Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 51071 |
| ensemblid | ENSG00000023697.13 |
| hgncid | 24269 |
| symbol | DERA |
| name | deoxyribose-phosphate aldolase |
| refseq_nuc | NM_015954.4 |
| refseq_prot | NP_057038.2 |
| ensembl_nuc | ENST00000428559.7 |
| ensembl_prot | ENSP00000416583.2 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 15911332 |
| end | 16037381 |
| strand | + |
| ver | v1.2 |
| region | chr12:15911332-16037381 |
| region5000 | chr12:15906332-16042381 |
| regionname0 | DERA_chr12_15911332_16037381 |
| regionname5000 | DERA_chr12_15906332_16042381 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 318 | 255 | 80 | 52 | 92 | 4 | 25 | 66 | DERA_chr12_15906332_16042381 | DERA | MSAHN others(313): Show |
chr12 | 15906332 | 16042381 |
| a0002 | 0/0 | 318 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | MSAHN others(313): Show |
chr12 | 15906332 | 16042381 |
| a0003 | 0/0 | 318 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | DERA_chr12_15906332_16042381 | DERA | MSAHN others(313): Show |
chr12 | 15906332 | 16042381 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 954 | 253 | 78 | 52 | 92 | 4 | 25 | DERA_chr12_15906332_16042381 | DERA | ATGTC others(949): Show |
chr12 | 15906332 | 16042381 | ||
| a0001c0003 | 0/0 | 954 | 2 | 2 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | ATGTC others(949): Show |
chr12 | 15906332 | 16042381 | ||
| a0002c0002 | 0/0 | 954 | 2 | 2 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | ATGTC others(949): Show |
chr12 | 15906332 | 16042381 | ||
| a0003c0004 | 0/0 | 954 | 1 | 0 | 0 | 0 | 0 | 1 | DERA_chr12_15906332_16042381 | DERA | ATGTC others(949): Show |
chr12 | 15906332 | 16042381 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1644 | 204 | 57 | 49 | 67 | 4 | 25 | DERA_chr12_15906332_16042381 | DERA | GCGGC others(1639): Show |
chr12 | 15906332 | 16042381 |
| a0001c0001t0002 | 0/0 | 1644 | 27 | 1 | 1 | 25 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | GCGGC others(1639): Show |
chr12 | 15906332 | 16042381 |
| a0001c0001t0003 | 0/0 | 1644 | 13 | 12 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | GCGGC others(1639): Show |
chr12 | 15906332 | 16042381 |
| a0001c0001t0004 | 0/0 | 1644 | 4 | 4 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | GCGGC others(1639): Show |
chr12 | 15906332 | 16042381 |
| a0001c0001t0005 | 0/0 | 1644 | 4 | 3 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | ACGGC others(1639): Show |
chr12 | 15906332 | 16042381 |
| a0001c0001t0006 | 0/0 | 1644 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | GCGGC others(1639): Show |
chr12 | 15906332 | 16042381 |
| a0001c0003t0001 | 0/0 | 1644 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | GCGGC others(1639): Show |
chr12 | 15906332 | 16042381 |
| a0001c0003t0004 | 0/0 | 1644 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | GCGGC others(1639): Show |
chr12 | 15906332 | 16042381 |
| a0002c0002t0003 | 0/0 | 1644 | 2 | 2 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | GCGGC others(1639): Show |
chr12 | 15906332 | 16042381 |
| a0003c0004t0001 | 0/0 | 1644 | 1 | 0 | 0 | 0 | 0 | 1 | DERA_chr12_15906332_16042381 | DERA | GCGGC others(1639): Show |
chr12 | 15906332 | 16042381 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0086 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0192 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0003g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0003g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0003g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0003g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0003g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0003g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0003g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0003g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0003g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0003g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0003g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0003g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0003g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0004g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0004g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0004g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0004g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0005g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0005g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0005g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0005g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0006g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0003t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0003t0004g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0002c0002t0003g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0002c0002t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0003c0004t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0132 | EUR | FIN | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0133 | EUR | FIN | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | CHS | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | CHS | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | CHS | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | CHS | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | CHS | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | CHS | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0154 | EAS | CHS | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | CHS | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | PUR | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0250 | AMR | PUR | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | PUR | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG01109 | hp1 | a0001 | c0001 | t0005 | g0038 | AMR | PUR | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0247 | AMR | PUR | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | PUR | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | CLM | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | CLM | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | CLM | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | CLM | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | CLM | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | CLM | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0237 | AMR | CLM | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | CLM | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | CLM | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0226 | EUR | IBS | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0155 | EUR | IBS | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | ACB | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | ACB | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0006 | AMR | PEL | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | PEL | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | PEL | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PEL | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0234 | AMR | PEL | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | KHV | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | KHV | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0161 | EAS | KHV | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | KHV | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0020 | AFR | ACB | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02055 | hp2 | a0001 | c0001 | t0005 | g0037 | AFR | ACB | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | KHV | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | KHV | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | KHV | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | KHV | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | KHV | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | KHV | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | KHV | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0239 | EAS | KHV | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | KHV | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | KHV | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | PEL | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | PEL | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0147 | EAS | CDX | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | CDX | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | ACB | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | ACB | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | ACB | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | ACB | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PEL | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | PEL | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0090 | AMR | PEL | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | PEL | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PEL | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | PEL | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | GWD | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | GWD | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0227 | SAS | PJL | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0246 | AFR | GWD | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | GWD | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | GWD | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02630 | hp2 | a0002 | c0002 | t0003 | g0021 | AFR | GWD | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0018 | AFR | GWD | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0176 | SAS | PJL | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0164 | SAS | PJL | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | GWD | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0241 | SAS | PJL | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0055 | SAS | PJL | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | GWD | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | GWD | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | GWD | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | GWD | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | GWD | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | GWD | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0251 | AFR | GWD | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02897 | hp2 | a0001 | c0001 | t0004 | g0058 | AFR | GWD | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ESN | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | ESN | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02965 | hp1 | a0001 | c0001 | t0006 | g0011 | AFR | ESN | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | ESN | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | ESN | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02976 | hp2 | a0001 | c0001 | t0004 | g0089 | AFR | ESN | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | GWD | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG03098 | hp1 | a0002 | c0002 | t0003 | g0019 | AFR | MSL | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | MSL | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | ESN | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | ESN | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | ESN | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0015 | AFR | ESN | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG03195 | hp1 | a0001 | c0001 | t0004 | g0116 | AFR | ESN | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | ESN | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | MSL | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0014 | AFR | MSL | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | MSL | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0137 | SAS | PJL | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0175 | SAS | PJL | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0060 | SAS | PJL | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0045 | SAS | PJL | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0165 | SAS | PJL | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0151 | SAS | PJL | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG03516 | hp1 | a0001 | c0001 | t0003 | g0003 | AFR | ESN | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0012 | AFR | ESN | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | GWD | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG03540 | hp2 | a0001 | c0001 | t0004 | g0213 | AFR | GWD | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG03579 | hp1 | a0001 | c0001 | t0003 | g0013 | AFR | MSL | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | MSL | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0145 | SAS | PJL | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0150 | SAS | PJL | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0162 | SAS | STU | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0101 | SAS | STU | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | BEB | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG03834 | hp2 | a0003 | c0004 | t0001 | g0225 | SAS | BEB | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0166 | SAS | STU | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0125 | SAS | STU | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0149 | SAS | STU | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0209 | SAS | STU | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA18522 | hp1 | a0001 | c0003 | t0001 | g0073 | AFR | YRI | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | YRI | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0139 | EAS | CHB | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | CHB | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA18906 | hp1 | a0001 | c0001 | t0005 | g0035 | AFR | YRI | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | YRI | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0256 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0017 | AFR | LWK | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA19030 | hp2 | a0001 | c0001 | t0003 | g0005 | AFR | LWK | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | LWK | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | LWK | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA19078 | hp2 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA19240 | hp1 | a0001 | c0001 | t0005 | g0036 | AFR | YRI | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | YRI | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0177 | SAS | GIH | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0252 | SAS | GIH | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | CLM | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | ACB | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0016 | AFR | ACB | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | ACB | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | ACB | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0004 | AFR | ACB | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | MSL | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | MSL | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG06807 | hp1 | a0001 | c0003 | t0004 | g0072 | AFR | USA | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | USA | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0010 | AFR | USA | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | USA | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0078 | AFR | LWK | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | LWK | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0192 | REF | REF | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0086 | REF | REF | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:15958297 | G | A | 1 | a0002 | 2 | HG02630.hp2 HG03098.hp1 |
missense_variant | MODERATE | c.239G>A | p.Arg80Gln | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 3/9 | 291/1644 | 239/957 | 80/318 | chr12 | 15958297 | |||
| chr12:15982416 | G | A | 1 | a0003 | 1 | HG03834.hp2 | missense_variant | MODERATE | c.617G>A | p.Ser206Asn | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/9 | 669/1644 | 617/957 | 206/318 | chr12 | 15982416 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:15959842 | C | T | 1 | a0001c0003 | 2 | HG06807.hp1 NA18522.hp1 |
synonymous_variant | LOW | c.291C>T | p.Ala97Ala | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 4/9 | 343/1644 | 291/957 | 97/318 | chr12 | 15959842 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:15911332 | G | A | 1 | a0001c0001t0005 | 4 | HG01109.hp1 HG02055.hp2 NA18906.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-52G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/9 | 52 | chr12 | 15911332 | ||||||
| chr12:15911377 | C | T | 3 | a0001c0001t0003 a0001c0001t0006 a0002c0002t0003 |
16 | HG01934.hp1 HG02055.hp1 HG02109.hp2 others(13): Show |
5_prime_UTR_variant | MODIFIER | c.-7C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/9 | 7 | chr12 | 15911377 | ||||||
| chr12:16036760 | T | A | 1 | a0001c0001t0002 | 27 | HG00438.hp1 HG00621.hp1 HG02027.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*14T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 9/9 | 14 | chr12 | 16036760 | ||||||
| chr12:16037283 | T | A | 3 | a0001c0001t0004 a0001c0001t0006 a0001c0003t0004 |
6 | HG02897.hp2 HG02965.hp1 HG02976.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*537T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 9/9 | 537 | chr12 | 16037283 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:15912020 | CT | C | 39 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(36): Show |
39 | HG00733.hp1 HG01070.hp1 HG01109.hp2 others(36): Show |
intron_variant | MODIFIER | c.31+622delT | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15912020 | ||||||
| chr12:15912112 | T | A | 42 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(39): Show |
42 | HG00733.hp1 HG01109.hp1 HG01109.hp2 others(39): Show |
intron_variant | MODIFIER | c.31+698T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15912112 | |||||||
| chr12:15912114 | A | G | 5 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(2): Show |
5 | HG01243.hp1 HG02622.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.31+700A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15912114 | |||||||
| chr12:15912251 | T | G | 1 | a0001c0001t0001g0045 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.31+837T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15912251 | |||||||
| chr12:15912713 | G | T | 5 | a0001c0001t0001g0039 a0001c0001t0005g0035 a0001c0001t0005g0036 others(2): Show |
5 | HG00733.hp1 HG01109.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.31+1299G>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15912713 | |||||||
| chr12:15912747 | G | T | 9 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(6): Show |
9 | HG01109.hp2 HG01891.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.31+1333G>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15912747 | |||||||
| chr12:15912827 | C | T | 1 | a0001c0001t0002g0256 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.31+1413C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15912827 | |||||||
| chr12:15912982 | T | C | 24 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(21): Show |
24 | HG00733.hp1 HG01109.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.31+1568T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15912982 | |||||||
| chr12:15913112 | A | G | 42 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(39): Show |
42 | HG00733.hp1 HG01109.hp1 HG01109.hp2 others(39): Show |
intron_variant | MODIFIER | c.31+1698A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15913112 | |||||||
| chr12:15913153 | T | C | 1 | a0001c0001t0001g0046 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.31+1739T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15913153 | |||||||
| chr12:15913492 | G | A | 2 | a0001c0001t0001g0047 a0001c0001t0001g0048 |
2 | HG01261.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.31+2078G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15913492 | |||||||
| chr12:15913677 | A | AGG | 4 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0005 others(1): Show |
4 | HG01934.hp1 HG02559.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.31+2263_31+2264ins others(2): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15913677 | |||||||
| chr12:15913680 | G | T | 4 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0005 others(1): Show |
4 | HG01934.hp1 HG02559.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.31+2266G>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15913680 | |||||||
| chr12:15913939 | T | A | 5 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(2): Show |
5 | HG01243.hp1 HG02622.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.31+2525T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15913939 | |||||||
| chr12:15913979 | A | T | 2 | a0001c0001t0001g0254 a0001c0001t0001g0255 |
2 | HG00544.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.31+2565A>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15913979 | |||||||
| chr12:15914123 | A | G | 1 | a0001c0001t0002g0253 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.31+2709A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15914123 | |||||||
| chr12:15914137 | T | A | 3 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 |
3 | HG01884.hp2 HG03041.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.31+2723T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15914137 | |||||||
| chr12:15914335 | T | C | 23 | a0001c0001t0001g0022 a0001c0001t0001g0025 a0001c0001t0001g0026 others(20): Show |
23 | HG00733.hp1 HG01109.hp1 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.31+2921T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15914335 | |||||||
| chr12:15914387 | A | G | 1 | a0001c0001t0001g0252 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.31+2973A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15914387 | |||||||
| chr12:15914392 | A | AT | 7 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(4): Show |
7 | HG01884.hp2 HG01934.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.31+2979dupT | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15914392 | ||||||
| chr12:15914393 | T | TA | 9 | a0001c0001t0001g0046 a0001c0001t0001g0050 a0001c0001t0001g0051 others(6): Show |
9 | HG00438.hp1 HG00558.hp2 HG02074.hp1 others(6): Show |
intron_variant | MODIFIER | c.31+2998dupA | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15914393 | ||||||
| chr12:15914393 | TA | T | 7 | a0001c0001t0001g0247 a0001c0001t0001g0248 a0001c0001t0001g0249 others(4): Show |
7 | HG00438.hp2 HG00544.hp2 HG01070.hp2 others(4): Show |
intron_variant | MODIFIER | c.31+2998delA | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15914393 | ||||||
| chr12:15914394 | A | T | 35 | a0001c0001t0001g0022 a0001c0001t0001g0025 a0001c0001t0001g0026 others(32): Show |
35 | HG00733.hp1 HG01109.hp1 HG01109.hp2 others(32): Show |
intron_variant | MODIFIER | c.31+2980A>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15914394 | |||||||
| chr12:15914793 | C | T | 3 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 |
3 | HG01884.hp2 HG03041.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.31+3379C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15914793 | |||||||
| chr12:15914922 | C | T | 1 | a0001c0001t0001g0246 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.31+3508C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15914922 | |||||||
| chr12:15915024 | A | G | 1 | a0001c0001t0001g0245 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.31+3610A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15915024 | |||||||
| chr12:15915480 | A | G | 1 | a0001c0001t0001g0039 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.31+4066A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15915480 | |||||||
| chr12:15915510 | T | G | 44 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(41): Show |
44 | HG00733.hp1 HG01109.hp1 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.31+4096T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15915510 | |||||||
| chr12:15915582 | A | T | 2 | a0001c0001t0001g0057 a0001c0001t0004g0058 |
2 | HG02897.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.31+4168A>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15915582 | |||||||
| chr12:15915886 | T | C | 6 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(3): Show |
6 | HG01109.hp2 HG02486.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.31+4472T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15915886 | |||||||
| chr12:15916446 | C | CT | 12 | a0001c0001t0001g0055 a0001c0001t0001g0235 a0001c0001t0001g0236 others(9): Show |
12 | HG00621.hp2 HG01361.hp2 HG02132.hp2 others(9): Show |
intron_variant | MODIFIER | c.31+5054dupT | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15916446 | ||||||
| chr12:15916446 | CT | C | 41 | a0001c0001t0001g0022 a0001c0001t0001g0026 a0001c0001t0001g0027 others(38): Show |
41 | HG01109.hp1 HG01109.hp2 HG01167.hp1 others(38): Show |
intron_variant | MODIFIER | c.31+5054delT | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15916446 | ||||||
| chr12:15916450 | T | C | 2 | a0001c0001t0002g0023 a0001c0001t0002g0024 |
2 | NA18967.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.31+5036T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15916450 | |||||||
| chr12:15916451 | T | C | 32 | a0001c0001t0001g0022 a0001c0001t0001g0026 a0001c0001t0001g0027 others(29): Show |
32 | HG01109.hp2 HG01243.hp1 HG01891.hp2 others(29): Show |
intron_variant | MODIFIER | c.31+5037T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15916451 | |||||||
| chr12:15916452 | T | C | 1 | a0001c0001t0001g0025 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.31+5038T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15916452 | |||||||
| chr12:15916519 | C | T | 3 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 |
3 | HG01884.hp2 HG03041.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.31+5105C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15916519 | |||||||
| chr12:15916557 | C | T | 27 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0045 others(24): Show |
29 | HG00558.hp1 HG00621.hp2 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.31+5143C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15916557 | |||||||
| chr12:15916650 | A | T | 36 | a0001c0001t0001g0022 a0001c0001t0001g0025 a0001c0001t0001g0026 others(33): Show |
36 | HG01109.hp2 HG01243.hp1 HG01891.hp2 others(33): Show |
intron_variant | MODIFIER | c.31+5236A>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15916650 | |||||||
| chr12:15917005 | G | A | 1 | a0001c0001t0001g0063 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.31+5591G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15917005 | |||||||
| chr12:15917166 | ATTTTGCC others(6): Show |
A | 1 | a0001c0001t0001g0040 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.31+5755_31+5767del others(13): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15917166 | ||||||
| chr12:15917202 | A | G | 5 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0216 others(2): Show |
5 | HG02717.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.31+5788A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15917202 | |||||||
| chr12:15917445 | C | G | 1 | a0001c0001t0001g0212 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.31+6031C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15917445 | |||||||
| chr12:15917497 | C | G | 1 | a0001c0001t0001g0211 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.31+6083C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15917497 | |||||||
| chr12:15917688 | C | T | 1 | a0001c0001t0001g0210 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.31+6274C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15917688 | |||||||
| chr12:15917771 | A | G | 9 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(6): Show |
9 | HG01109.hp2 HG01891.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.31+6357A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15917771 | |||||||
| chr12:15917787 | A | G | 1 | a0001c0001t0001g0210 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.31+6373A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15917787 | |||||||
| chr12:15917793 | T | TA | 4 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0005 others(1): Show |
4 | HG01934.hp1 HG02559.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.31+6381dupA | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15917793 | ||||||
| chr12:15917795 | A | C | 1 | a0001c0001t0001g0209 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.31+6381A>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15917795 | |||||||
| chr12:15917818 | T | G | 1 | a0001c0001t0004g0213 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.31+6404T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15917818 | |||||||
| chr12:15917835 | C | T | 4 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0001t0001g0208 others(1): Show |
4 | HG02258.hp2 HG02615.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.31+6421C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15917835 | |||||||
| chr12:15917857 | C | T | 5 | a0001c0001t0001g0039 a0001c0001t0005g0035 a0001c0001t0005g0036 others(2): Show |
5 | HG00733.hp1 HG01109.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.31+6443C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15917857 | |||||||
| chr12:15917997 | T | C | 45 | a0001c0001t0001g0022 a0001c0001t0001g0025 a0001c0001t0001g0026 others(42): Show |
45 | HG01109.hp2 HG01243.hp1 HG01891.hp2 others(42): Show |
intron_variant | MODIFIER | c.31+6583T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15917997 | |||||||
| chr12:15918049 | G | A | 1 | a0001c0001t0001g0074 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.31+6635G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15918049 | |||||||
| chr12:15918176 | C | G | 9 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 others(6): Show |
9 | HG02109.hp1 HG02257.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.31+6762C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15918176 | |||||||
| chr12:15918186 | T | G | 54 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(51): Show |
54 | HG00733.hp1 HG01109.hp1 HG01109.hp2 others(51): Show |
intron_variant | MODIFIER | c.31+6772T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15918186 | |||||||
| chr12:15918203 | G | A | 3 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0005 |
3 | HG02559.hp2 HG03516.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.31+6789G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15918203 | |||||||
| chr12:15918243 | A | G | 1 | a0001c0001t0001g0205 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.31+6829A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15918243 | |||||||
| chr12:15918399 | T | C | 1 | a0001c0001t0002g0049 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.31+6985T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15918399 | |||||||
| chr12:15918435 | T | C | 1 | a0001c0001t0001g0075 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.31+7021T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15918435 | |||||||
| chr12:15918457 | C | T | 6 | a0001c0001t0001g0039 a0001c0001t0003g0006 a0001c0001t0005g0035 others(3): Show |
6 | HG00733.hp1 HG01109.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.31+7043C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15918457 | |||||||
| chr12:15918459 | G | A | 1 | a0001c0001t0001g0064 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.31+7045G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15918459 | |||||||
| chr12:15918520 | C | T | 1 | a0001c0001t0001g0204 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.31+7106C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15918520 | |||||||
| chr12:15918582 | A | T | 1 | a0001c0001t0001g0216 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.31+7168A>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15918582 | |||||||
| chr12:15918642 | C | T | 44 | a0001c0001t0001g0022 a0001c0001t0001g0025 a0001c0001t0001g0027 others(41): Show |
44 | HG01243.hp1 HG01891.hp2 HG02055.hp1 others(41): Show |
intron_variant | MODIFIER | c.31+7228C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15918642 | |||||||
| chr12:15918748 | G | A | 24 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 others(21): Show |
24 | HG02055.hp1 HG02109.hp1 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.31+7334G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15918748 | |||||||
| chr12:15918810 | A | G | 54 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(51): Show |
54 | HG00733.hp1 HG01109.hp1 HG01109.hp2 others(51): Show |
intron_variant | MODIFIER | c.31+7396A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15918810 | |||||||
| chr12:15918930 | G | A | 45 | a0001c0001t0001g0022 a0001c0001t0001g0025 a0001c0001t0001g0026 others(42): Show |
45 | HG01109.hp2 HG01243.hp1 HG01891.hp2 others(42): Show |
intron_variant | MODIFIER | c.31+7516G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15918930 | |||||||
| chr12:15918940 | C | T | 9 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(6): Show |
9 | HG01109.hp2 HG01891.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.31+7526C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15918940 | |||||||
| chr12:15918949 | A | G | 3 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 |
3 | HG01884.hp2 HG03041.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.31+7535A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15918949 | |||||||
| chr12:15918990 | A | G | 1 | a0001c0001t0001g0203 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.31+7576A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15918990 | |||||||
| chr12:15919028 | C | G | 4 | a0001c0001t0001g0200 a0001c0001t0001g0202 a0001c0001t0001g0245 others(1): Show |
4 | NA18942.hp2 NA18950.hp2 NA18968.hp2 others(1): Show |
intron_variant | MODIFIER | c.31+7614C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15919028 | |||||||
| chr12:15919199 | G | T | 1 | a0001c0001t0001g0234 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.31+7785G>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15919199 | |||||||
| chr12:15919273 | A | T | 2 | a0001c0001t0001g0057 a0001c0001t0004g0058 |
2 | HG02897.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.31+7859A>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15919273 | |||||||
| chr12:15919686 | A | C | 32 | a0001c0001t0001g0053 a0001c0001t0001g0061 a0001c0001t0001g0074 others(29): Show |
32 | HG00735.hp2 HG01070.hp2 HG01074.hp1 others(29): Show |
intron_variant | MODIFIER | c.31+8272A>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15919686 | |||||||
| chr12:15919970 | A | ATG | 185 | a0001c0001t0001g0022 a0001c0001t0001g0026 a0001c0001t0001g0027 others(182): Show |
185 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(182): Show |
intron_variant | MODIFIER | c.31+8578_31+8579dup others(2): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15919970 | ||||||
| chr12:15919970 | A | ATGTG | 15 | a0001c0001t0001g0025 a0001c0001t0001g0039 a0001c0001t0001g0065 others(12): Show |
15 | HG00733.hp1 HG01934.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.31+8576_31+8579dup others(4): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15919970 | ||||||
| chr12:15919994 | C | G | 3 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 |
3 | HG01884.hp2 HG03041.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.31+8580C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15919994 | |||||||
| chr12:15919998 | G | GTC | 3 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 |
3 | HG01884.hp2 HG03041.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.31+8585_31+8586ins others(2): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15919998 | ||||||
| chr12:15920007 | A | T | 3 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 |
3 | HG01884.hp2 HG03041.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.31+8593A>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15920007 | |||||||
| chr12:15920009 | A | T | 3 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 |
3 | HG01884.hp2 HG03041.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.31+8595A>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15920009 | |||||||
| chr12:15920014 | A | G | 3 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 |
3 | HG01884.hp2 HG03041.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.31+8600A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15920014 | |||||||
| chr12:15920018 | G | A | 3 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 |
3 | HG01884.hp2 HG03041.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.31+8604G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15920018 | |||||||
| chr12:15920110 | TATAG | T | 148 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 others(145): Show |
148 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(145): Show |
intron_variant | MODIFIER | c.31+8702_31+8705del others(4): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15920110 | ||||||
| chr12:15920527 | A | G | 1 | a0001c0001t0001g0171 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.31+9113A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15920527 | |||||||
| chr12:15920561 | G | T | 1 | a0001c0001t0001g0233 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.31+9147G>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15920561 | |||||||
| chr12:15920639 | C | A | 3 | a0001c0001t0001g0025 a0001c0001t0002g0023 a0001c0001t0002g0024 |
3 | NA18964.hp1 NA18967.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.31+9225C>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15920639 | |||||||
| chr12:15920783 | C | T | 2 | a0001c0001t0001g0055 a0001c0001t0001g0170 |
2 | HG01358.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.31+9369C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15920783 | |||||||
| chr12:15920834 | C | T | 3 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0005 |
3 | HG02559.hp2 HG03516.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.31+9420C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15920834 | |||||||
| chr12:15921127 | T | G | 1 | a0001c0001t0001g0205 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.31+9713T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15921127 | |||||||
| chr12:15921130 | G | A | 3 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 |
3 | HG01884.hp2 HG03041.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.31+9716G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15921130 | |||||||
| chr12:15921473 | A | G | 48 | a0001c0001t0001g0022 a0001c0001t0001g0025 a0001c0001t0001g0026 others(45): Show |
48 | HG01109.hp1 HG01109.hp2 HG01243.hp1 others(45): Show |
intron_variant | MODIFIER | c.31+10059A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15921473 | |||||||
| chr12:15921595 | A | G | 8 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(5): Show |
8 | HG01109.hp1 HG01243.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.31+10181A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15921595 | |||||||
| chr12:15921813 | C | G | 1 | a0001c0001t0001g0212 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.31+10399C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15921813 | |||||||
| chr12:15921819 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.31+10405G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15921819 | |||||||
| chr12:15921894 | C | T | 5 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(2): Show |
5 | HG00733.hp1 HG01884.hp2 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.31+10480C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15921894 | |||||||
| chr12:15921926 | GATA | G | 205 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(202): Show |
205 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(202): Show |
