): Show |
103 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.720+1435_720+1440d others(8): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 5/13 | chr21 | 41916664 | |||||||
| chr21:41916664 | TACACACA others(1): Show |
T | 41 | a0001c0001t0001g0027 a0001c0001t0001g0035 a0001c0001t0001g0050 others(38): Show |
41 | HG00280.hp2 HG00609.hp2 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.720+1433_720+1440d others(10): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 5/13 | chr21 | 41916664 | |||||||
| chr21:41916664 | TACACACA others(3): Show |
T | 19 | a0001c0001t0002g0088 a0001c0002t0001g0202 a0001c0003t0001g0349 others(16): Show |
20 | HG02258.hp1 HG02559.hp2 HG02615.hp1 others(17): Show |
intron_variant | MODIFIER | c.720+1431_720+1440d others(12): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 5/13 | chr21 | 41916664 | |||||||
| chr21:41916664 | TACACACA others(11): Show |
T | 2 | a0001c0002t0004g0087 a0001c0002t0004g0206 |
2 | NA19078.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.720+1423_720+1440d others(20): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 5/13 | chr21 | 41916664 | |||||||
| chr21:41916664 | TACACACA others(15): Show |
T | 4 | a0001c0003t0009g0043 a0002c0012t0012g0241 a0002c0012t0012g0262 others(1): Show |
4 | HG02486.hp1 HG03098.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.720+1419_720+1440d others(24): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 5/13 | chr21 | 41916664 | |||||||
| chr21:41916780 | T | G | 1 | a0001c0002t0003g0182 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.720+1325A>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 5/13 | chr21 | 41916780 | |||||||
| chr21:41916901 | T | C | 1 | a0003c0031t0018g0158 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.720+1204A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 5/13 | chr21 | 41916901 | |||||||
| chr21:41917123 | C | T | 19 | a0002c0008t0001g0225 a0002c0008t0005g0249 a0002c0008t0005g0251 others(16): Show |
19 | HG00639.hp1 HG00642.hp2 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.720+982G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 5/13 | chr21 | 41917123 | |||||||
| chr21:41917174 | T | C | 24 | a0001c0003t0010g0153 a0002c0008t0001g0225 a0002c0008t0005g0249 others(21): Show |
24 | HG00639.hp1 HG00642.hp2 HG01167.hp1 others(21): Show |
intron_variant | MODIFIER | c.720+931A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 5/13 | chr21 | 41917174 | |||||||
| chr21:41917229 | A | C | 2 | a0001c0001t0002g0300 a0001c0001t0002g0301 |
2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.720+876T>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 5/13 | chr21 | 41917229 | |||||||
| chr21:41917574 | C | A | 2 | a0001c0002t0004g0181 a0001c0002t0004g0195 |
2 | NA18943.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.720+531G>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 5/13 | chr21 | 41917574 | |||||||
| chr21:41917832 | G | C | 1 | a0001c0021t0005g0235 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.720+273C>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 5/13 | chr21 | 41917832 | |||||||
| chr21:41918025 | C | T | 4 | a0001c0003t0001g0224 a0001c0003t0003g0268 a0001c0003t0005g0061 others(1): Show |
4 | HG01361.hp2 HG01952.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.720+80G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 5/13 | chr21 | 41918025 | |||||||
| chr21:41918066 | C | T | 56 | a0001c0001t0001g0027 a0001c0001t0001g0035 a0001c0001t0001g0066 others(53): Show |
56 | HG00280.hp2 HG00597.hp2 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.720+39G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 5/13 | chr21 | 41918066 | |||||||
| chr21:41918067 | G | A | 3 | a0001c0003t0035g0240 a0001c0006t0005g0242 a0001c0032t0010g0355 |
3 | HG02280.hp2 HG02559.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.720+38C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 5/13 | chr21 | 41918067 | |||||||
| chr21:41918291 | C | T | 89 | a0001c0001t0001g0027 a0001c0001t0001g0035 a0001c0001t0001g0066 others(86): Show |
90 | HG00280.hp2 HG00597.hp2 HG00609.hp2 others(87): Show |
intron_variant | MODIFIER | c.598-64G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 4/13 | chr21 | 41918291 | |||||||
| chr21:41918344 | G | A | 1 | a0001c0001t0003g0081 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.598-117C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 4/13 | chr21 | 41918344 | |||||||
| chr21:41918465 | C | T | 1 | a0001c0007t0005g0041 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.598-238G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 4/13 | chr21 | 41918465 | |||||||
| chr21:41918483 | G | C | 1 | a0001c0001t0002g0386 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.598-256C>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 4/13 | chr21 | 41918483 | |||||||
| chr21:41918520 | CAT | C | 3 | a0002c0008t0005g0260 a0002c0008t0005g0354 a0002c0008t0045g0226 |
3 | HG01884.hp2 HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.598-295_598-294del others(2): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 4/13 | chr21 | 41918520 | |||||||
| chr21:41918589 | G | GT | 6 | a0001c0001t0002g0373 a0001c0002t0002g0382 a0001c0002t0003g0145 others(3): Show |
6 | HG00621.hp2 HG01169.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.597+266dupA | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 4/13 | chr21 | 41918589 | |||||||
| chr21:41918681 | C | CT | 3 | a0002c0012t0012g0241 a0002c0012t0012g0262 a0002c0012t0012g0282 |
3 | HG02486.hp1 HG03540.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.597+174_597+175ins others(1): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 4/13 | chr21 | 41918681 | |||||||
| chr21:41918734 | G | A | 2 | a0001c0003t0020g0323 a0003c0031t0018g0158 |
2 | HG02486.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.597+122C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 4/13 | chr21 | 41918734 | |||||||
| chr21:41918746 | G | C | 73 | a0001c0001t0001g0027 a0001c0001t0001g0035 a0001c0001t0001g0066 others(70): Show |
74 | HG00280.hp2 HG00597.hp2 HG00609.hp2 others(71): Show |
intron_variant | MODIFIER | c.597+110C>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 4/13 | chr21 | 41918746 | |||||||
| chr21:41918789 | C | T | 2 | a0001c0001t0003g0092 a0001c0001t0003g0193 |
2 | NA18939.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.597+67G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 4/13 | chr21 | 41918789 | |||||||
| chr21:41918824 | A | T | 73 | a0001c0001t0001g0027 a0001c0001t0001g0035 a0001c0001t0001g0066 others(70): Show |
74 | HG00280.hp2 HG00597.hp2 HG00609.hp2 others(71): Show |
intron_variant | MODIFIER | c.597+32T>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 4/13 | chr21 | 41918824 | |||||||
| chr21:41918839 | A | C | 50 | a0001c0001t0001g0027 a0001c0001t0001g0035 a0001c0001t0001g0066 others(47): Show |
50 | HG00280.hp2 HG00597.hp2 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.597+17T>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 4/13 | chr21 | 41918839 | |||||||
| chr21:41919032 | G | A | 1 | a0001c0006t0008g0387 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.493-72C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 3/13 | chr21 | 41919032 | |||||||
| chr21:41919034 | C | CTGTG | 88 | a0001c0001t0001g0027 a0001c0001t0001g0035 a0001c0001t0001g0066 others(85): Show |
89 | HG00280.hp2 HG00597.hp2 HG00609.hp2 others(86): Show |
intron_variant | MODIFIER | c.493-78_493-75dupCA others(2): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 3/13 | chr21 | 41919034 | |||||||
| chr21:41919041 | A | T | 1 | a0001c0002t0004g0343 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.493-81T>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 3/13 | chr21 | 41919041 | |||||||
| chr21:41919043 | C | T | 1 | a0001c0002t0004g0343 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.493-83G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 3/13 | chr21 | 41919043 | |||||||
| chr21:41919044 | A | G | 1 | a0001c0002t0004g0343 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.493-84T>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 3/13 | chr21 | 41919044 | |||||||
| chr21:41919045 | T | A | 1 | a0001c0002t0004g0343 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.493-85A>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 3/13 | chr21 | 41919045 | |||||||
| chr21:41919045 | T | C | 88 | a0001c0001t0001g0027 a0001c0001t0001g0035 a0001c0001t0001g0066 others(85): Show |
89 | HG00280.hp2 HG00597.hp2 HG00609.hp2 others(86): Show |
intron_variant | MODIFIER | c.493-85A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 3/13 | chr21 | 41919045 | |||||||
| chr21:41919047 | T | C | 1 | a0001c0002t0004g0343 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.493-87A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 3/13 | chr21 | 41919047 | |||||||
| chr21:41919048 | G | A | 1 | a0001c0002t0004g0343 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.493-88C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 3/13 | chr21 | 41919048 | |||||||
| chr21:41919049 | T | C | 1 | a0001c0002t0004g0343 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.493-89A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 3/13 | chr21 | 41919049 | |||||||
| chr21:41919196 | A | G | 92 | a0001c0001t0001g0027 a0001c0001t0001g0035 a0001c0001t0001g0066 others(89): Show |
93 | HG00280.hp2 HG00597.hp2 HG00609.hp2 others(90): Show |
intron_variant | MODIFIER | c.493-236T>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 3/13 | chr21 | 41919196 | |||||||
| chr21:41919268 | G | A | 2 | a0002c0008t0009g0161 a0002c0027t0009g0325 |
2 | HG02257.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.493-308C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 3/13 | chr21 | 41919268 | |||||||
| chr21:41919283 | C | T | 74 | a0001c0001t0001g0027 a0001c0001t0001g0035 a0001c0001t0001g0066 others(71): Show |
75 | HG00280.hp2 HG00597.hp2 HG00609.hp2 others(72): Show |
intron_variant | MODIFIER | c.493-323G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 3/13 | chr21 | 41919283 | |||||||
| chr21:41919360 | T | C | 1 | a0001c0040t0008g0305 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.493-400A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 3/13 | chr21 | 41919360 | |||||||
| chr21:41919621 | G | A | 89 | a0001c0001t0001g0027 a0001c0001t0001g0035 a0001c0001t0001g0066 others(86): Show |
90 | HG00280.hp2 HG00597.hp2 HG00609.hp2 others(87): Show |
intron_variant | MODIFIER | c.493-661C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 3/13 | chr21 | 41919621 | |||||||
| chr21:41919795 | C | G | 17 | a0001c0003t0001g0349 a0001c0003t0005g0024 a0001c0003t0005g0263 others(14): Show |
18 | HG02258.hp1 HG02280.hp2 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.493-835G>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 3/13 | chr21 | 41919795 | |||||||
| chr21:41919843 | G | A | 1 | a0001c0006t0003g0344 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.493-883C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 3/13 | chr21 | 41919843 | |||||||
| chr21:41919857 | T | G | 1 | a0001c0001t0001g0132 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.493-897A>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 3/13 | chr21 | 41919857 | |||||||
| chr21:41919944 | G | C | 1 | a0001c0001t0001g0005 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.493-984C>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 3/13 | chr21 | 41919944 | |||||||
| chr21:41919951 | C | T | 1 | a0001c0007t0005g0041 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.493-991G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 3/13 | chr21 | 41919951 | |||||||
| chr21:41920001 | C | T | 6 | a0002c0008t0001g0225 a0002c0008t0005g0249 a0002c0008t0005g0251 others(3): Show |
6 | HG01884.hp2 HG02723.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.493-1041G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 3/13 | chr21 | 41920001 | |||||||
| chr21:41920172 | CG | C | 8 | a0002c0012t0009g0062 a0002c0012t0012g0241 a0002c0012t0012g0262 others(5): Show |
8 | HG01167.hp1 HG01169.hp1 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.493-1213delC | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 3/13 | chr21 | 41920172 | |||||||
| chr21:41920188 | C | T | 5 | a0001c0004t0004g0280 a0001c0004t0004g0281 a0001c0004t0006g0392 others(2): Show |
5 | HG02630.hp2 HG02647.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.493-1228G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 3/13 | chr21 | 41920188 | |||||||
| chr21:41920491 | T | A | 3 | a0001c0003t0020g0323 a0001c0006t0034g0289 a0003c0031t0018g0158 |
3 | HG02486.hp2 HG03130.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.492+1481A>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 3/13 | chr21 | 41920491 | |||||||
| chr21:41920592 | G | A | 48 | a0001c0001t0001g0027 a0001c0001t0001g0035 a0001c0001t0001g0066 others(45): Show |
48 | HG00280.hp2 HG00597.hp2 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.492+1380C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 3/13 | chr21 | 41920592 | |||||||
| chr21:41920637 | G | A | 2 | a0001c0002t0004g0087 a0001c0002t0004g0206 |
2 | NA19078.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.492+1335C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 3/13 | chr21 | 41920637 | |||||||
| chr21:41920715 | T | A | 8 | a0002c0010t0001g0131 a0002c0010t0007g0111 a0002c0010t0008g0023 others(5): Show |
8 | HG00639.hp1 HG00642.hp2 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.492+1257A>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 3/13 | chr21 | 41920715 | |||||||
| chr21:41920718 | T | C | 1 | a0001c0003t0001g0294 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.492+1254A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 3/13 | chr21 | 41920718 | |||||||
| chr21:41920822 | A | G | 3 | a0001c0002t0002g0083 a0001c0002t0002g0086 a0001c0002t0002g0304 |
3 | NA18983.hp1 NA19000.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.492+1150T>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 3/13 | chr21 | 41920822 | |||||||
| chr21:41921055 | C | T | 69 | a0001c0001t0001g0027 a0001c0001t0001g0035 a0001c0001t0001g0066 others(66): Show |
70 | HG00280.hp2 HG00597.hp2 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.492+917G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 3/13 | chr21 | 41921055 | |||||||
| chr21:41921221 | A | G | 1 | a0001c0003t0006g0010 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.492+751T>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 3/13 | chr21 | 41921221 | |||||||
| chr21:41921253 | T | C | 114 | a0001c0001t0001g0005 a0001c0001t0001g0025 a0001c0001t0001g0037 others(111): Show |
114 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.492+719A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 3/13 | chr21 | 41921253 | |||||||
| chr21:41921304 | T | A | 5 | a0001c0002t0002g0004 a0001c0003t0002g0030 a0001c0003t0003g0094 others(2): Show |
5 | HG00408.hp2 HG00438.hp1 HG02523.hp2 others(2): Show |
intron_variant | MODIFIER | c.492+668A>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 3/13 | chr21 | 41921304 | |||||||
| chr21:41921340 | G | A | 1 | a0001c0001t0003g0383 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.492+632C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 3/13 | chr21 | 41921340 | |||||||
| chr21:41921383 | A | G | 2 | a0001c0003t0015g0312 a0001c0003t0015g0328 |
2 | HG02965.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.492+589T>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 3/13 | chr21 | 41921383 | |||||||
| chr21:41921540 | G | A | 2 | a0001c0003t0015g0312 a0001c0003t0015g0328 |
2 | HG02965.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.492+432C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 3/13 | chr21 | 41921540 | |||||||
| chr21:41921597 | G | C | 1 | a0001c0001t0003g0383 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.492+375C>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 3/13 | chr21 | 41921597 | |||||||
| chr21:41921672 | A | G | 8 | a0002c0010t0001g0131 a0002c0010t0007g0111 a0002c0010t0008g0023 others(5): Show |
8 | HG00639.hp1 HG00642.hp2 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.492+300T>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 3/13 | chr21 | 41921672 | |||||||
| chr21:41921754 | A | ATG | 70 | a0001c0001t0001g0027 a0001c0001t0001g0035 a0001c0001t0001g0066 others(67): Show |
71 | HG00280.hp2 HG00597.hp2 HG00609.hp2 others(68): Show |
intron_variant | MODIFIER | c.492+216_492+217dup others(2): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 3/13 | chr21 | 41921754 | |||||||
| chr21:41921766 | G | A | 7 | a0002c0010t0001g0131 a0002c0010t0007g0111 a0002c0010t0008g0023 others(4): Show |
7 | HG00639.hp1 HG00642.hp2 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.492+206C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 3/13 | chr21 | 41921766 | |||||||
| chr21:41921937 | G | A | 69 | a0001c0001t0001g0027 a0001c0001t0001g0035 a0001c0001t0001g0066 others(66): Show |
70 | HG00280.hp2 HG00597.hp2 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.492+35C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 3/13 | chr21 | 41921937 | |||||||
| chr21:41922136 | C | T | 11 | a0001c0003t0005g0024 a0001c0003t0009g0043 a0001c0003t0015g0141 others(8): Show |
12 | HG02280.hp2 HG02559.hp2 HG02965.hp1 others(9): Show |
intron_variant | MODIFIER | c.379-51G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41922136 | |||||||
| chr21:41922160 | C | CT | 59 | a0001c0001t0001g0066 a0001c0001t0001g0085 a0001c0001t0001g0132 others(56): Show |
60 | HG00280.hp2 HG00597.hp2 HG00609.hp2 others(57): Show |
intron_variant | MODIFIER | c.379-76dupA | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41922160 | |||||||
| chr21:41922163 | C | T | 82 | a0001c0001t0001g0066 a0001c0001t0001g0085 a0001c0001t0001g0132 others(79): Show |
83 | HG00280.hp2 HG00597.hp2 HG00609.hp2 others(80): Show |
intron_variant | MODIFIER | c.379-78G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41922163 | |||||||
| chr21:41922242 | T | TCCA | 51 | a0001c0001t0001g0027 a0001c0001t0001g0035 a0001c0001t0001g0066 others(48): Show |
51 | HG00280.hp2 HG00597.hp2 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.379-160_379-158dup others(3): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41922242 | |||||||
| chr21:41922321 | C | T | 1 | a0001c0001t0001g0380 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.379-236G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41922321 | |||||||
| chr21:41922429 | T | C | 7 | a0002c0010t0001g0131 a0002c0010t0007g0111 a0002c0010t0008g0023 others(4): Show |
7 | HG00639.hp1 HG00642.hp2 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.379-344A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41922429 | |||||||
| chr21:41922476 | C | CT | 11 | a0001c0001t0005g0379 a0001c0002t0006g0381 a0001c0003t0011g0108 others(8): Show |
11 | HG00438.hp2 HG01891.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.379-392dupA | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41922476 | |||||||
| chr21:41922476 | CT | C | 88 | a0001c0001t0002g0316 a0001c0001t0002g0367 a0001c0001t0004g0297 others(85): Show |
88 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.379-392delA | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41922476 | |||||||
