Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 115811 |
| ensemblid | ENSG00000166578.10 |
| hgncid | 25168 |
| symbol | IQCD |
| name | IQ motif containing D |
| refseq_nuc | NM_001330452.2 |
| refseq_prot | NP_001317381.1 |
| ensembl_nuc | ENST00000416617.3 |
| ensembl_prot | ENSP00000400669.2 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 113195446 |
| end | 113221094 |
| strand | - |
| ver | v1.2 |
| region | chr12:113195446-113221094 |
| region5000 | chr12:113190446-113226094 |
| regionname0 | IQCD_chr12_113195446_113221094 |
| regionname5000 | IQCD_chr12_113190446_113226094 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 449 | 285 | 81 | 50 | 111 | 10 | 31 | 82 | IQCD_chr12_113190446_113226094 | IQCD | MALDI others(444): Show |
chr12 | 113190446 | 113226094 |
| a0002 | 0/0 | 449 | 40 | 2 | 0 | 37 | 0 | 1 | 30 | IQCD_chr12_113190446_113226094 | IQCD | MALDI others(444): Show |
chr12 | 113190446 | 113226094 |
| a0003 | 0/0 | 449 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | MALDI others(444): Show |
chr12 | 113190446 | 113226094 |
| a0004 | 0/0 | 449 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | IQCD_chr12_113190446_113226094 | IQCD | MALDI others(444): Show |
chr12 | 113190446 | 113226094 |
| a0005 | 0/0 | 449 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | MALDI others(444): Show |
chr12 | 113190446 | 113226094 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1347 | 274 | 72 | 50 | 110 | 10 | 30 | IQCD_chr12_113190446_113226094 | IQCD | ATGGC others(1342): Show |
chr12 | 113190446 | 113226094 | ||
| a0001c0003 | 0/0 | 1347 | 8 | 8 | 0 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | ATGGC others(1342): Show |
chr12 | 113190446 | 113226094 | ||
| a0001c0006 | 0/0 | 1347 | 1 | 0 | 0 | 0 | 0 | 1 | IQCD_chr12_113190446_113226094 | IQCD | ATGGC others(1342): Show |
chr12 | 113190446 | 113226094 | ||
| a0001c0008 | 0/0 | 1347 | 1 | 1 | 0 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | ATGGC others(1342): Show |
chr12 | 113190446 | 113226094 | ||
| a0001c0009 | 0/0 | 1347 | 1 | 0 | 0 | 1 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | ATGGC others(1342): Show |
chr12 | 113190446 | 113226094 | ||
| a0002c0002 | 0/0 | 1347 | 40 | 2 | 0 | 37 | 0 | 1 | IQCD_chr12_113190446_113226094 | IQCD | ATGGC others(1342): Show |
chr12 | 113190446 | 113226094 | ||
| a0003c0004 | 0/0 | 1347 | 4 | 4 | 0 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | ATGGC others(1342): Show |
chr12 | 113190446 | 113226094 | ||
| a0004c0005 | 0/0 | 1347 | 2 | 0 | 0 | 0 | 0 | 2 | IQCD_chr12_113190446_113226094 | IQCD | ATGGC others(1342): Show |
chr12 | 113190446 | 113226094 | ||
| a0005c0007 | 0/0 | 1347 | 1 | 1 | 0 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | ATGGC others(1342): Show |
chr12 | 113190446 | 113226094 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1670 | 241 | 69 | 48 | 86 | 9 | 27 | IQCD_chr12_113190446_113226094 | IQCD | AGACA others(1665): Show |
chr12 | 113190446 | 113226094 |
| a0001c0001t0002 | 0/0 | 1670 | 26 | 0 | 1 | 23 | 0 | 2 | IQCD_chr12_113190446_113226094 | IQCD | AGACA others(1665): Show |
chr12 | 113190446 | 113226094 |
| a0001c0001t0004 | 0/0 | 1670 | 3 | 1 | 1 | 0 | 1 | 0 | IQCD_chr12_113190446_113226094 | IQCD | AGACA others(1665): Show |
chr12 | 113190446 | 113226094 |
| a0001c0001t0005 | 0/0 | 1670 | 2 | 2 | 0 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | AGACA others(1665): Show |
chr12 | 113190446 | 113226094 |
| a0001c0001t0006 | 0/0 | 1670 | 1 | 0 | 0 | 0 | 0 | 1 | IQCD_chr12_113190446_113226094 | IQCD | AGACA others(1665): Show |
chr12 | 113190446 | 113226094 |
| a0001c0001t0007 | 0/0 | 1670 | 1 | 0 | 0 | 1 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | AGACA others(1665): Show |
chr12 | 113190446 | 113226094 |
| a0001c0003t0001 | 0/0 | 1670 | 8 | 8 | 0 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | AGACA others(1665): Show |
chr12 | 113190446 | 113226094 |
| a0001c0006t0001 | 0/0 | 1670 | 1 | 0 | 0 | 0 | 0 | 1 | IQCD_chr12_113190446_113226094 | IQCD | AGACA others(1665): Show |
chr12 | 113190446 | 113226094 |
| a0001c0008t0001 | 0/0 | 1670 | 1 | 1 | 0 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | AGACA others(1665): Show |
chr12 | 113190446 | 113226094 |
| a0001c0009t0001 | 0/0 | 1670 | 1 | 0 | 0 | 1 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | AGACA others(1665): Show |
chr12 | 113190446 | 113226094 |
| a0002c0002t0001 | 0/0 | 1670 | 25 | 2 | 0 | 23 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | AGACA others(1665): Show |
chr12 | 113190446 | 113226094 |
| a0002c0002t0003 | 0/0 | 1670 | 15 | 0 | 0 | 14 | 0 | 1 | IQCD_chr12_113190446_113226094 | IQCD | AGACA others(1665): Show |
chr12 | 113190446 | 113226094 |
| a0003c0004t0001 | 0/0 | 1670 | 4 | 4 | 0 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | AGACA others(1665): Show |
chr12 | 113190446 | 113226094 |
| a0004c0005t0001 | 0/0 | 1670 | 2 | 0 | 0 | 0 | 0 | 2 | IQCD_chr12_113190446_113226094 | IQCD | AGACA others(1665): Show |
chr12 | 113190446 | 113226094 |
| a0005c0007t0001 | 0/0 | 1670 | 1 | 1 | 0 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | AGACA others(1665): Show |
chr12 | 113190446 | 113226094 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 1/0 | 16 | 0 | 2 | 7 | 1 | 5 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0002 | 0/0 | 12 | 2 | 2 | 4 | 0 | 4 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0006 | 0/0 | 6 | 5 | 1 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0007 | 0/0 | 6 | 0 | 0 | 5 | 0 | 1 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0008 | 0/0 | 5 | 2 | 3 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0009 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0010 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0012 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0029 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0031 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0043 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0002g0003 | 0/0 | 8 | 0 | 0 | 7 | 0 | 1 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0004g0036 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0004g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0005g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0005g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0006g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0001t0007g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0003t0001g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0003t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0003t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0003t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0003t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0006t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0008t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0001c0009t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0002c0002t0001g0005 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0002c0002t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0002c0002t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0002c0002t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0002c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0002c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0002c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0002c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0002c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0002c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0002c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0002c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0002c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0002c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0002c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0002c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0002c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0002c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0002c0002t0003g0004 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0002c0002t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0002c0002t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0002c0002t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0002c0002t0003g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0002c0002t0003g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0002c0002t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0002c0002t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0002c0002t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0003c0004t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0003c0004t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0003c0004t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0003c0004t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0004c0005t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0004c0005t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| a0005c0007t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0022 | EUR | GBR | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0019 | EUR | GBR | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0034 | EUR | GBR | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0058 | EUR | GBR | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG00280 | hp1 | a0001 | c0001 | t0004 | g0231 | EUR | FIN | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0052 | EUR | FIN | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0034 | EUR | FIN | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0027 | EUR | FIN | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG00408 | hp1 | a0002 | c0002 | t0001 | g0218 | EAS | CHS | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | CHS | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | CHS | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG00423 | hp2 | a0002 | c0002 | t0001 | g0219 | EAS | CHS | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | CHS | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG00438 | hp2 | a0002 | c0002 | t0001 | g0213 | EAS | CHS | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | CHS | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | CHS | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | CHS | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | CHS | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | CHS | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | CHS | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | CHS | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | CHS | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | PUR | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG01168 | hp1 | a0001 | c0001 | t0004 | g0036 | AMR | PUR | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | CLM | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | CLM | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | CLM | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | CLM | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | CLM | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | CLM | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | ACB | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG01891 | hp1 | a0003 | c0004 | t0001 | g0152 | AFR | ACB | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | PEL | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PEL | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | PEL | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PEL | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | PEL | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG02027 | hp1 | a0002 | c0002 | t0003 | g0176 | EAS | KHV | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG02027 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | KHV | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0166 | EAS | KHV | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0157 | EAS | KHV | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG02055 | hp1 | a0003 | c0004 | t0001 | g0151 | AFR | ACB | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | ACB | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | KHV | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | KHV | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | KHV | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG02071 | hp2 | a0002 | c0002 | t0003 | g0216 | EAS | KHV | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | KHV | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0164 | EAS | KHV | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | KHV | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | KHV | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | ACB | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PEL | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | PEL | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | CDX | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG02155 | hp2 | a0002 | c0002 | t0003 | g0004 | EAS | CDX | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | CDX | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | CDX | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | ACB | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | ACB | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | ACB | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | ACB | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | ACB | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG02280 | hp2 | a0001 | c0003 | t0001 | g0017 | AFR | ACB | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PEL | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0165 | AMR | PEL | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG02451 | hp1 | a0001 | c0003 | t0001 | g0174 | AFR | ACB | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | ACB | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | KHV | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | KHV | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG02572 | hp1 | a0001 | c0001 | t0005 | g0122 | AFR | GWD | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | GWD | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | GWD | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | GWD | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | GWD | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | GWD | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | GWD | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | GWD | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0070 | SAS | PJL | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0226 | AFR | GWD | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | GWD | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | GWD | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | GWD | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0196 | SAS | PJL | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG02809 | hp1 | a0001 | c0003 | t0001 | g0032 | AFR | GWD | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | GWD | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | GWD | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | GWD | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | GWD | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | GWD | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG02922 | hp1 | a0001 | c0003 | t0001 | g0017 | AFR | ESN | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | ESN | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | ESN | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG02970 | hp1 | a0001 | c0003 | t0001 | g0175 | AFR | ESN | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | ESN | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | MSL | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG03098 | hp2 | a0001 | c0003 | t0001 | g0177 | AFR | MSL | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG03130 | hp2 | a0001 | c0003 | t0001 | g0032 | AFR | ESN | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG03139 | hp1 | a0002 | c0002 | t0001 | g0203 | AFR | ESN | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | ESN | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0227 | AFR | ESN | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG03195 | hp2 | a0001 | c0008 | t0001 | g0044 | AFR | ESN | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG03209 | hp1 | a0003 | c0004 | t0001 | g0153 | AFR | MSL | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | MSL | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | MSL | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | MSL | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | MSL | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | MSL | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | MSL | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | MSL | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG03540 | hp1 | a0001 | c0003 | t0001 | g0017 | AFR | GWD | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | GWD | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | MSL | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | MSL | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG03669 | hp1 | a0004 | c0005 | t0001 | g0097 | SAS | PJL | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0053 | SAS | PJL | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG03688 | hp1 | a0001 | c0001 | t0006 | g0037 | SAS | STU | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0161 | SAS | BEB | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | BEB | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0073 | SAS | BEB | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0064 | SAS | BEB | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG04115 | hp1 | a0002 | c0002 | t0003 | g0214 | SAS | STU | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | STU | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG04184 | hp1 | a0001 | c0006 | t0001 | g0192 | SAS | BEB | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG04184 | hp2 | a0004 | c0005 | t0001 | g0114 | SAS | BEB | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0145 | SAS | STU | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | YRI | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | YRI | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | YRI | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | YRI | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA18945 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0162 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA18946 | hp2 | a0002 | c0002 | t0003 | g0210 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA18947 | hp2 | a0001 | c0001 | t0007 | g0067 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA18948 | hp2 | a0002 | c0002 | t0001 | g0222 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA18951 | hp2 | a0002 | c0002 | t0003 | g0004 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA18960 | hp2 | a0002 | c0002 | t0001 | g0204 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA18961 | hp1 | a0002 | c0002 | t0003 | g0004 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA18962 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA18968 | hp1 | a0002 | c0002 | t0001 | g0205 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA18969 | hp1 | a0002 | c0002 | t0003 | g0215 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA18974 | hp1 | a0002 | c0002 | t0003 | g0004 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA18979 | hp1 | a0002 | c0002 | t0001 | g0208 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA18982 | hp2 | a0002 | c0002 | t0003 | g0004 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA18984 | hp1 | a0002 | c0002 | t0001 | g0212 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA18992 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA18994 | hp2 | a0001 | c0009 | t0001 | g0140 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA18998 | hp2 | a0002 | c0002 | t0001 | g0220 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0160 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA19012 | hp2 | a0002 | c0002 | t0001 | g0206 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | LWK | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | LWK | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | LWK | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA19043 | hp2 | a0002 | c0002 | t0001 | g0184 | AFR | LWK | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA19063 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA19065 | hp1 | a0002 | c0002 | t0001 | g0035 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA19065 | hp2 | a0002 | c0002 | t0003 | g0004 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA19066 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA19067 | hp2 | a0002 | c0002 | t0001 | g0217 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA19070 | hp1 | a0002 | c0002 | t0001 | g0230 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA19074 | hp2 | a0002 | c0002 | t0003 | g0221 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA19075 | hp2 | a0002 | c0002 | t0001 | g0223 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA19076 | hp2 | a0002 | c0002 | t0001 | g0035 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA19079 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA19083 | hp1 | a0002 | c0002 | t0001 | g0209 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA19084 | hp1 | a0002 | c0002 | t0003 | g0004 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA19085 | hp1 | a0002 | c0002 | t0003 | g0211 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA19089 | hp2 | a0002 | c0002 | t0003 | g0207 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | YRI | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA19240 | hp2 | a0001 | c0001 | t0005 | g0109 | AFR | YRI | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ASW | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | ASW | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0056 | EUR | TSI | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | ACB | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | ACB | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | ACB | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG02559 | hp2 | a0003 | c0004 | t0001 | g0154 | AFR | ACB | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | MSL | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | MSL | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | USA | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| HG06807 | hp2 | a0001 | c0001 | t0004 | g0036 | AFR | USA | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | USA | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| NA20300 | hp2 | a0005 | c0007 | t0001 | g0091 | AFR | USA | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0043 | REF | REF | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0001 | REF | REF | IQCD_chr12_113190446_113226094 | IQCD | chr12 | 113190446 | 113226094 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:113200761 | A | G | 1 | a0004 | 2 | HG03669.hp1 HG04184.hp2 |
missense_variant | MODERATE | c.782T>C | p.Val261Ala | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 3/5 | 973/1670 | 782/1350 | 261/449 | chr12 | 113200761 | |||
| chr12:113207704 | C | T | 1 | a0005 | 1 | NA20300.hp2 | missense_variant | MODERATE | c.463G>A | p.Val155Ile | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 2/5 | 654/1670 | 463/1350 | 155/449 | chr12 | 113207704 | |||
| chr12:113207761 | G | C | 1 | a0003 | 4 | HG01891.hp1 HG02055.hp1 HG02559.hp2 others(1): Show |
missense_variant | MODERATE | c.406C>G | p.Leu136Val | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 2/5 | 597/1670 | 406/1350 | 136/449 | chr12 | 113207761 | |||
| chr12:113208111 | C | T | 1 | a0002 | 40 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(37): Show |
missense_variant | MODERATE | c.56G>A | p.Arg19Lys | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 2/5 | 247/1670 | 56/1350 | 19/449 | chr12 | 113208111 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:113195794 | C | T | 1 | a0001c0008 | 1 | HG03195.hp2 | synonymous_variant | LOW | c.1131G>A | p.Ala377Ala | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 5/5 | 1322/1670 | 1131/1350 | 377/449 | chr12 | 113195794 | |||
| chr12:113207843 | C | T | 1 | a0001c0006 | 1 | HG04184.hp1 | synonymous_variant | LOW | c.324G>A | p.Leu108Leu | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 2/5 | 515/1670 | 324/1350 | 108/449 | chr12 | 113207843 | |||
| chr12:113207909 | G | A | 1 | a0001c0009 | 1 | NA18994.hp2 | synonymous_variant | LOW | c.258C>T | p.Asp86Asp | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 2/5 | 449/1670 | 258/1350 | 86/449 | chr12 | 113207909 | |||
| chr12:113207927 | C | T | 1 | a0001c0003 | 8 | HG02280.hp2 HG02451.hp1 HG02809.hp1 others(5): Show |
synonymous_variant | LOW | c.240G>A | p.Glu80Glu | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 2/5 | 431/1670 | 240/1350 | 80/449 | chr12 | 113207927 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:113195507 | C | T | 2 | a0001c0001t0005 a0001c0001t0007 |
3 | HG02572.hp1 NA18947.hp2 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*68G>A | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 5/5 | 68 | chr12 | 113195507 | ||||||
| chr12:113208231 | G | A | 1 | a0002c0002t0003 | 15 | HG02027.hp1 HG02071.hp2 HG02155.hp2 others(12): Show |
5_prime_UTR_variant | MODIFIER | c.-65C>T | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 2/5 | 65 | chr12 | 113208231 | ||||||
| chr12:113208239 | C | A | 2 | a0001c0001t0002 a0001c0001t0007 |
27 | HG02040.hp1 HG02040.hp2 HG02080.hp1 others(24): Show |
5_prime_UTR_variant | MODIFIER | c.-73G>T | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 2/5 | 73 | chr12 | 113208239 | ||||||
| chr12:113221042 | G | A | 1 | a0001c0001t0004 | 3 | HG00280.hp1 HG01168.hp1 HG06807.hp2 |
5_prime_UTR_variant | MODIFIER | c.-139C>T | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/5 | 12876 | chr12 | 113221042 | ||||||
| chr12:113221056 | A | G | 1 | a0001c0001t0006 | 1 | HG03688.hp1 | 5_prime_UTR_variant | MODIFIER | c.-153T>C | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/5 | 12890 | chr12 | 113221056 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:113196025 | G | A | 29 | a0001c0001t0001g0132 a0001c0001t0001g0134 a0001c0001t0004g0036 others(26): Show |
43 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.1036-136C>T | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 4/4 | chr12 | 113196025 | |||||||
| chr12:113196031 | A | C | 1 | a0001c0001t0001g0101 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1036-142T>G | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 4/4 | chr12 | 113196031 | |||||||
| chr12:113196037 | A | G | 4 | a0003c0004t0001g0151 a0003c0004t0001g0152 a0003c0004t0001g0153 others(1): Show |
4 | HG01891.hp1 HG02055.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.1036-148T>C | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 4/4 | chr12 | 113196037 | |||||||
| chr12:113196110 | A | G | 1 | a0001c0001t0001g0200 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1036-221T>C | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 4/4 | chr12 | 113196110 | |||||||
