Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 124152 |
| ensemblid | ENSG00000174628.17 |
| hgncid | 28556 |
| symbol | IQCK |
| name | IQ motif containing K |
| refseq_nuc | NM_153208.3 |
| refseq_prot | NP_694940.1 |
| ensembl_nuc | ENST00000695302.1 |
| ensembl_prot | ENSP00000511791.1 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 19718271 |
| end | 19858467 |
| strand | + |
| ver | v1.2 |
| region | chr16:19718271-19858467 |
| region5000 | chr16:19713271-19863467 |
| regionname0 | IQCK_chr16_19718271_19858467 |
| regionname5000 | IQCK_chr16_19713271_19863467 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 287 | 185 | 83 | 36 | 39 | 8 | 17 | 28 | IQCK_chr16_19713271_19863467 | IQCK | MAAPR others(282): Show |
chr16 | 19713271 | 19863467 |
| a0002 | 0/0 | 287 | 58 | 6 | 6 | 33 | 2 | 11 | 24 | IQCK_chr16_19713271_19863467 | IQCK | MAAPR others(282): Show |
chr16 | 19713271 | 19863467 |
| a0003 | 0/0 | 287 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | MAAPR others(282): Show |
chr16 | 19713271 | 19863467 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 861 | 184 | 82 | 36 | 39 | 8 | 17 | IQCK_chr16_19713271_19863467 | IQCK | ATGGC others(856): Show |
chr16 | 19713271 | 19863467 | ||
| a0001c0003 | 0/0 | 861 | 1 | 1 | 0 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | ATGGC others(856): Show |
chr16 | 19713271 | 19863467 | ||
| a0002c0002 | 0/0 | 861 | 58 | 6 | 6 | 33 | 2 | 11 | IQCK_chr16_19713271_19863467 | IQCK | ATGGC others(856): Show |
chr16 | 19713271 | 19863467 | ||
| a0003c0004 | 0/0 | 861 | 1 | 1 | 0 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | ATGGC others(856): Show |
chr16 | 19713271 | 19863467 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2819 | 89 | 40 | 14 | 28 | 2 | 5 | IQCK_chr16_19713271_19863467 | IQCK | CTTCC others(2814): Show |
chr16 | 19713271 | 19863467 |
| a0001c0001t0002 | 0/1 | 2819 | 41 | 7 | 12 | 10 | 5 | 6 | IQCK_chr16_19713271_19863467 | IQCK | CTTCC others(2814): Show |
chr16 | 19713271 | 19863467 |
| a0001c0001t0003 | 0/0 | 2818 | 9 | 6 | 2 | 0 | 0 | 1 | IQCK_chr16_19713271_19863467 | IQCK | CTTCC others(2813): Show |
chr16 | 19713271 | 19863467 |
| a0001c0001t0004 | 0/0 | 2816 | 9 | 7 | 2 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | CTTCC others(2811): Show |
chr16 | 19713271 | 19863467 |
| a0001c0001t0005 | 0/0 | 2817 | 8 | 8 | 0 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | CTTCC others(2812): Show |
chr16 | 19713271 | 19863467 |
| a0001c0001t0006 | 0/0 | 2820 | 7 | 0 | 3 | 0 | 0 | 4 | IQCK_chr16_19713271_19863467 | IQCK | CTTCC others(2815): Show |
chr16 | 19713271 | 19863467 |
| a0001c0001t0007 | 0/0 | 2819 | 6 | 6 | 0 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | CTTCC others(2814): Show |
chr16 | 19713271 | 19863467 |
| a0001c0001t0008 | 1/0 | 2819 | 4 | 1 | 1 | 0 | 1 | 0 | IQCK_chr16_19713271_19863467 | IQCK | CTTCC others(2814): Show |
chr16 | 19713271 | 19863467 |
| a0001c0001t0009 | 0/0 | 2818 | 1 | 1 | 0 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | CTTCC others(2813): Show |
chr16 | 19713271 | 19863467 |
| a0001c0001t0010 | 0/0 | 2820 | 3 | 1 | 1 | 1 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | CTTCC others(2815): Show |
chr16 | 19713271 | 19863467 |
| a0001c0001t0011 | 0/0 | 2819 | 1 | 1 | 0 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | CTTCC others(2814): Show |
chr16 | 19713271 | 19863467 |
| a0001c0001t0012 | 0/0 | 2819 | 1 | 1 | 0 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | CTTCC others(2814): Show |
chr16 | 19713271 | 19863467 |
| a0001c0001t0014 | 0/0 | 2819 | 1 | 0 | 1 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | CTTCC others(2814): Show |
chr16 | 19713271 | 19863467 |
| a0001c0001t0015 | 0/0 | 2818 | 1 | 1 | 0 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | CTTCC others(2813): Show |
chr16 | 19713271 | 19863467 |
| a0001c0001t0016 | 0/0 | 2818 | 1 | 0 | 0 | 0 | 0 | 1 | IQCK_chr16_19713271_19863467 | IQCK | CTTCC others(2813): Show |
chr16 | 19713271 | 19863467 |
| a0001c0001t0018 | 0/0 | 2820 | 1 | 1 | 0 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | CTTCC others(2815): Show |
chr16 | 19713271 | 19863467 |
| a0001c0001t0019 | 0/0 | 2820 | 1 | 1 | 0 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | CTTCC others(2815): Show |
chr16 | 19713271 | 19863467 |
| a0001c0003t0003 | 0/0 | 2818 | 1 | 1 | 0 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | CTTCC others(2813): Show |
chr16 | 19713271 | 19863467 |
| a0002c0002t0001 | 0/0 | 2819 | 43 | 1 | 2 | 29 | 0 | 11 | IQCK_chr16_19713271_19863467 | IQCK | CTTCC others(2814): Show |
chr16 | 19713271 | 19863467 |
| a0002c0002t0002 | 0/0 | 2819 | 2 | 0 | 0 | 2 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | CTTCC others(2814): Show |
chr16 | 19713271 | 19863467 |
| a0002c0002t0003 | 0/0 | 2818 | 10 | 3 | 4 | 1 | 2 | 0 | IQCK_chr16_19713271_19863467 | IQCK | CTTCC others(2813): Show |
chr16 | 19713271 | 19863467 |
| a0002c0002t0009 | 0/0 | 2818 | 2 | 2 | 0 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | CTTCC others(2813): Show |
chr16 | 19713271 | 19863467 |
| a0002c0002t0017 | 0/0 | 2820 | 1 | 0 | 0 | 1 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | CTTCC others(2815): Show |
chr16 | 19713271 | 19863467 |
| a0003c0004t0013 | 0/0 | 2819 | 1 | 1 | 0 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | CTTCC others(2814): Show |
chr16 | 19713271 | 19863467 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0002g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0002g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0002g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0002g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0002g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0002g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0002g0071 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0003g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0003g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0003g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0003g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0003g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0003g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0003g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0004g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0004g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0004g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0004g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0004g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0004g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0004g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0004g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0004g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0005g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0005g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0005g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0005g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0005g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0005g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0005g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0005g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0006g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0006g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0006g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0006g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0006g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0006g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0006g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0007g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0007g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0007g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0007g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0007g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0007g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0008g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0008g0080 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0008g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0008g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0009g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0010g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0010g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0010g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0011g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0012g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0014g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0015g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0016g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0018g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0001t0019g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0001c0003t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0002c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0002c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0002c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0002c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0002c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0002c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0002c0002t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0002c0002t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0002c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0002c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0002c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0002c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0002c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0002c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0002c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0002c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0002c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0002c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0002c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0002c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0002c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0002c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0002c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0002c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0002c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0002c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0002c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0002c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0002c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0002c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0002c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0002c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0002c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0002c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0002c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0002c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0002c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0002c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0002c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0002c0002t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0002c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0002c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0002c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0002c0002t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0002c0002t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0002c0002t0003g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0002c0002t0003g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0002c0002t0003g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0002c0002t0003g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0002c0002t0003g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0002c0002t0003g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0002c0002t0003g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0002c0002t0003g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0002c0002t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0002c0002t0003g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0002c0002t0009g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0002c0002t0009g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0002c0002t0017g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| a0003c0004t0013g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0052 | EUR | GBR | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0092 | EUR | GBR | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0077 | EUR | GBR | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0047 | EUR | GBR | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0086 | EUR | FIN | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0130 | EUR | FIN | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | CHS | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG00597 | hp2 | a0002 | c0002 | t0001 | g0204 | EAS | CHS | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG00609 | hp1 | a0002 | c0002 | t0017 | g0212 | EAS | CHS | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG00639 | hp1 | a0001 | c0001 | t0003 | g0096 | AMR | PUR | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0093 | AMR | PUR | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG00733 | hp1 | a0002 | c0002 | t0003 | g0199 | AMR | PUR | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0244 | AMR | PUR | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG00735 | hp2 | a0001 | c0001 | t0010 | g0124 | AMR | PUR | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG00738 | hp1 | a0001 | c0001 | t0006 | g0041 | AMR | PUR | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0035 | AMR | PUR | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0042 | AMR | PUR | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG01081 | hp1 | a0002 | c0002 | t0001 | g0186 | AMR | PUR | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0088 | AMR | PUR | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG01109 | hp2 | a0001 | c0001 | t0004 | g0022 | AMR | PUR | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0079 | AMR | PUR | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG01255 | hp1 | a0002 | c0002 | t0003 | g0235 | AMR | CLM | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG01255 | hp2 | a0001 | c0001 | t0014 | g0049 | AMR | CLM | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG01261 | hp1 | a0001 | c0001 | t0008 | g0102 | AMR | CLM | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG01261 | hp2 | a0002 | c0002 | t0001 | g0232 | AMR | CLM | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0046 | AMR | CLM | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | CLM | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG01358 | hp1 | a0001 | c0001 | t0006 | g0099 | AMR | CLM | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG01358 | hp2 | a0001 | c0001 | t0006 | g0076 | AMR | CLM | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | CLM | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG01433 | hp2 | a0002 | c0002 | t0003 | g0200 | AMR | CLM | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | CLM | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | CLM | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG01884 | hp1 | a0001 | c0001 | t0007 | g0166 | AFR | ACB | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG01884 | hp2 | a0001 | c0001 | t0004 | g0025 | AFR | ACB | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | ACB | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | ACB | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PEL | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | PEL | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG01934 | hp2 | a0001 | c0001 | t0004 | g0012 | AMR | PEL | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG01943 | hp1 | a0001 | c0001 | t0003 | g0068 | AMR | PEL | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0095 | AMR | PEL | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PEL | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | PEL | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0094 | AMR | PEL | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | PEL | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG02015 | hp1 | a0002 | c0002 | t0001 | g0209 | EAS | KHV | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | KHV | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | ACB | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG02055 | hp2 | a0001 | c0001 | t0005 | g0033 | AFR | ACB | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG02056 | hp1 | a0002 | c0002 | t0001 | g0234 | EAS | KHV | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0084 | EAS | KHV | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG02074 | hp1 | a0002 | c0002 | t0002 | g0218 | EAS | KHV | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | KHV | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | KHV | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG02083 | hp2 | a0002 | c0002 | t0001 | g0213 | EAS | KHV | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG02135 | hp1 | a0002 | c0002 | t0001 | g0206 | EAS | KHV | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | KHV | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG02145 | hp1 | a0001 | c0001 | t0005 | g0037 | AFR | ACB | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | ACB | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG02155 | hp1 | a0002 | c0002 | t0001 | g0205 | EAS | CDX | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | CDX | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | ACB | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG02257 | hp2 | a0001 | c0001 | t0007 | g0168 | AFR | ACB | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG02258 | hp1 | a0001 | c0001 | t0007 | g0170 | AFR | ACB | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG02258 | hp2 | a0001 | c0001 | t0005 | g0019 | AFR | ACB | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | ACB | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0015 | AFR | ACB | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0113 | AMR | PEL | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG02300 | hp2 | a0002 | c0002 | t0003 | g0191 | AMR | PEL | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | ACB | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0237 | AFR | ACB | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | KHV | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | KHV | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG02572 | hp2 | a0001 | c0001 | t0004 | g0028 | AFR | GWD | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG02615 | hp1 | a0001 | c0001 | t0004 | g0178 | AFR | GWD | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | GWD | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0242 | AFR | GWD | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | GWD | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG02647 | hp1 | a0001 | c0001 | t0010 | g0147 | AFR | GWD | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0119 | AFR | GWD | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0055 | SAS | PJL | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0081 | SAS | PJL | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG02698 | hp1 | a0002 | c0002 | t0001 | g0225 | SAS | PJL | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG02698 | hp2 | a0001 | c0001 | t0006 | g0118 | SAS | PJL | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | GWD | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG02723 | hp1 | a0001 | c0001 | t0007 | g0169 | AFR | GWD | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | GWD | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG02735 | hp1 | a0002 | c0002 | t0001 | g0228 | SAS | PJL | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG02735 | hp2 | a0001 | c0001 | t0016 | g0089 | SAS | PJL | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG02738 | hp1 | a0001 | c0001 | t0006 | g0073 | SAS | PJL | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0069 | SAS | PJL | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG02809 | hp1 | a0002 | c0002 | t0003 | g0192 | AFR | GWD | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG02809 | hp2 | a0001 | c0001 | t0007 | g0163 | AFR | GWD | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG02818 | hp1 | a0001 | c0001 | t0012 | g0243 | AFR | GWD | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0241 | AFR | GWD | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0029 | AFR | GWD | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG02895 | hp2 | a0001 | c0001 | t0009 | g0239 | AFR | GWD | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | GWD | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | GWD | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG02922 | hp1 | a0001 | c0001 | t0005 | g0039 | AFR | ESN | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ESN | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG02965 | hp1 | a0001 | c0001 | t0005 | g0043 | AFR | ESN | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | ESN | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG02970 | hp1 | a0002 | c0002 | t0003 | g0198 | AFR | ESN | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | ESN | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG02976 | hp1 | a0001 | c0001 | t0005 | g0044 | AFR | ESN | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0136 | AFR | ESN | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG03098 | hp1 | a0001 | c0001 | t0018 | g0164 | AFR | MSL | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | MSL | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | ESN | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | ESN | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG03139 | hp1 | a0001 | c0001 | t0007 | g0165 | AFR | ESN | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG03195 | hp1 | a0001 | c0001 | t0011 | g0132 | AFR | ESN | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG03195 | hp2 | a0002 | c0002 | t0003 | g0197 | AFR | ESN | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | MSL | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0123 | AFR | MSL | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | MSL | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG03239 | hp1 | a0002 | c0002 | t0001 | g0208 | SAS | PJL | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0036 | SAS | PJL | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG03453 | hp1 | a0001 | c0001 | t0004 | g0023 | AFR | MSL | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG03453 | hp2 | a0001 | c0001 | t0003 | g0120 | AFR | MSL | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG03486 | hp1 | a0002 | c0002 | t0001 | g0185 | AFR | MSL | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0016 | AFR | MSL | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG03516 | hp1 | a0001 | c0003 | t0003 | g0021 | AFR | ESN | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG03516 | hp2 | a0001 | c0001 | t0019 | g0238 | AFR | ESN | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0027 | AFR | GWD | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | GWD | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | MSL | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG03579 | hp2 | a0001 | c0001 | t0005 | g0038 | AFR | MSL | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG03688 | hp1 | a0002 | c0002 | t0001 | g0226 | SAS | STU | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0129 | SAS | STU | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG03704 | hp1 | a0002 | c0002 | t0001 | g0183 | SAS | PJL | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG03710 | hp1 | a0002 | c0002 | t0001 | g0227 | SAS | PJL | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0034 | SAS | BEB | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG03834 | hp2 | a0002 | c0002 | t0001 | g0193 | SAS | BEB | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG03942 | hp1 | a0002 | c0002 | t0001 | g0230 | SAS | BEB | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0054 | SAS | BEB | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG04184 | hp1 | a0002 | c0002 | t0001 | g0202 | SAS | BEB | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG04184 | hp2 | a0001 | c0001 | t0006 | g0007 | SAS | BEB | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG04199 | hp1 | a0001 | c0001 | t0006 | g0117 | SAS | STU | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG04199 | hp2 | a0002 | c0002 | t0001 | g0214 | SAS | STU | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0103 | SAS | STU | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | STU | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0188 | SAS | STU | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG04228 | hp2 | a0002 | c0002 | t0001 | g0221 | SAS | STU | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | CHB | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| NA18612 | hp2 | a0002 | c0002 | t0001 | g0184 | EAS | CHB | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| NA18943 | hp2 | a0002 | c0002 | t0001 | g0236 | EAS | JPT | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| NA18944 | hp1 | a0002 | c0002 | t0001 | g0215 | EAS | JPT | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| NA18946 | hp1 | a0002 | c0002 | t0001 | g0187 | EAS | JPT | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| NA18948 | hp2 | a0002 | c0002 | t0001 | g0223 | EAS | JPT | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| NA18952 | hp1 | a0002 | c0002 | t0001 | g0177 | EAS | JPT | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| NA18954 | hp2 | a0002 | c0002 | t0001 | g0211 | EAS | JPT | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| NA18961 | hp1 | a0002 | c0002 | t0001 | g0229 | EAS | JPT | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| NA18963 | hp2 | a0002 | c0002 | t0001 | g0222 | EAS | JPT | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| NA18966 | hp2 | a0002 | c0002 | t0001 | g0210 | EAS | JPT | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| NA18967 | hp2 | a0002 | c0002 | t0001 | g0189 | EAS | JPT | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| NA18968 | hp1 | a0002 | c0002 | t0001 | g0182 | EAS | JPT | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| NA18971 | hp1 | a0002 | c0002 | t0001 | g0216 | EAS | JPT | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| NA18974 | hp1 | a0002 | c0002 | t0001 | g0181 | EAS | JPT | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| NA18980 | hp2 | a0002 | c0002 | t0001 | g0217 | EAS | JPT | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| NA18983 | hp1 | a0002 | c0002 | t0001 | g0219 | EAS | JPT | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| NA18993 | hp2 | a0002 | c0002 | t0001 | g0231 | EAS | JPT | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| NA19002 | hp1 | a0002 | c0002 | t0002 | g0180 | EAS | JPT | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| NA19003 | hp1 | a0002 | c0002 | t0003 | g0203 | EAS | JPT | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| NA19004 | hp1 | a0001 | c0001 | t0010 | g0032 | EAS | JPT | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| NA19004 | hp2 | a0002 | c0002 | t0001 | g0207 | EAS | JPT | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| NA19007 | hp2 | a0002 | c0002 | t0001 | g0224 | EAS | JPT | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| NA19030 | hp1 | a0001 | c0001 | t0008 | g0110 | AFR | LWK | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | LWK | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| NA19043 | hp1 | a0001 | c0001 | t0015 | g0179 | AFR | LWK | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | LWK | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| NA19056 | hp1 | a0002 | c0002 | t0001 | g0176 | EAS | JPT | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| NA19062 | hp1 | a0002 | c0002 | t0001 | g0201 | EAS | JPT | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| NA19067 | hp1 | a0002 | c0002 | t0001 | g0220 | EAS | JPT | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| NA19088 | hp2 | a0002 | c0002 | t0001 | g0233 | EAS | JPT | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| NA19240 | hp1 | a0001 | c0001 | t0003 | g0045 | AFR | YRI | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | YRI | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| NA20129 | hp1 | a0001 | c0001 | t0004 | g0024 | AFR | ASW | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | ASW | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| NA20752 | hp1 | a0001 | c0001 | t0008 | g0074 | EUR | TSI | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| NA20752 | hp2 | a0002 | c0002 | t0003 | g0190 | EUR | TSI | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| NA20805 | hp1 | a0002 | c0002 | t0003 | g0196 | EUR | TSI | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0085 | EUR | TSI | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG02486 | hp1 | a0001 | c0001 | t0004 | g0026 | AFR | ACB | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG02486 | hp2 | a0002 | c0002 | t0009 | g0194 | AFR | ACB | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | ACB | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG02559 | hp2 | a0001 | c0001 | t0005 | g0020 | AFR | ACB | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | MSL | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG03471 | hp2 | a0002 | c0002 | t0009 | g0195 | AFR | MSL | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | USA | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | USA | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| NA20300 | hp1 | a0001 | c0001 | t0004 | g0005 | AFR | USA | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | USA | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| NA21309 | hp1 | a0003 | c0004 | t0013 | g0240 | AFR | LWK | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | LWK | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0071 | REF | REF | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0008 | g0080 | REF | REF | IQCK_chr16_19713271_19863467 | IQCK | chr16 | 19713271 | 19863467 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:19718445 | A | G | 1 | a0003 | 1 | NA21309.hp1 | missense_variant | MODERATE | c.139A>G | p.Thr47Ala | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/9 | 175/2819 | 139/864 | 47/287 | chr16 | 19718445 | |||
| chr16:19788891 | T | C | 1 | a0002 | 58 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(55): Show |
missense_variant | MODERATE | c.659T>C | p.Leu220Pro | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/9 | 695/2819 | 659/864 | 220/287 | chr16 | 19788891 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:19788907 | C | T | 1 | a0001c0003 | 1 | HG03516.hp1 | synonymous_variant | LOW | c.675C>T | p.Phe225Phe | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/9 | 711/2819 | 675/864 | 225/287 | chr16 | 19788907 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:19856759 | T | C | 2 | a0001c0001t0009 a0002c0002t0009 |
3 | HG02486.hp2 HG02895.hp2 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*211T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 9/9 | 211 | chr16 | 19856759 | ||||||
| chr16:19856759 | TC | T | 1 | a0001c0001t0005 | 8 | HG02055.hp2 HG02145.hp1 HG02258.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*215delC | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 9/9 | 215 | INFO_REALIGN_3_PRIME | chr16 | 19856759 | |||||
| chr16:19856808 | G | A | 2 | a0001c0001t0009 a0002c0002t0009 |
3 | HG02486.hp2 HG02895.hp2 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*260G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 9/9 | 260 | chr16 | 19856808 | ||||||
| chr16:19856860 | G | A | 1 | a0001c0001t0011 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*312G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 9/9 | 312 | chr16 | 19856860 | ||||||
| chr16:19857253 | A | T | 3 | a0001c0001t0007 a0001c0001t0018 a0001c0001t0019 |
8 | HG01884.hp1 HG02257.hp2 HG02258.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*705A>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 9/9 | 705 | chr16 | 19857253 | ||||||
| chr16:19857365 | G | C | 23 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(20): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
3_prime_UTR_variant | MODIFIER | c.*817G>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 9/9 | 817 | chr16 | 19857365 | ||||||
| chr16:19857371 | A | T | 1 | a0001c0001t0019 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*823A>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 9/9 | 823 | chr16 | 19857371 | ||||||
| chr16:19857733 | C | T | 1 | a0002c0002t0017 | 1 | HG00609.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1185C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 9/9 | 1185 | chr16 | 19857733 | ||||||
| chr16:19857745 | T | TA | 5 | a0001c0001t0006 a0001c0001t0010 a0001c0001t0018 others(2): Show |
13 | HG00609.hp1 HG00735.hp2 HG00738.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1217dupA | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 9/9 | 1218 | INFO_REALIGN_3_PRIME | chr16 | 19857745 | |||||
| chr16:19857745 | TA | T | 8 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0009 others(5): Show |
33 | HG00639.hp1 HG00733.hp1 HG01255.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*1217delA | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 9/9 | 1217 | INFO_REALIGN_3_PRIME | chr16 | 19857745 | |||||
| chr16:19857745 | TAAA | T | 1 | a0001c0001t0004 | 9 | HG01109.hp2 HG01884.hp2 HG01934.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1215_*1217delAAA | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 9/9 | 1215 | INFO_REALIGN_3_PRIME | chr16 | 19857745 | |||||
| chr16:19858052 | C | T | 1 | a0001c0001t0014 | 1 | HG01255.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1504C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 9/9 | 1504 | chr16 | 19858052 | ||||||
| chr16:19858069 | C | A | 19 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(16): Show |
189 | HG00099.hp2 HG00140.hp1 HG00597.hp1 others(186): Show |
3_prime_UTR_variant | MODIFIER | c.*1521C>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 9/9 | 1521 | chr16 | 19858069 | ||||||
| chr16:19858328 | G | T | 1 | a0003c0004t0013 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1780G>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 9/9 | 1780 | chr16 | 19858328 | ||||||
| chr16:19858435 | T | C | 1 | a0001c0001t0012 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1887T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 9/9 | 1887 | chr16 | 19858435 | ||||||
| chr16:19858452 | G | T | 1 | a0001c0001t0015 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1904G>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 9/9 | 1904 | chr16 | 19858452 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:19718913 | C | T | 1 | a0001c0001t0001g0244 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.181+426C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19718913 | |||||||
| chr16:19719013 | C | T | 3 | a0001c0001t0002g0241 a0001c0001t0002g0242 a0001c0001t0012g0243 |
3 | HG02622.hp2 HG02818.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.181+526C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19719013 | |||||||
| chr16:19719042 | C | G | 1 | a0003c0004t0013g0240 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.181+555C>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19719042 | |||||||
| chr16:19719232 | A | C | 64 | a0001c0001t0002g0237 a0001c0001t0003g0188 a0001c0001t0004g0178 others(61): Show |
64 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(61): Show |
intron_variant | MODIFIER | c.181+745A>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19719232 | |||||||
| chr16:19719235 | C | G | 1 | a0001c0001t0001g0175 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.181+748C>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19719235 | |||||||
| chr16:19719326 | A | G | 3 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0174 |
3 | NA18943.hp1 NA18944.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.181+839A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19719326 | |||||||
| chr16:19719427 | A | G | 9 | a0001c0001t0001g0167 a0001c0001t0001g0171 a0001c0001t0007g0163 others(6): Show |
9 | HG01884.hp1 HG02257.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.181+940A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19719427 | |||||||
| chr16:19719591 | A | C | 36 | a0001c0001t0001g0131 a0001c0001t0001g0133 a0001c0001t0001g0134 others(33): Show |
36 | HG00733.hp2 HG01175.hp1 HG01496.hp1 others(33): Show |
intron_variant | MODIFIER | c.181+1104A>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19719591 | |||||||
| chr16:19719592 | A | C | 4 | a0001c0001t0001g0162 a0001c0001t0002g0237 a0001c0001t0009g0239 others(1): Show |
4 | HG02451.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.181+1105A>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19719592 | |||||||
| chr16:19719662 | G | T | 1 | a0001c0001t0002g0130 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.181+1175G>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19719662 | |||||||
| chr16:19719670 | A | AT | 8 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(5): Show |
8 | HG01255.hp1 HG01928.hp1 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.181+1205dupT | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr16 | 19719670 | ||||||
| chr16:19719670 | AT | A | 28 | a0001c0001t0001g0003 a0001c0001t0001g0131 a0001c0001t0001g0133 others(25): Show |
28 | HG00733.hp2 HG01175.hp1 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.181+1205delT | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr16 | 19719670 | ||||||
| chr16:19719670 | ATTTTTTT others(4): Show |
A | 1 | a0003c0004t0013g0240 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.181+1195_181+1205d others(13): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr16 | 19719670 | ||||||
| chr16:19719724 | G | T | 9 | a0001c0001t0001g0167 a0001c0001t0001g0171 a0001c0001t0007g0163 others(6): Show |
9 | HG01884.hp1 HG02257.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.181+1237G>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19719724 | |||||||
| chr16:19719972 | C | T | 1 | a0001c0001t0010g0124 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.181+1485C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19719972 | |||||||
| chr16:19720109 | G | A | 27 | a0001c0001t0001g0131 a0001c0001t0001g0133 a0001c0001t0001g0134 others(24): Show |
27 | HG00733.hp2 HG01175.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.181+1622G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19720109 | |||||||
| chr16:19720294 | T | C | 2 | a0001c0001t0004g0178 a0001c0001t0015g0179 |
2 | HG02615.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.181+1807T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19720294 | |||||||
| chr16:19720870 | A | G | 1 | a0003c0004t0013g0240 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.181+2383A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19720870 | |||||||
| chr16:19721006 | C | T | 6 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(3): Show |
6 | HG01496.hp1 HG01891.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.181+2519C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19721006 | |||||||
| chr16:19721012 | G | GA | 8 | a0001c0001t0001g0008 a0001c0001t0001g0131 a0001c0001t0002g0006 others(5): Show |