| chr21:41922476 | CTT | C | 50 | a0001c0001t0001g0027 a0001c0001t0001g0035 a0001c0001t0001g0066 others(47): Show |
50 | HG00280.hp2 HG00597.hp2 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.379-393_379-392del others(2): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41922476 | |||||||
| chr21:41922476 | CTTT | C | 13 | a0001c0003t0001g0349 a0001c0003t0005g0024 a0001c0003t0005g0263 others(10): Show |
14 | HG02258.hp1 HG02280.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.379-394_379-392del others(3): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41922476 | |||||||
| chr21:41922497 | C | T | 1 | a0001c0002t0002g0129 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.379-412G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41922497 | |||||||
| chr21:41922970 | C | A | 6 | a0002c0008t0001g0225 a0002c0008t0005g0249 a0002c0008t0005g0251 others(3): Show |
6 | HG01884.hp2 HG02723.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.379-885G>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41922970 | |||||||
| chr21:41922986 | TAC | T | 4 | a0002c0010t0001g0131 a0002c0010t0007g0111 a0002c0010t0008g0023 others(1): Show |
4 | HG02602.hp1 HG03688.hp2 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.379-903_379-902del others(2): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41922986 | |||||||
| chr21:41922999 | CT | C | 319 | a0001c0001t0001g0005 a0001c0001t0001g0025 a0001c0001t0001g0037 others(316): Show |
320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.379-915delA | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41922999 | |||||||
| chr21:41923081 | C | T | 85 | a0001c0001t0001g0025 a0001c0001t0001g0037 a0001c0001t0001g0042 others(82): Show |
85 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.379-996G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41923081 | |||||||
| chr21:41923213 | T | C | 1 | a0002c0008t0005g0354 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.379-1128A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41923213 | |||||||
| chr21:41923240 | A | G | 10 | a0001c0001t0001g0353 a0001c0001t0049g0220 a0001c0001t0053g0395 others(7): Show |
10 | HG01891.hp1 HG02132.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.379-1155T>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41923240 | |||||||
| chr21:41923267 | A | C | 1 | a0001c0003t0002g0200 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.379-1182T>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41923267 | |||||||
| chr21:41923288 | C | T | 2 | a0001c0002t0005g0247 a0001c0003t0005g0024 |
2 | HG03195.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.379-1203G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41923288 | |||||||
| chr21:41923364 | G | A | 2 | a0002c0008t0009g0161 a0002c0027t0009g0325 |
2 | HG02257.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.379-1279C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41923364 | |||||||
| chr21:41923364 | G | T | 10 | a0001c0002t0005g0303 a0002c0012t0009g0062 a0002c0012t0012g0241 others(7): Show |
10 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.379-1279C>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41923364 | |||||||
| chr21:41923376 | A | G | 2 | a0001c0021t0005g0235 a0001c0028t0020g0244 |
2 | HG02717.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.379-1291T>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41923376 | |||||||
| chr21:41923397 | C | G | 2 | a0002c0008t0009g0161 a0002c0027t0009g0325 |
2 | HG02257.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.379-1312G>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41923397 | |||||||
| chr21:41923401 | G | C | 38 | a0001c0002t0005g0303 a0001c0003t0001g0349 a0001c0003t0005g0024 others(35): Show |
39 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(36): Show |
intron_variant | MODIFIER | c.379-1316C>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41923401 | |||||||
| chr21:41923773 | A | T | 2 | a0001c0004t0024g0284 a0001c0004t0024g0286 |
2 | HG06807.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.379-1688T>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41923773 | |||||||
| chr21:41923789 | T | A | 1 | a0001c0001t0008g0267 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.379-1704A>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41923789 | |||||||
| chr21:41923950 | C | T | 1 | a0001c0001t0011g0210 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.379-1865G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41923950 | |||||||
| chr21:41923958 | G | A | 2 | a0001c0003t0010g0153 a0002c0018t0010g0150 |
2 | HG01243.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.379-1873C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41923958 | |||||||
| chr21:41924063 | G | C | 1 | a0001c0002t0006g0381 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.379-1978C>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41924063 | |||||||
| chr21:41924164 | G | A | 22 | a0001c0003t0005g0024 a0001c0003t0009g0043 a0001c0003t0015g0141 others(19): Show |
23 | HG01884.hp2 HG02280.hp2 HG02559.hp2 others(20): Show |
intron_variant | MODIFIER | c.379-2079C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41924164 | |||||||
| chr21:41924235 | C | A | 8 | a0001c0002t0005g0303 a0001c0003t0010g0153 a0002c0012t0009g0062 others(5): Show |
8 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.379-2150G>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41924235 | |||||||
| chr21:41924236 | A | G | 8 | a0001c0002t0005g0303 a0001c0003t0010g0153 a0002c0012t0009g0062 others(5): Show |
8 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.379-2151T>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41924236 | |||||||
| chr21:41924258 | T | C | 2 | a0001c0003t0010g0153 a0002c0018t0010g0150 |
2 | HG01243.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.379-2173A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41924258 | |||||||
| chr21:41924278 | C | T | 1 | a0001c0007t0005g0009 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.379-2193G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41924278 | |||||||
| chr21:41924315 | C | T | 1 | a0001c0003t0003g0105 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.379-2230G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41924315 | |||||||
| chr21:41924329 | C | T | 2 | a0001c0002t0002g0216 a0001c0002t0003g0217 |
2 | NA18945.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.379-2244G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41924329 | |||||||
| chr21:41924533 | T | C | 4 | a0001c0003t0001g0180 a0001c0003t0001g0209 a0001c0003t0001g0218 others(1): Show |
4 | NA18971.hp1 NA19003.hp2 NA19078.hp1 others(1): Show |
intron_variant | MODIFIER | c.379-2448A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41924533 | |||||||
| chr21:41924597 | T | C | 4 | a0002c0010t0001g0131 a0002c0010t0007g0111 a0002c0010t0008g0023 others(1): Show |
4 | HG02602.hp1 HG03688.hp2 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.379-2512A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41924597 | |||||||
| chr21:41924693 | GTAAAAAA | G | 17 | a0001c0002t0005g0303 a0001c0005t0005g0156 a0001c0005t0005g0348 others(14): Show |
17 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.379-2615_379-2609d others(9): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41924693 | |||||||
| chr21:41924720 | T | A | 9 | a0001c0001t0039g0346 a0001c0002t0002g0083 a0001c0002t0002g0086 others(6): Show |
9 | HG01952.hp1 HG02145.hp2 HG02735.hp1 others(6): Show |
intron_variant | MODIFIER | c.379-2635A>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41924720 | |||||||
| chr21:41924807 | C | T | 1 | a0003c0009t0007g0352 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.379-2722G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41924807 | |||||||
| chr21:41924944 | G | C | 293 | a0001c0001t0001g0025 a0001c0001t0001g0037 a0001c0001t0001g0038 others(290): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.379-2859C>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41924944 | |||||||
| chr21:41925051 | G | C | 32 | a0001c0001t0052g0394 a0001c0002t0005g0247 a0001c0002t0005g0248 others(29): Show |
33 | HG01884.hp1 HG01884.hp2 HG02109.hp2 others(30): Show |
intron_variant | MODIFIER | c.379-2966C>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41925051 | |||||||
| chr21:41925098 | A | G | 91 | a0001c0001t0001g0005 a0001c0001t0001g0027 a0001c0001t0001g0035 others(88): Show |
91 | HG00280.hp2 HG00621.hp1 HG00673.hp2 others(88): Show |
intron_variant | MODIFIER | c.379-3013T>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41925098 | |||||||
| chr21:41925143 | C | T | 1 | a0001c0003t0006g0010 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.379-3058G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41925143 | |||||||
| chr21:41925154 | T | C | 15 | a0001c0003t0020g0323 a0001c0004t0005g0138 a0001c0004t0005g0358 others(12): Show |
15 | HG01243.hp2 HG02451.hp1 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.379-3069A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41925154 | |||||||
| chr21:41925321 | T | TA | 15 | a0001c0001t0005g0379 a0001c0001t0011g0077 a0001c0001t0013g0142 others(12): Show |
15 | HG01167.hp1 HG01169.hp1 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.379-3237dupT | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41925321 | |||||||
| chr21:41925321 | T | TAA | 142 | a0001c0001t0001g0005 a0001c0001t0001g0050 a0001c0001t0001g0085 others(139): Show |
142 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.379-3238_379-3237d others(4): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41925321 | |||||||
| chr21:41925329 | A | G | 4 | a0001c0001t0001g0380 a0001c0001t0002g0296 a0001c0001t0003g0384 others(1): Show |
4 | HG01433.hp2 HG02683.hp1 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.379-3244T>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41925329 | |||||||
| chr21:41925354 | T | G | 1 | a0001c0001t0007g0175 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.379-3269A>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41925354 | |||||||
| chr21:41925455 | G | T | 1 | a0001c0001t0002g0154 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.379-3370C>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41925455 | |||||||
| chr21:41925466 | C | G | 6 | a0001c0001t0001g0132 a0001c0001t0001g0380 a0001c0001t0002g0296 others(3): Show |
6 | HG01106.hp2 HG01192.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.379-3381G>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41925466 | |||||||
| chr21:41925562 | G | A | 1 | a0001c0028t0020g0244 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.379-3477C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41925562 | |||||||
| chr21:41925675 | G | A | 1 | a0001c0001t0002g0112 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.379-3590C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41925675 | |||||||
| chr21:41925754 | C | A | 5 | a0001c0003t0001g0064 a0001c0003t0005g0061 a0001c0003t0009g0139 others(2): Show |
5 | HG02145.hp2 HG02451.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.379-3669G>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41925754 | |||||||
| chr21:41925771 | G | T | 3 | a0001c0001t0005g0287 a0001c0001t0026g0322 a0002c0010t0008g0023 |
3 | HG02602.hp1 HG03942.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.379-3686C>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41925771 | |||||||
| chr21:41926019 | T | C | 1 | a0001c0003t0001g0064 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.379-3934A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41926019 | |||||||
| chr21:41926041 | A | T | 6 | a0001c0002t0005g0303 a0002c0012t0012g0241 a0002c0012t0012g0262 others(3): Show |
6 | HG01109.hp1 HG02258.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.379-3956T>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41926041 | |||||||
| chr21:41926046 | G | A | 1 | a0001c0001t0001g0027 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.379-3961C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41926046 | |||||||
| chr21:41926068 | G | A | 1 | a0001c0002t0002g0126 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.379-3983C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41926068 | |||||||
| chr21:41926132 | A | G | 2 | a0001c0014t0021g0227 a0002c0008t0009g0161 |
2 | HG03130.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.379-4047T>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41926132 | |||||||
| chr21:41926175 | C | T | 1 | a0001c0003t0008g0347 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.379-4090G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41926175 | |||||||
| chr21:41926339 | C | T | 1 | a0001c0001t0004g0152 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.379-4254G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41926339 | |||||||
| chr21:41926402 | C | T | 10 | a0001c0003t0005g0024 a0001c0004t0009g0350 a0001c0004t0017g0232 others(7): Show |
10 | HG02109.hp1 HG02647.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.379-4317G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41926402 | |||||||
| chr21:41926434 | C | T | 2 | a0001c0003t0005g0061 a0002c0008t0045g0226 |
2 | HG01884.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.379-4349G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41926434 | |||||||
| chr21:41926502 | G | A | 1 | a0003c0009t0007g0352 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.379-4417C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41926502 | |||||||
| chr21:41926557 | C | T | 12 | a0001c0001t0002g0296 a0001c0001t0002g0386 a0001c0001t0036g0356 others(9): Show |
12 | HG01069.hp2 HG01070.hp2 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.379-4472G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41926557 | |||||||
| chr21:41926596 | A | C | 1 | a0001c0005t0005g0221 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.379-4511T>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41926596 | |||||||
| chr21:41926802 | G | A | 33 | a0001c0001t0002g0212 a0001c0001t0002g0386 a0001c0001t0003g0072 others(30): Show |
33 | HG00597.hp2 HG00673.hp2 HG01168.hp2 others(30): Show |
intron_variant | MODIFIER | c.379-4717C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41926802 | |||||||
| chr21:41926829 | G | A | 1 | a0003c0031t0018g0158 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.379-4744C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41926829 | |||||||
| chr21:41927022 | G | A | 1 | a0001c0007t0012g0230 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.379-4937C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41927022 | |||||||
| chr21:41927262 | T | C | 1 | a0001c0004t0022g0391 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.379-5177A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41927262 | |||||||
| chr21:41927447 | C | T | 59 | a0001c0001t0001g0005 a0001c0001t0001g0178 a0001c0001t0001g0380 others(56): Show |
59 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.379-5362G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41927447 | |||||||
| chr21:41927588 | A | G | 6 | a0001c0002t0017g0279 a0001c0004t0004g0280 a0001c0004t0004g0281 others(3): Show |
6 | HG02486.hp1 HG02630.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.379-5503T>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41927588 | |||||||
| chr21:41927622 | C | T | 2 | a0001c0004t0005g0390 a0001c0004t0017g0028 |
2 | HG02451.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.379-5537G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41927622 | |||||||
| chr21:41927786 | A | G | 1 | a0001c0004t0006g0392 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.379-5701T>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41927786 | |||||||
| chr21:41927886 | C | T | 2 | a0001c0001t0005g0259 a0001c0004t0022g0391 |
2 | HG03579.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.379-5801G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41927886 | |||||||
| chr21:41928017 | A | G | 1 | a0001c0001t0005g0379 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.379-5932T>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41928017 | |||||||
| chr21:41928078 | C | T | 1 | a0001c0025t0004g0273 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.379-5993G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41928078 | |||||||
| chr21:41928255 | C | A | 2 | a0001c0001t0005g0259 a0001c0004t0022g0391 |
2 | HG03579.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.379-6170G>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41928255 | |||||||
| chr21:41928303 | T | C | 37 | a0001c0001t0001g0035 a0001c0001t0001g0042 a0001c0001t0002g0212 others(34): Show |
37 | HG00597.hp2 HG00639.hp1 HG02056.hp1 others(34): Show |
intron_variant | MODIFIER | c.379-6218A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41928303 | |||||||
| chr21:41928315 | C | T | 1 | a0002c0018t0022g0285 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.379-6230G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41928315 | |||||||
| chr21:41928347 | G | C | 1 | a0002c0008t0009g0161 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.379-6262C>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41928347 | |||||||
| chr21:41928544 | C | CA | 12 | a0001c0001t0002g0367 a0001c0002t0011g0337 a0001c0003t0001g0103 others(9): Show |
12 | HG01981.hp1 HG02109.hp1 HG02300.hp2 others(9): Show |
intron_variant | MODIFIER | c.379-6460dupT | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41928544 | |||||||
| chr21:41928544 | C | CAAA | 13 | a0001c0003t0001g0008 a0001c0003t0005g0332 a0001c0003t0005g0335 others(10): Show |
13 | HG01070.hp1 HG01071.hp1 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.379-6462_379-6460d others(5): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41928544 | |||||||
| chr21:41928544 | CA | C | 81 | a0001c0001t0001g0353 a0001c0001t0002g0058 a0001c0001t0002g0146 others(78): Show |
81 | HG00099.hp1 HG00140.hp1 HG00741.hp2 others(78): Show |
intron_variant | MODIFIER | c.379-6460delT | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41928544 | |||||||
| chr21:41928544 | CAA | C | 118 | a0001c0001t0001g0005 a0001c0001t0001g0025 a0001c0001t0001g0027 others(115): Show |
119 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.379-6461_379-6460d others(4): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41928544 | |||||||
| chr21:41928566 | A | T | 1 | a0002c0027t0009g0325 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.379-6481T>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41928566 | |||||||
| chr21:41928580 | C | T | 1 | a0001c0004t0022g0391 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.379-6495G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41928580 | |||||||
| chr21:41928599 | T | C | 1 | a0001c0006t0009g0256 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.379-6514A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41928599 | |||||||
| chr21:41928695 | C | A | 2 | a0001c0002t0011g0336 a0001c0002t0011g0337 |
2 | NA18951.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.379-6610G>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41928695 | |||||||
| chr21:41928721 | G | A | 1 | a0001c0025t0004g0273 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.379-6636C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41928721 | |||||||