| chr12:113196222 | C | T | 1 | a0005c0007t0001g0091 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1036-333G>A | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 4/4 | chr12 | 113196222 | |||||||
| chr12:113196359 | AGAG | A | 20 | a0001c0001t0002g0003 a0001c0001t0002g0066 a0001c0001t0002g0068 others(17): Show |
27 | HG02040.hp1 HG02040.hp2 HG02080.hp1 others(24): Show |
intron_variant | MODIFIER | c.1036-473_1036-471d others(5): Show |
IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 4/4 | chr12 | 113196359 | |||||||
| chr12:113196360 | G | C | 1 | a0001c0001t0001g0076 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1036-471C>G | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 4/4 | chr12 | 113196360 | |||||||
| chr12:113196924 | T | C | 1 | a0002c0002t0001g0217 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1035+617A>G | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 4/4 | chr12 | 113196924 | |||||||
| chr12:113197166 | G | A | 1 | a0001c0001t0001g0099 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1035+375C>T | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 4/4 | chr12 | 113197166 | |||||||
| chr12:113197182 | G | A | 1 | a0001c0001t0001g0121 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1035+359C>T | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 4/4 | chr12 | 113197182 | |||||||
| chr12:113197190 | CT | C | 42 | a0001c0001t0001g0009 a0001c0001t0001g0033 a0001c0001t0001g0034 others(39): Show |
49 | HG00140.hp1 HG00323.hp1 HG01069.hp2 others(46): Show |
intron_variant | MODIFIER | c.1035+350delA | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 4/4 | chr12 | 113197190 | |||||||
| chr12:113197190 | CTT | C | 49 | a0001c0001t0001g0132 a0001c0001t0001g0134 a0001c0001t0001g0189 others(46): Show |
71 | HG00408.hp1 HG00438.hp2 HG02027.hp1 others(68): Show |
intron_variant | MODIFIER | c.1035+349_1035+350d others(4): Show |
IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 4/4 | chr12 | 113197190 | |||||||
| chr12:113197212 | A | T | 1 | a0001c0001t0001g0135 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1035+329T>A | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 4/4 | chr12 | 113197212 | |||||||
| chr12:113197250 | C | T | 6 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(3): Show |
7 | HG00280.hp1 HG01168.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1035+291G>A | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 4/4 | chr12 | 113197250 | |||||||
| chr12:113197522 | C | A | 1 | a0001c0001t0001g0173 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1035+19G>T | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 4/4 | chr12 | 113197522 | |||||||
| chr12:113197619 | A | G | 22 | a0001c0001t0002g0003 a0001c0001t0002g0066 a0001c0001t0002g0068 others(19): Show |
30 | HG00280.hp1 HG01168.hp1 HG02040.hp1 others(27): Show |
splice_region_variant&intron_variant | LOW | c.964-7T>C | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 3/4 | chr12 | 113197619 | |||||||
| chr12:113197674 | A | G | 3 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 |
3 | HG02717.hp1 HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.964-62T>C | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 3/4 | chr12 | 113197674 | |||||||
| chr12:113197676 | T | A | 3 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 |
3 | HG02717.hp1 HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.964-64A>T | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 3/4 | chr12 | 113197676 | |||||||
| chr12:113197716 | C | T | 2 | a0001c0001t0001g0186 a0001c0001t0001g0187 |
2 | HG02809.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.964-104G>A | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 3/4 | chr12 | 113197716 | |||||||
| chr12:113197717 | G | T | 2 | a0001c0001t0001g0103 a0001c0001t0001g0104 |
2 | NA18980.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.964-105C>A | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 3/4 | chr12 | 113197717 | |||||||
| chr12:113197721 | A | G | 1 | a0001c0001t0001g0089 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.964-109T>C | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 3/4 | chr12 | 113197721 | |||||||
| chr12:113197768 | G | A | 1 | a0001c0001t0001g0051 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.964-156C>T | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 3/4 | chr12 | 113197768 | |||||||
| chr12:113197875 | G | A | 1 | a0001c0001t0001g0075 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.964-263C>T | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 3/4 | chr12 | 113197875 | |||||||
| chr12:113197992 | G | A | 1 | a0001c0001t0001g0135 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.964-380C>T | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 3/4 | chr12 | 113197992 | |||||||
| chr12:113198148 | C | T | 1 | a0002c0002t0001g0184 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.964-536G>A | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 3/4 | chr12 | 113198148 | |||||||
| chr12:113198205 | A | G | 2 | a0001c0001t0001g0089 a0001c0001t0001g0229 |
2 | HG02486.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.964-593T>C | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 3/4 | chr12 | 113198205 | |||||||
| chr12:113198229 | A | T | 1 | a0001c0001t0001g0202 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.964-617T>A | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 3/4 | chr12 | 113198229 | |||||||
| chr12:113198248 | A | G | 5 | a0001c0001t0001g0018 a0001c0001t0001g0039 a0001c0001t0001g0048 others(2): Show |
6 | HG01069.hp1 HG01175.hp2 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.964-636T>C | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 3/4 | chr12 | 113198248 | |||||||
| chr12:113198323 | G | A | 1 | a0001c0001t0001g0121 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.964-711C>T | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 3/4 | chr12 | 113198323 | |||||||
| chr12:113198460 | G | A | 64 | a0001c0001t0001g0132 a0001c0001t0001g0134 a0001c0001t0001g0183 others(61): Show |
88 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.964-848C>T | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 3/4 | chr12 | 113198460 | |||||||
| chr12:113198521 | A | G | 3 | a0001c0001t0001g0041 a0001c0001t0001g0046 a0001c0001t0001g0051 |
3 | HG00408.hp2 NA18982.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.964-909T>C | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 3/4 | chr12 | 113198521 | |||||||
| chr12:113198538 | C | T | 1 | a0001c0001t0001g0070 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.964-926G>A | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 3/4 | chr12 | 113198538 | |||||||
| chr12:113198667 | T | C | 27 | a0001c0001t0001g0132 a0001c0001t0001g0134 a0002c0002t0001g0005 others(24): Show |
40 | HG00408.hp1 HG00438.hp2 HG02027.hp1 others(37): Show |
intron_variant | MODIFIER | c.964-1055A>G | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 3/4 | chr12 | 113198667 | |||||||
| chr12:113198779 | G | A | 26 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(23): Show |
34 | HG00280.hp1 HG01168.hp1 HG02040.hp1 others(31): Show |
intron_variant | MODIFIER | c.964-1167C>T | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 3/4 | chr12 | 113198779 | |||||||
| chr12:113198939 | CT | C | 58 | a0001c0001t0001g0132 a0001c0001t0001g0134 a0001c0001t0001g0224 others(55): Show |
79 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.964-1328delA | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 3/4 | chr12 | 113198939 | |||||||
| chr12:113199007 | G | A | 5 | a0001c0003t0001g0017 a0001c0003t0001g0032 a0001c0003t0001g0174 others(2): Show |
8 | HG02280.hp2 HG02451.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.964-1395C>T | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 3/4 | chr12 | 113199007 | |||||||
| chr12:113199076 | T | C | 1 | a0001c0001t0001g0072 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.964-1464A>G | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 3/4 | chr12 | 113199076 | |||||||
| chr12:113199179 | C | T | 2 | a0001c0001t0004g0036 a0001c0001t0004g0231 |
3 | HG00280.hp1 HG01168.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.963+1401G>A | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 3/4 | chr12 | 113199179 | |||||||
| chr12:113199180 | G | A | 1 | a0001c0001t0001g0049 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.963+1400C>T | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 3/4 | chr12 | 113199180 | |||||||
| chr12:113199383 | G | A | 22 | a0001c0001t0002g0003 a0001c0001t0002g0066 a0001c0001t0002g0068 others(19): Show |
30 | HG00280.hp1 HG01168.hp1 HG02040.hp1 others(27): Show |
intron_variant | MODIFIER | c.963+1197C>T | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 3/4 | chr12 | 113199383 | |||||||
| chr12:113199399 | C | CATAA | 12 | a0001c0001t0001g0038 a0001c0001t0001g0056 a0001c0001t0001g0078 others(9): Show |
15 | HG02280.hp2 HG02451.hp1 HG02735.hp1 others(12): Show |
intron_variant | MODIFIER | c.963+1177_963+1180d others(6): Show |
IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 3/4 | chr12 | 113199399 | |||||||
| chr12:113199399 | C | CATAAATA others(1): Show |
25 | a0001c0001t0001g0132 a0001c0001t0001g0134 a0001c0001t0002g0166 others(22): Show |
37 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(34): Show |
intron_variant | MODIFIER | c.963+1173_963+1180d others(10): Show |
IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 3/4 | chr12 | 113199399 | |||||||
| chr12:113199399 | C | CATAAATA others(5): Show |
22 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(19): Show |
30 | HG01168.hp1 HG02040.hp2 HG02080.hp1 others(27): Show |
intron_variant | MODIFIER | c.963+1169_963+1180d others(14): Show |
IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 3/4 | chr12 | 113199399 | |||||||
| chr12:113199399 | C | CATAAATA others(9): Show |
5 | a0001c0001t0001g0224 a0001c0001t0002g0066 a0001c0001t0002g0068 others(2): Show |
6 | HG02559.hp1 NA18947.hp2 NA18969.hp2 others(3): Show |
intron_variant | MODIFIER | c.963+1165_963+1180d others(18): Show |
IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 3/4 | chr12 | 113199399 | |||||||
| chr12:113199399 | C | CATAAATA others(13): Show |
1 | a0002c0002t0001g0204 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.963+1161_963+1180d others(22): Show |
IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 3/4 | chr12 | 113199399 | |||||||
| chr12:113199399 | CATAA | C | 6 | a0001c0001t0001g0088 a0001c0001t0001g0183 a0003c0004t0001g0151 others(3): Show |
6 | HG01891.hp1 HG02055.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.963+1177_963+1180d others(6): Show |
IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 3/4 | chr12 | 113199399 | |||||||
| chr12:113199475 | T | G | 5 | a0001c0003t0001g0017 a0001c0003t0001g0032 a0001c0003t0001g0174 others(2): Show |
8 | HG02280.hp2 HG02451.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.963+1105A>C | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 3/4 | chr12 | 113199475 | |||||||
| chr12:113199564 | C | T | 1 | a0001c0001t0001g0186 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.963+1016G>A | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 3/4 | chr12 | 113199564 | |||||||
| chr12:113199628 | T | C | 1 | a0001c0001t0001g0117 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.963+952A>G | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 3/4 | chr12 | 113199628 | |||||||
| chr12:113199638 | A | G | 64 | a0001c0001t0001g0132 a0001c0001t0001g0134 a0001c0001t0001g0183 others(61): Show |
88 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.963+942T>C | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 3/4 | chr12 | 113199638 | |||||||
| chr12:113199701 | G | T | 26 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(23): Show |
34 | HG00280.hp1 HG01168.hp1 HG02040.hp1 others(31): Show |
intron_variant | MODIFIER | c.963+879C>A | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 3/4 | chr12 | 113199701 | |||||||
| chr12:113199722 | G | GT | 17 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0045 others(14): Show |
21 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(18): Show |
intron_variant | MODIFIER | c.963+857dupA | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 3/4 | chr12 | 113199722 | |||||||
| chr12:113199722 | G | T | 2 | a0001c0001t0001g0186 a0001c0001t0001g0187 |
2 | HG02809.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.963+858C>A | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 3/4 | chr12 | 113199722 | |||||||
| chr12:113199779 | A | G | 63 | a0001c0001t0001g0132 a0001c0001t0001g0134 a0001c0001t0001g0224 others(60): Show |
87 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.963+801T>C | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 3/4 | chr12 | 113199779 | |||||||
| chr12:113200336 | G | A | 1 | a0001c0001t0001g0047 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.963+244C>T | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 3/4 | chr12 | 113200336 | |||||||
| chr12:113200413 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.963+167C>T | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 3/4 | chr12 | 113200413 | |||||||
| chr12:113200483 | G | C | 1 | a0002c0002t0003g0221 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.963+97C>G | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 3/4 | chr12 | 113200483 | |||||||
| chr12:113200500 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.963+80G>A | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 3/4 | chr12 | 113200500 | |||||||