8 | HG00609.hp2 HG01175.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.181+2539dupA | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr16 | 19721012 | ||||||
| chr16:19721012 | GA | G | 8 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0002g0119 others(5): Show |
8 | HG02622.hp1 HG02622.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.181+2539delA | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr16 | 19721012 | ||||||
| chr16:19721026 | A | G | 6 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(3): Show |
6 | HG01496.hp1 HG01891.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.181+2539A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19721026 | |||||||
| chr16:19721027 | C | A | 10 | a0001c0001t0001g0167 a0001c0001t0001g0171 a0001c0001t0002g0004 others(7): Show |
10 | HG01884.hp1 HG02257.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.181+2540C>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19721027 | |||||||
| chr16:19721046 | T | C | 9 | a0001c0001t0001g0167 a0001c0001t0001g0171 a0001c0001t0007g0163 others(6): Show |
9 | HG01884.hp1 HG02257.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.181+2559T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19721046 | |||||||
| chr16:19721055 | T | G | 6 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(3): Show |
6 | HG01496.hp1 HG01891.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.181+2568T>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19721055 | |||||||
| chr16:19721076 | G | T | 2 | a0001c0001t0006g0117 a0001c0001t0006g0118 |
2 | HG02698.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.181+2589G>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19721076 | |||||||
| chr16:19721133 | T | C | 3 | a0001c0001t0001g0011 a0001c0001t0002g0009 a0001c0001t0002g0010 |
3 | HG01928.hp2 HG01934.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.181+2646T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19721133 | |||||||
| chr16:19721223 | C | CT | 8 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0002g0119 others(5): Show |
8 | HG02622.hp1 HG02622.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.181+2738dupT | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr16 | 19721223 | ||||||
| chr16:19721282 | C | T | 1 | a0001c0001t0001g0116 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.181+2795C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19721282 | |||||||
| chr16:19721437 | A | C | 1 | a0001c0001t0003g0123 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.181+2950A>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19721437 | |||||||
| chr16:19721587 | CT | C | 135 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(132): Show |
135 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(132): Show |
intron_variant | MODIFIER | c.181+3116delT | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr16 | 19721587 | ||||||
| chr16:19721690 | A | G | 64 | a0001c0001t0002g0237 a0001c0001t0003g0188 a0001c0001t0004g0178 others(61): Show |
64 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(61): Show |
intron_variant | MODIFIER | c.181+3203A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19721690 | |||||||
| chr16:19721759 | G | A | 8 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0002g0119 others(5): Show |
8 | HG02622.hp1 HG02622.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.181+3272G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19721759 | |||||||
| chr16:19721868 | G | A | 1 | a0001c0001t0002g0004 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.181+3381G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19721868 | |||||||
| chr16:19721899 | T | C | 10 | a0001c0001t0001g0167 a0001c0001t0001g0171 a0001c0001t0007g0163 others(7): Show |
10 | HG01884.hp1 HG02257.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.181+3412T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19721899 | |||||||
| chr16:19721950 | T | TAATC | 136 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(133): Show |
136 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(133): Show |
intron_variant | MODIFIER | c.181+3466_181+3469d others(6): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr16 | 19721950 | ||||||
| chr16:19722078 | G | C | 2 | a0001c0001t0002g0002 a0001c0001t0002g0031 |
2 | NA18946.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.181+3591G>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19722078 | |||||||
| chr16:19722179 | C | T | 9 | a0001c0001t0001g0167 a0001c0001t0001g0171 a0001c0001t0007g0163 others(6): Show |
9 | HG01884.hp1 HG02257.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.181+3692C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19722179 | |||||||
| chr16:19722219 | G | A | 1 | a0001c0001t0001g0152 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.181+3732G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19722219 | |||||||
| chr16:19722229 | A | T | 27 | a0001c0001t0001g0131 a0001c0001t0001g0133 a0001c0001t0001g0134 others(24): Show |
27 | HG00733.hp2 HG01175.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.181+3742A>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19722229 | |||||||
| chr16:19722230 | G | T | 27 | a0001c0001t0001g0131 a0001c0001t0001g0133 a0001c0001t0001g0134 others(24): Show |
27 | HG00733.hp2 HG01175.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.181+3743G>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19722230 | |||||||
| chr16:19722231 | A | C | 27 | a0001c0001t0001g0131 a0001c0001t0001g0133 a0001c0001t0001g0134 others(24): Show |
27 | HG00733.hp2 HG01175.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.181+3744A>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19722231 | |||||||
| chr16:19722232 | A | T | 27 | a0001c0001t0001g0131 a0001c0001t0001g0133 a0001c0001t0001g0134 others(24): Show |
27 | HG00733.hp2 HG01175.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.181+3745A>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19722232 | |||||||
| chr16:19722264 | T | C | 136 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(133): Show |
136 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(133): Show |
intron_variant | MODIFIER | c.181+3777T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19722264 | |||||||
| chr16:19722390 | G | A | 1 | a0001c0001t0010g0032 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.181+3903G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19722390 | |||||||
| chr16:19722674 | C | T | 1 | a0001c0001t0001g0129 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.181+4187C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19722674 | |||||||
| chr16:19722694 | T | G | 1 | a0002c0002t0001g0183 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.181+4207T>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19722694 | |||||||
| chr16:19722711 | CT | C | 16 | a0001c0001t0001g0040 a0001c0001t0001g0048 a0001c0001t0002g0034 others(13): Show |
16 | HG00140.hp2 HG00738.hp1 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.181+4238delT | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr16 | 19722711 | ||||||
| chr16:19722751 | C | T | 2 | a0001c0001t0001g0151 a0001c0001t0001g0155 |
2 | HG00733.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.181+4264C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19722751 | |||||||
| chr16:19722932 | G | A | 2 | a0002c0002t0001g0176 a0002c0002t0001g0184 |
2 | NA18612.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.181+4445G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19722932 | |||||||
| chr16:19722982 | G | A | 2 | a0002c0002t0001g0185 a0002c0002t0001g0186 |
2 | HG01081.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.181+4495G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19722982 | |||||||
| chr16:19723231 | C | A | 1 | a0002c0002t0001g0187 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.181+4744C>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19723231 | |||||||
| chr16:19723232 | T | G | 1 | a0002c0002t0001g0187 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.181+4745T>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19723232 | |||||||
| chr16:19723236 | G | T | 1 | a0002c0002t0001g0187 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.181+4749G>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19723236 | |||||||
| chr16:19723266 | C | G | 9 | a0001c0001t0001g0167 a0001c0001t0001g0171 a0001c0001t0007g0163 others(6): Show |
9 | HG01884.hp1 HG02257.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.181+4779C>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19723266 | |||||||
| chr16:19723519 | T | G | 1 | a0001c0001t0001g0175 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.181+5032T>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19723519 | |||||||
| chr16:19723532 | C | T | 135 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(132): Show |
135 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(132): Show |
intron_variant | MODIFIER | c.181+5045C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19723532 | |||||||
| chr16:19723716 | G | A | 1 | a0001c0001t0001g0162 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.181+5229G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19723716 | |||||||
| chr16:19723960 | C | CA | 8 | a0001c0001t0002g0006 a0001c0001t0002g0119 a0001c0001t0002g0237 others(5): Show |
8 | HG01175.hp2 HG01255.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.181+5489dupA | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr16 | 19723960 | ||||||
| chr16:19724052 | A | G | 3 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0002g0113 |
3 | HG01975.hp1 HG02300.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.181+5565A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19724052 | |||||||
| chr16:19724061 | T | C | 1 | a0003c0004t0013g0240 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.181+5574T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19724061 | |||||||
| chr16:19724208 | C | T | 46 | a0002c0002t0001g0176 a0002c0002t0001g0177 a0002c0002t0001g0181 others(43): Show |
46 | HG00597.hp2 HG00609.hp1 HG01081.hp1 others(43): Show |
intron_variant | MODIFIER | c.181+5721C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19724208 | |||||||
| chr16:19724209 | G | A | 1 | a0001c0001t0004g0012 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.181+5722G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19724209 | |||||||
| chr16:19724303 | A | G | 46 | a0002c0002t0001g0176 a0002c0002t0001g0177 a0002c0002t0001g0181 others(43): Show |
46 | HG00597.hp2 HG00609.hp1 HG01081.hp1 others(43): Show |
intron_variant | MODIFIER | c.181+5816A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19724303 | |||||||
| chr16:19724338 | C | A | 1 | a0001c0001t0001g0013 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.181+5851C>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19724338 | |||||||
| chr16:19724375 | T | C | 135 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(132): Show |
135 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(132): Show |
intron_variant | MODIFIER | c.181+5888T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19724375 | |||||||
| chr16:19724404 | C | A | 2 | a0001c0001t0007g0163 a0001c0001t0018g0164 |
2 | HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.181+5917C>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19724404 | |||||||
| chr16:19724472 | C | A | 6 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(3): Show |
6 | HG01496.hp1 HG01891.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.182-5958C>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19724472 | |||||||
| chr16:19724495 | G | A | 1 | a0001c0001t0002g0050 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.182-5935G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19724495 | |||||||
| chr16:19724520 | T | C | 1 | a0001c0001t0001g0125 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.182-5910T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19724520 | |||||||
| chr16:19724524 | G | T | 1 | a0001c0001t0001g0112 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.182-5906G>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19724524 | |||||||
| chr16:19724563 | C | G | 1 | a0001c0001t0001g0112 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.182-5867C>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19724563 | |||||||
| chr16:19724578 | C | G | 127 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(124): Show |
127 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(124): Show |
intron_variant | MODIFIER | c.182-5852C>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19724578 | |||||||
| chr16:19724634 | T | C | 2 | a0001c0001t0001g0051 a0001c0001t0001g0126 |
2 | HG02083.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.182-5796T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19724634 | |||||||
| chr16:19724682 | C | G | 9 | a0001c0001t0001g0167 a0001c0001t0001g0171 a0001c0001t0007g0163 others(6): Show |
9 | HG01884.hp1 HG02257.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.182-5748C>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19724682 | |||||||
| chr16:19724709 | T | C | 1 | a0001c0001t0002g0052 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.182-5721T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19724709 | |||||||
| chr16:19724753 | C | T | 9 | a0001c0001t0001g0167 a0001c0001t0001g0171 a0001c0001t0007g0163 others(6): Show |
9 | HG01884.hp1 HG02257.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.182-5677C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19724753 | |||||||
| chr16:19725198 | A | C | 21 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(18): Show |
21 | HG01109.hp2 HG01884.hp2 HG01934.hp2 others(18): Show |
intron_variant | MODIFIER | c.182-5232A>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19725198 | |||||||
| chr16:19725200 | T | A | 2 | a0001c0001t0001g0133 a0001c0001t0011g0132 |
2 | HG02630.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.182-5230T>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19725200 | |||||||
| chr16:19725242 | G | C | 21 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(18): Show |
21 | HG01109.hp2 HG01884.hp2 HG01934.hp2 others(18): Show |
intron_variant | MODIFIER | c.182-5188G>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19725242 | |||||||
| chr16:19725330 | G | A | 21 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(18): Show |
21 | HG01109.hp2 HG01884.hp2 HG01934.hp2 others(18): Show |
intron_variant | MODIFIER | c.182-5100G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19725330 | |||||||
| chr16:19725341 | C | T | 1 | a0001c0001t0001g0150 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.182-5089C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19725341 | |||||||
| chr16:19725801 | C | T | 1 | a0001c0001t0001g0112 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.182-4629C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19725801 | |||||||
| chr16:19725911 | CT | C | 21 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(18): Show |
21 | HG01109.hp2 HG01884.hp2 HG01934.hp2 others(18): Show |
intron_variant | MODIFIER | c.182-4511delT | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr16 | 19725911 | ||||||
| chr16:19726060 | C | T | 9 | a0001c0001t0001g0167 a0001c0001t0001g0171 a0001c0001t0007g0163 others(6): Show |
9 | HG01884.hp1 HG02257.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.182-4370C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19726060 | |||||||
| chr16:19726103 | A | G | 69 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(66): Show |
69 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(66): Show |
intron_variant | MODIFIER | c.182-4327A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19726103 | |||||||
| chr16:19726138 | T | A | 1 | a0001c0001t0001g0053 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.182-4292T>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19726138 | |||||||
| chr16:19726183 | G | GGATTACA others(1): Show |
21 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(18): Show |
21 | HG01109.hp2 HG01884.hp2 HG01934.hp2 others(18): Show |
intron_variant | MODIFIER | c.182-4245_182-4238d others(10): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr16 | 19726183 | ||||||
| chr16:19726219 | C | T | 1 | a0001c0001t0001g0111 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.182-4211C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19726219 | |||||||
| chr16:19726326 | A | G | 3 | a0001c0001t0002g0237 a0001c0001t0009g0239 a0001c0001t0019g0238 |
3 | HG02451.hp2 HG02895.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.182-4104A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19726326 | |||||||
| chr16:19726517 | G | A | 1 | a0001c0001t0007g0165 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.182-3913G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19726517 | |||||||
| chr16:19726712 | G | GT | 3 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0003g0120 |
3 | HG02622.hp1 HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.182-3717dupT | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr16 | 19726712 | ||||||
| chr16:19726817 | C | A | 1 | a0003c0004t0013g0240 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.182-3613C>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19726817 | |||||||
| chr16:19726825 | T | C | 3 | a0001c0001t0002g0241 a0001c0001t0002g0242 a0001c0001t0012g0243 |
3 | HG02622.hp2 HG02818.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.182-3605T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19726825 | |||||||
| chr16:19726898 | C | T | 12 | a0002c0002t0001g0193 a0002c0002t0003g0190 a0002c0002t0003g0191 others(9): Show |
12 | HG00733.hp1 HG01255.hp1 HG01433.hp2 others(9): Show |
intron_variant | MODIFIER | c.182-3532C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19726898 | |||||||
| chr16:19727108 | G | A | 1 | a0003c0004t0013g0240 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.182-3322G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19727108 | |||||||
| chr16:19727110 | G | A | 21 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(18): Show |
21 | HG01109.hp2 HG01884.hp2 HG01934.hp2 others(18): Show |
intron_variant | MODIFIER | c.182-3320G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19727110 | |||||||
| chr16:19727125 | G | A | 1 | a0001c0001t0001g0134 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.182-3305G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19727125 | |||||||
| chr16:19727129 | T | A | 6 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(3): Show |
6 | HG01496.hp1 HG01891.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.182-3301T>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19727129 | |||||||
| chr16:19727130 | C | A | 6 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(3): Show |
6 | HG01496.hp1 HG01891.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.182-3300C>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19727130 | |||||||
| chr16:19727130 | C | CA | 8 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(5): Show |
8 | HG01175.hp2 HG02280.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.182-3287dupA | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr16 | 19727130 | ||||||
| chr16:19727164 | T | TA | 21 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(18): Show |
21 | HG01109.hp2 HG01884.hp2 HG01934.hp2 others(18): Show |
intron_variant | MODIFIER | c.182-3265dupA | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr16 | 19727164 | ||||||
| chr16:19727195 | G | A | 21 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(18): Show |
21 | HG01109.hp2 HG01884.hp2 HG01934.hp2 others(18): Show |
intron_variant | MODIFIER | c.182-3235G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19727195 | |||||||
| chr16:19727215 | T | A | 1 | a0001c0001t0001g0112 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.182-3215T>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19727215 | |||||||
| chr16:19727227 | A | G | 1 | a0002c0002t0001g0177 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.182-3203A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19727227 | |||||||
| chr16:19727364 | A | T | 1 | a0001c0001t0001g0112 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.182-3066A>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19727364 | |||||||
| chr16:19727375 | T | G | 1 | a0003c0004t0013g0240 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.182-3055T>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19727375 | |||||||
| chr16:19727435 | A | C | 21 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(18): Show |
21 | HG01109.hp2 HG01884.hp2 HG01934.hp2 others(18): Show |
intron_variant | MODIFIER | c.182-2995A>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19727435 | |||||||
| chr16:19727585 | A | AC | 35 | a0001c0001t0001g0003 a0001c0001t0001g0048 a0001c0001t0001g0098 others(32): Show |
35 | HG00099.hp1 HG00140.hp2 HG00597.hp1 others(32): Show |
intron_variant | MODIFIER | c.182-2833dupC | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr16 | 19727585 | ||||||
| chr16:19727585 | AC | A | 68 | a0001c0001t0001g0018 a0001c0001t0001g0111 a0001c0001t0001g0121 others(65): Show |
68 | HG00597.hp2 HG00609.hp1 HG01081.hp1 others(65): Show |
intron_variant | MODIFIER | c.182-2833delC | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr16 | 19727585 | ||||||
| chr16:19727585 | ACC | A | 20 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(17): Show |
20 | HG01109.hp2 HG01884.hp2 HG01934.hp2 others(17): Show |
intron_variant | MODIFIER | c.182-2834_182-2833d others(4): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr16 | 19727585 | ||||||
| chr16:19727598 | A | C | 27 | a0001c0001t0001g0131 a0001c0001t0001g0133 a0001c0001t0001g0134 others(24): Show |
27 | HG00733.hp2 HG01175.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.182-2832A>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19727598 | |||||||
| chr16:19727639 | G | A | 2 | a0001c0001t0005g0019 a0001c0001t0005g0020 |
2 | HG02258.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.182-2791G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19727639 | |||||||
| chr16:19727680 | C | G | 63 | a0001c0001t0002g0237 a0001c0001t0004g0178 a0001c0001t0009g0239 others(60): Show |
63 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(60): Show |
intron_variant | MODIFIER | c.182-2750C>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19727680 | |||||||
| chr16:19727930 | G | A | 3 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0174 |
3 | NA18943.hp1 NA18944.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.182-2500G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19727930 | |||||||
| chr16:19727958 | C | T | 9 | a0001c0001t0001g0167 a0001c0001t0001g0171 a0001c0001t0007g0163 others(6): Show |
9 | HG01884.hp1 HG02257.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.182-2472C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19727958 | |||||||
| chr16:19728104 | TCTC | T | 27 | a0001c0001t0001g0131 a0001c0001t0001g0133 a0001c0001t0001g0134 others(24): Show |
27 | HG00733.hp2 HG01175.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.182-2323_182-2321d others(5): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr16 | 19728104 | ||||||
| chr16:19728115 | C | T | 6 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(3): Show |
6 | HG02717.hp2 HG02886.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.182-2315C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19728115 | |||||||
| chr16:19728151 | T | A | 1 | a0002c0002t0002g0180 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.182-2279T>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19728151 | |||||||
| chr16:19728206 | A | G | 1 | a0001c0001t0001g0097 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.182-2224A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19728206 | |||||||
| chr16:19728283 | C | G | 1 | a0001c0001t0002g0052 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.182-2147C>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19728283 | |||||||
| chr16:19728413 | C | A | 1 | a0001c0001t0001g0145 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.182-2017C>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19728413 | |||||||
| chr16:19728740 | T | C | 9 | a0001c0001t0001g0167 a0001c0001t0001g0171 a0001c0001t0007g0163 others(6): Show |
9 | HG01884.hp1 HG02257.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.182-1690T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19728740 | |||||||
| chr16:19728915 | A | G | 136 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(133): Show |
136 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(133): Show |
intron_variant | MODIFIER | c.182-1515A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19728915 | |||||||
| chr16:19728921 | A | G | 70 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(67): Show |
70 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(67): Show |
intron_variant | MODIFIER | c.182-1509A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19728921 | |||||||
| chr16:19729047 | G | A | 8 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0002g0119 others(5): Show |
8 | HG02622.hp1 HG02622.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.182-1383G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19729047 | |||||||
| chr16:19729058 | A | G | 1 | a0001c0001t0003g0096 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.182-1372A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19729058 | |||||||
| chr16:19729071 | A | T | 9 | a0001c0001t0001g0167 a0001c0001t0001g0171 a0001c0001t0007g0163 others(6): Show |
9 | HG01884.hp1 HG02257.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.182-1359A>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19729071 | |||||||
| chr16:19729097 | T | C | 1 | a0001c0001t0001g0098 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.182-1333T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19729097 | |||||||
| chr16:19729169 | C | T | 2 | a0001c0001t0002g0094 a0001c0001t0002g0095 |
2 | HG01943.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.182-1261C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19729169 | |||||||
| chr16:19729259 | C | T | 3 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0003g0120 |
3 | HG02622.hp1 HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.182-1171C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19729259 | |||||||
| chr16:19729327 | C | T | 1 | a0002c0002t0001g0181 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.182-1103C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19729327 | |||||||
| chr16:19729399 | C | T | 5 | a0001c0001t0002g0237 a0001c0001t0004g0178 a0001c0001t0009g0239 others(2): Show |
5 | HG02451.hp2 HG02615.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.182-1031C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19729399 | |||||||
| chr16:19729403 | G | A | 1 | a0001c0001t0001g0055 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.182-1027G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19729403 | |||||||
| chr16:19729450 | G | A | 8 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0002g0119 others(5): Show |
8 | HG02622.hp1 HG02622.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.182-980G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19729450 | |||||||
| chr16:19729486 | C | G | 1 | a0001c0001t0001g0097 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.182-944C>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19729486 | |||||||
| chr16:19729565 | G | C | 1 | a0002c0002t0003g0190 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.182-865G>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19729565 | |||||||
| chr16:19729684 | G | A | 1 | a0001c0003t0003g0021 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.182-746G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19729684 | |||||||
| chr16:19729705 | C | T | 58 | a0002c0002t0001g0176 a0002c0002t0001g0177 a0002c0002t0001g0181 others(55): Show |
58 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(55): Show |
intron_variant | MODIFIER | c.182-725C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19729705 | |||||||
| chr16:19729738 | G | A | 6 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(3): Show |
6 | HG01496.hp1 HG01891.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.182-692G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19729738 | |||||||
| chr16:19729765 | T | C | 135 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(132): Show |
135 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(132): Show |
intron_variant | MODIFIER | c.182-665T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19729765 | |||||||
| chr16:19729784 | A | G | 63 | a0001c0001t0002g0237 a0001c0001t0004g0178 a0001c0001t0009g0239 others(60): Show |
63 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(60): Show |
intron_variant | MODIFIER | c.182-646A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19729784 | |||||||
| chr16:19729916 | T | C | 2 | a0001c0001t0001g0135 a0001c0001t0003g0136 |
2 | HG02451.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.182-514T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19729916 | |||||||
| chr16:19729940 | G | A | 9 | a0001c0001t0001g0167 a0001c0001t0001g0171 a0001c0001t0007g0163 others(6): Show |
9 | HG01884.hp1 HG02257.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.182-490G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19729940 | |||||||
| chr16:19730151 | T | C | 9 | a0001c0001t0001g0167 a0001c0001t0001g0171 a0001c0001t0007g0163 others(6): Show |
9 | HG01884.hp1 HG02257.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.182-279T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 1/8 | chr16 | 19730151 | |||||||
| chr16:19730519 | G | A | 3 | a0001c0001t0005g0033 a0001c0001t0005g0043 a0001c0001t0005g0044 |
3 | HG02055.hp2 HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.246+25G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 2/8 | chr16 | 19730519 | |||||||
| chr16:19730549 | T | C | 21 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(18): Show |
21 | HG01109.hp2 HG01884.hp2 HG01934.hp2 others(18): Show |
intron_variant | MODIFIER | c.246+55T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 2/8 | chr16 | 19730549 | |||||||
| chr16:19730709 | T | C | 6 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(3): Show |
6 | HG01496.hp1 HG01891.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.246+215T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 2/8 | chr16 | 19730709 | |||||||
| chr16:19730715 | G | GTCTA | 101 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(98): Show |
101 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(98): Show |
intron_variant | MODIFIER | c.246+229_246+232dup others(4): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 19730715 | ||||||
| chr16:19730715 | G | GTCTATCT others(1): Show |
11 | a0001c0001t0002g0001 a0001c0001t0002g0027 a0001c0001t0002g0029 others(8): Show |
11 | HG01109.hp2 HG01884.hp2 HG01934.hp2 others(8): Show |
intron_variant | MODIFIER | c.246+225_246+232dup others(8): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 19730715 | ||||||
| chr16:19730717 | C | CTATG | 10 | a0001c0001t0001g0167 a0001c0001t0001g0171 a0001c0001t0007g0163 others(7): Show |
10 | HG01884.hp1 HG02257.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.246+226_246+227ins others(4): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 19730717 | ||||||
| chr16:19730719 | A | ATCTG | 3 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0003g0120 |
3 | HG02622.hp1 HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.246+228_246+229ins others(4): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 19730719 | ||||||
| chr16:19730723 | A | ATCTG | 6 | a0001c0001t0002g0241 a0001c0001t0002g0242 a0001c0001t0003g0123 others(3): Show |
6 | HG02258.hp2 HG02559.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.246+249_246+252dup others(4): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 19730723 | ||||||
| chr16:19730723 | A | G | 3 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0003g0120 |
3 | HG02622.hp1 HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.246+229A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 2/8 | chr16 | 19730723 | |||||||
| chr16:19730727 | G | A | 1 | a0002c0002t0001g0228 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.246+233G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 2/8 | chr16 | 19730727 | |||||||
| chr16:19730747 | A | G | 1 | a0002c0002t0001g0228 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.246+253A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 2/8 | chr16 | 19730747 | |||||||
| chr16:19730762 | CT | C | 135 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(132): Show |
135 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(132): Show |
intron_variant | MODIFIER | c.246+270delT | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 19730762 | ||||||
| chr16:19730813 | C | G | 3 | a0002c0002t0001g0225 a0002c0002t0001g0226 a0002c0002t0001g0227 |
3 | HG02698.hp1 HG03688.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.246+319C>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 2/8 | chr16 | 19730813 | |||||||
| chr16:19730907 | C | T | 1 | a0002c0002t0001g0228 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.246+413C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 2/8 | chr16 | 19730907 | |||||||
| chr16:19730908 | G | A | 12 | a0002c0002t0001g0193 a0002c0002t0003g0190 a0002c0002t0003g0191 others(9): Show |
12 | HG00733.hp1 HG01255.hp1 HG01433.hp2 others(9): Show |
intron_variant | MODIFIER | c.246+414G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 2/8 | chr16 | 19730908 | |||||||
| chr16:19731063 | C | G | 1 | a0001c0001t0001g0111 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.246+569C>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 2/8 | chr16 | 19731063 | |||||||
| chr16:19731190 | A | G | 27 | a0001c0001t0001g0131 a0001c0001t0001g0133 a0001c0001t0001g0134 others(24): Show |
27 | HG00733.hp2 HG01175.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.246+696A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 2/8 | chr16 | 19731190 | |||||||
| chr16:19731255 | C | T | 1 | a0001c0001t0001g0111 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.246+761C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 2/8 | chr16 | 19731255 | |||||||
| chr16:19731383 | T | C | 27 | a0001c0001t0001g0131 a0001c0001t0001g0133 a0001c0001t0001g0134 others(24): Show |
27 | HG00733.hp2 HG01175.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.246+889T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 2/8 | chr16 | 19731383 | |||||||
| chr16:19731487 | T | C | 1 | a0001c0001t0003g0045 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.246+993T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 2/8 | chr16 | 19731487 | |||||||
| chr16:19731539 | C | T | 1 | a0003c0004t0013g0240 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.246+1045C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 2/8 | chr16 | 19731539 | |||||||
| chr16:19731552 | G | A | 1 | a0003c0004t0013g0240 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.246+1058G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 2/8 | chr16 | 19731552 | |||||||
| chr16:19731582 | A | G | 27 | a0001c0001t0001g0131 a0001c0001t0001g0133 a0001c0001t0001g0134 others(24): Show |
27 | HG00733.hp2 HG01175.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.246+1088A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 2/8 | chr16 | 19731582 | |||||||
| chr16:19731914 | A | G | 1 | a0002c0002t0001g0234 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.246+1420A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 2/8 | chr16 | 19731914 | |||||||
| chr16:19731991 | A | G | 1 | a0001c0001t0001g0141 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.246+1497A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 2/8 | chr16 | 19731991 | |||||||
| chr16:19732088 | C | T | 1 | a0002c0002t0001g0228 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.246+1594C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 2/8 | chr16 | 19732088 | |||||||
| chr16:19732121 | A | G | 1 | a0001c0001t0001g0017 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.247-1577A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 2/8 | chr16 | 19732121 | |||||||
| chr16:19732134 | A | T | 27 | a0001c0001t0001g0131 a0001c0001t0001g0133 a0001c0001t0001g0134 others(24): Show |
27 | HG00733.hp2 HG01175.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.247-1564A>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 2/8 | chr16 | 19732134 | |||||||
| chr16:19732225 | C | T | 3 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0002g0093 |
3 | HG00099.hp2 HG00639.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.247-1473C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 2/8 | chr16 | 19732225 | |||||||
| chr16:19732327 | T | C | 63 | a0001c0001t0002g0237 a0001c0001t0004g0178 a0001c0001t0009g0239 others(60): Show |
63 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(60): Show |
intron_variant | MODIFIER | c.247-1371T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 2/8 | chr16 | 19732327 | |||||||
| chr16:19732381 | C | A | 198 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0013 others(195): Show |
198 | HG00099.hp2 HG00140.hp2 HG00597.hp1 others(195): Show |
intron_variant | MODIFIER | c.247-1317C>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 2/8 | chr16 | 19732381 | |||||||
| chr16:19732461 | G | A | 1 | a0002c0002t0001g0229 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.247-1237G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 2/8 | chr16 | 19732461 | |||||||
| chr16:19732488 | T | A | 7 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(4): Show |
7 | HG01496.hp1 HG01891.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.247-1210T>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 2/8 | chr16 | 19732488 | |||||||
| chr16:19732573 | G | T | 1 | a0001c0001t0007g0165 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.247-1125G>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 2/8 | chr16 | 19732573 | |||||||
| chr16:19732606 | G | A | 4 | a0001c0001t0001g0137 a0001c0001t0002g0241 a0001c0001t0002g0242 others(1): Show |
4 | HG02622.hp2 HG02818.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.247-1092G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 2/8 | chr16 | 19732606 | |||||||
| chr16:19732624 | C | A | 3 | a0001c0001t0002g0241 a0001c0001t0002g0242 a0001c0001t0012g0243 |
3 | HG02622.hp2 HG02818.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.247-1074C>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 2/8 | chr16 | 19732624 | |||||||
| chr16:19732912 | C | G | 1 | a0001c0001t0002g0050 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.247-786C>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 2/8 | chr16 | 19732912 | |||||||
| chr16:19732970 | G | A | 1 | a0001c0001t0003g0123 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.247-728G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 2/8 | chr16 | 19732970 | |||||||
| chr16:19733076 | A | G | 7 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(4): Show |
7 | HG01496.hp1 HG01891.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.247-622A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 2/8 | chr16 | 19733076 | |||||||
| chr16:19733143 | A | T | 26 | a0001c0001t0001g0131 a0001c0001t0001g0133 a0001c0001t0001g0134 others(23): Show |