| chr21:41928835 | C | T | 2 | a0001c0014t0005g0243 a0001c0014t0005g0250 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.379-6750G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41928835 | |||||||
| chr21:41928911 | A | G | 18 | a0001c0002t0005g0303 a0001c0003t0001g0008 a0001c0003t0001g0272 others(15): Show |
18 | HG01070.hp1 HG01071.hp1 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.379-6826T>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41928911 | |||||||
| chr21:41928931 | G | A | 99 | a0001c0001t0001g0005 a0001c0001t0001g0035 a0001c0001t0001g0042 others(96): Show |
99 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.379-6846C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41928931 | |||||||
| chr21:41928979 | T | TA | 99 | a0001c0001t0001g0005 a0001c0001t0001g0035 a0001c0001t0001g0042 others(96): Show |
99 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.379-6895dupT | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41928979 | |||||||
| chr21:41929040 | A | G | 1 | a0001c0001t0005g0379 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.379-6955T>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41929040 | |||||||
| chr21:41929102 | T | TA | 17 | a0001c0001t0005g0259 a0001c0002t0011g0336 a0001c0002t0011g0337 others(14): Show |
17 | HG01516.hp1 HG01981.hp1 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.379-7018dupT | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41929102 | |||||||
| chr21:41929221 | G | A | 1 | a0002c0010t0016g0340 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.379-7136C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41929221 | |||||||
| chr21:41929399 | C | T | 3 | a0001c0001t0005g0259 a0001c0004t0022g0391 a0008c0043t0041g0012 |
3 | HG02572.hp2 HG03579.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.379-7314G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41929399 | |||||||
| chr21:41929504 | GC | G | 28 | a0001c0001t0001g0025 a0001c0001t0001g0027 a0001c0001t0001g0050 others(25): Show |
28 | HG00639.hp2 HG00642.hp1 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.379-7420delG | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41929504 | |||||||
| chr21:41929556 | CT | C | 28 | a0001c0001t0001g0025 a0001c0001t0001g0027 a0001c0001t0001g0050 others(25): Show |
28 | HG00639.hp2 HG00642.hp1 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.379-7472delA | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41929556 | |||||||
| chr21:41929564 | A | C | 28 | a0001c0001t0001g0025 a0001c0001t0001g0027 a0001c0001t0001g0050 others(25): Show |
28 | HG00639.hp2 HG00642.hp1 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.379-7479T>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41929564 | |||||||
| chr21:41929586 | T | C | 1 | a0001c0001t0002g0367 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.379-7501A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41929586 | |||||||
| chr21:41929790 | C | T | 2 | a0001c0002t0002g0003 a0001c0002t0004g0087 |
2 | NA18944.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.379-7705G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41929790 | |||||||
| chr21:41929938 | G | A | 1 | a0002c0018t0022g0285 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.379-7853C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41929938 | |||||||
| chr21:41929943 | C | T | 8 | a0001c0003t0001g0349 a0001c0004t0024g0284 a0001c0004t0024g0286 others(5): Show |
8 | HG02145.hp1 HG03130.hp1 HG03209.hp2 others(5): Show |
intron_variant | MODIFIER | c.379-7858G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41929943 | |||||||
| chr21:41929953 | T | C | 28 | a0001c0001t0001g0025 a0001c0001t0001g0027 a0001c0001t0001g0050 others(25): Show |
28 | HG00639.hp2 HG00642.hp1 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.379-7868A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41929953 | |||||||
| chr21:41930007 | GGAGGAAG others(3362): Show |
G | 28 | a0001c0001t0001g0025 a0001c0001t0001g0027 a0001c0001t0001g0050 others(25): Show |
28 | HG00639.hp2 HG00642.hp1 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.378+8771_379-7923d others(2): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41930007 | |||||||
| chr21:41930216 | C | T | 1 | a0001c0002t0006g0071 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.379-8131G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41930216 | |||||||
| chr21:41930437 | T | C | 7 | a0001c0003t0005g0024 a0001c0004t0006g0392 a0001c0004t0017g0232 others(4): Show |
7 | HG02109.hp1 HG02451.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.379-8352A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41930437 | |||||||
| chr21:41930478 | G | A | 1 | a0001c0007t0005g0041 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.379-8393C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41930478 | |||||||
| chr21:41930633 | C | T | 8 | a0001c0005t0044g0254 a0001c0007t0001g0231 a0001c0007t0006g0255 others(5): Show |
8 | HG02615.hp2 HG02809.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.379-8548G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41930633 | |||||||
| chr21:41930711 | C | CA | 13 | a0001c0001t0001g0132 a0001c0001t0002g0168 a0001c0001t0002g0197 others(10): Show |
13 | HG00099.hp1 HG00140.hp2 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.379-8627dupT | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41930711 | |||||||
| chr21:41930933 | C | T | 8 | a0001c0001t0004g0113 a0001c0001t0006g0007 a0001c0002t0001g0095 others(5): Show |
8 | HG02071.hp2 HG02135.hp2 HG02293.hp1 others(5): Show |
intron_variant | MODIFIER | c.379-8848G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41930933 | |||||||
| chr21:41931081 | G | A | 1 | a0001c0025t0004g0273 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.379-8996C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41931081 | |||||||
| chr21:41931147 | G | A | 1 | a0001c0007t0005g0041 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.379-9062C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41931147 | |||||||
| chr21:41931319 | C | T | 1 | a0001c0025t0004g0273 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.379-9234G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41931319 | |||||||
| chr21:41931395 | G | A | 2 | a0001c0003t0005g0332 a0001c0003t0005g0335 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.379-9310C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41931395 | |||||||
| chr21:41931426 | C | CT | 259 | a0001c0001t0001g0005 a0001c0001t0001g0035 a0001c0001t0001g0042 others(256): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.379-9342dupA | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41931426 | |||||||
| chr21:41931446 | C | A | 8 | a0001c0003t0001g0349 a0001c0004t0024g0284 a0001c0004t0024g0286 others(5): Show |
8 | HG02145.hp1 HG03130.hp1 HG03209.hp2 others(5): Show |
intron_variant | MODIFIER | c.379-9361G>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41931446 | |||||||
| chr21:41931567 | C | T | 3 | a0001c0001t0002g0291 a0001c0001t0003g0290 a0002c0010t0016g0292 |
3 | HG00642.hp2 HG01255.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.379-9482G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41931567 | |||||||
| chr21:41931569 | C | A | 4 | a0001c0003t0001g0224 a0001c0003t0005g0263 a0001c0005t0005g0001 others(1): Show |
5 | HG01361.hp2 HG02258.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.379-9484G>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41931569 | |||||||
| chr21:41931638 | G | A | 2 | a0001c0002t0003g0299 a0002c0041t0033g0308 |
2 | HG01168.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.379-9553C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41931638 | |||||||
| chr21:41931670 | C | T | 37 | a0001c0001t0001g0035 a0001c0001t0001g0042 a0001c0001t0002g0212 others(34): Show |
37 | HG00597.hp2 HG00639.hp1 HG02056.hp1 others(34): Show |
intron_variant | MODIFIER | c.379-9585G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41931670 | |||||||
| chr21:41931715 | C | T | 2 | a0001c0004t0006g0392 a0003c0017t0018g0331 |
2 | HG02109.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.379-9630G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41931715 | |||||||
| chr21:41931751 | G | T | 4 | a0001c0001t0002g0154 a0001c0003t0010g0153 a0001c0011t0005g0140 others(1): Show |
4 | HG01074.hp2 HG02559.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.379-9666C>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41931751 | |||||||
| chr21:41931829 | TACCCCAC others(59): Show |
T | 1 | a0001c0025t0004g0273 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.379-9810_379-9745d others(68): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41931829 | |||||||
| chr21:41931864 | ACATCCCA others(15): Show |
A | 20 | a0001c0001t0002g0342 a0001c0001t0005g0051 a0001c0002t0007g0318 others(17): Show |
20 | HG00738.hp1 HG01070.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.379-9801_379-9780d others(24): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41931864 | |||||||
| chr21:41931864 | ACATCCCA others(37): Show |
A | 100 | a0001c0001t0001g0005 a0001c0001t0001g0035 a0001c0001t0001g0042 others(97): Show |
100 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.379-9823_379-9780d others(46): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41931864 | |||||||
| chr21:41931918 | ACCCCACC others(59): Show |
A | 2 | a0001c0003t0011g0108 a0001c0037t0004g0021 |
2 | HG00438.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.379-9899_379-9834d others(68): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41931918 | |||||||
| chr21:41931940 | A | ACCCCACC others(81): Show |
1 | a0001c0002t0002g0172 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.379-9856_379-9855i others(90): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41931940 | |||||||
| chr21:41931940 | A | T | 2 | a0001c0001t0004g0149 a0001c0001t0019g0157 |
2 | HG01106.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.379-9855T>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41931940 | |||||||
| chr21:41931941 | C | A | 2 | a0004c0016t0004g0134 a0004c0016t0004g0135 |
2 | HG00741.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.379-9856G>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41931941 | |||||||
| chr21:41931962 | A | T | 265 | a0001c0001t0001g0005 a0001c0001t0001g0035 a0001c0001t0001g0042 others(262): Show |
265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.379-9877T>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41931962 | |||||||
| chr21:41931974 | G | A | 29 | a0001c0002t0005g0303 a0001c0003t0001g0008 a0001c0003t0001g0272 others(26): Show |
29 | HG01070.hp1 HG01071.hp1 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.379-9889C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41931974 | |||||||
| chr21:41931974 | G | GCATCCCA others(15): Show |
1 | a0002c0008t0009g0161 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.379-9890_379-9889i others(24): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41931974 | |||||||
| chr21:41932005 | C | T | 1 | a0001c0004t0009g0137 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.379-9920G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41932005 | |||||||
| chr21:41932038 | A | C | 1 | a0003c0015t0010g0270 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.379-9953T>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41932038 | |||||||
| chr21:41932290 | G | A | 5 | a0001c0003t0001g0224 a0001c0003t0005g0263 a0001c0005t0005g0001 others(2): Show |
6 | HG01361.hp2 HG01516.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.378+9857C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41932290 | |||||||
| chr21:41932413 | C | T | 2 | a0001c0002t0025g0002 a0001c0003t0006g0070 |
2 | HG02165.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.378+9734G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41932413 | |||||||
| chr21:41932445 | CAGAT | C | 208 | a0001c0001t0001g0005 a0001c0001t0001g0035 a0001c0001t0001g0042 others(205): Show |
208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.378+9698_378+9701d others(6): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41932445 | |||||||
| chr21:41932528 | C | T | 2 | a0001c0002t0001g0073 a0001c0003t0006g0010 |
2 | HG03669.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.378+9619G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41932528 | |||||||
| chr21:41932541 | T | C | 2 | a0001c0001t0006g0375 a0001c0002t0002g0376 |
2 | NA18983.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.378+9606A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41932541 | |||||||
| chr21:41932586 | C | T | 1 | a0001c0002t0007g0345 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.378+9561G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41932586 | |||||||
| chr21:41932691 | C | T | 1 | a0001c0001t0003g0081 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.378+9456G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41932691 | |||||||
| chr21:41932709 | G | A | 1 | a0003c0015t0005g0361 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.378+9438C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41932709 | |||||||
| chr21:41932750 | T | TC | 6 | a0001c0003t0001g0224 a0001c0003t0005g0263 a0001c0005t0005g0001 others(3): Show |
7 | HG01361.hp2 HG01516.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.378+9396_378+9397i others(3): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41932750 | |||||||
| chr21:41932751 | G | C | 6 | a0001c0003t0001g0224 a0001c0003t0005g0263 a0001c0005t0005g0001 others(3): Show |
7 | HG01361.hp2 HG01516.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.378+9396C>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41932751 | |||||||
| chr21:41932752 | A | G | 6 | a0001c0003t0001g0224 a0001c0003t0005g0263 a0001c0005t0005g0001 others(3): Show |
7 | HG01361.hp2 HG01516.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.378+9395T>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41932752 | |||||||
| chr21:41932909 | C | G | 271 | a0001c0001t0001g0005 a0001c0001t0001g0035 a0001c0001t0001g0042 others(268): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.378+9238G>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41932909 | |||||||
| chr21:41933009 | C | G | 1 | a0001c0002t0004g0343 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.378+9138G>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41933009 | |||||||
| chr21:41933032 | G | A | 5 | a0001c0005t0005g0360 a0001c0014t0021g0227 a0002c0008t0009g0161 others(2): Show |
5 | HG01884.hp2 HG02622.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.378+9115C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41933032 | |||||||
| chr21:41933142 | G | A | 50 | a0001c0001t0002g0291 a0001c0001t0002g0300 a0001c0001t0002g0301 others(47): Show |
50 | HG00280.hp2 HG00323.hp1 HG00642.hp2 others(47): Show |
intron_variant | MODIFIER | c.378+9005C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41933142 | |||||||
| chr21:41933154 | TGAC | T | 51 | a0001c0001t0002g0291 a0001c0001t0002g0300 a0001c0001t0002g0301 others(48): Show |
51 | HG00280.hp2 HG00323.hp1 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.378+8990_378+8992d others(5): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41933154 | |||||||
| chr21:41933213 | T | C | 1 | a0001c0004t0005g0138 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.378+8934A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41933213 | |||||||
| chr21:41933260 | G | GT | 51 | a0001c0001t0002g0291 a0001c0001t0002g0300 a0001c0001t0002g0301 others(48): Show |
51 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.378+8886dupA | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41933260 | |||||||
| chr21:41933322 | G | A | 2 | a0001c0003t0020g0323 a0009c0026t0004g0271 |
2 | HG02486.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.378+8825C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41933322 | |||||||
| chr21:41933358 | T | C | 11 | a0001c0001t0002g0291 a0001c0001t0002g0300 a0001c0001t0002g0301 others(8): Show |
11 | HG00642.hp2 HG00735.hp2 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.378+8789A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41933358 | |||||||
| chr21:41933361 | C | T | 48 | a0001c0001t0002g0291 a0001c0001t0002g0300 a0001c0001t0002g0301 others(45): Show |
48 | HG00280.hp2 HG00323.hp1 HG00642.hp2 others(45): Show |
intron_variant | MODIFIER | c.378+8786G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41933361 | |||||||
| chr21:41933390 | G | A | 1 | a0001c0001t0004g0266 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.378+8757C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41933390 | |||||||
| chr21:41933461 | C | G | 267 | a0001c0001t0001g0005 a0001c0001t0001g0035 a0001c0001t0001g0042 others(264): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.378+8686G>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41933461 | |||||||
| chr21:41933501 | T | C | 51 | a0001c0001t0002g0291 a0001c0001t0002g0300 a0001c0001t0002g0301 others(48): Show |
51 | HG00280.hp2 HG00323.hp1 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.378+8646A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41933501 | |||||||
| chr21:41933539 | T | C | 100 | a0001c0001t0001g0005 a0001c0001t0001g0035 a0001c0001t0001g0042 others(97): Show |
100 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.378+8608A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41933539 | |||||||
| chr21:41933616 | A | G | 78 | a0001c0001t0001g0085 a0001c0001t0001g0132 a0001c0001t0001g0353 others(75): Show |
78 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(75): Show |
intron_variant | MODIFIER | c.378+8531T>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41933616 | |||||||
| chr21:41933755 | G | A | 1 | a0001c0006t0048g0357 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.378+8392C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41933755 | |||||||
| chr21:41933804 | T | C | 278 | a0001c0001t0001g0005 a0001c0001t0001g0035 a0001c0001t0001g0042 others(275): Show |
279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.378+8343A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41933804 | |||||||
| chr21:41934620 | T | C | 1 | a0001c0005t0002g0327 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.378+7527A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41934620 | |||||||
| chr21:41934631 | A | G | 2 | a0001c0003t0005g0332 a0001c0003t0005g0335 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.378+7516T>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41934631 | |||||||
| chr21:41934719 | T | C | 203 | a0001c0001t0001g0005 a0001c0001t0001g0035 a0001c0001t0001g0042 others(200): Show |
204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.378+7428A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41934719 | |||||||
| chr21:41934767 | G | A | 104 | a0001c0001t0001g0005 a0001c0001t0001g0035 a0001c0001t0001g0042 others(101): Show |
104 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.378+7380C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41934767 | |||||||
| chr21:41934857 | T | TG | 81 | a0001c0001t0001g0085 a0001c0001t0001g0132 a0001c0001t0001g0353 others(78): Show |
81 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(78): Show |