| chr12:113200543 | G | A | 23 | a0001c0001t0001g0132 a0001c0001t0001g0134 a0002c0002t0001g0005 others(20): Show |
35 | HG00408.hp1 HG00438.hp2 HG02027.hp1 others(32): Show |
intron_variant | MODIFIER | c.963+37C>T | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 3/4 | chr12 | 113200543 | |||||||
| chr12:113200551 | C | A | 4 | a0001c0001t0001g0026 a0001c0001t0001g0073 a0001c0001t0001g0081 others(1): Show |
5 | HG02258.hp1 HG02280.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.963+29G>T | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 3/4 | chr12 | 113200551 | |||||||
| chr12:113200860 | C | T | 1 | a0001c0001t0001g0135 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.730-47G>A | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 2/4 | chr12 | 113200860 | |||||||
| chr12:113200877 | G | A | 1 | a0001c0001t0001g0080 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.730-64C>T | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 2/4 | chr12 | 113200877 | |||||||
| chr12:113200883 | A | G | 22 | a0001c0001t0002g0003 a0001c0001t0002g0066 a0001c0001t0002g0068 others(19): Show |
30 | HG00280.hp1 HG01168.hp1 HG02040.hp1 others(27): Show |
intron_variant | MODIFIER | c.730-70T>C | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 2/4 | chr12 | 113200883 | |||||||
| chr12:113200967 | C | T | 3 | a0001c0001t0001g0100 a0001c0001t0004g0036 a0001c0001t0004g0231 |
4 | HG00280.hp1 HG01168.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.730-154G>A | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 2/4 | chr12 | 113200967 | |||||||
| chr12:113201140 | C | CA | 9 | a0001c0001t0001g0134 a0001c0001t0001g0224 a0001c0001t0001g0225 others(6): Show |
9 | HG01891.hp1 HG02055.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.730-328dupT | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 2/4 | chr12 | 113201140 | |||||||
| chr12:113201151 | G | A | 58 | a0001c0001t0001g0132 a0001c0001t0001g0134 a0001c0001t0001g0183 others(55): Show |
79 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.730-338C>T | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 2/4 | chr12 | 113201151 | |||||||
| chr12:113201151 | G | C | 4 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(1): Show |
4 | HG02559.hp1 HG02717.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.730-338C>G | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 2/4 | chr12 | 113201151 | |||||||
| chr12:113201216 | G | C | 1 | a0001c0001t0001g0129 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.730-403C>G | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 2/4 | chr12 | 113201216 | |||||||
| chr12:113201402 | T | C | 2 | a0001c0001t0001g0106 a0001c0001t0001g0108 |
2 | NA18977.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.730-589A>G | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 2/4 | chr12 | 113201402 | |||||||
| chr12:113201413 | T | C | 1 | a0001c0001t0001g0183 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.730-600A>G | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 2/4 | chr12 | 113201413 | |||||||
| chr12:113201418 | C | T | 1 | a0001c0001t0001g0042 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.730-605G>A | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 2/4 | chr12 | 113201418 | |||||||
| chr12:113201449 | G | T | 1 | a0001c0001t0001g0171 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.730-636C>A | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 2/4 | chr12 | 113201449 | |||||||
| chr12:113201600 | G | A | 2 | a0001c0001t0001g0186 a0001c0001t0001g0187 |
2 | HG02809.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.730-787C>T | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 2/4 | chr12 | 113201600 | |||||||
| chr12:113201696 | A | G | 1 | a0001c0001t0001g0190 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.730-883T>C | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 2/4 | chr12 | 113201696 | |||||||
| chr12:113201779 | C | T | 3 | a0003c0004t0001g0151 a0003c0004t0001g0152 a0003c0004t0001g0153 |
3 | HG01891.hp1 HG02055.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.730-966G>A | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 2/4 | chr12 | 113201779 | |||||||
| chr12:113201880 | T | C | 21 | a0001c0001t0002g0003 a0001c0001t0002g0066 a0001c0001t0002g0068 others(18): Show |
28 | HG02040.hp1 HG02040.hp2 HG02080.hp1 others(25): Show |
intron_variant | MODIFIER | c.730-1067A>G | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 2/4 | chr12 | 113201880 | |||||||
| chr12:113201884 | C | T | 1 | a0001c0001t0001g0080 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.730-1071G>A | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 2/4 | chr12 | 113201884 | |||||||
| chr12:113202000 | G | C | 59 | a0001c0001t0001g0171 a0001c0001t0001g0183 a0001c0001t0001g0224 others(56): Show |
83 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.730-1187C>G | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 2/4 | chr12 | 113202000 | |||||||
| chr12:113202013 | C | G | 26 | a0001c0001t0001g0171 a0002c0002t0001g0005 a0002c0002t0001g0035 others(23): Show |
39 | HG00408.hp1 HG00438.hp2 HG02027.hp1 others(36): Show |
intron_variant | MODIFIER | c.730-1200G>C | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 2/4 | chr12 | 113202013 | |||||||
| chr12:113202027 | A | C | 1 | a0001c0001t0001g0119 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.730-1214T>G | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 2/4 | chr12 | 113202027 | |||||||
| chr12:113202288 | T | TATGTTAT others(16): Show |
1 | a0002c0002t0001g0203 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.730-1498_730-1476d others(25): Show |
IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 2/4 | chr12 | 113202288 | |||||||
| chr12:113202417 | C | T | 25 | a0001c0001t0001g0034 a0001c0001t0001g0150 a0001c0001t0001g0183 others(22): Show |
29 | HG00140.hp1 HG00323.hp1 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.730-1604G>A | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 2/4 | chr12 | 113202417 | |||||||
| chr12:113202493 | C | G | 6 | a0001c0001t0001g0096 a0001c0001t0001g0110 a0001c0001t0001g0111 others(3): Show |
6 | HG01943.hp2 HG02572.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.730-1680G>C | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 2/4 | chr12 | 113202493 | |||||||
| chr12:113202496 | G | A | 1 | a0001c0001t0001g0107 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.730-1683C>T | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 2/4 | chr12 | 113202496 | |||||||
| chr12:113202542 | G | A | 24 | a0001c0001t0002g0003 a0001c0001t0002g0066 a0001c0001t0002g0068 others(21): Show |
32 | HG00280.hp1 HG01168.hp1 HG02040.hp1 others(29): Show |
intron_variant | MODIFIER | c.730-1729C>T | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 2/4 | chr12 | 113202542 | |||||||
| chr12:113202618 | T | C | 2 | a0003c0004t0001g0152 a0003c0004t0001g0153 |
2 | HG01891.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.730-1805A>G | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 2/4 | chr12 | 113202618 | |||||||
| chr12:113202824 | C | T | 1 | a0001c0001t0001g0054 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.730-2011G>A | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 2/4 | chr12 | 113202824 | |||||||
| chr12:113202828 | G | A | 22 | a0001c0001t0002g0003 a0001c0001t0002g0066 a0001c0001t0002g0068 others(19): Show |
30 | HG00280.hp1 HG01168.hp1 HG02040.hp1 others(27): Show |
intron_variant | MODIFIER | c.730-2015C>T | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 2/4 | chr12 | 113202828 | |||||||
| chr12:113202923 | C | G | 22 | a0001c0001t0002g0003 a0001c0001t0002g0066 a0001c0001t0002g0068 others(19): Show |
30 | HG00280.hp1 HG01168.hp1 HG02040.hp1 others(27): Show |
intron_variant | MODIFIER | c.730-2110G>C | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 2/4 | chr12 | 113202923 | |||||||
| chr12:113203101 | C | G | 2 | a0001c0001t0001g0188 a0001c0001t0001g0194 |
2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.730-2288G>C | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 2/4 | chr12 | 113203101 | |||||||
| chr12:113203122 | C | T | 4 | a0003c0004t0001g0151 a0003c0004t0001g0152 a0003c0004t0001g0153 others(1): Show |
4 | HG01891.hp1 HG02055.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.730-2309G>A | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 2/4 | chr12 | 113203122 | |||||||
| chr12:113203141 | T | C | 2 | a0003c0004t0001g0152 a0003c0004t0001g0153 |
2 | HG01891.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.730-2328A>G | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 2/4 | chr12 | 113203141 | |||||||
| chr12:113203260 | A | C | 2 | a0001c0001t0001g0084 a0001c0001t0001g0087 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.730-2447T>G | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 2/4 | chr12 | 113203260 | |||||||
| chr12:113203304 | C | T | 4 | a0003c0004t0001g0151 a0003c0004t0001g0152 a0003c0004t0001g0153 others(1): Show |
4 | HG01891.hp1 HG02055.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.730-2491G>A | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 2/4 | chr12 | 113203304 | |||||||
| chr12:113203379 | T | C | 2 | a0001c0001t0002g0163 a0001c0001t0002g0164 |
2 | HG02083.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.730-2566A>G | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 2/4 | chr12 | 113203379 | |||||||
| chr12:113203428 | G | A | 3 | a0001c0001t0001g0150 a0001c0001t0001g0185 a0001c0001t0001g0189 |
3 | HG03471.hp1 HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.730-2615C>T | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 2/4 | chr12 | 113203428 | |||||||
| chr12:113203468 | C | T | 1 | a0001c0001t0002g0157 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.730-2655G>A | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 2/4 | chr12 | 113203468 | |||||||
| chr12:113203515 | G | A | 6 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0053 others(3): Show |
8 | HG00099.hp2 HG00639.hp2 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.730-2702C>T | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 2/4 | chr12 | 113203515 | |||||||
| chr12:113203529 | A | G | 1 | a0001c0001t0001g0063 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.730-2716T>C | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 2/4 | chr12 | 113203529 | |||||||
| chr12:113203599 | C | T | 1 | a0001c0001t0006g0037 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.730-2786G>A | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 2/4 | chr12 | 113203599 | |||||||
| chr12:113203644 | T | G | 1 | a0001c0001t0001g0083 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.730-2831A>C | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 2/4 | chr12 | 113203644 | |||||||
| chr12:113203701 | C | A | 1 | a0001c0001t0001g0145 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.730-2888G>T | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 2/4 | chr12 | 113203701 | |||||||
| chr12:113203742 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.730-2929G>A | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 2/4 | chr12 | 113203742 | |||||||
| chr12:113203777 | A | AT | 59 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0011 others(56): Show |
75 | HG00140.hp1 HG00323.hp1 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.730-2965dupA | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 2/4 | chr12 | 113203777 | |||||||
| chr12:113203777 | A | ATT | 18 | a0001c0001t0001g0033 a0001c0001t0001g0054 a0001c0001t0001g0129 others(15): Show |
27 | HG01168.hp1 HG02040.hp1 HG02040.hp2 others(24): Show |
intron_variant | MODIFIER | c.730-2966_730-2965d others(4): Show |
IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 2/4 | chr12 | 113203777 | |||||||
| chr12:113203777 | A | ATTT | 7 | a0001c0001t0002g0066 a0001c0001t0002g0155 a0001c0001t0002g0156 others(4): Show |
7 | HG00280.hp1 NA18943.hp2 NA18945.hp2 others(4): Show |
intron_variant | MODIFIER | c.730-2967_730-2965d others(5): Show |
IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 2/4 | chr12 | 113203777 | |||||||
| chr12:113203777 | AT | A | 9 | a0001c0001t0001g0083 a0001c0001t0001g0108 a0001c0001t0001g0183 others(6): Show |
9 | HG00423.hp2 HG00438.hp2 HG02071.hp2 others(6): Show |
intron_variant | MODIFIER | c.730-2965delA | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 2/4 | chr12 | 113203777 | |||||||
| chr12:113203777 | ATT | A | 27 | a0001c0003t0001g0017 a0001c0003t0001g0032 a0001c0003t0001g0174 others(24): Show |
43 | HG00408.hp1 HG02027.hp1 HG02027.hp2 others(40): Show |
intron_variant | MODIFIER | c.730-2966_730-2965d others(4): Show |
IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 2/4 | chr12 | 113203777 | |||||||
| chr12:113203803 | G | T | 1 | a0001c0001t0001g0129 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.730-2990C>A | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 2/4 | chr12 | 113203803 | |||||||
| chr12:113203820 | C | T | 1 | a0002c0002t0003g0214 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.730-3007G>A | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 2/4 | chr12 | 113203820 | |||||||
| chr12:113203852 | C | A | 1 | a0001c0001t0001g0183 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.730-3039G>T | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 2/4 | chr12 | 113203852 | |||||||
| chr12:113204033 | G | A | 1 | a0001c0001t0001g0028 | 2 | NA18962.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.730-3220C>T | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 2/4 | chr12 | 113204033 | |||||||
| chr12:113204304 | T | A | 5 | a0001c0003t0001g0017 a0001c0003t0001g0032 a0001c0003t0001g0174 others(2): Show |