26 | HG00733.hp2 HG01175.hp1 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.247-555A>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 2/8 | chr16 | 19733143 | |||||||
| chr16:19733147 | T | A | 7 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0172 others(4): Show |
7 | HG02622.hp1 HG02809.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.247-551T>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 2/8 | chr16 | 19733147 | |||||||
| chr16:19733423 | G | A | 2 | a0001c0001t0001g0056 a0001c0001t0002g0050 |
2 | NA18954.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.247-275G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 2/8 | chr16 | 19733423 | |||||||
| chr16:19733546 | A | T | 6 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(3): Show |
6 | HG01496.hp1 HG01891.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.247-152A>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 2/8 | chr16 | 19733546 | |||||||
| chr16:19733692 | C | T | 1 | a0002c0002t0001g0224 | 1 | NA19007.hp2 | splice_region_variant&intron_variant | LOW | c.247-6C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 2/8 | chr16 | 19733692 | |||||||
| chr16:19733856 | A | G | 1 | a0001c0001t0001g0072 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.376+29A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 3/8 | chr16 | 19733856 | |||||||
| chr16:19734201 | A | T | 2 | a0002c0002t0001g0183 a0002c0002t0001g0230 |
2 | HG03704.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.376+374A>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 3/8 | chr16 | 19734201 | |||||||
| chr16:19734459 | C | CA | 73 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(70): Show |
73 | HG00140.hp2 HG00733.hp2 HG00738.hp2 others(70): Show |
intron_variant | MODIFIER | c.376+652dupA | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 19734459 | ||||||
| chr16:19734459 | C | CAA | 11 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0139 others(8): Show |
11 | HG01496.hp1 HG01934.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.376+651_376+652dup others(2): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 19734459 | ||||||
| chr16:19734479 | A | AAG | 6 | a0002c0002t0001g0183 a0002c0002t0001g0201 a0002c0002t0001g0202 others(3): Show |
6 | HG02300.hp2 HG03704.hp1 HG03942.hp1 others(3): Show |
intron_variant | MODIFIER | c.376+652_376+653ins others(2): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 3/8 | chr16 | 19734479 | |||||||
| chr16:19734479 | A | AG | 58 | a0001c0001t0002g0237 a0001c0001t0003g0188 a0001c0001t0004g0178 others(55): Show |
58 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(55): Show |
intron_variant | MODIFIER | c.376+652_376+653ins others(1): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 3/8 | chr16 | 19734479 | |||||||
| chr16:19734664 | T | C | 22 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(19): Show |
22 | HG01109.hp2 HG01884.hp2 HG01934.hp2 others(19): Show |
intron_variant | MODIFIER | c.377-689T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 3/8 | chr16 | 19734664 | |||||||
| chr16:19734712 | T | C | 4 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0031 others(1): Show |
4 | NA18612.hp1 NA18946.hp2 NA18961.hp2 others(1): Show |
intron_variant | MODIFIER | c.377-641T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 3/8 | chr16 | 19734712 | |||||||
| chr16:19734780 | CA | C | 12 | a0001c0001t0001g0115 a0001c0001t0001g0121 a0001c0001t0001g0122 others(9): Show |
12 | HG00733.hp2 HG01175.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.377-556delA | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 19734780 | ||||||
| chr16:19734786 | A | AG | 3 | a0001c0001t0002g0241 a0001c0001t0002g0242 a0001c0001t0012g0243 |
3 | HG02622.hp2 HG02818.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.377-567_377-566ins others(1): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 3/8 | chr16 | 19734786 | |||||||
| chr16:19734875 | C | T | 1 | a0003c0004t0013g0240 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.377-478C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 3/8 | chr16 | 19734875 | |||||||
| chr16:19734876 | G | A | 1 | a0001c0001t0007g0166 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.377-477G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 3/8 | chr16 | 19734876 | |||||||
| chr16:19735014 | A | T | 1 | a0001c0001t0008g0110 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.377-339A>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 3/8 | chr16 | 19735014 | |||||||
| chr16:19735225 | A | G | 2 | a0001c0001t0004g0178 a0001c0001t0015g0179 |
2 | HG02615.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.377-128A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 3/8 | chr16 | 19735225 | |||||||
| chr16:19735226 | A | T | 2 | a0001c0001t0004g0178 a0001c0001t0015g0179 |
2 | HG02615.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.377-127A>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 3/8 | chr16 | 19735226 | |||||||
| chr16:19735272 | T | C | 1 | a0001c0001t0001g0053 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.377-81T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 3/8 | chr16 | 19735272 | |||||||
| chr16:19735318 | G | T | 1 | a0001c0001t0004g0028 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.377-35G>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 3/8 | chr16 | 19735318 | |||||||
| chr16:19735654 | G | C | 1 | a0001c0001t0002g0119 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.474+204G>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19735654 | |||||||
| chr16:19735660 | C | T | 58 | a0002c0002t0001g0176 a0002c0002t0001g0177 a0002c0002t0001g0181 others(55): Show |
58 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(55): Show |
intron_variant | MODIFIER | c.474+210C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19735660 | |||||||
| chr16:19735995 | G | A | 1 | a0001c0001t0002g0119 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.474+545G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19735995 | |||||||
| chr16:19736079 | A | G | 27 | a0001c0001t0001g0131 a0001c0001t0001g0133 a0001c0001t0001g0134 others(24): Show |
27 | HG00733.hp2 HG01175.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.474+629A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19736079 | |||||||
| chr16:19736132 | T | C | 3 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0141 |
3 | HG02572.hp1 HG03130.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.474+682T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19736132 | |||||||
| chr16:19736174 | CAG | C | 9 | a0001c0001t0001g0167 a0001c0001t0001g0171 a0001c0001t0007g0163 others(6): Show |
9 | HG01884.hp1 HG02257.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.474+729_474+730del others(2): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 19736174 | ||||||
| chr16:19736419 | C | T | 3 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0003g0120 |
3 | HG02622.hp1 HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.474+969C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19736419 | |||||||
| chr16:19736426 | C | CTGAT | 14 | a0001c0001t0008g0074 a0001c0001t0008g0102 a0002c0002t0001g0193 others(11): Show |
14 | HG00733.hp1 HG01255.hp1 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.474+999_474+1002du others(5): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 19736426 | ||||||
| chr16:19736522 | A | T | 1 | a0001c0001t0001g0056 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.474+1072A>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19736522 | |||||||
| chr16:19736538 | C | G | 6 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(3): Show |
6 | HG02717.hp2 HG02886.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.474+1088C>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19736538 | |||||||
| chr16:19736556 | C | T | 1 | a0003c0004t0013g0240 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.474+1106C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19736556 | |||||||
| chr16:19736600 | T | C | 64 | a0001c0001t0002g0237 a0001c0001t0003g0188 a0001c0001t0004g0178 others(61): Show |
64 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(61): Show |
intron_variant | MODIFIER | c.474+1150T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19736600 | |||||||
| chr16:19736629 | G | A | 1 | a0001c0001t0001g0244 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.474+1179G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19736629 | |||||||
| chr16:19736637 | A | C | 2 | a0002c0002t0003g0197 a0002c0002t0003g0198 |
2 | HG02970.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.474+1187A>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19736637 | |||||||
| chr16:19736638 | C | A | 2 | a0002c0002t0003g0197 a0002c0002t0003g0198 |
2 | HG02970.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.474+1188C>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19736638 | |||||||
| chr16:19736741 | C | CTAT | 15 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(12): Show |
15 | HG01496.hp1 HG01884.hp1 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.474+1301_474+1303d others(5): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 19736741 | ||||||
| chr16:19736869 | C | T | 1 | a0002c0002t0001g0177 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.474+1419C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19736869 | |||||||
| chr16:19736984 | C | CA | 43 | a0001c0001t0001g0014 a0001c0001t0001g0017 a0001c0001t0001g0018 others(40): Show |
43 | HG00733.hp2 HG00735.hp1 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.474+1551dupA | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 19736984 | ||||||
| chr16:19737154 | C | T | 1 | a0001c0001t0001g0244 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.474+1704C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19737154 | |||||||
| chr16:19737379 | G | A | 1 | a0001c0001t0001g0161 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.474+1929G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19737379 | |||||||
| chr16:19737676 | A | G | 1 | a0002c0002t0001g0228 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.474+2226A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19737676 | |||||||
| chr16:19737688 | G | T | 4 | a0001c0001t0001g0156 a0001c0001t0001g0158 a0001c0001t0001g0159 others(1): Show |
4 | HG01496.hp1 HG01891.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.474+2238G>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19737688 | |||||||
| chr16:19737793 | C | T | 6 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(3): Show |
6 | HG02717.hp2 HG02886.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.474+2343C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19737793 | |||||||
| chr16:19737794 | G | A | 7 | a0001c0001t0004g0012 a0001c0001t0004g0022 a0001c0001t0004g0023 others(4): Show |
7 | HG01109.hp2 HG01884.hp2 HG01934.hp2 others(4): Show |
intron_variant | MODIFIER | c.474+2344G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19737794 | |||||||
| chr16:19737915 | A | G | 2 | a0001c0001t0001g0056 a0001c0001t0002g0050 |
2 | NA18954.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.474+2465A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19737915 | |||||||
| chr16:19737967 | T | A | 1 | a0002c0002t0001g0204 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.474+2517T>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19737967 | |||||||
| chr16:19738257 | A | G | 3 | a0001c0001t0007g0166 a0001c0001t0007g0168 a0001c0001t0007g0169 |
3 | HG01884.hp1 HG02257.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.474+2807A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19738257 | |||||||
| chr16:19738296 | A | G | 28 | a0001c0001t0001g0053 a0001c0001t0001g0131 a0001c0001t0001g0133 others(25): Show |
28 | HG00733.hp2 HG01175.hp1 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.474+2846A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19738296 | |||||||
| chr16:19738387 | A | G | 136 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(133): Show |
136 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(133): Show |
intron_variant | MODIFIER | c.474+2937A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19738387 | |||||||
| chr16:19738729 | A | G | 63 | a0001c0001t0002g0237 a0001c0001t0004g0178 a0001c0001t0009g0239 others(60): Show |
63 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(60): Show |
intron_variant | MODIFIER | c.474+3279A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19738729 | |||||||
| chr16:19738806 | A | G | 2 | a0001c0001t0004g0178 a0001c0001t0015g0179 |
2 | HG02615.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.474+3356A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19738806 | |||||||
| chr16:19738864 | A | C | 1 | a0002c0002t0001g0184 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.474+3414A>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19738864 | |||||||
| chr16:19738953 | G | A | 135 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(132): Show |
135 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(132): Show |
intron_variant | MODIFIER | c.474+3503G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19738953 | |||||||
| chr16:19739051 | C | G | 1 | a0001c0001t0003g0045 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.474+3601C>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19739051 | |||||||
| chr16:19739083 | G | A | 1 | a0001c0001t0001g0017 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.474+3633G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19739083 | |||||||
| chr16:19739585 | C | T | 1 | a0001c0001t0001g0090 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.474+4135C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19739585 | |||||||
| chr16:19739609 | G | T | 21 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(18): Show |
21 | HG01109.hp2 HG01884.hp2 HG01934.hp2 others(18): Show |
intron_variant | MODIFIER | c.474+4159G>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19739609 | |||||||
| chr16:19739660 | C | T | 1 | a0001c0001t0008g0110 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.474+4210C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19739660 | |||||||
| chr16:19739814 | C | CA | 10 | a0001c0001t0001g0167 a0001c0001t0001g0171 a0001c0001t0004g0005 others(7): Show |
10 | HG01884.hp1 HG02257.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.474+4375dupA | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 19739814 | ||||||
| chr16:19739878 | A | G | 1 | a0002c0002t0001g0224 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.474+4428A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19739878 | |||||||
| chr16:19739888 | T | C | 12 | a0002c0002t0001g0193 a0002c0002t0003g0190 a0002c0002t0003g0191 others(9): Show |
12 | HG00733.hp1 HG01255.hp1 HG01433.hp2 others(9): Show |
intron_variant | MODIFIER | c.474+4438T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19739888 | |||||||
| chr16:19739903 | A | C | 1 | a0001c0001t0003g0016 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.474+4453A>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19739903 | |||||||
| chr16:19740012 | C | G | 9 | a0001c0001t0001g0167 a0001c0001t0001g0171 a0001c0001t0007g0163 others(6): Show |
9 | HG01884.hp1 HG02257.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.474+4562C>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19740012 | |||||||
| chr16:19740034 | C | A | 3 | a0001c0001t0005g0033 a0001c0001t0005g0043 a0001c0001t0005g0044 |
3 | HG02055.hp2 HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.474+4584C>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19740034 | |||||||
| chr16:19740080 | G | A | 2 | a0001c0001t0002g0001 a0001c0001t0002g0029 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.474+4630G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19740080 | |||||||
| chr16:19740299 | A | G | 5 | a0001c0001t0007g0165 a0001c0001t0007g0166 a0001c0001t0007g0168 others(2): Show |
5 | HG01884.hp1 HG02257.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.474+4849A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19740299 | |||||||
| chr16:19740308 | A | G | 1 | a0002c0002t0001g0223 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.474+4858A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19740308 | |||||||
| chr16:19740453 | C | T | 1 | a0001c0001t0001g0172 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.474+5003C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19740453 | |||||||
| chr16:19740520 | G | A | 1 | a0001c0001t0001g0056 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.474+5070G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19740520 | |||||||
| chr16:19740565 | G | A | 21 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(18): Show |
21 | HG01109.hp2 HG01884.hp2 HG01934.hp2 others(18): Show |
intron_variant | MODIFIER | c.474+5115G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19740565 | |||||||
| chr16:19740660 | C | G | 1 | a0001c0001t0002g0119 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.474+5210C>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19740660 | |||||||
| chr16:19740663 | T | C | 2 | a0001c0001t0001g0157 a0001c0001t0001g0161 |
2 | HG03540.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.474+5213T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19740663 | |||||||
| chr16:19740892 | C | T | 21 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(18): Show |
21 | HG01109.hp2 HG01884.hp2 HG01934.hp2 others(18): Show |
intron_variant | MODIFIER | c.474+5442C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19740892 | |||||||
| chr16:19740966 | T | TA | 55 | a0001c0001t0001g0040 a0001c0001t0003g0188 a0001c0001t0004g0178 others(52): Show |
55 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.474+5533dupA | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 19740966 | ||||||
| chr16:19740966 | T | TAA | 9 | a0001c0001t0009g0239 a0001c0001t0019g0238 a0002c0002t0001g0181 others(6): Show |
9 | HG02135.hp1 HG02155.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.474+5532_474+5533d others(4): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 19740966 | ||||||
| chr16:19740966 | TAA | T | 21 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(18): Show |
21 | HG01109.hp2 HG01884.hp2 HG01934.hp2 others(18): Show |
intron_variant | MODIFIER | c.474+5532_474+5533d others(4): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 19740966 | ||||||
| chr16:19741018 | G | A | 6 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(3): Show |
6 | HG02717.hp2 HG02886.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.474+5568G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19741018 | |||||||
| chr16:19741229 | C | T | 1 | a0003c0004t0013g0240 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.474+5779C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19741229 | |||||||
| chr16:19741341 | G | A | 1 | a0001c0001t0001g0075 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.474+5891G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19741341 | |||||||
| chr16:19741504 | A | G | 10 | a0001c0001t0001g0030 a0001c0001t0002g0027 a0001c0001t0004g0005 others(7): Show |
10 | HG01109.hp2 HG01884.hp2 HG01934.hp2 others(7): Show |
intron_variant | MODIFIER | c.474+6054A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19741504 | |||||||
| chr16:19741506 | A | G | 1 | a0002c0002t0001g0221 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.474+6056A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19741506 | |||||||
| chr16:19741541 | T | C | 7 | a0001c0001t0001g0048 a0001c0001t0002g0034 a0001c0001t0002g0035 others(4): Show |
7 | HG00140.hp2 HG00738.hp2 HG01074.hp1 others(4): Show |
intron_variant | MODIFIER | c.474+6091T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19741541 | |||||||
| chr16:19741565 | A | G | 1 | a0001c0001t0001g0149 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.474+6115A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19741565 | |||||||
| chr16:19741609 | T | A | 1 | a0001c0001t0001g0053 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.474+6159T>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19741609 | |||||||
| chr16:19741617 | G | C | 47 | a0001c0001t0003g0188 a0002c0002t0001g0176 a0002c0002t0001g0177 others(44): Show |
47 | HG00597.hp2 HG00609.hp1 HG01081.hp1 others(44): Show |
intron_variant | MODIFIER | c.474+6167G>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19741617 | |||||||
| chr16:19741646 | T | A | 27 | a0001c0001t0001g0131 a0001c0001t0001g0133 a0001c0001t0001g0134 others(24): Show |
27 | HG00733.hp2 HG01175.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.474+6196T>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19741646 | |||||||
| chr16:19741755 | G | T | 4 | a0002c0002t0003g0190 a0002c0002t0003g0191 a0002c0002t0003g0196 others(1): Show |
4 | HG01433.hp2 HG02300.hp2 NA20752.hp2 others(1): Show |
intron_variant | MODIFIER | c.474+6305G>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19741755 | |||||||
| chr16:19741784 | C | T | 1 | a0002c0002t0001g0221 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.474+6334C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19741784 | |||||||
| chr16:19741891 | T | G | 136 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(133): Show |
136 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(133): Show |
intron_variant | MODIFIER | c.474+6441T>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19741891 | |||||||
| chr16:19741945 | T | C | 136 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(133): Show |
136 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(133): Show |
intron_variant | MODIFIER | c.474+6495T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19741945 | |||||||
| chr16:19742012 | T | C | 136 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(133): Show |
136 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(133): Show |
intron_variant | MODIFIER | c.474+6562T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19742012 | |||||||
| chr16:19742058 | A | C | 1 | a0002c0002t0003g0203 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.474+6608A>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19742058 | |||||||
| chr16:19742134 | G | A | 136 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(133): Show |
136 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(133): Show |
intron_variant | MODIFIER | c.474+6684G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19742134 | |||||||
| chr16:19742269 | T | C | 27 | a0001c0001t0001g0131 a0001c0001t0001g0133 a0001c0001t0001g0134 others(24): Show |
27 | HG00733.hp2 HG01175.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.474+6819T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19742269 | |||||||
| chr16:19742368 | G | A | 1 | a0001c0001t0002g0119 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.474+6918G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19742368 | |||||||
| chr16:19742479 | A | AT | 21 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(18): Show |
21 | HG01109.hp2 HG01884.hp2 HG01934.hp2 others(18): Show |
intron_variant | MODIFIER | c.474+7031dupT | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 19742479 | ||||||
| chr16:19742636 | G | A | 1 | a0001c0001t0001g0129 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.474+7186G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19742636 | |||||||
| chr16:19743023 | T | A | 3 | a0001c0001t0002g0237 a0001c0001t0009g0239 a0001c0001t0019g0238 |
3 | HG02451.hp2 HG02895.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.474+7573T>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19743023 | |||||||
| chr16:19743170 | C | CAAAT | 64 | a0001c0001t0002g0237 a0001c0001t0003g0188 a0001c0001t0004g0178 others(61): Show |
64 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(61): Show |
intron_variant | MODIFIER | c.474+7740_474+7743d others(6): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 19743170 | ||||||
| chr16:19743349 | A | G | 3 | a0001c0001t0001g0148 a0001c0001t0001g0151 a0001c0001t0001g0155 |
3 | HG00733.hp2 HG01175.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.474+7899A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19743349 | |||||||
| chr16:19743491 | T | A | 1 | a0002c0002t0001g0208 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.474+8041T>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19743491 | |||||||
| chr16:19743721 | C | T | 3 | a0001c0001t0002g0237 a0001c0001t0009g0239 a0001c0001t0019g0238 |
3 | HG02451.hp2 HG02895.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.474+8271C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19743721 | |||||||
| chr16:19743966 | T | C | 8 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0002g0119 others(5): Show |
8 | HG02622.hp1 HG02622.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.474+8516T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19743966 | |||||||
| chr16:19744164 | A | G | 2 | a0002c0002t0001g0185 a0002c0002t0001g0186 |
2 | HG01081.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.474+8714A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19744164 | |||||||
| chr16:19744195 | G | T | 1 | a0001c0001t0002g0027 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.474+8745G>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19744195 | |||||||
| chr16:19744346 | G | A | 1 | a0003c0004t0013g0240 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.474+8896G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19744346 | |||||||
| chr16:19744564 | A | G | 4 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0031 others(1): Show |
4 | NA18612.hp1 NA18946.hp2 NA18961.hp2 others(1): Show |
intron_variant | MODIFIER | c.474+9114A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19744564 | |||||||
| chr16:19744737 | A | G | 21 | a0001c0001t0001g0011 a0001c0001t0001g0067 a0001c0001t0001g0070 others(18): Show |
21 | HG00099.hp2 HG00639.hp2 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.474+9287A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19744737 | |||||||
| chr16:19745026 | A | G | 151 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(148): Show |
151 | HG00140.hp2 HG00597.hp2 HG00609.hp1 others(148): Show |
intron_variant | MODIFIER | c.474+9576A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19745026 | |||||||
| chr16:19745259 | T | C | 1 | a0001c0001t0002g0119 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.474+9809T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19745259 | |||||||
| chr16:19745471 | T | A | 1 | a0001c0001t0001g0150 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.474+10021T>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19745471 | |||||||
| chr16:19745679 | C | T | 150 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(147): Show |
150 | HG00140.hp2 HG00597.hp2 HG00609.hp1 others(147): Show |
intron_variant | MODIFIER | c.474+10229C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19745679 | |||||||
| chr16:19745818 | CAT | C | 21 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(18): Show |
21 | HG01109.hp2 HG01884.hp2 HG01934.hp2 others(18): Show |
intron_variant | MODIFIER | c.474+10369_474+1037 others(6): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19745818 | |||||||
| chr16:19745932 | G | T | 1 | a0001c0001t0003g0123 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.474+10482G>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19745932 | |||||||
| chr16:19746153 | C | CA | 8 | a0001c0001t0001g0133 a0001c0001t0001g0139 a0001c0001t0001g0145 others(5): Show |
8 | HG01358.hp1 HG02055.hp1 HG02056.hp1 others(5): Show |
intron_variant | MODIFIER | c.474+10723dupA | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 19746153 | ||||||
| chr16:19746153 | CA | C | 18 | a0001c0001t0001g0014 a0001c0001t0001g0017 a0001c0001t0001g0018 others(15): Show |
18 | HG00639.hp2 HG02074.hp1 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.474+10723delA | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 19746153 | ||||||
| chr16:19746153 | CAA | C | 8 | a0001c0001t0001g0013 a0001c0001t0002g0027 a0001c0001t0004g0012 others(5): Show |
8 | HG01109.hp2 HG01884.hp2 HG01934.hp2 others(5): Show |
intron_variant | MODIFIER | c.474+10722_474+1072 others(6): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 19746153 | ||||||
| chr16:19746153 | CAAAAAAA others(4): Show |
C | 3 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0174 |
3 | NA18943.hp1 NA18944.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.474+10713_474+1072 others(15): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 19746153 | ||||||
| chr16:19746171 | AAAG | A | 17 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(14): Show |
17 | HG00597.hp2 HG01496.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.474+10723_474+1072 others(7): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 19746171 | ||||||
| chr16:19746172 | AAG | A | 8 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0002g0119 others(5): Show |
8 | HG02622.hp1 HG02622.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.474+10725_474+1072 others(6): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 19746172 | ||||||
| chr16:19746190 | CT | C | 132 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(129): Show |
132 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(129): Show |
intron_variant | MODIFIER | c.474+10751delT | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 19746190 | ||||||
| chr16:19746325 | TACAA | T | 23 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0156 others(20): Show |
23 | HG01496.hp1 HG01884.hp1 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.474+10880_474+1088 others(8): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 19746325 | ||||||
| chr16:19746536 | G | A | 1 | a0002c0002t0001g0209 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.474+11086G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19746536 | |||||||
| chr16:19746601 | T | C | 27 | a0001c0001t0001g0131 a0001c0001t0001g0133 a0001c0001t0001g0134 others(24): Show |
27 | HG00733.hp2 HG01175.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.474+11151T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19746601 | |||||||
| chr16:19747005 | A | C | 1 | a0001c0001t0001g0138 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.474+11555A>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19747005 | |||||||
| chr16:19747324 | C | G | 2 | a0001c0001t0004g0023 a0001c0001t0004g0028 |
2 | HG02572.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.474+11874C>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19747324 | |||||||
| chr16:19747328 | G | A | 32 | a0001c0001t0003g0188 a0002c0002t0001g0176 a0002c0002t0001g0177 others(29): Show |
32 | HG00597.hp2 HG00609.hp1 HG01261.hp2 others(29): Show |
intron_variant | MODIFIER | c.474+11878G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19747328 | |||||||
| chr16:19747375 | C | A | 27 | a0001c0001t0001g0131 a0001c0001t0001g0133 a0001c0001t0001g0134 others(24): Show |
27 | HG00733.hp2 HG01175.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.474+11925C>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19747375 | |||||||
| chr16:19747411 | A | G | 27 | a0001c0001t0001g0131 a0001c0001t0001g0133 a0001c0001t0001g0134 others(24): Show |
27 | HG00733.hp2 HG01175.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.474+11961A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19747411 | |||||||
| chr16:19747553 | G | T | 1 | a0002c0002t0001g0217 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.474+12103G>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19747553 | |||||||
| chr16:19747563 | A | C | 136 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(133): Show |
136 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(133): Show |
intron_variant | MODIFIER | c.474+12113A>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19747563 | |||||||
| chr16:19747640 | C | T | 62 | a0001c0001t0002g0237 a0001c0001t0004g0178 a0001c0001t0009g0239 others(59): Show |
62 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(59): Show |
intron_variant | MODIFIER | c.474+12190C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19747640 | |||||||
| chr16:19747681 | C | G | 21 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(18): Show |
21 | HG01109.hp2 HG01884.hp2 HG01934.hp2 others(18): Show |
intron_variant | MODIFIER | c.474+12231C>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19747681 | |||||||
| chr16:19747685 | A | C | 136 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(133): Show |
136 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(133): Show |
intron_variant | MODIFIER | c.474+12235A>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19747685 | |||||||
| chr16:19748008 | A | G | 1 | a0001c0001t0015g0179 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.474+12558A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19748008 | |||||||
| chr16:19748072 | C | CT | 39 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0030 others(36): Show |
39 | HG00609.hp2 HG01081.hp2 HG01109.hp2 others(36): Show |
intron_variant | MODIFIER | c.474+12642dupT | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 19748072 | ||||||
| chr16:19748072 | C | CTT | 66 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0135 others(63): Show |
66 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(63): Show |
intron_variant | MODIFIER | c.474+12641_474+1264 others(6): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 19748072 | ||||||
| chr16:19748072 | C | CTTT | 24 | a0001c0001t0001g0131 a0001c0001t0001g0133 a0001c0001t0001g0134 others(21): Show |
24 | HG00733.hp2 HG01175.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.474+12640_474+1264 others(7): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 19748072 | ||||||
| chr16:19748072 | C | CTTTT | 6 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(3): Show |
6 | HG02647.hp2 HG02717.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.474+12639_474+1264 others(8): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 19748072 | ||||||
| chr16:19748253 | T | C | 127 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(124): Show |
127 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(124): Show |
intron_variant | MODIFIER | c.474+12803T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19748253 | |||||||
| chr16:19748264 | A | G | 9 | a0001c0001t0001g0167 a0001c0001t0001g0171 a0001c0001t0007g0163 others(6): Show |
9 | HG01884.hp1 HG02257.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.474+12814A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19748264 | |||||||
| chr16:19748300 | T | C | 136 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(133): Show |
136 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(133): Show |
intron_variant | MODIFIER | c.474+12850T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19748300 | |||||||
| chr16:19748654 | A | G | 1 | a0001c0001t0002g0087 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.474+13204A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19748654 | |||||||
| chr16:19748670 | A | C | 1 | a0001c0001t0002g0052 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.474+13220A>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19748670 | |||||||
| chr16:19748707 | A | G | 1 | a0003c0004t0013g0240 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.474+13257A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19748707 | |||||||
| chr16:19748849 | C | T | 21 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(18): Show |
21 | HG01109.hp2 HG01884.hp2 HG01934.hp2 others(18): Show |
intron_variant | MODIFIER | c.474+13399C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19748849 | |||||||
| chr16:19749314 | A | T | 1 | a0001c0001t0001g0065 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.474+13864A>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19749314 | |||||||
| chr16:19749484 | G | C | 1 | a0001c0001t0002g0237 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.474+14034G>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19749484 | |||||||
| chr16:19749563 | C | A | 1 | a0001c0001t0002g0103 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.474+14113C>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19749563 | |||||||
| chr16:19749771 | G | GA | 21 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(18): Show |
21 | HG01109.hp2 HG01884.hp2 HG01934.hp2 others(18): Show |
intron_variant | MODIFIER | c.475-14065dupA | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 19749771 | ||||||
| chr16:19749778 | A | G | 8 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0002g0119 others(5): Show |
8 | HG02622.hp1 HG02622.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.475-14070A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19749778 | |||||||
| chr16:19749812 | T | C | 2 | a0002c0002t0001g0185 a0002c0002t0001g0186 |
2 | HG01081.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.475-14036T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19749812 | |||||||
| chr16:19750188 | G | A | 1 | a0002c0002t0001g0208 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.475-13660G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19750188 | |||||||
| chr16:19750328 | T | C | 3 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0003g0120 |
3 | HG02622.hp1 HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.475-13520T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19750328 | |||||||
| chr16:19750426 | C | G | 1 | a0001c0001t0001g0137 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.475-13422C>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19750426 | |||||||
| chr16:19750470 | G | GT | 23 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(20): Show |
23 | HG01109.hp2 HG01884.hp2 HG01934.hp2 others(20): Show |
intron_variant | MODIFIER | c.475-13369dupT | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 19750470 | ||||||
| chr16:19750536 | G | A | 135 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(132): Show |
135 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(132): Show |
intron_variant | MODIFIER | c.475-13312G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19750536 | |||||||
| chr16:19750729 | C | T | 1 | a0001c0001t0003g0016 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.475-13119C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19750729 | |||||||
| chr16:19751196 | T | C | 2 | a0001c0001t0001g0158 a0001c0001t0001g0159 |
2 | HG01891.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.475-12652T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19751196 | |||||||
| chr16:19751234 | C | T | 21 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(18): Show |
21 | HG01109.hp2 HG01884.hp2 HG01934.hp2 others(18): Show |
intron_variant | MODIFIER | c.475-12614C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19751234 | |||||||
| chr16:19751262 | G | A | 5 | a0001c0001t0007g0165 a0001c0001t0007g0166 a0001c0001t0007g0168 others(2): Show |
5 | HG01884.hp1 HG02257.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.475-12586G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19751262 | |||||||
| chr16:19751370 | C | T | 48 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(45): Show |
48 | HG00733.hp2 HG01109.hp2 HG01175.hp1 others(45): Show |
intron_variant | MODIFIER | c.475-12478C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19751370 | |||||||
| chr16:19751395 | T | C | 1 | a0002c0002t0001g0202 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.475-12453T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19751395 | |||||||