intron_variant | MODIFIER | c.378+7289_378+7290i others(3): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41934857 | |||||||
| chr21:41935180 | G | A | 1 | a0003c0015t0005g0361 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.378+6967C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41935180 | |||||||
| chr21:41935182 | G | A | 109 | a0001c0001t0001g0005 a0001c0001t0001g0035 a0001c0001t0001g0042 others(106): Show |
110 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.378+6965C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41935182 | |||||||
| chr21:41935354 | T | C | 110 | a0001c0001t0001g0005 a0001c0001t0001g0035 a0001c0001t0001g0042 others(107): Show |
111 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.378+6793A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41935354 | |||||||
| chr21:41935355 | G | C | 4 | a0001c0003t0001g0224 a0001c0003t0005g0263 a0001c0005t0005g0001 others(1): Show |
5 | HG01361.hp2 HG02258.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.378+6792C>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41935355 | |||||||
| chr21:41935593 | G | A | 1 | a0002c0018t0005g0252 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.378+6554C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41935593 | |||||||
| chr21:41935632 | C | T | 1 | a0001c0001t0001g0038 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.378+6515G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41935632 | |||||||
| chr21:41935695 | T | C | 1 | a0001c0004t0022g0391 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.378+6452A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41935695 | |||||||
| chr21:41935699 | A | C | 109 | a0001c0001t0001g0005 a0001c0001t0001g0035 a0001c0001t0001g0042 others(106): Show |
110 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.378+6448T>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41935699 | |||||||
| chr21:41935729 | G | A | 2 | a0001c0003t0020g0323 a0009c0026t0004g0271 |
2 | HG02486.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.378+6418C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41935729 | |||||||
| chr21:41935807 | G | A | 6 | a0001c0001t0001g0353 a0001c0001t0039g0346 a0001c0001t0053g0395 others(3): Show |
6 | HG01106.hp1 HG01346.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.378+6340C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41935807 | |||||||
| chr21:41935849 | A | T | 2 | a0001c0002t0001g0073 a0001c0003t0006g0010 |
2 | HG03669.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.378+6298T>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41935849 | |||||||
| chr21:41935855 | C | T | 3 | a0001c0003t0001g0064 a0001c0003t0005g0061 a0001c0003t0009g0139 |
3 | HG02145.hp2 HG02965.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.378+6292G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41935855 | |||||||
| chr21:41935997 | GA | G | 111 | a0001c0001t0001g0005 a0001c0001t0001g0035 a0001c0001t0001g0042 others(108): Show |
112 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.378+6149delT | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41935997 | |||||||
| chr21:41936045 | A | AT | 113 | a0001c0001t0001g0005 a0001c0001t0001g0035 a0001c0001t0001g0037 others(110): Show |
114 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.378+6101dupA | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41936045 | |||||||
| chr21:41936050 | T | A | 4 | a0001c0001t0004g0125 a0001c0002t0002g0102 a0001c0002t0003g0101 others(1): Show |
4 | HG03239.hp1 NA18949.hp1 NA18961.hp2 others(1): Show |
intron_variant | MODIFIER | c.378+6097A>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41936050 | |||||||
| chr21:41936110 | C | T | 112 | a0001c0001t0001g0005 a0001c0001t0001g0035 a0001c0001t0001g0037 others(109): Show |
113 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(110): Show |
intron_variant | MODIFIER | c.378+6037G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41936110 | |||||||
| chr21:41936149 | G | A | 2 | a0001c0003t0020g0323 a0009c0026t0004g0271 |
2 | HG02486.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.378+5998C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41936149 | |||||||
| chr21:41936168 | C | T | 113 | a0001c0001t0001g0005 a0001c0001t0001g0035 a0001c0001t0001g0037 others(110): Show |
114 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.378+5979G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41936168 | |||||||
| chr21:41936180 | C | A | 113 | a0001c0001t0001g0005 a0001c0001t0001g0035 a0001c0001t0001g0037 others(110): Show |
114 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.378+5967G>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41936180 | |||||||
| chr21:41936301 | A | G | 73 | a0001c0001t0001g0085 a0001c0001t0001g0132 a0001c0001t0001g0353 others(70): Show |
73 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(70): Show |
intron_variant | MODIFIER | c.378+5846T>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41936301 | |||||||
| chr21:41936420 | T | G | 1 | a0007c0030t0001g0118 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.378+5727A>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41936420 | |||||||
| chr21:41936574 | G | A | 43 | a0001c0001t0001g0005 a0001c0001t0001g0380 a0001c0001t0002g0017 others(40): Show |
43 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(40): Show |
intron_variant | MODIFIER | c.378+5573C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41936574 | |||||||
| chr21:41936614 | G | A | 1 | a0002c0008t0009g0161 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.378+5533C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41936614 | |||||||
| chr21:41936652 | T | TA | 6 | a0001c0003t0001g0224 a0001c0003t0005g0263 a0001c0005t0005g0001 others(3): Show |
7 | HG01361.hp2 HG02258.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.378+5494_378+5495i others(3): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41936652 | |||||||
| chr21:41936778 | G | A | 1 | a0001c0004t0017g0232 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.378+5369C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41936778 | |||||||
| chr21:41936815 | C | CT | 15 | a0001c0001t0002g0088 a0001c0001t0005g0051 a0001c0001t0006g0173 others(12): Show |
15 | HG01167.hp2 HG01891.hp1 HG01934.hp2 others(12): Show |
intron_variant | MODIFIER | c.378+5331dupA | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41936815 | |||||||
| chr21:41936815 | CT | C | 37 | a0001c0001t0002g0154 a0001c0001t0002g0183 a0001c0001t0002g0211 others(34): Show |
38 | HG00280.hp2 HG01069.hp2 HG01070.hp1 others(35): Show |
intron_variant | MODIFIER | c.378+5331delA | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41936815 | |||||||
| chr21:41936815 | CTT | C | 146 | a0001c0001t0001g0005 a0001c0001t0001g0035 a0001c0001t0001g0037 others(143): Show |
146 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.378+5330_378+5331d others(4): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41936815 | |||||||
| chr21:41936928 | C | T | 1 | a0001c0001t0003g0072 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.378+5219G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41936928 | |||||||
| chr21:41936938 | C | A | 1 | a0001c0001t0004g0190 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.378+5209G>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41936938 | |||||||
| chr21:41936965 | C | T | 1 | a0002c0008t0001g0225 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.378+5182G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41936965 | |||||||
| chr21:41936982 | C | T | 2 | a0001c0006t0009g0256 a0001c0014t0021g0227 |
2 | HG02622.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.378+5165G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41936982 | |||||||
| chr21:41937000 | G | A | 1 | a0001c0005t0005g0156 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.378+5147C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41937000 | |||||||
| chr21:41937007 | TGG | T | 5 | a0001c0003t0001g0224 a0001c0003t0005g0263 a0001c0005t0005g0001 others(2): Show |
6 | HG01361.hp2 HG02258.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.378+5138_378+5139d others(4): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41937007 | |||||||
| chr21:41937077 | T | C | 18 | a0001c0003t0001g0224 a0001c0003t0001g0272 a0001c0003t0005g0263 others(15): Show |
19 | HG01070.hp1 HG01071.hp1 HG01257.hp1 others(16): Show |
intron_variant | MODIFIER | c.378+5070A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41937077 | |||||||
| chr21:41937094 | T | C | 13 | a0001c0003t0001g0272 a0001c0003t0005g0332 a0001c0003t0005g0335 others(10): Show |
13 | HG01070.hp1 HG01071.hp1 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.378+5053A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41937094 | |||||||
| chr21:41937264 | C | T | 1 | a0001c0002t0030g0106 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.378+4883G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41937264 | |||||||
| chr21:41937456 | A | C | 10 | a0001c0003t0001g0064 a0001c0003t0001g0349 a0001c0003t0005g0061 others(7): Show |
10 | HG02145.hp1 HG02145.hp2 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.378+4691T>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41937456 | |||||||
| chr21:41937481 | C | T | 18 | a0001c0003t0001g0224 a0001c0003t0001g0272 a0001c0003t0005g0263 others(15): Show |
19 | HG01070.hp1 HG01071.hp1 HG01257.hp1 others(16): Show |
intron_variant | MODIFIER | c.378+4666G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41937481 | |||||||
| chr21:41937494 | T | A | 1 | a0001c0025t0004g0273 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.378+4653A>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41937494 | |||||||
| chr21:41937517 | C | T | 2 | a0001c0002t0003g0160 a0001c0002t0004g0368 |
2 | NA19056.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.378+4630G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41937517 | |||||||
| chr21:41937520 | C | T | 14 | a0001c0003t0001g0272 a0001c0003t0005g0332 a0001c0003t0005g0335 others(11): Show |
14 | HG01070.hp1 HG01071.hp1 HG01257.hp1 others(11): Show |
intron_variant | MODIFIER | c.378+4627G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41937520 | |||||||
| chr21:41937522 | G | C | 68 | a0001c0001t0001g0035 a0001c0001t0001g0037 a0001c0001t0001g0042 others(65): Show |
68 | HG00438.hp1 HG00609.hp1 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.378+4625C>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41937522 | |||||||
| chr21:41937565 | G | A | 2 | a0001c0004t0006g0392 a0003c0017t0018g0331 |
2 | HG02109.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.378+4582C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41937565 | |||||||
| chr21:41937776 | A | G | 16 | a0001c0003t0001g0224 a0001c0003t0001g0272 a0001c0003t0005g0263 others(13): Show |
17 | HG01070.hp1 HG01071.hp1 HG01361.hp2 others(14): Show |
intron_variant | MODIFIER | c.378+4371T>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41937776 | |||||||
| chr21:41937945 | G | A | 1 | a0001c0025t0004g0273 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.378+4202C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41937945 | |||||||
| chr21:41937962 | G | A | 16 | a0001c0003t0001g0224 a0001c0003t0001g0272 a0001c0003t0005g0263 others(13): Show |
17 | HG01070.hp1 HG01071.hp1 HG01361.hp2 others(14): Show |
intron_variant | MODIFIER | c.378+4185C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41937962 | |||||||
| chr21:41937964 | C | T | 2 | a0001c0005t0005g0360 a0002c0008t0045g0226 |
2 | HG01884.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.378+4183G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41937964 | |||||||
| chr21:41938011 | C | T | 1 | a0001c0004t0022g0391 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.378+4136G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41938011 | |||||||
| chr21:41938024 | T | A | 1 | a0001c0004t0022g0391 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.378+4123A>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41938024 | |||||||
| chr21:41938034 | C | A | 1 | a0001c0004t0022g0391 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.378+4113G>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41938034 | |||||||
| chr21:41938082 | A | G | 1 | a0001c0003t0001g0377 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.378+4065T>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41938082 | |||||||
| chr21:41938164 | C | CGT | 18 | a0001c0003t0001g0224 a0001c0003t0001g0272 a0001c0003t0005g0263 others(15): Show |
19 | HG01070.hp1 HG01071.hp1 HG01257.hp1 others(16): Show |
intron_variant | MODIFIER | c.378+3981_378+3982d others(4): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41938164 | |||||||
| chr21:41938167 | G | GTA | 13 | a0001c0002t0002g0083 a0001c0002t0002g0136 a0001c0003t0005g0024 others(10): Show |
13 | HG02004.hp2 HG02109.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.378+3978_378+3979d others(4): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41938167 | |||||||
| chr21:41938270 | C | A | 36 | a0001c0001t0001g0005 a0001c0001t0001g0380 a0001c0001t0002g0017 others(33): Show |
36 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(33): Show |
intron_variant | MODIFIER | c.378+3877G>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41938270 | |||||||
| chr21:41938422 | A | G | 72 | a0001c0001t0001g0085 a0001c0001t0001g0132 a0001c0001t0001g0353 others(69): Show |
72 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(69): Show |
intron_variant | MODIFIER | c.378+3725T>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41938422 | |||||||
| chr21:41938486 | C | T | 64 | a0001c0001t0001g0035 a0001c0001t0001g0037 a0001c0001t0001g0042 others(61): Show |
64 | HG00438.hp1 HG00609.hp1 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.378+3661G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41938486 | |||||||
| chr21:41938505 | C | T | 215 | a0001c0001t0001g0005 a0001c0001t0001g0085 a0001c0001t0001g0132 others(212): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.378+3642G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41938505 | |||||||
| chr21:41938742 | C | CT | 6 | a0001c0001t0002g0264 a0001c0002t0002g0086 a0001c0002t0003g0016 others(3): Show |
6 | HG00738.hp1 NA18948.hp1 NA18988.hp2 others(3): Show |
intron_variant | MODIFIER | c.378+3404dupA | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41938742 | |||||||
| chr21:41938742 | CT | C | 62 | a0001c0001t0001g0178 a0001c0001t0002g0011 a0001c0001t0002g0058 others(59): Show |
63 | HG00140.hp1 HG00438.hp1 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.378+3404delA | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41938742 | |||||||
| chr21:41938781 | A | G | 2 | a0001c0003t0001g0064 a0001c0003t0005g0061 |
2 | HG02145.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.378+3366T>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41938781 | |||||||
| chr21:41938802 | C | T | 10 | a0001c0003t0001g0272 a0001c0003t0005g0332 a0001c0003t0005g0335 others(7): Show |
10 | HG01070.hp1 HG01071.hp1 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.378+3345G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41938802 | |||||||
| chr21:41938941 | A | G | 4 | a0001c0003t0020g0323 a0001c0025t0004g0273 a0003c0015t0005g0361 others(1): Show |
4 | HG01516.hp1 HG02486.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.378+3206T>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41938941 | |||||||
| chr21:41939023 | C | T | 24 | a0001c0001t0001g0178 a0001c0001t0002g0011 a0001c0001t0002g0183 others(21): Show |
24 | HG00438.hp1 HG00609.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.378+3124G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41939023 | |||||||
| chr21:41939038 | G | C | 1 | a0001c0001t0052g0394 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.378+3109C>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41939038 | |||||||
| chr21:41939084 | G | A | 5 | a0001c0003t0005g0024 a0001c0004t0017g0232 a0001c0007t0012g0230 others(2): Show |
5 | HG02647.hp1 HG02886.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.378+3063C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41939084 | |||||||
| chr21:41939197 | G | A | 1 | a0001c0003t0007g0370 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.378+2950C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41939197 | |||||||
| chr21:41939252 | T | C | 1 | a0001c0025t0004g0273 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.378+2895A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41939252 | |||||||
| chr21:41939367 | A | G | 1 | a0001c0002t0006g0071 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.378+2780T>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41939367 | |||||||
| chr21:41939371 | C | T | 1 | a0001c0003t0009g0043 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.378+2776G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41939371 | |||||||
| chr21:41939463 | A | C | 6 | a0001c0003t0001g0064 a0001c0003t0005g0061 a0001c0003t0020g0323 others(3): Show |
6 | HG01516.hp1 HG02145.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.378+2684T>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41939463 | |||||||
| chr21:41939503 | T | C | 26 | a0001c0003t0001g0064 a0001c0003t0001g0224 a0001c0003t0001g0272 others(23): Show |
27 | HG01070.hp1 HG01071.hp1 HG01257.hp1 others(24): Show |
intron_variant | MODIFIER | c.378+2644A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41939503 | |||||||
| chr21:41939571 | A | C | 112 | a0001c0001t0001g0132 a0001c0001t0001g0353 a0001c0001t0002g0058 others(109): Show |
113 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(110): Show |
intron_variant | MODIFIER | c.378+2576T>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41939571 | |||||||
| chr21:41939577 | A | G | 112 | a0001c0001t0001g0132 a0001c0001t0001g0353 a0001c0001t0002g0058 others(109): Show |
113 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(110): Show |
intron_variant | MODIFIER | c.378+2570T>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41939577 | |||||||
| chr21:41939660 | T | C | 110 | a0001c0001t0001g0132 a0001c0001t0001g0353 a0001c0001t0002g0058 others(107): Show |
111 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.378+2487A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41939660 | |||||||
| chr21:41939711 | T | C | 10 | a0001c0001t0005g0259 a0001c0003t0005g0024 a0001c0004t0006g0392 others(7): Show |
10 | HG02109.hp1 HG02451.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.378+2436A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41939711 | |||||||
| chr21:41939798 | C | T | 1 | a0001c0003t0006g0214 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.378+2349G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41939798 | |||||||
| chr21:41939860 | T | C | 4 | a0001c0021t0005g0235 a0001c0023t0005g0234 a0001c0024t0012g0233 others(1): Show |
4 | HG02258.hp2 HG02717.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.378+2287A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41939860 | |||||||
| chr21:41939972 | C | A | 4 | a0001c0001t0002g0295 a0001c0001t0002g0316 a0001c0001t0026g0322 others(1): Show |
4 | HG03710.hp2 HG03942.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.378+2175G>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41939972 | |||||||