8 | HG02280.hp2 HG02451.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.729+3134A>T | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 2/4 | chr12 | 113204304 | |||||||
| chr12:113204391 | CT | C | 22 | a0001c0001t0002g0003 a0001c0001t0002g0066 a0001c0001t0002g0068 others(19): Show |
30 | HG00280.hp1 HG01168.hp1 HG02040.hp1 others(27): Show |
intron_variant | MODIFIER | c.729+3046delA | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 2/4 | chr12 | 113204391 | |||||||
| chr12:113204604 | G | A | 6 | a0001c0001t0001g0096 a0001c0001t0001g0110 a0001c0001t0001g0111 others(3): Show |
6 | HG01943.hp2 HG02572.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.729+2834C>T | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 2/4 | chr12 | 113204604 | |||||||
| chr12:113204656 | C | T | 27 | a0002c0002t0001g0005 a0002c0002t0001g0035 a0002c0002t0001g0184 others(24): Show |
40 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.729+2782G>A | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 2/4 | chr12 | 113204656 | |||||||
| chr12:113204756 | T | C | 1 | a0001c0001t0001g0048 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.729+2682A>G | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 2/4 | chr12 | 113204756 | |||||||
| chr12:113204857 | A | G | 1 | a0001c0001t0001g0049 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.729+2581T>C | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 2/4 | chr12 | 113204857 | |||||||
| chr12:113204861 | G | A | 1 | a0001c0001t0001g0199 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.729+2577C>T | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 2/4 | chr12 | 113204861 | |||||||
| chr12:113204925 | C | CA | 24 | a0001c0001t0001g0139 a0001c0001t0001g0227 a0001c0001t0002g0003 others(21): Show |
32 | HG00280.hp1 HG01168.hp1 HG02040.hp1 others(29): Show |
intron_variant | MODIFIER | c.729+2512dupT | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 2/4 | chr12 | 113204925 | |||||||
| chr12:113204937 | AAT | A | 26 | a0002c0002t0001g0005 a0002c0002t0001g0035 a0002c0002t0001g0184 others(23): Show |
39 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.729+2499_729+2500d others(4): Show |
IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 2/4 | chr12 | 113204937 | |||||||
| chr12:113204944 | C | T | 59 | a0001c0001t0001g0183 a0001c0001t0001g0224 a0001c0001t0001g0225 others(56): Show |
83 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.729+2494G>A | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 2/4 | chr12 | 113204944 | |||||||
| chr12:113205222 | AT | A | 22 | a0002c0002t0001g0005 a0002c0002t0001g0206 a0002c0002t0001g0208 others(19): Show |
34 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(31): Show |
intron_variant | MODIFIER | c.729+2215delA | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 2/4 | chr12 | 113205222 | |||||||
| chr12:113205230 | T | A | 22 | a0001c0001t0002g0003 a0001c0001t0002g0066 a0001c0001t0002g0068 others(19): Show |
30 | HG00280.hp1 HG01168.hp1 HG02040.hp1 others(27): Show |
intron_variant | MODIFIER | c.729+2208A>T | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 2/4 | chr12 | 113205230 | |||||||
| chr12:113205231 | T | A | 56 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0023 others(53): Show |
83 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.729+2207A>T | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 2/4 | chr12 | 113205231 | |||||||
| chr12:113205232 | A | T | 11 | a0001c0001t0001g0006 a0001c0001t0001g0022 a0001c0001t0001g0062 others(8): Show |
17 | HG00099.hp1 HG01167.hp2 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.729+2206T>A | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 2/4 | chr12 | 113205232 | |||||||
| chr12:113205233 | A | T | 4 | a0002c0002t0001g0035 a0002c0002t0001g0184 a0002c0002t0001g0204 others(1): Show |
5 | NA18960.hp2 NA18968.hp1 NA19043.hp2 others(2): Show |
intron_variant | MODIFIER | c.729+2205T>A | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 2/4 | chr12 | 113205233 | |||||||
| chr12:113205303 | C | A | 1 | a0001c0001t0002g0165 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.729+2135G>T | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 2/4 | chr12 | 113205303 | |||||||
| chr12:113205304 | G | A | 1 | a0001c0001t0001g0200 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.729+2134C>T | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 2/4 | chr12 | 113205304 | |||||||
| chr12:113205472 | G | A | 1 | a0001c0001t0001g0061 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.729+1966C>T | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 2/4 | chr12 | 113205472 | |||||||
| chr12:113205476 | T | C | 1 | a0002c0002t0001g0203 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.729+1962A>G | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 2/4 | chr12 | 113205476 | |||||||
| chr12:113205556 | C | T | 1 | a0001c0001t0001g0060 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.729+1882G>A | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 2/4 | chr12 | 113205556 | |||||||
| chr12:113205627 | T | C | 62 | a0001c0001t0001g0183 a0001c0001t0001g0224 a0001c0001t0001g0225 others(59): Show |
86 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.729+1811A>G | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 2/4 | chr12 | 113205627 | |||||||
| chr12:113205631 | A | T | 63 | a0001c0001t0001g0183 a0001c0001t0001g0224 a0001c0001t0001g0225 others(60): Show |
87 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.729+1807T>A | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 2/4 | chr12 | 113205631 | |||||||
| chr12:113205717 | G | A | 5 | a0001c0001t0001g0133 a0001c0001t0001g0137 a0001c0001t0001g0139 others(2): Show |
5 | HG02132.hp1 NA18981.hp1 NA18986.hp2 others(2): Show |
intron_variant | MODIFIER | c.729+1721C>T | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 2/4 | chr12 | 113205717 | |||||||
| chr12:113205746 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.729+1692C>T | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 2/4 | chr12 | 113205746 | |||||||
| chr12:113205758 | G | A | 2 | a0001c0001t0001g0185 a0001c0001t0001g0189 |
2 | HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.729+1680C>T | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 2/4 | chr12 | 113205758 | |||||||
| chr12:113205764 | C | T | 5 | a0001c0003t0001g0017 a0001c0003t0001g0032 a0001c0003t0001g0174 others(2): Show |
8 | HG02280.hp2 HG02451.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.729+1674G>A | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 2/4 | chr12 | 113205764 | |||||||
| chr12:113205902 | C | CA | 13 | a0001c0001t0001g0020 a0001c0001t0001g0050 a0001c0001t0001g0051 others(10): Show |
14 | HG00140.hp2 HG00735.hp1 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.729+1535dupT | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 2/4 | chr12 | 113205902 | |||||||
| chr12:113205902 | CA | C | 37 | a0001c0001t0001g0041 a0001c0001t0001g0074 a0001c0001t0001g0080 others(34): Show |
50 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.729+1535delT | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 2/4 | chr12 | 113205902 | |||||||
| chr12:113205902 | CAA | C | 31 | a0001c0001t0001g0183 a0001c0001t0002g0003 a0001c0001t0002g0066 others(28): Show |
42 | HG00280.hp1 HG01168.hp1 HG01891.hp1 others(39): Show |
intron_variant | MODIFIER | c.729+1534_729+1535d others(4): Show |
IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 2/4 | chr12 | 113205902 | |||||||
| chr12:113205931 | A | G | 1 | a0001c0001t0001g0229 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.729+1507T>C | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 2/4 | chr12 | 113205931 | |||||||
| chr12:113206060 | C | CA | 33 | a0001c0001t0001g0009 a0001c0001t0001g0033 a0001c0001t0001g0034 others(30): Show |
41 | HG00140.hp1 HG00323.hp1 HG01069.hp2 others(38): Show |
intron_variant | MODIFIER | c.729+1377dupT | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 2/4 | chr12 | 113206060 | |||||||
| chr12:113206073 | A | G | 27 | a0002c0002t0001g0005 a0002c0002t0001g0035 a0002c0002t0001g0184 others(24): Show |
40 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.729+1365T>C | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 2/4 | chr12 | 113206073 | |||||||
| chr12:113206144 | T | C | 1 | a0001c0001t0001g0118 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.729+1294A>G | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 2/4 | chr12 | 113206144 | |||||||
| chr12:113206214 | G | A | 1 | a0001c0001t0001g0052 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.729+1224C>T | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 2/4 | chr12 | 113206214 | |||||||
| chr12:113206218 | C | CA | 22 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0033 others(19): Show |
33 | HG00621.hp2 HG01255.hp1 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.729+1219dupT | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 2/4 | chr12 | 113206218 | |||||||
| chr12:113206218 | CA | C | 50 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0074 others(47): Show |
73 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.729+1219delT | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 2/4 | chr12 | 113206218 | |||||||
| chr12:113206233 | A | G | 1 | a0001c0001t0001g0062 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.729+1205T>C | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 2/4 | chr12 | 113206233 | |||||||
| chr12:113206406 | T | C | 53 | a0001c0001t0002g0003 a0001c0001t0002g0066 a0001c0001t0002g0068 others(50): Show |
74 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.729+1032A>G | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 2/4 | chr12 | 113206406 | |||||||
| chr12:113206490 | A | G | 4 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(1): Show |
4 | HG02559.hp1 HG02717.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.729+948T>C | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 2/4 | chr12 | 113206490 | |||||||
| chr12:113206516 | G | A | 1 | a0001c0001t0001g0183 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.729+922C>T | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 2/4 | chr12 | 113206516 | |||||||
| chr12:113206522 | G | A | 2 | a0001c0001t0004g0036 a0001c0001t0004g0231 |
3 | HG00280.hp1 HG01168.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.729+916C>T | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 2/4 | chr12 | 113206522 | |||||||
| chr12:113206541 | C | T | 1 | a0001c0001t0001g0053 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.729+897G>A | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 2/4 | chr12 | 113206541 | |||||||
| chr12:113206660 | C | T | 2 | a0001c0001t0001g0185 a0001c0001t0001g0189 |
2 | HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.729+778G>A | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 2/4 | chr12 | 113206660 | |||||||
| chr12:113206688 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.729+750C>T | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 2/4 | chr12 | 113206688 | |||||||
| chr12:113206754 | T | TA | 30 | a0001c0001t0001g0150 a0001c0001t0001g0185 a0001c0001t0001g0186 others(27): Show |
37 | HG00423.hp2 HG01891.hp1 HG02040.hp1 others(34): Show |
intron_variant | MODIFIER | c.729+683dupT | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 2/4 | chr12 | 113206754 | |||||||
| chr12:113207129 | C | T | 1 | a0002c0002t0001g0213 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.729+309G>A | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 2/4 | chr12 | 113207129 | |||||||
| chr12:113207263 | G | T | 1 | a0001c0001t0001g0093 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.729+175C>A | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 2/4 | chr12 | 113207263 | |||||||
| chr12:113207426 | A | G | 6 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0069 others(3): Show |
10 | HG01081.hp1 HG01255.hp2 HG01256.hp2 others(7): Show |
intron_variant | MODIFIER | c.729+12T>C | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 2/4 | chr12 | 113207426 | |||||||
| chr12:113208410 | T | G | 4 | a0003c0004t0001g0151 a0003c0004t0001g0152 a0003c0004t0001g0153 others(1): Show |
4 | HG01891.hp1 HG02055.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.-93-151A>C | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113208410 | |||||||
| chr12:113208418 | G | A | 1 | a0001c0001t0001g0197 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-93-159C>T | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113208418 | |||||||
| chr12:113208466 | G | A | 1 | a0001c0001t0001g0090 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-93-207C>T | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113208466 | |||||||
| chr12:113208505 | G | C | 29 | a0001c0001t0001g0183 a0001c0001t0002g0003 a0001c0001t0002g0066 others(26): Show |
40 | HG00280.hp1 HG01168.hp1 HG02040.hp1 others(37): Show |
intron_variant | MODIFIER | c.-93-246C>G | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113208505 | |||||||
| chr12:113208751 | C | T | 1 | a0001c0001t0006g0037 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-93-492G>A | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113208751 | |||||||
| chr12:113208922 | T | G | 4 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0071 others(1): Show |
6 | HG00544.hp1 NA18953.hp2 NA18992.hp2 others(3): Show |
intron_variant | MODIFIER | c.-93-663A>C | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113208922 | |||||||