| chr16:19751606 | C | T | 1 | a0001c0001t0001g0090 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.475-12242C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19751606 | |||||||
| chr16:19751613 | A | G | 64 | a0001c0001t0002g0237 a0001c0001t0003g0188 a0001c0001t0004g0178 others(61): Show |
64 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(61): Show |
intron_variant | MODIFIER | c.475-12235A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19751613 | |||||||
| chr16:19751654 | A | G | 2 | a0002c0002t0001g0182 a0002c0002t0001g0229 |
2 | NA18961.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.475-12194A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19751654 | |||||||
| chr16:19751680 | A | G | 1 | a0001c0001t0002g0103 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.475-12168A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19751680 | |||||||
| chr16:19751858 | A | G | 1 | a0001c0001t0004g0178 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.475-11990A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19751858 | |||||||
| chr16:19751869 | C | A | 3 | a0001c0001t0002g0241 a0001c0001t0002g0242 a0001c0001t0012g0243 |
3 | HG02622.hp2 HG02818.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.475-11979C>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19751869 | |||||||
| chr16:19751928 | C | T | 1 | a0001c0001t0001g0055 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.475-11920C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19751928 | |||||||
| chr16:19751932 | C | G | 1 | a0002c0002t0001g0229 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.475-11916C>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19751932 | |||||||
| chr16:19752096 | CTG | C | 21 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(18): Show |
21 | HG01109.hp2 HG01884.hp2 HG01934.hp2 others(18): Show |
intron_variant | MODIFIER | c.475-11751_475-1175 others(6): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19752096 | |||||||
| chr16:19752204 | C | T | 6 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(3): Show |
6 | HG01496.hp1 HG01891.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.475-11644C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19752204 | |||||||
| chr16:19752504 | A | G | 8 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0002g0119 others(5): Show |
8 | HG02622.hp1 HG02622.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.475-11344A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19752504 | |||||||
| chr16:19752604 | T | C | 1 | a0001c0001t0006g0041 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.475-11244T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19752604 | |||||||
| chr16:19752744 | T | C | 1 | a0001c0001t0007g0170 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.475-11104T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19752744 | |||||||
| chr16:19752783 | C | T | 2 | a0001c0001t0006g0117 a0001c0001t0006g0118 |
2 | HG02698.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.475-11065C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19752783 | |||||||
| chr16:19752827 | G | C | 9 | a0001c0001t0001g0167 a0001c0001t0001g0171 a0001c0001t0007g0163 others(6): Show |
9 | HG01884.hp1 HG02257.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.475-11021G>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19752827 | |||||||
| chr16:19752931 | A | G | 4 | a0002c0002t0001g0176 a0002c0002t0001g0184 a0002c0002t0001g0187 others(1): Show |
4 | NA18612.hp2 NA18946.hp1 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.475-10917A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19752931 | |||||||
| chr16:19753052 | C | CAG | 40 | a0001c0001t0001g0131 a0001c0001t0001g0133 a0001c0001t0001g0134 others(37): Show |
40 | HG00733.hp2 HG01175.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.475-10775_475-1077 others(6): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 19753052 | ||||||
| chr16:19753058 | G | A | 1 | a0001c0001t0003g0123 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.475-10790G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19753058 | |||||||
| chr16:19753247 | C | CA | 5 | a0001c0001t0004g0022 a0001c0001t0010g0124 a0002c0002t0001g0205 others(2): Show |
5 | HG00735.hp2 HG01109.hp2 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.475-10586dupA | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 19753247 | ||||||
| chr16:19753247 | CA | C | 9 | a0001c0001t0001g0092 a0001c0001t0001g0121 a0001c0001t0001g0122 others(6): Show |
9 | HG00099.hp1 HG00099.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.475-10586delA | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 19753247 | ||||||
| chr16:19753262 | A | C | 4 | a0002c0002t0001g0201 a0002c0002t0001g0216 a0002c0002t0001g0217 others(1): Show |
4 | NA18963.hp2 NA18971.hp1 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.475-10586A>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19753262 | |||||||
| chr16:19753262 | A | T | 2 | a0001c0001t0001g0111 a0001c0001t0002g0237 |
2 | HG01496.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.475-10586A>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19753262 | |||||||
| chr16:19753263 | T | A | 27 | a0001c0001t0001g0131 a0001c0001t0001g0133 a0001c0001t0001g0134 others(24): Show |
27 | HG00733.hp2 HG01175.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.475-10585T>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19753263 | |||||||
| chr16:19753630 | A | T | 3 | a0001c0001t0001g0011 a0001c0001t0001g0114 a0001c0001t0002g0010 |
3 | HG01928.hp2 HG01934.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.475-10218A>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19753630 | |||||||
| chr16:19753752 | A | G | 1 | a0001c0001t0001g0048 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.475-10096A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19753752 | |||||||
| chr16:19753961 | C | A | 1 | a0001c0001t0005g0037 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.475-9887C>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19753961 | |||||||
| chr16:19753992 | A | T | 1 | a0001c0001t0002g0002 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.475-9856A>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19753992 | |||||||
| chr16:19754156 | C | T | 1 | a0001c0001t0002g0002 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.475-9692C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19754156 | |||||||
| chr16:19754170 | G | A | 12 | a0001c0001t0001g0030 a0001c0001t0002g0001 a0001c0001t0002g0027 others(9): Show |
12 | HG01109.hp2 HG01884.hp2 HG01934.hp2 others(9): Show |
intron_variant | MODIFIER | c.475-9678G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19754170 | |||||||
| chr16:19754564 | C | G | 6 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(3): Show |
6 | HG02717.hp2 HG02886.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.475-9284C>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19754564 | |||||||
| chr16:19754600 | G | A | 21 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(18): Show |
21 | HG01109.hp2 HG01884.hp2 HG01934.hp2 others(18): Show |
intron_variant | MODIFIER | c.475-9248G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19754600 | |||||||
| chr16:19754604 | A | T | 1 | a0001c0001t0015g0179 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.475-9244A>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19754604 | |||||||
| chr16:19754637 | CT | C | 135 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(132): Show |
135 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(132): Show |
intron_variant | MODIFIER | c.475-9201delT | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 19754637 | ||||||
| chr16:19754712 | A | T | 126 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(123): Show |
126 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(123): Show |
intron_variant | MODIFIER | c.475-9136A>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19754712 | |||||||
| chr16:19754893 | C | T | 3 | a0001c0001t0002g0241 a0001c0001t0002g0242 a0001c0001t0012g0243 |
3 | HG02622.hp2 HG02818.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.475-8955C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19754893 | |||||||
| chr16:19754900 | A | G | 1 | a0002c0002t0009g0195 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.475-8948A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19754900 | |||||||
| chr16:19754992 | T | C | 6 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(3): Show |
6 | HG01496.hp1 HG01891.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.475-8856T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19754992 | |||||||
| chr16:19755556 | G | A | 7 | a0001c0001t0004g0012 a0001c0001t0004g0022 a0001c0001t0004g0023 others(4): Show |
7 | HG01109.hp2 HG01884.hp2 HG01934.hp2 others(4): Show |
intron_variant | MODIFIER | c.475-8292G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19755556 | |||||||
| chr16:19755570 | C | T | 1 | a0001c0001t0003g0123 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.475-8278C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19755570 | |||||||
| chr16:19755807 | T | G | 151 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(148): Show |
151 | HG00140.hp2 HG00597.hp2 HG00609.hp1 others(148): Show |
intron_variant | MODIFIER | c.475-8041T>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19755807 | |||||||
| chr16:19755955 | G | T | 1 | a0003c0004t0013g0240 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.475-7893G>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19755955 | |||||||
| chr16:19755956 | G | T | 1 | a0003c0004t0013g0240 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.475-7892G>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19755956 | |||||||
| chr16:19756051 | T | G | 136 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(133): Show |
136 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(133): Show |
intron_variant | MODIFIER | c.475-7797T>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19756051 | |||||||
| chr16:19756145 | C | G | 1 | a0001c0001t0002g0237 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.475-7703C>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19756145 | |||||||
| chr16:19756355 | CAAGAT | C | 21 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(18): Show |
21 | HG01109.hp2 HG01884.hp2 HG01934.hp2 others(18): Show |
intron_variant | MODIFIER | c.475-7489_475-7485d others(7): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 19756355 | ||||||
| chr16:19756615 | A | G | 6 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(3): Show |
6 | HG01496.hp1 HG01891.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.475-7233A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19756615 | |||||||
| chr16:19756624 | C | T | 1 | a0001c0001t0007g0165 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.475-7224C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19756624 | |||||||
| chr16:19756725 | A | G | 127 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(124): Show |
127 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(124): Show |
intron_variant | MODIFIER | c.475-7123A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19756725 | |||||||
| chr16:19756757 | C | T | 1 | a0001c0001t0005g0020 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.475-7091C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19756757 | |||||||
| chr16:19756803 | A | C | 1 | a0001c0001t0001g0140 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.475-7045A>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19756803 | |||||||
| chr16:19756896 | C | CA | 119 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(116): Show |
119 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(116): Show |
intron_variant | MODIFIER | c.475-6934dupA | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 19756896 | ||||||
| chr16:19756896 | CAAAAAAA others(2): Show |
C | 6 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(3): Show |
6 | HG01496.hp1 HG01891.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.475-6942_475-6934d others(11): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 19756896 | ||||||
| chr16:19756911 | A | G | 1 | a0001c0001t0001g0064 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.475-6937A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19756911 | |||||||
| chr16:19756937 | C | A | 1 | a0002c0002t0001g0208 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.475-6911C>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19756937 | |||||||
| chr16:19756955 | G | A | 1 | a0002c0002t0003g0196 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.475-6893G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19756955 | |||||||
| chr16:19756991 | C | T | 8 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0002g0119 others(5): Show |
8 | HG02622.hp1 HG02622.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.475-6857C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19756991 | |||||||
| chr16:19756992 | A | G | 1 | a0001c0001t0001g0098 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.475-6856A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19756992 | |||||||
| chr16:19756996 | C | G | 21 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(18): Show |
21 | HG01109.hp2 HG01884.hp2 HG01934.hp2 others(18): Show |
intron_variant | MODIFIER | c.475-6852C>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19756996 | |||||||
| chr16:19757018 | C | T | 59 | a0001c0001t0003g0188 a0002c0002t0001g0176 a0002c0002t0001g0177 others(56): Show |
59 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(56): Show |
intron_variant | MODIFIER | c.475-6830C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19757018 | |||||||
| chr16:19757108 | G | A | 1 | a0003c0004t0013g0240 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.475-6740G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19757108 | |||||||
| chr16:19757211 | C | CT | 3 | a0001c0001t0002g0237 a0001c0001t0009g0239 a0001c0001t0019g0238 |
3 | HG02451.hp2 HG02895.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.475-6633dupT | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 19757211 | ||||||
| chr16:19757432 | G | T | 8 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0002g0119 others(5): Show |
8 | HG02622.hp1 HG02622.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.475-6416G>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19757432 | |||||||
| chr16:19757435 | G | T | 2 | a0001c0001t0001g0135 a0001c0001t0003g0136 |
2 | HG02451.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.475-6413G>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19757435 | |||||||
| chr16:19757475 | C | A | 21 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(18): Show |
21 | HG01109.hp2 HG01884.hp2 HG01934.hp2 others(18): Show |
intron_variant | MODIFIER | c.475-6373C>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19757475 | |||||||
| chr16:19757602 | G | A | 2 | a0001c0001t0002g0001 a0001c0001t0002g0029 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.475-6246G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19757602 | |||||||
| chr16:19757716 | A | G | 9 | a0001c0001t0001g0167 a0001c0001t0001g0171 a0001c0001t0007g0163 others(6): Show |
9 | HG01884.hp1 HG02257.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.475-6132A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19757716 | |||||||
| chr16:19757911 | C | T | 1 | a0001c0001t0003g0123 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.475-5937C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19757911 | |||||||
| chr16:19758072 | A | G | 136 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(133): Show |
136 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(133): Show |
intron_variant | MODIFIER | c.475-5776A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19758072 | |||||||
| chr16:19758239 | T | C | 1 | a0001c0001t0001g0100 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.475-5609T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19758239 | |||||||
| chr16:19758383 | C | T | 27 | a0001c0001t0001g0131 a0001c0001t0001g0133 a0001c0001t0001g0134 others(24): Show |
27 | HG00733.hp2 HG01175.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.475-5465C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19758383 | |||||||
| chr16:19758412 | G | A | 1 | a0001c0001t0001g0155 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.475-5436G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19758412 | |||||||
| chr16:19758496 | C | T | 3 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0149 |
3 | HG02717.hp2 HG02886.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.475-5352C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19758496 | |||||||
| chr16:19758501 | T | C | 136 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(133): Show |
136 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(133): Show |
intron_variant | MODIFIER | c.475-5347T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19758501 | |||||||
| chr16:19758656 | A | C | 12 | a0001c0001t0001g0030 a0001c0001t0002g0001 a0001c0001t0002g0027 others(9): Show |
12 | HG01109.hp2 HG01884.hp2 HG01934.hp2 others(9): Show |
intron_variant | MODIFIER | c.475-5192A>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19758656 | |||||||
| chr16:19758698 | A | G | 1 | a0001c0001t0002g0093 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.475-5150A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19758698 | |||||||
| chr16:19759060 | A | C | 2 | a0001c0001t0007g0163 a0001c0001t0018g0164 |
2 | HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.475-4788A>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19759060 | |||||||
| chr16:19759400 | G | T | 1 | a0001c0001t0002g0119 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.475-4448G>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19759400 | |||||||
| chr16:19759451 | C | T | 9 | a0001c0001t0001g0167 a0001c0001t0001g0171 a0001c0001t0007g0163 others(6): Show |
9 | HG01884.hp1 HG02257.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.475-4397C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19759451 | |||||||
| chr16:19759452 | G | A | 3 | a0001c0001t0001g0067 a0001c0001t0001g0101 a0001c0001t0003g0068 |
3 | HG01433.hp1 HG01943.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.475-4396G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19759452 | |||||||
| chr16:19759555 | T | C | 1 | a0001c0001t0006g0076 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.475-4293T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19759555 | |||||||
| chr16:19759608 | T | C | 1 | a0001c0001t0001g0014 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.475-4240T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19759608 | |||||||
| chr16:19759638 | A | G | 1 | a0001c0001t0005g0039 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.475-4210A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19759638 | |||||||
| chr16:19759725 | C | T | 9 | a0001c0001t0001g0167 a0001c0001t0001g0171 a0001c0001t0007g0163 others(6): Show |
9 | HG01884.hp1 HG02257.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.475-4123C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19759725 | |||||||
| chr16:19759766 | G | A | 8 | a0001c0001t0001g0040 a0001c0001t0003g0045 a0001c0001t0005g0033 others(5): Show |
8 | HG02055.hp2 HG02145.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.475-4082G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19759766 | |||||||
| chr16:19759860 | G | A | 125 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(122): Show |
125 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(122): Show |
intron_variant | MODIFIER | c.475-3988G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19759860 | |||||||
| chr16:19760167 | A | G | 1 | a0001c0001t0001g0134 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.475-3681A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19760167 | |||||||
| chr16:19760255 | G | A | 64 | a0001c0001t0002g0237 a0001c0001t0003g0188 a0001c0001t0004g0178 others(61): Show |
64 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(61): Show |
intron_variant | MODIFIER | c.475-3593G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19760255 | |||||||
| chr16:19760280 | C | T | 15 | a0001c0001t0001g0040 a0001c0001t0001g0048 a0001c0001t0002g0034 others(12): Show |
15 | HG00140.hp2 HG00738.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.475-3568C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19760280 | |||||||
| chr16:19760288 | C | T | 2 | a0001c0001t0002g0001 a0001c0001t0002g0029 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.475-3560C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19760288 | |||||||
| chr16:19760651 | T | A | 7 | a0001c0001t0001g0048 a0001c0001t0002g0034 a0001c0001t0002g0035 others(4): Show |
7 | HG00140.hp2 HG00738.hp2 HG01074.hp1 others(4): Show |
intron_variant | MODIFIER | c.475-3197T>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19760651 | |||||||
| chr16:19760731 | T | C | 21 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(18): Show |
21 | HG01109.hp2 HG01884.hp2 HG01934.hp2 others(18): Show |
intron_variant | MODIFIER | c.475-3117T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19760731 | |||||||
| chr16:19760754 | A | G | 136 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(133): Show |
136 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(133): Show |
intron_variant | MODIFIER | c.475-3094A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19760754 | |||||||
| chr16:19760853 | T | C | 8 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0002g0119 others(5): Show |
8 | HG02622.hp1 HG02622.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.475-2995T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19760853 | |||||||
| chr16:19760875 | A | T | 8 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0002g0119 others(5): Show |
8 | HG02622.hp1 HG02622.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.475-2973A>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19760875 | |||||||
| chr16:19760946 | A | G | 4 | a0001c0001t0001g0040 a0001c0001t0005g0037 a0001c0001t0005g0038 others(1): Show |
4 | HG02145.hp1 HG02922.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.475-2902A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19760946 | |||||||
| chr16:19761015 | C | T | 3 | a0002c0002t0001g0225 a0002c0002t0001g0226 a0002c0002t0001g0227 |
3 | HG02698.hp1 HG03688.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.475-2833C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19761015 | |||||||
| chr16:19761173 | A | G | 1 | a0001c0001t0001g0064 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.475-2675A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19761173 | |||||||
| chr16:19761271 | T | C | 13 | a0002c0002t0001g0181 a0002c0002t0001g0183 a0002c0002t0001g0202 others(10): Show |
13 | HG02074.hp1 HG02135.hp1 HG02155.hp1 others(10): Show |
intron_variant | MODIFIER | c.475-2577T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19761271 | |||||||
| chr16:19761523 | G | A | 1 | a0001c0001t0001g0162 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.475-2325G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19761523 | |||||||
| chr16:19761679 | C | G | 1 | a0001c0001t0001g0137 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.475-2169C>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19761679 | |||||||
| chr16:19762174 | G | T | 4 | a0001c0001t0001g0140 a0001c0001t0001g0146 a0001c0001t0001g0153 others(1): Show |
4 | HG01891.hp2 HG02280.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.475-1674G>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19762174 | |||||||
| chr16:19762202 | G | A | 1 | a0003c0004t0013g0240 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.475-1646G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19762202 | |||||||
| chr16:19762283 | G | A | 2 | a0001c0001t0001g0133 a0001c0001t0011g0132 |
2 | HG02630.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.475-1565G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19762283 | |||||||
| chr16:19762304 | G | T | 27 | a0001c0001t0001g0131 a0001c0001t0001g0133 a0001c0001t0001g0134 others(24): Show |
27 | HG00733.hp2 HG01175.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.475-1544G>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19762304 | |||||||
| chr16:19762739 | G | T | 1 | a0003c0004t0013g0240 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.475-1109G>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19762739 | |||||||
| chr16:19763074 | T | C | 9 | a0001c0001t0001g0167 a0001c0001t0001g0171 a0001c0001t0007g0163 others(6): Show |
9 | HG01884.hp1 HG02257.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.475-774T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19763074 | |||||||
| chr16:19763335 | A | T | 3 | a0001c0001t0002g0241 a0001c0001t0002g0242 a0001c0001t0012g0243 |
3 | HG02622.hp2 HG02818.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.475-513A>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19763335 | |||||||
| chr16:19763391 | A | G | 135 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(132): Show |
135 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(132): Show |
intron_variant | MODIFIER | c.475-457A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19763391 | |||||||
| chr16:19763543 | A | G | 21 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(18): Show |
21 | HG01109.hp2 HG01884.hp2 HG01934.hp2 others(18): Show |
intron_variant | MODIFIER | c.475-305A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19763543 | |||||||
| chr16:19763678 | A | G | 1 | a0001c0001t0003g0188 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.475-170A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19763678 | |||||||
| chr16:19763760 | A | G | 1 | a0001c0001t0001g0112 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.475-88A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 4/8 | chr16 | 19763760 | |||||||
| chr16:19763921 | T | C | 3 | a0001c0001t0002g0237 a0001c0001t0009g0239 a0001c0001t0019g0238 |
3 | HG02451.hp2 HG02895.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.527+21T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 5/8 | chr16 | 19763921 | |||||||
| chr16:19763947 | G | C | 3 | a0001c0001t0001g0077 a0001c0001t0001g0111 a0001c0001t0001g0244 |
3 | HG00140.hp1 HG00735.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.527+47G>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 5/8 | chr16 | 19763947 | |||||||
| chr16:19763967 | T | G | 21 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(18): Show |
21 | HG01109.hp2 HG01884.hp2 HG01934.hp2 others(18): Show |
intron_variant | MODIFIER | c.527+67T>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 5/8 | chr16 | 19763967 | |||||||
| chr16:19764371 | C | T | 1 | a0002c0002t0001g0186 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.605+259C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19764371 | |||||||
| chr16:19764660 | A | G | 21 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(18): Show |
21 | HG01109.hp2 HG01884.hp2 HG01934.hp2 others(18): Show |
intron_variant | MODIFIER | c.605+548A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19764660 | |||||||
| chr16:19764692 | C | CT | 28 | a0001c0001t0001g0131 a0001c0001t0001g0133 a0001c0001t0001g0134 others(25): Show |
28 | HG00733.hp2 HG01175.hp1 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.605+596dupT | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr16 | 19764692 | ||||||
| chr16:19764692 | CT | C | 7 | a0001c0001t0001g0048 a0001c0001t0001g0111 a0001c0001t0002g0042 others(4): Show |
7 | HG01074.hp1 HG01074.hp2 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.605+596delT | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr16 | 19764692 | ||||||
| chr16:19764744 | G | A | 2 | a0001c0001t0002g0001 a0001c0001t0002g0029 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.605+632G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19764744 | |||||||
| chr16:19764773 | C | T | 1 | a0001c0001t0001g0011 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.605+661C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19764773 | |||||||
| chr16:19764889 | C | T | 1 | a0001c0001t0002g0086 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.605+777C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19764889 | |||||||
| chr16:19764921 | G | A | 1 | a0001c0001t0006g0041 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.605+809G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19764921 | |||||||
| chr16:19764949 | T | A | 21 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(18): Show |
21 | HG01109.hp2 HG01884.hp2 HG01934.hp2 others(18): Show |
intron_variant | MODIFIER | c.605+837T>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19764949 | |||||||
| chr16:19764950 | C | T | 1 | a0001c0001t0002g0242 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.605+838C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19764950 | |||||||
| chr16:19765049 | C | T | 3 | a0001c0001t0002g0241 a0001c0001t0002g0242 a0001c0001t0012g0243 |
3 | HG02622.hp2 HG02818.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.605+937C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19765049 | |||||||
| chr16:19765221 | CA | C | 81 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(78): Show |
81 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.605+1130delA | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr16 | 19765221 | ||||||
| chr16:19765221 | CAA | C | 14 | a0001c0001t0001g0030 a0001c0001t0002g0001 a0001c0001t0002g0027 others(11): Show |
14 | HG01109.hp2 HG01884.hp2 HG01934.hp2 others(11): Show |
intron_variant | MODIFIER | c.605+1129_605+1130d others(4): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr16 | 19765221 | ||||||
| chr16:19765259 | C | T | 1 | a0001c0001t0001g0008 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.605+1147C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19765259 | |||||||
| chr16:19765260 | G | A | 1 | a0001c0001t0002g0119 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.605+1148G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19765260 | |||||||
| chr16:19765304 | G | A | 6 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(3): Show |
6 | HG01496.hp1 HG01891.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.605+1192G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19765304 | |||||||
| chr16:19765400 | C | T | 32 | a0001c0001t0003g0188 a0002c0002t0001g0176 a0002c0002t0001g0177 others(29): Show |
32 | HG00597.hp2 HG00609.hp1 HG01261.hp2 others(29): Show |
intron_variant | MODIFIER | c.605+1288C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19765400 | |||||||
| chr16:19765422 | C | T | 3 | a0001c0001t0001g0148 a0001c0001t0001g0151 a0001c0001t0001g0155 |
3 | HG00733.hp2 HG01175.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.605+1310C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19765422 | |||||||
| chr16:19765537 | CA | C | 10 | a0001c0001t0001g0167 a0001c0001t0001g0171 a0001c0001t0007g0163 others(7): Show |
10 | HG01884.hp1 HG02257.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.605+1435delA | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr16 | 19765537 | ||||||
| chr16:19765875 | A | T | 127 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(124): Show |
127 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(124): Show |
intron_variant | MODIFIER | c.605+1763A>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19765875 | |||||||
| chr16:19765909 | T | A | 59 | a0001c0001t0003g0188 a0002c0002t0001g0176 a0002c0002t0001g0177 others(56): Show |
59 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(56): Show |
intron_variant | MODIFIER | c.605+1797T>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19765909 | |||||||
| chr16:19765915 | A | T | 59 | a0001c0001t0003g0188 a0002c0002t0001g0176 a0002c0002t0001g0177 others(56): Show |
59 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(56): Show |
intron_variant | MODIFIER | c.605+1803A>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19765915 | |||||||
| chr16:19766117 | C | G | 1 | a0003c0004t0013g0240 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.605+2005C>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19766117 | |||||||
| chr16:19766383 | C | A | 127 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(124): Show |
127 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(124): Show |
intron_variant | MODIFIER | c.605+2271C>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19766383 | |||||||
| chr16:19766494 | G | A | 1 | a0001c0001t0001g0112 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.605+2382G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19766494 | |||||||
| chr16:19766691 | G | GT | 9 | a0001c0001t0001g0167 a0001c0001t0001g0171 a0001c0001t0007g0163 others(6): Show |
9 | HG01884.hp1 HG02257.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.605+2579_605+2580i others(3): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19766691 | |||||||
| chr16:19766692 | C | G | 9 | a0001c0001t0001g0167 a0001c0001t0001g0171 a0001c0001t0007g0163 others(6): Show |
9 | HG01884.hp1 HG02257.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.605+2580C>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19766692 | |||||||
| chr16:19766695 | C | A | 9 | a0001c0001t0001g0167 a0001c0001t0001g0171 a0001c0001t0007g0163 others(6): Show |
9 | HG01884.hp1 HG02257.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.605+2583C>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19766695 | |||||||
| chr16:19766696 | C | A | 9 | a0001c0001t0001g0167 a0001c0001t0001g0171 a0001c0001t0007g0163 others(6): Show |
9 | HG01884.hp1 HG02257.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.605+2584C>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19766696 | |||||||
| chr16:19766905 | G | A | 3 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0003g0120 |
3 | HG02622.hp1 HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.605+2793G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19766905 | |||||||
| chr16:19767044 | C | G | 1 | a0001c0001t0007g0165 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.605+2932C>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19767044 | |||||||
| chr16:19767074 | G | A | 21 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(18): Show |
21 | HG01109.hp2 HG01884.hp2 HG01934.hp2 others(18): Show |
intron_variant | MODIFIER | c.605+2962G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19767074 | |||||||
| chr16:19767253 | A | G | 8 | a0002c0002t0003g0190 a0002c0002t0003g0191 a0002c0002t0003g0196 others(5): Show |
8 | HG00733.hp1 HG01255.hp1 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.605+3141A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19767253 | |||||||
| chr16:19767472 | G | A | 27 | a0001c0001t0001g0131 a0001c0001t0001g0133 a0001c0001t0001g0134 others(24): Show |
27 | HG00733.hp2 HG01175.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.605+3360G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19767472 | |||||||
| chr16:19767526 | G | T | 1 | a0001c0001t0001g0070 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.605+3414G>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19767526 | |||||||
| chr16:19767766 | G | A | 4 | a0001c0001t0002g0034 a0001c0001t0002g0036 a0001c0001t0002g0046 others(1): Show |
4 | HG00140.hp2 HG01346.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.605+3654G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19767766 | |||||||
| chr16:19767787 | G | A | 7 | a0002c0002t0001g0189 a0002c0002t0001g0201 a0002c0002t0001g0211 others(4): Show |
7 | NA18954.hp2 NA18963.hp2 NA18967.hp2 others(4): Show |
intron_variant | MODIFIER | c.605+3675G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19767787 | |||||||
| chr16:19767867 | G | A | 1 | a0001c0001t0001g0040 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.605+3755G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19767867 | |||||||
| chr16:19767875 | A | G | 1 | a0002c0002t0001g0202 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.605+3763A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19767875 | |||||||
| chr16:19768014 | G | T | 1 | a0001c0001t0001g0151 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.605+3902G>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19768014 | |||||||
| chr16:19768015 | C | G | 1 | a0001c0001t0001g0151 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.605+3903C>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19768015 | |||||||
| chr16:19768015 | CT | C | 31 | a0001c0001t0001g0131 a0001c0001t0001g0133 a0001c0001t0001g0134 others(28): Show |
31 | HG01175.hp1 HG01891.hp2 HG02055.hp1 others(28): Show |
intron_variant | MODIFIER | c.605+3919delT | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr16 | 19768015 | ||||||
| chr16:19768016 | T | C | 1 | a0001c0001t0001g0151 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.605+3904T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19768016 | |||||||
| chr16:19768216 | G | A | 2 | a0001c0001t0004g0178 a0001c0001t0015g0179 |
2 | HG02615.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.605+4104G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19768216 | |||||||
| chr16:19768449 | T | C | 21 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(18): Show |
21 | HG01109.hp2 HG01884.hp2 HG01934.hp2 others(18): Show |
intron_variant | MODIFIER | c.605+4337T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19768449 | |||||||
| chr16:19768613 | G | A | 15 | a0001c0001t0001g0040 a0001c0001t0001g0048 a0001c0001t0002g0034 others(12): Show |
15 | HG00140.hp2 HG00738.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.605+4501G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19768613 | |||||||
| chr16:19769210 | A | G | 9 | a0001c0001t0001g0167 a0001c0001t0001g0171 a0001c0001t0007g0163 others(6): Show |
9 | HG01884.hp1 HG02257.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.605+5098A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19769210 | |||||||
| chr16:19769265 | T | C | 5 | a0001c0001t0002g0237 a0001c0001t0004g0178 a0001c0001t0009g0239 others(2): Show |
5 | HG02451.hp2 HG02615.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.605+5153T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19769265 | |||||||
| chr16:19769416 | C | T | 7 | a0001c0001t0007g0163 a0001c0001t0007g0165 a0001c0001t0007g0166 others(4): Show |
7 | HG01884.hp1 HG02257.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.605+5304C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19769416 | |||||||
| chr16:19769777 | T | C | 4 | a0001c0001t0001g0040 a0001c0001t0005g0037 a0001c0001t0005g0038 others(1): Show |
4 | HG02145.hp1 HG02922.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.605+5665T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19769777 | |||||||
| chr16:19769915 | G | A | 27 | a0001c0001t0001g0131 a0001c0001t0001g0133 a0001c0001t0001g0134 others(24): Show |
27 | HG00733.hp2 HG01175.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.605+5803G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19769915 | |||||||
| chr16:19770112 | G | A | 1 | a0001c0001t0001g0161 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.605+6000G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19770112 | |||||||
| chr16:19770276 | G | A | 5 | a0001c0001t0001g0140 a0001c0001t0001g0146 a0001c0001t0001g0153 others(2): Show |