| chr21:41940272 | T | C | 1 | a0001c0003t0003g0065 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.378+1875A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41940272 | |||||||
| chr21:41940318 | G | C | 7 | a0001c0003t0001g0349 a0001c0004t0024g0284 a0001c0004t0024g0286 others(4): Show |
7 | HG02145.hp1 HG03209.hp2 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.378+1829C>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41940318 | |||||||
| chr21:41940363 | C | T | 11 | a0001c0003t0001g0272 a0001c0003t0005g0332 a0001c0003t0005g0335 others(8): Show |
11 | HG01070.hp1 HG01071.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.378+1784G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41940363 | |||||||
| chr21:41940393 | T | G | 4 | a0001c0003t0001g0224 a0001c0003t0005g0263 a0001c0005t0005g0001 others(1): Show |
5 | HG01361.hp2 HG02258.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.378+1754A>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41940393 | |||||||
| chr21:41940396 | A | C | 1 | a0001c0001t0006g0007 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.378+1751T>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41940396 | |||||||
| chr21:41940486 | G | A | 2 | a0001c0003t0007g0370 a0001c0004t0024g0286 |
2 | HG02698.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.378+1661C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41940486 | |||||||
| chr21:41940543 | C | T | 1 | a0001c0002t0001g0393 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.378+1604G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41940543 | |||||||
| chr21:41940559 | G | C | 388 | a0001c0001t0001g0005 a0001c0001t0001g0025 a0001c0001t0001g0027 others(385): Show |
389 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(386): Show |
intron_variant | MODIFIER | c.378+1588C>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41940559 | |||||||
| chr21:41940779 | C | G | 85 | a0001c0001t0001g0132 a0001c0001t0001g0353 a0001c0001t0002g0058 others(82): Show |
86 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(83): Show |
intron_variant | MODIFIER | c.378+1368G>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41940779 | |||||||
| chr21:41940863 | A | T | 8 | a0001c0002t0005g0247 a0001c0002t0005g0248 a0001c0003t0001g0258 others(5): Show |
8 | HG01167.hp2 HG01891.hp1 HG02027.hp2 others(5): Show |
intron_variant | MODIFIER | c.378+1284T>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41940863 | |||||||
| chr21:41941161 | C | T | 2 | a0001c0001t0004g0317 a0001c0001t0049g0220 |
2 | HG01496.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.378+986G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41941161 | |||||||
| chr21:41941235 | C | T | 2 | a0001c0004t0004g0280 a0001c0004t0004g0281 |
2 | HG02809.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.378+912G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41941235 | |||||||
| chr21:41941396 | A | G | 3 | a0001c0003t0001g0064 a0001c0003t0005g0061 a0001c0025t0004g0273 |
3 | HG01516.hp1 HG02145.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.378+751T>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41941396 | |||||||
| chr21:41941575 | C | T | 1 | a0001c0002t0004g0343 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.378+572G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41941575 | |||||||
| chr21:41941600 | A | G | 2 | a0001c0003t0001g0064 a0001c0003t0005g0061 |
2 | HG02145.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.378+547T>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41941600 | |||||||
| chr21:41941696 | G | T | 1 | a0002c0008t0005g0260 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.378+451C>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41941696 | |||||||
| chr21:41941795 | G | A | 3 | a0001c0001t0002g0017 a0001c0001t0040g0018 a0001c0002t0002g0015 |
3 | NA18989.hp1 NA19056.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.378+352C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41941795 | |||||||
| chr21:41941796 | A | C | 9 | a0001c0002t0005g0247 a0001c0002t0005g0248 a0001c0003t0001g0258 others(6): Show |
9 | HG01167.hp2 HG01516.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.378+351T>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41941796 | |||||||
| chr21:41941889 | C | T | 1 | a0003c0036t0051g0143 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.378+258G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41941889 | |||||||
| chr21:41941942 | G | A | 2 | a0001c0001t0006g0173 a0001c0002t0001g0122 |
2 | HG01934.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.378+205C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41941942 | |||||||
| chr21:41941958 | G | T | 5 | a0001c0003t0005g0024 a0001c0004t0017g0232 a0001c0007t0012g0230 others(2): Show |
5 | HG02647.hp1 HG02886.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.378+189C>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41941958 | |||||||
| chr21:41942093 | C | T | 2 | a0001c0005t0005g0360 a0002c0008t0045g0226 |
2 | HG01884.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.378+54G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41942093 | |||||||
| chr21:41942094 | G | A | 24 | a0001c0001t0001g0025 a0001c0001t0001g0027 a0001c0001t0001g0050 others(21): Show |
24 | HG00639.hp2 HG00642.hp1 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.378+53C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41942094 | |||||||
| chr21:41942095 | T | C | 24 | a0001c0001t0001g0025 a0001c0001t0001g0027 a0001c0001t0001g0050 others(21): Show |
24 | HG00639.hp2 HG00642.hp1 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.378+52A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41942095 | |||||||
| chr21:41942127 | G | A | 1 | a0001c0001t0001g0085 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.378+20C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 2/13 | chr21 | 41942127 | |||||||
| chr21:41942404 | C | G | 131 | a0001c0001t0001g0025 a0001c0001t0001g0037 a0001c0001t0001g0050 others(128): Show |
131 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.280-159G>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41942404 | |||||||
| chr21:41942414 | C | G | 1 | a0001c0002t0001g0319 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.280-169G>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41942414 | |||||||
| chr21:41942492 | C | T | 8 | a0001c0001t0001g0037 a0001c0002t0001g0315 a0001c0002t0002g0304 others(5): Show |
8 | HG02135.hp1 NA18945.hp2 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.280-247G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41942492 | |||||||
| chr21:41942548 | T | A | 13 | a0001c0003t0001g0008 a0001c0003t0012g0239 a0001c0007t0005g0009 others(10): Show |
13 | HG01243.hp2 HG02258.hp2 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.280-303A>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41942548 | |||||||
| chr21:41942548 | T | C | 1 | a0001c0002t0030g0106 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.280-303A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41942548 | |||||||
| chr21:41942596 | G | C | 1 | a0001c0001t0013g0371 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.280-351C>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41942596 | |||||||
| chr21:41942634 | C | T | 1 | a0001c0003t0001g0294 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.280-389G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41942634 | |||||||
| chr21:41942676 | A | G | 9 | a0001c0005t0005g0221 a0001c0005t0044g0254 a0001c0006t0009g0256 others(6): Show |
9 | HG02615.hp2 HG02622.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.280-431T>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41942676 | |||||||
| chr21:41942680 | A | T | 2 | a0001c0002t0025g0002 a0001c0003t0006g0070 |
2 | HG02165.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.280-435T>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41942680 | |||||||
| chr21:41942687 | T | C | 1 | a0001c0002t0001g0122 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.280-442A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41942687 | |||||||
| chr21:41942715 | C | T | 1 | a0002c0008t0001g0225 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.280-470G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41942715 | |||||||
| chr21:41942723 | G | A | 1 | a0001c0003t0003g0056 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.280-478C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41942723 | |||||||
| chr21:41942738 | T | C | 12 | a0001c0002t0001g0275 a0001c0002t0002g0274 a0001c0003t0001g0272 others(9): Show |
12 | HG01069.hp2 HG01071.hp2 HG01516.hp1 others(9): Show |
intron_variant | MODIFIER | c.280-493A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41942738 | |||||||
| chr21:41942755 | C | T | 4 | a0001c0002t0001g0275 a0001c0002t0001g0339 a0001c0002t0002g0274 others(1): Show |
4 | HG01069.hp2 HG01071.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.280-510G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41942755 | |||||||
| chr21:41942756 | C | T | 9 | a0001c0003t0001g0272 a0001c0003t0020g0323 a0001c0004t0005g0390 others(6): Show |
9 | HG01884.hp2 HG02451.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.280-511G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41942756 | |||||||
| chr21:41942871 | C | T | 1 | a0001c0003t0006g0174 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.280-626G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41942871 | |||||||
| chr21:41942887 | A | C | 2 | a0001c0014t0005g0243 a0001c0014t0005g0250 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.280-642T>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41942887 | |||||||
| chr21:41943000 | G | A | 56 | a0001c0001t0001g0005 a0001c0001t0001g0380 a0001c0001t0002g0342 others(53): Show |
56 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(53): Show |
intron_variant | MODIFIER | c.280-755C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41943000 | |||||||
| chr21:41943025 | G | C | 1 | a0001c0007t0005g0041 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.280-780C>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41943025 | |||||||
| chr21:41943034 | C | T | 10 | a0001c0002t0017g0279 a0001c0004t0004g0280 a0001c0004t0004g0281 others(7): Show |
10 | HG01243.hp2 HG02145.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.280-789G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41943034 | |||||||
| chr21:41943176 | G | A | 2 | a0001c0001t0006g0276 a0001c0001t0006g0277 |
2 | HG00639.hp2 HG00642.hp1 |
intron_variant | MODIFIER | c.280-931C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41943176 | |||||||
| chr21:41943364 | C | T | 12 | a0001c0001t0001g0050 a0001c0001t0002g0058 a0001c0001t0002g0060 others(9): Show |
12 | HG00140.hp1 HG00741.hp2 HG01496.hp1 others(9): Show |
intron_variant | MODIFIER | c.280-1119G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41943364 | |||||||
| chr21:41943370 | A | T | 54 | a0001c0001t0002g0017 a0001c0001t0005g0259 a0001c0001t0040g0018 others(51): Show |
55 | HG01167.hp1 HG01167.hp2 HG01169.hp1 others(52): Show |
intron_variant | MODIFIER | c.280-1125T>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41943370 | |||||||
| chr21:41943432 | G | A | 3 | a0001c0003t0001g0272 a0001c0003t0020g0323 a0009c0026t0004g0271 |
3 | HG02486.hp2 HG02896.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.280-1187C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41943432 | |||||||
| chr21:41943465 | C | T | 1 | a0001c0001t0052g0394 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.280-1220G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41943465 | |||||||
| chr21:41943577 | C | T | 135 | a0001c0001t0001g0132 a0001c0001t0001g0353 a0001c0001t0002g0133 others(132): Show |
135 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.280-1332G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41943577 | |||||||
| chr21:41943594 | G | A | 104 | a0001c0001t0001g0132 a0001c0001t0001g0353 a0001c0001t0002g0133 others(101): Show |
104 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.280-1349C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41943594 | |||||||
| chr21:41943621 | G | A | 2 | a0001c0003t0001g0272 a0009c0026t0004g0271 |
2 | HG02896.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.280-1376C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41943621 | |||||||
| chr21:41943627 | G | A | 11 | a0001c0001t0001g0050 a0001c0001t0002g0058 a0001c0001t0002g0060 others(8): Show |
11 | HG00140.hp1 HG00741.hp2 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.280-1382C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41943627 | |||||||
| chr21:41943662 | C | T | 1 | a0001c0003t0002g0030 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.280-1417G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41943662 | |||||||
| chr21:41943938 | C | G | 1 | a0001c0003t0003g0196 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.280-1693G>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41943938 | |||||||
| chr21:41943948 | G | A | 1 | a0001c0001t0003g0384 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.280-1703C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41943948 | |||||||
| chr21:41944064 | G | A | 1 | a0001c0003t0001g0385 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.280-1819C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41944064 | |||||||
| chr21:41944162 | A | G | 5 | a0001c0001t0004g0266 a0001c0001t0008g0267 a0001c0003t0003g0268 others(2): Show |
5 | HG00323.hp1 HG01952.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.280-1917T>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41944162 | |||||||
| chr21:41944165 | C | T | 10 | a0001c0002t0017g0279 a0001c0004t0004g0280 a0001c0004t0004g0281 others(7): Show |
10 | HG01243.hp2 HG02145.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.280-1920G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41944165 | |||||||
| chr21:41944287 | C | T | 5 | a0001c0001t0004g0266 a0001c0001t0008g0267 a0001c0003t0003g0268 others(2): Show |
5 | HG00323.hp1 HG01952.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.280-2042G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41944287 | |||||||
| chr21:41944336 | C | T | 5 | a0001c0001t0004g0266 a0001c0001t0008g0267 a0001c0003t0003g0268 others(2): Show |
5 | HG00323.hp1 HG01952.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.280-2091G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41944336 | |||||||
| chr21:41944345 | TATTAAAA others(16): Show |
T | 1 | a0001c0002t0001g0120 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.280-2123_280-2101d others(25): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41944345 | |||||||
| chr21:41944364 | C | A | 42 | a0001c0001t0001g0132 a0001c0001t0002g0121 a0001c0001t0002g0133 others(39): Show |
42 | HG00280.hp2 HG00323.hp2 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.280-2119G>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41944364 | |||||||
| chr21:41944366 | A | C | 189 | a0001c0001t0001g0005 a0001c0001t0001g0025 a0001c0001t0001g0027 others(186): Show |
190 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.280-2121T>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41944366 | |||||||
| chr21:41944368 | A | C | 3 | a0001c0001t0005g0051 a0001c0003t0009g0043 a0001c0007t0005g0041 |
3 | HG03098.hp2 HG03831.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.280-2123T>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41944368 | |||||||
| chr21:41944392 | G | A | 1 | a0001c0002t0019g0147 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.280-2147C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41944392 | |||||||
| chr21:41944437 | G | C | 1 | a0001c0004t0005g0390 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.280-2192C>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41944437 | |||||||
| chr21:41944460 | T | G | 156 | a0001c0001t0001g0025 a0001c0001t0001g0027 a0001c0001t0001g0035 others(153): Show |
157 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(154): Show |
intron_variant | MODIFIER | c.280-2215A>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41944460 | |||||||
| chr21:41944478 | T | C | 32 | a0001c0003t0001g0008 a0001c0003t0001g0064 a0001c0003t0001g0224 others(29): Show |
33 | HG01167.hp1 HG01169.hp1 HG01361.hp2 others(30): Show |
intron_variant | MODIFIER | c.280-2233A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41944478 | |||||||
| chr21:41944488 | C | G | 3 | a0001c0021t0005g0235 a0001c0023t0005g0234 a0003c0022t0042g0236 |
3 | HG02258.hp2 HG03516.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.280-2243G>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41944488 | |||||||
| chr21:41944501 | G | A | 11 | a0001c0001t0005g0259 a0001c0005t0005g0221 a0001c0005t0044g0254 others(8): Show |
11 | HG02615.hp2 HG02622.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.280-2256C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41944501 | |||||||
| chr21:41944521 | C | CA | 147 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0066 others(144): Show |
147 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.280-2277dupT | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41944521 | |||||||
| chr21:41944521 | C | CAA | 12 | a0001c0001t0053g0395 a0001c0002t0011g0336 a0001c0002t0011g0337 others(9): Show |
12 | HG00438.hp2 HG02129.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.280-2278_280-2277d others(4): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41944521 | |||||||
| chr21:41944521 | CA | C | 39 | a0001c0001t0001g0005 a0001c0001t0001g0380 a0001c0001t0002g0367 others(36): Show |
39 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(36): Show |
intron_variant | MODIFIER | c.280-2277delT | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41944521 | |||||||
| chr21:41944533 | A | AAAAAG | 5 | a0001c0003t0001g0224 a0001c0003t0005g0263 a0001c0004t0009g0223 others(2): Show |
6 | HG01361.hp2 HG01884.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.280-2289_280-2288i others(7): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41944533 | |||||||
| chr21:41944538 | A | AAAAAG | 17 | a0001c0002t0002g0022 a0001c0002t0003g0053 a0001c0003t0001g0047 others(14): Show |
17 | HG02056.hp2 HG02145.hp2 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.280-2298_280-2294d others(7): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41944538 | |||||||
| chr21:41944538 | A | AAAAG | 130 | a0001c0001t0001g0025 a0001c0001t0001g0027 a0001c0001t0001g0035 others(127): Show |
130 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.280-2294_280-2293i others(6): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41944538 | |||||||
| chr21:41944538 | A | AG | 9 | a0001c0002t0017g0279 a0001c0004t0004g0280 a0001c0004t0004g0281 others(6): Show |
9 | HG02145.hp1 HG02486.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.280-2294_280-2293i others(3): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41944538 | |||||||
| chr21:41944538 | A | G | 5 | a0001c0003t0001g0224 a0001c0003t0005g0263 a0001c0004t0009g0223 others(2): Show |
6 | HG01361.hp2 HG01884.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.280-2293T>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41944538 | |||||||
| chr21:41944571 | A | G | 4 | a0001c0003t0001g0064 a0001c0003t0005g0061 a0002c0012t0009g0062 others(1): Show |