| chr12:113208958 | G | C | 1 | a0001c0001t0001g0077 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-93-699C>G | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113208958 | |||||||
| chr12:113209010 | C | T | 2 | a0001c0001t0001g0006 a0001c0001t0001g0079 |
7 | HG01167.hp2 HG02109.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-93-751G>A | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113209010 | |||||||
| chr12:113209066 | G | A | 22 | a0002c0002t0001g0005 a0002c0002t0001g0206 a0002c0002t0001g0208 others(19): Show |
34 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(31): Show |
intron_variant | MODIFIER | c.-93-807C>T | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113209066 | |||||||
| chr12:113209100 | C | T | 58 | a0001c0001t0001g0183 a0001c0001t0001g0224 a0001c0001t0001g0225 others(55): Show |
79 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.-93-841G>A | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113209100 | |||||||
| chr12:113209152 | A | AAAATCCT others(11): Show |
1 | a0001c0001t0001g0183 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-93-894_-93-893ins others(18): Show |
IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113209152 | |||||||
| chr12:113209152 | A | AAACTCCT others(11): Show |
70 | a0001c0001t0001g0150 a0001c0001t0001g0185 a0001c0001t0001g0186 others(67): Show |
94 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.-93-894_-93-893ins others(18): Show |
IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113209152 | |||||||
| chr12:113209348 | G | A | 1 | a0001c0001t0001g0183 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-93-1089C>T | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113209348 | |||||||
| chr12:113209413 | T | C | 1 | a0005c0007t0001g0091 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-93-1154A>G | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113209413 | |||||||
| chr12:113209470 | C | A | 5 | a0001c0003t0001g0017 a0001c0003t0001g0032 a0001c0003t0001g0174 others(2): Show |
8 | HG02280.hp2 HG02451.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.-93-1211G>T | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113209470 | |||||||
| chr12:113209510 | G | C | 1 | a0002c0002t0001g0230 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.-93-1251C>G | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113209510 | |||||||
| chr12:113209532 | T | C | 91 | a0001c0001t0001g0009 a0001c0001t0001g0033 a0001c0001t0001g0034 others(88): Show |
121 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.-93-1273A>G | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113209532 | |||||||
| chr12:113209715 | T | C | 1 | a0001c0001t0001g0115 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.-93-1456A>G | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113209715 | |||||||
| chr12:113209759 | C | T | 5 | a0001c0003t0001g0017 a0001c0003t0001g0032 a0001c0003t0001g0174 others(2): Show |
8 | HG02280.hp2 HG02451.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.-93-1500G>A | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113209759 | |||||||
| chr12:113209946 | C | T | 5 | a0001c0003t0001g0017 a0001c0003t0001g0032 a0001c0003t0001g0174 others(2): Show |
8 | HG02280.hp2 HG02451.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.-93-1687G>A | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113209946 | |||||||
| chr12:113209996 | C | T | 1 | a0001c0001t0001g0080 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-93-1737G>A | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113209996 | |||||||
| chr12:113210105 | C | T | 5 | a0001c0003t0001g0017 a0001c0003t0001g0032 a0001c0003t0001g0174 others(2): Show |
8 | HG02280.hp2 HG02451.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.-93-1846G>A | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113210105 | |||||||
| chr12:113210166 | T | C | 1 | a0001c0001t0001g0129 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.-93-1907A>G | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113210166 | |||||||
| chr12:113210278 | G | T | 4 | a0003c0004t0001g0151 a0003c0004t0001g0152 a0003c0004t0001g0153 others(1): Show |
4 | HG01891.hp1 HG02055.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.-93-2019C>A | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113210278 | |||||||
| chr12:113210493 | G | A | 26 | a0001c0001t0002g0003 a0001c0001t0002g0066 a0001c0001t0002g0068 others(23): Show |
34 | HG00280.hp1 HG01168.hp1 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.-93-2234C>T | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113210493 | |||||||
| chr12:113210604 | G | T | 27 | a0002c0002t0001g0005 a0002c0002t0001g0035 a0002c0002t0001g0184 others(24): Show |
40 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.-93-2345C>A | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113210604 | |||||||
| chr12:113210611 | AG | A | 18 | a0001c0001t0002g0003 a0001c0001t0002g0066 a0001c0001t0002g0068 others(15): Show |
25 | HG02040.hp1 HG02040.hp2 HG02080.hp1 others(22): Show |
intron_variant | MODIFIER | c.-93-2353delC | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113210611 | |||||||
| chr12:113210612 | G | A | 2 | a0001c0001t0002g0161 a0001c0001t0002g0168 |
2 | HG03831.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.-93-2353C>T | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113210612 | |||||||
| chr12:113210612 | GA | G | 39 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0009 others(36): Show |
47 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(44): Show |
intron_variant | MODIFIER | c.-93-2354delT | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113210612 | |||||||
| chr12:113210625 | A | T | 1 | a0002c0002t0001g0184 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-93-2366T>A | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113210625 | |||||||
| chr12:113210713 | C | A | 1 | a0001c0001t0001g0124 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-93-2454G>T | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113210713 | |||||||
| chr12:113210770 | C | T | 1 | a0001c0001t0001g0198 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-93-2511G>A | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113210770 | |||||||
| chr12:113210937 | A | G | 3 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 |
3 | HG02717.hp1 HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-93-2678T>C | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113210937 | |||||||
| chr12:113211046 | G | A | 26 | a0002c0002t0001g0005 a0002c0002t0001g0035 a0002c0002t0001g0184 others(23): Show |
39 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.-93-2787C>T | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113211046 | |||||||
| chr12:113211167 | G | A | 26 | a0001c0001t0002g0003 a0001c0001t0002g0066 a0001c0001t0002g0068 others(23): Show |
34 | HG00280.hp1 HG01168.hp1 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.-93-2908C>T | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113211167 | |||||||
| chr12:113211239 | T | G | 36 | a0001c0001t0001g0183 a0001c0001t0001g0224 a0001c0001t0001g0225 others(33): Show |
47 | HG00280.hp1 HG01168.hp1 HG01891.hp1 others(44): Show |
intron_variant | MODIFIER | c.-93-2980A>C | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113211239 | |||||||
| chr12:113211375 | G | T | 4 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(1): Show |
4 | HG02559.hp1 HG02717.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-93-3116C>A | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113211375 | |||||||
| chr12:113211506 | G | A | 8 | a0001c0001t0001g0029 a0001c0001t0001g0092 a0001c0001t0001g0116 others(5): Show |
9 | HG01081.hp2 HG01109.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.-93-3247C>T | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113211506 | |||||||
| chr12:113211588 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-93-3329G>A | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113211588 | |||||||
| chr12:113211638 | C | CA | 6 | a0001c0001t0001g0129 a0001c0003t0001g0017 a0001c0003t0001g0032 others(3): Show |
9 | HG02280.hp2 HG02451.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.-93-3380dupT | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113211638 | |||||||
| chr12:113211945 | G | T | 4 | a0003c0004t0001g0151 a0003c0004t0001g0152 a0003c0004t0001g0153 others(1): Show |
4 | HG01891.hp1 HG02055.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.-93-3686C>A | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113211945 | |||||||
| chr12:113212014 | A | G | 63 | a0001c0001t0001g0183 a0001c0001t0001g0224 a0001c0001t0001g0225 others(60): Show |
87 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.-93-3755T>C | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113212014 | |||||||
| chr12:113212043 | T | C | 3 | a0001c0001t0001g0030 a0001c0001t0001g0119 a0001c0001t0001g0127 |
4 | HG02523.hp2 NA18961.hp2 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.-93-3784A>G | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113212043 | |||||||
| chr12:113212069 | C | CT | 49 | a0001c0001t0001g0079 a0001c0001t0001g0129 a0001c0001t0002g0003 others(46): Show |
70 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.-93-3811dupA | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113212069 | |||||||
| chr12:113212215 | G | A | 31 | a0001c0001t0001g0183 a0001c0001t0001g0224 a0001c0001t0001g0225 others(28): Show |
39 | HG00280.hp1 HG01168.hp1 HG01891.hp1 others(36): Show |
intron_variant | MODIFIER | c.-93-3956C>T | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113212215 | |||||||
| chr12:113212391 | A | G | 5 | a0001c0003t0001g0017 a0001c0003t0001g0032 a0001c0003t0001g0174 others(2): Show |
8 | HG02280.hp2 HG02451.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.-93-4132T>C | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113212391 | |||||||
| chr12:113212440 | G | A | 1 | a0002c0002t0003g0215 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-93-4181C>T | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113212440 | |||||||
| chr12:113212562 | C | T | 5 | a0001c0003t0001g0017 a0001c0003t0001g0032 a0001c0003t0001g0174 others(2): Show |
8 | HG02280.hp2 HG02451.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.-93-4303G>A | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113212562 | |||||||
| chr12:113212610 | C | T | 5 | a0001c0001t0002g0156 a0001c0001t0002g0157 a0001c0001t0002g0158 others(2): Show |
5 | HG02040.hp2 NA18943.hp2 NA18946.hp1 others(2): Show |
intron_variant | MODIFIER | c.-93-4351G>A | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113212610 | |||||||
| chr12:113212709 | C | T | 1 | a0002c0002t0001g0203 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-93-4450G>A | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113212709 | |||||||
| chr12:113212819 | C | T | 1 | a0002c0002t0001g0206 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-93-4560G>A | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113212819 | |||||||
| chr12:113213016 | C | A | 31 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(28): Show |
44 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(41): Show |
intron_variant | MODIFIER | c.-93-4757G>T | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113213016 | |||||||
| chr12:113213109 | G | A | 4 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(1): Show |
4 | HG02559.hp1 HG02717.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-93-4850C>T | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113213109 | |||||||
| chr12:113213176 | T | TA | 23 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0031 others(20): Show |
28 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(25): Show |
intron_variant | MODIFIER | c.-93-4918dupT | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113213176 | |||||||
| chr12:113213176 | T | TAAAAAAA others(7): Show |
1 | a0001c0001t0001g0129 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.-93-4931_-93-4918d others(16): Show |
IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113213176 | |||||||
| chr12:113213176 | TA | T | 59 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0010 others(56): Show |
79 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.-93-4918delT | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113213176 | |||||||
| chr12:113213176 | TAA | T | 24 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(21): Show |
37 | HG00408.hp1 HG00423.hp2 HG01891.hp1 others(34): Show |
intron_variant | MODIFIER | c.-93-4919_-93-4918d others(4): Show |
IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113213176 | |||||||
| chr12:113213183 | A | C | 1 | a0001c0006t0001g0192 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-93-4924T>G | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113213183 | |||||||
| chr12:113213184 | A | C | 1 | a0001c0001t0001g0178 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-93-4925T>G | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113213184 | |||||||
| chr12:113213189 | A | AC | 2 | a0001c0001t0001g0034 a0001c0001t0001g0191 |
3 | HG00140.hp1 HG00323.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.-93-4931_-93-4930i others(3): Show |
IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113213189 | |||||||
| chr12:113213190 | A | C | 17 | a0001c0001t0001g0009 a0001c0001t0001g0033 a0001c0001t0001g0171 others(14): Show |
22 | HG01069.hp2 HG01071.hp2 HG01943.hp1 others(19): Show |
intron_variant | MODIFIER | c.-93-4931T>G | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113213190 | |||||||
| chr12:113213195 | A | C | 1 | a0001c0001t0001g0191 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-93-4936T>G | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113213195 | |||||||