intron_variant | MODIFIER | c.31+10529_31+10531d others(5): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15921926 | ||||||
| chr12:15922195 | C | T | 54 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(51): Show |
54 | HG00733.hp1 HG01109.hp1 HG01109.hp2 others(51): Show |
intron_variant | MODIFIER | c.31+10781C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15922195 | |||||||
| chr12:15922217 | C | T | 1 | a0001c0001t0001g0199 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.31+10803C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15922217 | |||||||
| chr12:15922265 | C | G | 2 | a0001c0001t0001g0039 a0001c0001t0003g0006 |
2 | HG00733.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.31+10851C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15922265 | |||||||
| chr12:15922375 | T | C | 1 | a0001c0001t0001g0064 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.31+10961T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15922375 | |||||||
| chr12:15922557 | G | A | 3 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 |
3 | HG01884.hp2 HG03041.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.31+11143G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15922557 | |||||||
| chr12:15922720 | GAT | G | 10 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(7): Show |
10 | HG01109.hp2 HG01891.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.31+11308_31+11309d others(4): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15922720 | ||||||
| chr12:15922731 | G | T | 5 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(2): Show |
5 | HG00733.hp1 HG01884.hp2 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.31+11317G>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15922731 | |||||||
| chr12:15922756 | C | T | 54 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(51): Show |
54 | HG00733.hp1 HG01109.hp1 HG01109.hp2 others(51): Show |
intron_variant | MODIFIER | c.31+11342C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15922756 | |||||||
| chr12:15922876 | A | G | 205 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(202): Show |
205 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(202): Show |
intron_variant | MODIFIER | c.31+11462A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15922876 | |||||||
| chr12:15923017 | C | CT | 60 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0025 others(57): Show |
61 | HG00438.hp2 HG00642.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.31+11626dupT | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15923017 | ||||||
| chr12:15923017 | CTTTTTTT | C | 12 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 others(9): Show |
12 | HG02109.hp1 HG02257.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.31+11620_31+11626d others(9): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15923017 | ||||||
| chr12:15923017 | CTTTTTTT others(3): Show |
C | 10 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(7): Show |
10 | HG01109.hp2 HG01891.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.31+11617_31+11626d others(12): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15923017 | ||||||
| chr12:15923085 | C | G | 49 | a0001c0001t0001g0022 a0001c0001t0001g0025 a0001c0001t0001g0026 others(46): Show |
49 | HG01109.hp1 HG01109.hp2 HG01243.hp1 others(46): Show |
intron_variant | MODIFIER | c.31+11671C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15923085 | |||||||
| chr12:15923086 | G | T | 1 | a0001c0001t0001g0211 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.31+11672G>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15923086 | |||||||
| chr12:15923108 | C | T | 49 | a0001c0001t0001g0022 a0001c0001t0001g0025 a0001c0001t0001g0026 others(46): Show |
49 | HG01109.hp1 HG01109.hp2 HG01243.hp1 others(46): Show |
intron_variant | MODIFIER | c.31+11694C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15923108 | |||||||
| chr12:15923148 | A | G | 2 | a0001c0001t0001g0060 a0001c0001t0001g0156 |
2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.31+11734A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15923148 | |||||||
| chr12:15923297 | C | T | 2 | a0001c0001t0001g0172 a0001c0001t0001g0173 |
2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.31+11883C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15923297 | |||||||
| chr12:15923320 | C | T | 24 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 others(21): Show |
24 | HG02055.hp1 HG02109.hp1 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.31+11906C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15923320 | |||||||
| chr12:15923461 | AC | A | 9 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 others(6): Show |
9 | HG02109.hp1 HG02257.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.31+12049delC | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15923461 | ||||||
| chr12:15923464 | T | A | 9 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 others(6): Show |
9 | HG02109.hp1 HG02257.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.31+12050T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15923464 | |||||||
| chr12:15923578 | C | A | 1 | a0001c0001t0001g0157 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.31+12164C>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15923578 | |||||||
| chr12:15923578 | C | T | 49 | a0001c0001t0001g0022 a0001c0001t0001g0025 a0001c0001t0001g0026 others(46): Show |
49 | HG01109.hp1 HG01109.hp2 HG01243.hp1 others(46): Show |
intron_variant | MODIFIER | c.31+12164C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15923578 | |||||||
| chr12:15923701 | C | CT | 108 | a0001c0001t0001g0009 a0001c0001t0001g0039 a0001c0001t0001g0046 others(105): Show |
108 | HG00438.hp2 HG00558.hp2 HG00642.hp2 others(105): Show |
intron_variant | MODIFIER | c.31+12300dupT | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15923701 | ||||||
| chr12:15923701 | C | CTT | 43 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0055 others(40): Show |
43 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(40): Show |
intron_variant | MODIFIER | c.31+12299_31+12300d others(4): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15923701 | ||||||
| chr12:15923701 | CTT | C | 49 | a0001c0001t0001g0022 a0001c0001t0001g0025 a0001c0001t0001g0026 others(46): Show |
49 | HG01109.hp1 HG01109.hp2 HG01243.hp1 others(46): Show |
intron_variant | MODIFIER | c.31+12299_31+12300d others(4): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15923701 | ||||||
| chr12:15923908 | C | A | 1 | a0001c0001t0001g0027 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.31+12494C>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15923908 | |||||||
| chr12:15924176 | C | T | 49 | a0001c0001t0001g0022 a0001c0001t0001g0025 a0001c0001t0001g0026 others(46): Show |
49 | HG01109.hp1 HG01109.hp2 HG01243.hp1 others(46): Show |
intron_variant | MODIFIER | c.31+12762C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15924176 | |||||||
| chr12:15924238 | G | A | 2 | a0001c0001t0001g0039 a0001c0001t0003g0006 |
2 | HG00733.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.31+12824G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15924238 | |||||||
| chr12:15924475 | A | G | 9 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 others(6): Show |
9 | HG02109.hp1 HG02257.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.31+13061A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15924475 | |||||||
| chr12:15924529 | T | C | 3 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0005 |
3 | HG02559.hp2 HG03516.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.31+13115T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15924529 | |||||||
| chr12:15924543 | A | G | 1 | a0001c0001t0001g0064 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.31+13129A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15924543 | |||||||
| chr12:15924644 | A | G | 2 | a0001c0001t0001g0215 a0001c0001t0001g0251 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.31+13230A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15924644 | |||||||
| chr12:15924741 | T | G | 10 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(7): Show |
10 | HG01109.hp2 HG01891.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.31+13327T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15924741 | |||||||
| chr12:15924955 | A | G | 12 | a0001c0001t0003g0010 a0001c0001t0003g0012 a0001c0001t0003g0013 others(9): Show |
12 | HG02055.hp1 HG02109.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.31+13541A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15924955 | |||||||
| chr12:15925044 | G | A | 49 | a0001c0001t0001g0022 a0001c0001t0001g0025 a0001c0001t0001g0026 others(46): Show |
49 | HG01109.hp1 HG01109.hp2 HG01243.hp1 others(46): Show |
intron_variant | MODIFIER | c.31+13630G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15925044 | |||||||
| chr12:15925160 | G | A | 1 | a0001c0001t0001g0064 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.31+13746G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15925160 | |||||||
| chr12:15925163 | G | C | 5 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(2): Show |
5 | HG00733.hp1 HG01884.hp2 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.31+13749G>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15925163 | |||||||
| chr12:15925274 | C | T | 1 | a0001c0001t0001g0155 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.31+13860C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15925274 | |||||||
| chr12:15925316 | T | G | 49 | a0001c0001t0001g0022 a0001c0001t0001g0025 a0001c0001t0001g0026 others(46): Show |
49 | HG01109.hp1 HG01109.hp2 HG01243.hp1 others(46): Show |
intron_variant | MODIFIER | c.31+13902T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15925316 | |||||||
| chr12:15925374 | T | G | 6 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(3): Show |
6 | HG00733.hp2 HG01884.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.31+13960T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15925374 | |||||||
| chr12:15925409 | C | T | 2 | a0001c0001t0001g0057 a0001c0001t0004g0058 |
2 | HG02897.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.31+13995C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15925409 | |||||||
| chr12:15925429 | A | T | 1 | a0001c0001t0001g0064 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.31+14015A>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15925429 | |||||||
| chr12:15925452 | C | T | 48 | a0001c0001t0001g0022 a0001c0001t0001g0025 a0001c0001t0001g0026 others(45): Show |
48 | HG01109.hp1 HG01109.hp2 HG01243.hp1 others(45): Show |
intron_variant | MODIFIER | c.31+14038C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15925452 | |||||||
| chr12:15925594 | C | G | 4 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0030 others(1): Show |
4 | HG01109.hp2 HG02486.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.31+14180C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15925594 | |||||||
| chr12:15925822 | C | CT | 26 | a0001c0001t0001g0051 a0001c0001t0001g0055 a0001c0001t0001g0077 others(23): Show |
26 | HG00558.hp2 HG00621.hp1 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.31+14431dupT | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15925822 | ||||||
| chr12:15925822 | CT | C | 19 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(16): Show |
19 | HG01109.hp2 HG01261.hp1 HG02015.hp1 others(16): Show |
intron_variant | MODIFIER | c.31+14431delT | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15925822 | ||||||
| chr12:15925822 | CTTT | C | 20 | a0001c0001t0001g0022 a0001c0001t0001g0025 a0001c0001t0001g0044 others(17): Show |
20 | HG01109.hp1 HG01243.hp1 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.31+14429_31+14431d others(5): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15925822 | ||||||
| chr12:15925822 | CTTTT | C | 18 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0040 others(15): Show |
18 | HG01884.hp2 HG02109.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.31+14428_31+14431d others(6): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15925822 | ||||||
| chr12:15925954 | T | TG | 54 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(51): Show |
54 | HG00733.hp1 HG01109.hp1 HG01109.hp2 others(51): Show |
intron_variant | MODIFIER | c.31+14542dupG | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15925954 | ||||||
| chr12:15926188 | G | T | 42 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(39): Show |
42 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(39): Show |
intron_variant | MODIFIER | c.31+14774G>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15926188 | |||||||
| chr12:15926433 | G | A | 9 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 others(6): Show |
9 | HG02109.hp1 HG02257.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.31+15019G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15926433 | |||||||
| chr12:15926458 | C | T | 1 | a0001c0001t0001g0248 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.31+15044C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15926458 | |||||||
| chr12:15926472 | C | T | 1 | a0001c0001t0001g0127 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.31+15058C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15926472 | |||||||
| chr12:15926532 | C | T | 1 | a0002c0002t0003g0019 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.31+15118C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15926532 | |||||||
| chr12:15926561 | A | C | 16 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(13): Show |
16 | HG01109.hp2 HG01243.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.31+15147A>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15926561 | |||||||
| chr12:15926563 | C | G | 3 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0004g0089 |
3 | HG02809.hp2 HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.31+15149C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15926563 | |||||||
| chr12:15926566 | C | G | 40 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(37): Show |
40 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.31+15152C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15926566 | |||||||
| chr12:15926598 | T | C | 3 | a0001c0001t0005g0036 a0001c0001t0005g0037 a0001c0001t0005g0038 |
3 | HG01109.hp1 HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.31+15184T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15926598 | |||||||
| chr12:15926599 | G | A | 14 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(11): Show |
14 | HG00733.hp1 HG01109.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.31+15185G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15926599 | |||||||
| chr12:15926626 | C | A | 7 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(4): Show |
7 | HG01891.hp2 HG02486.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.31+15212C>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15926626 | |||||||
| chr12:15926645 | G | A | 7 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(4): Show |
7 | HG01891.hp2 HG02486.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.31+15231G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15926645 | |||||||
| chr12:15926691 | C | G | 1 | a0001c0001t0002g0187 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.31+15277C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15926691 | |||||||
| chr12:15926693 | A | C | 7 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(4): Show |
7 | HG01891.hp2 HG02486.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.31+15279A>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15926693 | |||||||
| chr12:15926693 | A | G | 1 | a0001c0001t0002g0187 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.31+15279A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15926693 | |||||||
| chr12:15926706 | C | A | 1 | a0001c0001t0002g0187 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.31+15292C>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15926706 | |||||||
| chr12:15926742 | G | GA | 164 | a0001c0001t0001g0025 a0001c0001t0001g0033 a0001c0001t0001g0046 others(161): Show |
164 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(161): Show |
intron_variant | MODIFIER | c.31+15347dupA | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15926742 | ||||||
| chr12:15926742 | G | GAA | 13 | a0001c0001t0001g0027 a0001c0001t0001g0077 a0001c0001t0001g0160 others(10): Show |
13 | HG01109.hp1 HG02027.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.31+15346_31+15347d others(4): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15926742 | ||||||
| chr12:15926930 | C | T | 2 | a0001c0001t0001g0059 a0001c0001t0001g0091 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.31+15516C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15926930 | |||||||
| chr12:15927018 | T | G | 2 | a0001c0001t0001g0059 a0001c0001t0001g0091 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.31+15604T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15927018 | |||||||
| chr12:15927193 | A | G | 24 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(21): Show |
24 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.31+15779A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15927193 | |||||||
| chr12:15927413 | C | T | 2 | a0001c0001t0001g0126 a0001c0001t0001g0226 |
2 | HG01071.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.31+15999C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15927413 | |||||||
| chr12:15927414 | G | A | 55 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0028 others(52): Show |
56 | HG00733.hp2 HG01071.hp2 HG01123.hp2 others(53): Show |
intron_variant | MODIFIER | c.31+16000G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15927414 | |||||||
| chr12:15927490 | T | C | 1 | a0001c0001t0002g0217 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.31+16076T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15927490 | |||||||
| chr12:15927715 | T | C | 67 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(64): Show |
68 | HG00280.hp1 HG00280.hp2 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.31+16301T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15927715 | |||||||
| chr12:15927753 | T | G | 2 | a0001c0001t0001g0172 a0001c0001t0001g0173 |
2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.31+16339T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15927753 | |||||||
| chr12:15927781 | A | G | 1 | a0001c0001t0001g0129 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.31+16367A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15927781 | |||||||
| chr12:15927828 | T | A | 7 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 others(4): Show |
7 | HG02109.hp1 HG02257.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.31+16414T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15927828 | |||||||
| chr12:15927899 | G | A | 1 | a0001c0001t0001g0136 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.31+16485G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15927899 | |||||||
| chr12:15927934 | C | T | 1 | a0001c0001t0001g0041 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.31+16520C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15927934 | |||||||
| chr12:15927966 | A | G | 1 | a0001c0001t0001g0001 | 2 | HG01123.hp2 HG01256.hp2 |
intron_variant | MODIFIER | c.31+16552A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15927966 | |||||||
| chr12:15928030 | T | TTG | 61 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(58): Show |
62 | HG00280.hp1 HG00280.hp2 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.31+16617_31+16618i others(4): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15928030 | ||||||
| chr12:15928041 | G | T | 61 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(58): Show |
62 | HG00280.hp1 HG00280.hp2 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.31+16627G>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15928041 | |||||||
| chr12:15928093 | C | A | 1 | a0001c0001t0002g0217 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.31+16679C>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15928093 | |||||||
| chr12:15928101 | G | T | 73 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(70): Show |
74 | HG00280.hp1 HG00280.hp2 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.31+16687G>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15928101 | |||||||
| chr12:15928166 | G | A | 2 | a0001c0001t0002g0023 a0001c0001t0002g0024 |
2 | NA18967.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.31+16752G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15928166 | |||||||
| chr12:15928360 | T | C | 8 | a0001c0001t0003g0010 a0001c0001t0003g0012 a0001c0001t0003g0013 others(5): Show |
8 | HG02055.hp1 HG02109.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.31+16946T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15928360 | |||||||
| chr12:15928375 | C | T | 45 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(42): Show |
46 | HG00280.hp1 HG00280.hp2 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.31+16961C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15928375 | |||||||
| chr12:15928689 | GAGA | G | 8 | a0001c0001t0003g0010 a0001c0001t0003g0012 a0001c0001t0003g0013 others(5): Show |
8 | HG02055.hp1 HG02109.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.31+17280_31+17282d others(5): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15928689 | ||||||
| chr12:15928707 | G | A | 61 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(58): Show |
62 | HG00280.hp1 HG00280.hp2 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.31+17293G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15928707 | |||||||
| chr12:15928826 | G | T | 1 | a0001c0001t0002g0256 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.31+17412G>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15928826 | |||||||
| chr12:15928979 | C | T | 1 | a0001c0001t0001g0129 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.31+17565C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15928979 | |||||||
| chr12:15929259 | G | C | 1 | a0001c0001t0001g0107 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.31+17845G>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15929259 | |||||||
| chr12:15929342 | G | C | 61 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(58): Show |
62 | HG00280.hp1 HG00280.hp2 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.31+17928G>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15929342 | |||||||
| chr12:15929388 | C | T | 1 | a0001c0001t0004g0089 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.31+17974C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15929388 | |||||||
| chr12:15929516 | GTCA | G | 7 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0174 others(4): Show |
7 | HG02257.hp2 HG02559.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.31+18103_31+18105d others(5): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15929516 | |||||||
| chr12:15929532 | A | C | 7 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 others(4): Show |
7 | HG02109.hp1 HG02257.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.31+18118A>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15929532 | |||||||
| chr12:15929583 | C | T | 2 | a0001c0001t0001g0129 a0001c0001t0003g0018 |
2 | HG02486.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.31+18169C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15929583 | |||||||
| chr12:15929637 | G | T | 4 | a0001c0001t0001g0009 a0001c0001t0001g0207 a0001c0001t0001g0208 others(1): Show |
4 | HG02258.hp2 HG02615.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.31+18223G>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15929637 | |||||||
| chr12:15929652 | T | A | 73 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(70): Show |
74 | HG00280.hp1 HG00280.hp2 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.31+18238T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15929652 | |||||||
| chr12:15929809 | G | A | 2 | a0001c0001t0001g0063 a0001c0001t0003g0018 |
2 | HG02647.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.31+18395G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15929809 | |||||||
| chr12:15929842 | G | A | 2 | a0002c0002t0003g0019 a0002c0002t0003g0021 |
2 | HG02630.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.31+18428G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15929842 | |||||||
| chr12:15929999 | T | G | 1 | a0001c0001t0001g0227 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.31+18585T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15929999 | |||||||
| chr12:15930040 | T | C | 5 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0087 others(2): Show |
5 | HG02559.hp1 HG02809.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.31+18626T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15930040 | |||||||
| chr12:15930581 | G | A | 25 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(22): Show |
25 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.31+19167G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15930581 | |||||||
| chr12:15930762 | T | G | 2 | a0002c0002t0003g0019 a0002c0002t0003g0021 |
2 | HG02630.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.31+19348T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15930762 | |||||||
| chr12:15931179 | G | A | 1 | a0001c0001t0002g0078 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.31+19765G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15931179 | |||||||
| chr12:15931261 | CAG | C | 4 | a0001c0001t0001g0125 a0001c0001t0001g0130 a0001c0001t0001g0163 others(1): Show |
4 | HG00642.hp2 HG00738.hp1 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.31+19850_31+19851d others(4): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15931261 | ||||||
| chr12:15931535 | G | A | 2 | a0001c0001t0001g0032 a0001c0001t0001g0064 |
2 | HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.31+20121G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15931535 | |||||||
| chr12:15931870 | C | G | 1 | a0001c0001t0001g0071 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.31+20456C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15931870 | |||||||
| chr12:15932121 | C | T | 7 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 others(4): Show |
7 | HG02109.hp1 HG02257.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.31+20707C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15932121 | |||||||
| chr12:15932320 | T | C | 2 | a0001c0001t0001g0100 a0001c0001t0001g0101 |
2 | HG03491.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.31+20906T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15932320 | |||||||
| chr12:15932355 | C | A | 5 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0030 others(2): Show |
5 | HG01109.hp2 HG01891.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.31+20941C>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15932355 | |||||||
| chr12:15932434 | G | A | 1 | a0001c0001t0001g0177 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.31+21020G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15932434 | |||||||
| chr12:15932438 | C | T | 4 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0046 others(1): Show |
4 | HG02647.hp1 HG03130.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.31+21024C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15932438 | |||||||
| chr12:15932444 | G | A | 1 | a0001c0001t0001g0224 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.31+21030G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15932444 | |||||||
| chr12:15932507 | G | A | 2 | a0001c0001t0002g0023 a0001c0001t0002g0024 |
2 | NA18967.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.31+21093G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15932507 | |||||||
| chr12:15932523 | G | C | 11 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0174 others(8): Show |
11 | HG02257.hp2 HG02559.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.31+21109G>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15932523 | |||||||
| chr12:15932640 | TA | T | 7 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0174 others(4): Show |
7 | HG02257.hp2 HG02559.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.31+21238delA | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15932640 | ||||||
| chr12:15932641 | A | T | 8 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 others(5): Show |
8 | HG02109.hp1 HG02257.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.31+21227A>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15932641 | |||||||
| chr12:15932659 | C | G | 19 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0174 others(16): Show |
19 | HG02055.hp1 HG02109.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.31+21245C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15932659 | |||||||
| chr12:15932727 | C | T | 1 | a0001c0001t0001g0249 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.31+21313C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15932727 | |||||||
| chr12:15932847 | G | T | 1 | a0001c0001t0001g0233 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.31+21433G>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15932847 | |||||||
| chr12:15932881 | A | ACT | 65 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(62): Show |
66 | HG00280.hp1 HG00280.hp2 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.31+21470_31+21471d others(4): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15932881 | ||||||
| chr12:15933061 | A | G | 8 | a0001c0001t0003g0010 a0001c0001t0003g0012 a0001c0001t0003g0013 others(5): Show |
8 | HG02055.hp1 HG02109.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.31+21647A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15933061 | |||||||
| chr12:15933246 | T | C | 4 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0046 others(1): Show |
4 | HG02647.hp1 HG03130.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.31+21832T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15933246 | |||||||
| chr12:15933273 | C | T | 1 | a0001c0001t0001g0227 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.31+21859C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15933273 | |||||||
| chr12:15933615 | G | A | 64 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(61): Show |
65 | HG00280.hp1 HG00280.hp2 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.31+22201G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15933615 | |||||||
| chr12:15933667 | T | C | 1 | a0001c0001t0001g0241 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.31+22253T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15933667 | |||||||
| chr12:15933671 | G | A | 8 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 others(5): Show |
8 | HG02109.hp1 HG02257.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.31+22257G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15933671 | |||||||
| chr12:15933939 | G | A | 15 | a0001c0001t0001g0053 a0001c0001t0001g0055 a0001c0001t0001g0098 others(12): Show |
15 | HG01358.hp2 HG02738.hp2 HG03834.hp1 others(12): Show |
intron_variant | MODIFIER | c.31+22525G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15933939 | |||||||
| chr12:15934000 | G | T | 1 | a0001c0001t0001g0093 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.31+22586G>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15934000 | |||||||
| chr12:15934260 | C | A | 1 | a0001c0001t0001g0022 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.32-22676C>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15934260 | |||||||
| chr12:15934381 | T | A | 41 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(38): Show |
42 | HG00280.hp1 HG00280.hp2 HG00621.hp1 others(39): Show |
intron_variant | MODIFIER | c.32-22555T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15934381 | |||||||
| chr12:15934638 | A | C | 5 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0030 others(2): Show |
5 | HG01109.hp2 HG01891.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.32-22298A>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15934638 | |||||||
| chr12:15934957 | A | C | 11 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(8): Show |
11 | HG01109.hp2 HG01891.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.32-21979A>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15934957 | |||||||
| chr12:15935162 | A | G | 7 | a0001c0001t0001g0053 a0001c0001t0001g0157 a0001c0001t0001g0178 others(4): Show |
7 | NA18942.hp1 NA18950.hp1 NA18975.hp1 others(4): Show |
intron_variant | MODIFIER | c.32-21774A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15935162 | |||||||
| chr12:15935169 | T | A | 4 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0046 others(1): Show |
4 | HG02647.hp1 HG03130.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.32-21767T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15935169 | |||||||
| chr12:15935229 | G | C | 6 | a0001c0001t0001g0198 a0001c0001t0001g0200 a0001c0001t0001g0202 others(3): Show |
6 | HG02080.hp1 HG02135.hp2 NA18942.hp2 others(3): Show |
intron_variant | MODIFIER | c.32-21707G>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15935229 | |||||||
| chr12:15935540 | A | G | 46 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(43): Show |
47 | HG00280.hp1 HG00280.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.32-21396A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15935540 | |||||||
| chr12:15935547 | G | A | 7 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0174 others(4): Show |
7 | HG02257.hp2 HG02559.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.32-21389G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15935547 | |||||||
| chr12:15935606 | G | A | 4 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0046 others(1): Show |
4 | HG02647.hp1 HG03130.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.32-21330G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15935606 | |||||||
| chr12:15935870 | T | G | 1 | a0001c0001t0001g0129 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.32-21066T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15935870 | |||||||
| chr12:15935874 | A | T | 1 | a0001c0001t0001g0211 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.32-21062A>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15935874 | |||||||
| chr12:15935988 | A | G | 4 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0046 others(1): Show |
4 | HG02647.hp1 HG03130.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.32-20948A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15935988 | |||||||
| chr12:15936130 | G | A | 4 | a0001c0001t0002g0147 a0001c0001t0002g0148 a0001c0001t0002g0154 others(1): Show |
4 | HG00621.hp1 HG02165.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.32-20806G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15936130 | |||||||
| chr12:15936456 | G | T | 1 | a0001c0001t0002g0201 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.32-20480G>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15936456 | |||||||
| chr12:15936761 | A | G | 4 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0046 others(1): Show |
4 | HG02647.hp1 HG03130.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.32-20175A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15936761 | |||||||
| chr12:15936850 | G | GTTGTC | 80 | a0001c0001t0001g0009 a0001c0001t0001g0025 a0001c0001t0001g0039 others(77): Show |
80 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.32-20050_32-20046d others(7): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15936850 | ||||||
| chr12:15936850 | G | GTTGTCTT others(3): Show |
9 | a0001c0001t0001g0052 a0001c0001t0001g0061 a0001c0001t0001g0062 others(6): Show |
9 | HG02027.hp2 HG02074.hp2 HG02083.hp2 others(6): Show |
intron_variant | MODIFIER | c.32-20055_32-20046d others(12): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15936850 | ||||||
| chr12:15936850 | G | GTTGTCTT others(8): Show |
3 | a0001c0001t0001g0135 a0001c0001t0001g0146 a0001c0001t0001g0227 |
3 | HG01168.hp1 HG01169.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.32-20060_32-20046d others(17): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15936850 | ||||||
| chr12:15936850 | G | GTTGTCTT others(13): Show |
1 | a0001c0001t0001g0046 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.32-20065_32-20046d others(22): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15936850 | ||||||
| chr12:15936850 | GTTGTC | G | 9 | a0001c0001t0001g0096 a0001c0001t0003g0010 a0001c0001t0003g0012 others(6): Show |
9 | HG02055.hp1 HG02109.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.32-20050_32-20046d others(7): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15936850 | ||||||
| chr12:15936855 | C | CTTGTG | 2 | a0001c0003t0001g0073 a0001c0003t0004g0072 |
2 | HG06807.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.32-20077_32-20076i others(7): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15936855 | ||||||
| chr12:15936861 | T | C | 2 | a0001c0001t0002g0023 a0001c0001t0002g0024 |
2 | NA18967.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.32-20075T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15936861 | |||||||
| chr12:15936865 | C | G | 2 | a0001c0001t0002g0023 a0001c0001t0002g0024 |
2 | NA18967.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.32-20071C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15936865 | |||||||
| chr12:15936871 | TTGTCTTG others(18): Show |
T | 4 | a0001c0001t0002g0023 a0001c0001t0002g0024 a0002c0002t0003g0019 others(1): Show |
4 | HG02630.hp2 HG03098.hp1 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.32-20060_32-20036d others(27): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15936871 | ||||||
| chr12:15936876 | TTGTCTTG others(23): Show |
T | 3 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0005 |
3 | HG02559.hp2 HG03516.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.32-20055_32-20026d others(32): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15936876 | ||||||
| chr12:15936876 | TTGTCTTG others(28): Show |
T | 3 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0235 |
3 | HG02257.hp2 HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.32-20055_32-20021d others(37): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15936876 | ||||||
| chr12:15936876 | TTGTCTTG others(33): Show |
T | 1 | a0001c0001t0001g0174 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.32-20055_32-20016d others(42): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15936876 | ||||||
| chr12:15936881 | T | TTGTCCTG others(13): Show |
1 | a0001c0001t0001g0129 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.32-20051_32-20050i others(22): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15936881 | ||||||
| chr12:15936881 | T | TTGTCCTG others(18): Show |
6 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 others(3): Show |
6 | HG02109.hp1 HG02257.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.32-20051_32-20050i others(27): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15936881 | ||||||
| chr12:15936881 | T | TTGTCCTG others(23): Show |
1 | a0001c0001t0001g0069 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.32-20051_32-20050i others(32): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15936881 | ||||||
| chr12:15936886 | T | C | 9 | a0001c0001t0001g0034 a0001c0001t0001g0065 a0001c0001t0001g0066 others(6): Show |
9 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.32-20050T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15936886 | |||||||
| chr12:15936886 | T | TTGTCC | 2 | a0001c0001t0001g0220 a0001c0001t0002g0256 |
2 | NA19003.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.32-20005_32-20001d others(7): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15936886 | ||||||
| chr12:15936886 | T | TTGTCCTG others(13): Show |
1 | a0001c0001t0001g0083 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.32-20020_32-20001d others(22): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15936886 | ||||||
| chr12:15936886 | T | TTGTCCTG others(18): Show |