5 | HG01891.hp2 HG02280.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.605+6164G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19770276 | |||||||
| chr16:19770406 | G | A | 1 | a0001c0001t0001g0055 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.605+6294G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19770406 | |||||||
| chr16:19770527 | C | T | 3 | a0001c0001t0002g0237 a0001c0001t0009g0239 a0001c0001t0019g0238 |
3 | HG02451.hp2 HG02895.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.605+6415C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19770527 | |||||||
| chr16:19770638 | G | T | 120 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(117): Show |
120 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(117): Show |
intron_variant | MODIFIER | c.605+6526G>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19770638 | |||||||
| chr16:19770768 | A | C | 1 | a0001c0001t0003g0123 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.605+6656A>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19770768 | |||||||
| chr16:19771015 | C | G | 2 | a0001c0001t0002g0069 a0001c0001t0002g0085 |
2 | HG02738.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.605+6903C>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19771015 | |||||||
| chr16:19771155 | A | G | 1 | a0001c0001t0002g0242 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.605+7043A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19771155 | |||||||
| chr16:19771331 | A | G | 59 | a0001c0001t0003g0188 a0002c0002t0001g0176 a0002c0002t0001g0177 others(56): Show |
59 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(56): Show |
intron_variant | MODIFIER | c.605+7219A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19771331 | |||||||
| chr16:19771480 | C | A | 73 | a0001c0001t0001g0167 a0001c0001t0001g0171 a0001c0001t0002g0237 others(70): Show |
73 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(70): Show |
intron_variant | MODIFIER | c.605+7368C>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19771480 | |||||||
| chr16:19771702 | A | G | 1 | a0002c0002t0001g0208 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.605+7590A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19771702 | |||||||
| chr16:19771885 | G | A | 6 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(3): Show |
6 | HG01496.hp1 HG01891.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.605+7773G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19771885 | |||||||
| chr16:19771897 | A | C | 28 | a0001c0001t0001g0131 a0001c0001t0001g0133 a0001c0001t0001g0134 others(25): Show |
28 | HG00733.hp2 HG01175.hp1 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.605+7785A>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19771897 | |||||||
| chr16:19771999 | T | A | 3 | a0001c0001t0001g0115 a0001c0001t0002g0009 a0001c0001t0002g0113 |
3 | HG01975.hp2 HG02300.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.605+7887T>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19771999 | |||||||
| chr16:19772210 | C | T | 1 | a0001c0001t0002g0119 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.605+8098C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19772210 | |||||||
| chr16:19772713 | T | C | 2 | a0001c0001t0001g0145 a0001c0001t0001g0150 |
2 | HG02055.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.605+8601T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19772713 | |||||||
| chr16:19772729 | G | T | 1 | a0001c0001t0002g0086 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.605+8617G>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19772729 | |||||||
| chr16:19772875 | C | T | 33 | a0001c0001t0001g0131 a0001c0001t0001g0133 a0001c0001t0001g0134 others(30): Show |
33 | HG00733.hp2 HG01175.hp1 HG01496.hp1 others(30): Show |
intron_variant | MODIFIER | c.605+8763C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19772875 | |||||||
| chr16:19772963 | G | A | 11 | a0001c0001t0001g0167 a0001c0001t0001g0171 a0001c0001t0004g0178 others(8): Show |
11 | HG01884.hp1 HG02257.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.605+8851G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19772963 | |||||||
| chr16:19773020 | A | T | 3 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0003g0120 |
3 | HG02622.hp1 HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.605+8908A>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19773020 | |||||||
| chr16:19773135 | G | A | 1 | a0001c0001t0001g0167 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.605+9023G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19773135 | |||||||
| chr16:19773369 | A | G | 135 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(132): Show |
135 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(132): Show |
intron_variant | MODIFIER | c.605+9257A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19773369 | |||||||
| chr16:19773724 | C | T | 8 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0002g0119 others(5): Show |
8 | HG02622.hp1 HG02622.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.605+9612C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19773724 | |||||||
| chr16:19773805 | T | G | 34 | a0001c0001t0001g0131 a0001c0001t0001g0133 a0001c0001t0001g0134 others(31): Show |
34 | HG00733.hp2 HG01175.hp1 HG01496.hp1 others(31): Show |
intron_variant | MODIFIER | c.605+9693T>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19773805 | |||||||
| chr16:19774074 | A | G | 1 | a0001c0001t0004g0005 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.605+9962A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19774074 | |||||||
| chr16:19774075 | A | T | 1 | a0002c0002t0002g0180 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.605+9963A>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19774075 | |||||||
| chr16:19774105 | T | C | 1 | a0001c0001t0002g0242 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.605+9993T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19774105 | |||||||
| chr16:19774134 | A | T | 46 | a0002c0002t0001g0176 a0002c0002t0001g0177 a0002c0002t0001g0181 others(43): Show |
46 | HG00597.hp2 HG00609.hp1 HG01081.hp1 others(43): Show |
intron_variant | MODIFIER | c.605+10022A>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19774134 | |||||||
| chr16:19774297 | C | T | 45 | a0001c0001t0001g0003 a0001c0001t0001g0066 a0001c0001t0001g0075 others(42): Show |
45 | HG00140.hp1 HG00323.hp1 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.605+10185C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19774297 | |||||||
| chr16:19774320 | C | A | 1 | a0001c0001t0005g0039 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.605+10208C>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19774320 | |||||||
| chr16:19774334 | CATTATTG others(6): Show |
C | 1 | a0001c0001t0005g0039 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.605+10225_605+1023 others(17): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr16 | 19774334 | ||||||
| chr16:19774398 | C | CT | 17 | a0001c0001t0001g0008 a0001c0001t0001g0077 a0001c0001t0001g0090 others(14): Show |
17 | HG00140.hp1 HG00609.hp2 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.605+10313dupT | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr16 | 19774398 | ||||||
| chr16:19774398 | C | CTT | 8 | a0001c0001t0001g0133 a0001c0001t0001g0156 a0001c0001t0001g0160 others(5): Show |
8 | HG01496.hp1 HG02630.hp1 HG02735.hp1 others(5): Show |
intron_variant | MODIFIER | c.605+10312_605+1031 others(6): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr16 | 19774398 | ||||||
| chr16:19774398 | C | CTTT | 51 | a0001c0001t0001g0131 a0001c0001t0001g0134 a0001c0001t0001g0135 others(48): Show |
51 | HG00597.hp2 HG00609.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.605+10311_605+1031 others(7): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr16 | 19774398 | ||||||
| chr16:19774398 | C | CTTTT | 20 | a0001c0001t0001g0140 a0001c0001t0001g0145 a0001c0001t0001g0146 others(17): Show |
20 | HG01261.hp2 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.605+10310_605+1031 others(8): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr16 | 19774398 | ||||||
| chr16:19774398 | CTT | C | 12 | a0001c0001t0005g0039 a0002c0002t0001g0193 a0002c0002t0003g0190 others(9): Show |
12 | HG00733.hp1 HG01255.hp1 HG02300.hp2 others(9): Show |
intron_variant | MODIFIER | c.605+10312_605+1031 others(6): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr16 | 19774398 | ||||||
| chr16:19774398 | CTTTTTTT others(2): Show |
C | 7 | a0001c0001t0007g0163 a0001c0001t0007g0165 a0001c0001t0007g0166 others(4): Show |
7 | HG01884.hp1 HG02257.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.605+10305_605+1031 others(13): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr16 | 19774398 | ||||||
| chr16:19774398 | CTTTTTTT others(3): Show |
C | 3 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0141 |
3 | HG02572.hp1 HG03130.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.605+10304_605+1031 others(14): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr16 | 19774398 | ||||||
| chr16:19774398 | CTTTTTTT others(5): Show |
C | 21 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(18): Show |
21 | HG01109.hp2 HG01884.hp2 HG01934.hp2 others(18): Show |
intron_variant | MODIFIER | c.605+10302_605+1031 others(16): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr16 | 19774398 | ||||||
| chr16:19774655 | C | T | 1 | a0001c0001t0002g0042 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.605+10543C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19774655 | |||||||
| chr16:19774785 | C | T | 8 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0002g0119 others(5): Show |
8 | HG02622.hp1 HG02622.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.605+10673C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19774785 | |||||||
| chr16:19775051 | T | C | 73 | a0001c0001t0001g0167 a0001c0001t0001g0171 a0001c0001t0002g0237 others(70): Show |
73 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(70): Show |
intron_variant | MODIFIER | c.605+10939T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19775051 | |||||||
| chr16:19775226 | CA | C | 46 | a0001c0001t0001g0040 a0001c0001t0001g0048 a0001c0001t0001g0131 others(43): Show |
46 | HG00140.hp2 HG00733.hp2 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.605+11133delA | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr16 | 19775226 | ||||||
| chr16:19775226 | CAA | C | 14 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0156 others(11): Show |
14 | HG01496.hp1 HG01891.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.605+11132_605+1113 others(6): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr16 | 19775226 | ||||||
| chr16:19775308 | G | A | 8 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0002g0119 others(5): Show |
8 | HG02622.hp1 HG02622.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.605+11196G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19775308 | |||||||
| chr16:19775417 | T | C | 2 | a0001c0001t0004g0178 a0001c0001t0015g0179 |
2 | HG02615.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.605+11305T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19775417 | |||||||
| chr16:19775635 | CAAAAAGA others(8): Show |
C | 1 | a0001c0001t0006g0099 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.605+11524_605+1153 others(19): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19775635 | |||||||
| chr16:19775685 | T | C | 1 | a0001c0001t0001g0014 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.605+11573T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19775685 | |||||||
| chr16:19775844 | GCTGTT | G | 136 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(133): Show |
136 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(133): Show |
intron_variant | MODIFIER | c.605+11741_605+1174 others(9): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr16 | 19775844 | ||||||
| chr16:19775866 | C | CT | 6 | a0001c0001t0001g0112 a0001c0001t0007g0166 a0002c0002t0001g0193 others(3): Show |
6 | HG01884.hp1 HG03471.hp2 HG03834.hp2 others(3): Show |
intron_variant | MODIFIER | c.605+11787dupT | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr16 | 19775866 | ||||||
| chr16:19775866 | C | CTT | 27 | a0001c0001t0001g0121 a0001c0001t0003g0120 a0002c0002t0001g0176 others(24): Show |
27 | HG00609.hp1 HG01081.hp1 HG02074.hp1 others(24): Show |
intron_variant | MODIFIER | c.605+11786_605+1178 others(6): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr16 | 19775866 | ||||||
| chr16:19775866 | C | CTTT | 16 | a0001c0001t0003g0188 a0002c0002t0001g0182 a0002c0002t0001g0189 others(13): Show |
16 | HG01433.hp2 HG02015.hp1 HG02056.hp1 others(13): Show |
intron_variant | MODIFIER | c.605+11785_605+1178 others(7): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr16 | 19775866 | ||||||
| chr16:19775866 | C | CTTTT | 12 | a0001c0001t0001g0122 a0002c0002t0001g0177 a0002c0002t0001g0222 others(9): Show |
12 | HG00733.hp1 HG01255.hp1 HG02698.hp1 others(9): Show |
intron_variant | MODIFIER | c.605+11784_605+1178 others(8): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr16 | 19775866 | ||||||
| chr16:19775866 | CT | C | 27 | a0001c0001t0001g0008 a0001c0001t0001g0040 a0001c0001t0001g0053 others(24): Show |
27 | HG00140.hp2 HG00609.hp2 HG01255.hp2 others(24): Show |
intron_variant | MODIFIER | c.605+11787delT | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr16 | 19775866 | ||||||
| chr16:19775866 | CTT | C | 79 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0048 others(76): Show |
79 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(76): Show |
intron_variant | MODIFIER | c.605+11786_605+1178 others(6): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr16 | 19775866 | ||||||
| chr16:19775866 | CTTT | C | 15 | a0001c0001t0001g0017 a0001c0001t0001g0051 a0001c0001t0001g0056 others(12): Show |
15 | HG01109.hp2 HG01891.hp1 HG02083.hp1 others(12): Show |
intron_variant | MODIFIER | c.605+11785_605+1178 others(7): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr16 | 19775866 | ||||||
| chr16:19775866 | CTTTT | C | 22 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0018 others(19): Show |
22 | HG01496.hp1 HG01884.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.605+11784_605+1178 others(8): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr16 | 19775866 | ||||||
| chr16:19775866 | CTTTTT | C | 27 | a0001c0001t0001g0131 a0001c0001t0001g0133 a0001c0001t0001g0134 others(24): Show |
27 | HG00733.hp2 HG01175.hp1 HG02145.hp2 others(24): Show |
intron_variant | MODIFIER | c.605+11783_605+1178 others(9): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr16 | 19775866 | ||||||
| chr16:19776089 | G | C | 136 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(133): Show |
136 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(133): Show |
intron_variant | MODIFIER | c.605+11977G>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19776089 | |||||||
| chr16:19776098 | C | G | 1 | a0001c0001t0001g0134 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.605+11986C>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19776098 | |||||||
| chr16:19776304 | C | T | 1 | a0002c0002t0001g0206 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.605+12192C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19776304 | |||||||
| chr16:19776333 | C | G | 1 | a0003c0004t0013g0240 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.605+12221C>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19776333 | |||||||
| chr16:19776550 | C | A | 1 | a0003c0004t0013g0240 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.606-12288C>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19776550 | |||||||
| chr16:19776627 | G | A | 59 | a0001c0001t0003g0188 a0002c0002t0001g0176 a0002c0002t0001g0177 others(56): Show |
59 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(56): Show |
intron_variant | MODIFIER | c.606-12211G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19776627 | |||||||
| chr16:19776634 | G | A | 1 | a0001c0001t0006g0076 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.606-12204G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19776634 | |||||||
| chr16:19776657 | C | T | 2 | a0002c0002t0001g0204 a0002c0002t0001g0213 |
2 | HG00597.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.606-12181C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19776657 | |||||||
| chr16:19776877 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.606-11961C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19776877 | |||||||
| chr16:19776897 | A | G | 1 | a0001c0001t0002g0042 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.606-11941A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19776897 | |||||||
| chr16:19777605 | A | G | 13 | a0002c0002t0001g0181 a0002c0002t0001g0183 a0002c0002t0001g0202 others(10): Show |
13 | HG02074.hp1 HG02135.hp1 HG02155.hp1 others(10): Show |
intron_variant | MODIFIER | c.606-11233A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19777605 | |||||||
| chr16:19777702 | C | T | 27 | a0001c0001t0001g0131 a0001c0001t0001g0133 a0001c0001t0001g0134 others(24): Show |
27 | HG00733.hp2 HG01175.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.606-11136C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19777702 | |||||||
| chr16:19777985 | A | G | 136 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(133): Show |
136 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(133): Show |
intron_variant | MODIFIER | c.606-10853A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19777985 | |||||||
| chr16:19778052 | C | CA | 11 | a0001c0001t0001g0167 a0001c0001t0001g0171 a0001c0001t0004g0178 others(8): Show |
11 | HG01884.hp1 HG02257.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.606-10777dupA | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr16 | 19778052 | ||||||
| chr16:19778066 | A | G | 1 | a0001c0001t0003g0136 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.606-10772A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19778066 | |||||||
| chr16:19778126 | T | C | 241 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(238): Show |
241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.606-10712T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19778126 | |||||||
| chr16:19778270 | T | G | 1 | a0003c0004t0013g0240 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.606-10568T>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19778270 | |||||||
| chr16:19778415 | G | A | 30 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0053 others(27): Show |
30 | HG00099.hp1 HG00099.hp2 HG00609.hp2 others(27): Show |
intron_variant | MODIFIER | c.606-10423G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19778415 | |||||||
| chr16:19778441 | G | A | 1 | a0002c0002t0001g0202 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.606-10397G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19778441 | |||||||
| chr16:19778543 | G | C | 3 | a0001c0001t0001g0057 a0001c0001t0001g0060 a0001c0001t0001g0061 |
3 | NA18983.hp2 NA18993.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.606-10295G>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19778543 | |||||||
| chr16:19778556 | C | T | 2 | a0001c0001t0006g0117 a0001c0001t0006g0118 |
2 | HG02698.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.606-10282C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19778556 | |||||||
| chr16:19778610 | A | G | 230 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(227): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.606-10228A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19778610 | |||||||
| chr16:19778677 | A | G | 1 | a0001c0003t0003g0021 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.606-10161A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19778677 | |||||||
| chr16:19778779 | G | A | 1 | a0002c0002t0001g0208 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.606-10059G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19778779 | |||||||
| chr16:19778852 | T | C | 2 | a0001c0001t0001g0131 a0001c0001t0001g0154 |
2 | HG02145.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.606-9986T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19778852 | |||||||
| chr16:19778872 | A | C | 34 | a0001c0001t0001g0131 a0001c0001t0001g0133 a0001c0001t0001g0134 others(31): Show |
34 | HG00733.hp2 HG01175.hp1 HG01496.hp1 others(31): Show |
intron_variant | MODIFIER | c.606-9966A>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19778872 | |||||||
| chr16:19778889 | T | C | 1 | a0001c0001t0005g0039 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.606-9949T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19778889 | |||||||
| chr16:19778927 | A | C | 1 | a0001c0001t0003g0123 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.606-9911A>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19778927 | |||||||
| chr16:19778984 | C | A | 2 | a0001c0001t0002g0001 a0001c0001t0002g0029 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.606-9854C>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19778984 | |||||||
| chr16:19779057 | A | G | 8 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0002g0119 others(5): Show |
8 | HG02622.hp1 HG02622.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.606-9781A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19779057 | |||||||
| chr16:19779171 | C | A | 8 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0002g0119 others(5): Show |
8 | HG02622.hp1 HG02622.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.606-9667C>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19779171 | |||||||
| chr16:19779300 | T | C | 21 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(18): Show |
21 | HG01109.hp2 HG01884.hp2 HG01934.hp2 others(18): Show |
intron_variant | MODIFIER | c.606-9538T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19779300 | |||||||
| chr16:19779361 | G | C | 33 | a0001c0001t0001g0131 a0001c0001t0001g0133 a0001c0001t0001g0134 others(30): Show |
33 | HG00733.hp2 HG01175.hp1 HG01496.hp1 others(30): Show |
intron_variant | MODIFIER | c.606-9477G>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19779361 | |||||||
| chr16:19779634 | C | T | 1 | a0003c0004t0013g0240 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.606-9204C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19779634 | |||||||
| chr16:19779690 | T | A | 1 | a0002c0002t0001g0227 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.606-9148T>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19779690 | |||||||
| chr16:19779727 | A | T | 18 | a0001c0001t0001g0040 a0001c0001t0001g0048 a0001c0001t0001g0157 others(15): Show |
18 | HG00140.hp2 HG00738.hp2 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.606-9111A>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19779727 | |||||||
| chr16:19779781 | G | A | 21 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(18): Show |
21 | HG01109.hp2 HG01884.hp2 HG01934.hp2 others(18): Show |
intron_variant | MODIFIER | c.606-9057G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19779781 | |||||||
| chr16:19779794 | T | C | 8 | a0001c0001t0002g0027 a0001c0001t0004g0012 a0001c0001t0004g0022 others(5): Show |
8 | HG01109.hp2 HG01884.hp2 HG01934.hp2 others(5): Show |
intron_variant | MODIFIER | c.606-9044T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19779794 | |||||||
| chr16:19779840 | C | T | 1 | a0001c0001t0002g0079 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.606-8998C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19779840 | |||||||
| chr16:19779952 | C | T | 1 | a0003c0004t0013g0240 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.606-8886C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19779952 | |||||||
| chr16:19780018 | C | CTTAT | 6 | a0001c0001t0001g0125 a0001c0001t0003g0096 a0001c0001t0006g0041 others(3): Show |
6 | HG00639.hp1 HG00738.hp1 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.606-8781_606-8778d others(6): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr16 | 19780018 | ||||||
| chr16:19780018 | CTTAT | C | 102 | a0001c0001t0001g0013 a0001c0001t0001g0040 a0001c0001t0001g0048 others(99): Show |
102 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(99): Show |
intron_variant | MODIFIER | c.606-8781_606-8778d others(6): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr16 | 19780018 | ||||||
| chr16:19780018 | CTTATTTA others(1): Show |
C | 67 | a0001c0001t0001g0030 a0001c0001t0001g0051 a0001c0001t0001g0055 others(64): Show |
67 | HG00733.hp2 HG01109.hp2 HG01175.hp1 others(64): Show |
intron_variant | MODIFIER | c.606-8785_606-8778d others(10): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr16 | 19780018 | ||||||
| chr16:19780018 | CTTATTTA others(5): Show |
C | 1 | a0001c0001t0003g0123 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.606-8789_606-8778d others(14): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr16 | 19780018 | ||||||
| chr16:19780341 | C | T | 72 | a0001c0001t0001g0167 a0001c0001t0001g0171 a0001c0001t0002g0237 others(69): Show |
72 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(69): Show |
intron_variant | MODIFIER | c.606-8497C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19780341 | |||||||
| chr16:19780377 | C | G | 8 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0002g0119 others(5): Show |
8 | HG02622.hp1 HG02622.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.606-8461C>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19780377 | |||||||
| chr16:19780502 | A | G | 1 | a0002c0002t0001g0234 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.606-8336A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19780502 | |||||||
| chr16:19780694 | G | A | 1 | a0001c0001t0003g0123 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.606-8144G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19780694 | |||||||
| chr16:19780696 | G | A | 1 | a0001c0001t0003g0123 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.606-8142G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19780696 | |||||||
| chr16:19780849 | G | A | 8 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0002g0119 others(5): Show |
8 | HG02622.hp1 HG02622.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.606-7989G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19780849 | |||||||
| chr16:19780858 | A | G | 2 | a0002c0002t0009g0194 a0002c0002t0009g0195 |
2 | HG02486.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.606-7980A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19780858 | |||||||
| chr16:19781075 | C | T | 1 | a0001c0001t0002g0103 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.606-7763C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19781075 | |||||||
| chr16:19781193 | C | T | 58 | a0002c0002t0001g0176 a0002c0002t0001g0177 a0002c0002t0001g0181 others(55): Show |
58 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(55): Show |
intron_variant | MODIFIER | c.606-7645C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19781193 | |||||||
| chr16:19781212 | C | A | 58 | a0002c0002t0001g0176 a0002c0002t0001g0177 a0002c0002t0001g0181 others(55): Show |
58 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(55): Show |
intron_variant | MODIFIER | c.606-7626C>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19781212 | |||||||
| chr16:19781213 | T | C | 1 | a0001c0001t0001g0100 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.606-7625T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19781213 | |||||||
| chr16:19781261 | A | T | 9 | a0001c0001t0001g0167 a0001c0001t0001g0171 a0001c0001t0007g0163 others(6): Show |
9 | HG01884.hp1 HG02257.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.606-7577A>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19781261 | |||||||
| chr16:19781276 | C | T | 72 | a0001c0001t0001g0167 a0001c0001t0001g0171 a0001c0001t0002g0237 others(69): Show |
72 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(69): Show |
intron_variant | MODIFIER | c.606-7562C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19781276 | |||||||
| chr16:19781651 | C | T | 1 | a0002c0002t0003g0196 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.606-7187C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19781651 | |||||||
| chr16:19781689 | C | T | 135 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(132): Show |
135 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(132): Show |
intron_variant | MODIFIER | c.606-7149C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19781689 | |||||||
| chr16:19781711 | G | A | 1 | a0001c0001t0003g0123 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.606-7127G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19781711 | |||||||
| chr16:19781726 | C | T | 1 | a0001c0001t0010g0147 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.606-7112C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19781726 | |||||||
| chr16:19781747 | G | T | 3 | a0001c0001t0002g0241 a0001c0001t0002g0242 a0001c0001t0012g0243 |
3 | HG02622.hp2 HG02818.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.606-7091G>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19781747 | |||||||
| chr16:19781856 | G | T | 11 | a0001c0001t0001g0167 a0001c0001t0001g0171 a0001c0001t0004g0178 others(8): Show |
11 | HG01884.hp1 HG02257.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.606-6982G>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19781856 | |||||||
| chr16:19782340 | C | T | 2 | a0001c0001t0001g0075 a0003c0004t0013g0240 |
2 | HG02523.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.606-6498C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19782340 | |||||||
| chr16:19782449 | G | A | 1 | a0001c0001t0003g0123 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.606-6389G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19782449 | |||||||
| chr16:19782642 | AAGAG | A | 21 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(18): Show |
21 | HG01109.hp2 HG01884.hp2 HG01934.hp2 others(18): Show |
intron_variant | MODIFIER | c.606-6192_606-6189d others(6): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr16 | 19782642 | ||||||
| chr16:19782658 | T | G | 135 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(132): Show |
135 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(132): Show |
intron_variant | MODIFIER | c.606-6180T>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19782658 | |||||||
| chr16:19782675 | C | A | 1 | a0001c0001t0001g0067 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.606-6163C>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19782675 | |||||||
| chr16:19782848 | C | G | 1 | a0001c0001t0002g0119 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.606-5990C>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19782848 | |||||||
| chr16:19782991 | C | CT | 132 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(129): Show |
132 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(129): Show |
intron_variant | MODIFIER | c.606-5840dupT | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr16 | 19782991 | ||||||
| chr16:19782997 | T | TTG | 4 | a0001c0001t0002g0094 a0001c0001t0002g0095 a0001c0001t0008g0074 others(1): Show |
4 | HG01261.hp1 HG01943.hp2 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.606-5822_606-5821d others(4): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr16 | 19782997 | ||||||
| chr16:19782999 | G | T | 157 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(154): Show |
157 | HG00597.hp1 HG00597.hp2 HG00609.hp1 others(154): Show |
intron_variant | MODIFIER | c.606-5839G>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19782999 | |||||||
| chr16:19783001 | G | T | 136 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(133): Show |
136 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(133): Show |
intron_variant | MODIFIER | c.606-5837G>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19783001 | |||||||
| chr16:19783003 | G | T | 134 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(131): Show |
134 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(131): Show |
intron_variant | MODIFIER | c.606-5835G>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19783003 | |||||||
| chr16:19783011 | G | T | 1 | a0002c0002t0003g0203 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.606-5827G>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19783011 | |||||||
| chr16:19783014 | T | C | 1 | a0001c0001t0001g0097 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.606-5824T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19783014 | |||||||
| chr16:19783025 | G | A | 72 | a0001c0001t0001g0167 a0001c0001t0001g0171 a0001c0001t0002g0237 others(69): Show |
72 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(69): Show |
intron_variant | MODIFIER | c.606-5813G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19783025 | |||||||
| chr16:19783052 | A | G | 135 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(132): Show |
135 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(132): Show |
intron_variant | MODIFIER | c.606-5786A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19783052 | |||||||
| chr16:19783076 | G | A | 6 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(3): Show |
6 | HG01496.hp1 HG01891.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.606-5762G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19783076 | |||||||
| chr16:19783102 | G | A | 8 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0002g0119 others(5): Show |
8 | HG02622.hp1 HG02622.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.606-5736G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19783102 | |||||||
| chr16:19783319 | A | T | 3 | a0001c0001t0002g0237 a0001c0001t0009g0239 a0001c0001t0019g0238 |
3 | HG02451.hp2 HG02895.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.606-5519A>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19783319 | |||||||
| chr16:19783381 | C | T | 135 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(132): Show |
135 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(132): Show |
intron_variant | MODIFIER | c.606-5457C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19783381 | |||||||
| chr16:19783421 | C | T | 2 | a0001c0001t0004g0178 a0001c0001t0015g0179 |
2 | HG02615.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.606-5417C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19783421 | |||||||
| chr16:19783439 | C | T | 1 | a0001c0001t0002g0119 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.606-5399C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19783439 | |||||||
| chr16:19783469 | C | T | 2 | a0001c0001t0007g0163 a0001c0001t0018g0164 |
2 | HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.606-5369C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19783469 | |||||||
| chr16:19783542 | CA | C | 29 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0053 others(26): Show |
29 | HG00099.hp1 HG00099.hp2 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.606-5295delA | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19783542 | |||||||
| chr16:19783545 | T | A | 29 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0053 others(26): Show |
29 | HG00099.hp1 HG00099.hp2 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.606-5293T>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19783545 | |||||||
| chr16:19783547 | G | T | 29 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0053 others(26): Show |
29 | HG00099.hp1 HG00099.hp2 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.606-5291G>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19783547 | |||||||
| chr16:19783548 | C | G | 29 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0053 others(26): Show |
29 | HG00099.hp1 HG00099.hp2 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.606-5290C>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19783548 | |||||||
| chr16:19783581 | C | T | 1 | a0002c0002t0001g0181 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.606-5257C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19783581 | |||||||
| chr16:19783959 | G | A | 1 | a0001c0001t0016g0089 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.606-4879G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19783959 | |||||||
| chr16:19784004 | GA | G | 72 | a0001c0001t0001g0167 a0001c0001t0001g0171 a0001c0001t0002g0237 others(69): Show |
72 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(69): Show |
intron_variant | MODIFIER | c.606-4829delA | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr16 | 19784004 | ||||||
| chr16:19784048 | C | A | 1 | a0001c0001t0005g0039 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.606-4790C>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19784048 | |||||||
| chr16:19784087 | A | T | 72 | a0001c0001t0001g0167 a0001c0001t0001g0171 a0001c0001t0002g0237 others(69): Show |
72 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(69): Show |
intron_variant | MODIFIER | c.606-4751A>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19784087 | |||||||
| chr16:19784480 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.606-4358G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19784480 | |||||||
| chr16:19784923 | C | A | 3 | a0001c0001t0002g0237 a0001c0001t0009g0239 a0001c0001t0019g0238 |
3 | HG02451.hp2 HG02895.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.606-3915C>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19784923 | |||||||
| chr16:19785021 | G | A | 58 | a0002c0002t0001g0176 a0002c0002t0001g0177 a0002c0002t0001g0181 others(55): Show |
58 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(55): Show |
intron_variant | MODIFIER | c.606-3817G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19785021 | |||||||
| chr16:19785509 | A | G | 3 | a0001c0001t0001g0011 a0001c0001t0001g0114 a0001c0001t0002g0010 |
3 | HG01928.hp2 HG01934.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.606-3329A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19785509 | |||||||
| chr16:19785579 | A | G | 141 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(138): Show |
141 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(138): Show |
intron_variant | MODIFIER | c.606-3259A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19785579 | |||||||
| chr16:19785807 | G | A | 70 | a0001c0001t0001g0167 a0001c0001t0001g0171 a0001c0001t0002g0237 others(67): Show |
70 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(67): Show |
intron_variant | MODIFIER | c.606-3031G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19785807 | |||||||
| chr16:19786275 | C | T | 27 | a0001c0001t0001g0131 a0001c0001t0001g0133 a0001c0001t0001g0134 others(24): Show |
27 | HG00733.hp2 HG01175.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.606-2563C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19786275 | |||||||
| chr16:19786276 | G | A | 6 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(3): Show |
6 | HG01496.hp1 HG01891.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.606-2562G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19786276 | |||||||
| chr16:19786425 | C | T | 6 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(3): Show |
6 | HG01496.hp1 HG01891.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.606-2413C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19786425 | |||||||
| chr16:19786556 | A | G | 141 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(138): Show |
141 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(138): Show |
intron_variant | MODIFIER | c.606-2282A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19786556 | |||||||
| chr16:19786568 | G | A | 1 | a0003c0004t0013g0240 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.606-2270G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19786568 | |||||||