4 | HG01167.hp1 HG01169.hp1 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.280-2326T>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41944571 | |||||||
| chr21:41944704 | C | T | 89 | a0001c0001t0001g0025 a0001c0001t0001g0027 a0001c0001t0001g0035 others(86): Show |
89 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.280-2459G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41944704 | |||||||
| chr21:41944758 | C | T | 6 | a0001c0001t0004g0266 a0001c0001t0008g0267 a0001c0001t0052g0394 others(3): Show |
6 | HG00323.hp1 HG01952.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.280-2513G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41944758 | |||||||
| chr21:41944887 | C | A | 4 | a0001c0001t0001g0027 a0001c0001t0001g0050 a0001c0001t0014g0054 others(1): Show |
4 | NA18955.hp1 NA18979.hp1 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.280-2642G>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41944887 | |||||||
| chr21:41945337 | G | A | 70 | a0001c0001t0001g0025 a0001c0001t0001g0035 a0001c0001t0001g0042 others(67): Show |
70 | HG00099.hp1 HG00438.hp1 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.280-3092C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41945337 | |||||||
| chr21:41945569 | C | T | 71 | a0001c0001t0001g0025 a0001c0001t0001g0035 a0001c0001t0001g0042 others(68): Show |
71 | HG00099.hp1 HG00438.hp1 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.280-3324G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41945569 | |||||||
| chr21:41945585 | C | T | 5 | a0001c0001t0004g0266 a0001c0001t0008g0267 a0001c0001t0052g0394 others(2): Show |
5 | HG00323.hp1 HG02109.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.280-3340G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41945585 | |||||||
| chr21:41945804 | C | T | 1 | a0002c0012t0012g0262 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.280-3559G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41945804 | |||||||
| chr21:41945805 | G | A | 1 | a0001c0005t0002g0327 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.280-3560C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41945805 | |||||||
| chr21:41945974 | T | C | 1 | a0001c0003t0001g0209 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.280-3729A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41945974 | |||||||
| chr21:41946157 | A | T | 1 | a0001c0001t0052g0394 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.280-3912T>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41946157 | |||||||
| chr21:41946178 | G | A | 12 | a0001c0003t0001g0008 a0001c0003t0012g0239 a0001c0004t0017g0232 others(9): Show |
12 | HG02451.hp2 HG02647.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.280-3933C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41946178 | |||||||
| chr21:41946281 | A | G | 4 | a0001c0001t0004g0266 a0001c0001t0008g0267 a0001c0003t0003g0268 others(1): Show |
4 | HG00323.hp1 HG01952.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.280-4036T>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41946281 | |||||||
| chr21:41946344 | T | G | 10 | a0001c0001t0004g0266 a0001c0001t0008g0267 a0001c0001t0052g0394 others(7): Show |
10 | HG00323.hp1 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.280-4099A>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41946344 | |||||||
| chr21:41946462 | T | C | 4 | a0001c0003t0001g0064 a0001c0003t0005g0061 a0002c0012t0009g0062 others(1): Show |
4 | HG01167.hp1 HG01169.hp1 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.280-4217A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41946462 | |||||||
| chr21:41946476 | C | A | 5 | a0001c0001t0004g0266 a0001c0001t0008g0267 a0001c0003t0003g0268 others(2): Show |
5 | HG00323.hp1 HG01952.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.280-4231G>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41946476 | |||||||
| chr21:41946533 | G | T | 1 | a0001c0001t0052g0394 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.280-4288C>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41946533 | |||||||
| chr21:41946590 | G | C | 3 | a0001c0003t0001g0272 a0003c0015t0010g0270 a0009c0026t0004g0271 |
3 | HG02818.hp2 HG02896.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.280-4345C>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41946590 | |||||||
| chr21:41946793 | T | G | 2 | a0001c0002t0002g0382 a0001c0002t0006g0381 |
2 | NA18992.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.280-4548A>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41946793 | |||||||
| chr21:41946835 | A | G | 6 | a0001c0001t0004g0266 a0001c0001t0008g0267 a0001c0001t0052g0394 others(3): Show |
6 | HG00323.hp1 HG01952.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.280-4590T>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41946835 | |||||||
| chr21:41946876 | T | C | 10 | a0001c0002t0017g0279 a0001c0004t0004g0280 a0001c0004t0004g0281 others(7): Show |
10 | HG01243.hp2 HG02145.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.280-4631A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41946876 | |||||||
| chr21:41947049 | G | A | 26 | a0001c0001t0002g0017 a0001c0001t0002g0300 a0001c0001t0002g0301 others(23): Show |
26 | HG01168.hp2 HG01169.hp2 HG01516.hp2 others(23): Show |
intron_variant | MODIFIER | c.280-4804C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41947049 | |||||||
| chr21:41947110 | T | TTCTCTCT others(25): Show |
1 | a0001c0002t0004g0368 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.280-4866_280-4865i others(34): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41947110 | |||||||
| chr21:41947112 | T | C | 32 | a0001c0001t0001g0380 a0001c0001t0002g0367 a0001c0001t0002g0373 others(29): Show |
32 | HG00280.hp1 HG00673.hp1 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.280-4867A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41947112 | |||||||
| chr21:41947112 | T | TCTCTCTC others(18): Show |
3 | a0001c0002t0002g0172 a0001c0003t0001g0047 a0001c0006t0003g0344 |
3 | HG01993.hp2 HG03654.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.280-4868_280-4867i others(27): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41947112 | |||||||
| chr21:41947112 | T | TCTCTCTC others(20): Show |
4 | a0001c0001t0001g0027 a0001c0001t0004g0298 a0003c0009t0007g0293 others(1): Show |
4 | HG01169.hp2 HG02135.hp1 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.280-4868_280-4867i others(29): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41947112 | |||||||
| chr21:41947112 | T | TCTCTCTC others(22): Show |
3 | a0001c0001t0002g0296 a0001c0002t0003g0014 a0002c0018t0005g0252 |
3 | HG02622.hp2 HG02683.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.280-4868_280-4867i others(31): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41947112 | |||||||
| chr21:41947112 | T | TCTCTCTC others(30): Show |
1 | a0001c0003t0037g0257 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.280-4868_280-4867i others(39): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41947112 | |||||||
| chr21:41947112 | T | TTCTCTCC others(11): Show |
5 | a0001c0001t0002g0342 a0001c0001t0004g0317 a0001c0002t0007g0318 others(2): Show |
5 | HG00639.hp1 HG01070.hp2 HG01243.hp1 others(2): Show |
intron_variant | MODIFIER | c.280-4868_280-4867i others(20): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41947112 | |||||||
| chr21:41947112 | T | TTCTCTCC others(37): Show |
1 | a0006c0035t0003g0116 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.280-4868_280-4867i others(46): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41947112 | |||||||
| chr21:41947112 | T | TTCTCTCC others(51): Show |
1 | a0001c0003t0016g0117 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.280-4868_280-4867i others(60): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41947112 | |||||||
| chr21:41947112 | T | TTCTCTCC others(13): Show |
1 | a0008c0043t0041g0012 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.280-4868_280-4867i others(22): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41947112 | |||||||
| chr21:41947112 | T | TTCTCTCC others(45): Show |
1 | a0001c0005t0002g0327 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.280-4868_280-4867i others(54): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41947112 | |||||||
| chr21:41947112 | T | TTCTCTCC others(15): Show |
2 | a0001c0002t0001g0362 a0001c0006t0048g0357 |
2 | HG03017.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.280-4868_280-4867i others(24): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41947112 | |||||||
| chr21:41947112 | T | TTCTCTCC others(17): Show |
1 | a0001c0002t0001g0339 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.280-4868_280-4867i others(26): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41947112 | |||||||
| chr21:41947112 | T | TTCTCTCC others(19): Show |
17 | a0001c0001t0002g0121 a0001c0001t0002g0154 a0001c0001t0002g0295 others(14): Show |
17 | HG01070.hp1 HG01071.hp1 HG01074.hp2 others(14): Show |
intron_variant | MODIFIER | c.280-4868_280-4867i others(28): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41947112 | |||||||
| chr21:41947112 | T | TTCTCTCC others(21): Show |
5 | a0001c0002t0001g0127 a0001c0002t0002g0129 a0001c0004t0009g0137 others(2): Show |
5 | HG01358.hp2 HG01943.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.280-4868_280-4867i others(30): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41947112 | |||||||
| chr21:41947112 | T | TTCTCTCC others(23): Show |
7 | a0001c0001t0001g0132 a0001c0001t0002g0133 a0001c0001t0002g0264 others(4): Show |
7 | HG01192.hp2 HG01978.hp2 HG02148.hp2 others(4): Show |
intron_variant | MODIFIER | c.280-4868_280-4867i others(32): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41947112 | |||||||
| chr21:41947112 | T | TTCTCTCC others(25): Show |
6 | a0001c0001t0007g0159 a0001c0002t0003g0145 a0001c0003t0003g0151 others(3): Show |
6 | HG00280.hp2 HG00741.hp1 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.280-4868_280-4867i others(34): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41947112 | |||||||
| chr21:41947112 | T | TTCTCTCC others(27): Show |
6 | a0001c0001t0002g0146 a0001c0001t0004g0288 a0001c0001t0005g0287 others(3): Show |
6 | HG00099.hp2 HG01074.hp1 HG03688.hp1 others(3): Show |
intron_variant | MODIFIER | c.280-4868_280-4867i others(36): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41947112 | |||||||
| chr21:41947112 | T | TTCTCTCC others(29): Show |
5 | a0001c0001t0001g0353 a0001c0001t0026g0322 a0001c0002t0004g0321 others(2): Show |
5 | HG01257.hp1 HG03017.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.280-4868_280-4867i others(38): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41947112 | |||||||
| chr21:41947112 | T | TTCTCTCC others(31): Show |
7 | a0001c0002t0004g0343 a0001c0003t0015g0328 a0001c0003t0020g0323 others(4): Show |
7 | HG01258.hp2 HG02080.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.280-4868_280-4867i others(40): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41947112 | |||||||
| chr21:41947112 | T | TTCTCTCC others(33): Show |
4 | a0001c0001t0039g0346 a0001c0001t0053g0395 a0001c0002t0005g0303 others(1): Show |
4 | HG01109.hp1 HG02738.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.280-4868_280-4867i others(42): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41947112 | |||||||
| chr21:41947112 | T | TTCTCTCC others(37): Show |
2 | a0001c0003t0001g0294 a0001c0006t0003g0324 |
2 | HG02280.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.280-4868_280-4867i others(46): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41947112 | |||||||
| chr21:41947112 | T | TTCTCTCC others(12): Show |
1 | a0001c0003t0008g0341 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.280-4868_280-4867i others(21): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41947112 | |||||||
| chr21:41947112 | T | TTCTCTCC others(20): Show |
1 | a0001c0011t0005g0306 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.280-4868_280-4867i others(29): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41947112 | |||||||
| chr21:41947112 | T | TTCTCTCC others(22): Show |
1 | a0001c0002t0002g0136 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.280-4868_280-4867i others(31): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41947112 | |||||||
| chr21:41947112 | T | TTCTCTCC others(24): Show |
1 | a0004c0016t0004g0135 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.280-4868_280-4867i others(33): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41947112 | |||||||
| chr21:41947112 | T | TTCTCTCC others(26): Show |
1 | a0001c0002t0021g0320 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.280-4868_280-4867i others(35): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41947112 | |||||||
| chr21:41947112 | T | TTCTCTCC others(36): Show |
1 | a0001c0002t0001g0319 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.280-4868_280-4867i others(45): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41947112 | |||||||
| chr21:41947112 | T | TTCTCTCT others(7): Show |
1 | a0001c0004t0004g0280 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.280-4881_280-4868d others(16): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41947112 | |||||||
| chr21:41947112 | T | TTCTCTCT others(9): Show |
1 | a0002c0010t0008g0023 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.280-4883_280-4868d others(18): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41947112 | |||||||
| chr21:41947112 | T | TTCTCTCT others(11): Show |
1 | a0003c0009t0007g0169 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.280-4885_280-4868d others(20): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41947112 | |||||||
| chr21:41947112 | T | TTCTCTCT others(13): Show |
1 | a0001c0003t0005g0061 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.280-4887_280-4868d others(22): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41947112 | |||||||
| chr21:41947112 | T | TTCTCTCT others(15): Show |
6 | a0001c0003t0001g0064 a0001c0003t0003g0065 a0001c0003t0004g0170 others(3): Show |
6 | HG01167.hp1 HG01496.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.280-4889_280-4868d others(24): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41947112 | |||||||
| chr21:41947112 | T | TTCTCTCT others(17): Show |
5 | a0001c0004t0024g0286 a0001c0006t0034g0289 a0002c0012t0009g0062 others(2): Show |
5 | HG01169.hp1 HG02486.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.280-4891_280-4868d others(26): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41947112 | |||||||
| chr21:41947112 | T | TTCTCTCT others(19): Show |
5 | a0001c0001t0003g0046 a0001c0001t0003g0290 a0001c0001t0004g0297 others(2): Show |
5 | HG00735.hp2 HG01168.hp2 HG01243.hp2 others(2): Show |
intron_variant | MODIFIER | c.280-4893_280-4868d others(28): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41947112 | |||||||
| chr21:41947112 | T | TTCTCTCT others(21): Show |
2 | a0001c0001t0002g0291 a0001c0007t0001g0283 |
2 | HG01255.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.280-4895_280-4868d others(30): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41947112 | |||||||
| chr21:41947112 | T | TTCTCTCT others(23): Show |
3 | a0002c0010t0016g0292 a0003c0031t0018g0158 a0009c0026t0004g0271 |
3 | HG00642.hp2 HG03130.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.280-4868_280-4867i others(32): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41947112 | |||||||
| chr21:41947112 | T | TTCTCTCT others(25): Show |
3 | a0001c0002t0011g0337 a0001c0004t0024g0284 a0002c0018t0022g0285 |
3 | HG02145.hp1 NA18906.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.280-4868_280-4867i others(34): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41947112 | |||||||
| chr21:41947112 | T | TTCTCTCT others(27): Show |
3 | a0001c0002t0011g0336 a0001c0003t0001g0272 a0001c0003t0003g0334 |
3 | HG02896.hp1 NA18945.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.280-4868_280-4867i others(36): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41947112 | |||||||
| chr21:41947112 | T | TTCTCTCT others(29): Show |
1 | a0001c0002t0002g0304 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.280-4868_280-4867i others(38): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41947112 | |||||||
| chr21:41947112 | T | TTCTCTCT others(31): Show |
1 | a0003c0015t0010g0270 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.280-4868_280-4867i others(40): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41947112 | |||||||
| chr21:41947112 | T | TTTTCTCT others(19): Show |
1 | a0001c0001t0001g0025 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.280-4868_280-4867i others(28): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41947112 | |||||||
| chr21:41947119 | T | C | 5 | a0001c0001t0002g0316 a0001c0001t0004g0125 a0001c0001t0004g0338 others(2): Show |
5 | HG00735.hp1 HG01978.hp1 HG02015.hp2 others(2): Show |
intron_variant | MODIFIER | c.280-4874A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41947119 | |||||||
| chr21:41947133 | T | C | 1 | a0001c0003t0016g0117 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.280-4888A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41947133 | |||||||
| chr21:41947137 | T | C | 82 | a0001c0001t0001g0025 a0001c0001t0001g0027 a0001c0001t0001g0132 others(79): Show |
82 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.280-4892A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41947137 | |||||||
| chr21:41947137 | T | TCTCTCC | 6 | a0001c0001t0002g0373 a0001c0001t0002g0374 a0001c0001t0006g0375 others(3): Show |
6 | HG00673.hp1 NA18983.hp2 NA19007.hp2 others(3): Show |
intron_variant | MODIFIER | c.280-4893_280-4892i others(8): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41947137 | |||||||
| chr21:41947137 | T | TCTCTCTC others(7): Show |
2 | a0001c0002t0002g0022 a0001c0028t0020g0244 |
2 | HG02717.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.280-4893_280-4892i others(16): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41947137 | |||||||
| chr21:41947137 | T | TCTCTCTC others(11): Show |
1 | a0001c0003t0001g0008 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.280-4893_280-4892i others(20): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41947137 | |||||||
| chr21:41947137 | T | TCTCTCTC others(15): Show |
1 | a0001c0005t0005g0360 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.280-4893_280-4892i others(24): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41947137 | |||||||
| chr21:41947137 | T | TCTCTCTC others(9): Show |
2 | a0001c0004t0017g0028 a0001c0004t0022g0391 |
2 | HG02572.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.280-4893_280-4892i others(18): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41947137 | |||||||
| chr21:41947137 | T | TCTCTCTC others(13): Show |
5 | a0001c0021t0005g0235 a0002c0008t0005g0260 a0003c0017t0005g0238 others(2): Show |
5 | HG02258.hp2 HG02976.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.280-4893_280-4892i others(22): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41947137 | |||||||
| chr21:41947137 | T | TCTCTCTC others(11): Show |
6 | a0001c0001t0004g0266 a0001c0001t0006g0173 a0001c0002t0007g0378 others(3): Show |
6 | HG00323.hp1 HG01261.hp1 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.280-4893_280-4892i others(20): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41947137 | |||||||
| chr21:41947137 | T | TCTCTCTC others(15): Show |
6 | a0001c0003t0001g0218 a0001c0003t0012g0239 a0001c0007t0005g0009 others(3): Show |