1 | a0001c0001t0001g0180 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.32-20025_32-20001d others(27): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15936886 | ||||||
| chr12:15936886 | T | TTGTCTTG others(3): Show |
8 | a0001c0001t0001g0122 a0001c0001t0001g0178 a0001c0001t0001g0198 others(5): Show |
8 | HG02080.hp1 HG02135.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.32-20046_32-20045i others(12): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15936886 | ||||||
| chr12:15936886 | T | TTGTCTTG others(8): Show |
3 | a0001c0001t0001g0092 a0001c0001t0001g0123 a0001c0001t0001g0218 |
3 | HG02300.hp1 HG02602.hp2 NA18949.hp1 |
intron_variant | MODIFIER | c.32-20046_32-20045i others(17): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15936886 | ||||||
| chr12:15936886 | T | TTGTCTTG others(8): Show |
2 | a0001c0001t0001g0130 a0001c0001t0001g0211 |
2 | HG01496.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.32-20046_32-20045i others(17): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15936886 | ||||||
| chr12:15936886 | T | TTGTCTTG others(18): Show |
2 | a0001c0001t0001g0028 a0001c0001t0001g0029 |
2 | HG03130.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.32-20046_32-20045i others(27): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15936886 | ||||||
| chr12:15936886 | TTGTCC | T | 7 | a0001c0001t0001g0041 a0001c0001t0001g0079 a0001c0001t0004g0058 others(4): Show |
7 | HG01109.hp1 HG02055.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.32-20005_32-20001d others(7): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15936886 | ||||||
| chr12:15936887 | T | TGTCCCGT others(53): Show |
1 | a0001c0001t0001g0034 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.32-20045_32-20044i others(62): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15936887 | ||||||
| chr12:15936891 | C | T | 53 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(50): Show |
54 | HG00280.hp1 HG00280.hp2 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.32-20045C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15936891 | |||||||
| chr12:15936892 | T | C | 1 | a0001c0001t0001g0034 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.32-20044T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15936892 | |||||||
| chr12:15936896 | C | T | 50 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(47): Show |
51 | HG00280.hp1 HG00280.hp2 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.32-20040C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15936896 | |||||||
| chr12:15936897 | T | C | 1 | a0001c0001t0001g0034 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.32-20039T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15936897 | |||||||
| chr12:15936901 | C | T | 41 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(38): Show |
42 | HG00280.hp1 HG00280.hp2 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.32-20035C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15936901 | |||||||
| chr12:15936902 | T | C | 8 | a0001c0001t0001g0034 a0001c0001t0001g0210 a0001c0001t0002g0023 others(5): Show |
8 | HG00621.hp1 HG01891.hp2 HG02165.hp1 others(5): Show |
intron_variant | MODIFIER | c.32-20034T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15936902 | |||||||
| chr12:15936906 | C | T | 37 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(34): Show |
38 | HG00280.hp2 HG00735.hp1 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.32-20030C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15936906 | |||||||
| chr12:15936907 | T | C | 11 | a0001c0001t0001g0034 a0001c0001t0001g0102 a0001c0001t0001g0132 others(8): Show |
11 | HG00280.hp1 HG00621.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.32-20029T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15936907 | |||||||
| chr12:15936911 | C | T | 6 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(3): Show |
6 | HG01516.hp2 HG01884.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.32-20025C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15936911 | |||||||
| chr12:15936911 | CTGTCCTG others(18): Show |
C | 1 | a0001c0001t0001g0032 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.32-20014_32-19990d others(27): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15936911 | ||||||
| chr12:15936912 | T | C | 44 | a0001c0001t0001g0002 a0001c0001t0001g0034 a0001c0001t0001g0060 others(41): Show |
45 | HG00280.hp1 HG00280.hp2 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.32-20024T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15936912 | |||||||
| chr12:15936916 | C | T | 3 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0033 |
3 | HG01884.hp2 HG02258.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.32-20020C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15936916 | |||||||
| chr12:15936916 | CTGTCCTG others(13): Show |
C | 1 | a0001c0001t0001g0064 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.32-20009_32-19990d others(22): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15936916 | ||||||
| chr12:15936917 | T | C | 57 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0034 others(54): Show |
58 | HG00280.hp1 HG00280.hp2 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.32-20019T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15936917 | |||||||
| chr12:15936921 | C | T | 3 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0033 |
3 | HG01884.hp2 HG02258.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.32-20015C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15936921 | |||||||
| chr12:15936922 | T | C | 58 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0034 others(55): Show |
59 | HG00280.hp1 HG00280.hp2 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.32-20014T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15936922 | |||||||
| chr12:15936926 | C | T | 3 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0033 |
3 | HG01884.hp2 HG02258.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.32-20010C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15936926 | |||||||
| chr12:15936926 | CTGTCCTG others(3): Show |
C | 1 | a0001c0001t0001g0210 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.32-20000_32-19991d others(12): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15936926 | ||||||
| chr12:15936927 | T | C | 59 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0034 others(56): Show |
60 | HG00280.hp1 HG00280.hp2 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.32-20009T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15936927 | |||||||
| chr12:15936931 | C | T | 3 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0033 |
3 | HG01884.hp2 HG02258.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.32-20005C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15936931 | |||||||
| chr12:15936931 | CTGTCT | C | 8 | a0001c0001t0001g0102 a0001c0001t0001g0132 a0001c0001t0001g0208 others(5): Show |
8 | HG00280.hp1 HG00621.hp1 HG01167.hp2 others(5): Show |
intron_variant | MODIFIER | c.32-20000_32-19996d others(7): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15936931 | ||||||
| chr12:15936932 | T | C | 51 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0034 others(48): Show |
52 | HG00280.hp2 HG00735.hp1 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.32-20004T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15936932 | |||||||
| chr12:15936936 | T | C | 59 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0026 others(56): Show |
60 | HG00280.hp2 HG00735.hp1 HG00738.hp2 others(57): Show |
intron_variant | MODIFIER | c.32-20000T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15936936 | |||||||
| chr12:15936937 | T | C | 62 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0032 others(59): Show |
63 | HG00280.hp1 HG00280.hp2 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.32-19999T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15936937 | |||||||
| chr12:15936937 | T | TGTCCCGT others(28): Show |
1 | a0001c0001t0001g0007 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.32-19995_32-19994i others(37): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15936937 | ||||||
| chr12:15936937 | T | TGTCTTGT others(43): Show |
1 | a0001c0001t0001g0033 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.32-19996_32-19995i others(52): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15936937 | ||||||
| chr12:15936937 | T | TGTCTTGT others(53): Show |
1 | a0001c0001t0001g0008 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.32-19996_32-19995i others(62): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15936937 | ||||||
| chr12:15936942 | T | C | 65 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(62): Show |
66 | HG00280.hp1 HG00280.hp2 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.32-19994T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15936942 | |||||||
| chr12:15936947 | C | T | 8 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(5): Show |
8 | HG01109.hp2 HG02486.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.32-19989C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15936947 | |||||||
| chr12:15936952 | T | C | 69 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(66): Show |
70 | HG00280.hp1 HG00280.hp2 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.32-19984T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15936952 | |||||||
| chr12:15936953 | G | A | 4 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0174 others(1): Show |
4 | HG02257.hp2 HG02630.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.32-19983G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15936953 | |||||||
| chr12:15936957 | T | C | 20 | a0001c0001t0001g0034 a0001c0001t0001g0172 a0001c0001t0001g0173 others(17): Show |
20 | HG01891.hp2 HG02055.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.32-19979T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15936957 | |||||||
| chr12:15936957 | T | TGTCCTGT others(38): Show |
2 | a0001c0001t0001g0030 a0001c0001t0001g0031 |
2 | HG02886.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.32-19978_32-19977i others(47): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15936957 | ||||||
| chr12:15936957 | T | TGTCCTGT others(33): Show |
1 | a0001c0001t0001g0027 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.32-19978_32-19977i others(42): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15936957 | ||||||
| chr12:15936957 | T | TGTCCTGT others(28): Show |
1 | a0001c0001t0001g0026 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.32-19978_32-19977i others(37): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15936957 | ||||||
| chr12:15936959 | C | T | 21 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(18): Show |
21 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.32-19977C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15936959 | |||||||
| chr12:15936969 | C | T | 7 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0174 others(4): Show |
7 | HG02257.hp2 HG02559.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.32-19967C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15936969 | |||||||
| chr12:15936971 | C | T | 7 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0174 others(4): Show |
7 | HG02257.hp2 HG02559.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.32-19965C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15936971 | |||||||
| chr12:15937020 | C | T | 2 | a0002c0002t0003g0019 a0002c0002t0003g0021 |
2 | HG02630.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.32-19916C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15937020 | |||||||
| chr12:15937103 | C | T | 5 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0030 others(2): Show |
5 | HG01109.hp2 HG01891.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.32-19833C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15937103 | |||||||
| chr12:15937105 | C | A | 1 | a0001c0001t0005g0035 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.32-19831C>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15937105 | |||||||
| chr12:15937152 | C | T | 1 | a0001c0001t0001g0044 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.32-19784C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15937152 | |||||||
| chr12:15937459 | A | G | 1 | a0001c0001t0001g0129 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.32-19477A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15937459 | |||||||
| chr12:15937462 | G | C | 5 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0191 others(2): Show |
5 | HG01070.hp2 HG01074.hp2 HG01243.hp2 others(2): Show |
intron_variant | MODIFIER | c.32-19474G>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15937462 | |||||||
| chr12:15937677 | G | T | 1 | a0001c0001t0003g0018 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.32-19259G>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15937677 | |||||||
| chr12:15937796 | G | A | 2 | a0001c0001t0002g0023 a0001c0001t0002g0024 |
2 | NA18967.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.32-19140G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15937796 | |||||||
| chr12:15937966 | A | T | 5 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0030 others(2): Show |
5 | HG01109.hp2 HG01891.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.32-18970A>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15937966 | |||||||
| chr12:15938039 | C | T | 3 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0235 |
3 | HG02257.hp2 HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.32-18897C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15938039 | |||||||
| chr12:15938393 | C | G | 4 | a0001c0001t0001g0009 a0001c0001t0001g0207 a0001c0001t0001g0208 others(1): Show |
4 | HG02258.hp2 HG02615.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.32-18543C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15938393 | |||||||
| chr12:15938488 | A | T | 65 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(62): Show |
66 | HG00280.hp1 HG00280.hp2 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.32-18448A>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15938488 | |||||||
| chr12:15938698 | T | C | 1 | a0001c0001t0001g0103 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.32-18238T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15938698 | |||||||
| chr12:15938699 | G | A | 2 | a0001c0001t0002g0023 a0001c0001t0002g0024 |
2 | NA18967.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.32-18237G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15938699 | |||||||
| chr12:15939034 | A | G | 1 | a0001c0001t0001g0144 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.32-17902A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15939034 | |||||||
| chr12:15939624 | T | A | 1 | a0001c0001t0001g0133 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.32-17312T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15939624 | |||||||
| chr12:15940063 | C | T | 2 | a0001c0001t0001g0215 a0001c0001t0001g0251 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.32-16873C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15940063 | |||||||
| chr12:15940149 | C | T | 8 | a0001c0001t0003g0010 a0001c0001t0003g0012 a0001c0001t0003g0013 others(5): Show |
8 | HG02055.hp1 HG02109.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.32-16787C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15940149 | |||||||
| chr12:15940264 | C | G | 1 | a0001c0001t0001g0211 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.32-16672C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15940264 | |||||||
| chr12:15940341 | T | A | 2 | a0001c0001t0001g0206 a0001c0001t0005g0035 |
2 | HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.32-16595T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15940341 | |||||||
| chr12:15940444 | C | T | 1 | a0001c0001t0002g0097 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.32-16492C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15940444 | |||||||
| chr12:15940497 | G | A | 7 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0030 others(4): Show |
7 | HG01109.hp2 HG01891.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.32-16439G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15940497 | |||||||
| chr12:15940512 | T | C | 82 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(79): Show |
83 | HG00280.hp1 HG00280.hp2 HG00621.hp1 others(80): Show |
intron_variant | MODIFIER | c.32-16424T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15940512 | |||||||
| chr12:15940513 | G | A | 2 | a0001c0001t0001g0032 a0001c0001t0001g0064 |
2 | HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.32-16423G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15940513 | |||||||
| chr12:15940537 | G | A | 2 | a0001c0001t0002g0023 a0001c0001t0002g0024 |
2 | NA18967.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.32-16399G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15940537 | |||||||
| chr12:15940568 | G | C | 1 | a0001c0001t0001g0032 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.32-16368G>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15940568 | |||||||
| chr12:15940641 | G | A | 7 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0174 others(4): Show |
7 | HG02257.hp2 HG02559.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.32-16295G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15940641 | |||||||
| chr12:15941196 | G | A | 5 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0030 others(2): Show |
5 | HG01109.hp2 HG01891.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.32-15740G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15941196 | |||||||
| chr12:15941227 | G | A | 82 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(79): Show |
83 | HG00280.hp1 HG00280.hp2 HG00621.hp1 others(80): Show |
intron_variant | MODIFIER | c.32-15709G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15941227 | |||||||
| chr12:15941242 | C | G | 2 | a0001c0001t0002g0023 a0001c0001t0002g0024 |
2 | NA18967.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.32-15694C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15941242 | |||||||
| chr12:15941448 | A | G | 1 | a0001c0001t0001g0155 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.32-15488A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15941448 | |||||||
| chr12:15941565 | C | A | 4 | a0001c0001t0001g0009 a0001c0001t0001g0207 a0001c0001t0001g0208 others(1): Show |
4 | HG02258.hp2 HG02615.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.32-15371C>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15941565 | |||||||
| chr12:15941625 | G | A | 2 | a0002c0002t0003g0019 a0002c0002t0003g0021 |
2 | HG02630.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.32-15311G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15941625 | |||||||
| chr12:15941661 | C | T | 8 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0046 others(5): Show |
8 | HG02630.hp2 HG02647.hp1 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.32-15275C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15941661 | |||||||
| chr12:15941683 | A | G | 2 | a0002c0002t0003g0019 a0002c0002t0003g0021 |
2 | HG02630.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.32-15253A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15941683 | |||||||
| chr12:15941793 | T | C | 3 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0033 |
3 | HG01884.hp2 HG02258.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.32-15143T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15941793 | |||||||
| chr12:15941795 | C | T | 1 | a0001c0001t0001g0034 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.32-15141C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15941795 | |||||||
| chr12:15941890 | A | G | 8 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0046 others(5): Show |
8 | HG02630.hp2 HG02647.hp1 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.32-15046A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15941890 | |||||||
| chr12:15942014 | A | G | 2 | a0002c0002t0003g0019 a0002c0002t0003g0021 |
2 | HG02630.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.32-14922A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15942014 | |||||||
| chr12:15942159 | C | G | 1 | a0001c0001t0001g0001 | 2 | HG01123.hp2 HG01256.hp2 |
intron_variant | MODIFIER | c.32-14777C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15942159 | |||||||
| chr12:15942470 | T | C | 1 | a0001c0001t0001g0104 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.32-14466T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15942470 | |||||||
| chr12:15942614 | A | G | 6 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0046 others(3): Show |
6 | HG02647.hp1 HG03130.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.32-14322A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15942614 | |||||||
| chr12:15942676 | T | G | 7 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0174 others(4): Show |
7 | HG02257.hp2 HG02559.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.32-14260T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15942676 | |||||||
| chr12:15942771 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.32-14165G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15942771 | |||||||
| chr12:15942783 | G | C | 1 | a0001c0001t0001g0120 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.32-14153G>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15942783 | |||||||
| chr12:15942820 | G | C | 2 | a0001c0001t0002g0023 a0001c0001t0002g0024 |
2 | NA18967.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.32-14116G>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15942820 | |||||||
| chr12:15942938 | C | A | 1 | a0001c0001t0001g0118 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.32-13998C>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15942938 | |||||||
| chr12:15943059 | C | T | 67 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(64): Show |
68 | HG00280.hp1 HG00280.hp2 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.32-13877C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15943059 | |||||||
| chr12:15943276 | C | G | 1 | a0001c0001t0001g0136 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.32-13660C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15943276 | |||||||
| chr12:15943294 | T | G | 3 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0005 |
3 | HG02559.hp2 HG03516.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.32-13642T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15943294 | |||||||
| chr12:15943492 | A | T | 6 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0046 others(3): Show |
6 | HG02647.hp1 HG03130.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.32-13444A>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15943492 | |||||||
| chr12:15943561 | C | T | 2 | a0001c0001t0001g0039 a0001c0001t0003g0006 |
2 | HG00733.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.32-13375C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15943561 | |||||||
| chr12:15943563 | T | G | 82 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(79): Show |
83 | HG00280.hp1 HG00280.hp2 HG00621.hp1 others(80): Show |
intron_variant | MODIFIER | c.32-13373T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15943563 | |||||||
| chr12:15943576 | T | C | 1 | a0001c0001t0001g0079 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.32-13360T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15943576 | |||||||
| chr12:15943701 | T | A | 1 | a0001c0001t0001g0218 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.32-13235T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15943701 | |||||||
| chr12:15943703 | A | T | 1 | a0001c0001t0001g0218 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.32-13233A>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15943703 | |||||||
| chr12:15943705 | T | TTTATTTA others(4): Show |
1 | a0001c0001t0001g0218 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.32-13229_32-13228i others(13): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15943705 | ||||||
| chr12:15943705 | T | TTTTA | 71 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(68): Show |
72 | HG00280.hp1 HG00280.hp2 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.32-13199_32-13196d others(6): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15943705 | ||||||
| chr12:15943705 | T | TTTTATTT others(1): Show |
31 | a0001c0001t0001g0022 a0001c0001t0001g0026 a0001c0001t0001g0030 others(28): Show |
31 | HG00735.hp2 HG01070.hp2 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.32-13203_32-13196d others(10): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15943705 | ||||||
| chr12:15943705 | T | TTTTATTT others(5): Show |
2 | a0001c0001t0001g0182 a0001c0001t0001g0183 |
2 | HG01081.hp2 NA18949.hp2 |
intron_variant | MODIFIER | c.32-13207_32-13196d others(14): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15943705 | ||||||
| chr12:15943705 | T | TTTTATTT others(9): Show |
1 | a0001c0001t0001g0120 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.32-13211_32-13196d others(18): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15943705 | ||||||
| chr12:15943705 | TTTTA | T | 15 | a0001c0001t0001g0107 a0001c0001t0001g0128 a0001c0001t0001g0172 others(12): Show |
15 | HG02015.hp1 HG02257.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.32-13199_32-13196d others(6): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15943705 | ||||||
| chr12:15943705 | TTTTATTT others(5): Show |
T | 2 | a0002c0002t0003g0019 a0002c0002t0003g0021 |
2 | HG02630.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.32-13207_32-13196d others(14): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15943705 | ||||||
| chr12:15943835 | C | T | 3 | a0001c0001t0005g0036 a0001c0001t0005g0037 a0001c0001t0005g0038 |
3 | HG01109.hp1 HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.32-13101C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15943835 | |||||||
| chr12:15943877 | C | G | 2 | a0002c0002t0003g0019 a0002c0002t0003g0021 |
2 | HG02630.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.32-13059C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15943877 | |||||||
| chr12:15943920 | T | G | 48 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(45): Show |
49 | HG00280.hp1 HG00280.hp2 HG00621.hp1 others(46): Show |
intron_variant | MODIFIER | c.32-13016T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15943920 | |||||||
| chr12:15943942 | T | C | 1 | a0001c0001t0001g0034 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.32-12994T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15943942 | |||||||
| chr12:15944036 | T | C | 12 | a0001c0001t0001g0075 a0001c0001t0001g0107 a0001c0001t0001g0113 others(9): Show |
12 | HG00621.hp2 HG02015.hp1 HG02132.hp2 others(9): Show |
intron_variant | MODIFIER | c.32-12900T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15944036 | |||||||
| chr12:15944074 | C | G | 1 | a0001c0001t0001g0183 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.32-12862C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15944074 | |||||||
| chr12:15944078 | T | A | 1 | a0001c0001t0006g0011 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.32-12858T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15944078 | |||||||
| chr12:15944141 | G | A | 41 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(38): Show |
42 | HG00280.hp1 HG00280.hp2 HG00621.hp1 others(39): Show |
intron_variant | MODIFIER | c.32-12795G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15944141 | |||||||
| chr12:15944197 | A | C | 4 | a0001c0001t0001g0009 a0001c0001t0001g0207 a0001c0001t0001g0208 others(1): Show |
4 | HG02258.hp2 HG02615.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.32-12739A>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15944197 | |||||||
| chr12:15944299 | G | A | 1 | a0001c0001t0001g0254 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.32-12637G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15944299 | |||||||
| chr12:15944377 | C | T | 8 | a0001c0001t0003g0010 a0001c0001t0003g0012 a0001c0001t0003g0013 others(5): Show |
8 | HG02055.hp1 HG02109.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.32-12559C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15944377 | |||||||
| chr12:15944416 | C | A | 1 | a0001c0001t0003g0018 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.32-12520C>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15944416 | |||||||
| chr12:15944556 | G | A | 1 | a0001c0001t0001g0092 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.32-12380G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15944556 | |||||||
| chr12:15944791 | T | G | 8 | a0001c0001t0003g0010 a0001c0001t0003g0012 a0001c0001t0003g0013 others(5): Show |
8 | HG02055.hp1 HG02109.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.32-12145T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15944791 | |||||||
| chr12:15945335 | C | G | 7 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0174 others(4): Show |
7 | HG02257.hp2 HG02559.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.32-11601C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15945335 | |||||||
| chr12:15945462 | A | T | 1 | a0001c0001t0001g0210 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.32-11474A>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15945462 | |||||||
| chr12:15945492 | A | G | 1 | a0001c0001t0002g0253 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.32-11444A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15945492 | |||||||
| chr12:15945595 | G | T | 5 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0030 others(2): Show |
5 | HG01109.hp2 HG01891.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.32-11341G>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15945595 | |||||||
| chr12:15945659 | G | A | 4 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0174 others(1): Show |
4 | HG02257.hp2 HG02630.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.32-11277G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15945659 | |||||||
| chr12:15945746 | G | A | 1 | a0001c0001t0003g0018 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.32-11190G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15945746 | |||||||
| chr12:15946191 | C | T | 3 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0005 |
3 | HG02559.hp2 HG03516.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.32-10745C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15946191 | |||||||
| chr12:15946291 | T | A | 5 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0030 others(2): Show |
5 | HG01109.hp2 HG01891.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.32-10645T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15946291 | |||||||
| chr12:15946569 | G | T | 8 | a0001c0001t0003g0010 a0001c0001t0003g0012 a0001c0001t0003g0013 others(5): Show |
8 | HG02055.hp1 HG02109.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.32-10367G>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15946569 | |||||||
| chr12:15946580 | T | C | 12 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0046 others(9): Show |
12 | HG02257.hp2 HG02559.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.32-10356T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15946580 | |||||||
| chr12:15946612 | C | G | 1 | a0001c0001t0001g0211 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.32-10324C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15946612 | |||||||
| chr12:15946777 | G | A | 1 | a0001c0001t0002g0168 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.32-10159G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15946777 | |||||||
| chr12:15946782 | C | T | 6 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0046 others(3): Show |
6 | HG02647.hp1 HG03130.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.32-10154C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15946782 | |||||||
| chr12:15946954 | T | A | 2 | a0002c0002t0003g0019 a0002c0002t0003g0021 |
2 | HG02630.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.32-9982T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15946954 | |||||||
| chr12:15947294 | G | A | 67 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(64): Show |
68 | HG00280.hp1 HG00280.hp2 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.32-9642G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15947294 | |||||||
| chr12:15947403 | C | T | 1 | a0001c0001t0001g0022 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.32-9533C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15947403 | |||||||
| chr12:15947436 | G | A | 1 | a0001c0001t0001g0102 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.32-9500G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15947436 | |||||||
| chr12:15947542 | A | T | 83 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(80): Show |
84 | HG00280.hp1 HG00280.hp2 HG00621.hp1 others(81): Show |
intron_variant | MODIFIER | c.32-9394A>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15947542 | |||||||
| chr12:15947566 | T | C | 1 | a0001c0001t0001g0252 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.32-9370T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15947566 | |||||||
| chr12:15947615 | A | G | 6 | a0001c0001t0001g0198 a0001c0001t0001g0200 a0001c0001t0001g0202 others(3): Show |
6 | HG02080.hp1 HG02135.hp2 NA18942.hp2 others(3): Show |
intron_variant | MODIFIER | c.32-9321A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15947615 | |||||||
| chr12:15947623 | C | T | 1 | a0001c0001t0001g0174 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.32-9313C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15947623 | |||||||
| chr12:15947649 | T | C | 1 | a0001c0001t0001g0052 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.32-9287T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15947649 | |||||||
| chr12:15947737 | T | C | 1 | a0001c0001t0001g0057 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.32-9199T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15947737 | |||||||
| chr12:15947744 | C | T | 8 | a0001c0001t0003g0010 a0001c0001t0003g0012 a0001c0001t0003g0013 others(5): Show |
8 | HG02055.hp1 HG02109.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.32-9192C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15947744 | |||||||
| chr12:15947811 | C | G | 1 | a0001c0001t0001g0088 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.32-9125C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15947811 | |||||||
| chr12:15947862 | A | G | 3 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0246 |
3 | HG02258.hp2 HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.32-9074A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15947862 | |||||||
| chr12:15947945 | A | T | 2 | a0001c0003t0001g0073 a0001c0003t0004g0072 |
2 | HG06807.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.32-8991A>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15947945 | |||||||
| chr12:15948035 | T | G | 2 | a0001c0001t0001g0151 a0001c0001t0001g0165 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.32-8901T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15948035 | |||||||
| chr12:15948198 | G | A | 1 | a0001c0001t0001g0219 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.32-8738G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15948198 | |||||||
| chr12:15948240 | A | G | 1 | a0001c0001t0003g0005 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.32-8696A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15948240 | |||||||
| chr12:15948285 | T | A | 2 | a0001c0001t0001g0039 a0001c0001t0003g0006 |
2 | HG00733.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.32-8651T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15948285 | |||||||
| chr12:15948365 | C | T | 11 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(8): Show |
11 | HG01109.hp2 HG01891.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.32-8571C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15948365 | |||||||
| chr12:15948686 | T | G | 1 | a0001c0001t0001g0001 | 2 | HG01123.hp2 HG01256.hp2 |
intron_variant | MODIFIER | c.32-8250T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15948686 | |||||||
| chr12:15948708 | C | G | 5 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0030 others(2): Show |
5 | HG01109.hp2 HG01891.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.32-8228C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15948708 | |||||||
| chr12:15948712 | C | G | 1 | a0001c0001t0001g0249 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.32-8224C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15948712 | |||||||
| chr12:15948719 | C | T | 2 | a0002c0002t0003g0019 a0002c0002t0003g0021 |
2 | HG02630.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.32-8217C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15948719 | |||||||
| chr12:15948784 | A | T | 1 | a0001c0001t0001g0205 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.32-8152A>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15948784 | |||||||
| chr12:15949012 | C | T | 5 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0030 others(2): Show |
5 | HG01109.hp2 HG01891.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.32-7924C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15949012 | |||||||
| chr12:15949353 | C | T | 6 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0046 others(3): Show |
6 | HG02647.hp1 HG03130.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.32-7583C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15949353 | |||||||
| chr12:15949458 | A | AGGCTCCG others(2): Show |
52 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(49): Show |
53 | HG00280.hp1 HG00280.hp2 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.32-7477_32-7476ins others(9): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15949458 | ||||||
| chr12:15949460 | C | G | 52 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(49): Show |
53 | HG00280.hp1 HG00280.hp2 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.32-7476C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15949460 | |||||||
| chr12:15949461 | A | C | 52 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(49): Show |
53 | HG00280.hp1 HG00280.hp2 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.32-7475A>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15949461 | |||||||
| chr12:15949462 | A | G | 52 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(49): Show |
53 | HG00280.hp1 HG00280.hp2 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.32-7474A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15949462 | |||||||
| chr12:15949482 | G | A | 8 | a0001c0001t0001g0085 a0001c0001t0001g0172 a0001c0001t0001g0173 others(5): Show |
8 | HG02257.hp2 HG02559.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.32-7454G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15949482 | |||||||
| chr12:15949493 | T | C | 82 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(79): Show |
83 | HG00280.hp1 HG00280.hp2 HG00621.hp1 others(80): Show |
intron_variant | MODIFIER | c.32-7443T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15949493 | |||||||
| chr12:15949540 | G | A | 3 | a0001c0001t0001g0041 a0001c0001t0001g0215 a0001c0001t0001g0251 |
3 | HG02647.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.32-7396G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15949540 | |||||||
| chr12:15949674 | C | T | 5 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0030 others(2): Show |
5 | HG01109.hp2 HG01891.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.32-7262C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15949674 | |||||||
| chr12:15949739 | G | A | 1 | a0003c0004t0001g0225 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.32-7197G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15949739 | |||||||
| chr12:15949815 | C | T | 1 | a0001c0001t0004g0116 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.32-7121C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15949815 | |||||||