| chr16:19786647 | G | A | 58 | a0002c0002t0001g0176 a0002c0002t0001g0177 a0002c0002t0001g0181 others(55): Show |
58 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(55): Show |
intron_variant | MODIFIER | c.606-2191G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19786647 | |||||||
| chr16:19786701 | GAAGA | G | 27 | a0001c0001t0001g0131 a0001c0001t0001g0133 a0001c0001t0001g0134 others(24): Show |
27 | HG00733.hp2 HG01175.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.606-2128_606-2125d others(6): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr16 | 19786701 | ||||||
| chr16:19786706 | AAGAAAGA others(1): Show |
A | 3 | a0001c0001t0001g0018 a0001c0001t0003g0015 a0001c0001t0003g0016 |
3 | HG02280.hp2 HG02615.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.606-2121_606-2114d others(10): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr16 | 19786706 | ||||||
| chr16:19786753 | G | GA | 21 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(18): Show |
21 | HG01109.hp2 HG01884.hp2 HG01934.hp2 others(18): Show |
intron_variant | MODIFIER | c.606-2078dupA | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr16 | 19786753 | ||||||
| chr16:19786810 | AGAGAAGG others(1): Show |
A | 10 | a0001c0001t0001g0040 a0001c0001t0002g0119 a0001c0001t0003g0045 others(7): Show |
10 | HG02055.hp2 HG02145.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.606-2027_606-2020d others(10): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19786810 | |||||||
| chr16:19786811 | G | A | 1 | a0001c0001t0002g0034 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.606-2027G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19786811 | |||||||
| chr16:19786814 | AAGGG | A | 130 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(127): Show |
130 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(127): Show |
intron_variant | MODIFIER | c.606-2007_606-2004d others(6): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr16 | 19786814 | ||||||
| chr16:19786815 | A | G | 1 | a0002c0002t0001g0189 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.606-2023A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19786815 | |||||||
| chr16:19786856 | GGAAA | G | 7 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(4): Show |
7 | HG01496.hp1 HG01891.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.606-1969_606-1966d others(6): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr16 | 19786856 | ||||||
| chr16:19786969 | C | G | 9 | a0001c0001t0001g0167 a0001c0001t0001g0171 a0001c0001t0007g0163 others(6): Show |
9 | HG01884.hp1 HG02257.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.606-1869C>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19786969 | |||||||
| chr16:19787410 | C | T | 21 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(18): Show |
21 | HG01109.hp2 HG01884.hp2 HG01934.hp2 others(18): Show |
intron_variant | MODIFIER | c.606-1428C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19787410 | |||||||
| chr16:19787425 | G | A | 1 | a0001c0001t0003g0045 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.606-1413G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19787425 | |||||||
| chr16:19787726 | A | G | 1 | a0001c0001t0001g0106 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.606-1112A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19787726 | |||||||
| chr16:19787819 | T | TA | 58 | a0001c0001t0001g0112 a0001c0001t0001g0137 a0002c0002t0001g0176 others(55): Show |
58 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(55): Show |
intron_variant | MODIFIER | c.606-1005dupA | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr16 | 19787819 | ||||||
| chr16:19787989 | A | C | 1 | a0003c0004t0013g0240 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.606-849A>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19787989 | |||||||
| chr16:19788193 | G | T | 1 | a0001c0001t0016g0089 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.606-645G>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19788193 | |||||||
| chr16:19788489 | C | T | 4 | a0002c0002t0003g0190 a0002c0002t0003g0191 a0002c0002t0003g0196 others(1): Show |
4 | HG01433.hp2 HG02300.hp2 NA20752.hp2 others(1): Show |
intron_variant | MODIFIER | c.606-349C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19788489 | |||||||
| chr16:19788640 | T | A | 239 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(236): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.606-198T>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19788640 | |||||||
| chr16:19788811 | G | A | 107 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(104): Show |
107 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(104): Show |
intron_variant | MODIFIER | c.606-27G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 6/8 | chr16 | 19788811 | |||||||
| chr16:19789221 | C | CA | 35 | a0001c0001t0001g0075 a0001c0001t0001g0131 a0001c0001t0001g0133 others(32): Show |
35 | HG00733.hp2 HG01175.hp1 HG01891.hp1 others(32): Show |
intron_variant | MODIFIER | c.690+311dupA | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19789221 | ||||||
| chr16:19789278 | C | T | 1 | a0001c0001t0001g0070 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.690+356C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19789278 | |||||||
| chr16:19789411 | C | CA | 50 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 others(47): Show |
50 | HG00597.hp1 HG00733.hp1 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.690+514dupA | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19789411 | ||||||
| chr16:19789411 | C | CAAA | 17 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0138 others(14): Show |
17 | HG00733.hp2 HG02280.hp1 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.690+512_690+514dup others(3): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19789411 | ||||||
| chr16:19789411 | C | CAAAA | 11 | a0001c0001t0001g0131 a0001c0001t0001g0137 a0001c0001t0001g0145 others(8): Show |
11 | HG01175.hp1 HG01496.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.690+511_690+514dup others(4): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19789411 | ||||||
| chr16:19789411 | CA | C | 6 | a0001c0001t0001g0083 a0001c0001t0001g0128 a0001c0001t0002g0088 others(3): Show |
6 | HG01081.hp2 HG01167.hp2 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.690+514delA | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19789411 | ||||||
| chr16:19789626 | C | T | 2 | a0001c0001t0019g0238 a0003c0004t0013g0240 |
2 | HG03516.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.690+704C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19789626 | |||||||
| chr16:19789651 | A | G | 71 | a0001c0001t0001g0167 a0001c0001t0001g0171 a0001c0001t0002g0237 others(68): Show |
71 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(68): Show |
intron_variant | MODIFIER | c.690+729A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19789651 | |||||||
| chr16:19789701 | C | T | 8 | a0002c0002t0003g0190 a0002c0002t0003g0191 a0002c0002t0003g0196 others(5): Show |
8 | HG00733.hp1 HG01255.hp1 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.690+779C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19789701 | |||||||
| chr16:19789908 | A | G | 142 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(139): Show |
142 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(139): Show |
intron_variant | MODIFIER | c.690+986A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19789908 | |||||||
| chr16:19790228 | CA | C | 109 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(106): Show |
109 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(106): Show |
intron_variant | MODIFIER | c.690+1319delA | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19790228 | ||||||
| chr16:19790429 | A | G | 2 | a0001c0001t0001g0135 a0001c0001t0003g0136 |
2 | HG02451.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.690+1507A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19790429 | |||||||
| chr16:19790527 | T | C | 142 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(139): Show |
142 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(139): Show |
intron_variant | MODIFIER | c.690+1605T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19790527 | |||||||
| chr16:19790536 | C | T | 3 | a0001c0001t0002g0069 a0001c0001t0002g0085 a0001c0001t0006g0118 |
3 | HG02698.hp2 HG02738.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.690+1614C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19790536 | |||||||
| chr16:19790539 | A | G | 142 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(139): Show |
142 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(139): Show |
intron_variant | MODIFIER | c.690+1617A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19790539 | |||||||
| chr16:19790605 | C | A | 21 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(18): Show |
21 | HG01109.hp2 HG01884.hp2 HG01934.hp2 others(18): Show |
intron_variant | MODIFIER | c.690+1683C>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19790605 | |||||||
| chr16:19790624 | T | TC | 151 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(148): Show |
151 | HG00140.hp2 HG00597.hp2 HG00609.hp1 others(148): Show |
intron_variant | MODIFIER | c.690+1702_690+1703i others(3): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19790624 | |||||||
| chr16:19790692 | G | A | 144 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(141): Show |
144 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(141): Show |
intron_variant | MODIFIER | c.690+1770G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19790692 | |||||||
| chr16:19790727 | T | C | 2 | a0002c0002t0001g0185 a0002c0002t0001g0186 |
2 | HG01081.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.690+1805T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19790727 | |||||||
| chr16:19790781 | G | A | 3 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0003g0120 |
3 | HG02622.hp1 HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.690+1859G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19790781 | |||||||
| chr16:19790801 | G | A | 231 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(228): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.690+1879G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19790801 | |||||||
| chr16:19790832 | AAAC | A | 19 | a0001c0001t0001g0014 a0001c0001t0001g0017 a0001c0001t0001g0018 others(16): Show |
19 | HG01884.hp1 HG02257.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.690+1925_690+1927d others(5): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19790832 | ||||||
| chr16:19790867 | A | G | 2 | a0002c0002t0001g0185 a0002c0002t0001g0186 |
2 | HG01081.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.690+1945A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19790867 | |||||||
| chr16:19791065 | C | A | 3 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0003g0120 |
3 | HG02622.hp1 HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.690+2143C>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19791065 | |||||||
| chr16:19791180 | C | T | 2 | a0002c0002t0003g0197 a0002c0002t0003g0198 |
2 | HG02970.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.690+2258C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19791180 | |||||||
| chr16:19791442 | A | G | 142 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(139): Show |
142 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(139): Show |
intron_variant | MODIFIER | c.690+2520A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19791442 | |||||||
| chr16:19791676 | A | G | 27 | a0001c0001t0001g0131 a0001c0001t0001g0133 a0001c0001t0001g0134 others(24): Show |
27 | HG00733.hp2 HG01175.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.690+2754A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19791676 | |||||||
| chr16:19791877 | G | T | 70 | a0001c0001t0001g0167 a0001c0001t0001g0171 a0001c0001t0002g0237 others(67): Show |
70 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(67): Show |
intron_variant | MODIFIER | c.690+2955G>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19791877 | |||||||
| chr16:19791978 | T | G | 4 | a0001c0001t0002g0069 a0001c0001t0002g0085 a0001c0001t0003g0188 others(1): Show |
4 | HG02698.hp2 HG02738.hp2 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.690+3056T>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19791978 | |||||||
| chr16:19792214 | C | T | 2 | a0002c0002t0001g0185 a0002c0002t0001g0186 |
2 | HG01081.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.690+3292C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19792214 | |||||||
| chr16:19792260 | G | A | 3 | a0001c0001t0002g0237 a0001c0001t0009g0239 a0001c0001t0019g0238 |
3 | HG02451.hp2 HG02895.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.690+3338G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19792260 | |||||||
| chr16:19792351 | G | A | 2 | a0001c0001t0004g0178 a0001c0001t0015g0179 |
2 | HG02615.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.690+3429G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19792351 | |||||||
| chr16:19792435 | T | C | 1 | a0002c0002t0001g0177 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.690+3513T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19792435 | |||||||
| chr16:19792524 | C | T | 141 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(138): Show |
141 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(138): Show |
intron_variant | MODIFIER | c.690+3602C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19792524 | |||||||
| chr16:19792569 | C | CT | 29 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(26): Show |
29 | HG01109.hp2 HG01496.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.690+3666dupT | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19792569 | ||||||
| chr16:19792569 | CT | C | 68 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0167 others(65): Show |
68 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(65): Show |
intron_variant | MODIFIER | c.690+3666delT | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19792569 | ||||||
| chr16:19792675 | G | A | 2 | a0001c0001t0001g0133 a0001c0001t0011g0132 |
2 | HG02630.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.690+3753G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19792675 | |||||||
| chr16:19792681 | C | T | 16 | a0001c0001t0001g0040 a0001c0001t0001g0121 a0001c0001t0001g0122 others(13): Show |
16 | HG02055.hp2 HG02145.hp1 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.690+3759C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19792681 | |||||||
| chr16:19792760 | C | CG | 13 | a0001c0001t0002g0119 a0001c0001t0002g0237 a0001c0001t0005g0033 others(10): Show |
13 | HG01433.hp2 HG02055.hp2 HG02135.hp1 others(10): Show |
intron_variant | MODIFIER | c.690+3840dupG | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19792760 | ||||||
| chr16:19792760 | C | CGG | 7 | a0001c0001t0005g0044 a0001c0001t0007g0163 a0001c0001t0009g0239 others(4): Show |
7 | HG02809.hp2 HG02895.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.690+3839_690+3840d others(4): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19792760 | ||||||
| chr16:19792761 | G | C | 34 | a0001c0001t0001g0131 a0001c0001t0001g0133 a0001c0001t0001g0134 others(31): Show |
34 | HG00733.hp2 HG01175.hp1 HG01496.hp1 others(31): Show |
intron_variant | MODIFIER | c.690+3839G>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19792761 | |||||||
| chr16:19792763 | A | G | 141 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(138): Show |
141 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(138): Show |
intron_variant | MODIFIER | c.690+3841A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19792763 | |||||||
| chr16:19792901 | A | C | 2 | a0001c0001t0001g0104 a0001c0001t0006g0041 |
2 | HG00738.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.690+3979A>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19792901 | |||||||
| chr16:19792909 | G | A | 1 | a0001c0001t0008g0110 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.690+3987G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19792909 | |||||||
| chr16:19792934 | G | A | 141 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(138): Show |
141 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(138): Show |
intron_variant | MODIFIER | c.690+4012G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19792934 | |||||||
| chr16:19793048 | T | C | 70 | a0001c0001t0001g0167 a0001c0001t0001g0171 a0001c0001t0002g0237 others(67): Show |
70 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(67): Show |
intron_variant | MODIFIER | c.690+4126T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19793048 | |||||||
| chr16:19793473 | C | T | 1 | a0001c0001t0004g0028 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.690+4551C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19793473 | |||||||
| chr16:19793643 | G | GT | 45 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0055 others(42): Show |
45 | HG00323.hp1 HG00639.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.690+4751dupT | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19793643 | ||||||
| chr16:19793643 | G | GTT | 26 | a0001c0001t0001g0051 a0001c0001t0001g0053 a0001c0001t0001g0056 others(23): Show |
26 | HG00099.hp1 HG00099.hp2 HG00597.hp1 others(23): Show |
intron_variant | MODIFIER | c.690+4750_690+4751d others(4): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19793643 | ||||||
| chr16:19793643 | G | GTTT | 6 | a0001c0001t0001g0008 a0001c0001t0001g0127 a0001c0001t0001g0244 others(3): Show |
6 | HG00609.hp2 HG00735.hp1 HG00735.hp2 others(3): Show |
intron_variant | MODIFIER | c.690+4749_690+4751d others(5): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19793643 | ||||||
| chr16:19793643 | G | GTTTTTTT others(13): Show |
1 | a0001c0001t0015g0179 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.690+4732_690+4751d others(22): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19793643 | ||||||
| chr16:19793643 | GT | G | 28 | a0001c0001t0001g0121 a0001c0001t0002g0001 a0001c0001t0002g0027 others(25): Show |
28 | HG01255.hp1 HG01884.hp2 HG02145.hp1 others(25): Show |
intron_variant | MODIFIER | c.690+4751delT | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19793643 | ||||||
| chr16:19793643 | GTT | G | 40 | a0001c0001t0001g0030 a0001c0001t0001g0040 a0001c0001t0001g0057 others(37): Show |
40 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(37): Show |
intron_variant | MODIFIER | c.690+4750_690+4751d others(4): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19793643 | ||||||
| chr16:19793643 | GTTT | G | 13 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0002g0237 others(10): Show |
13 | HG01884.hp1 HG02055.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.690+4749_690+4751d others(5): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19793643 | ||||||
| chr16:19793643 | GTTTT | G | 7 | a0001c0001t0001g0014 a0001c0001t0002g0242 a0001c0001t0003g0123 others(4): Show |
7 | HG02258.hp2 HG02622.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.690+4748_690+4751d others(6): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19793643 | ||||||
| chr16:19793643 | GTTTTT | G | 7 | a0001c0001t0001g0013 a0001c0001t0001g0017 a0001c0001t0001g0018 others(4): Show |
7 | HG02280.hp2 HG02559.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.690+4747_690+4751d others(7): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19793643 | ||||||
| chr16:19793643 | GTTTTTTT others(2): Show |
G | 12 | a0002c0002t0001g0181 a0002c0002t0001g0183 a0002c0002t0001g0205 others(9): Show |
12 | HG02074.hp1 HG02135.hp1 HG02155.hp1 others(9): Show |
intron_variant | MODIFIER | c.690+4743_690+4751d others(11): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19793643 | ||||||
| chr16:19793643 | GTTTTTTT others(3): Show |
G | 1 | a0002c0002t0001g0202 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.690+4742_690+4751d others(12): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19793643 | ||||||
| chr16:19793652 | T | TTG | 6 | a0001c0001t0001g0138 a0001c0001t0001g0141 a0001c0001t0001g0148 others(3): Show |
6 | HG00733.hp2 HG01175.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.690+4731_690+4732i others(4): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19793652 | ||||||
| chr16:19793655 | T | G | 1 | a0003c0004t0013g0240 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.690+4733T>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19793655 | |||||||
| chr16:19793656 | T | A | 1 | a0002c0002t0001g0214 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.690+4734T>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19793656 | |||||||
| chr16:19793656 | T | G | 6 | a0001c0001t0001g0138 a0001c0001t0001g0141 a0001c0001t0001g0148 others(3): Show |
6 | HG00733.hp2 HG01175.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.690+4734T>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19793656 | |||||||
| chr16:19793656 | T | TTG | 27 | a0001c0001t0001g0131 a0001c0001t0001g0133 a0001c0001t0001g0134 others(24): Show |
27 | HG01496.hp1 HG01891.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.690+4735_690+4736i others(4): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19793656 | ||||||
| chr16:19793660 | T | A | 1 | a0002c0002t0001g0214 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.690+4738T>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19793660 | |||||||
| chr16:19793660 | T | G | 27 | a0001c0001t0001g0131 a0001c0001t0001g0133 a0001c0001t0001g0134 others(24): Show |
27 | HG00733.hp2 HG01175.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.690+4738T>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19793660 | |||||||
| chr16:19793663 | T | G | 6 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(3): Show |
6 | HG01496.hp1 HG01891.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.690+4741T>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19793663 | |||||||
| chr16:19793664 | T | G | 27 | a0001c0001t0001g0131 a0001c0001t0001g0133 a0001c0001t0001g0134 others(24): Show |
27 | HG00733.hp2 HG01175.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.690+4742T>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19793664 | |||||||
| chr16:19793927 | G | C | 16 | a0001c0001t0001g0040 a0001c0001t0001g0121 a0001c0001t0001g0122 others(13): Show |
16 | HG02055.hp2 HG02145.hp1 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.690+5005G>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19793927 | |||||||
| chr16:19794064 | AAATG | A | 70 | a0001c0001t0001g0167 a0001c0001t0001g0171 a0001c0001t0002g0237 others(67): Show |
70 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(67): Show |
intron_variant | MODIFIER | c.690+5145_690+5148d others(6): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19794064 | ||||||
| chr16:19794114 | A | G | 4 | a0001c0001t0001g0125 a0001c0001t0002g0042 a0001c0001t0002g0059 others(1): Show |
4 | HG01074.hp2 HG01167.hp1 HG01928.hp1 others(1): Show |
intron_variant | MODIFIER | c.690+5192A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19794114 | |||||||
| chr16:19794294 | T | C | 4 | a0001c0001t0002g0119 a0001c0001t0002g0241 a0001c0001t0002g0242 others(1): Show |
4 | HG02622.hp2 HG02647.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.690+5372T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19794294 | |||||||
| chr16:19794720 | A | G | 1 | a0001c0001t0001g0072 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.690+5798A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19794720 | |||||||
| chr16:19794842 | G | A | 70 | a0001c0001t0001g0167 a0001c0001t0001g0171 a0001c0001t0002g0237 others(67): Show |
70 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(67): Show |
intron_variant | MODIFIER | c.690+5920G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19794842 | |||||||
| chr16:19794930 | A | G | 141 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(138): Show |
141 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(138): Show |
intron_variant | MODIFIER | c.690+6008A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19794930 | |||||||
| chr16:19795030 | A | G | 1 | a0002c0002t0001g0193 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.690+6108A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19795030 | |||||||
| chr16:19795036 | A | G | 1 | a0001c0001t0005g0038 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.690+6114A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19795036 | |||||||
| chr16:19795196 | C | T | 1 | a0001c0001t0002g0035 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.690+6274C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19795196 | |||||||
| chr16:19795202 | C | CA | 6 | a0001c0001t0001g0055 a0001c0001t0001g0244 a0001c0001t0002g0081 others(3): Show |
6 | HG00735.hp1 HG00735.hp2 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.690+6294dupA | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19795202 | ||||||
| chr16:19795251 | A | T | 1 | a0002c0002t0001g0214 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.690+6329A>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19795251 | |||||||
| chr16:19795312 | G | A | 3 | a0001c0001t0002g0237 a0001c0001t0009g0239 a0001c0001t0019g0238 |
3 | HG02451.hp2 HG02895.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.690+6390G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19795312 | |||||||
| chr16:19795402 | T | A | 1 | a0003c0004t0013g0240 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.690+6480T>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19795402 | |||||||
| chr16:19795440 | C | T | 1 | a0003c0004t0013g0240 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.690+6518C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19795440 | |||||||
| chr16:19795477 | A | G | 1 | a0001c0001t0002g0004 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.690+6555A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19795477 | |||||||
| chr16:19795599 | C | T | 13 | a0001c0001t0001g0030 a0001c0001t0001g0075 a0001c0001t0002g0001 others(10): Show |
13 | HG01109.hp2 HG01884.hp2 HG01934.hp2 others(10): Show |
intron_variant | MODIFIER | c.690+6677C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19795599 | |||||||
| chr16:19795684 | C | T | 2 | a0001c0001t0002g0001 a0001c0001t0002g0029 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.690+6762C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19795684 | |||||||
| chr16:19795696 | C | T | 1 | a0001c0001t0002g0034 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.690+6774C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19795696 | |||||||
| chr16:19795697 | G | A | 2 | a0001c0001t0009g0239 a0001c0001t0019g0238 |
2 | HG02895.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.690+6775G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19795697 | |||||||
| chr16:19795824 | G | GT | 10 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0018 others(7): Show |
10 | HG01255.hp2 HG01261.hp2 HG01934.hp1 others(7): Show |
intron_variant | MODIFIER | c.690+6915dupT | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19795824 | ||||||
| chr16:19796018 | C | A | 3 | a0001c0001t0007g0166 a0001c0001t0007g0168 a0001c0001t0007g0169 |
3 | HG01884.hp1 HG02257.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.690+7096C>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19796018 | |||||||
| chr16:19796087 | T | C | 1 | a0001c0001t0001g0125 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.690+7165T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19796087 | |||||||
| chr16:19796436 | AG | A | 16 | a0001c0001t0001g0040 a0001c0001t0001g0121 a0001c0001t0001g0122 others(13): Show |
16 | HG02055.hp2 HG02145.hp1 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.690+7515delG | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19796436 | |||||||
| chr16:19796439 | A | T | 1 | a0003c0004t0013g0240 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.690+7517A>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19796439 | |||||||
| chr16:19796445 | A | G | 141 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(138): Show |
141 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(138): Show |
intron_variant | MODIFIER | c.690+7523A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19796445 | |||||||
| chr16:19796458 | T | C | 1 | a0001c0001t0001g0116 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.690+7536T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19796458 | |||||||
| chr16:19796470 | G | A | 1 | a0001c0001t0002g0107 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.690+7548G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19796470 | |||||||
| chr16:19796841 | T | C | 143 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(140): Show |
143 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(140): Show |
intron_variant | MODIFIER | c.690+7919T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19796841 | |||||||
| chr16:19797032 | C | T | 46 | a0002c0002t0001g0176 a0002c0002t0001g0177 a0002c0002t0001g0181 others(43): Show |
46 | HG00597.hp2 HG00609.hp1 HG01081.hp1 others(43): Show |
intron_variant | MODIFIER | c.690+8110C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19797032 | |||||||
| chr16:19797051 | C | G | 6 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(3): Show |
6 | HG01496.hp1 HG01891.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.690+8129C>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19797051 | |||||||
| chr16:19797242 | A | G | 1 | a0002c0002t0003g0192 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.690+8320A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19797242 | |||||||
| chr16:19797277 | T | C | 3 | a0002c0002t0001g0177 a0002c0002t0001g0204 a0002c0002t0001g0213 |
3 | HG00597.hp2 HG02083.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.690+8355T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19797277 | |||||||
| chr16:19797287 | G | A | 141 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(138): Show |
141 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(138): Show |
intron_variant | MODIFIER | c.690+8365G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19797287 | |||||||
| chr16:19797398 | G | A | 1 | a0001c0001t0002g0108 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.690+8476G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19797398 | |||||||
| chr16:19797496 | A | G | 7 | a0001c0001t0001g0040 a0001c0001t0005g0033 a0001c0001t0005g0037 others(4): Show |
7 | HG02055.hp2 HG02145.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.690+8574A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19797496 | |||||||
| chr16:19797613 | C | CA | 35 | a0001c0001t0001g0070 a0001c0001t0001g0125 a0001c0001t0001g0127 others(32): Show |
35 | HG00733.hp1 HG00733.hp2 HG01175.hp1 others(32): Show |
intron_variant | MODIFIER | c.690+8707dupA | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19797613 | ||||||
| chr16:19797613 | CA | C | 29 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(26): Show |
29 | HG00140.hp2 HG00738.hp2 HG01358.hp1 others(26): Show |
intron_variant | MODIFIER | c.690+8707delA | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19797613 | ||||||
| chr16:19797613 | CAA | C | 5 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0003g0120 others(2): Show |
5 | HG02258.hp2 HG02559.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.690+8706_690+8707d others(4): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19797613 | ||||||
| chr16:19797623 | A | C | 2 | a0001c0001t0002g0069 a0001c0001t0002g0085 |
2 | HG02738.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.690+8701A>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19797623 | |||||||
| chr16:19797627 | A | C | 6 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(3): Show |
6 | HG01496.hp1 HG01891.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.690+8705A>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19797627 | |||||||
| chr16:19797628 | AAC | A | 18 | a0002c0002t0001g0182 a0002c0002t0001g0201 a0002c0002t0001g0205 others(15): Show |
18 | HG00609.hp1 HG01261.hp2 HG02015.hp1 others(15): Show |
intron_variant | MODIFIER | c.690+8708_690+8709d others(4): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19797628 | ||||||
| chr16:19797629 | AC | A | 26 | a0001c0001t0004g0023 a0001c0001t0004g0024 a0001c0001t0004g0025 others(23): Show |
26 | HG00597.hp2 HG01081.hp1 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.690+8708delC | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19797629 | |||||||
| chr16:19797630 | C | A | 40 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(37): Show |
40 | HG00733.hp1 HG01109.hp2 HG01255.hp1 others(37): Show |
intron_variant | MODIFIER | c.690+8708C>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19797630 | |||||||
| chr16:19797730 | C | A | 3 | a0002c0002t0001g0219 a0002c0002t0001g0220 a0002c0002t0002g0218 |
3 | HG02074.hp1 NA18983.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.690+8808C>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19797730 | |||||||
| chr16:19798285 | G | A | 20 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(17): Show |
20 | HG01109.hp2 HG01884.hp2 HG01934.hp2 others(17): Show |
intron_variant | MODIFIER | c.690+9363G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19798285 | |||||||
| chr16:19798291 | G | A | 2 | a0001c0001t0002g0009 a0001c0001t0002g0113 |
2 | HG01975.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.690+9369G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19798291 | |||||||
| chr16:19798373 | A | G | 141 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(138): Show |
141 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(138): Show |
intron_variant | MODIFIER | c.690+9451A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19798373 | |||||||
| chr16:19798416 | C | CAAAAAAA others(3): Show |
4 | a0001c0001t0002g0119 a0001c0001t0002g0241 a0001c0001t0002g0242 others(1): Show |
4 | HG02622.hp2 HG02647.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.690+9500_690+9501i others(12): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19798416 | ||||||
| chr16:19798421 | A | AAAAAAAA others(28): Show |
1 | a0001c0001t0003g0045 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.690+9500_690+9501i others(37): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19798421 | ||||||
| chr16:19798421 | A | AAAAAAAA others(35): Show |
1 | a0001c0001t0005g0039 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.690+9500_690+9501i others(44): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19798421 | ||||||
| chr16:19798421 | A | AAAAAAAA others(37): Show |
1 | a0001c0001t0001g0040 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.690+9500_690+9501i others(46): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19798421 | ||||||
| chr16:19798421 | A | AAAAAAAA others(26): Show |
1 | a0001c0001t0003g0123 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.690+9500_690+9501i others(35): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19798421 | ||||||
| chr16:19798421 | A | AAAAAAAA others(37): Show |
1 | a0001c0001t0005g0038 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.690+9500_690+9501i others(46): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19798421 | ||||||
| chr16:19798421 | A | AAAAAAAA others(40): Show |
1 | a0001c0001t0005g0037 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.690+9500_690+9501i others(49): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19798421 | ||||||
| chr16:19798421 | A | AAAAAAAA others(43): Show |
1 | a0003c0004t0013g0240 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.690+9500_690+9501i others(52): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19798421 | ||||||
| chr16:19798421 | A | AAAAAAAA others(9): Show |
1 | a0001c0001t0001g0150 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.690+9500_690+9501i others(18): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19798421 | ||||||
| chr16:19798421 | A | AAAAAAAA others(31): Show |
1 | a0001c0001t0005g0043 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.690+9500_690+9501i others(40): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19798421 | ||||||
| chr16:19798421 | A | AAAAAAAA others(41): Show |
1 | a0001c0001t0005g0033 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.690+9500_690+9501i others(50): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19798421 | ||||||
| chr16:19798421 | A | AAAAAAAA others(8): Show |
2 | a0001c0001t0001g0137 a0001c0001t0001g0145 |
2 | HG02559.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.690+9500_690+9501i others(17): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19798421 | ||||||
| chr16:19798421 | A | AAAAAAAA others(30): Show |
1 | a0001c0001t0005g0044 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.690+9500_690+9501i others(39): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19798421 | ||||||
| chr16:19798421 | A | AAAAAAAA others(9): Show |
2 | a0001c0001t0001g0133 a0001c0001t0011g0132 |
2 | HG02630.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.690+9500_690+9501i others(18): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19798421 | ||||||
| chr16:19798421 | A | AAAAAAAA others(6): Show |
1 | a0001c0001t0001g0151 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.690+9500_690+9501i others(15): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19798421 | ||||||
| chr16:19798421 | A | AAAAAAAA others(8): Show |
7 | a0001c0001t0001g0131 a0001c0001t0001g0142 a0001c0001t0001g0146 others(4): Show |
7 | HG01175.hp1 HG02145.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.690+9500_690+9501i others(17): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19798421 | ||||||
| chr16:19798421 | A | AAAAAAAA others(14): Show |
1 | a0001c0001t0001g0162 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.690+9500_690+9501i others(23): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19798421 | ||||||
| chr16:19798421 | A | AAAAAAAA others(8): Show |
8 | a0001c0001t0001g0135 a0001c0001t0001g0140 a0001c0001t0001g0143 others(5): Show |
8 | HG01891.hp2 HG02451.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.690+9500_690+9501i others(17): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19798421 | ||||||
| chr16:19798421 | A | AAAAAAAA others(12): Show |
1 | a0001c0001t0001g0139 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.690+9500_690+9501i others(21): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19798421 | ||||||
| chr16:19798421 | A | AAAAAAAA others(14): Show |
1 | a0001c0001t0001g0138 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.690+9500_690+9501i others(23): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19798421 | ||||||
| chr16:19798421 | A | AAAAAAAA others(16): Show |
1 | a0001c0001t0001g0141 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.690+9500_690+9501i others(25): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19798421 | ||||||
| chr16:19798421 | A | AAAAAAAA others(9): Show |
1 | a0001c0001t0001g0134 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.690+9500_690+9501i others(18): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19798421 | ||||||
| chr16:19798421 | A | AAAAAAAA others(11): Show |
1 | a0001c0001t0010g0147 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.690+9500_690+9501i others(20): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19798421 | ||||||
| chr16:19798421 | A | AAAAAAAA others(25): Show |
1 | a0001c0001t0001g0161 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.690+9500_690+9501i others(34): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19798421 | ||||||