6 | HG02451.hp2 HG03098.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.280-4893_280-4892i others(24): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41947137 | |||||||
| chr21:41947137 | T | TCTCTCTC others(19): Show |
2 | a0002c0008t0045g0226 a0003c0015t0005g0361 |
2 | HG01884.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.280-4893_280-4892i others(28): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41947137 | |||||||
| chr21:41947137 | T | TCTCTCTC others(13): Show |
12 | a0001c0001t0003g0177 a0001c0001t0007g0175 a0001c0002t0001g0176 others(9): Show |
12 | HG00099.hp1 HG00597.hp1 HG00738.hp1 others(9): Show |
intron_variant | MODIFIER | c.280-4893_280-4892i others(22): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41947137 | |||||||
| chr21:41947137 | T | TCTCTCTC others(17): Show |
5 | a0001c0003t0005g0263 a0001c0007t0001g0231 a0001c0007t0012g0230 others(2): Show |
5 | HG02258.hp1 HG02886.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.280-4893_280-4892i others(26): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41947137 | |||||||
| chr21:41947137 | T | TCTCTCTC others(14): Show |
1 | a0001c0003t0005g0024 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.280-4893_280-4892i others(23): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41947137 | |||||||
| chr21:41947137 | T | TCTCTCTC others(15): Show |
13 | a0001c0001t0001g0050 a0001c0001t0001g0178 a0001c0001t0002g0300 others(10): Show |
13 | HG01167.hp2 HG01516.hp2 HG02723.hp1 others(10): Show |
intron_variant | MODIFIER | c.280-4893_280-4892i others(24): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41947137 | |||||||
| chr21:41947137 | T | TCTCTCTC others(19): Show |
5 | a0001c0004t0009g0223 a0001c0004t0017g0232 a0001c0005t0005g0001 others(2): Show |
6 | HG01884.hp1 HG02647.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.280-4893_280-4892i others(28): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41947137 | |||||||
| chr21:41947137 | T | TCTCTCTC others(23): Show |
1 | a0001c0001t0003g0044 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.280-4893_280-4892i others(32): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41947137 | |||||||
| chr21:41947137 | T | TCTCTCTC others(17): Show |
26 | a0001c0001t0002g0011 a0001c0001t0002g0183 a0001c0001t0002g0301 others(23): Show |
26 | HG00323.hp2 HG00609.hp1 HG01358.hp1 others(23): Show |
intron_variant | MODIFIER | c.280-4893_280-4892i others(26): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41947137 | |||||||
| chr21:41947137 | T | TCTCTCTC others(21): Show |
2 | a0001c0001t0002g0367 a0001c0003t0004g0219 |
2 | HG02300.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.280-4893_280-4892i others(30): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41947137 | |||||||
| chr21:41947137 | T | TCTCTCTC others(18): Show |
1 | a0001c0001t0002g0212 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.280-4893_280-4892i others(27): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41947137 | |||||||
| chr21:41947137 | T | TCTCTCTC others(19): Show |
34 | a0001c0001t0001g0035 a0001c0001t0001g0037 a0001c0001t0001g0038 others(31): Show |
34 | HG00438.hp1 HG00621.hp1 HG00621.hp2 others(31): Show |
intron_variant | MODIFIER | c.280-4893_280-4892i others(28): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41947137 | |||||||
| chr21:41947137 | T | TCTCTCTC others(23): Show |
3 | a0001c0003t0001g0224 a0001c0006t0008g0387 a0001c0011t0010g0269 |
3 | HG01123.hp2 HG01361.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.280-4893_280-4892i others(32): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41947137 | |||||||
| chr21:41947137 | T | TCTCTCTC others(20): Show |
1 | a0001c0013t0004g0171 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.280-4893_280-4892i others(29): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41947137 | |||||||
| chr21:41947137 | T | TCTCTCTC others(21): Show |
23 | a0001c0001t0001g0380 a0001c0001t0002g0058 a0001c0001t0002g0168 others(20): Show |
23 | HG00140.hp1 HG00738.hp2 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.280-4893_280-4892i others(30): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41947137 | |||||||
| chr21:41947137 | T | TCTCTCTC others(22): Show |
4 | a0001c0001t0036g0356 a0001c0002t0001g0120 a0001c0002t0002g0013 others(1): Show |
4 | HG01099.hp2 HG01978.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.280-4893_280-4892i others(31): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41947137 | |||||||
| chr21:41947137 | T | TCTCTCTC others(23): Show |
14 | a0001c0001t0001g0042 a0001c0001t0002g0017 a0001c0001t0003g0366 others(11): Show |
14 | HG00741.hp2 HG01175.hp2 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.280-4893_280-4892i others(32): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41947137 | |||||||
| chr21:41947137 | T | TCTCTCTC others(24): Show |
2 | a0001c0001t0002g0316 a0001c0002t0002g0119 |
2 | HG00735.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.280-4893_280-4892i others(33): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41947137 | |||||||
| chr21:41947137 | T | TCTCTCTC others(25): Show |
9 | a0001c0001t0002g0060 a0001c0001t0002g0211 a0001c0001t0004g0148 others(6): Show |
9 | HG00280.hp1 HG01175.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.280-4893_280-4892i others(34): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41947137 | |||||||
| chr21:41947137 | T | TCTCTCTC others(29): Show |
1 | a0001c0002t0001g0359 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.280-4893_280-4892i others(38): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41947137 | |||||||
| chr21:41947137 | T | TCTCTCTC others(26): Show |
1 | a0001c0001t0004g0125 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.280-4893_280-4892i others(35): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41947137 | |||||||
| chr21:41947137 | T | TCTCTCTC others(27): Show |
4 | a0001c0001t0002g0386 a0001c0001t0004g0149 a0001c0003t0003g0372 others(1): Show |
4 | HG00609.hp2 HG01106.hp2 HG02129.hp1 others(1): Show |
intron_variant | MODIFIER | c.280-4893_280-4892i others(36): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41947137 | |||||||
| chr21:41947137 | T | TCTCTCTC others(31): Show |
1 | a0001c0003t0009g0043 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.280-4893_280-4892i others(40): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41947137 | |||||||
| chr21:41947137 | T | TCTCTCTC others(36): Show |
1 | a0001c0001t0004g0338 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.280-4893_280-4892i others(45): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41947137 | |||||||
| chr21:41947139 | T | TCTCTCTC others(11): Show |
3 | a0001c0002t0001g0275 a0001c0002t0002g0274 a0001c0025t0004g0273 |
3 | HG01069.hp2 HG01071.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.280-4895_280-4894i others(20): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41947139 | |||||||
| chr21:41947139 | T | TCTCTCTC others(15): Show |
1 | a0001c0001t0006g0276 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.280-4895_280-4894i others(24): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41947139 | |||||||
| chr21:41947139 | T | TCTCTCTC others(17): Show |
2 | a0001c0001t0006g0277 a0002c0010t0031g0278 |
2 | HG00642.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.280-4895_280-4894i others(26): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41947139 | |||||||
| chr21:41947141 | C | T | 10 | a0001c0002t0017g0279 a0001c0004t0004g0280 a0001c0004t0004g0281 others(7): Show |
10 | HG01243.hp2 HG02145.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.280-4896G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41947141 | |||||||
| chr21:41947144 | C | CTCTCTCT others(16): Show |
1 | a0001c0002t0017g0279 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.280-4900_280-4899i others(25): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41947144 | |||||||
| chr21:41947218 | C | T | 1 | a0001c0001t0053g0395 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.280-4973G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41947218 | |||||||
| chr21:41947227 | G | C | 29 | a0001c0001t0002g0017 a0001c0001t0005g0259 a0001c0001t0040g0018 others(26): Show |
29 | HG01167.hp2 HG01891.hp1 HG02027.hp2 others(26): Show |
intron_variant | MODIFIER | c.280-4982C>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41947227 | |||||||
| chr21:41947332 | A | T | 1 | a0001c0001t0052g0394 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.280-5087T>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41947332 | |||||||
| chr21:41947399 | C | T | 1 | a0001c0001t0002g0168 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.280-5154G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41947399 | |||||||
| chr21:41947496 | T | C | 13 | a0001c0002t0017g0279 a0001c0003t0001g0272 a0001c0004t0004g0280 others(10): Show |
13 | HG01243.hp2 HG02145.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.280-5251A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41947496 | |||||||
| chr21:41947606 | C | T | 1 | a0001c0003t0001g0008 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.280-5361G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41947606 | |||||||
| chr21:41947668 | C | T | 2 | a0001c0001t0005g0259 a0002c0018t0005g0252 |
2 | HG02622.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.280-5423G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41947668 | |||||||
| chr21:41947822 | G | A | 5 | a0001c0003t0001g0224 a0001c0003t0005g0263 a0001c0004t0009g0223 others(2): Show |
6 | HG01361.hp2 HG01884.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.279+5548C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41947822 | |||||||
| chr21:41947996 | C | A | 91 | a0001c0001t0001g0025 a0001c0001t0001g0027 a0001c0001t0001g0035 others(88): Show |
91 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.279+5374G>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41947996 | |||||||
| chr21:41948123 | A | G | 1 | a0001c0002t0002g0022 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.279+5247T>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41948123 | |||||||
| chr21:41948269 | G | C | 1 | a0001c0005t0002g0327 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.279+5101C>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41948269 | |||||||
| chr21:41948277 | C | T | 3 | a0001c0002t0001g0275 a0001c0002t0002g0274 a0001c0025t0004g0273 |
3 | HG01069.hp2 HG01071.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.279+5093G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41948277 | |||||||
| chr21:41948283 | G | A | 2 | a0001c0003t0004g0109 a0002c0008t0009g0161 |
2 | HG03130.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.279+5087C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41948283 | |||||||
| chr21:41948298 | A | G | 9 | a0001c0002t0005g0303 a0001c0003t0001g0294 a0001c0003t0015g0312 others(6): Show |
9 | HG01109.hp1 HG01257.hp1 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.279+5072T>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41948298 | |||||||
| chr21:41948304 | TCTGGCTC others(14): Show |
T | 24 | a0001c0001t0001g0132 a0001c0001t0002g0121 a0001c0001t0002g0133 others(21): Show |
24 | HG00280.hp2 HG00323.hp2 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.279+5045_279+5065d others(23): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41948304 | |||||||
| chr21:41948382 | G | C | 6 | a0001c0001t0006g0276 a0001c0001t0006g0277 a0001c0002t0001g0275 others(3): Show |
6 | HG00639.hp2 HG00642.hp1 HG01069.hp2 others(3): Show |
intron_variant | MODIFIER | c.279+4988C>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41948382 | |||||||
| chr21:41948404 | C | T | 1 | a0001c0001t0052g0394 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.279+4966G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41948404 | |||||||
| chr21:41948851 | T | C | 1 | a0002c0008t0009g0161 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.279+4519A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41948851 | |||||||
| chr21:41948870 | C | CT | 71 | a0001c0001t0001g0025 a0001c0001t0001g0027 a0001c0001t0001g0035 others(68): Show |
71 | HG00099.hp1 HG00438.hp1 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.279+4499dupA | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41948870 | |||||||
| chr21:41948870 | C | CTTTTT | 16 | a0001c0001t0001g0380 a0001c0001t0002g0373 a0001c0001t0002g0374 others(13): Show |
16 | HG01123.hp2 HG01433.hp2 HG02040.hp1 others(13): Show |
intron_variant | MODIFIER | c.279+4495_279+4499d others(7): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41948870 | |||||||
| chr21:41948870 | C | CTTTTTT | 8 | a0001c0001t0013g0371 a0001c0002t0001g0393 a0001c0002t0004g0368 others(5): Show |
8 | HG00280.hp1 HG00673.hp1 HG00738.hp2 others(5): Show |
intron_variant | MODIFIER | c.279+4494_279+4499d others(8): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41948870 | |||||||
| chr21:41948870 | C | CTTTTTTT | 6 | a0001c0001t0001g0353 a0001c0001t0002g0367 a0001c0001t0003g0366 others(3): Show |
6 | HG01515.hp1 HG02300.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.279+4493_279+4499d others(9): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41948870 | |||||||
| chr21:41948870 | C | CTTTTTTT others(1): Show |
35 | a0001c0001t0002g0154 a0001c0001t0002g0342 a0001c0001t0003g0351 others(32): Show |
35 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(32): Show |
intron_variant | MODIFIER | c.279+4492_279+4499d others(10): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41948870 | |||||||
| chr21:41948870 | C | CTTTTTTT others(2): Show |
28 | a0001c0001t0002g0146 a0001c0001t0002g0316 a0001c0001t0004g0148 others(25): Show |
28 | HG01106.hp1 HG01106.hp2 HG01175.hp1 others(25): Show |
intron_variant | MODIFIER | c.279+4491_279+4499d others(11): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41948870 | |||||||
| chr21:41948870 | C | CTTTTTTT others(3): Show |
13 | a0001c0001t0008g0309 a0001c0001t0013g0142 a0001c0002t0002g0304 others(10): Show |
13 | HG00738.hp1 HG01070.hp2 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.279+4490_279+4499d others(12): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41948870 | |||||||
| chr21:41948870 | C | CTTTTTTT others(4): Show |
5 | a0001c0001t0002g0300 a0001c0001t0002g0301 a0001c0002t0003g0299 others(2): Show |
5 | HG01361.hp1 HG01516.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.279+4489_279+4499d others(13): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41948870 | |||||||
| chr21:41948870 | C | CTTTTTTT others(5): Show |
15 | a0001c0001t0001g0132 a0001c0001t0002g0133 a0001c0001t0004g0125 others(12): Show |
15 | HG00741.hp1 HG01168.hp2 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.279+4488_279+4499d others(14): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41948870 | |||||||
| chr21:41948870 | C | CTTTTTTT others(6): Show |
8 | a0001c0001t0002g0121 a0001c0001t0002g0264 a0001c0001t0002g0296 others(5): Show |
8 | HG00735.hp1 HG01978.hp1 HG01978.hp2 others(5): Show |
intron_variant | MODIFIER | c.279+4487_279+4499d others(15): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41948870 | |||||||
| chr21:41948870 | C | CTTTTTTT others(7): Show |
3 | a0001c0001t0002g0295 a0001c0003t0001g0294 a0007c0030t0001g0118 |
3 | HG02165.hp1 HG02280.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.279+4486_279+4499d others(16): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41948870 | |||||||
| chr21:41948870 | C | CTTTTTTT others(8): Show |
3 | a0001c0001t0002g0291 a0002c0010t0016g0292 a0003c0009t0007g0293 |
3 | HG00642.hp2 HG01255.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.279+4485_279+4499d others(17): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41948870 | |||||||
| chr21:41948870 | C | CTTTTTTT others(9): Show |
1 | a0001c0001t0003g0290 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.279+4484_279+4499d others(18): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41948870 | |||||||
| chr21:41948870 | C | CTTTTTTT others(10): Show |
1 | a0001c0003t0016g0117 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.279+4483_279+4499d others(19): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41948870 | |||||||
| chr21:41948870 | C | CTTTTTTT others(12): Show |
1 | a0006c0035t0003g0116 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.279+4481_279+4499d others(21): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41948870 | |||||||
| chr21:41948870 | C | G | 1 | a0001c0001t0052g0394 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.279+4500G>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41948870 | |||||||
| chr21:41948870 | CT | C | 25 | a0001c0001t0002g0112 a0001c0001t0004g0113 a0001c0001t0005g0259 others(22): Show |
25 | HG01167.hp1 HG01167.hp2 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.279+4499delA | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41948870 | |||||||
| chr21:41948870 | CTT | C | 8 | a0001c0004t0017g0232 a0001c0006t0009g0256 a0001c0007t0001g0231 others(5): Show |
8 | HG02451.hp2 HG02622.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.279+4498_279+4499d others(4): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41948870 | |||||||
| chr21:41948870 | CTTT | C | 9 | a0001c0003t0001g0008 a0001c0003t0012g0239 a0001c0007t0005g0009 others(6): Show |
9 | HG02258.hp2 HG02572.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.279+4497_279+4499d others(5): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41948870 | |||||||
| chr21:41948877 | TTTTTTTT others(9): Show |
T | 1 | a0001c0001t0052g0394 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.279+4477_279+4492d others(18): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41948877 | |||||||
| chr21:41948882 | TTTTTTTT others(4): Show |
T | 7 | a0001c0001t0006g0276 a0001c0001t0006g0277 a0001c0001t0036g0356 others(4): Show |
7 | HG00639.hp2 HG00642.hp1 HG01069.hp2 others(4): Show |
intron_variant | MODIFIER | c.279+4477_279+4487d others(13): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41948882 | |||||||
| chr21:41948883 | TTTTTTTT others(3): Show |
T | 1 | a0002c0008t0009g0161 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.279+4477_279+4486d others(12): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41948883 | |||||||
| chr21:41948891 | TTC | T | 10 | a0001c0001t0008g0267 a0001c0002t0017g0279 a0001c0003t0003g0268 others(7): Show |
10 | HG01952.hp1 HG02145.hp1 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.279+4477_279+4478d others(4): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41948891 | |||||||
| chr21:41948893 | C | T | 145 | a0001c0001t0001g0132 a0001c0001t0001g0353 a0001c0001t0001g0380 others(142): Show |
145 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.279+4477G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41948893 | |||||||
| chr21:41948950 | A | T | 327 | a0001c0001t0001g0025 a0001c0001t0001g0027 a0001c0001t0001g0035 others(324): Show |
328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.279+4420T>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41948950 | |||||||
| chr21:41948994 | C | T | 1 | a0001c0037t0004g0021 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.279+4376G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41948994 | |||||||