| chr12:15949872 | C | T | 67 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(64): Show |
68 | HG00280.hp1 HG00280.hp2 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.32-7064C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15949872 | |||||||
| chr12:15949894 | T | G | 6 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0046 others(3): Show |
6 | HG02647.hp1 HG03130.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.32-7042T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15949894 | |||||||
| chr12:15949983 | G | A | 12 | a0001c0001t0001g0075 a0001c0001t0001g0107 a0001c0001t0001g0113 others(9): Show |
12 | HG00621.hp2 HG02015.hp1 HG02132.hp2 others(9): Show |
intron_variant | MODIFIER | c.32-6953G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15949983 | |||||||
| chr12:15950270 | A | G | 1 | a0001c0001t0003g0018 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.32-6666A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15950270 | |||||||
| chr12:15950281 | A | G | 82 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(79): Show |
83 | HG00280.hp1 HG00280.hp2 HG00621.hp1 others(80): Show |
intron_variant | MODIFIER | c.32-6655A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15950281 | |||||||
| chr12:15950407 | C | G | 2 | a0001c0001t0002g0023 a0001c0001t0002g0024 |
2 | NA18967.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.32-6529C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15950407 | |||||||
| chr12:15950478 | A | G | 2 | a0001c0001t0001g0254 a0001c0001t0001g0255 |
2 | HG00544.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.32-6458A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15950478 | |||||||
| chr12:15950723 | C | T | 1 | a0001c0001t0001g0050 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.32-6213C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15950723 | |||||||
| chr12:15950795 | A | T | 4 | a0001c0001t0002g0147 a0001c0001t0002g0148 a0001c0001t0002g0154 others(1): Show |
4 | HG00621.hp1 HG02165.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.32-6141A>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15950795 | |||||||
| chr12:15950876 | A | T | 13 | a0001c0001t0001g0075 a0001c0001t0001g0107 a0001c0001t0001g0113 others(10): Show |
13 | HG00621.hp2 HG02015.hp1 HG02132.hp2 others(10): Show |
intron_variant | MODIFIER | c.32-6060A>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15950876 | |||||||
| chr12:15950878 | C | T | 13 | a0001c0001t0001g0075 a0001c0001t0001g0107 a0001c0001t0001g0113 others(10): Show |
13 | HG00621.hp2 HG02015.hp1 HG02132.hp2 others(10): Show |
intron_variant | MODIFIER | c.32-6058C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15950878 | |||||||
| chr12:15951017 | T | A | 1 | a0001c0001t0001g0255 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.32-5919T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15951017 | |||||||
| chr12:15951137 | A | C | 1 | a0001c0001t0001g0069 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.32-5799A>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15951137 | |||||||
| chr12:15951226 | C | T | 1 | a0001c0001t0001g0162 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.32-5710C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15951226 | |||||||
| chr12:15951256 | T | G | 3 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0110 |
3 | HG02818.hp1 HG02895.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.32-5680T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15951256 | |||||||
| chr12:15951257 | G | C | 4 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0174 others(1): Show |
4 | HG02257.hp2 HG02630.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.32-5679G>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15951257 | |||||||
| chr12:15951357 | T | G | 10 | a0001c0001t0001g0094 a0001c0001t0001g0096 a0001c0001t0001g0099 others(7): Show |
10 | HG00642.hp2 HG00738.hp1 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.32-5579T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15951357 | |||||||
| chr12:15951514 | C | T | 1 | a0001c0001t0001g0197 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.32-5422C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15951514 | |||||||
| chr12:15951518 | T | G | 1 | a0001c0001t0001g0233 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.32-5418T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15951518 | |||||||
| chr12:15951737 | T | C | 5 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0030 others(2): Show |
5 | HG01109.hp2 HG01891.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.32-5199T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15951737 | |||||||
| chr12:15951938 | G | C | 1 | a0001c0001t0001g0064 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.32-4998G>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15951938 | |||||||
| chr12:15951972 | G | A | 1 | a0001c0001t0001g0195 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.32-4964G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15951972 | |||||||
| chr12:15951995 | A | C | 1 | a0001c0001t0001g0129 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.32-4941A>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15951995 | |||||||
| chr12:15952024 | C | T | 5 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0046 others(2): Show |
5 | HG03130.hp2 HG03471.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.32-4912C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15952024 | |||||||
| chr12:15952118 | C | G | 4 | a0001c0001t0002g0147 a0001c0001t0002g0148 a0001c0001t0002g0154 others(1): Show |
4 | HG00621.hp1 HG02165.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.32-4818C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15952118 | |||||||
| chr12:15952134 | C | T | 52 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(49): Show |
53 | HG00280.hp1 HG00280.hp2 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.32-4802C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15952134 | |||||||
| chr12:15952255 | A | G | 2 | a0002c0002t0003g0019 a0002c0002t0003g0021 |
2 | HG02630.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.32-4681A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15952255 | |||||||
| chr12:15952311 | G | A | 1 | a0001c0001t0001g0113 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.32-4625G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15952311 | |||||||
| chr12:15952433 | C | T | 1 | a0001c0001t0001g0144 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.32-4503C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15952433 | |||||||
| chr12:15952610 | T | C | 1 | a0001c0001t0001g0052 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.32-4326T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15952610 | |||||||
| chr12:15952635 | C | A | 3 | a0001c0001t0002g0140 a0001c0001t0002g0152 a0001c0001t0002g0217 |
3 | NA19000.hp1 NA19070.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.32-4301C>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15952635 | |||||||
| chr12:15952636 | G | A | 1 | a0001c0001t0001g0133 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.32-4300G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15952636 | |||||||
| chr12:15952816 | A | G | 1 | a0001c0001t0001g0249 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.32-4120A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15952816 | |||||||
| chr12:15953168 | T | G | 2 | a0001c0003t0001g0073 a0001c0003t0004g0072 |
2 | HG06807.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.32-3768T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15953168 | |||||||
| chr12:15953296 | G | A | 3 | a0001c0001t0001g0074 a0001c0001t0001g0177 a0001c0001t0001g0183 |
3 | HG01074.hp1 HG01081.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.32-3640G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15953296 | |||||||
| chr12:15953589 | A | G | 52 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(49): Show |
53 | HG00280.hp1 HG00280.hp2 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.32-3347A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15953589 | |||||||
| chr12:15953614 | A | C | 5 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0030 others(2): Show |
5 | HG01109.hp2 HG01891.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.32-3322A>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15953614 | |||||||
| chr12:15953813 | A | G | 1 | a0001c0001t0001g0077 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.32-3123A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15953813 | |||||||
| chr12:15953942 | T | C | 7 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0174 others(4): Show |
7 | HG02257.hp2 HG02559.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.32-2994T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15953942 | |||||||
| chr12:15954034 | T | C | 2 | a0001c0001t0001g0084 a0001c0001t0001g0214 |
2 | HG02559.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.32-2902T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15954034 | |||||||
| chr12:15954038 | T | C | 2 | a0001c0001t0001g0055 a0001c0001t0001g0170 |
2 | HG01358.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.32-2898T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15954038 | |||||||
| chr12:15954279 | A | G | 1 | a0001c0001t0001g0102 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.32-2657A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15954279 | |||||||
| chr12:15954280 | T | C | 1 | a0001c0001t0001g0051 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.32-2656T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15954280 | |||||||
| chr12:15954412 | C | G | 7 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0174 others(4): Show |
7 | HG02257.hp2 HG02559.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.32-2524C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15954412 | |||||||
| chr12:15954772 | G | A | 6 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0046 others(3): Show |
6 | HG02647.hp1 HG03130.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.32-2164G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15954772 | |||||||
| chr12:15954801 | G | T | 1 | a0001c0001t0001g0193 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.32-2135G>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15954801 | |||||||
| chr12:15954866 | C | T | 1 | a0001c0001t0003g0014 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.32-2070C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15954866 | |||||||
| chr12:15955078 | T | C | 2 | a0001c0001t0001g0083 a0001c0001t0001g0129 |
2 | HG02486.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.32-1858T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15955078 | |||||||
| chr12:15955089 | C | T | 2 | a0002c0002t0003g0019 a0002c0002t0003g0021 |
2 | HG02630.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.32-1847C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15955089 | |||||||
| chr12:15955117 | T | C | 2 | a0001c0001t0001g0032 a0001c0001t0001g0064 |
2 | HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.32-1819T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15955117 | |||||||
| chr12:15955166 | G | C | 3 | a0001c0001t0001g0074 a0001c0001t0001g0177 a0001c0001t0001g0183 |
3 | HG01074.hp1 HG01081.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.32-1770G>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15955166 | |||||||
| chr12:15955170 | C | T | 4 | a0001c0001t0001g0085 a0001c0001t0001g0087 a0001c0001t0001g0088 others(1): Show |
4 | HG02809.hp2 HG02965.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.32-1766C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15955170 | |||||||
| chr12:15955254 | G | T | 1 | a0001c0001t0001g0041 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.32-1682G>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15955254 | |||||||
| chr12:15955261 | T | G | 2 | a0001c0001t0001g0172 a0001c0001t0001g0173 |
2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.32-1675T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15955261 | |||||||
| chr12:15955296 | GA | G | 6 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0046 others(3): Show |
6 | HG01261.hp1 HG03130.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.32-1626delA | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15955296 | ||||||
| chr12:15955795 | A | G | 4 | a0001c0001t0002g0147 a0001c0001t0002g0148 a0001c0001t0002g0154 others(1): Show |
4 | HG00621.hp1 HG02165.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.32-1141A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15955795 | |||||||
| chr12:15956013 | T | C | 1 | a0001c0001t0001g0129 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.32-923T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15956013 | |||||||
| chr12:15956070 | A | G | 2 | a0002c0002t0003g0019 a0002c0002t0003g0021 |
2 | HG02630.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.32-866A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15956070 | |||||||
| chr12:15956416 | A | T | 1 | a0001c0001t0001g0176 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.32-520A>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15956416 | |||||||
| chr12:15956483 | G | A | 2 | a0001c0001t0001g0144 a0001c0001t0001g0167 |
2 | HG02273.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.32-453G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15956483 | |||||||
| chr12:15956525 | A | G | 6 | a0001c0001t0001g0094 a0001c0001t0001g0096 a0001c0001t0001g0099 others(3): Show |
6 | NA18747.hp1 NA18943.hp2 NA18975.hp2 others(3): Show |
intron_variant | MODIFIER | c.32-411A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15956525 | |||||||
| chr12:15956739 | T | G | 21 | a0001c0001t0001g0022 a0001c0001t0001g0048 a0001c0001t0001g0074 others(18): Show |
21 | HG00735.hp2 HG01070.hp2 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.32-197T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15956739 | |||||||
| chr12:15957240 | T | A | 48 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(45): Show |
49 | HG00280.hp1 HG00280.hp2 HG00621.hp1 others(46): Show |
intron_variant | MODIFIER | c.129+207T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 2/8 | chr12 | 15957240 | |||||||
| chr12:15957324 | G | A | 5 | a0001c0001t0001g0094 a0001c0001t0001g0096 a0001c0001t0001g0099 others(2): Show |
5 | NA18943.hp2 NA18975.hp2 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.129+291G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 2/8 | chr12 | 15957324 | |||||||
| chr12:15957516 | G | A | 2 | a0001c0001t0002g0023 a0001c0001t0002g0024 |
2 | NA18967.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.129+483G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 2/8 | chr12 | 15957516 | |||||||
| chr12:15957551 | C | T | 1 | a0001c0001t0001g0098 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.129+518C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 2/8 | chr12 | 15957551 | |||||||
| chr12:15957675 | G | A | 8 | a0001c0001t0003g0010 a0001c0001t0003g0012 a0001c0001t0003g0013 others(5): Show |
8 | HG02055.hp1 HG02109.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.130-513G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 2/8 | chr12 | 15957675 | |||||||
| chr12:15957918 | G | A | 5 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0030 others(2): Show |
5 | HG01109.hp2 HG01891.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.130-270G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 2/8 | chr12 | 15957918 | |||||||
| chr12:15958514 | CT | C | 164 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(161): Show |
165 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(162): Show |
intron_variant | MODIFIER | c.277+198delT | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 15958514 | ||||||
| chr12:15958663 | C | T | 1 | a0001c0001t0003g0018 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.277+328C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 3/8 | chr12 | 15958663 | |||||||
| chr12:15959131 | G | A | 1 | a0001c0001t0001g0209 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.278-698G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 3/8 | chr12 | 15959131 | |||||||
| chr12:15959426 | T | C | 1 | a0001c0001t0001g0145 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.278-403T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 3/8 | chr12 | 15959426 | |||||||
| chr12:15959820 | T | C | 2 | a0002c0002t0003g0019 a0002c0002t0003g0021 |
2 | HG02630.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.278-9T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 3/8 | chr12 | 15959820 | |||||||
| chr12:15959958 | T | A | 1 | a0001c0001t0002g0161 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.373+34T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 4/8 | chr12 | 15959958 | |||||||
| chr12:15959964 | T | C | 7 | a0001c0001t0001g0057 a0001c0001t0001g0084 a0001c0001t0001g0085 others(4): Show |
7 | HG02559.hp1 HG02809.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.373+40T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 4/8 | chr12 | 15959964 | |||||||
| chr12:15960020 | A | G | 2 | a0001c0001t0001g0095 a0001c0001t0001g0230 |
2 | HG00735.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.373+96A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 4/8 | chr12 | 15960020 | |||||||
| chr12:15960207 | T | C | 77 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(74): Show |
78 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.373+283T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 4/8 | chr12 | 15960207 | |||||||
| chr12:15960273 | T | C | 2 | a0001c0001t0001g0055 a0001c0001t0001g0170 |
2 | HG01358.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.373+349T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 4/8 | chr12 | 15960273 | |||||||
| chr12:15960362 | G | A | 1 | a0001c0001t0001g0189 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.373+438G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 4/8 | chr12 | 15960362 | |||||||
| chr12:15960636 | C | CA | 52 | a0001c0001t0001g0041 a0001c0001t0001g0043 a0001c0001t0001g0044 others(49): Show |
52 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.373+739dupA | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | 15960636 | ||||||
| chr12:15960636 | C | CAA | 18 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0042 others(15): Show |
18 | HG01168.hp1 HG01516.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.373+738_373+739dup others(2): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | 15960636 | ||||||
| chr12:15960636 | C | CAAA | 20 | a0001c0001t0001g0029 a0001c0001t0001g0040 a0001c0001t0001g0065 others(17): Show |
20 | HG00280.hp1 HG00280.hp2 HG00642.hp2 others(17): Show |
intron_variant | MODIFIER | c.373+737_373+739dup others(3): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | 15960636 | ||||||
| chr12:15960636 | C | CAAAA | 23 | a0001c0001t0001g0009 a0001c0001t0001g0028 a0001c0001t0001g0032 others(20): Show |
23 | HG00738.hp2 HG01361.hp2 HG01978.hp2 others(20): Show |
intron_variant | MODIFIER | c.373+736_373+739dup others(4): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | 15960636 | ||||||
| chr12:15960636 | C | CAAAAA | 6 | a0001c0001t0001g0002 a0001c0001t0001g0084 a0001c0001t0001g0130 others(3): Show |
7 | HG01070.hp1 HG01071.hp1 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.373+735_373+739dup others(5): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | 15960636 | ||||||
| chr12:15960636 | CA | C | 14 | a0001c0001t0001g0001 a0001c0001t0001g0026 a0001c0001t0001g0027 others(11): Show |
15 | HG00642.hp1 HG01071.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.373+739delA | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | 15960636 | ||||||
| chr12:15960636 | CAAAAAAA others(4): Show |
C | 6 | a0001c0001t0001g0206 a0001c0001t0002g0147 a0001c0001t0002g0148 others(3): Show |
6 | HG00621.hp1 HG02165.hp1 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.373+729_373+739del others(11): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | 15960636 | ||||||
| chr12:15960691 | C | T | 4 | a0001c0001t0001g0009 a0001c0001t0001g0207 a0001c0001t0001g0208 others(1): Show |
4 | HG02258.hp2 HG02615.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.373+767C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 4/8 | chr12 | 15960691 | |||||||
| chr12:15960849 | C | T | 4 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0174 others(1): Show |
4 | HG02257.hp2 HG02630.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.373+925C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 4/8 | chr12 | 15960849 | |||||||
| chr12:15960887 | G | T | 1 | a0001c0001t0002g0024 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.373+963G>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 4/8 | chr12 | 15960887 | |||||||
| chr12:15961293 | A | G | 15 | a0001c0001t0001g0009 a0001c0001t0001g0053 a0001c0001t0001g0157 others(12): Show |
15 | HG02080.hp1 HG02135.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.373+1369A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 4/8 | chr12 | 15961293 | |||||||
| chr12:15961393 | G | C | 1 | a0001c0001t0001g0079 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.374-1420G>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 4/8 | chr12 | 15961393 | |||||||
| chr12:15961446 | C | T | 5 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0082 others(2): Show |
5 | HG00733.hp2 HG01081.hp1 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.374-1367C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 4/8 | chr12 | 15961446 | |||||||
| chr12:15961506 | AAAAAT | A | 11 | a0001c0001t0001g0085 a0001c0001t0001g0115 a0001c0001t0003g0010 others(8): Show |
11 | HG02055.hp1 HG02109.hp2 HG02965.hp1 others(8): Show |
intron_variant | MODIFIER | c.374-1299_374-1295d others(7): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | 15961506 | ||||||
| chr12:15961596 | A | G | 1 | a0001c0001t0001g0033 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.374-1217A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 4/8 | chr12 | 15961596 | |||||||
| chr12:15961664 | A | G | 53 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(50): Show |
54 | HG00280.hp1 HG00280.hp2 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.374-1149A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 4/8 | chr12 | 15961664 | |||||||
| chr12:15961962 | T | G | 1 | a0001c0001t0001g0079 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.374-851T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 4/8 | chr12 | 15961962 | |||||||
| chr12:15962430 | G | A | 1 | a0001c0001t0001g0022 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.374-383G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 4/8 | chr12 | 15962430 | |||||||
| chr12:15962617 | C | T | 1 | a0001c0001t0001g0102 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.374-196C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 4/8 | chr12 | 15962617 | |||||||
| chr12:15962808 | A | C | 5 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0191 others(2): Show |
5 | HG01070.hp2 HG01074.hp2 HG01243.hp2 others(2): Show |
splice_region_variant&intron_variant | LOW | c.374-5A>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 4/8 | chr12 | 15962808 | |||||||
| chr12:15963022 | A | G | 1 | a0001c0001t0001g0033 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.508+75A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15963022 | |||||||
| chr12:15963243 | C | A | 7 | a0001c0001t0001g0053 a0001c0001t0001g0157 a0001c0001t0001g0178 others(4): Show |
7 | NA18942.hp1 NA18950.hp1 NA18975.hp1 others(4): Show |
intron_variant | MODIFIER | c.508+296C>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15963243 | |||||||
| chr12:15963257 | A | T | 9 | a0001c0001t0001g0085 a0001c0001t0003g0010 a0001c0001t0003g0012 others(6): Show |
9 | HG02055.hp1 HG02109.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.508+310A>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15963257 | |||||||
| chr12:15963270 | C | G | 3 | a0001c0001t0005g0036 a0001c0001t0005g0037 a0001c0001t0005g0038 |
3 | HG01109.hp1 HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.508+323C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15963270 | |||||||
| chr12:15963444 | G | A | 1 | a0001c0001t0001g0026 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.508+497G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15963444 | |||||||
| chr12:15963685 | C | T | 102 | a0001c0001t0001g0025 a0001c0001t0001g0039 a0001c0001t0001g0040 others(99): Show |
102 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.508+738C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15963685 | |||||||
| chr12:15963722 | A | G | 14 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0030 others(11): Show |
14 | HG01109.hp2 HG01891.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.508+775A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15963722 | |||||||
| chr12:15963876 | TCTGTATC others(8): Show |
T | 5 | a0001c0001t0001g0009 a0001c0001t0001g0083 a0001c0001t0003g0003 others(2): Show |
5 | HG02559.hp2 HG02886.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.508+932_508+946del others(15): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 15963876 | ||||||
| chr12:15963976 | G | C | 1 | a0001c0001t0001g0033 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.508+1029G>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15963976 | |||||||
| chr12:15964053 | G | A | 1 | a0001c0001t0001g0033 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.508+1106G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15964053 | |||||||
| chr12:15964177 | A | T | 252 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(249): Show |
254 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(251): Show |
intron_variant | MODIFIER | c.508+1230A>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15964177 | |||||||
| chr12:15964205 | A | G | 1 | a0001c0001t0001g0220 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.508+1258A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15964205 | |||||||
| chr12:15964246 | C | T | 3 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0145 |
3 | HG03491.hp1 HG03669.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.508+1299C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15964246 | |||||||
| chr12:15964367 | T | C | 205 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(202): Show |
206 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(203): Show |
intron_variant | MODIFIER | c.508+1420T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15964367 | |||||||
| chr12:15964502 | T | G | 1 | a0001c0001t0001g0144 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.508+1555T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15964502 | |||||||
| chr12:15964624 | A | G | 1 | a0001c0001t0001g0033 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.508+1677A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15964624 | |||||||
| chr12:15964700 | A | G | 4 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0174 others(1): Show |
4 | HG02257.hp2 HG02630.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.508+1753A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15964700 | |||||||
| chr12:15964874 | T | A | 10 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0065 others(7): Show |
10 | HG01884.hp2 HG02109.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.508+1927T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15964874 | |||||||
| chr12:15965048 | C | A | 1 | a0001c0001t0002g0188 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.508+2101C>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15965048 | |||||||
| chr12:15965211 | C | T | 3 | a0001c0001t0001g0129 a0001c0003t0001g0073 a0001c0003t0004g0072 |
3 | HG02486.hp2 HG06807.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.508+2264C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15965211 | |||||||
| chr12:15965259 | G | A | 5 | a0001c0001t0001g0040 a0001c0001t0001g0042 a0001c0001t0001g0043 others(2): Show |
5 | HG01243.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.508+2312G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15965259 | |||||||
| chr12:15965355 | A | G | 4 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0174 others(1): Show |
4 | HG02257.hp2 HG02630.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.508+2408A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15965355 | |||||||
| chr12:15965370 | G | T | 1 | a0001c0001t0001g0062 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.508+2423G>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15965370 | |||||||
| chr12:15965604 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.508+2657C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15965604 | |||||||
| chr12:15965605 | G | C | 10 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0065 others(7): Show |
10 | HG01884.hp2 HG02109.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.508+2658G>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15965605 | |||||||
| chr12:15965625 | G | A | 1 | a0001c0001t0001g0033 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.508+2678G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15965625 | |||||||
| chr12:15965820 | C | T | 3 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0246 |
3 | HG02258.hp2 HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.508+2873C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15965820 | |||||||
| chr12:15965876 | C | G | 1 | a0001c0001t0001g0033 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.508+2929C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15965876 | |||||||
| chr12:15965936 | G | A | 5 | a0001c0001t0001g0025 a0001c0001t0002g0124 a0001c0001t0002g0140 others(2): Show |
5 | NA18964.hp1 NA19000.hp1 NA19007.hp1 others(2): Show |
intron_variant | MODIFIER | c.508+2989G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15965936 | |||||||
| chr12:15965989 | A | G | 10 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0003g0010 others(7): Show |
10 | HG02055.hp1 HG02109.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.508+3042A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15965989 | |||||||
| chr12:15965996 | C | T | 2 | a0001c0001t0001g0032 a0001c0001t0001g0064 |
2 | HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.508+3049C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15965996 | |||||||
| chr12:15966063 | T | G | 5 | a0001c0001t0001g0009 a0001c0001t0001g0083 a0001c0001t0003g0003 others(2): Show |
5 | HG02559.hp2 HG02886.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.508+3116T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15966063 | |||||||
| chr12:15966110 | C | T | 2 | a0002c0002t0003g0019 a0002c0002t0003g0021 |
2 | HG02630.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.508+3163C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15966110 | |||||||
| chr12:15966280 | A | G | 1 | a0001c0001t0001g0007 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.508+3333A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15966280 | |||||||
| chr12:15966317 | C | T | 3 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0110 |
3 | HG02818.hp1 HG02895.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.508+3370C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15966317 | |||||||
| chr12:15966318 | G | A | 1 | a0001c0001t0001g0063 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.508+3371G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15966318 | |||||||
| chr12:15966337 | G | T | 2 | a0001c0001t0001g0095 a0001c0001t0001g0230 |
2 | HG00735.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.508+3390G>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15966337 | |||||||
| chr12:15966421 | G | A | 1 | a0001c0001t0001g0009 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.508+3474G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15966421 | |||||||
| chr12:15966438 | T | C | 2 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
2 | HG01884.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.508+3491T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15966438 | |||||||
| chr12:15966613 | GC | G | 3 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0004g0089 |
3 | HG02809.hp2 HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.508+3667delC | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15966613 | |||||||
| chr12:15966670 | C | T | 14 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0030 others(11): Show |
14 | HG01109.hp2 HG01891.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.508+3723C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15966670 | |||||||
| chr12:15966840 | C | T | 1 | a0001c0001t0001g0045 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.508+3893C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15966840 | |||||||
| chr12:15966916 | G | C | 1 | a0001c0001t0001g0177 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.508+3969G>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15966916 | |||||||
| chr12:15966950 | G | A | 1 | a0001c0001t0001g0130 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.508+4003G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15966950 | |||||||
| chr12:15967071 | C | T | 1 | a0001c0001t0001g0033 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.508+4124C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15967071 | |||||||
| chr12:15967202 | T | A | 1 | a0001c0001t0001g0170 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.508+4255T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15967202 | |||||||
| chr12:15967208 | A | C | 10 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0003g0010 others(7): Show |
10 | HG02055.hp1 HG02109.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.508+4261A>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15967208 | |||||||
| chr12:15967464 | C | T | 102 | a0001c0001t0001g0025 a0001c0001t0001g0039 a0001c0001t0001g0040 others(99): Show |
102 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.508+4517C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15967464 | |||||||
| chr12:15967723 | C | T | 1 | a0001c0001t0002g0222 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.508+4776C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15967723 | |||||||
| chr12:15967728 | C | T | 1 | a0001c0001t0001g0077 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.508+4781C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15967728 | |||||||
| chr12:15967788 | G | A | 4 | a0001c0001t0001g0009 a0001c0001t0003g0003 a0001c0001t0003g0004 others(1): Show |
4 | HG02559.hp2 HG03225.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.508+4841G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15967788 | |||||||
| chr12:15967886 | T | C | 1 | a0001c0001t0001g0155 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.508+4939T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15967886 | |||||||
| chr12:15968086 | C | CT | 52 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(49): Show |
53 | HG00280.hp1 HG00280.hp2 HG00558.hp2 others(50): Show |
intron_variant | MODIFIER | c.508+5153dupT | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 15968086 | ||||||
| chr12:15968372 | A | C | 3 | a0001c0001t0001g0193 a0001c0001t0002g0023 a0001c0001t0002g0024 |
3 | NA18967.hp2 NA19010.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.508+5425A>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15968372 | |||||||
| chr12:15968799 | C | G | 3 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0246 |
3 | HG02258.hp2 HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.508+5852C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15968799 | |||||||
| chr12:15968909 | T | C | 5 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0191 others(2): Show |
5 | HG01070.hp2 HG01074.hp2 HG01243.hp2 others(2): Show |
intron_variant | MODIFIER | c.508+5962T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15968909 | |||||||
| chr12:15969024 | C | T | 3 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0005 |
3 | HG02559.hp2 HG03516.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.508+6077C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15969024 | |||||||
| chr12:15969102 | G | A | 1 | a0001c0001t0001g0033 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.508+6155G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15969102 | |||||||
| chr12:15969244 | T | A | 173 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(170): Show |
174 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(171): Show |
intron_variant | MODIFIER | c.508+6297T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15969244 | |||||||
| chr12:15969480 | G | A | 3 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0110 |
3 | HG02818.hp1 HG02895.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.508+6533G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15969480 | |||||||
| chr12:15969512 | C | T | 1 | a0001c0001t0001g0033 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.508+6565C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15969512 | |||||||
| chr12:15969684 | C | T | 185 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(182): Show |
186 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(183): Show |
intron_variant | MODIFIER | c.508+6737C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15969684 | |||||||
| chr12:15969780 | A | G | 3 | a0001c0001t0001g0193 a0001c0001t0002g0023 a0001c0001t0002g0024 |
3 | NA18967.hp2 NA19010.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.508+6833A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15969780 | |||||||
| chr12:15969809 | G | T | 10 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0003g0010 others(7): Show |
10 | HG02055.hp1 HG02109.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.508+6862G>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15969809 | |||||||
| chr12:15969920 | CAG | C | 4 | a0001c0001t0001g0009 a0001c0001t0003g0003 a0001c0001t0003g0004 others(1): Show |
4 | HG02559.hp2 HG03225.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.508+6975_508+6976d others(4): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 15969920 | ||||||
| chr12:15969937 | C | G | 106 | a0001c0001t0001g0025 a0001c0001t0001g0039 a0001c0001t0001g0040 others(103): Show |
106 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(103): Show |
intron_variant | MODIFIER | c.508+6990C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15969937 | |||||||
| chr12:15970048 | G | T | 4 | a0001c0001t0001g0009 a0001c0001t0003g0003 a0001c0001t0003g0004 others(1): Show |
4 | HG02559.hp2 HG03225.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.508+7101G>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15970048 | |||||||
| chr12:15970138 | T | G | 3 | a0001c0001t0001g0129 a0001c0003t0001g0073 a0001c0003t0004g0072 |
3 | HG02486.hp2 HG06807.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.508+7191T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15970138 | |||||||
| chr12:15970277 | G | A | 1 | a0001c0001t0001g0209 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.508+7330G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15970277 | |||||||
| chr12:15970359 | C | G | 1 | a0001c0001t0001g0191 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.508+7412C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15970359 | |||||||
| chr12:15970366 | C | T | 1 | a0001c0001t0003g0010 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.508+7419C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15970366 | |||||||
| chr12:15970421 | T | C | 1 | a0001c0001t0001g0079 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.508+7474T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15970421 | |||||||
| chr12:15970540 | T | A | 174 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(171): Show |
175 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(172): Show |