| chr16:19798421 | A | AAAAAAT | 8 | a0001c0001t0002g0027 a0001c0001t0004g0012 a0001c0001t0004g0022 others(5): Show |
8 | HG01109.hp2 HG01884.hp2 HG01934.hp2 others(5): Show |
intron_variant | MODIFIER | c.690+9500_690+9501i others(8): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19798421 | ||||||
| chr16:19798421 | A | AAAAAATA others(1): Show |
5 | a0001c0001t0001g0014 a0001c0001t0001g0030 a0001c0001t0002g0001 others(2): Show |
5 | HG02895.hp1 HG02897.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.690+9500_690+9501i others(10): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19798421 | ||||||
| chr16:19798421 | A | AAAAAATA others(3): Show |
4 | a0001c0001t0001g0013 a0001c0001t0001g0018 a0001c0001t0003g0015 others(1): Show |
4 | HG02280.hp2 HG02615.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.690+9500_690+9501i others(12): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19798421 | ||||||
| chr16:19798421 | A | AAAAAATA others(23): Show |
1 | a0001c0001t0001g0157 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.690+9500_690+9501i others(32): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19798421 | ||||||
| chr16:19798421 | A | AAAAAATA others(25): Show |
2 | a0001c0001t0001g0158 a0001c0001t0001g0159 |
2 | HG01891.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.690+9500_690+9501i others(34): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19798421 | ||||||
| chr16:19798421 | A | AAAAAATA others(27): Show |
1 | a0001c0001t0001g0156 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.690+9500_690+9501i others(36): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19798421 | ||||||
| chr16:19798421 | A | AAAAAATA others(35): Show |
1 | a0001c0003t0003g0021 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.690+9500_690+9501i others(44): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19798421 | ||||||
| chr16:19798421 | A | AAAATATA others(3): Show |
2 | a0001c0001t0005g0019 a0001c0001t0005g0020 |
2 | HG02258.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.690+9500_690+9501i others(12): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19798421 | ||||||
| chr16:19798421 | A | AAT | 4 | a0001c0001t0001g0008 a0001c0001t0001g0115 a0001c0001t0001g0127 others(1): Show |
4 | HG00609.hp2 HG01346.hp1 NA19067.hp2 others(1): Show |
intron_variant | MODIFIER | c.690+9522_690+9523d others(4): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19798421 | ||||||
| chr16:19798421 | A | T | 2 | a0001c0001t0001g0090 a0001c0001t0001g0112 |
2 | NA18967.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.690+9499A>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19798421 | |||||||
| chr16:19798421 | AAT | A | 12 | a0001c0001t0001g0167 a0001c0001t0001g0171 a0001c0001t0002g0237 others(9): Show |
12 | HG01884.hp1 HG02257.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.690+9522_690+9523d others(4): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19798421 | ||||||
| chr16:19798422 | AT | A | 46 | a0002c0002t0001g0176 a0002c0002t0001g0181 a0002c0002t0001g0182 others(43): Show |
46 | HG00609.hp1 HG01081.hp1 HG01261.hp2 others(43): Show |
intron_variant | MODIFIER | c.690+9501delT | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19798422 | |||||||
| chr16:19798423 | T | A | 19 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0002g0119 others(16): Show |
19 | HG00597.hp2 HG00733.hp1 HG01255.hp1 others(16): Show |
intron_variant | MODIFIER | c.690+9501T>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19798423 | |||||||
| chr16:19798425 | T | A | 62 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0167 others(59): Show |
62 | HG00609.hp1 HG01081.hp1 HG01261.hp2 others(59): Show |
intron_variant | MODIFIER | c.690+9503T>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19798425 | |||||||
| chr16:19798427 | T | A | 18 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0167 others(15): Show |
18 | HG01884.hp1 HG02257.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.690+9505T>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19798427 | |||||||
| chr16:19798429 | T | A | 3 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0003g0120 |
3 | HG02622.hp1 HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.690+9507T>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19798429 | |||||||
| chr16:19798431 | T | A | 4 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0003g0120 others(1): Show |
4 | HG02622.hp1 HG03098.hp2 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.690+9509T>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19798431 | |||||||
| chr16:19798433 | T | A | 3 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0003g0120 |
3 | HG02622.hp1 HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.690+9511T>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19798433 | |||||||
| chr16:19798435 | T | A | 3 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0003g0120 |
3 | HG02622.hp1 HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.690+9513T>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19798435 | |||||||
| chr16:19798437 | T | A | 2 | a0001c0001t0001g0122 a0001c0001t0003g0120 |
2 | HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.690+9515T>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19798437 | |||||||
| chr16:19798627 | G | T | 19 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(16): Show |
19 | HG01109.hp2 HG01884.hp2 HG01934.hp2 others(16): Show |
intron_variant | MODIFIER | c.690+9705G>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19798627 | |||||||
| chr16:19798676 | C | T | 1 | a0001c0001t0002g0079 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.690+9754C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19798676 | |||||||
| chr16:19798887 | A | G | 1 | a0003c0004t0013g0240 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.690+9965A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19798887 | |||||||
| chr16:19798916 | TA | T | 6 | a0001c0001t0001g0003 a0001c0001t0001g0162 a0001c0001t0005g0044 others(3): Show |
6 | HG02897.hp2 HG02976.hp1 NA18946.hp1 others(3): Show |
intron_variant | MODIFIER | c.690+10006delA | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19798916 | ||||||
| chr16:19799028 | C | T | 1 | a0001c0001t0006g0076 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.690+10106C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19799028 | |||||||
| chr16:19799163 | G | GCCTA | 134 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(131): Show |
134 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(131): Show |
intron_variant | MODIFIER | c.690+10243_690+1024 others(8): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19799163 | ||||||
| chr16:19799245 | C | A | 16 | a0001c0001t0001g0040 a0001c0001t0001g0121 a0001c0001t0001g0122 others(13): Show |
16 | HG02055.hp2 HG02145.hp1 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.690+10323C>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19799245 | |||||||
| chr16:19799262 | A | T | 63 | a0001c0001t0001g0051 a0001c0001t0001g0126 a0001c0001t0002g0009 others(60): Show |
63 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(60): Show |
intron_variant | MODIFIER | c.690+10340A>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19799262 | |||||||
| chr16:19799264 | T | A | 11 | a0001c0001t0001g0040 a0001c0001t0001g0156 a0001c0001t0001g0157 others(8): Show |
11 | HG01496.hp1 HG01891.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.690+10342T>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19799264 | |||||||
| chr16:19799266 | T | A | 7 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(4): Show |
7 | HG01496.hp1 HG01891.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.690+10344T>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19799266 | |||||||
| chr16:19799268 | T | A | 1 | a0001c0001t0001g0157 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.690+10346T>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19799268 | |||||||
| chr16:19799271 | A | T | 6 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(3): Show |
6 | HG01496.hp1 HG01891.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.690+10349A>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19799271 | |||||||
| chr16:19799278 | A | T | 7 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(4): Show |
7 | HG01496.hp1 HG01891.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.690+10356A>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19799278 | |||||||
| chr16:19799358 | G | A | 2 | a0001c0001t0003g0045 a0001c0001t0003g0123 |
2 | HG03225.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.690+10436G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19799358 | |||||||
| chr16:19799490 | C | T | 4 | a0002c0002t0001g0210 a0002c0002t0001g0215 a0002c0002t0001g0236 others(1): Show |
4 | NA18943.hp2 NA18944.hp1 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.690+10568C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19799490 | |||||||
| chr16:19799582 | T | TTA | 6 | a0001c0001t0001g0171 a0001c0001t0002g0035 a0001c0001t0002g0047 others(3): Show |
6 | HG00140.hp2 HG00738.hp2 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.690+10675_690+1067 others(6): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19799582 | ||||||
| chr16:19799582 | TTA | T | 18 | a0001c0001t0001g0051 a0001c0001t0001g0055 a0001c0001t0001g0056 others(15): Show |
18 | HG00597.hp1 HG01081.hp2 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.690+10675_690+1067 others(6): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19799582 | ||||||
| chr16:19799593 | TATATACA others(7): Show |
T | 1 | a0001c0001t0001g0134 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.690+10673_690+1068 others(18): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19799593 | ||||||
| chr16:19799593 | TATATACA others(11): Show |
T | 1 | a0001c0001t0001g0161 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.690+10673_690+1069 others(22): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19799593 | ||||||
| chr16:19799593 | TATATACA others(13): Show |
T | 5 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(2): Show |
5 | HG01496.hp1 HG01891.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.690+10673_690+1069 others(24): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19799593 | ||||||
| chr16:19799595 | TATAC | T | 15 | a0001c0001t0005g0037 a0002c0002t0001g0193 a0002c0002t0001g0227 others(12): Show |
15 | HG00733.hp1 HG01255.hp1 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.690+10675_690+1067 others(8): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19799595 | ||||||
| chr16:19799595 | TATACACA others(3): Show |
T | 1 | a0001c0001t0002g0237 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.690+10675_690+1068 others(14): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19799595 | ||||||
| chr16:19799595 | TATACACA others(5): Show |
T | 1 | a0001c0001t0001g0175 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.690+10675_690+1068 others(16): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19799595 | ||||||
| chr16:19799595 | TATACACA others(7): Show |
T | 25 | a0001c0001t0001g0131 a0001c0001t0001g0133 a0001c0001t0001g0135 others(22): Show |
25 | HG00733.hp2 HG01175.hp1 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.690+10675_690+1068 others(18): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19799595 | ||||||
| chr16:19799597 | T | C | 9 | a0001c0001t0001g0017 a0001c0001t0001g0057 a0001c0001t0001g0072 others(6): Show |
9 | HG01167.hp1 HG01167.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.690+10675T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19799597 | |||||||
| chr16:19799597 | T | TAC | 3 | a0001c0001t0001g0075 a0001c0001t0002g0034 a0001c0001t0002g0036 |
3 | HG02523.hp2 HG03239.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.690+10718_690+1071 others(6): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19799597 | ||||||
| chr16:19799597 | TAC | T | 63 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0030 others(60): Show |
63 | HG00140.hp1 HG00323.hp1 HG00735.hp1 others(60): Show |
intron_variant | MODIFIER | c.690+10718_690+1071 others(6): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19799597 | ||||||
| chr16:19799597 | TACAC | T | 44 | a0001c0001t0001g0040 a0001c0001t0001g0125 a0001c0001t0002g0006 others(41): Show |
44 | HG00597.hp2 HG00609.hp1 HG01081.hp1 others(41): Show |
intron_variant | MODIFIER | c.690+10716_690+1071 others(8): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19799597 | ||||||
| chr16:19799597 | TACACAC | T | 6 | a0001c0001t0002g0130 a0001c0001t0003g0120 a0001c0001t0009g0239 others(3): Show |
6 | HG00323.hp2 HG01261.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.690+10714_690+1071 others(10): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19799597 | ||||||
| chr16:19799597 | TACACACA others(1): Show |
T | 4 | a0001c0001t0007g0166 a0001c0001t0007g0168 a0001c0001t0007g0169 others(1): Show |
4 | HG01884.hp1 HG02257.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.690+10712_690+1071 others(12): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19799597 | ||||||
| chr16:19799597 | TACACACA others(3): Show |
T | 2 | a0001c0001t0001g0121 a0001c0001t0001g0122 |
2 | HG02622.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.690+10710_690+1071 others(14): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19799597 | ||||||
| chr16:19799597 | TACACACA others(5): Show |
T | 1 | a0001c0001t0001g0105 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.690+10708_690+1071 others(16): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19799597 | ||||||
| chr16:19799597 | TACACACA others(13): Show |
T | 1 | a0001c0001t0005g0039 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.690+10700_690+1071 others(24): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19799597 | ||||||
| chr16:19799597 | TACACACA others(21): Show |
T | 3 | a0001c0001t0005g0033 a0001c0001t0005g0043 a0001c0001t0005g0044 |
3 | HG02055.hp2 HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.690+10692_690+1071 others(32): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19799597 | ||||||
| chr16:19799599 | C | T | 10 | a0001c0001t0001g0092 a0001c0001t0001g0097 a0001c0001t0001g0116 others(7): Show |
10 | HG00099.hp1 HG00099.hp2 HG00639.hp1 others(7): Show |
intron_variant | MODIFIER | c.690+10677C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19799599 | |||||||
| chr16:19799601 | C | T | 6 | a0001c0001t0001g0064 a0001c0001t0001g0129 a0001c0001t0002g0241 others(3): Show |
6 | HG02523.hp1 HG02818.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.690+10679C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19799601 | |||||||
| chr16:19799603 | C | T | 1 | a0001c0001t0003g0045 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.690+10681C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19799603 | |||||||
| chr16:19799640 | A | ACC | 4 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(1): Show |
4 | HG02615.hp2 HG02630.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.690+10720_690+1072 others(6): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19799640 | ||||||
| chr16:19799640 | A | C | 13 | a0001c0001t0001g0030 a0001c0001t0002g0001 a0001c0001t0002g0027 others(10): Show |
13 | HG01109.hp2 HG01884.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.690+10718A>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19799640 | |||||||
| chr16:19799673 | T | C | 1 | a0001c0001t0001g0105 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.690+10751T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19799673 | |||||||
| chr16:19800128 | G | A | 16 | a0001c0001t0001g0040 a0001c0001t0001g0121 a0001c0001t0001g0122 others(13): Show |
16 | HG02055.hp2 HG02145.hp1 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.690+11206G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19800128 | |||||||
| chr16:19800375 | G | A | 21 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(18): Show |
21 | HG01109.hp2 HG01884.hp2 HG01934.hp2 others(18): Show |
intron_variant | MODIFIER | c.690+11453G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19800375 | |||||||
| chr16:19800449 | C | T | 2 | a0001c0001t0004g0178 a0001c0001t0015g0179 |
2 | HG02615.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.690+11527C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19800449 | |||||||
| chr16:19800560 | CAAT | C | 16 | a0001c0001t0001g0040 a0001c0001t0001g0121 a0001c0001t0001g0122 others(13): Show |
16 | HG02055.hp2 HG02145.hp1 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.690+11648_690+1165 others(7): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19800560 | ||||||
| chr16:19800589 | G | A | 1 | a0001c0001t0001g0011 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.690+11667G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19800589 | |||||||
| chr16:19800883 | C | CTTTA | 141 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(138): Show |
141 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(138): Show |
intron_variant | MODIFIER | c.690+11962_690+1196 others(8): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19800883 | ||||||
| chr16:19801092 | C | T | 1 | a0001c0003t0003g0021 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.690+12170C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19801092 | |||||||
| chr16:19801093 | A | G | 27 | a0001c0001t0001g0131 a0001c0001t0001g0133 a0001c0001t0001g0134 others(24): Show |
27 | HG00733.hp2 HG01175.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.690+12171A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19801093 | |||||||
| chr16:19801284 | TTC | T | 57 | a0001c0001t0001g0040 a0001c0001t0001g0167 a0001c0001t0001g0171 others(54): Show |
57 | HG00597.hp2 HG00609.hp1 HG01081.hp1 others(54): Show |
intron_variant | MODIFIER | c.690+12380_690+1238 others(6): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19801284 | ||||||
| chr16:19801284 | TTCTC | T | 5 | a0001c0001t0002g0029 a0001c0001t0002g0069 a0001c0001t0002g0085 others(2): Show |
5 | HG02615.hp1 HG02738.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.690+12378_690+1238 others(8): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19801284 | ||||||
| chr16:19801299 | TC | T | 14 | a0002c0002t0001g0193 a0002c0002t0001g0220 a0002c0002t0001g0228 others(11): Show |
14 | HG00733.hp1 HG01255.hp1 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.690+12378delC | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19801299 | |||||||
| chr16:19801299 | TCTC | T | 34 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(31): Show |
34 | HG01109.hp2 HG01884.hp2 HG01934.hp2 others(31): Show |
intron_variant | MODIFIER | c.690+12378_690+1238 others(7): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19801299 | |||||||
| chr16:19801302 | C | CT | 38 | a0001c0001t0001g0067 a0001c0001t0001g0131 a0001c0001t0001g0133 others(35): Show |
38 | HG00733.hp2 HG01175.hp1 HG01891.hp1 others(35): Show |
intron_variant | MODIFIER | c.690+12396dupT | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19801302 | ||||||
| chr16:19801302 | C | T | 71 | a0001c0001t0001g0040 a0001c0001t0001g0167 a0001c0001t0001g0171 others(68): Show |
71 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(68): Show |
intron_variant | MODIFIER | c.690+12380C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19801302 | |||||||
| chr16:19801563 | C | T | 108 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(105): Show |
108 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(105): Show |
intron_variant | MODIFIER | c.690+12641C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19801563 | |||||||
| chr16:19801567 | T | C | 27 | a0001c0001t0001g0131 a0001c0001t0001g0133 a0001c0001t0001g0134 others(24): Show |
27 | HG00733.hp2 HG01175.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.690+12645T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19801567 | |||||||
| chr16:19801833 | A | T | 9 | a0001c0001t0001g0167 a0001c0001t0001g0171 a0001c0001t0007g0163 others(6): Show |
9 | HG01884.hp1 HG02257.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.690+12911A>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19801833 | |||||||
| chr16:19801875 | A | G | 1 | a0001c0001t0001g0157 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.690+12953A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19801875 | |||||||
| chr16:19801918 | G | A | 1 | a0002c0002t0001g0193 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.690+12996G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19801918 | |||||||
| chr16:19801930 | C | T | 33 | a0001c0001t0001g0131 a0001c0001t0001g0133 a0001c0001t0001g0134 others(30): Show |
33 | HG00733.hp2 HG01175.hp1 HG01496.hp1 others(30): Show |
intron_variant | MODIFIER | c.690+13008C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19801930 | |||||||
| chr16:19802183 | A | T | 1 | a0001c0001t0001g0077 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.690+13261A>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19802183 | |||||||
| chr16:19802283 | T | C | 70 | a0001c0001t0001g0167 a0001c0001t0001g0171 a0001c0001t0002g0237 others(67): Show |
70 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(67): Show |
intron_variant | MODIFIER | c.690+13361T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19802283 | |||||||
| chr16:19802319 | G | A | 1 | a0001c0001t0001g0171 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.690+13397G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19802319 | |||||||
| chr16:19802361 | G | C | 7 | a0001c0001t0001g0040 a0001c0001t0005g0033 a0001c0001t0005g0037 others(4): Show |
7 | HG02055.hp2 HG02145.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.690+13439G>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19802361 | |||||||
| chr16:19802409 | C | A | 3 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0003g0120 |
3 | HG02622.hp1 HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.690+13487C>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19802409 | |||||||
| chr16:19802735 | A | G | 1 | a0001c0001t0002g0050 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.690+13813A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19802735 | |||||||
| chr16:19802737 | A | G | 33 | a0001c0001t0001g0131 a0001c0001t0001g0133 a0001c0001t0001g0134 others(30): Show |
33 | HG00733.hp2 HG01175.hp1 HG01496.hp1 others(30): Show |
intron_variant | MODIFIER | c.690+13815A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19802737 | |||||||
| chr16:19802761 | C | G | 1 | a0001c0001t0007g0170 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.690+13839C>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19802761 | |||||||
| chr16:19802943 | G | A | 16 | a0001c0001t0001g0040 a0001c0001t0001g0121 a0001c0001t0001g0122 others(13): Show |
16 | HG02055.hp2 HG02145.hp1 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.690+14021G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19802943 | |||||||
| chr16:19803148 | T | G | 2 | a0002c0002t0003g0199 a0002c0002t0003g0235 |
2 | HG00733.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.690+14226T>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19803148 | |||||||
| chr16:19803150 | T | G | 1 | a0001c0003t0003g0021 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.690+14228T>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19803150 | |||||||
| chr16:19803232 | T | G | 21 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(18): Show |
21 | HG01109.hp2 HG01884.hp2 HG01934.hp2 others(18): Show |
intron_variant | MODIFIER | c.690+14310T>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19803232 | |||||||
| chr16:19803291 | C | T | 1 | a0001c0001t0003g0045 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.690+14369C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19803291 | |||||||
| chr16:19803422 | T | C | 141 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(138): Show |
141 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(138): Show |
intron_variant | MODIFIER | c.690+14500T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19803422 | |||||||
| chr16:19803655 | T | C | 1 | a0001c0001t0001g0175 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.690+14733T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19803655 | |||||||
| chr16:19803746 | G | C | 1 | a0001c0001t0001g0152 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.690+14824G>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19803746 | |||||||
| chr16:19803810 | A | G | 3 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0003g0120 |
3 | HG02622.hp1 HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.690+14888A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19803810 | |||||||
| chr16:19803867 | C | T | 10 | a0001c0001t0002g0001 a0001c0001t0002g0027 a0001c0001t0002g0029 others(7): Show |
10 | HG01109.hp2 HG01884.hp2 HG01934.hp2 others(7): Show |
intron_variant | MODIFIER | c.690+14945C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19803867 | |||||||
| chr16:19803906 | C | T | 108 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(105): Show |
108 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(105): Show |
intron_variant | MODIFIER | c.690+14984C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19803906 | |||||||
| chr16:19804078 | C | T | 1 | a0001c0001t0002g0088 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.690+15156C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19804078 | |||||||
| chr16:19804084 | C | G | 16 | a0001c0001t0001g0040 a0001c0001t0001g0121 a0001c0001t0001g0122 others(13): Show |
16 | HG02055.hp2 HG02145.hp1 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.690+15162C>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19804084 | |||||||
| chr16:19804089 | G | A | 108 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(105): Show |
108 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(105): Show |
intron_variant | MODIFIER | c.690+15167G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19804089 | |||||||
| chr16:19804091 | C | T | 4 | a0001c0001t0002g0034 a0001c0001t0002g0036 a0001c0001t0002g0046 others(1): Show |
4 | HG00140.hp2 HG01346.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.690+15169C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19804091 | |||||||
| chr16:19804182 | C | T | 1 | a0001c0001t0004g0022 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.690+15260C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19804182 | |||||||
| chr16:19804228 | C | G | 21 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(18): Show |
21 | HG01109.hp2 HG01884.hp2 HG01934.hp2 others(18): Show |
intron_variant | MODIFIER | c.690+15306C>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19804228 | |||||||
| chr16:19804302 | C | T | 1 | a0001c0001t0006g0041 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.690+15380C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19804302 | |||||||
| chr16:19804761 | G | A | 3 | a0001c0001t0002g0237 a0001c0001t0009g0239 a0001c0001t0019g0238 |
3 | HG02451.hp2 HG02895.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.690+15839G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19804761 | |||||||
| chr16:19804855 | T | G | 6 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(3): Show |
6 | HG01496.hp1 HG01891.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.690+15933T>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19804855 | |||||||
| chr16:19805227 | C | A | 2 | a0001c0001t0009g0239 a0001c0001t0019g0238 |
2 | HG02895.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.690+16305C>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19805227 | |||||||
| chr16:19805240 | G | GAC | 135 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(132): Show |
135 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(132): Show |
intron_variant | MODIFIER | c.690+16319_690+1632 others(6): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19805240 | ||||||
| chr16:19805455 | C | T | 5 | a0001c0001t0004g0012 a0001c0001t0004g0022 a0001c0001t0004g0024 others(2): Show |
5 | HG01109.hp2 HG01884.hp2 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.690+16533C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19805455 | |||||||
| chr16:19805517 | A | G | 1 | a0001c0001t0001g0062 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.690+16595A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19805517 | |||||||
| chr16:19805584 | A | G | 1 | a0001c0001t0001g0070 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.690+16662A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19805584 | |||||||
| chr16:19805662 | A | G | 1 | a0001c0001t0002g0006 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.690+16740A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19805662 | |||||||
| chr16:19805870 | G | C | 12 | a0001c0001t0001g0030 a0001c0001t0002g0001 a0001c0001t0002g0027 others(9): Show |
12 | HG01109.hp2 HG01884.hp2 HG01934.hp2 others(9): Show |
intron_variant | MODIFIER | c.690+16948G>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19805870 | |||||||
| chr16:19805876 | G | A | 1 | a0001c0001t0008g0074 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.690+16954G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19805876 | |||||||
| chr16:19805924 | G | T | 1 | a0001c0001t0001g0055 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.690+17002G>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19805924 | |||||||
| chr16:19806241 | A | C | 1 | a0001c0001t0002g0130 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.690+17319A>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19806241 | |||||||
| chr16:19806450 | C | T | 2 | a0002c0002t0001g0182 a0002c0002t0001g0229 |
2 | NA18961.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.690+17528C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19806450 | |||||||
| chr16:19806531 | C | CA | 131 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(128): Show |
131 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(128): Show |
intron_variant | MODIFIER | c.690+17619dupA | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19806531 | ||||||
| chr16:19806546 | T | C | 1 | a0001c0001t0001g0162 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.690+17624T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19806546 | |||||||
| chr16:19806716 | A | C | 1 | a0001c0003t0003g0021 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.690+17794A>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19806716 | |||||||
| chr16:19807672 | T | C | 1 | a0002c0002t0001g0201 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.690+18750T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19807672 | |||||||
| chr16:19807887 | G | C | 1 | a0001c0001t0001g0097 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.690+18965G>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19807887 | |||||||
| chr16:19807913 | A | G | 1 | a0001c0001t0001g0083 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.690+18991A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19807913 | |||||||
| chr16:19807927 | T | C | 1 | a0001c0001t0001g0104 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.690+19005T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19807927 | |||||||
| chr16:19808157 | G | C | 10 | a0001c0001t0001g0131 a0001c0001t0001g0135 a0001c0001t0001g0140 others(7): Show |
10 | HG01891.hp2 HG02055.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.691-18869G>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19808157 | |||||||
| chr16:19808262 | G | C | 2 | a0001c0001t0004g0178 a0001c0001t0015g0179 |
2 | HG02615.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.691-18764G>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19808262 | |||||||
| chr16:19808918 | C | T | 2 | a0001c0001t0001g0121 a0001c0001t0001g0122 |
2 | HG02622.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.691-18108C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19808918 | |||||||
| chr16:19808919 | G | A | 58 | a0002c0002t0001g0176 a0002c0002t0001g0177 a0002c0002t0001g0181 others(55): Show |
58 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(55): Show |
intron_variant | MODIFIER | c.691-18107G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19808919 | |||||||
| chr16:19809000 | G | A | 1 | a0001c0003t0003g0021 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.691-18026G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19809000 | |||||||
| chr16:19809372 | T | C | 58 | a0002c0002t0001g0176 a0002c0002t0001g0177 a0002c0002t0001g0181 others(55): Show |
58 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(55): Show |
intron_variant | MODIFIER | c.691-17654T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19809372 | |||||||
| chr16:19809656 | A | G | 1 | a0001c0001t0001g0152 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.691-17370A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19809656 | |||||||
| chr16:19809761 | C | A | 8 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(5): Show |
8 | HG02258.hp2 HG02280.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.691-17265C>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19809761 | |||||||
| chr16:19809894 | C | T | 2 | a0001c0001t0004g0012 a0001c0001t0004g0025 |
2 | HG01884.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.691-17132C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19809894 | |||||||
| chr16:19809932 | G | A | 6 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(3): Show |
6 | HG01496.hp1 HG01891.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.691-17094G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19809932 | |||||||
| chr16:19809980 | C | T | 4 | a0001c0001t0002g0119 a0001c0001t0002g0241 a0001c0001t0002g0242 others(1): Show |
4 | HG02622.hp2 HG02647.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.691-17046C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19809980 | |||||||
| chr16:19810031 | G | A | 1 | a0001c0001t0001g0140 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.691-16995G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19810031 | |||||||
| chr16:19810082 | G | C | 27 | a0001c0001t0001g0131 a0001c0001t0001g0133 a0001c0001t0001g0134 others(24): Show |
27 | HG00733.hp2 HG01175.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.691-16944G>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19810082 | |||||||
| chr16:19810143 | A | G | 3 | a0001c0001t0005g0033 a0001c0001t0005g0043 a0001c0001t0005g0044 |
3 | HG02055.hp2 HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.691-16883A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19810143 | |||||||
| chr16:19810186 | C | T | 1 | a0002c0002t0001g0187 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.691-16840C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19810186 | |||||||
| chr16:19810214 | C | T | 52 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(49): Show |
52 | HG00733.hp2 HG01175.hp1 HG01891.hp2 others(49): Show |
intron_variant | MODIFIER | c.691-16812C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19810214 | |||||||
| chr16:19810235 | G | A | 71 | a0001c0001t0001g0167 a0001c0001t0001g0171 a0001c0001t0002g0237 others(68): Show |
71 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(68): Show |
intron_variant | MODIFIER | c.691-16791G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19810235 | |||||||
| chr16:19810313 | G | A | 2 | a0001c0001t0001g0057 a0001c0001t0001g0060 |
2 | NA18983.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.691-16713G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19810313 | |||||||
| chr16:19810496 | C | CA | 84 | a0001c0001t0001g0131 a0001c0001t0001g0133 a0001c0001t0001g0134 others(81): Show |
84 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(81): Show |
intron_variant | MODIFIER | c.691-16517dupA | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19810496 | ||||||
| chr16:19810633 | C | T | 4 | a0001c0001t0001g0040 a0001c0001t0005g0037 a0001c0001t0005g0038 others(1): Show |
4 | HG02145.hp1 HG02922.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.691-16393C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19810633 | |||||||
| chr16:19810803 | C | CA | 15 | a0001c0001t0001g0040 a0001c0001t0001g0121 a0001c0001t0001g0122 others(12): Show |
15 | HG02055.hp2 HG02145.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.691-16209dupA | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19810803 | ||||||
| chr16:19810838 | A | G | 3 | a0001c0001t0001g0057 a0001c0001t0001g0060 a0001c0001t0001g0061 |
3 | NA18983.hp2 NA18993.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.691-16188A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19810838 | |||||||
| chr16:19811209 | C | T | 1 | a0001c0001t0001g0100 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.691-15817C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19811209 | |||||||
| chr16:19811210 | G | A | 2 | a0001c0001t0009g0239 a0001c0001t0019g0238 |
2 | HG02895.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.691-15816G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19811210 | |||||||
| chr16:19811342 | A | G | 1 | a0001c0001t0001g0137 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.691-15684A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19811342 | |||||||
| chr16:19811420 | C | T | 1 | a0001c0001t0002g0081 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.691-15606C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19811420 | |||||||
| chr16:19811615 | A | G | 1 | a0001c0001t0001g0106 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.691-15411A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19811615 | |||||||
| chr16:19811985 | A | AT | 6 | a0001c0001t0001g0127 a0001c0001t0004g0012 a0001c0001t0004g0022 others(3): Show |
6 | HG01109.hp2 HG01884.hp2 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.691-15021dupT | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19811985 | ||||||
| chr16:19811985 | AT | A | 48 | a0001c0001t0001g0048 a0001c0001t0001g0090 a0001c0001t0001g0131 others(45): Show |
48 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(45): Show |
intron_variant | MODIFIER | c.691-15021delT | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19811985 | ||||||
| chr16:19811985 | ATT | A | 89 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(86): Show |
89 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(86): Show |
intron_variant | MODIFIER | c.691-15022_691-1502 others(6): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19811985 | ||||||
| chr16:19812024 | G | C | 1 | a0002c0002t0001g0177 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.691-15002G>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19812024 | |||||||
| chr16:19812057 | G | A | 1 | a0001c0001t0001g0151 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.691-14969G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19812057 | |||||||
| chr16:19812080 | C | T | 3 | a0001c0001t0001g0065 a0001c0001t0005g0019 a0001c0001t0005g0020 |
3 | HG02135.hp2 HG02258.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.691-14946C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19812080 | |||||||
| chr16:19812558 | G | A | 1 | a0001c0001t0001g0171 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.691-14468G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19812558 | |||||||
| chr16:19812764 | G | A | 15 | a0001c0001t0001g0040 a0001c0001t0001g0121 a0001c0001t0001g0122 others(12): Show |
15 | HG02055.hp2 HG02145.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.691-14262G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19812764 | |||||||