| chr12:113213198 | A | AC | 3 | a0001c0001t0002g0168 a0001c0001t0002g0169 a0001c0001t0002g0170 |
3 | NA19002.hp2 NA19066.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.-93-4940_-93-4939i others(3): Show |
IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113213198 | |||||||
| chr12:113213198 | A | C | 27 | a0001c0001t0001g0183 a0001c0001t0002g0003 a0001c0001t0002g0066 others(24): Show |
37 | HG00280.hp1 HG01168.hp1 HG01891.hp1 others(34): Show |
intron_variant | MODIFIER | c.-93-4939T>G | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113213198 | |||||||
| chr12:113213528 | G | A | 5 | a0001c0003t0001g0017 a0001c0003t0001g0032 a0001c0003t0001g0174 others(2): Show |
8 | HG02280.hp2 HG02451.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.-93-5269C>T | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113213528 | |||||||
| chr12:113213622 | C | T | 3 | a0002c0002t0001g0035 a0002c0002t0001g0204 a0002c0002t0001g0205 |
4 | NA18960.hp2 NA18968.hp1 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.-93-5363G>A | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113213622 | |||||||
| chr12:113213685 | G | A | 5 | a0001c0001t0001g0150 a0001c0001t0001g0185 a0001c0001t0001g0186 others(2): Show |
5 | HG02809.hp2 HG02886.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.-93-5426C>T | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113213685 | |||||||
| chr12:113213775 | A | C | 1 | a0001c0001t0001g0190 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-93-5516T>G | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113213775 | |||||||
| chr12:113213842 | G | C | 26 | a0001c0001t0002g0003 a0001c0001t0002g0066 a0001c0001t0002g0068 others(23): Show |
34 | HG00280.hp1 HG01168.hp1 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.-93-5583C>G | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113213842 | |||||||
| chr12:113213850 | G | A | 1 | a0002c0002t0001g0203 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-93-5591C>T | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113213850 | |||||||
| chr12:113213893 | G | C | 13 | a0002c0002t0001g0005 a0002c0002t0001g0206 a0002c0002t0001g0208 others(10): Show |
19 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(16): Show |
intron_variant | MODIFIER | c.-93-5634C>G | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113213893 | |||||||
| chr12:113213952 | C | A | 1 | a0001c0001t0001g0129 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.-93-5693G>T | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113213952 | |||||||
| chr12:113213986 | A | G | 1 | a0001c0001t0001g0078 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-93-5727T>C | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113213986 | |||||||
| chr12:113214301 | G | C | 1 | a0001c0001t0001g0128 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-93-6042C>G | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113214301 | |||||||
| chr12:113214436 | A | T | 1 | a0001c0001t0001g0078 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-93-6177T>A | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113214436 | |||||||
| chr12:113214507 | C | CA | 29 | a0001c0001t0001g0129 a0001c0001t0004g0036 a0001c0001t0004g0231 others(26): Show |
43 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(40): Show |
intron_variant | MODIFIER | c.-93-6249dupT | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113214507 | |||||||
| chr12:113214507 | C | CAA | 20 | a0001c0001t0001g0183 a0001c0001t0002g0003 a0001c0001t0002g0066 others(17): Show |
27 | HG02040.hp1 HG02040.hp2 HG02080.hp1 others(24): Show |
intron_variant | MODIFIER | c.-93-6250_-93-6249d others(4): Show |
IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113214507 | |||||||
| chr12:113214507 | CA | C | 9 | a0001c0001t0001g0025 a0001c0001t0001g0040 a0001c0001t0001g0132 others(6): Show |
10 | HG01069.hp2 HG02809.hp2 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.-93-6249delT | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113214507 | |||||||
| chr12:113214545 | A | G | 1 | a0002c0002t0001g0223 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-93-6286T>C | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113214545 | |||||||
| chr12:113214546 | G | A | 1 | a0002c0002t0001g0223 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-93-6287C>T | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113214546 | |||||||
| chr12:113214809 | T | C | 1 | a0001c0001t0001g0146 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-94+6188A>G | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113214809 | |||||||
| chr12:113214946 | G | T | 2 | a0001c0001t0001g0186 a0001c0001t0001g0187 |
2 | HG02809.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.-94+6051C>A | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113214946 | |||||||
| chr12:113215013 | C | T | 2 | a0002c0002t0001g0208 a0002c0002t0001g0209 |
2 | NA18979.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.-94+5984G>A | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113215013 | |||||||
| chr12:113215130 | G | A | 1 | a0001c0001t0001g0059 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-94+5867C>T | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113215130 | |||||||
| chr12:113215411 | C | T | 27 | a0002c0002t0001g0005 a0002c0002t0001g0035 a0002c0002t0001g0184 others(24): Show |
40 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.-94+5586G>A | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113215411 | |||||||
| chr12:113215855 | G | A | 1 | a0001c0001t0001g0224 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-94+5142C>T | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113215855 | |||||||
| chr12:113215860 | C | G | 1 | a0002c0002t0003g0207 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-94+5137G>C | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113215860 | |||||||
| chr12:113215862 | G | A | 1 | a0001c0001t0001g0065 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-94+5135C>T | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113215862 | |||||||
| chr12:113216202 | A | G | 1 | a0001c0001t0001g0185 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-94+4795T>C | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113216202 | |||||||
| chr12:113216206 | G | T | 8 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0069 others(5): Show |
12 | HG00558.hp2 HG01081.hp1 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.-94+4791C>A | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113216206 | |||||||
| chr12:113216336 | A | G | 1 | a0001c0001t0001g0073 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-94+4661T>C | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113216336 | |||||||
| chr12:113216558 | T | C | 1 | a0001c0001t0001g0202 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-94+4439A>G | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113216558 | |||||||
| chr12:113216764 | G | A | 1 | a0001c0001t0001g0224 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-94+4233C>T | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113216764 | |||||||
| chr12:113216786 | G | C | 3 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 |
3 | HG02717.hp1 HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-94+4211C>G | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113216786 | |||||||
| chr12:113216854 | G | A | 3 | a0002c0002t0001g0035 a0002c0002t0001g0204 a0002c0002t0001g0205 |
4 | NA18960.hp2 NA18968.hp1 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.-94+4143C>T | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113216854 | |||||||
| chr12:113217324 | AT | A | 28 | a0001c0001t0001g0060 a0001c0001t0001g0183 a0001c0001t0002g0003 others(25): Show |
36 | HG00280.hp1 HG01168.hp1 HG01891.hp1 others(33): Show |
intron_variant | MODIFIER | c.-94+3672delA | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113217324 | |||||||
| chr12:113217401 | G | T | 4 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(1): Show |
4 | HG02559.hp1 HG02717.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-94+3596C>A | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113217401 | |||||||
| chr12:113217418 | T | C | 4 | a0003c0004t0001g0151 a0003c0004t0001g0152 a0003c0004t0001g0153 others(1): Show |
4 | HG01891.hp1 HG02055.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.-94+3579A>G | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113217418 | |||||||
| chr12:113217619 | C | A | 3 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0148 |
3 | HG00609.hp2 HG02071.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.-94+3378G>T | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113217619 | |||||||
| chr12:113217621 | C | A | 27 | a0002c0002t0001g0005 a0002c0002t0001g0035 a0002c0002t0001g0184 others(24): Show |
40 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.-94+3376G>T | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113217621 | |||||||
| chr12:113217633 | G | C | 1 | a0001c0001t0001g0065 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-94+3364C>G | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113217633 | |||||||
| chr12:113217691 | T | C | 20 | a0001c0001t0002g0003 a0001c0001t0002g0066 a0001c0001t0002g0068 others(17): Show |
27 | HG02040.hp1 HG02040.hp2 HG02080.hp1 others(24): Show |
intron_variant | MODIFIER | c.-94+3306A>G | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113217691 | |||||||
| chr12:113217706 | G | A | 20 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0023 others(17): Show |
38 | HG00544.hp1 HG00673.hp2 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.-94+3291C>T | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113217706 | |||||||
| chr12:113217723 | G | C | 2 | a0001c0001t0004g0036 a0001c0001t0004g0231 |
3 | HG00280.hp1 HG01168.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-94+3274C>G | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113217723 | |||||||
| chr12:113217759 | C | T | 3 | a0001c0001t0001g0022 a0001c0001t0001g0062 a0001c0001t0001g0063 |
4 | HG00099.hp1 HG01358.hp2 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.-94+3238G>A | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113217759 | |||||||
| chr12:113217826 | C | A | 1 | a0001c0001t0001g0228 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-94+3171G>T | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113217826 | |||||||
| chr12:113217916 | C | T | 1 | a0001c0001t0001g0039 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-94+3081G>A | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113217916 | |||||||
| chr12:113218022 | T | C | 1 | a0001c0001t0001g0147 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-94+2975A>G | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113218022 | |||||||
| chr12:113218137 | C | CT | 29 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(26): Show |
42 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(39): Show |
intron_variant | MODIFIER | c.-94+2859dupA | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113218137 | |||||||
| chr12:113218137 | CT | C | 28 | a0001c0001t0001g0071 a0001c0001t0001g0183 a0001c0001t0002g0003 others(25): Show |
36 | HG00280.hp1 HG01168.hp1 HG01891.hp1 others(33): Show |
intron_variant | MODIFIER | c.-94+2859delA | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113218137 | |||||||
| chr12:113218173 | G | A | 1 | a0001c0001t0001g0148 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-94+2824C>T | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113218173 | |||||||
| chr12:113218190 | G | T | 1 | a0001c0001t0001g0072 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-94+2807C>A | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113218190 | |||||||
| chr12:113218239 | C | T | 1 | a0001c0001t0001g0013 | 3 | HG01891.hp2 HG02976.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-94+2758G>A | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113218239 | |||||||
| chr12:113218303 | A | AT | 8 | a0001c0001t0001g0009 a0001c0001t0001g0033 a0001c0001t0001g0171 others(5): Show |
13 | HG02055.hp2 HG02109.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.-94+2693dupA | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113218303 | |||||||
| chr12:113218303 | AT | A | 62 | a0001c0001t0001g0183 a0001c0001t0001g0224 a0001c0001t0001g0225 others(59): Show |
86 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.-94+2693delA | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113218303 | |||||||
| chr12:113218678 | C | G | 1 | a0001c0001t0001g0183 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-94+2319G>C | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113218678 | |||||||
| chr12:113218923 | T | G | 1 | a0002c0002t0001g0206 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-94+2074A>C | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113218923 | |||||||
| chr12:113218928 | T | A | 1 | a0002c0002t0001g0206 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-94+2069A>T | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113218928 | |||||||
| chr12:113218929 | T | G | 1 | a0002c0002t0001g0206 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-94+2068A>C | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113218929 | |||||||
| chr12:113218930 | G | A | 1 | a0002c0002t0001g0206 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-94+2067C>T | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113218930 | |||||||
| chr12:113218933 | A | G | 1 | a0002c0002t0001g0206 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-94+2064T>C | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113218933 | |||||||