intron_variant | MODIFIER | c.508+7593T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15970540 | |||||||
| chr12:15970732 | G | C | 1 | a0001c0001t0001g0033 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.508+7785G>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15970732 | |||||||
| chr12:15970732 | G | T | 186 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(183): Show |
187 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(184): Show |
intron_variant | MODIFIER | c.508+7785G>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15970732 | |||||||
| chr12:15971119 | G | C | 187 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(184): Show |
188 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(185): Show |
intron_variant | MODIFIER | c.508+8172G>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15971119 | |||||||
| chr12:15971120 | G | A | 187 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(184): Show |
188 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(185): Show |
intron_variant | MODIFIER | c.508+8173G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15971120 | |||||||
| chr12:15971201 | A | G | 1 | a0001c0001t0001g0173 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.508+8254A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15971201 | |||||||
| chr12:15971208 | G | A | 187 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(184): Show |
188 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(185): Show |
intron_variant | MODIFIER | c.508+8261G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15971208 | |||||||
| chr12:15971275 | A | G | 156 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(153): Show |
157 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(154): Show |
intron_variant | MODIFIER | c.508+8328A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15971275 | |||||||
| chr12:15971346 | A | G | 3 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0235 |
3 | HG02257.hp2 HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.508+8399A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15971346 | |||||||
| chr12:15971476 | G | A | 187 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(184): Show |
188 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(185): Show |
intron_variant | MODIFIER | c.508+8529G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15971476 | |||||||
| chr12:15971491 | A | G | 1 | a0001c0001t0001g0176 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.508+8544A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15971491 | |||||||
| chr12:15971498 | T | G | 187 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(184): Show |
188 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(185): Show |
intron_variant | MODIFIER | c.508+8551T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15971498 | |||||||
| chr12:15971508 | CT | C | 28 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0029 others(25): Show |
29 | HG00642.hp1 HG01070.hp2 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.508+8586delT | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 15971508 | ||||||
| chr12:15971508 | CTTTT | C | 102 | a0001c0001t0001g0025 a0001c0001t0001g0039 a0001c0001t0001g0040 others(99): Show |
102 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.508+8583_508+8586d others(6): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 15971508 | ||||||
| chr12:15971508 | CTTTTT | C | 11 | a0001c0001t0001g0043 a0001c0001t0001g0065 a0001c0001t0001g0066 others(8): Show |
11 | HG02074.hp2 HG02109.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.508+8582_508+8586d others(7): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 15971508 | ||||||
| chr12:15971508 | CTTTTTT | C | 68 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(65): Show |
69 | HG00280.hp1 HG00280.hp2 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.508+8581_508+8586d others(8): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 15971508 | ||||||
| chr12:15971527 | T | C | 10 | a0001c0001t0001g0001 a0001c0001t0001g0045 a0001c0001t0001g0126 others(7): Show |
11 | HG00642.hp1 HG01071.hp2 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.508+8580T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15971527 | |||||||
| chr12:15971529 | T | G | 3 | a0001c0001t0001g0193 a0001c0001t0002g0023 a0001c0001t0002g0024 |
3 | NA18967.hp2 NA19010.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.508+8582T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15971529 | |||||||
| chr12:15971530 | T | A | 3 | a0001c0001t0001g0193 a0001c0001t0002g0023 a0001c0001t0002g0024 |
3 | NA18967.hp2 NA19010.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.508+8583T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15971530 | |||||||
| chr12:15971531 | T | G | 3 | a0001c0001t0001g0193 a0001c0001t0002g0023 a0001c0001t0002g0024 |
3 | NA18967.hp2 NA19010.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.508+8584T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15971531 | |||||||
| chr12:15971532 | T | A | 3 | a0001c0001t0001g0193 a0001c0001t0002g0023 a0001c0001t0002g0024 |
3 | NA18967.hp2 NA19010.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.508+8585T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15971532 | |||||||
| chr12:15971533 | TGA | T | 3 | a0001c0001t0001g0193 a0001c0001t0002g0023 a0001c0001t0002g0024 |
3 | NA18967.hp2 NA19010.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.508+8589_508+8590d others(4): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 15971533 | ||||||
| chr12:15971551 | T | C | 187 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(184): Show |
188 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(185): Show |
intron_variant | MODIFIER | c.508+8604T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15971551 | |||||||
| chr12:15971723 | G | A | 4 | a0001c0001t0001g0009 a0001c0001t0003g0003 a0001c0001t0003g0004 others(1): Show |
4 | HG02559.hp2 HG03225.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.508+8776G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15971723 | |||||||
| chr12:15971758 | C | T | 187 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(184): Show |
188 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(185): Show |
intron_variant | MODIFIER | c.508+8811C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15971758 | |||||||
| chr12:15971859 | G | A | 187 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(184): Show |
188 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(185): Show |
intron_variant | MODIFIER | c.508+8912G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15971859 | |||||||
| chr12:15972014 | C | T | 187 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(184): Show |
188 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(185): Show |
intron_variant | MODIFIER | c.508+9067C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15972014 | |||||||
| chr12:15972017 | G | C | 187 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(184): Show |
188 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(185): Show |
intron_variant | MODIFIER | c.508+9070G>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15972017 | |||||||
| chr12:15972140 | G | A | 187 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(184): Show |
188 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(185): Show |
intron_variant | MODIFIER | c.508+9193G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15972140 | |||||||
| chr12:15972340 | C | T | 4 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0174 others(1): Show |
4 | HG02257.hp2 HG02630.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.508+9393C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15972340 | |||||||
| chr12:15972436 | C | T | 187 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(184): Show |
188 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(185): Show |
intron_variant | MODIFIER | c.508+9489C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15972436 | |||||||
| chr12:15972488 | T | C | 187 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(184): Show |
188 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(185): Show |
intron_variant | MODIFIER | c.508+9541T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15972488 | |||||||
| chr12:15972506 | A | AG | 9 | a0001c0001t0001g0085 a0001c0001t0003g0010 a0001c0001t0003g0012 others(6): Show |
9 | HG02055.hp1 HG02109.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.508+9561dupG | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 15972506 | ||||||
| chr12:15972638 | T | C | 187 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(184): Show |
188 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(185): Show |
intron_variant | MODIFIER | c.509-9670T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15972638 | |||||||
| chr12:15972662 | C | T | 187 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(184): Show |
188 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(185): Show |
intron_variant | MODIFIER | c.509-9646C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15972662 | |||||||
| chr12:15972711 | G | A | 187 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(184): Show |
188 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(185): Show |
intron_variant | MODIFIER | c.509-9597G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15972711 | |||||||
| chr12:15972718 | C | T | 187 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(184): Show |
188 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(185): Show |
intron_variant | MODIFIER | c.509-9590C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15972718 | |||||||
| chr12:15972836 | A | G | 1 | a0001c0001t0001g0040 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.509-9472A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15972836 | |||||||
| chr12:15972886 | G | A | 1 | a0001c0001t0001g0033 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.509-9422G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15972886 | |||||||
| chr12:15972987 | G | A | 1 | a0001c0001t0001g0248 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.509-9321G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15972987 | |||||||
| chr12:15973199 | T | C | 3 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0246 |
3 | HG02258.hp2 HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.509-9109T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15973199 | |||||||
| chr12:15973215 | CT | C | 9 | a0001c0001t0001g0085 a0001c0001t0003g0010 a0001c0001t0003g0012 others(6): Show |
9 | HG02055.hp1 HG02109.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.509-9092delT | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15973215 | |||||||
| chr12:15973428 | A | ATAATAGC others(20): Show |
187 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(184): Show |
188 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(185): Show |
intron_variant | MODIFIER | c.509-8875_509-8874i others(29): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 15973428 | ||||||
| chr12:15973444 | A | G | 3 | a0001c0001t0005g0036 a0001c0001t0005g0037 a0001c0001t0005g0038 |
3 | HG01109.hp1 HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.509-8864A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15973444 | |||||||
| chr12:15973541 | G | A | 5 | a0001c0001t0001g0002 a0001c0001t0001g0117 a0001c0001t0001g0232 others(2): Show |
6 | HG00738.hp2 HG01070.hp1 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.509-8767G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15973541 | |||||||
| chr12:15973564 | C | T | 1 | a0001c0001t0003g0014 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.509-8744C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15973564 | |||||||
| chr12:15973683 | C | G | 1 | a0001c0001t0002g0090 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.509-8625C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15973683 | |||||||
| chr12:15973916 | T | G | 1 | a0003c0004t0001g0225 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.509-8392T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15973916 | |||||||
| chr12:15973973 | C | T | 187 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(184): Show |
188 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(185): Show |
intron_variant | MODIFIER | c.509-8335C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15973973 | |||||||
| chr12:15974104 | G | A | 187 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(184): Show |
188 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(185): Show |
intron_variant | MODIFIER | c.509-8204G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15974104 | |||||||
| chr12:15974230 | A | G | 187 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(184): Show |
188 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(185): Show |
intron_variant | MODIFIER | c.509-8078A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15974230 | |||||||
| chr12:15974247 | G | A | 187 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(184): Show |
188 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(185): Show |
intron_variant | MODIFIER | c.509-8061G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15974247 | |||||||
| chr12:15974254 | C | T | 187 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(184): Show |
188 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(185): Show |
intron_variant | MODIFIER | c.509-8054C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15974254 | |||||||
| chr12:15974318 | G | A | 1 | a0001c0001t0001g0002 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.509-7990G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15974318 | |||||||
| chr12:15974398 | T | G | 14 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0030 others(11): Show |
14 | HG01109.hp2 HG01891.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.509-7910T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15974398 | |||||||
| chr12:15974417 | G | A | 187 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(184): Show |
188 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(185): Show |
intron_variant | MODIFIER | c.509-7891G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15974417 | |||||||
| chr12:15974516 | C | T | 2 | a0001c0001t0001g0084 a0001c0001t0001g0214 |
2 | HG02559.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.509-7792C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15974516 | |||||||
| chr12:15974717 | A | T | 187 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(184): Show |
188 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(185): Show |
intron_variant | MODIFIER | c.509-7591A>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15974717 | |||||||
| chr12:15974920 | CCCTT | C | 3 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0005 |
3 | HG02559.hp2 HG03516.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.509-7376_509-7373d others(6): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 15974920 | ||||||
| chr12:15974968 | C | G | 9 | a0001c0001t0001g0085 a0001c0001t0003g0010 a0001c0001t0003g0012 others(6): Show |
9 | HG02055.hp1 HG02109.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.509-7340C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15974968 | |||||||
| chr12:15975035 | G | A | 5 | a0001c0001t0001g0048 a0001c0001t0001g0120 a0001c0001t0001g0169 others(2): Show |
5 | HG00735.hp2 HG01168.hp2 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.509-7273G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15975035 | |||||||
| chr12:15975202 | A | G | 1 | a0001c0001t0001g0028 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.509-7106A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15975202 | |||||||
| chr12:15975229 | G | A | 1 | a0001c0001t0001g0236 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.509-7079G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15975229 | |||||||
| chr12:15975291 | ATTAT | A | 187 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(184): Show |
188 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(185): Show |
intron_variant | MODIFIER | c.509-7014_509-7011d others(6): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 15975291 | ||||||
| chr12:15975365 | G | A | 1 | a0001c0001t0001g0211 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.509-6943G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15975365 | |||||||
| chr12:15975425 | A | G | 187 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(184): Show |
188 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(185): Show |
intron_variant | MODIFIER | c.509-6883A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15975425 | |||||||
| chr12:15975488 | G | A | 2 | a0001c0001t0001g0200 a0001c0001t0001g0244 |
2 | NA18950.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.509-6820G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15975488 | |||||||
| chr12:15975524 | C | T | 14 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0030 others(11): Show |
14 | HG01109.hp2 HG01891.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.509-6784C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15975524 | |||||||
| chr12:15975743 | C | T | 10 | a0001c0001t0001g0001 a0001c0001t0001g0045 a0001c0001t0001g0126 others(7): Show |
11 | HG00642.hp1 HG01071.hp2 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.509-6565C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15975743 | |||||||
| chr12:15975771 | T | G | 10 | a0001c0001t0001g0001 a0001c0001t0001g0045 a0001c0001t0001g0126 others(7): Show |
11 | HG00642.hp1 HG01071.hp2 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.509-6537T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15975771 | |||||||
| chr12:15975834 | C | T | 187 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(184): Show |
188 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(185): Show |
intron_variant | MODIFIER | c.509-6474C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15975834 | |||||||
| chr12:15975851 | C | G | 50 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(47): Show |
51 | HG00280.hp1 HG00280.hp2 HG00558.hp2 others(48): Show |
intron_variant | MODIFIER | c.509-6457C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15975851 | |||||||
| chr12:15975856 | C | T | 1 | a0001c0001t0001g0132 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.509-6452C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15975856 | |||||||
| chr12:15975865 | G | A | 1 | a0001c0001t0001g0174 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.509-6443G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15975865 | |||||||
| chr12:15975911 | CTG | C | 8 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0030 others(5): Show |
8 | HG01109.hp2 HG01891.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.509-6395_509-6394d others(4): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 15975911 | ||||||
| chr12:15976185 | C | T | 187 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(184): Show |
188 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(185): Show |
intron_variant | MODIFIER | c.509-6123C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15976185 | |||||||
| chr12:15976265 | A | G | 2 | a0001c0001t0001g0169 a0001c0001t0001g0189 |
2 | HG00735.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.509-6043A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15976265 | |||||||
| chr12:15976343 | G | T | 33 | a0001c0001t0001g0025 a0001c0001t0001g0052 a0001c0001t0001g0092 others(30): Show |
33 | HG02027.hp1 HG02080.hp1 HG02080.hp2 others(30): Show |
intron_variant | MODIFIER | c.509-5965G>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15976343 | |||||||
| chr12:15976424 | T | C | 5 | a0001c0001t0001g0002 a0001c0001t0001g0117 a0001c0001t0001g0232 others(2): Show |
6 | HG00738.hp2 HG01070.hp1 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.509-5884T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15976424 | |||||||
| chr12:15976808 | GA | G | 4 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0046 others(1): Show |
4 | HG03130.hp2 HG03471.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.509-5495delA | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 15976808 | ||||||
| chr12:15976946 | G | C | 2 | a0001c0001t0001g0186 a0001c0001t0001g0220 |
2 | NA19012.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.509-5362G>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15976946 | |||||||
| chr12:15977088 | C | A | 187 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(184): Show |
188 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(185): Show |
intron_variant | MODIFIER | c.509-5220C>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15977088 | |||||||
| chr12:15977231 | G | A | 54 | a0001c0001t0001g0039 a0001c0001t0001g0047 a0001c0001t0001g0050 others(51): Show |
54 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.509-5077G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15977231 | |||||||
| chr12:15977268 | G | T | 2 | a0002c0002t0003g0019 a0002c0002t0003g0021 |
2 | HG02630.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.509-5040G>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15977268 | |||||||
| chr12:15977299 | G | A | 119 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(116): Show |
119 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(116): Show |
intron_variant | MODIFIER | c.509-5009G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15977299 | |||||||
| chr12:15977315 | G | A | 1 | a0001c0001t0001g0065 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.509-4993G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15977315 | |||||||
| chr12:15977375 | C | T | 2 | a0002c0002t0003g0019 a0002c0002t0003g0021 |
2 | HG02630.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.509-4933C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15977375 | |||||||
| chr12:15977646 | C | T | 187 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(184): Show |
188 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(185): Show |
intron_variant | MODIFIER | c.509-4662C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15977646 | |||||||
| chr12:15977826 | G | A | 3 | a0001c0001t0001g0193 a0001c0001t0002g0023 a0001c0001t0002g0024 |
3 | NA18967.hp2 NA19010.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.509-4482G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15977826 | |||||||
| chr12:15977887 | A | G | 3 | a0001c0001t0001g0074 a0001c0001t0001g0177 a0001c0001t0001g0183 |
3 | HG01074.hp1 HG01081.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.509-4421A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15977887 | |||||||
| chr12:15977917 | A | T | 28 | a0001c0001t0001g0025 a0001c0001t0001g0052 a0001c0001t0001g0122 others(25): Show |
28 | HG02027.hp1 HG02080.hp1 HG02080.hp2 others(25): Show |
intron_variant | MODIFIER | c.509-4391A>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15977917 | |||||||
| chr12:15977918 | T | G | 10 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0003g0010 others(7): Show |
10 | HG02055.hp1 HG02109.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.509-4390T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15977918 | |||||||
| chr12:15977947 | T | C | 1 | a0001c0001t0001g0033 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.509-4361T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15977947 | |||||||
| chr12:15978008 | C | T | 187 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(184): Show |
188 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(185): Show |
intron_variant | MODIFIER | c.509-4300C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15978008 | |||||||
| chr12:15978023 | TCCTACCA others(9): Show |
T | 1 | a0001c0001t0001g0026 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.509-4284_509-4269d others(18): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15978023 | |||||||
| chr12:15978040 | A | T | 1 | a0001c0001t0001g0026 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.509-4268A>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15978040 | |||||||
| chr12:15978096 | T | C | 187 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(184): Show |
188 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(185): Show |
intron_variant | MODIFIER | c.509-4212T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15978096 | |||||||
| chr12:15978151 | A | G | 4 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0046 others(1): Show |
4 | HG03130.hp2 HG03471.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.509-4157A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15978151 | |||||||
| chr12:15978194 | A | G | 1 | a0001c0001t0004g0213 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.509-4114A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15978194 | |||||||
| chr12:15978228 | A | G | 5 | a0001c0001t0001g0009 a0001c0001t0001g0083 a0001c0001t0003g0003 others(2): Show |
5 | HG02559.hp2 HG02886.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.509-4080A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15978228 | |||||||
| chr12:15978358 | C | T | 10 | a0001c0001t0001g0001 a0001c0001t0001g0045 a0001c0001t0001g0126 others(7): Show |
11 | HG00642.hp1 HG01071.hp2 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.509-3950C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15978358 | |||||||
| chr12:15978370 | C | T | 7 | a0001c0001t0001g0053 a0001c0001t0001g0157 a0001c0001t0001g0178 others(4): Show |
7 | NA18942.hp1 NA18950.hp1 NA18975.hp1 others(4): Show |
intron_variant | MODIFIER | c.509-3938C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15978370 | |||||||
| chr12:15978371 | G | A | 4 | a0001c0001t0001g0009 a0001c0001t0003g0003 a0001c0001t0003g0004 others(1): Show |
4 | HG02559.hp2 HG03225.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.509-3937G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15978371 | |||||||
| chr12:15978545 | C | A | 9 | a0001c0001t0001g0085 a0001c0001t0003g0010 a0001c0001t0003g0012 others(6): Show |
9 | HG02055.hp1 HG02109.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.509-3763C>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15978545 | |||||||
| chr12:15978552 | T | A | 9 | a0001c0001t0001g0085 a0001c0001t0003g0010 a0001c0001t0003g0012 others(6): Show |
9 | HG02055.hp1 HG02109.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.509-3756T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15978552 | |||||||
| chr12:15978792 | C | G | 7 | a0001c0001t0001g0053 a0001c0001t0001g0157 a0001c0001t0001g0178 others(4): Show |
7 | NA18942.hp1 NA18950.hp1 NA18975.hp1 others(4): Show |
intron_variant | MODIFIER | c.509-3516C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15978792 | |||||||
| chr12:15978824 | C | T | 50 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(47): Show |
51 | HG00280.hp1 HG00280.hp2 HG00558.hp2 others(48): Show |
intron_variant | MODIFIER | c.509-3484C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15978824 | |||||||
| chr12:15979077 | C | T | 187 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(184): Show |
188 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(185): Show |
intron_variant | MODIFIER | c.509-3231C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15979077 | |||||||
| chr12:15979196 | A | G | 3 | a0001c0001t0001g0193 a0001c0001t0002g0023 a0001c0001t0002g0024 |
3 | NA18967.hp2 NA19010.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.509-3112A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15979196 | |||||||
| chr12:15979232 | G | A | 187 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(184): Show |
188 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(185): Show |
intron_variant | MODIFIER | c.509-3076G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15979232 | |||||||
| chr12:15979252 | C | T | 187 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(184): Show |
188 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(185): Show |
intron_variant | MODIFIER | c.509-3056C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15979252 | |||||||
| chr12:15979457 | G | A | 3 | a0001c0001t0001g0159 a0001c0001t0001g0218 a0001c0001t0001g0228 |
3 | NA18949.hp1 NA19062.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.509-2851G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15979457 | |||||||
| chr12:15979457 | G | T | 1 | a0001c0001t0001g0252 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.509-2851G>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15979457 | |||||||
| chr12:15979614 | A | G | 10 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0003g0010 others(7): Show |
10 | HG02055.hp1 HG02109.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.509-2694A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15979614 | |||||||
| chr12:15979680 | G | T | 3 | a0001c0001t0001g0129 a0001c0003t0001g0073 a0001c0003t0004g0072 |
3 | HG02486.hp2 HG06807.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.509-2628G>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15979680 | |||||||
| chr12:15980100 | A | G | 8 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0030 others(5): Show |
8 | HG01109.hp2 HG01891.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.509-2208A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15980100 | |||||||
| chr12:15980225 | A | G | 3 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0110 |
3 | HG02818.hp1 HG02895.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.509-2083A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15980225 | |||||||
| chr12:15980409 | G | A | 173 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(170): Show |
174 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(171): Show |
intron_variant | MODIFIER | c.509-1899G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15980409 | |||||||
| chr12:15980441 | T | G | 3 | a0001c0001t0001g0193 a0001c0001t0002g0023 a0001c0001t0002g0024 |
3 | NA18967.hp2 NA19010.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.509-1867T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15980441 | |||||||
| chr12:15980555 | T | C | 3 | a0001c0001t0001g0193 a0001c0001t0002g0023 a0001c0001t0002g0024 |
3 | NA18967.hp2 NA19010.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.509-1753T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15980555 | |||||||
| chr12:15980577 | T | A | 7 | a0001c0001t0001g0053 a0001c0001t0001g0157 a0001c0001t0001g0178 others(4): Show |
7 | NA18942.hp1 NA18950.hp1 NA18975.hp1 others(4): Show |
intron_variant | MODIFIER | c.509-1731T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15980577 | |||||||
| chr12:15980682 | A | G | 10 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0003g0010 others(7): Show |
10 | HG02055.hp1 HG02109.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.509-1626A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15980682 | |||||||
| chr12:15980706 | A | G | 10 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0003g0010 others(7): Show |
10 | HG02055.hp1 HG02109.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.509-1602A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15980706 | |||||||
| chr12:15980821 | C | A | 1 | a0001c0001t0002g0139 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.509-1487C>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15980821 | |||||||
| chr12:15981086 | C | T | 10 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0003g0010 others(7): Show |
10 | HG02055.hp1 HG02109.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.509-1222C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15981086 | |||||||
| chr12:15981123 | C | T | 1 | a0001c0001t0001g0001 | 2 | HG01123.hp2 HG01256.hp2 |
intron_variant | MODIFIER | c.509-1185C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15981123 | |||||||
| chr12:15981158 | T | C | 2 | a0001c0001t0001g0132 a0001c0001t0001g0237 |
2 | HG00280.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.509-1150T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15981158 | |||||||
| chr12:15981396 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.509-912C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15981396 | |||||||
| chr12:15981471 | C | T | 1 | a0001c0001t0001g0255 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.509-837C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15981471 | |||||||
| chr12:15981728 | T | G | 2 | a0002c0002t0003g0019 a0002c0002t0003g0021 |
2 | HG02630.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.509-580T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15981728 | |||||||
| chr12:15981866 | C | T | 174 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(171): Show |
175 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(172): Show |
intron_variant | MODIFIER | c.509-442C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15981866 | |||||||
| chr12:15981974 | C | T | 9 | a0001c0001t0001g0085 a0001c0001t0003g0010 a0001c0001t0003g0012 others(6): Show |
9 | HG02055.hp1 HG02109.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.509-334C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15981974 | |||||||
| chr12:15981983 | T | G | 9 | a0001c0001t0001g0085 a0001c0001t0003g0010 a0001c0001t0003g0012 others(6): Show |
9 | HG02055.hp1 HG02109.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.509-325T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15981983 | |||||||
| chr12:15982492 | A | G | 8 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 others(5): Show |
8 | HG02109.hp1 HG02257.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.637+56A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15982492 | |||||||
| chr12:15982565 | A | G | 9 | a0001c0001t0001g0085 a0001c0001t0003g0010 a0001c0001t0003g0012 others(6): Show |
9 | HG02055.hp1 HG02109.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.637+129A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15982565 | |||||||
| chr12:15982660 | C | T | 9 | a0001c0001t0001g0085 a0001c0001t0003g0010 a0001c0001t0003g0012 others(6): Show |
9 | HG02055.hp1 HG02109.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.637+224C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15982660 | |||||||
| chr12:15982767 | A | T | 1 | a0001c0001t0001g0092 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.637+331A>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15982767 | |||||||
| chr12:15982770 | C | T | 1 | a0001c0001t0001g0079 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.637+334C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15982770 | |||||||
| chr12:15982798 | C | G | 14 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0030 others(11): Show |
14 | HG01109.hp2 HG01891.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.637+362C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15982798 | |||||||
| chr12:15982956 | A | G | 8 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0046 others(5): Show |
8 | HG02257.hp2 HG02630.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.637+520A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15982956 | |||||||
| chr12:15983018 | G | C | 204 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(201): Show |
205 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(202): Show |
intron_variant | MODIFIER | c.637+582G>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15983018 | |||||||
| chr12:15983170 | T | A | 1 | a0001c0001t0002g0253 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.637+734T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15983170 | |||||||
| chr12:15983443 | C | T | 4 | a0001c0001t0002g0147 a0001c0001t0002g0148 a0001c0001t0002g0154 others(1): Show |
4 | HG00621.hp1 HG02165.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.637+1007C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15983443 | |||||||
| chr12:15983516 | C | T | 3 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0005 |
3 | HG02559.hp2 HG03516.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.637+1080C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15983516 | |||||||
| chr12:15983539 | G | A | 187 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(184): Show |
188 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(185): Show |
intron_variant | MODIFIER | c.637+1103G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15983539 | |||||||
| chr12:15983771 | T | G | 1 | a0001c0001t0001g0034 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.637+1335T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15983771 | |||||||
| chr12:15983817 | C | T | 4 | a0001c0001t0001g0202 a0001c0001t0001g0223 a0001c0001t0001g0231 others(1): Show |
4 | NA18971.hp1 NA18978.hp1 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.637+1381C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15983817 | |||||||
| chr12:15983848 | T | C | 109 | a0001c0001t0001g0025 a0001c0001t0001g0039 a0001c0001t0001g0040 others(106): Show |
109 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(106): Show |
intron_variant | MODIFIER | c.637+1412T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15983848 | |||||||
| chr12:15983903 | C | T | 4 | a0001c0001t0001g0060 a0001c0001t0001g0135 a0001c0001t0001g0146 others(1): Show |
4 | HG01168.hp1 HG01169.hp1 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.637+1467C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15983903 | |||||||
| chr12:15984023 | C | G | 1 | a0001c0001t0001g0045 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.637+1587C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15984023 | |||||||
| chr12:15984123 | T | C | 2 | a0001c0001t0001g0059 a0001c0001t0001g0091 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.637+1687T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15984123 | |||||||
| chr12:15984147 | T | C | 3 | a0001c0001t0001g0193 a0001c0001t0002g0023 a0001c0001t0002g0024 |
3 | NA18967.hp2 NA19010.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.637+1711T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15984147 | |||||||
| chr12:15984277 | C | T | 2 | a0001c0001t0001g0157 a0001c0001t0002g0256 |
2 | NA18950.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.637+1841C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15984277 | |||||||
| chr12:15984530 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.637+2094C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15984530 | |||||||
| chr12:15984633 | T | A | 8 | a0001c0001t0001g0085 a0001c0001t0003g0010 a0001c0001t0003g0012 others(5): Show |
8 | HG02055.hp1 HG02109.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.637+2197T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15984633 | |||||||
| chr12:15984962 | T | C | 55 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(52): Show |
56 | HG00280.hp2 HG00621.hp1 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.637+2526T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15984962 | |||||||
| chr12:15985364 | T | C | 2 | a0001c0001t0001g0007 a0001c0001t0001g0174 |
2 | HG01884.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.637+2928T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15985364 | |||||||
| chr12:15985575 | T | C | 2 | a0001c0001t0001g0121 a0002c0002t0003g0021 |
2 | HG01934.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.637+3139T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15985575 | |||||||
| chr12:15985581 | CTTTTCAG others(3): Show |
C | 130 | a0001c0001t0001g0002 a0001c0001t0001g0025 a0001c0001t0001g0026 others(127): Show |
131 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(128): Show |
intron_variant | MODIFIER | c.637+3146_637+3155d others(12): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15985581 | |||||||
| chr12:15985595 | T | A | 1 | a0001c0001t0001g0033 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.637+3159T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15985595 | |||||||
| chr12:15985853 | G | C | 108 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0026 others(105): Show |