| chr21:41949084 | C | T | 4 | a0001c0004t0022g0391 a0001c0014t0047g0261 a0002c0008t0005g0260 others(1): Show |
4 | HG02922.hp1 HG03540.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.279+4286G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41949084 | |||||||
| chr21:41949207 | G | A | 1 | a0002c0008t0009g0161 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.279+4163C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41949207 | |||||||
| chr21:41949329 | T | G | 1 | a0001c0001t0052g0394 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.279+4041A>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41949329 | |||||||
| chr21:41949467 | G | C | 3 | a0001c0003t0001g0272 a0003c0015t0010g0270 a0009c0026t0004g0271 |
3 | HG02818.hp2 HG02896.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.279+3903C>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41949467 | |||||||
| chr21:41949490 | T | C | 174 | a0001c0001t0001g0132 a0001c0001t0001g0353 a0001c0001t0001g0380 others(171): Show |
174 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.279+3880A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41949490 | |||||||
| chr21:41949719 | C | T | 6 | a0001c0001t0006g0276 a0001c0001t0006g0277 a0001c0002t0001g0275 others(3): Show |
6 | HG00639.hp2 HG00642.hp1 HG01069.hp2 others(3): Show |
intron_variant | MODIFIER | c.279+3651G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41949719 | |||||||
| chr21:41949755 | T | C | 1 | a0001c0003t0004g0162 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.279+3615A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41949755 | |||||||
| chr21:41949960 | G | A | 1 | a0001c0001t0052g0394 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.279+3410C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41949960 | |||||||
| chr21:41949998 | G | A | 3 | a0001c0003t0001g0272 a0003c0015t0010g0270 a0009c0026t0004g0271 |
3 | HG02818.hp2 HG02896.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.279+3372C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41949998 | |||||||
| chr21:41950077 | C | T | 388 | a0001c0001t0001g0005 a0001c0001t0001g0025 a0001c0001t0001g0027 others(385): Show |
389 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(386): Show |
intron_variant | MODIFIER | c.279+3293G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41950077 | |||||||
| chr21:41950081 | T | C | 16 | a0001c0001t0004g0266 a0001c0001t0008g0267 a0001c0001t0052g0394 others(13): Show |
16 | HG00323.hp1 HG01952.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.279+3289A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41950081 | |||||||
| chr21:41950139 | T | TA | 10 | a0001c0001t0002g0017 a0001c0001t0040g0018 a0001c0001t0052g0394 others(7): Show |
10 | HG02027.hp2 HG02056.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.279+3230dupT | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41950139 | |||||||
| chr21:41950182 | G | A | 53 | a0001c0001t0001g0178 a0001c0001t0002g0011 a0001c0001t0002g0168 others(50): Show |
53 | HG00099.hp1 HG00438.hp1 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.279+3188C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41950182 | |||||||
| chr21:41950208 | C | T | 1 | a0001c0002t0002g0020 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.279+3162G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41950208 | |||||||
| chr21:41950231 | A | T | 15 | a0001c0001t0004g0266 a0001c0001t0008g0267 a0001c0002t0017g0279 others(12): Show |
15 | HG00323.hp1 HG01952.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.279+3139T>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41950231 | |||||||
| chr21:41950265 | G | A | 21 | a0001c0001t0005g0259 a0001c0002t0005g0247 a0001c0002t0005g0248 others(18): Show |
21 | HG01167.hp2 HG01891.hp1 HG02027.hp2 others(18): Show |
intron_variant | MODIFIER | c.279+3105C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41950265 | |||||||
| chr21:41950284 | G | A | 1 | a0001c0001t0005g0259 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.279+3086C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41950284 | |||||||
| chr21:41950591 | C | T | 1 | a0001c0003t0003g0019 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.279+2779G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41950591 | |||||||
| chr21:41950628 | C | G | 55 | a0001c0001t0002g0017 a0001c0001t0005g0259 a0001c0001t0040g0018 others(52): Show |
56 | HG01167.hp2 HG01361.hp2 HG01884.hp1 others(53): Show |
intron_variant | MODIFIER | c.279+2742G>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41950628 | |||||||
| chr21:41950730 | A | C | 1 | a0001c0001t0052g0394 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.279+2640T>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41950730 | |||||||
| chr21:41950872 | T | C | 1 | a0001c0001t0049g0220 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.279+2498A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41950872 | |||||||
| chr21:41951026 | G | A | 3 | a0001c0014t0047g0261 a0002c0008t0005g0260 a0002c0012t0012g0262 |
3 | HG02922.hp1 HG03540.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.279+2344C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41951026 | |||||||
| chr21:41951094 | C | T | 1 | a0001c0001t0002g0011 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.279+2276G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41951094 | |||||||
| chr21:41951222 | C | T | 2 | a0001c0001t0004g0288 a0001c0001t0005g0287 |
2 | HG01074.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.279+2148G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41951222 | |||||||
| chr21:41951236 | G | A | 1 | a0001c0003t0005g0263 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.279+2134C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41951236 | |||||||
| chr21:41951239 | G | A | 1 | a0001c0013t0001g0389 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.279+2131C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41951239 | |||||||
| chr21:41951364 | C | T | 1 | a0001c0003t0006g0010 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.279+2006G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41951364 | |||||||
| chr21:41951453 | T | G | 6 | a0001c0001t0006g0276 a0001c0001t0006g0277 a0001c0002t0001g0275 others(3): Show |
6 | HG00639.hp2 HG00642.hp1 HG01069.hp2 others(3): Show |
intron_variant | MODIFIER | c.279+1917A>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41951453 | |||||||
| chr21:41951542 | A | G | 1 | a0001c0005t0005g0221 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.279+1828T>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41951542 | |||||||
| chr21:41951563 | G | A | 48 | a0001c0001t0005g0259 a0001c0002t0005g0247 a0001c0002t0005g0248 others(45): Show |
49 | HG01167.hp2 HG01361.hp2 HG01884.hp1 others(46): Show |
intron_variant | MODIFIER | c.279+1807C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41951563 | |||||||
| chr21:41951600 | C | A | 8 | a0001c0002t0017g0279 a0001c0004t0004g0280 a0001c0004t0004g0281 others(5): Show |
8 | HG02145.hp1 HG02486.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.279+1770G>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41951600 | |||||||
| chr21:41951669 | T | C | 22 | a0001c0001t0004g0266 a0001c0001t0006g0276 a0001c0001t0006g0277 others(19): Show |
22 | HG00323.hp1 HG00639.hp2 HG00642.hp1 others(19): Show |
intron_variant | MODIFIER | c.279+1701A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41951669 | |||||||
| chr21:41951879 | G | A | 1 | a0001c0002t0001g0362 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.279+1491C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41951879 | |||||||
| chr21:41952045 | T | C | 1 | a0001c0001t0002g0264 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.279+1325A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41952045 | |||||||
| chr21:41952110 | T | C | 29 | a0001c0001t0001g0380 a0001c0001t0002g0367 a0001c0001t0002g0373 others(26): Show |
29 | HG00280.hp1 HG00673.hp1 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.279+1260A>G | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41952110 | |||||||
| chr21:41952122 | C | A | 1 | a0001c0002t0001g0265 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.279+1248G>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41952122 | |||||||
| chr21:41952123 | T | A | 1 | a0001c0002t0001g0265 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.279+1247A>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41952123 | |||||||
| chr21:41952124 | C | G | 1 | a0001c0002t0001g0265 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.279+1246G>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41952124 | |||||||
| chr21:41952125 | T | A | 1 | a0001c0002t0001g0265 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.279+1245A>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41952125 | |||||||
| chr21:41952126 | C | A | 1 | a0001c0002t0001g0265 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.279+1244G>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41952126 | |||||||
| chr21:41952127 | C | A | 1 | a0001c0002t0001g0265 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.279+1243G>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41952127 | |||||||
| chr21:41952130 | C | A | 1 | a0001c0002t0001g0265 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.279+1240G>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41952130 | |||||||
| chr21:41952131 | T | A | 1 | a0001c0002t0001g0265 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.279+1239A>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41952131 | |||||||
| chr21:41952132 | C | A | 1 | a0001c0002t0001g0265 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.279+1238G>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41952132 | |||||||
| chr21:41952137 | C | G | 1 | a0001c0002t0001g0265 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.279+1233G>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41952137 | |||||||
| chr21:41952140 | C | A | 1 | a0001c0002t0001g0265 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.279+1230G>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41952140 | |||||||
| chr21:41952144 | G | A | 1 | a0001c0002t0001g0265 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.279+1226C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41952144 | |||||||
| chr21:41952146 | C | A | 1 | a0001c0002t0001g0265 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.279+1224G>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41952146 | |||||||
| chr21:41952148 | C | A | 1 | a0001c0002t0001g0265 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.279+1222G>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41952148 | |||||||
| chr21:41952152 | T | A | 1 | a0001c0002t0001g0265 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.279+1218A>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41952152 | |||||||
| chr21:41952153 | T | A | 1 | a0001c0002t0001g0265 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.279+1217A>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41952153 | |||||||
| chr21:41952154 | C | G | 1 | a0001c0002t0001g0265 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.279+1216G>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41952154 | |||||||
| chr21:41952155 | T | A | 1 | a0001c0002t0001g0265 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.279+1215A>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41952155 | |||||||
| chr21:41952156 | G | A | 1 | a0001c0002t0001g0265 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.279+1214C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41952156 | |||||||
| chr21:41952159 | C | T | 1 | a0001c0002t0001g0265 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.279+1211G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41952159 | |||||||
| chr21:41952161 | C | A | 1 | a0001c0002t0001g0265 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.279+1209G>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41952161 | |||||||
| chr21:41952162 | C | G | 1 | a0001c0002t0001g0265 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.279+1208G>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41952162 | |||||||
| chr21:41952165 | G | A | 1 | a0001c0002t0001g0265 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.279+1205C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41952165 | |||||||
| chr21:41952167 | C | A | 1 | a0001c0002t0001g0265 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.279+1203G>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41952167 | |||||||
| chr21:41952170 | A | AAAGAGAA others(48): Show |
1 | a0001c0002t0001g0265 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.279+1199_279+1200i others(57): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41952170 | |||||||
| chr21:41952173 | T | A | 1 | a0001c0002t0001g0265 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.279+1197A>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41952173 | |||||||
| chr21:41952174 | C | A | 1 | a0001c0002t0001g0265 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.279+1196G>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41952174 | |||||||
| chr21:41952177 | T | A | 1 | a0001c0002t0001g0265 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.279+1193A>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41952177 | |||||||
| chr21:41952178 | C | A | 1 | a0001c0002t0001g0265 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.279+1192G>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41952178 | |||||||
| chr21:41952181 | C | T | 1 | a0001c0002t0001g0265 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.279+1189G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41952181 | |||||||
| chr21:41952185 | C | A | 1 | a0001c0002t0001g0265 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.279+1185G>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41952185 | |||||||
| chr21:41952186 | C | A | 1 | a0001c0002t0001g0265 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.279+1184G>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41952186 | |||||||
| chr21:41952187 | C | A | 1 | a0001c0002t0001g0265 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.279+1183G>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41952187 | |||||||
| chr21:41952188 | T | A | 1 | a0001c0002t0001g0265 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.279+1182A>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41952188 | |||||||
| chr21:41952192 | GCCTTTTT others(4): Show |
G | 1 | a0001c0002t0001g0265 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.279+1167_279+1177d others(13): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41952192 | |||||||
| chr21:41952204 | C | A | 1 | a0001c0002t0001g0265 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.279+1166G>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41952204 | |||||||
| chr21:41952211 | T | G | 1 | a0001c0002t0001g0265 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.279+1159A>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41952211 | |||||||
| chr21:41952213 | C | A | 1 | a0001c0002t0001g0265 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.279+1157G>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41952213 | |||||||
| chr21:41952216 | T | A | 1 | a0001c0002t0001g0265 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.279+1154A>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41952216 | |||||||
| chr21:41952217 | C | A | 1 | a0001c0002t0001g0265 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.279+1153G>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41952217 | |||||||
| chr21:41952218 | ATTTATGT others(50): Show |
A | 1 | a0001c0002t0001g0265 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.279+1095_279+1151d others(59): Show |
C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41952218 | |||||||
| chr21:41952278 | C | G | 1 | a0001c0002t0001g0265 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.279+1092G>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41952278 | |||||||
| chr21:41952279 | T | A | 1 | a0001c0002t0001g0265 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.279+1091A>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41952279 | |||||||
| chr21:41952282 | T | G | 1 | a0001c0002t0001g0265 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.279+1088A>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41952282 | |||||||
| chr21:41952344 | C | G | 2 | a0001c0003t0001g0008 a0001c0007t0005g0009 |
2 | HG03139.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.279+1026G>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41952344 | |||||||
| chr21:41952361 | A | G | 1 | a0001c0001t0006g0007 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.279+1009T>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41952361 | |||||||
| chr21:41952447 | G | A | 30 | a0001c0001t0001g0380 a0001c0001t0002g0367 a0001c0001t0002g0373 others(27): Show |
30 | HG00280.hp1 HG00673.hp1 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.279+923C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41952447 | |||||||
| chr21:41952451 | T | G | 22 | a0001c0001t0004g0266 a0001c0001t0006g0276 a0001c0001t0006g0277 others(19): Show |
22 | HG00323.hp1 HG00639.hp2 HG00642.hp1 others(19): Show |
intron_variant | MODIFIER | c.279+919A>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41952451 | |||||||
| chr21:41952613 | C | T | 1 | a0001c0006t0001g0006 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.279+757G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41952613 | |||||||
| chr21:41952724 | G | A | 77 | a0001c0001t0001g0353 a0001c0001t0002g0291 a0001c0001t0002g0295 others(74): Show |
77 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(74): Show |
intron_variant | MODIFIER | c.279+646C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41952724 | |||||||
| chr21:41952814 | G | A | 31 | a0001c0001t0001g0380 a0001c0001t0002g0367 a0001c0001t0002g0373 others(28): Show |
31 | HG00280.hp1 HG00673.hp1 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.279+556C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41952814 | |||||||
| chr21:41953066 | G | A | 1 | a0001c0001t0053g0395 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.279+304C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41953066 | |||||||
| chr21:41953072 | A | G | 28 | a0001c0001t0001g0380 a0001c0001t0002g0367 a0001c0001t0002g0373 others(25): Show |
28 | HG00280.hp1 HG00673.hp1 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.279+298T>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41953072 | |||||||
| chr21:41953181 | T | G | 1 | a0001c0002t0001g0393 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.279+189A>C | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41953181 | |||||||
| chr21:41953300 | G | A | 31 | a0001c0001t0001g0380 a0001c0001t0002g0367 a0001c0001t0002g0373 others(28): Show |
31 | HG00280.hp1 HG00673.hp1 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.279+70C>T | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41953300 | |||||||
| chr21:41953319 | C | T | 3 | a0001c0001t0001g0005 a0001c0002t0002g0003 a0001c0002t0002g0004 |
3 | HG00408.hp2 NA18944.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.279+51G>A | C2CD2 | ENSG00000157617.17 | transcript | ENST00000380486.4 | protein_coding | 1/13 | chr21 | 41953319 |