| chr12:113218936 | A | G | 1 | a0002c0002t0001g0206 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-94+2061T>C | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113218936 | |||||||
| chr12:113218937 | A | G | 1 | a0002c0002t0001g0206 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-94+2060T>C | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113218937 | |||||||
| chr12:113218939 | A | C | 1 | a0002c0002t0001g0206 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-94+2058T>G | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113218939 | |||||||
| chr12:113218940 | T | A | 1 | a0002c0002t0001g0206 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-94+2057A>T | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113218940 | |||||||
| chr12:113218941 | T | G | 1 | a0002c0002t0001g0206 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-94+2056A>C | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113218941 | |||||||
| chr12:113218942 | T | G | 1 | a0002c0002t0001g0206 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-94+2055A>C | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113218942 | |||||||
| chr12:113218943 | A | G | 1 | a0002c0002t0001g0206 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-94+2054T>C | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113218943 | |||||||
| chr12:113218944 | T | G | 1 | a0002c0002t0001g0206 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-94+2053A>C | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113218944 | |||||||
| chr12:113218945 | A | G | 1 | a0002c0002t0001g0206 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-94+2052T>C | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113218945 | |||||||
| chr12:113218946 | T | G | 1 | a0002c0002t0001g0206 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-94+2051A>C | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113218946 | |||||||
| chr12:113218952 | T | C | 1 | a0002c0002t0001g0206 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-94+2045A>G | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113218952 | |||||||
| chr12:113218953 | C | A | 1 | a0002c0002t0001g0206 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-94+2044G>T | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113218953 | |||||||
| chr12:113218954 | T | C | 1 | a0002c0002t0001g0206 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-94+2043A>G | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113218954 | |||||||
| chr12:113218955 | T | C | 1 | a0002c0002t0001g0206 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-94+2042A>G | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113218955 | |||||||
| chr12:113218965 | T | C | 1 | a0002c0002t0001g0206 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-94+2032A>G | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113218965 | |||||||
| chr12:113218966 | T | C | 1 | a0002c0002t0001g0206 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-94+2031A>G | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113218966 | |||||||
| chr12:113218968 | T | A | 1 | a0002c0002t0001g0206 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-94+2029A>T | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113218968 | |||||||
| chr12:113218970 | T | G | 1 | a0002c0002t0001g0206 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-94+2027A>C | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113218970 | |||||||
| chr12:113218971 | T | C | 1 | a0002c0002t0001g0206 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-94+2026A>G | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113218971 | |||||||
| chr12:113218972 | T | C | 1 | a0002c0002t0001g0206 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-94+2025A>G | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113218972 | |||||||
| chr12:113218973 | T | C | 1 | a0002c0002t0001g0206 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-94+2024A>G | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113218973 | |||||||
| chr12:113218977 | T | G | 1 | a0002c0002t0001g0206 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-94+2020A>C | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113218977 | |||||||
| chr12:113218980 | G | A | 1 | a0002c0002t0001g0206 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-94+2017C>T | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113218980 | |||||||
| chr12:113218985 | G | A | 1 | a0002c0002t0001g0206 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-94+2012C>T | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113218985 | |||||||
| chr12:113218987 | T | G | 1 | a0002c0002t0001g0206 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-94+2010A>C | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113218987 | |||||||
| chr12:113218990 | C | G | 1 | a0002c0002t0001g0206 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-94+2007G>C | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113218990 | |||||||
| chr12:113218991 | T | A | 1 | a0002c0002t0001g0206 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-94+2006A>T | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113218991 | |||||||
| chr12:113218992 | T | A | 1 | a0002c0002t0001g0206 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-94+2005A>T | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113218992 | |||||||
| chr12:113218993 | C | A | 1 | a0002c0002t0001g0206 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-94+2004G>T | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113218993 | |||||||
| chr12:113219000 | G | T | 1 | a0002c0002t0001g0206 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-94+1997C>A | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113219000 | |||||||
| chr12:113219001 | T | C | 1 | a0002c0002t0001g0206 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-94+1996A>G | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113219001 | |||||||
| chr12:113219002 | G | C | 1 | a0002c0002t0001g0206 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-94+1995C>G | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113219002 | |||||||
| chr12:113219003 | G | A | 1 | a0002c0002t0001g0206 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-94+1994C>T | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113219003 | |||||||
| chr12:113219004 | A | C | 1 | a0002c0002t0001g0206 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-94+1993T>G | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113219004 | |||||||
| chr12:113219005 | A | T | 1 | a0002c0002t0001g0206 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-94+1992T>A | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113219005 | |||||||
| chr12:113219008 | G | A | 1 | a0002c0002t0001g0206 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-94+1989C>T | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113219008 | |||||||
| chr12:113219009 | C | T | 1 | a0002c0002t0001g0206 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-94+1988G>A | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113219009 | |||||||
| chr12:113219011 | A | T | 1 | a0002c0002t0001g0206 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-94+1986T>A | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113219011 | |||||||
| chr12:113219012 | G | A | 1 | a0002c0002t0001g0206 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-94+1985C>T | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113219012 | |||||||
| chr12:113219013 | G | T | 1 | a0002c0002t0001g0206 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-94+1984C>A | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113219013 | |||||||
| chr12:113219503 | G | T | 1 | a0001c0001t0001g0228 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-94+1494C>A | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113219503 | |||||||
| chr12:113219504 | C | G | 1 | a0001c0001t0001g0228 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-94+1493G>C | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113219504 | |||||||
| chr12:113219533 | T | C | 1 | a0001c0001t0001g0149 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-94+1464A>G | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113219533 | |||||||
| chr12:113219642 | T | C | 22 | a0002c0002t0001g0005 a0002c0002t0001g0206 a0002c0002t0001g0208 others(19): Show |
34 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(31): Show |
intron_variant | MODIFIER | c.-94+1355A>G | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113219642 | |||||||
| chr12:113219667 | T | G | 1 | a0001c0003t0001g0177 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-94+1330A>C | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113219667 | |||||||
| chr12:113219742 | G | A | 4 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(1): Show |
4 | HG02559.hp1 HG02717.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-94+1255C>T | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113219742 | |||||||
| chr12:113219759 | G | A | 7 | a0001c0001t0001g0009 a0001c0001t0001g0033 a0001c0001t0001g0178 others(4): Show |
12 | HG02055.hp2 HG02109.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.-94+1238C>T | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113219759 | |||||||
| chr12:113219775 | C | T | 20 | a0001c0001t0002g0003 a0001c0001t0002g0066 a0001c0001t0002g0068 others(17): Show |
27 | HG02040.hp1 HG02040.hp2 HG02080.hp1 others(24): Show |
intron_variant | MODIFIER | c.-94+1222G>A | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113219775 | |||||||
| chr12:113219793 | C | CTTAT | 39 | a0001c0001t0001g0009 a0001c0001t0001g0023 a0001c0001t0001g0024 others(36): Show |
56 | HG02027.hp1 HG02040.hp1 HG02040.hp2 others(53): Show |
intron_variant | MODIFIER | c.-94+1200_-94+1203d others(6): Show |
IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113219793 | |||||||
| chr12:113219793 | C | CTTATTTA others(5): Show |
3 | a0003c0004t0001g0152 a0003c0004t0001g0153 a0003c0004t0001g0154 |
3 | HG01891.hp1 HG02559.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-94+1192_-94+1203d others(14): Show |
IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113219793 | |||||||
| chr12:113219793 | C | CTTATTTA others(13): Show |
1 | a0003c0004t0001g0151 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-94+1184_-94+1203d others(22): Show |
IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113219793 | |||||||
| chr12:113219793 | C | T | 1 | a0001c0001t0001g0150 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-94+1204G>A | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113219793 | |||||||
| chr12:113219920 | C | G | 1 | a0001c0001t0001g0228 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-94+1077G>C | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113219920 | |||||||
| chr12:113219921 | G | C | 1 | a0001c0001t0001g0228 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-94+1076C>G | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113219921 | |||||||
| chr12:113220009 | T | C | 1 | a0001c0001t0001g0061 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-94+988A>G | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113220009 | |||||||
| chr12:113220056 | C | T | 1 | a0001c0001t0001g0070 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-94+941G>A | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113220056 | |||||||
| chr12:113220298 | C | T | 1 | a0001c0001t0001g0069 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-94+699G>A | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113220298 | |||||||
| chr12:113220319 | T | G | 93 | a0001c0001t0001g0009 a0001c0001t0001g0033 a0001c0001t0001g0034 others(90): Show |
123 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.-94+678A>C | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113220319 | |||||||
| chr12:113220410 | T | A | 1 | a0001c0001t0001g0228 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-94+587A>T | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113220410 | |||||||
| chr12:113220643 | GC | G | 3 | a0001c0001t0002g0066 a0001c0001t0002g0068 a0001c0001t0007g0067 |
3 | NA18947.hp2 NA18969.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.-94+353delG | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113220643 | |||||||
| chr12:113220678 | C | A | 1 | a0001c0001t0001g0229 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-94+319G>T | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113220678 | |||||||
| chr12:113220759 | T | A | 1 | a0002c0002t0001g0230 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.-94+238A>T | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113220759 | |||||||
| chr12:113220797 | G | T | 1 | a0001c0001t0001g0065 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-94+200C>A | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113220797 | |||||||
| chr12:113220893 | A | T | 1 | a0001c0001t0001g0038 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-94+104T>A | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113220893 | |||||||
| chr12:113220958 | C | G | 4 | a0001c0001t0001g0022 a0001c0001t0001g0062 a0001c0001t0001g0063 others(1): Show |
5 | HG00099.hp1 HG01358.hp2 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.-94+39G>C | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113220958 | |||||||
| chr12:113220961 | C | T | 29 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0019 others(26): Show |
36 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(33): Show |
intron_variant | MODIFIER | c.-94+36G>A | IQCD | ENSG00000166578.10 | transcript | ENST00000416617.3 | protein_coding | 1/4 | chr12 | 113220961 |