109 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(106): Show |
intron_variant | MODIFIER | c.637+3417G>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15985853 | |||||||
| chr12:15985869 | G | A | 2 | a0001c0001t0001g0203 a0001c0001t0001g0219 |
2 | HG02015.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.637+3433G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15985869 | |||||||
| chr12:15985872 | T | C | 31 | a0001c0001t0001g0050 a0001c0001t0001g0053 a0001c0001t0001g0066 others(28): Show |
31 | HG00280.hp2 HG00558.hp1 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.637+3436T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15985872 | |||||||
| chr12:15985992 | C | T | 1 | a0001c0001t0001g0050 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.637+3556C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15985992 | |||||||
| chr12:15986054 | G | T | 14 | a0001c0001t0001g0051 a0001c0001t0001g0060 a0001c0001t0001g0079 others(11): Show |
14 | HG00558.hp2 HG01168.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.637+3618G>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15986054 | |||||||
| chr12:15986386 | G | T | 5 | a0001c0001t0001g0007 a0001c0001t0001g0033 a0001c0001t0001g0174 others(2): Show |
5 | HG01884.hp2 HG02258.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.637+3950G>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15986386 | |||||||
| chr12:15986453 | A | G | 3 | a0001c0001t0001g0069 a0001c0001t0001g0080 a0001c0001t0001g0081 |
3 | HG01884.hp1 HG02622.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.637+4017A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15986453 | |||||||
| chr12:15986480 | C | T | 1 | a0001c0001t0001g0236 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.637+4044C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15986480 | |||||||
| chr12:15986650 | A | C | 1 | a0001c0001t0002g0185 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.637+4214A>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15986650 | |||||||
| chr12:15986668 | T | A | 5 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0046 others(2): Show |
5 | HG03130.hp2 HG03471.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.637+4232T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15986668 | |||||||
| chr12:15986704 | CTT | C | 28 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0026 others(25): Show |
28 | HG01109.hp2 HG01884.hp2 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.637+4271_637+4272d others(4): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 15986704 | ||||||
| chr12:15986782 | T | C | 2 | a0001c0001t0001g0178 a0001c0001t0001g0179 |
2 | NA18942.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.637+4346T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15986782 | |||||||
| chr12:15986840 | T | C | 28 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0026 others(25): Show |
28 | HG01109.hp2 HG01884.hp2 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.637+4404T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15986840 | |||||||
| chr12:15986869 | A | C | 5 | a0001c0001t0001g0007 a0001c0001t0001g0033 a0001c0001t0001g0174 others(2): Show |
5 | HG01884.hp2 HG02258.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.637+4433A>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15986869 | |||||||
| chr12:15987042 | A | G | 1 | a0001c0001t0001g0195 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.637+4606A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15987042 | |||||||
| chr12:15987055 | C | G | 1 | a0001c0001t0001g0099 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.637+4619C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15987055 | |||||||
| chr12:15987229 | A | C | 1 | a0001c0001t0003g0005 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.637+4793A>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15987229 | |||||||
| chr12:15987230 | C | CT | 16 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0042 others(13): Show |
16 | HG00642.hp2 HG01243.hp1 HG02717.hp2 others(13): Show |
intron_variant | MODIFIER | c.637+4818dupT | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 15987230 | ||||||
| chr12:15987230 | CT | C | 12 | a0001c0001t0001g0008 a0001c0001t0001g0034 a0001c0001t0001g0047 others(9): Show |
12 | HG01071.hp2 HG01358.hp1 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.637+4818delT | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 15987230 | ||||||
| chr12:15987230 | CTTT | C | 10 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0030 others(7): Show |
10 | HG01109.hp2 HG02109.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.637+4816_637+4818d others(5): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 15987230 | ||||||
| chr12:15987230 | CTTTT | C | 18 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0033 others(15): Show |
18 | HG01884.hp2 HG02165.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.637+4815_637+4818d others(6): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 15987230 | ||||||
| chr12:15987384 | A | G | 28 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0026 others(25): Show |
28 | HG01109.hp2 HG01884.hp2 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.637+4948A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15987384 | |||||||
| chr12:15987446 | G | A | 28 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0026 others(25): Show |
28 | HG01109.hp2 HG01884.hp2 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.637+5010G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15987446 | |||||||
| chr12:15987479 | C | T | 1 | a0001c0001t0001g0118 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.637+5043C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15987479 | |||||||
| chr12:15987480 | G | A | 1 | a0001c0001t0001g0046 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.637+5044G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15987480 | |||||||
| chr12:15987695 | T | C | 1 | a0001c0001t0003g0013 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.637+5259T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15987695 | |||||||
| chr12:15987829 | G | A | 8 | a0001c0001t0001g0062 a0001c0001t0001g0099 a0001c0001t0001g0114 others(5): Show |
8 | HG02165.hp2 NA18949.hp2 NA18967.hp1 others(5): Show |
intron_variant | MODIFIER | c.637+5393G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15987829 | |||||||
| chr12:15987865 | C | T | 1 | a0001c0001t0001g0218 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.637+5429C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15987865 | |||||||
| chr12:15987921 | G | T | 28 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0026 others(25): Show |
28 | HG01109.hp2 HG01884.hp2 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.637+5485G>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15987921 | |||||||
| chr12:15987946 | C | G | 22 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0105 others(19): Show |
22 | HG00621.hp2 HG02027.hp1 HG02080.hp1 others(19): Show |
intron_variant | MODIFIER | c.637+5510C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15987946 | |||||||
| chr12:15987979 | G | A | 5 | a0001c0001t0001g0039 a0001c0001t0001g0214 a0001c0001t0003g0006 others(2): Show |
5 | HG00733.hp1 HG01934.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.637+5543G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15987979 | |||||||
| chr12:15988022 | G | A | 1 | a0001c0001t0001g0247 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.637+5586G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15988022 | |||||||
| chr12:15988134 | A | C | 18 | a0001c0001t0001g0059 a0001c0001t0001g0064 a0001c0001t0001g0085 others(15): Show |
18 | HG00642.hp1 HG01167.hp1 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.637+5698A>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15988134 | |||||||
| chr12:15988340 | G | A | 80 | a0001c0001t0001g0039 a0001c0001t0001g0045 a0001c0001t0001g0047 others(77): Show |
80 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.637+5904G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15988340 | |||||||
| chr12:15988461 | A | T | 10 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0030 others(7): Show |
10 | HG01109.hp2 HG02109.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.637+6025A>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15988461 | |||||||
| chr12:15988500 | C | T | 28 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0026 others(25): Show |
28 | HG01109.hp2 HG01884.hp2 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.637+6064C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15988500 | |||||||
| chr12:15988505 | A | G | 1 | a0001c0001t0001g0057 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.637+6069A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15988505 | |||||||
| chr12:15988508 | G | A | 1 | a0001c0001t0001g0157 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.637+6072G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15988508 | |||||||
| chr12:15988615 | C | T | 72 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(69): Show |
72 | HG00558.hp2 HG00642.hp1 HG01109.hp2 others(69): Show |
intron_variant | MODIFIER | c.637+6179C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15988615 | |||||||
| chr12:15988656 | G | A | 2 | a0001c0001t0001g0068 a0001c0001t0001g0173 |
2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.637+6220G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15988656 | |||||||
| chr12:15988809 | C | T | 28 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0026 others(25): Show |
28 | HG01109.hp2 HG01884.hp2 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.637+6373C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15988809 | |||||||
| chr12:15988868 | A | G | 1 | a0001c0001t0001g0138 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.637+6432A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15988868 | |||||||
| chr12:15988927 | C | T | 1 | a0001c0001t0001g0207 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.637+6491C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15988927 | |||||||
| chr12:15988941 | T | C | 28 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0026 others(25): Show |
28 | HG01109.hp2 HG01884.hp2 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.637+6505T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15988941 | |||||||
| chr12:15989174 | G | C | 1 | a0001c0001t0003g0013 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.637+6738G>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15989174 | |||||||
| chr12:15989220 | G | A | 8 | a0001c0001t0001g0136 a0001c0001t0001g0144 a0001c0001t0001g0167 others(5): Show |
8 | HG00544.hp1 HG01496.hp1 HG02273.hp1 others(5): Show |
intron_variant | MODIFIER | c.637+6784G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15989220 | |||||||
| chr12:15989228 | C | T | 5 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0046 others(2): Show |
5 | HG03130.hp2 HG03471.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.637+6792C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15989228 | |||||||
| chr12:15989296 | T | C | 28 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0026 others(25): Show |
28 | HG01109.hp2 HG01884.hp2 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.637+6860T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15989296 | |||||||
| chr12:15989316 | T | A | 8 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0046 others(5): Show |
8 | HG02615.hp1 HG02886.hp1 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.637+6880T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15989316 | |||||||
| chr12:15989462 | T | G | 1 | a0001c0001t0001g0129 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.637+7026T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15989462 | |||||||
| chr12:15989633 | T | C | 28 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0026 others(25): Show |
28 | HG01109.hp2 HG01884.hp2 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.637+7197T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15989633 | |||||||
| chr12:15989694 | A | G | 28 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0026 others(25): Show |
28 | HG01109.hp2 HG01884.hp2 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.637+7258A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15989694 | |||||||
| chr12:15989915 | A | G | 28 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0026 others(25): Show |
28 | HG01109.hp2 HG01884.hp2 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.637+7479A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15989915 | |||||||
| chr12:15989982 | C | T | 28 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0026 others(25): Show |
28 | HG01109.hp2 HG01884.hp2 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.637+7546C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15989982 | |||||||
| chr12:15990032 | G | A | 1 | a0001c0001t0001g0098 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.637+7596G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15990032 | |||||||
| chr12:15990187 | C | T | 1 | a0001c0001t0001g0227 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.637+7751C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15990187 | |||||||
| chr12:15990409 | C | T | 2 | a0001c0001t0001g0211 a0001c0001t0003g0018 |
2 | HG02647.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.637+7973C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15990409 | |||||||
| chr12:15990410 | G | A | 1 | a0001c0001t0001g0075 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.637+7974G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15990410 | |||||||
| chr12:15990425 | C | T | 28 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0026 others(25): Show |
28 | HG01109.hp2 HG01884.hp2 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.637+7989C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15990425 | |||||||
| chr12:15990427 | T | G | 1 | a0001c0001t0005g0035 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.637+7991T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15990427 | |||||||
| chr12:15990635 | T | C | 3 | a0001c0001t0001g0118 a0001c0001t0001g0132 a0001c0001t0001g0218 |
3 | HG00280.hp1 NA18949.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.637+8199T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15990635 | |||||||
| chr12:15990779 | A | T | 4 | a0001c0001t0001g0025 a0001c0001t0001g0113 a0001c0001t0001g0127 others(1): Show |
4 | NA18964.hp1 NA18989.hp1 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.637+8343A>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15990779 | |||||||
| chr12:15990802 | G | A | 1 | a0001c0001t0001g0025 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.637+8366G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15990802 | |||||||
| chr12:15990871 | C | G | 71 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(68): Show |
71 | HG00642.hp1 HG01109.hp2 HG01167.hp1 others(68): Show |
intron_variant | MODIFIER | c.637+8435C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15990871 | |||||||
| chr12:15990892 | G | A | 30 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0026 others(27): Show |
30 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.637+8456G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15990892 | |||||||
| chr12:15991159 | G | A | 2 | a0001c0001t0001g0120 a0001c0001t0001g0141 |
2 | HG01168.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.637+8723G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15991159 | |||||||
| chr12:15991191 | C | T | 30 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0026 others(27): Show |
30 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.637+8755C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15991191 | |||||||
| chr12:15991214 | T | A | 1 | a0001c0001t0004g0213 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.637+8778T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15991214 | |||||||
| chr12:15991703 | T | C | 24 | a0001c0001t0001g0009 a0001c0001t0001g0026 a0001c0001t0001g0027 others(21): Show |
24 | HG01109.hp2 HG02109.hp1 HG02165.hp2 others(21): Show |
intron_variant | MODIFIER | c.637+9267T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15991703 | |||||||
| chr12:15991704 | C | T | 1 | a0001c0001t0001g0048 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.637+9268C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15991704 | |||||||
| chr12:15991899 | C | T | 1 | a0001c0001t0003g0013 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.637+9463C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15991899 | |||||||
| chr12:15991949 | A | AATTTTAT others(20): Show |
1 | a0001c0001t0001g0118 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.637+9514_637+9515i others(29): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 15991949 | ||||||
| chr12:15991951 | C | A | 1 | a0001c0001t0001g0118 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.637+9515C>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15991951 | |||||||
| chr12:15992061 | C | T | 29 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0026 others(26): Show |
29 | HG01109.hp2 HG01884.hp2 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.637+9625C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15992061 | |||||||
| chr12:15992069 | A | AT | 45 | a0001c0001t0001g0009 a0001c0001t0001g0026 a0001c0001t0001g0027 others(42): Show |
45 | HG00558.hp2 HG01109.hp2 HG01168.hp1 others(42): Show |
intron_variant | MODIFIER | c.637+9647dupT | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 15992069 | ||||||
| chr12:15992318 | T | A | 4 | a0001c0001t0001g0107 a0001c0001t0001g0128 a0001c0001t0001g0160 others(1): Show |
4 | NA18943.hp1 NA18954.hp1 NA19006.hp2 others(1): Show |
intron_variant | MODIFIER | c.637+9882T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15992318 | |||||||
| chr12:15992322 | A | G | 2 | a0001c0001t0001g0094 a0001c0001t0001g0229 |
2 | NA18943.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.637+9886A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15992322 | |||||||
| chr12:15992330 | G | A | 29 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0026 others(26): Show |
29 | HG01109.hp2 HG01884.hp2 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.637+9894G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15992330 | |||||||
| chr12:15992586 | A | C | 1 | a0001c0001t0001g0009 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.637+10150A>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15992586 | |||||||
| chr12:15993060 | C | T | 1 | a0001c0001t0001g0009 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.637+10624C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15993060 | |||||||
| chr12:15993256 | T | TA | 30 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0026 others(27): Show |
30 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.637+10827dupA | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 15993256 | ||||||
| chr12:15993264 | T | A | 1 | a0001c0001t0001g0111 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.637+10828T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15993264 | |||||||
| chr12:15993444 | C | G | 1 | a0001c0001t0001g0220 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.637+11008C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15993444 | |||||||
| chr12:15993480 | C | CT | 16 | a0001c0001t0001g0060 a0001c0001t0001g0079 a0001c0001t0001g0094 others(13): Show |
16 | HG01168.hp1 HG01169.hp1 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.637+11059dupT | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 15993480 | ||||||
| chr12:15993480 | CT | C | 10 | a0001c0001t0001g0085 a0001c0001t0001g0099 a0001c0001t0001g0103 others(7): Show |
10 | HG01516.hp2 HG02273.hp1 HG02698.hp2 others(7): Show |
intron_variant | MODIFIER | c.637+11059delT | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 15993480 | ||||||
| chr12:15993480 | CTT | C | 5 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0046 others(2): Show |
5 | HG03130.hp2 HG03471.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.637+11058_637+1105 others(6): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 15993480 | ||||||
| chr12:15993492 | T | A | 1 | a0001c0001t0001g0009 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.637+11056T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15993492 | |||||||
| chr12:15993493 | T | A | 26 | a0001c0001t0001g0009 a0001c0001t0001g0026 a0001c0001t0001g0027 others(23): Show |
26 | HG01109.hp2 HG02109.hp1 HG02165.hp2 others(23): Show |
intron_variant | MODIFIER | c.637+11057T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15993493 | |||||||
| chr12:15993494 | T | A | 29 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0026 others(26): Show |
29 | HG01109.hp2 HG01884.hp2 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.637+11058T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15993494 | |||||||
| chr12:15993495 | T | A | 42 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0026 others(39): Show |
42 | HG01109.hp2 HG01358.hp2 HG01884.hp2 others(39): Show |
intron_variant | MODIFIER | c.637+11059T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15993495 | |||||||
| chr12:15993496 | A | T | 2 | a0001c0001t0001g0055 a0001c0001t0001g0190 |
2 | HG02300.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.637+11060A>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15993496 | |||||||
| chr12:15993634 | C | A | 30 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0026 others(27): Show |
30 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.637+11198C>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15993634 | |||||||
| chr12:15993710 | C | T | 5 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0046 others(2): Show |
5 | HG03130.hp2 HG03471.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.637+11274C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15993710 | |||||||
| chr12:15993745 | C | A | 1 | a0001c0001t0001g0034 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.637+11309C>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15993745 | |||||||
| chr12:15993822 | G | A | 14 | a0001c0001t0001g0051 a0001c0001t0001g0060 a0001c0001t0001g0079 others(11): Show |
14 | HG00558.hp2 HG01168.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.637+11386G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15993822 | |||||||
| chr12:15993978 | A | G | 1 | a0001c0001t0004g0116 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.637+11542A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15993978 | |||||||
| chr12:15994202 | A | G | 33 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0026 others(30): Show |
33 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(30): Show |
intron_variant | MODIFIER | c.637+11766A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15994202 | |||||||
| chr12:15994204 | A | C | 29 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0026 others(26): Show |
29 | HG01109.hp2 HG01884.hp2 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.637+11768A>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15994204 | |||||||
| chr12:15994438 | G | A | 1 | a0001c0001t0001g0234 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.637+12002G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15994438 | |||||||
| chr12:15994499 | G | A | 29 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0026 others(26): Show |
29 | HG01109.hp2 HG01884.hp2 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.637+12063G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15994499 | |||||||
| chr12:15994614 | T | C | 47 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0026 others(44): Show |
47 | HG00558.hp2 HG01109.hp2 HG01168.hp1 others(44): Show |
intron_variant | MODIFIER | c.637+12178T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15994614 | |||||||
| chr12:15994692 | A | C | 5 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0046 others(2): Show |
5 | HG03130.hp2 HG03471.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.637+12256A>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15994692 | |||||||
| chr12:15994705 | G | A | 1 | a0001c0001t0001g0125 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.637+12269G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15994705 | |||||||
| chr12:15994819 | A | G | 1 | a0001c0001t0001g0034 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.637+12383A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15994819 | |||||||
| chr12:15994821 | A | G | 1 | a0001c0001t0001g0034 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.637+12385A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15994821 | |||||||
| chr12:15994926 | G | A | 1 | a0001c0001t0001g0034 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.637+12490G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15994926 | |||||||
| chr12:15995379 | G | A | 10 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0030 others(7): Show |
10 | HG01109.hp2 HG02109.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.637+12943G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15995379 | |||||||
| chr12:15995416 | T | C | 30 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0026 others(27): Show |
30 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.637+12980T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15995416 | |||||||
| chr12:15995517 | G | A | 5 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0046 others(2): Show |
5 | HG03130.hp2 HG03471.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.637+13081G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15995517 | |||||||
| chr12:15995871 | C | G | 209 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(206): Show |
211 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(208): Show |
intron_variant | MODIFIER | c.637+13435C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15995871 | |||||||
| chr12:15996013 | C | T | 1 | a0001c0001t0001g0227 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.637+13577C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15996013 | |||||||
| chr12:15996087 | T | A | 30 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0026 others(27): Show |
30 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.637+13651T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15996087 | |||||||
| chr12:15996105 | T | C | 30 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0026 others(27): Show |
30 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.637+13669T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15996105 | |||||||
| chr12:15996106 | A | G | 1 | a0001c0001t0001g0232 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.637+13670A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15996106 | |||||||
| chr12:15996157 | A | ATG | 37 | a0001c0001t0001g0045 a0001c0001t0001g0059 a0001c0001t0001g0064 others(34): Show |
37 | HG00438.hp1 HG00621.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.637+13755_637+1375 others(6): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 15996157 | ||||||
| chr12:15996157 | A | ATGTG | 10 | a0001c0001t0001g0094 a0001c0001t0001g0126 a0001c0001t0001g0190 others(7): Show |
10 | HG00438.hp2 HG01071.hp2 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.637+13753_637+1375 others(8): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 15996157 | ||||||
| chr12:15996157 | ATG | A | 91 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0022 others(88): Show |
92 | HG00280.hp2 HG00544.hp2 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.637+13755_637+1375 others(6): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 15996157 | ||||||
| chr12:15996157 | ATGTG | A | 4 | a0001c0001t0001g0083 a0001c0001t0001g0208 a0001c0001t0001g0246 others(1): Show |
4 | HG02615.hp1 HG02886.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.637+13753_637+1375 others(8): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 15996157 | ||||||
| chr12:15996157 | ATGTGTGT others(1): Show |
A | 13 | a0001c0001t0001g0060 a0001c0001t0001g0079 a0001c0001t0001g0098 others(10): Show |
13 | HG01168.hp1 HG01169.hp1 HG02083.hp1 others(10): Show |
intron_variant | MODIFIER | c.637+13749_637+1375 others(12): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 15996157 | ||||||
| chr12:15996157 | ATGTGTGT others(5): Show |
A | 2 | a0001c0001t0001g0009 a0001c0001t0001g0108 |
2 | HG02818.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.637+13745_637+1375 others(16): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 15996157 | ||||||
| chr12:15996157 | ATGTGTGT others(7): Show |
A | 28 | a0001c0001t0001g0007 a0001c0001t0001g0026 a0001c0001t0001g0027 others(25): Show |
28 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.637+13743_637+1375 others(18): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 15996157 | ||||||
| chr12:15996330 | G | A | 30 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0026 others(27): Show |
30 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.637+13894G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15996330 | |||||||
| chr12:15996355 | G | A | 1 | a0002c0002t0003g0021 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.637+13919G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15996355 | |||||||
| chr12:15996401 | T | C | 79 | a0001c0001t0001g0039 a0001c0001t0001g0045 a0001c0001t0001g0047 others(76): Show |
79 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.637+13965T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15996401 | |||||||
| chr12:15996676 | C | A | 13 | a0001c0001t0001g0060 a0001c0001t0001g0079 a0001c0001t0001g0098 others(10): Show |
13 | HG01168.hp1 HG01169.hp1 HG02083.hp1 others(10): Show |
intron_variant | MODIFIER | c.637+14240C>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15996676 | |||||||
| chr12:15996685 | G | C | 2 | a0001c0001t0001g0061 a0001c0001t0001g0075 |
2 | NA18939.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.637+14249G>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15996685 | |||||||
| chr12:15996737 | A | T | 13 | a0001c0001t0001g0060 a0001c0001t0001g0079 a0001c0001t0001g0098 others(10): Show |
13 | HG01168.hp1 HG01169.hp1 HG02083.hp1 others(10): Show |
intron_variant | MODIFIER | c.637+14301A>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15996737 | |||||||
| chr12:15996805 | T | G | 30 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0026 others(27): Show |
30 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.637+14369T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15996805 | |||||||
| chr12:15996845 | A | G | 30 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0026 others(27): Show |
30 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.637+14409A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15996845 | |||||||
| chr12:15996935 | A | G | 30 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0026 others(27): Show |
30 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.637+14499A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15996935 | |||||||
| chr12:15997229 | A | G | 1 | a0001c0001t0001g0034 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.637+14793A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15997229 | |||||||
| chr12:15997298 | ATTTC | A | 10 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0030 others(7): Show |
10 | HG01109.hp2 HG02109.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.637+14866_637+1486 others(8): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 15997298 | ||||||
| chr12:15997360 | A | T | 1 | a0001c0001t0001g0174 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.637+14924A>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15997360 | |||||||
| chr12:15997386 | T | A | 30 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0026 others(27): Show |
30 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.637+14950T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15997386 | |||||||
| chr12:15997504 | C | T | 1 | a0001c0001t0001g0112 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.637+15068C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15997504 | |||||||
| chr12:15997555 | G | T | 2 | a0001c0001t0001g0008 a0001c0001t0001g0032 |
2 | HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.637+15119G>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15997555 | |||||||
| chr12:15997578 | G | A | 13 | a0001c0001t0001g0060 a0001c0001t0001g0079 a0001c0001t0001g0098 others(10): Show |
13 | HG01168.hp1 HG01169.hp1 HG02083.hp1 others(10): Show |
intron_variant | MODIFIER | c.637+15142G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15997578 | |||||||
| chr12:15997588 | G | A | 30 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0026 others(27): Show |
30 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.637+15152G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15997588 | |||||||
| chr12:15997592 | C | T | 1 | a0001c0001t0001g0034 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.637+15156C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15997592 | |||||||
| chr12:15997653 | C | CTCT | 29 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0026 others(26): Show |
29 | HG01109.hp2 HG01884.hp2 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.637+15219_637+1522 others(7): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 15997653 | ||||||
| chr12:15997661 | A | T | 29 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0026 others(26): Show |
29 | HG01109.hp2 HG01884.hp2 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.637+15225A>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15997661 | |||||||
| chr12:15997662 | A | T | 29 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0026 others(26): Show |
29 | HG01109.hp2 HG01884.hp2 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.637+15226A>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15997662 | |||||||
| chr12:15997715 | C | T | 1 | a0001c0001t0001g0032 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.637+15279C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15997715 | |||||||
| chr12:15997974 | C | T | 29 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0026 others(26): Show |
29 | HG01109.hp2 HG01884.hp2 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.637+15538C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15997974 | |||||||
| chr12:15998083 | C | T | 1 | a0002c0002t0003g0021 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.637+15647C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15998083 | |||||||
| chr12:15998112 | G | A | 30 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0026 others(27): Show |
30 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.637+15676G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15998112 | |||||||
| chr12:15998311 | CTTTATTT others(1): Show |
C | 30 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0026 others(27): Show |
30 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.637+15892_637+1589 others(12): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 15998311 | ||||||
| chr12:15998394 | G | A | 30 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0026 others(27): Show |
30 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.637+15958G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15998394 | |||||||
| chr12:15998403 | C | T | 1 | a0001c0001t0001g0070 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.637+15967C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15998403 | |||||||
| chr12:15998422 | G | A | 30 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0026 others(27): Show |
30 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.637+15986G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15998422 | |||||||
| chr12:15998429 | C | T | 30 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0026 others(27): Show |
30 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.637+15993C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15998429 | |||||||
| chr12:15998474 | T | C | 30 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0026 others(27): Show |
30 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.637+16038T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15998474 | |||||||
| chr12:15998478 | C | T | 4 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0046 others(1): Show |
4 | HG03130.hp2 HG03471.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.637+16042C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15998478 | |||||||
| chr12:15998523 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.637+16087G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15998523 | |||||||
| chr12:15998566 | C | T | 5 | a0001c0001t0001g0007 a0001c0001t0001g0033 a0001c0001t0001g0174 others(2): Show |
5 | HG01884.hp2 HG02258.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.637+16130C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15998566 | |||||||
| chr12:15998579 | T | A | 30 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0026 others(27): Show |
30 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.637+16143T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15998579 | |||||||
| chr12:15998675 | G | A | 30 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0026 others(27): Show |
30 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.637+16239G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15998675 | |||||||
| chr12:15998696 | T | G | 30 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0026 others(27): Show |
30 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.637+16260T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15998696 | |||||||
| chr12:15998754 | A | G | 41 | a0001c0001t0001g0008 a0001c0001t0001g0028 a0001c0001t0001g0029 others(38): Show |
41 | HG00642.hp1 HG01167.hp1 HG01168.hp1 others(38): Show |
intron_variant | MODIFIER | c.637+16318A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15998754 | |||||||
| chr12:15998780 | T | G | 1 | a0001c0001t0001g0048 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.637+16344T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15998780 | |||||||
| chr12:15998807 | A | C | 1 | a0001c0001t0001g0220 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.637+16371A>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15998807 | |||||||
| chr12:15998872 | T | G | 1 | a0001c0001t0001g0034 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.637+16436T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15998872 | |||||||
| chr12:15998898 | C | T | 1 | a0001c0001t0001g0223 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.637+16462C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15998898 | |||||||
| chr12:15998938 | T | C | 30 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0026 others(27): Show |
30 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.637+16502T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15998938 | |||||||
| chr12:15999080 | G | A | 2 | a0001c0001t0001g0207 a0001c0001t0003g0013 |
2 | HG02258.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.637+16644G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15999080 | |||||||
| chr12:15999235 | T | G | 30 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0026 others(27): Show |
30 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.637+16799T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15999235 | |||||||
| chr12:15999244 | C | T | 1 | a0001c0001t0001g0179 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.637+16808C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15999244 | |||||||
| chr12:15999288 | G | C | 1 | a0001c0001t0002g0253 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.637+16852G>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15999288 | |||||||
| chr12:15999475 | A | T | 4 | a0001c0001t0001g0041 a0001c0001t0001g0057 a0001c0001t0001g0115 others(1): Show |
4 | HG02647.hp2 HG03041.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.637+17039A>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15999475 | |||||||
| chr12:15999548 | G | A | 1 | a0001c0001t0001g0034 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.637+17112G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15999548 | |||||||
| chr12:15999722 | C | T | 1 | a0001c0001t0001g0034 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.637+17286C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15999722 | |||||||
| chr12:16000025 | T | C | 1 | a0001c0001t0001g0034 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.637+17589T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16000025 | |||||||
| chr12:16000172 | C | T | 29 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0026 others(26): Show |
29 | HG01109.hp2 HG01884.hp2 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.637+17736C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16000172 | |||||||
| chr12:16000191 | C | T | 1 | a0001c0001t0001g0142 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.637+17755C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16000191 | |||||||
| chr12:16000269 | C | T | 30 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0026 others(27): Show |
30 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.637+17833C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16000269 | |||||||
| chr12:16000434 | C | T | 30 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0026 others(27): Show |
30 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.637+17998C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16000434 | |||||||
| chr12:16000535 | G | A | 2 | a0001c0001t0001g0137 a0001c0001t0001g0164 |
2 | HG02698.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.637+18099G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16000535 | |||||||
| chr12:16000598 | C | T | 1 | a0001c0001t0001g0189 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.637+18162C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16000598 | |||||||
| chr12:16000624 | G | A | 30 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0026 others(27): Show |
30 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.637+18188G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16000624 | |||||||
| chr12:16000632 | A | C | 30 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0026 others(27): Show |
30 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.637+18196A>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16000632 | |||||||
| chr12:16000708 | C | T | 30 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0026 others(27): Show |
30 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.637+18272C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16000708 | |||||||
| chr12:16000852 | GT | G | 18 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0055 others(15): Show |
20 | HG00738.hp2 HG01070.hp1 HG01070.hp2 others(17): Show |
intron_variant | MODIFIER | c.637+18425delT | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 16000852 | ||||||
| chr12:16000854 | T | G | 18 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0055 others(15): Show |
20 | HG00738.hp2 HG01070.hp1 HG01070.hp2 others(17): Show |
intron_variant | MODIFIER | c.637+18418T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16000854 | |||||||
| chr12:16000958 | C | T | 24 | a0001c0001t0001g0009 a0001c0001t0001g0026 a0001c0001t0001g0027 others(21): Show |
24 | HG01109.hp2 HG02109.hp1 HG02165.hp2 others(21): Show |
intron_variant | MODIFIER | c.637+18522C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16000958 | |||||||
| chr12:16001161 | C | T | 2 | a0001c0001t0001g0135 a0001c0001t0001g0146 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.637+18725C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16001161 | |||||||
| chr12:16001200 | C | T | 2 | a0001c0001t0001g0108 a0001c0001t0005g0037 |
2 | HG02055.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.637+18764C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16001200 | |||||||
| chr12:16001304 | G | T | 20 | a0001c0001t0001g0008 a0001c0001t0001g0032 a0001c0001t0001g0059 others(17): Show |
20 | HG00642.hp1 HG01167.hp1 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.637+18868G>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16001304 | |||||||
| chr12:16001417 | G | A | 5 | a0001c0001t0001g0007 a0001c0001t0001g0033 a0001c0001t0001g0174 others(2): Show |
5 | HG01884.hp2 HG02258.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.637+18981G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16001417 | |||||||
| chr12:16001505 | A | G | 1 | a0002c0002t0003g0021 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.637+19069A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16001505 | |||||||
| chr12:16001830 | C | T | 1 | a0001c0001t0003g0005 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.637+19394C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16001830 | |||||||
| chr12:16002100 | C | T | 18 | a0001c0001t0001g0050 a0001c0001t0001g0053 a0001c0001t0001g0093 others(15): Show |
18 | HG00280.hp2 HG00558.hp1 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.637+19664C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16002100 | |||||||
| chr12:16002204 | A | G | 4 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0046 others(1): Show |
4 | HG03130.hp2 HG03471.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.637+19768A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16002204 | |||||||
| chr12:16002342 | AC | A | 60 | a0001c0001t0001g0045 a0001c0001t0001g0048 a0001c0001t0001g0050 others(57): Show |
60 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.637+19908delC | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 16002342 | ||||||
| chr12:16002349 | G | A | 60 | a0001c0001t0001g0045 a0001c0001t0001g0048 a0001c0001t0001g0050 others(57): Show |
60 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.637+19913G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16002349 | |||||||
| chr12:16002509 | T | C | 39 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0022 others(36): Show |
39 | HG01109.hp2 HG01167.hp2 HG01884.hp2 others(36): Show |
intron_variant | MODIFIER | c.637+20073T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16002509 | |||||||
| chr12:16002682 | T | A | 1 | a0001c0001t0001g0040 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.637+20246T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16002682 | |||||||
| chr12:16002687 | T | C | 117 | a0001c0001t0001g0032 a0001c0001t0001g0039 a0001c0001t0001g0045 others(114): Show |
117 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.637+20251T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16002687 | |||||||
| chr12:16002872 | C | A | 1 | a0001c0001t0005g0037 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.637+20436C>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16002872 | |||||||
| chr12:16002895 | A | C | 1 | a0001c0001t0003g0017 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.637+20459A>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16002895 | |||||||
| chr12:16002983 | C | A | 2 | a0001c0001t0002g0139 a0001c0001t0002g0256 |
2 | NA18747.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.637+20547C>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16002983 | |||||||
| chr12:16003105 | A | G | 47 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0022 others(44): Show |
47 | HG01109.hp2 HG01167.hp2 HG01884.hp2 others(44): Show |
intron_variant | MODIFIER | c.637+20669A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16003105 | |||||||
| chr12:16003114 | GT | G | 3 | a0001c0001t0001g0007 a0001c0001t0001g0033 a0001c0001t0001g0174 |
3 | HG01884.hp2 HG02258.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.637+20682delT | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 16003114 | ||||||
| chr12:16003196 | C | T | 1 | a0001c0001t0004g0089 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.637+20760C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16003196 | |||||||
| chr12:16003297 | G | C | 47 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0022 others(44): Show |
47 | HG01109.hp2 HG01167.hp2 HG01884.hp2 others(44): Show |
intron_variant | MODIFIER | c.637+20861G>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16003297 | |||||||
| chr12:16003508 | G | A | 1 | a0001c0001t0002g0078 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.637+21072G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16003508 | |||||||
| chr12:16003518 | C | T | 50 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0022 others(47): Show |
50 | HG01109.hp2 HG01167.hp2 HG01884.hp2 others(47): Show |
intron_variant | MODIFIER | c.637+21082C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16003518 | |||||||
| chr12:16003538 | CTG | C | 10 | a0001c0001t0001g0025 a0001c0001t0001g0061 a0001c0001t0001g0075 others(7): Show |
10 | HG02015.hp1 HG02132.hp1 NA18939.hp1 others(7): Show |
intron_variant | MODIFIER | c.637+21105_637+2110 others(6): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 16003538 | ||||||
| chr12:16003547 | G | C | 1 | a0001c0001t0001g0040 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.637+21111G>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16003547 | |||||||
| chr12:16003578 | G | T | 3 | a0001c0001t0001g0007 a0001c0001t0001g0033 a0001c0001t0001g0174 |
3 | HG01884.hp2 HG02258.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.637+21142G>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16003578 | |||||||
| chr12:16003670 | T | C | 162 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(159): Show |
162 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(159): Show |
intron_variant | MODIFIER | c.637+21234T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16003670 | |||||||
| chr12:16003922 | C | T | 9 | a0001c0001t0001g0007 a0001c0001t0001g0033 a0001c0001t0001g0084 others(6): Show |
9 | HG01884.hp2 HG02258.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.637+21486C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16003922 | |||||||
| chr12:16003933 | C | G | 1 | a0001c0001t0001g0082 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.637+21497C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16003933 | |||||||
| chr12:16004114 | T | C | 1 | a0001c0001t0001g0138 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.637+21678T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16004114 | |||||||
| chr12:16004158 | T | C | 1 | a0001c0001t0001g0121 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.637+21722T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16004158 | |||||||
| chr12:16004363 | A | AATCC | 47 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0022 others(44): Show |
47 | HG01109.hp2 HG01167.hp2 HG01884.hp2 others(44): Show |
intron_variant | MODIFIER | c.637+21928_637+2192 others(8): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 16004363 | ||||||
| chr12:16004365 | C | A | 47 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0022 others(44): Show |
47 | HG01109.hp2 HG01167.hp2 HG01884.hp2 others(44): Show |
intron_variant | MODIFIER | c.637+21929C>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16004365 | |||||||
| chr12:16004384 | T | TC | 50 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0022 others(47): Show |
50 | HG01109.hp2 HG01167.hp2 HG01884.hp2 others(47): Show |
intron_variant | MODIFIER | c.637+21948_637+2194 others(5): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16004384 | |||||||
| chr12:16004857 | A | G | 4 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0046 others(1): Show |
4 | HG03130.hp2 HG03471.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.637+22421A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16004857 | |||||||
| chr12:16005192 | C | A | 10 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0030 others(7): Show |
10 | HG01109.hp2 HG02109.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.637+22756C>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16005192 | |||||||
| chr12:16005224 | G | A | 1 | a0001c0001t0004g0116 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.637+22788G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16005224 | |||||||
| chr12:16005763 | G | A | 2 | a0001c0001t0001g0034 a0001c0001t0003g0013 |
2 | HG01891.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.637+23327G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16005763 | |||||||
| chr12:16005991 | A | G | 2 | a0001c0001t0001g0223 a0001c0001t0001g0231 |
2 | NA18971.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.637+23555A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16005991 | |||||||
| chr12:16006083 | G | C | 1 | a0001c0001t0001g0077 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.637+23647G>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16006083 | |||||||
| chr12:16006181 | C | T | 4 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0110 others(1): Show |
4 | HG02818.hp1 HG02895.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.637+23745C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16006181 | |||||||
| chr12:16006227 | T | C | 2 | a0001c0001t0001g0109 a0001c0001t0001g0110 |
2 | HG02895.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.637+23791T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16006227 | |||||||
| chr12:16006274 | CCAG | C | 47 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0022 others(44): Show |
47 | HG01109.hp2 HG01167.hp2 HG01884.hp2 others(44): Show |
intron_variant | MODIFIER | c.637+23839_637+2384 others(7): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16006274 | |||||||
| chr12:16006324 | C | T | 1 | a0001c0001t0001g0186 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.637+23888C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16006324 | |||||||
| chr12:16006471 | G | A | 2 | a0001c0001t0001g0205 a0001c0001t0001g0226 |
2 | HG01358.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.637+24035G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16006471 | |||||||
| chr12:16006489 | G | A | 2 | a0001c0001t0001g0211 a0001c0001t0003g0018 |
2 | HG02647.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.637+24053G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16006489 | |||||||
| chr12:16006529 | C | G | 1 | a0001c0001t0001g0131 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.637+24093C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16006529 | |||||||
| chr12:16006557 | C | T | 10 | a0001c0001t0001g0025 a0001c0001t0001g0061 a0001c0001t0001g0075 others(7): Show |
10 | HG02015.hp1 HG02132.hp1 NA18939.hp1 others(7): Show |
intron_variant | MODIFIER | c.637+24121C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16006557 | |||||||
| chr12:16006578 | G | A | 3 | a0001c0001t0001g0083 a0001c0001t0001g0208 a0001c0001t0001g0246 |
3 | HG02615.hp1 HG02886.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.637+24142G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16006578 | |||||||
| chr12:16006633 | C | A | 47 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0022 others(44): Show |
47 | HG01109.hp2 HG01167.hp2 HG01884.hp2 others(44): Show |
intron_variant | MODIFIER | c.637+24197C>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16006633 | |||||||
| chr12:16006664 | C | G | 48 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(45): Show |
48 | HG01109.hp2 HG01167.hp2 HG01884.hp2 others(45): Show |
intron_variant | MODIFIER | c.637+24228C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16006664 | |||||||
| chr12:16006763 | G | T | 1 | a0001c0001t0002g0097 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.637+24327G>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16006763 | |||||||
| chr12:16006963 | G | T | 47 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0022 others(44): Show |
47 | HG01109.hp2 HG01167.hp2 HG01884.hp2 others(44): Show |
intron_variant | MODIFIER | c.637+24527G>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16006963 | |||||||
| chr12:16007027 | C | T | 1 | a0001c0001t0001g0245 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.637+24591C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16007027 | |||||||
| chr12:16007175 | G | GT | 11 | a0001c0001t0001g0198 a0001c0001t0001g0244 a0001c0001t0002g0056 others(8): Show |
11 | HG00621.hp1 HG02027.hp1 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.637+24752dupT | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 16007175 | ||||||
| chr12:16007175 | GT | G | 5 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0046 others(2): Show |
5 | HG02630.hp2 HG03130.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.637+24752delT | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 16007175 | ||||||
| chr12:16007189 | G | GT | 6 | a0001c0001t0001g0008 a0001c0001t0001g0135 a0001c0001t0001g0146 others(3): Show |
6 | HG01123.hp1 HG01168.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.637+24765dupT | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 16007189 | ||||||
| chr12:16007189 | G | T | 7 | a0001c0001t0001g0083 a0001c0001t0001g0087 a0001c0001t0001g0088 others(4): Show |
7 | HG02257.hp2 HG02615.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.637+24753G>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16007189 | |||||||
| chr12:16007189 | GT | G | 46 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0022 others(43): Show |
46 | HG01109.hp2 HG01167.hp2 HG01884.hp2 others(43): Show |
intron_variant | MODIFIER | c.637+24765delT | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 16007189 | ||||||
| chr12:16007190 | T | G | 7 | a0001c0001t0001g0083 a0001c0001t0001g0087 a0001c0001t0001g0088 others(4): Show |
7 | HG02257.hp2 HG02615.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.637+24754T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16007190 | |||||||
| chr12:16007255 | C | T | 1 | a0001c0001t0001g0105 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.637+24819C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16007255 | |||||||
| chr12:16007260 | T | G | 19 | a0001c0001t0001g0007 a0001c0001t0001g0025 a0001c0001t0001g0033 others(16): Show |
19 | HG01884.hp2 HG02015.hp1 HG02132.hp1 others(16): Show |
intron_variant | MODIFIER | c.637+24824T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16007260 | |||||||
| chr12:16007290 | T | G | 1 | a0001c0001t0001g0170 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.637+24854T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16007290 | |||||||
| chr12:16007380 | C | T | 1 | a0001c0001t0001g0241 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.637+24944C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16007380 | |||||||
| chr12:16007702 | G | A | 85 | a0001c0001t0001g0032 a0001c0001t0001g0039 a0001c0001t0001g0045 others(82): Show |
85 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.638-24840G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16007702 | |||||||
| chr12:16007842 | GTGTTT | G | 49 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(46): Show |
51 | HG00558.hp1 HG00733.hp2 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.638-24676_638-2467 others(9): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 16007842 | ||||||
| chr12:16008223 | C | T | 1 | a0001c0001t0001g0008 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.638-24319C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16008223 | |||||||
| chr12:16008305 | C | G | 1 | a0001c0001t0001g0008 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.638-24237C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16008305 | |||||||
| chr12:16008319 | A | G | 28 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0026 others(25): Show |
28 | HG01109.hp2 HG01167.hp2 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.638-24223A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16008319 | |||||||
| chr12:16008402 | G | T | 47 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0022 others(44): Show |
47 | HG01109.hp2 HG01167.hp2 HG01884.hp2 others(44): Show |
intron_variant | MODIFIER | c.638-24140G>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16008402 | |||||||
| chr12:16008520 | C | G | 102 | a0001c0001t0001g0032 a0001c0001t0001g0039 a0001c0001t0001g0045 others(99): Show |
102 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.638-24022C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16008520 | |||||||
| chr12:16008634 | G | A | 1 | a0001c0001t0001g0155 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.638-23908G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16008634 | |||||||
| chr12:16009365 | T | A | 1 | a0001c0001t0001g0008 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.638-23177T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16009365 | |||||||
| chr12:16009440 | A | C | 6 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0046 others(3): Show |
6 | HG02630.hp2 HG03130.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.638-23102A>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16009440 | |||||||
| chr12:16010093 | A | G | 47 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0022 others(44): Show |
47 | HG01109.hp2 HG01167.hp2 HG01884.hp2 others(44): Show |
intron_variant | MODIFIER | c.638-22449A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16010093 | |||||||
| chr12:16010140 | T | G | 1 | a0001c0001t0001g0199 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.638-22402T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16010140 | |||||||
| chr12:16010268 | T | A | 2 | a0001c0001t0003g0012 a0002c0002t0003g0021 |
2 | HG02630.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.638-22274T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16010268 | |||||||
| chr12:16010356 | T | A | 10 | a0001c0001t0001g0025 a0001c0001t0001g0061 a0001c0001t0001g0075 others(7): Show |
10 | HG02015.hp1 HG02132.hp1 NA18939.hp1 others(7): Show |
intron_variant | MODIFIER | c.638-22186T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16010356 | |||||||
| chr12:16010449 | C | T | 102 | a0001c0001t0001g0032 a0001c0001t0001g0039 a0001c0001t0001g0045 others(99): Show |
102 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.638-22093C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16010449 | |||||||
| chr12:16010500 | C | T | 1 | a0001c0001t0001g0045 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.638-22042C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16010500 | |||||||
| chr12:16010527 | C | T | 10 | a0001c0001t0001g0025 a0001c0001t0001g0061 a0001c0001t0001g0075 others(7): Show |
10 | HG02015.hp1 HG02132.hp1 NA18939.hp1 others(7): Show |
intron_variant | MODIFIER | c.638-22015C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16010527 | |||||||
| chr12:16010570 | G | A | 1 | a0001c0001t0003g0014 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.638-21972G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16010570 | |||||||
| chr12:16010705 | A | G | 2 | a0001c0001t0001g0209 a0001c0001t0002g0090 |
2 | HG02293.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.638-21837A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16010705 | |||||||
| chr12:16010711 | T | C | 6 | a0001c0001t0001g0083 a0001c0001t0001g0087 a0001c0001t0001g0088 others(3): Show |
6 | HG02257.hp2 HG02615.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.638-21831T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16010711 | |||||||
| chr12:16010754 | T | C | 10 | a0001c0001t0001g0025 a0001c0001t0001g0061 a0001c0001t0001g0075 others(7): Show |
10 | HG02015.hp1 HG02132.hp1 NA18939.hp1 others(7): Show |
intron_variant | MODIFIER | c.638-21788T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16010754 | |||||||
| chr12:16010885 | CACTTATC others(27): Show |
C | 3 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0235 |
3 | HG02257.hp2 HG02809.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.638-21655_638-2162 others(38): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 16010885 | ||||||
| chr12:16011175 | G | C | 3 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0235 |
3 | HG02257.hp2 HG02809.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.638-21367G>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16011175 | |||||||
| chr12:16011176 | T | C | 1 | a0001c0001t0001g0053 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.638-21366T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16011176 | |||||||
| chr12:16011182 | T | G | 1 | a0001c0001t0001g0236 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.638-21360T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16011182 | |||||||
| chr12:16011266 | T | C | 47 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0022 others(44): Show |
47 | HG01109.hp2 HG01167.hp2 HG01884.hp2 others(44): Show |
intron_variant | MODIFIER | c.638-21276T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16011266 | |||||||
| chr12:16011696 | A | G | 3 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0235 |
3 | HG02257.hp2 HG02809.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.638-20846A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16011696 | |||||||
| chr12:16012006 | G | GA | 47 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0022 others(44): Show |
47 | HG01109.hp2 HG01167.hp2 HG01884.hp2 others(44): Show |
intron_variant | MODIFIER | c.638-20530dupA | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 16012006 | ||||||
| chr12:16012086 | G | C | 1 | a0001c0001t0001g0040 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.638-20456G>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16012086 | |||||||
| chr12:16012213 | A | G | 1 | a0001c0001t0004g0213 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.638-20329A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16012213 | |||||||
| chr12:16012280 | A | G | 16 | a0001c0001t0001g0050 a0001c0001t0001g0053 a0001c0001t0001g0095 others(13): Show |
16 | HG00558.hp1 HG00735.hp1 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.638-20262A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16012280 | |||||||
| chr12:16012331 | C | T | 1 | a0001c0001t0001g0061 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.638-20211C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16012331 | |||||||
| chr12:16012378 | A | G | 4 | a0001c0001t0001g0084 a0001c0001t0004g0089 a0001c0001t0004g0116 others(1): Show |
4 | HG02559.hp1 HG02976.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.638-20164A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16012378 | |||||||
| chr12:16012559 | G | A | 3 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0235 |
3 | HG02257.hp2 HG02809.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.638-19983G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16012559 | |||||||
| chr12:16012629 | A | G | 1 | a0001c0001t0003g0005 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.638-19913A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16012629 | |||||||
| chr12:16013146 | G | A | 1 | a0001c0001t0001g0082 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.638-19396G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16013146 | |||||||
| chr12:16013334 | A | G | 1 | a0001c0001t0001g0227 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.638-19208A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16013334 | |||||||
| chr12:16013365 | G | A | 2 | a0001c0001t0001g0137 a0001c0001t0001g0164 |
2 | HG02698.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.638-19177G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16013365 | |||||||
| chr12:16013431 | T | C | 6 | a0001c0001t0001g0083 a0001c0001t0001g0087 a0001c0001t0001g0088 others(3): Show |
6 | HG02257.hp2 HG02615.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.638-19111T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16013431 | |||||||
| chr12:16013482 | A | T | 2 | a0001c0001t0001g0009 a0001c0001t0001g0079 |
2 | HG02572.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.638-19060A>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16013482 | |||||||
| chr12:16013511 | C | T | 47 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0022 others(44): Show |
47 | HG01109.hp2 HG01167.hp2 HG01884.hp2 others(44): Show |
intron_variant | MODIFIER | c.638-19031C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16013511 | |||||||
| chr12:16013958 | C | T | 53 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0022 others(50): Show |
53 | HG01109.hp2 HG01167.hp2 HG01884.hp2 others(50): Show |
intron_variant | MODIFIER | c.638-18584C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16013958 | |||||||
| chr12:16013973 | G | C | 1 | a0001c0001t0001g0175 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.638-18569G>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16013973 | |||||||
| chr12:16014246 | C | T | 9 | a0001c0001t0001g0007 a0001c0001t0001g0033 a0001c0001t0001g0084 others(6): Show |
9 | HG01884.hp2 HG02258.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.638-18296C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16014246 | |||||||
| chr12:16014258 | T | C | 3 | a0001c0001t0001g0083 a0001c0001t0001g0208 a0001c0001t0001g0246 |
3 | HG02615.hp1 HG02886.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.638-18284T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16014258 | |||||||
| chr12:16014428 | T | C | 1 | a0001c0001t0001g0237 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.638-18114T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16014428 | |||||||
| chr12:16014480 | G | C | 1 | a0001c0001t0001g0166 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.638-18062G>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16014480 | |||||||
| chr12:16014545 | G | A | 14 | a0001c0001t0001g0022 a0001c0001t0001g0062 a0001c0001t0001g0099 others(11): Show |
14 | HG01167.hp2 HG02165.hp2 HG02818.hp1 others(11): Show |
intron_variant | MODIFIER | c.638-17997G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16014545 | |||||||
| chr12:16014560 | C | T | 1 | a0001c0001t0001g0112 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.638-17982C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16014560 | |||||||
| chr12:16014840 | T | C | 47 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0022 others(44): Show |
47 | HG01109.hp2 HG01167.hp2 HG01884.hp2 others(44): Show |
intron_variant | MODIFIER | c.638-17702T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16014840 | |||||||
| chr12:16014841 | G | A | 5 | a0001c0001t0001g0007 a0001c0001t0001g0033 a0001c0001t0001g0174 others(2): Show |
5 | HG01884.hp2 HG02258.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.638-17701G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16014841 | |||||||
| chr12:16015414 | G | A | 2 | a0001c0001t0001g0109 a0001c0001t0001g0110 |
2 | HG02895.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.638-17128G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16015414 | |||||||
| chr12:16015508 | C | A | 2 | a0001c0001t0001g0118 a0001c0001t0001g0245 |
2 | NA18968.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.638-17034C>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16015508 | |||||||
| chr12:16015556 | T | C | 1 | a0001c0001t0003g0013 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.638-16986T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16015556 | |||||||
| chr12:16015582 | C | A | 47 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0022 others(44): Show |
47 | HG01109.hp2 HG01167.hp2 HG01884.hp2 others(44): Show |
intron_variant | MODIFIER | c.638-16960C>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16015582 | |||||||
| chr12:16015687 | T | A | 1 | a0001c0001t0001g0008 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.638-16855T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16015687 | |||||||
| chr12:16015794 | C | G | 1 | a0001c0001t0002g0188 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.638-16748C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16015794 | |||||||
| chr12:16015795 | A | G | 5 | a0001c0001t0001g0041 a0001c0001t0001g0057 a0001c0001t0001g0087 others(2): Show |
5 | HG02647.hp2 HG02897.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.638-16747A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16015795 | |||||||
| chr12:16015865 | T | C | 1 | a0001c0001t0001g0183 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.638-16677T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16015865 | |||||||
| chr12:16015899 | T | G | 1 | a0002c0002t0003g0021 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.638-16643T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16015899 | |||||||
| chr12:16015934 | T | A | 1 | a0001c0001t0001g0226 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.638-16608T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16015934 | |||||||
| chr12:16016097 | A | T | 161 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(158): Show |
161 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(158): Show |
intron_variant | MODIFIER | c.638-16445A>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16016097 | |||||||
| chr12:16016353 | T | C | 2 | a0001c0001t0001g0163 a0001c0001t0001g0166 |
2 | HG00642.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.638-16189T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16016353 | |||||||
| chr12:16016569 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.638-15973G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16016569 | |||||||
| chr12:16016594 | G | A | 1 | a0001c0001t0001g0196 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.638-15948G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16016594 | |||||||
| chr12:16016791 | C | CA | 79 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(76): Show |
81 | HG00558.hp1 HG00621.hp2 HG00733.hp2 others(78): Show |
intron_variant | MODIFIER | c.638-15724dupA | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 16016791 | ||||||
| chr12:16016791 | C | CAA | 21 | a0001c0001t0001g0022 a0001c0001t0001g0030 a0001c0001t0001g0041 others(18): Show |
21 | HG01978.hp1 HG02109.hp1 HG02572.hp1 others(18): Show |
intron_variant | MODIFIER | c.638-15725_638-1572 others(6): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 16016791 | ||||||
| chr12:16016791 | C | CAAA | 8 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0031 others(5): Show |
8 | HG01109.hp2 HG02486.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.638-15726_638-1572 others(7): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 16016791 | ||||||
| chr12:16016791 | CA | C | 68 | a0001c0001t0001g0008 a0001c0001t0001g0032 a0001c0001t0001g0039 others(65): Show |
68 | HG00280.hp1 HG00280.hp2 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.638-15724delA | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 16016791 | ||||||
| chr12:16016791 | CAA | C | 8 | a0001c0001t0001g0074 a0001c0001t0001g0135 a0001c0001t0001g0169 others(5): Show |
8 | HG00738.hp1 HG01070.hp2 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.638-15725_638-1572 others(6): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 16016791 | ||||||
| chr12:16016913 | C | A | 1 | a0001c0001t0001g0022 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.638-15629C>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16016913 | |||||||
| chr12:16016940 | T | C | 6 | a0001c0001t0001g0050 a0001c0001t0001g0053 a0001c0001t0001g0159 others(3): Show |
6 | HG00558.hp1 HG02074.hp1 NA18964.hp2 others(3): Show |
intron_variant | MODIFIER | c.638-15602T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16016940 | |||||||
| chr12:16017052 | A | T | 5 | a0001c0001t0001g0002 a0001c0001t0001g0117 a0001c0001t0001g0194 others(2): Show |
6 | HG00738.hp2 HG01070.hp1 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.638-15490A>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16017052 | |||||||
| chr12:16017539 | C | T | 3 | a0001c0001t0001g0007 a0001c0001t0001g0033 a0001c0001t0001g0174 |
3 | HG01884.hp2 HG02258.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.638-15003C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16017539 | |||||||
| chr12:16017545 | G | C | 1 | a0001c0001t0001g0163 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.638-14997G>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16017545 | |||||||
| chr12:16017589 | C | T | 1 | a0001c0001t0001g0092 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.638-14953C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16017589 | |||||||
| chr12:16017640 | T | C | 28 | a0001c0001t0001g0094 a0001c0001t0001g0096 a0001c0001t0001g0103 others(25): Show |
28 | HG00621.hp2 HG01081.hp2 HG02027.hp1 others(25): Show |
intron_variant | MODIFIER | c.638-14902T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16017640 | |||||||
| chr12:16017963 | C | G | 10 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0030 others(7): Show |
10 | HG01109.hp2 HG02109.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.638-14579C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16017963 | |||||||
| chr12:16018041 | A | G | 1 | a0001c0001t0003g0017 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.638-14501A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16018041 | |||||||
| chr12:16018044 | A | C | 3 | a0001c0001t0001g0083 a0001c0001t0001g0208 a0001c0001t0001g0246 |
3 | HG02615.hp1 HG02886.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.638-14498A>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16018044 | |||||||
| chr12:16018044 | A | T | 50 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0022 others(47): Show |
50 | HG01109.hp2 HG01167.hp2 HG01884.hp2 others(47): Show |
intron_variant | MODIFIER | c.638-14498A>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16018044 | |||||||
| chr12:16018120 | T | A | 10 | a0001c0001t0001g0025 a0001c0001t0001g0061 a0001c0001t0001g0075 others(7): Show |
10 | HG02015.hp1 HG02132.hp1 NA18939.hp1 others(7): Show |
intron_variant | MODIFIER | c.638-14422T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16018120 | |||||||
| chr12:16018122 | C | T | 1 | a0001c0001t0002g0256 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.638-14420C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16018122 | |||||||
| chr12:16018146 | C | A | 6 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0046 others(3): Show |
6 | HG02630.hp2 HG03130.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.638-14396C>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16018146 | |||||||
| chr12:16018147 | T | A | 6 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0046 others(3): Show |
6 | HG02630.hp2 HG03130.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.638-14395T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16018147 | |||||||
| chr12:16018170 | T | A | 2 | a0001c0001t0001g0211 a0001c0001t0003g0018 |
2 | HG02647.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.638-14372T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16018170 | |||||||
| chr12:16018192 | G | A | 47 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0022 others(44): Show |
47 | HG01109.hp2 HG01167.hp2 HG01884.hp2 others(44): Show |
intron_variant | MODIFIER | c.638-14350G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16018192 | |||||||
| chr12:16018294 | C | G | 3 | a0001c0001t0001g0083 a0001c0001t0001g0208 a0001c0001t0001g0246 |
3 | HG02615.hp1 HG02886.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.638-14248C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16018294 | |||||||
| chr12:16018359 | A | C | 253 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(250): Show |
255 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(252): Show |
intron_variant | MODIFIER | c.638-14183A>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16018359 | |||||||
| chr12:16019062 | T | C | 1 | a0001c0001t0001g0051 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.638-13480T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16019062 | |||||||
| chr12:16019069 | TGGTGTTG others(46): Show |
T | 1 | a0001c0001t0001g0051 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.638-13471_638-1341 others(57): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 16019069 | ||||||
| chr12:16019083 | C | G | 1 | a0001c0001t0001g0189 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.638-13459C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16019083 | |||||||
| chr12:16019455 | G | A | 3 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0235 |
3 | HG02257.hp2 HG02809.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.638-13087G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16019455 | |||||||
| chr12:16019639 | T | C | 1 | a0001c0001t0005g0036 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.638-12903T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16019639 | |||||||
| chr12:16019705 | T | TC | 9 | a0001c0001t0001g0059 a0001c0001t0001g0064 a0001c0001t0001g0085 others(6): Show |
9 | HG01167.hp1 HG02055.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.638-12835dupC | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 16019705 | ||||||
| chr12:16019978 | G | T | 1 | a0001c0001t0001g0157 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.638-12564G>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16019978 | |||||||
| chr12:16020044 | C | G | 1 | a0001c0001t0001g0104 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.638-12498C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16020044 | |||||||
| chr12:16020357 | G | C | 60 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(57): Show |
60 | HG01109.hp2 HG01167.hp2 HG01884.hp2 others(57): Show |
intron_variant | MODIFIER | c.638-12185G>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16020357 | |||||||
| chr12:16020586 | G | A | 1 | a0001c0001t0001g0074 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.638-11956G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16020586 | |||||||
| chr12:16020921 | G | A | 2 | a0001c0001t0001g0008 a0003c0004t0001g0225 |
2 | HG03041.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.638-11621G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16020921 | |||||||
| chr12:16021154 | T | A | 3 | a0001c0001t0001g0064 a0001c0001t0003g0015 a0001c0001t0003g0020 |
3 | HG02055.hp1 HG02976.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.638-11388T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16021154 | |||||||
| chr12:16021166 | C | T | 1 | a0001c0001t0005g0037 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.638-11376C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16021166 | |||||||
| chr12:16021333 | A | G | 162 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(159): Show |
162 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(159): Show |
intron_variant | MODIFIER | c.638-11209A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16021333 | |||||||
| chr12:16021343 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.638-11199G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16021343 | |||||||
| chr12:16021362 | A | G | 1 | a0001c0001t0001g0132 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.638-11180A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16021362 | |||||||
| chr12:16021778 | C | T | 3 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0235 |
3 | HG02257.hp2 HG02809.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.638-10764C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16021778 | |||||||
| chr12:16021803 | A | G | 47 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0022 others(44): Show |
47 | HG01109.hp2 HG01167.hp2 HG01884.hp2 others(44): Show |
intron_variant | MODIFIER | c.638-10739A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16021803 | |||||||
| chr12:16022040 | A | G | 53 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0022 others(50): Show |
53 | HG01109.hp2 HG01167.hp2 HG01884.hp2 others(50): Show |
intron_variant | MODIFIER | c.638-10502A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16022040 | |||||||
| chr12:16022155 | A | G | 1 | a0001c0001t0001g0022 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.638-10387A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16022155 | |||||||
| chr12:16022480 | A | T | 162 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(159): Show |
162 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(159): Show |
intron_variant | MODIFIER | c.638-10062A>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16022480 | |||||||
| chr12:16022662 | A | G | 2 | a0001c0001t0001g0009 a0001c0001t0001g0079 |
2 | HG02572.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.638-9880A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16022662 | |||||||
| chr12:16022836 | C | T | 3 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0235 |
3 | HG02257.hp2 HG02809.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.638-9706C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16022836 | |||||||
| chr12:16022939 | C | T | 1 | a0001c0001t0001g0248 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.638-9603C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16022939 | |||||||
| chr12:16023061 | C | T | 4 | a0001c0001t0001g0001 a0001c0001t0001g0087 a0001c0001t0001g0088 others(1): Show |
5 | HG01123.hp2 HG01256.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.638-9481C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16023061 | |||||||
| chr12:16023136 | C | T | 47 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0022 others(44): Show |
47 | HG01109.hp2 HG01167.hp2 HG01884.hp2 others(44): Show |
intron_variant | MODIFIER | c.638-9406C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16023136 | |||||||
| chr12:16023266 | G | A | 3 | a0001c0001t0001g0083 a0001c0001t0001g0208 a0001c0001t0001g0246 |
3 | HG02615.hp1 HG02886.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.638-9276G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16023266 | |||||||
| chr12:16023473 | C | CT | 21 | a0001c0001t0001g0008 a0001c0001t0001g0055 a0001c0001t0001g0068 others(18): Show |
21 | HG01109.hp1 HG01361.hp2 HG01516.hp1 others(18): Show |
intron_variant | MODIFIER | c.638-9047dupT | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 16023473 | ||||||
| chr12:16023473 | C | CTT | 8 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0046 others(5): Show |
8 | HG02615.hp1 HG02886.hp1 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.638-9048_638-9047d others(4): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 16023473 | ||||||
| chr12:16023473 | C | CTTTT | 12 | a0001c0001t0001g0007 a0001c0001t0001g0033 a0001c0001t0001g0084 others(9): Show |
12 | HG01884.hp2 HG02257.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.638-9050_638-9047d others(6): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 16023473 | ||||||
| chr12:16023473 | CT | C | 18 | a0001c0001t0001g0009 a0001c0001t0001g0025 a0001c0001t0001g0030 others(15): Show |
18 | HG01261.hp1 HG02015.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.638-9047delT | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 16023473 | ||||||
| chr12:16023473 | CTT | C | 21 | a0001c0001t0001g0022 a0001c0001t0001g0026 a0001c0001t0001g0027 others(18): Show |
21 | HG01109.hp2 HG01891.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.638-9048_638-9047d others(4): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 16023473 | ||||||
| chr12:16023502 | G | A | 1 | a0001c0001t0001g0177 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.638-9040G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16023502 | |||||||
| chr12:16023508 | C | T | 1 | a0001c0001t0001g0008 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.638-9034C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16023508 | |||||||
| chr12:16023540 | G | C | 47 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0022 others(44): Show |
47 | HG01109.hp2 HG01167.hp2 HG01884.hp2 others(44): Show |
intron_variant | MODIFIER | c.638-9002G>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16023540 | |||||||
| chr12:16023547 | G | A | 2 | a0001c0001t0001g0034 a0001c0001t0003g0013 |
2 | HG01891.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.638-8995G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16023547 | |||||||
| chr12:16023578 | C | T | 1 | a0001c0001t0001g0106 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.638-8964C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16023578 | |||||||
| chr12:16023644 | A | T | 6 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0046 others(3): Show |
6 | HG02630.hp2 HG03130.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.638-8898A>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16023644 | |||||||
| chr12:16023723 | C | T | 2 | a0001c0001t0001g0009 a0001c0001t0001g0079 |
2 | HG02572.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.638-8819C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16023723 | |||||||
| chr12:16023784 | G | A | 1 | a0001c0001t0001g0209 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.638-8758G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16023784 | |||||||
| chr12:16023809 | G | T | 1 | a0001c0001t0001g0132 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.638-8733G>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16023809 | |||||||
| chr12:16024040 | G | A | 47 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0022 others(44): Show |
47 | HG01109.hp2 HG01167.hp2 HG01884.hp2 others(44): Show |
intron_variant | MODIFIER | c.638-8502G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16024040 | |||||||
| chr12:16024074 | T | A | 47 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0022 others(44): Show |
47 | HG01109.hp2 HG01167.hp2 HG01884.hp2 others(44): Show |
intron_variant | MODIFIER | c.638-8468T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16024074 | |||||||
| chr12:16024172 | G | A | 1 | a0001c0001t0001g0022 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.638-8370G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16024172 | |||||||
| chr12:16024347 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.638-8195C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16024347 | |||||||
| chr12:16024354 | T | C | 1 | a0001c0001t0001g0220 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.638-8188T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16024354 | |||||||
| chr12:16024497 | G | C | 2 | a0001c0001t0001g0118 a0001c0001t0001g0245 |
2 | NA18968.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.638-8045G>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16024497 | |||||||
| chr12:16024661 | AGCTGTAA others(14): Show |
A | 2 | a0001c0001t0003g0003 a0001c0001t0003g0004 |
2 | HG02559.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.638-7859_638-7839d others(23): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 16024661 | ||||||
| chr12:16024758 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.638-7784G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16024758 | |||||||
| chr12:16024784 | C | T | 1 | a0001c0001t0001g0203 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.638-7758C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16024784 | |||||||
| chr12:16025106 | A | G | 1 | a0001c0001t0001g0034 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.638-7436A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16025106 | |||||||
| chr12:16025163 | A | T | 1 | a0001c0001t0001g0062 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.638-7379A>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16025163 | |||||||
| chr12:16025390 | A | T | 5 | a0001c0001t0001g0083 a0001c0001t0001g0087 a0001c0001t0001g0088 others(2): Show |
5 | HG02615.hp1 HG02809.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.638-7152A>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16025390 | |||||||
| chr12:16025422 | C | T | 2 | a0001c0001t0002g0139 a0001c0001t0002g0256 |
2 | NA18747.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.638-7120C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16025422 | |||||||
| chr12:16025827 | A | G | 63 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(60): Show |
65 | HG00558.hp1 HG00642.hp1 HG00733.hp2 others(62): Show |
intron_variant | MODIFIER | c.638-6715A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16025827 | |||||||
| chr12:16025869 | T | A | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(164): Show |
169 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(166): Show |
intron_variant | MODIFIER | c.638-6673T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16025869 | |||||||
| chr12:16025941 | C | A | 6 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0046 others(3): Show |
6 | HG02630.hp2 HG03130.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.638-6601C>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16025941 | |||||||
| chr12:16025970 | C | T | 1 | a0001c0001t0001g0112 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.638-6572C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16025970 | |||||||
| chr12:16026261 | T | C | 3 | a0001c0001t0001g0083 a0001c0001t0001g0208 a0001c0001t0001g0246 |
3 | HG02615.hp1 HG02886.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.638-6281T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16026261 | |||||||
| chr12:16026295 | G | A | 67 | a0001c0001t0001g0041 a0001c0001t0001g0051 a0001c0001t0001g0062 others(64): Show |
67 | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.638-6247G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16026295 | |||||||
| chr12:16026371 | G | A | 49 | a0001c0001t0001g0041 a0001c0001t0001g0057 a0001c0001t0001g0062 others(46): Show |
49 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(46): Show |
intron_variant | MODIFIER | c.638-6171G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16026371 | |||||||
| chr12:16026386 | T | A | 201 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(198): Show |
203 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(200): Show |
intron_variant | MODIFIER | c.638-6156T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16026386 | |||||||
| chr12:16026437 | G | C | 5 | a0001c0001t0001g0002 a0001c0001t0001g0117 a0001c0001t0001g0194 others(2): Show |
6 | HG00738.hp2 HG01070.hp1 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.638-6105G>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16026437 | |||||||
| chr12:16026448 | A | G | 56 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0030 others(53): Show |
56 | HG00280.hp1 HG00558.hp2 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.638-6094A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16026448 | |||||||
| chr12:16026487 | A | G | 1 | a0001c0001t0002g0161 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.638-6055A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16026487 | |||||||
| chr12:16026594 | AC | A | 10 | a0001c0001t0001g0041 a0001c0001t0001g0062 a0001c0001t0001g0094 others(7): Show |
10 | HG01167.hp2 HG02647.hp2 NA18943.hp2 others(7): Show |
intron_variant | MODIFIER | c.638-5947delC | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16026594 | |||||||
| chr12:16026613 | A | G | 1 | a0001c0001t0001g0112 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.638-5929A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16026613 | |||||||
| chr12:16026614 | C | A | 133 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(130): Show |
135 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(132): Show |
intron_variant | MODIFIER | c.638-5928C>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16026614 | |||||||
| chr12:16026983 | G | A | 102 | a0001c0001t0001g0032 a0001c0001t0001g0041 a0001c0001t0001g0045 others(99): Show |
102 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.638-5559G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16026983 | |||||||
| chr12:16027045 | A | G | 2 | a0001c0001t0001g0068 a0001c0001t0001g0173 |
2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.638-5497A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16027045 | |||||||
| chr12:16027239 | A | G | 49 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(46): Show |
51 | HG00558.hp1 HG00735.hp1 HG00738.hp2 others(48): Show |
intron_variant | MODIFIER | c.638-5303A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16027239 | |||||||
| chr12:16027249 | C | G | 10 | a0001c0001t0001g0041 a0001c0001t0001g0062 a0001c0001t0001g0094 others(7): Show |
10 | HG01167.hp2 HG02647.hp2 NA18943.hp2 others(7): Show |
intron_variant | MODIFIER | c.638-5293C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16027249 | |||||||
| chr12:16027437 | T | G | 1 | a0001c0001t0001g0145 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.638-5105T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16027437 | |||||||
| chr12:16027446 | T | C | 4 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0212 others(1): Show |
4 | HG01081.hp1 HG01884.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.638-5096T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16027446 | |||||||
| chr12:16027452 | G | C | 1 | a0001c0001t0001g0233 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.638-5090G>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16027452 | |||||||
| chr12:16027711 | A | G | 1 | a0001c0003t0001g0073 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.638-4831A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16027711 | |||||||
| chr12:16027880 | C | T | 4 | a0001c0001t0001g0053 a0001c0001t0001g0159 a0001c0001t0001g0218 others(1): Show |
4 | NA18949.hp1 NA19055.hp1 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.638-4662C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16027880 | |||||||
| chr12:16027988 | A | G | 38 | a0001c0001t0001g0041 a0001c0001t0001g0062 a0001c0001t0001g0094 others(35): Show |
38 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.638-4554A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16027988 | |||||||
| chr12:16028050 | C | A | 8 | a0001c0001t0001g0026 a0001c0001t0001g0030 a0001c0001t0001g0031 others(5): Show |
8 | HG01109.hp2 HG02109.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.638-4492C>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16028050 | |||||||
| chr12:16028364 | A | T | 43 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0027 others(40): Show |
45 | HG00558.hp1 HG00735.hp1 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.638-4178A>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16028364 | |||||||
| chr12:16028448 | C | T | 1 | a0001c0001t0001g0163 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.638-4094C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16028448 | |||||||
| chr12:16028489 | T | C | 108 | a0001c0001t0001g0032 a0001c0001t0001g0041 a0001c0001t0001g0045 others(105): Show |
108 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.638-4053T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16028489 | |||||||
| chr12:16028565 | G | A | 1 | a0001c0001t0001g0193 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.638-3977G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16028565 | |||||||
| chr12:16029054 | T | G | 1 | a0001c0001t0002g0078 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.638-3488T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16029054 | |||||||
| chr12:16029280 | G | A | 66 | a0001c0001t0001g0032 a0001c0001t0001g0045 a0001c0001t0001g0047 others(63): Show |
66 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.638-3262G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16029280 | |||||||
| chr12:16029315 | C | T | 2 | a0001c0001t0002g0056 a0001c0001t0002g0185 |
2 | NA18995.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.638-3227C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16029315 | |||||||
| chr12:16029427 | A | AAAAT | 9 | a0001c0001t0001g0067 a0001c0001t0001g0070 a0001c0001t0001g0071 others(6): Show |
9 | HG02257.hp1 HG02615.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.638-3087_638-3084d others(6): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 16029427 | ||||||
| chr12:16029427 | A | AAAATAAA others(5): Show |
1 | a0001c0001t0001g0007 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.638-3095_638-3084d others(14): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 16029427 | ||||||
| chr12:16029427 | A | AAAATAAA others(9): Show |
1 | a0001c0001t0001g0174 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.638-3099_638-3084d others(18): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 16029427 | ||||||
| chr12:16029427 | AAAAT | A | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(152): Show |
157 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(154): Show |
intron_variant | MODIFIER | c.638-3087_638-3084d others(6): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 16029427 | ||||||
| chr12:16029589 | G | C | 2 | a0001c0001t0001g0094 a0001c0001t0001g0229 |
2 | NA18943.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.638-2953G>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16029589 | |||||||
| chr12:16029723 | A | G | 164 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(161): Show |
166 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(163): Show |
intron_variant | MODIFIER | c.638-2819A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16029723 | |||||||
| chr12:16029913 | C | CT | 35 | a0001c0001t0001g0022 a0001c0001t0001g0026 a0001c0001t0001g0030 others(32): Show |
35 | HG00544.hp1 HG00621.hp2 HG01109.hp1 others(32): Show |
intron_variant | MODIFIER | c.638-2602dupT | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 16029913 | ||||||
| chr12:16029913 | C | CTT | 26 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0033 others(23): Show |
26 | HG00438.hp1 HG02080.hp2 HG02132.hp2 others(23): Show |
intron_variant | MODIFIER | c.638-2603_638-2602d others(4): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 16029913 | ||||||
| chr12:16029913 | C | CTTT | 26 | a0001c0001t0001g0032 a0001c0001t0001g0051 a0001c0001t0001g0060 others(23): Show |
26 | HG00280.hp1 HG00558.hp2 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.638-2604_638-2602d others(5): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 16029913 | ||||||
| chr12:16029913 | C | CTTTT | 23 | a0001c0001t0001g0045 a0001c0001t0001g0098 a0001c0001t0001g0101 others(20): Show |
23 | HG00438.hp2 HG00621.hp1 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.638-2605_638-2602d others(6): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 16029913 | ||||||
| chr12:16029913 | C | CTTTTT | 21 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0054 others(18): Show |
21 | HG00738.hp1 HG01256.hp1 HG01261.hp2 others(18): Show |
intron_variant | MODIFIER | c.638-2606_638-2602d others(7): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 16029913 | ||||||
| chr12:16029913 | C | CTTTTTT | 8 | a0001c0001t0001g0063 a0001c0001t0001g0133 a0001c0001t0001g0175 others(5): Show |
8 | HG00280.hp2 HG00544.hp2 HG01123.hp1 others(5): Show |
intron_variant | MODIFIER | c.638-2607_638-2602d others(8): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 16029913 | ||||||
| chr12:16029913 | CT | C | 9 | a0001c0001t0001g0041 a0001c0001t0001g0077 a0001c0001t0001g0087 others(6): Show |
9 | HG01978.hp2 HG02027.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.638-2602delT | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 16029913 | ||||||
| chr12:16029913 | CTT | C | 44 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0027 others(41): Show |
46 | HG00558.hp1 HG00735.hp1 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.638-2603_638-2602d others(4): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 16029913 | ||||||
| chr12:16029913 | CTTTTTTT others(10): Show |
C | 1 | a0001c0001t0001g0193 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.638-2618_638-2602d others(19): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 16029913 | ||||||
| chr12:16030064 | A | T | 2 | a0001c0001t0001g0223 a0001c0001t0001g0231 |
2 | NA18971.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.638-2478A>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16030064 | |||||||
| chr12:16030089 | A | AT | 10 | a0001c0001t0001g0007 a0001c0001t0001g0026 a0001c0001t0001g0030 others(7): Show |
10 | HG01109.hp2 HG01884.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.638-2437dupT | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 16030089 | ||||||
| chr12:16030089 | AT | A | 7 | a0001c0001t0001g0051 a0001c0001t0001g0060 a0001c0001t0001g0156 others(4): Show |
7 | HG00558.hp2 HG01981.hp2 HG03490.hp1 others(4): Show |
intron_variant | MODIFIER | c.638-2437delT | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 16030089 | ||||||
| chr12:16030089 | ATT | A | 148 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(145): Show |
150 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.638-2438_638-2437d others(4): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 16030089 | ||||||
| chr12:16030092 | T | TC | 5 | a0001c0001t0001g0120 a0001c0001t0001g0149 a0001c0001t0001g0150 others(2): Show |
5 | HG01168.hp2 HG01358.hp2 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.638-2450_638-2449i others(3): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16030092 | |||||||
| chr12:16030105 | T | G | 2 | a0001c0001t0001g0207 a0001c0001t0001g0210 |
2 | HG02258.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.638-2437T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16030105 | |||||||
| chr12:16030130 | C | A | 2 | a0001c0001t0001g0120 a0001c0001t0001g0170 |
2 | HG01168.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.638-2412C>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16030130 | |||||||
| chr12:16030148 | G | T | 27 | a0001c0001t0002g0023 a0001c0001t0002g0024 a0001c0001t0002g0049 others(24): Show |
27 | HG00438.hp1 HG00621.hp1 HG02027.hp1 others(24): Show |
intron_variant | MODIFIER | c.638-2394G>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16030148 | |||||||
| chr12:16030221 | C | T | 2 | a0001c0001t0003g0012 a0002c0002t0003g0021 |
2 | HG02630.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.638-2321C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16030221 | |||||||
| chr12:16030224 | G | A | 1 | a0001c0001t0001g0240 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.638-2318G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16030224 | |||||||
| chr12:16030394 | T | C | 1 | a0001c0001t0003g0013 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.638-2148T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16030394 | |||||||
| chr12:16030607 | GATTA | G | 10 | a0001c0001t0001g0041 a0001c0001t0001g0062 a0001c0001t0001g0094 others(7): Show |
10 | HG01167.hp2 HG02647.hp2 NA18943.hp2 others(7): Show |
intron_variant | MODIFIER | c.638-1930_638-1927d others(6): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 16030607 | ||||||
| chr12:16030823 | G | C | 11 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0033 others(8): Show |
11 | HG01168.hp2 HG01358.hp2 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.638-1719G>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16030823 | |||||||
| chr12:16030894 | T | G | 1 | a0001c0001t0001g0068 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.638-1648T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16030894 | |||||||
| chr12:16030932 | C | T | 2 | a0001c0001t0001g0039 a0001c0001t0003g0006 |
2 | HG00733.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.638-1610C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16030932 | |||||||
| chr12:16031097 | G | A | 1 | a0001c0001t0001g0144 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.638-1445G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16031097 | |||||||
| chr12:16031218 | G | A | 1 | a0001c0001t0001g0138 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.638-1324G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16031218 | |||||||
| chr12:16031563 | G | A | 245 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(242): Show |
247 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(244): Show |
intron_variant | MODIFIER | c.638-979G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16031563 | |||||||
| chr12:16031636 | G | C | 195 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(192): Show |
197 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(194): Show |
intron_variant | MODIFIER | c.638-906G>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16031636 | |||||||
| chr12:16031683 | G | A | 1 | a0001c0001t0001g0238 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.638-859G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16031683 | |||||||
| chr12:16031703 | C | G | 27 | a0001c0001t0002g0023 a0001c0001t0002g0024 a0001c0001t0002g0049 others(24): Show |
27 | HG00438.hp1 HG00621.hp1 HG02027.hp1 others(24): Show |
intron_variant | MODIFIER | c.638-839C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16031703 | |||||||
| chr12:16031850 | C | T | 1 | a0001c0001t0001g0211 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.638-692C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16031850 | |||||||
| chr12:16031905 | G | T | 1 | a0001c0001t0001g0093 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.638-637G>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16031905 | |||||||
| chr12:16032283 | C | T | 1 | a0001c0001t0001g0155 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.638-259C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16032283 | |||||||
| chr12:16032529 | CTT | C | 62 | a0001c0001t0001g0032 a0001c0001t0001g0045 a0001c0001t0001g0047 others(59): Show |
62 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(59): Show |
splice_region_variant&intron_variant | LOW | c.638-9_638-8delTT | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 16032529 | ||||||
| chr12:16032781 | T | A | 1 | a0001c0001t0001g0182 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.750+127T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 7/8 | chr12 | 16032781 | |||||||
| chr12:16032998 | T | C | 195 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(192): Show |
197 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(194): Show |
intron_variant | MODIFIER | c.750+344T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 7/8 | chr12 | 16032998 | |||||||
| chr12:16033057 | T | A | 1 | a0001c0001t0001g0128 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.750+403T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 7/8 | chr12 | 16033057 | |||||||
| chr12:16033187 | C | A | 8 | a0001c0001t0001g0026 a0001c0001t0001g0030 a0001c0001t0001g0031 others(5): Show |
8 | HG01109.hp2 HG02109.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.750+533C>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 7/8 | chr12 | 16033187 | |||||||
| chr12:16033213 | A | G | 1 | a0001c0001t0001g0082 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.750+559A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 7/8 | chr12 | 16033213 | |||||||
| chr12:16033333 | A | G | 2 | a0001c0001t0003g0012 a0002c0002t0003g0021 |
2 | HG02630.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.750+679A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 7/8 | chr12 | 16033333 | |||||||
| chr12:16033581 | T | TTG | 41 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0040 others(38): Show |
41 | HG00558.hp1 HG00735.hp1 HG01168.hp1 others(38): Show |
intron_variant | MODIFIER | c.750+969_750+970dup others(2): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr12 | 16033581 | ||||||
| chr12:16033581 | T | TTGTG | 49 | a0001c0001t0001g0032 a0001c0001t0001g0041 a0001c0001t0001g0050 others(46): Show |
49 | HG00280.hp1 HG00621.hp2 HG00642.hp1 others(46): Show |
intron_variant | MODIFIER | c.750+967_750+970dup others(4): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr12 | 16033581 | ||||||
| chr12:16033581 | T | TTGTGTG | 54 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0026 others(51): Show |
55 | HG00558.hp2 HG00738.hp1 HG00738.hp2 others(52): Show |
intron_variant | MODIFIER | c.750+965_750+970dup others(6): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr12 | 16033581 | ||||||
| chr12:16033581 | T | TTGTGTGT others(1): Show |
22 | a0001c0001t0001g0001 a0001c0001t0001g0054 a0001c0001t0001g0068 others(19): Show |
23 | HG00438.hp2 HG00642.hp2 HG01074.hp1 others(20): Show |
intron_variant | MODIFIER | c.750+963_750+970dup others(8): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr12 | 16033581 | ||||||
| chr12:16033581 | T | TTGTGTGT others(3): Show |
5 | a0001c0001t0001g0080 a0001c0001t0001g0153 a0001c0001t0001g0166 others(2): Show |
5 | HG01884.hp1 HG02055.hp2 HG04204.hp1 others(2): Show |
intron_variant | MODIFIER | c.750+961_750+970dup others(10): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr12 | 16033581 | ||||||
| chr12:16033581 | T | TTGTGTGT others(5): Show |
3 | a0001c0001t0001g0033 a0001c0001t0001g0254 a0001c0001t0001g0255 |
3 | HG00544.hp2 HG02135.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.750+959_750+970dup others(12): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr12 | 16033581 | ||||||
| chr12:16033581 | T | TTGTGTGT others(9): Show |
1 | a0001c0001t0001g0133 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.750+955_750+970dup others(16): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr12 | 16033581 | ||||||
| chr12:16033581 | TTG | T | 23 | a0001c0001t0001g0027 a0001c0001t0001g0029 a0001c0001t0001g0046 others(20): Show |
23 | HG02015.hp1 HG02080.hp2 HG02132.hp1 others(20): Show |
intron_variant | MODIFIER | c.750+969_750+970del others(2): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr12 | 16033581 | ||||||
| chr12:16033581 | TTGTGTGT others(5): Show |
T | 1 | a0001c0001t0001g0220 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.750+959_750+970del others(12): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr12 | 16033581 | ||||||
| chr12:16033624 | T | TGTG | 3 | a0001c0001t0001g0194 a0001c0001t0001g0238 a0001c0001t0001g0245 |
3 | HG01243.hp2 NA18968.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.750+970_750+971ins others(3): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 7/8 | chr12 | 16033624 | |||||||
| chr12:16033624 | T | TGTGTG | 3 | a0001c0001t0001g0123 a0001c0001t0001g0130 a0001c0001t0001g0164 |
3 | HG01496.hp2 HG02602.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.750+970_750+971ins others(5): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 7/8 | chr12 | 16033624 | |||||||
| chr12:16033624 | T | TGTGTGTG others(4): Show |
1 | a0001c0001t0001g0063 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.750+970_750+971ins others(11): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 7/8 | chr12 | 16033624 | |||||||
| chr12:16033742 | TGTAA | T | 6 | a0001c0001t0004g0058 a0001c0001t0004g0089 a0001c0001t0004g0116 others(3): Show |
6 | HG02897.hp2 HG02965.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.750+1091_750+1094d others(6): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr12 | 16033742 | ||||||
| chr12:16033833 | C | T | 1 | a0001c0001t0002g0078 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.750+1179C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 7/8 | chr12 | 16033833 | |||||||
| chr12:16034294 | G | A | 47 | a0001c0001t0001g0045 a0001c0001t0001g0048 a0001c0001t0001g0054 others(44): Show |
47 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.750+1640G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 7/8 | chr12 | 16034294 | |||||||
| chr12:16034466 | G | A | 27 | a0001c0001t0002g0023 a0001c0001t0002g0024 a0001c0001t0002g0049 others(24): Show |
27 | HG00438.hp1 HG00621.hp1 HG02027.hp1 others(24): Show |
intron_variant | MODIFIER | c.751-1766G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 7/8 | chr12 | 16034466 | |||||||
| chr12:16034698 | C | T | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(153): Show |
158 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(155): Show |
intron_variant | MODIFIER | c.751-1534C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 7/8 | chr12 | 16034698 | |||||||
| chr12:16034757 | TA | T | 98 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0025 others(95): Show |
98 | HG00544.hp1 HG00621.hp2 HG00642.hp1 others(95): Show |
intron_variant | MODIFIER | c.751-1463delA | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr12 | 16034757 | ||||||
| chr12:16034962 | T | TATAGAGT others(1): Show |
27 | a0001c0001t0002g0023 a0001c0001t0002g0024 a0001c0001t0002g0049 others(24): Show |
27 | HG00438.hp1 HG00621.hp1 HG02027.hp1 others(24): Show |
intron_variant | MODIFIER | c.751-1269_751-1268i others(10): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr12 | 16034962 | ||||||
| chr12:16034964 | C | CAGAGTCA others(1): Show |
226 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(223): Show |
228 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(225): Show |
intron_variant | MODIFIER | c.751-1266_751-1265i others(10): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr12 | 16034964 | ||||||
| chr12:16034964 | C | T | 27 | a0001c0001t0002g0023 a0001c0001t0002g0024 a0001c0001t0002g0049 others(24): Show |
27 | HG00438.hp1 HG00621.hp1 HG02027.hp1 others(24): Show |
intron_variant | MODIFIER | c.751-1268C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 7/8 | chr12 | 16034964 | |||||||
| chr12:16035004 | C | T | 44 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0027 others(41): Show |
46 | HG00558.hp1 HG00735.hp1 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.751-1228C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 7/8 | chr12 | 16035004 | |||||||
| chr12:16035033 | G | A | 60 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(57): Show |
62 | HG00558.hp1 HG00733.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.751-1199G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 7/8 | chr12 | 16035033 | |||||||
| chr12:16035156 | G | C | 2 | a0001c0001t0001g0009 a0001c0001t0001g0208 |
2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.751-1076G>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 7/8 | chr12 | 16035156 | |||||||
| chr12:16035459 | G | T | 26 | a0001c0001t0002g0023 a0001c0001t0002g0024 a0001c0001t0002g0049 others(23): Show |
26 | HG00438.hp1 HG00621.hp1 HG02027.hp1 others(23): Show |
intron_variant | MODIFIER | c.751-773G>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 7/8 | chr12 | 16035459 | |||||||
| chr12:16035855 | G | A | 8 | a0001c0001t0001g0026 a0001c0001t0001g0030 a0001c0001t0001g0031 others(5): Show |
8 | HG01109.hp2 HG02109.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.751-377G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 7/8 | chr12 | 16035855 | |||||||
| chr12:16035969 | A | G | 1 | a0001c0001t0002g0076 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.751-263A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 7/8 | chr12 | 16035969 | |||||||
| chr12:16036047 | A | G | 1 | a0001c0001t0002g0168 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.751-185A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 7/8 | chr12 | 16036047 | |||||||
| chr12:16036080 | A | T | 1 | a0001c0001t0001g0193 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.751-152A>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 7/8 | chr12 | 16036080 | |||||||
| chr12:16036393 | T | C | 1 | a0001c0001t0001g0074 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.900+12T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 8/8 | chr12 | 16036393 | |||||||
| chr12:16036459 | T | C | 1 | a0001c0001t0001g0208 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.900+78T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 8/8 | chr12 | 16036459 | |||||||
| chr12:16036544 | G | C | 4 | a0001c0001t0001g0067 a0001c0001t0001g0070 a0001c0001t0001g0071 others(1): Show |
4 | HG02257.hp1 HG02922.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.901-146G>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 8/8 | chr12 | 16036544 | |||||||
| chr12:16036608 | T | C | 65 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(62): Show |
67 | HG00558.hp1 HG00733.hp2 HG00735.hp1 others(64): Show |
intron_variant | MODIFIER | c.901-82T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 8/8 | chr12 | 16036608 |