| chr16:19812842 | T | TG | 7 | a0001c0001t0001g0175 a0001c0001t0003g0120 a0001c0001t0007g0165 others(4): Show |
7 | HG01884.hp1 HG02257.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.691-14184_691-1418 others(5): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19812842 | |||||||
| chr16:19812843 | A | G | 123 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(120): Show |
123 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(120): Show |
intron_variant | MODIFIER | c.691-14183A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19812843 | |||||||
| chr16:19812864 | A | T | 1 | a0001c0001t0002g0130 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.691-14162A>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19812864 | |||||||
| chr16:19813171 | G | C | 71 | a0001c0001t0001g0167 a0001c0001t0001g0171 a0001c0001t0002g0237 others(68): Show |
71 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(68): Show |
intron_variant | MODIFIER | c.691-13855G>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19813171 | |||||||
| chr16:19813233 | C | T | 1 | a0001c0001t0014g0049 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.691-13793C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19813233 | |||||||
| chr16:19813316 | T | C | 98 | a0001c0001t0001g0131 a0001c0001t0001g0133 a0001c0001t0001g0134 others(95): Show |
98 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(95): Show |
intron_variant | MODIFIER | c.691-13710T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19813316 | |||||||
| chr16:19813415 | G | C | 1 | a0001c0001t0001g0053 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.691-13611G>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19813415 | |||||||
| chr16:19813457 | A | AC | 123 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(120): Show |
123 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(120): Show |
intron_variant | MODIFIER | c.691-13569_691-1356 others(5): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19813457 | |||||||
| chr16:19813461 | T | C | 2 | a0001c0001t0002g0002 a0001c0001t0002g0031 |
2 | NA18946.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.691-13565T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19813461 | |||||||
| chr16:19813617 | G | A | 2 | a0001c0001t0002g0069 a0001c0001t0002g0085 |
2 | HG02738.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.691-13409G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19813617 | |||||||
| chr16:19813843 | G | A | 1 | a0001c0001t0003g0120 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.691-13183G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19813843 | |||||||
| chr16:19814104 | C | T | 1 | a0001c0003t0003g0021 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.691-12922C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19814104 | |||||||
| chr16:19814220 | C | CA | 70 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0040 others(67): Show |
70 | HG00140.hp2 HG00597.hp1 HG00597.hp2 others(67): Show |
intron_variant | MODIFIER | c.691-12780dupA | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19814220 | ||||||
| chr16:19814220 | C | CAA | 13 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0156 others(10): Show |
13 | HG01175.hp2 HG01496.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.691-12781_691-1278 others(6): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19814220 | ||||||
| chr16:19814220 | CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0002g0241 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.691-12792_691-1278 others(17): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19814220 | ||||||
| chr16:19814232 | A | C | 1 | a0003c0004t0013g0240 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.691-12794A>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19814232 | |||||||
| chr16:19814235 | A | AC | 3 | a0001c0001t0001g0148 a0001c0001t0001g0151 a0001c0001t0001g0155 |
3 | HG00733.hp2 HG01175.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.691-12791_691-1279 others(5): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19814235 | |||||||
| chr16:19814240 | A | AC | 21 | a0001c0001t0001g0131 a0001c0001t0001g0133 a0001c0001t0001g0134 others(18): Show |
21 | HG01891.hp2 HG02055.hp1 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.691-12786_691-1278 others(5): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19814240 | |||||||
| chr16:19814240 | A | C | 13 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(10): Show |
13 | HG00733.hp2 HG01175.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.691-12786A>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19814240 | |||||||
| chr16:19814246 | A | C | 1 | a0002c0002t0001g0186 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.691-12780A>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19814246 | |||||||
| chr16:19814326 | A | T | 1 | a0001c0001t0001g0098 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.691-12700A>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19814326 | |||||||
| chr16:19814554 | C | G | 1 | a0001c0003t0003g0021 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.691-12472C>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19814554 | |||||||
| chr16:19814739 | G | T | 1 | a0001c0001t0002g0035 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.691-12287G>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19814739 | |||||||
| chr16:19814786 | C | CT | 84 | a0001c0001t0001g0106 a0001c0001t0001g0131 a0001c0001t0001g0133 others(81): Show |
84 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(81): Show |
intron_variant | MODIFIER | c.691-12221dupT | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19814786 | ||||||
| chr16:19814786 | C | CTT | 12 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(9): Show |
12 | HG01175.hp1 HG02074.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.691-12222_691-1222 others(6): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19814786 | ||||||
| chr16:19814786 | C | CTTT | 10 | a0001c0001t0001g0167 a0001c0001t0001g0171 a0001c0001t0003g0120 others(7): Show |
10 | HG01884.hp1 HG02258.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.691-12223_691-1222 others(7): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19814786 | ||||||
| chr16:19814786 | CT | C | 5 | a0001c0001t0001g0075 a0001c0001t0005g0033 a0001c0001t0005g0043 others(2): Show |
5 | HG02055.hp2 HG02523.hp2 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.691-12221delT | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19814786 | ||||||
| chr16:19814799 | T | G | 3 | a0001c0001t0005g0033 a0001c0001t0005g0043 a0001c0001t0005g0044 |
3 | HG02055.hp2 HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.691-12227T>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19814799 | |||||||
| chr16:19814820 | G | C | 1 | a0001c0003t0003g0021 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.691-12206G>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19814820 | |||||||
| chr16:19814872 | G | A | 1 | a0001c0001t0006g0076 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.691-12154G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19814872 | |||||||
| chr16:19814916 | A | G | 1 | a0001c0001t0001g0162 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.691-12110A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19814916 | |||||||
| chr16:19815066 | C | T | 3 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0141 |
3 | HG02572.hp1 HG03130.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.691-11960C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19815066 | |||||||
| chr16:19815212 | C | G | 98 | a0001c0001t0001g0131 a0001c0001t0001g0133 a0001c0001t0001g0134 others(95): Show |
98 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(95): Show |
intron_variant | MODIFIER | c.691-11814C>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19815212 | |||||||
| chr16:19815278 | C | T | 1 | a0002c0002t0001g0230 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.691-11748C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19815278 | |||||||
| chr16:19815319 | A | G | 1 | a0001c0001t0006g0118 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.691-11707A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19815319 | |||||||
| chr16:19815373 | G | A | 1 | a0001c0001t0007g0170 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.691-11653G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19815373 | |||||||
| chr16:19815496 | A | AAAAAC | 18 | a0001c0001t0001g0040 a0001c0001t0001g0121 a0001c0001t0001g0122 others(15): Show |
18 | HG01175.hp1 HG02055.hp2 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.691-11504_691-1150 others(9): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19815496 | ||||||
| chr16:19815544 | G | A | 1 | a0001c0003t0003g0021 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.691-11482G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19815544 | |||||||
| chr16:19815595 | C | T | 27 | a0001c0001t0001g0131 a0001c0001t0001g0133 a0001c0001t0001g0134 others(24): Show |
27 | HG00733.hp2 HG01175.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.691-11431C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19815595 | |||||||
| chr16:19815622 | G | T | 1 | a0001c0001t0002g0093 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.691-11404G>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19815622 | |||||||
| chr16:19816107 | A | G | 1 | a0003c0004t0013g0240 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.691-10919A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19816107 | |||||||
| chr16:19816130 | A | T | 2 | a0001c0001t0001g0158 a0001c0001t0001g0159 |
2 | HG01891.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.691-10896A>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19816130 | |||||||
| chr16:19816226 | C | G | 15 | a0001c0001t0001g0040 a0001c0001t0001g0121 a0001c0001t0001g0122 others(12): Show |
15 | HG02055.hp2 HG02145.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.691-10800C>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19816226 | |||||||
| chr16:19816385 | G | A | 31 | a0002c0002t0001g0176 a0002c0002t0001g0177 a0002c0002t0001g0182 others(28): Show |
31 | HG00597.hp2 HG00609.hp1 HG01261.hp2 others(28): Show |
intron_variant | MODIFIER | c.691-10641G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19816385 | |||||||
| chr16:19816566 | G | A | 1 | a0001c0001t0002g0059 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.691-10460G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19816566 | |||||||
| chr16:19816641 | A | T | 4 | a0001c0001t0001g0067 a0001c0001t0001g0101 a0001c0001t0001g0115 others(1): Show |
4 | HG01433.hp1 HG01943.hp1 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.691-10385A>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19816641 | |||||||
| chr16:19816886 | C | G | 1 | a0003c0004t0013g0240 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.691-10140C>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19816886 | |||||||
| chr16:19816887 | C | T | 1 | a0001c0001t0002g0088 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.691-10139C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19816887 | |||||||
| chr16:19817261 | A | G | 3 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0174 |
3 | NA18943.hp1 NA18944.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.691-9765A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19817261 | |||||||
| chr16:19817462 | A | G | 8 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(5): Show |
8 | HG02258.hp2 HG02280.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.691-9564A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19817462 | |||||||
| chr16:19817593 | T | C | 27 | a0001c0001t0001g0131 a0001c0001t0001g0133 a0001c0001t0001g0134 others(24): Show |
27 | HG00733.hp2 HG01175.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.691-9433T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19817593 | |||||||
| chr16:19817674 | AAATT | A | 15 | a0001c0001t0001g0040 a0001c0001t0001g0121 a0001c0001t0001g0122 others(12): Show |
15 | HG02055.hp2 HG02145.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.691-9342_691-9339d others(6): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19817674 | ||||||
| chr16:19818055 | AG | A | 25 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(22): Show |
25 | HG02055.hp2 HG02145.hp1 HG02258.hp2 others(22): Show |
intron_variant | MODIFIER | c.691-8970delG | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19818055 | |||||||
| chr16:19818189 | G | A | 8 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(5): Show |
8 | HG02258.hp2 HG02280.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.691-8837G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19818189 | |||||||
| chr16:19818276 | G | T | 1 | a0001c0001t0010g0147 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.691-8750G>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19818276 | |||||||
| chr16:19818346 | T | TTG | 4 | a0001c0001t0001g0156 a0001c0001t0002g0086 a0001c0001t0005g0037 others(1): Show |
4 | HG00323.hp1 HG01496.hp1 HG02083.hp2 others(1): Show |
intron_variant | MODIFIER | c.691-8660_691-8659d others(4): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19818346 | ||||||
| chr16:19818382 | C | T | 2 | a0001c0001t0002g0094 a0001c0001t0002g0095 |
2 | HG01943.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.691-8644C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19818382 | |||||||
| chr16:19818474 | C | T | 25 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(22): Show |
25 | HG02055.hp2 HG02145.hp1 HG02258.hp2 others(22): Show |
intron_variant | MODIFIER | c.691-8552C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19818474 | |||||||
| chr16:19818672 | T | C | 151 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(148): Show |
151 | HG00140.hp2 HG00597.hp2 HG00609.hp1 others(148): Show |
intron_variant | MODIFIER | c.691-8354T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19818672 | |||||||
| chr16:19818677 | G | A | 71 | a0001c0001t0001g0167 a0001c0001t0001g0171 a0001c0001t0002g0237 others(68): Show |
71 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(68): Show |
intron_variant | MODIFIER | c.691-8349G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19818677 | |||||||
| chr16:19818998 | G | T | 1 | a0001c0001t0001g0152 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.691-8028G>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19818998 | |||||||
| chr16:19819135 | G | A | 98 | a0001c0001t0001g0131 a0001c0001t0001g0133 a0001c0001t0001g0134 others(95): Show |
98 | HG00597.hp2 HG00609.hp1 HG00733.hp1 others(95): Show |
intron_variant | MODIFIER | c.691-7891G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19819135 | |||||||
| chr16:19819349 | C | T | 1 | a0001c0001t0001g0098 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.691-7677C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19819349 | |||||||
| chr16:19819361 | C | T | 13 | a0001c0001t0001g0167 a0001c0001t0001g0171 a0001c0001t0002g0237 others(10): Show |
13 | HG01884.hp1 HG02257.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.691-7665C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19819361 | |||||||
| chr16:19819507 | T | A | 6 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(3): Show |
6 | HG01496.hp1 HG01891.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.691-7519T>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19819507 | |||||||
| chr16:19819534 | G | A | 2 | a0001c0001t0001g0063 a0001c0001t0001g0137 |
2 | HG02155.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.691-7492G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19819534 | |||||||
| chr16:19819595 | A | G | 2 | a0001c0001t0001g0151 a0001c0001t0001g0155 |
2 | HG00733.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.691-7431A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19819595 | |||||||
| chr16:19819657 | A | G | 4 | a0001c0001t0001g0067 a0001c0001t0001g0101 a0001c0001t0001g0115 others(1): Show |
4 | HG01433.hp1 HG01943.hp1 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.691-7369A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19819657 | |||||||
| chr16:19819681 | C | T | 1 | a0003c0004t0013g0240 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.691-7345C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19819681 | |||||||
| chr16:19819718 | C | T | 1 | a0001c0001t0006g0007 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.691-7308C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19819718 | |||||||
| chr16:19819756 | G | A | 1 | a0001c0001t0002g0242 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.691-7270G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19819756 | |||||||
| chr16:19819945 | G | A | 75 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(72): Show |
75 | HG00597.hp2 HG00609.hp1 HG01081.hp1 others(72): Show |
intron_variant | MODIFIER | c.691-7081G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19819945 | |||||||
| chr16:19819971 | G | A | 1 | a0002c0002t0001g0231 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.691-7055G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19819971 | |||||||
| chr16:19820010 | A | G | 34 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0131 others(31): Show |
34 | HG00733.hp2 HG01175.hp1 HG01496.hp1 others(31): Show |
intron_variant | MODIFIER | c.691-7016A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19820010 | |||||||
| chr16:19820073 | G | A | 240 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(237): Show |
240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.691-6953G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19820073 | |||||||
| chr16:19820086 | A | C | 3 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0141 |
3 | HG02572.hp1 HG03130.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.691-6940A>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19820086 | |||||||
| chr16:19820154 | A | G | 113 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0013 others(110): Show |
113 | HG00099.hp2 HG00597.hp2 HG00609.hp1 others(110): Show |
intron_variant | MODIFIER | c.691-6872A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19820154 | |||||||
| chr16:19820169 | A | G | 1 | a0003c0004t0013g0240 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.691-6857A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19820169 | |||||||
| chr16:19820210 | G | GA | 71 | a0001c0001t0001g0040 a0001c0001t0001g0091 a0001c0001t0001g0092 others(68): Show |
71 | HG00099.hp2 HG00597.hp2 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.691-6807dupA | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19820210 | ||||||
| chr16:19820299 | T | C | 9 | a0001c0001t0005g0019 a0001c0001t0005g0020 a0001c0001t0005g0033 others(6): Show |
9 | HG02055.hp2 HG02145.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.691-6727T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19820299 | |||||||
| chr16:19820451 | C | T | 10 | a0001c0001t0007g0163 a0001c0001t0007g0165 a0001c0001t0007g0166 others(7): Show |
10 | HG01884.hp1 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.691-6575C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19820451 | |||||||
| chr16:19820522 | G | A | 1 | a0003c0004t0013g0240 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.691-6504G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19820522 | |||||||
| chr16:19820566 | T | G | 36 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0013 others(33): Show |
36 | HG00609.hp2 HG00735.hp2 HG01433.hp1 others(33): Show |
intron_variant | MODIFIER | c.691-6460T>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19820566 | |||||||
| chr16:19820648 | C | CA | 119 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0013 others(116): Show |
119 | HG00099.hp2 HG00609.hp1 HG00609.hp2 others(116): Show |
intron_variant | MODIFIER | c.691-6361dupA | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19820648 | ||||||
| chr16:19820648 | C | CAA | 7 | a0001c0001t0007g0165 a0001c0001t0007g0166 a0001c0001t0007g0168 others(4): Show |
7 | HG00597.hp2 HG01884.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.691-6362_691-6361d others(4): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19820648 | ||||||
| chr16:19820710 | T | G | 116 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0013 others(113): Show |
116 | HG00099.hp2 HG00597.hp2 HG00609.hp1 others(113): Show |
intron_variant | MODIFIER | c.691-6316T>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19820710 | |||||||
| chr16:19820784 | T | C | 1 | a0001c0001t0002g0108 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.691-6242T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19820784 | |||||||
| chr16:19820946 | C | T | 1 | a0001c0001t0001g0153 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.691-6080C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19820946 | |||||||
| chr16:19821084 | T | C | 3 | a0001c0001t0007g0166 a0001c0001t0007g0168 a0001c0001t0007g0169 |
3 | HG01884.hp1 HG02257.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.691-5942T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19821084 | |||||||
| chr16:19821267 | G | A | 53 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0013 others(50): Show |
53 | HG00609.hp2 HG00733.hp1 HG00735.hp2 others(50): Show |
intron_variant | MODIFIER | c.691-5759G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19821267 | |||||||
| chr16:19821380 | G | A | 1 | a0001c0001t0012g0243 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.691-5646G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19821380 | |||||||
| chr16:19821476 | G | T | 13 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0015g0179 others(10): Show |
13 | HG00733.hp1 HG01255.hp1 HG01433.hp2 others(10): Show |
intron_variant | MODIFIER | c.691-5550G>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19821476 | |||||||
| chr16:19821611 | G | T | 3 | a0001c0001t0009g0239 a0002c0002t0009g0194 a0002c0002t0009g0195 |
3 | HG02486.hp2 HG02895.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.691-5415G>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19821611 | |||||||
| chr16:19821679 | A | G | 70 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0013 others(67): Show |
70 | HG00609.hp2 HG00733.hp1 HG00735.hp2 others(67): Show |
intron_variant | MODIFIER | c.691-5347A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19821679 | |||||||
| chr16:19821756 | G | C | 3 | a0001c0001t0009g0239 a0002c0002t0009g0194 a0002c0002t0009g0195 |
3 | HG02486.hp2 HG02895.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.691-5270G>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19821756 | |||||||
| chr16:19821858 | G | A | 29 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0053 others(26): Show |
29 | HG00609.hp2 HG00735.hp2 HG01433.hp1 others(26): Show |
intron_variant | MODIFIER | c.691-5168G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19821858 | |||||||
| chr16:19821934 | G | C | 1 | a0001c0001t0001g0101 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.691-5092G>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19821934 | |||||||
| chr16:19821950 | C | T | 1 | a0002c0002t0001g0228 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.691-5076C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19821950 | |||||||
| chr16:19822039 | A | G | 6 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(3): Show |
6 | HG01496.hp1 HG01891.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.691-4987A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19822039 | |||||||
| chr16:19822067 | C | CA | 10 | a0001c0001t0001g0075 a0001c0001t0002g0027 a0001c0001t0002g0059 others(7): Show |
10 | HG00597.hp2 HG00609.hp1 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.691-4943dupA | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19822067 | ||||||
| chr16:19822067 | CA | C | 79 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0013 others(76): Show |
79 | HG00609.hp2 HG00733.hp1 HG00733.hp2 others(76): Show |
intron_variant | MODIFIER | c.691-4943delA | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19822067 | ||||||
| chr16:19822072 | AAAAAAAA others(5): Show |
A | 8 | a0001c0001t0001g0156 a0001c0001t0001g0158 a0001c0001t0001g0159 others(5): Show |
8 | HG01496.hp1 HG01891.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.691-4932_691-4921d others(14): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19822072 | ||||||
| chr16:19822073 | AAAAAAAA others(4): Show |
A | 1 | a0001c0001t0001g0157 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.691-4942_691-4932d others(13): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19822073 | ||||||
| chr16:19822076 | A | C | 1 | a0001c0001t0004g0005 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.691-4950A>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19822076 | |||||||
| chr16:19822082 | A | AC | 4 | a0001c0001t0009g0239 a0001c0001t0019g0238 a0002c0002t0009g0194 others(1): Show |
4 | HG02486.hp2 HG02895.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.691-4944_691-4943i others(3): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19822082 | |||||||
| chr16:19822083 | A | C | 15 | a0001c0001t0004g0005 a0001c0001t0004g0012 a0001c0001t0004g0022 others(12): Show |
15 | HG01109.hp2 HG01884.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.691-4943A>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19822083 | |||||||
| chr16:19822084 | C | A | 19 | a0001c0001t0004g0005 a0001c0001t0004g0012 a0001c0001t0004g0022 others(16): Show |
19 | HG01109.hp2 HG01884.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.691-4942C>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19822084 | |||||||
| chr16:19822085 | A | C | 1 | a0001c0001t0003g0120 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.691-4941A>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19822085 | |||||||
| chr16:19822086 | A | C | 3 | a0001c0001t0009g0239 a0002c0002t0009g0194 a0002c0002t0009g0195 |
3 | HG02486.hp2 HG02895.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.691-4940A>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19822086 | |||||||
| chr16:19822091 | A | C | 1 | a0003c0004t0013g0240 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.691-4935A>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19822091 | |||||||
| chr16:19822092 | A | C | 1 | a0001c0001t0001g0060 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.691-4934A>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19822092 | |||||||
| chr16:19822096 | C | CA | 6 | a0001c0001t0001g0040 a0001c0001t0001g0139 a0001c0001t0002g0088 others(3): Show |
6 | HG01081.hp2 HG02258.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.691-4921dupA | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19822096 | ||||||
| chr16:19822138 | C | T | 7 | a0001c0001t0007g0163 a0001c0001t0007g0165 a0001c0001t0007g0166 others(4): Show |
7 | HG01884.hp1 HG02257.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.691-4888C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19822138 | |||||||
| chr16:19822183 | C | T | 1 | a0001c0001t0001g0008 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.691-4843C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19822183 | |||||||
| chr16:19822300 | T | C | 45 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0003g0096 others(42): Show |
45 | HG00099.hp2 HG00597.hp2 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.691-4726T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19822300 | |||||||
| chr16:19822385 | C | CA | 59 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0018 others(56): Show |
59 | HG00735.hp2 HG01109.hp2 HG01433.hp1 others(56): Show |
intron_variant | MODIFIER | c.691-4621dupA | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19822385 | ||||||
| chr16:19822385 | C | CAA | 5 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0127 others(2): Show |
5 | HG00609.hp2 HG01934.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.691-4622_691-4621d others(4): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19822385 | ||||||
| chr16:19822400 | A | T | 1 | a0001c0001t0002g0084 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.691-4626A>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19822400 | |||||||
| chr16:19822493 | A | G | 52 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0013 others(49): Show |
52 | HG00609.hp2 HG00735.hp2 HG01109.hp2 others(49): Show |
intron_variant | MODIFIER | c.691-4533A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19822493 | |||||||
| chr16:19822657 | A | G | 1 | a0002c0002t0001g0204 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.691-4369A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19822657 | |||||||
| chr16:19822762 | G | T | 10 | a0001c0001t0002g0006 a0001c0001t0002g0034 a0001c0001t0002g0035 others(7): Show |
10 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(7): Show |
intron_variant | MODIFIER | c.691-4264G>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19822762 | |||||||
| chr16:19822978 | C | T | 9 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(6): Show |
9 | HG01496.hp1 HG01891.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.691-4048C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19822978 | |||||||
| chr16:19823100 | G | A | 51 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0013 others(48): Show |
51 | HG00609.hp2 HG00733.hp1 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.691-3926G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19823100 | |||||||
| chr16:19823193 | T | C | 1 | a0002c0002t0001g0211 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.691-3833T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19823193 | |||||||
| chr16:19823208 | T | G | 7 | a0001c0001t0007g0163 a0001c0001t0007g0165 a0001c0001t0007g0166 others(4): Show |
7 | HG01884.hp1 HG02257.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.691-3818T>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19823208 | |||||||
| chr16:19823219 | T | C | 1 | a0001c0001t0001g0055 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.691-3807T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19823219 | |||||||
| chr16:19823253 | G | A | 1 | a0001c0001t0012g0243 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.691-3773G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19823253 | |||||||
| chr16:19823275 | T | C | 1 | a0001c0001t0006g0007 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.691-3751T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19823275 | |||||||
| chr16:19823323 | C | T | 3 | a0001c0001t0009g0239 a0002c0002t0009g0194 a0002c0002t0009g0195 |
3 | HG02486.hp2 HG02895.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.691-3703C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19823323 | |||||||
| chr16:19823562 | A | T | 5 | a0002c0002t0001g0181 a0002c0002t0001g0205 a0002c0002t0001g0206 others(2): Show |
5 | HG02135.hp1 HG02155.hp1 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.691-3464A>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19823562 | |||||||
| chr16:19823674 | C | T | 8 | a0001c0001t0005g0019 a0001c0001t0005g0020 a0001c0001t0005g0033 others(5): Show |
8 | HG02055.hp2 HG02145.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.691-3352C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19823674 | |||||||
| chr16:19823795 | G | T | 61 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0013 others(58): Show |
61 | HG00609.hp2 HG00733.hp1 HG00735.hp2 others(58): Show |
intron_variant | MODIFIER | c.691-3231G>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19823795 | |||||||
| chr16:19823826 | G | C | 1 | a0001c0001t0012g0243 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.691-3200G>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19823826 | |||||||
| chr16:19823932 | T | TAAAA | 9 | a0001c0001t0004g0005 a0001c0001t0004g0012 a0001c0001t0004g0022 others(6): Show |
9 | HG01109.hp2 HG01884.hp2 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.691-3091_691-3088d others(6): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19823932 | ||||||
| chr16:19823932 | TA | T | 14 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0015g0179 others(11): Show |
14 | HG00733.hp1 HG01255.hp1 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.691-3088delA | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19823932 | ||||||
| chr16:19823935 | A | AAAAT | 3 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0003g0096 |
3 | HG00099.hp2 HG00639.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.691-3063_691-3060d others(6): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19823935 | ||||||
| chr16:19823938 | AT | A | 47 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0013 others(44): Show |
47 | HG00609.hp2 HG00735.hp2 HG01433.hp1 others(44): Show |
intron_variant | MODIFIER | c.691-3087delT | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19823938 | |||||||
| chr16:19823939 | T | A | 45 | a0001c0001t0001g0040 a0001c0001t0001g0121 a0001c0001t0001g0122 others(42): Show |
45 | HG00733.hp2 HG01175.hp1 HG01496.hp1 others(42): Show |
intron_variant | MODIFIER | c.691-3087T>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19823939 | |||||||
| chr16:19823943 | T | A | 39 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0013 others(36): Show |
39 | HG00609.hp2 HG00735.hp2 HG01433.hp1 others(36): Show |
intron_variant | MODIFIER | c.691-3083T>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19823943 | |||||||
| chr16:19824007 | G | A | 1 | a0001c0001t0001g0048 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.691-3019G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19824007 | |||||||
| chr16:19824069 | G | A | 8 | a0001c0001t0005g0019 a0001c0001t0005g0020 a0001c0001t0005g0033 others(5): Show |
8 | HG02055.hp2 HG02145.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.691-2957G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19824069 | |||||||
| chr16:19824156 | C | T | 1 | a0003c0004t0013g0240 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.691-2870C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19824156 | |||||||
| chr16:19824642 | T | C | 1 | a0001c0001t0002g0108 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.691-2384T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19824642 | |||||||
| chr16:19825024 | G | C | 70 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0013 others(67): Show |
70 | HG00609.hp2 HG00733.hp1 HG00735.hp2 others(67): Show |
intron_variant | MODIFIER | c.691-2002G>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19825024 | |||||||
| chr16:19825139 | C | T | 4 | a0001c0001t0001g0067 a0001c0001t0001g0101 a0001c0001t0001g0115 others(1): Show |
4 | HG01433.hp1 HG01943.hp1 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.691-1887C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19825139 | |||||||
| chr16:19825181 | A | G | 1 | a0001c0001t0003g0188 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.691-1845A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19825181 | |||||||
| chr16:19825319 | G | A | 3 | a0001c0001t0009g0239 a0002c0002t0009g0194 a0002c0002t0009g0195 |
3 | HG02486.hp2 HG02895.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.691-1707G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19825319 | |||||||
| chr16:19825489 | C | T | 1 | a0002c0002t0001g0177 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.691-1537C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19825489 | |||||||
| chr16:19825520 | C | CA | 9 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0005g0033 others(6): Show |
9 | HG02055.hp2 HG02145.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.691-1493dupA | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 19825520 | ||||||
| chr16:19825713 | A | G | 3 | a0001c0001t0002g0119 a0001c0001t0002g0241 a0001c0001t0002g0242 |
3 | HG02622.hp2 HG02647.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.691-1313A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19825713 | |||||||
| chr16:19825842 | T | C | 3 | a0001c0001t0009g0239 a0002c0002t0009g0194 a0002c0002t0009g0195 |
3 | HG02486.hp2 HG02895.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.691-1184T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19825842 | |||||||
| chr16:19826155 | C | T | 1 | a0002c0002t0001g0182 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.691-871C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19826155 | |||||||
| chr16:19826207 | T | A | 1 | a0001c0001t0001g0077 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.691-819T>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19826207 | |||||||
| chr16:19826578 | A | G | 1 | a0001c0001t0006g0118 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.691-448A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19826578 | |||||||
| chr16:19826619 | C | A | 9 | a0001c0001t0004g0005 a0001c0001t0004g0012 a0001c0001t0004g0022 others(6): Show |
9 | HG01109.hp2 HG01884.hp2 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.691-407C>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19826619 | |||||||
| chr16:19826938 | G | A | 37 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0013 others(34): Show |
37 | HG00609.hp2 HG00735.hp2 HG01433.hp1 others(34): Show |
intron_variant | MODIFIER | c.691-88G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19826938 | |||||||
| chr16:19826980 | C | T | 36 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0013 others(33): Show |
36 | HG00609.hp2 HG00735.hp2 HG01433.hp1 others(33): Show |
intron_variant | MODIFIER | c.691-46C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19826980 | |||||||
| chr16:19826997 | G | C | 37 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0013 others(34): Show |
37 | HG00609.hp2 HG00735.hp2 HG01433.hp1 others(34): Show |
intron_variant | MODIFIER | c.691-29G>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 7/8 | chr16 | 19826997 | |||||||
| chr16:19827148 | G | A | 9 | a0001c0001t0004g0005 a0001c0001t0004g0012 a0001c0001t0004g0022 others(6): Show |
9 | HG01109.hp2 HG01884.hp2 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.802+11G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19827148 | |||||||
| chr16:19827366 | C | G | 1 | a0001c0001t0002g0086 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.802+229C>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19827366 | |||||||
| chr16:19827519 | T | C | 1 | a0001c0001t0005g0037 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.802+382T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19827519 | |||||||
| chr16:19827561 | C | G | 51 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0013 others(48): Show |
51 | HG00609.hp2 HG00733.hp1 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.802+424C>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19827561 | |||||||
| chr16:19827619 | CAGAG | C | 6 | a0001c0001t0001g0014 a0001c0001t0001g0017 a0001c0001t0001g0018 others(3): Show |
6 | HG02280.hp1 HG02615.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.802+486_802+489del others(4): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 19827619 | ||||||
| chr16:19827644 | T | G | 3 | a0001c0001t0003g0045 a0001c0001t0003g0120 a0001c0001t0003g0123 |
3 | HG03225.hp1 HG03453.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.802+507T>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19827644 | |||||||
| chr16:19827745 | G | C | 8 | a0001c0001t0004g0012 a0001c0001t0004g0022 a0001c0001t0004g0023 others(5): Show |
8 | HG01109.hp2 HG01884.hp2 HG01934.hp2 others(5): Show |
intron_variant | MODIFIER | c.802+608G>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19827745 | |||||||
| chr16:19827758 | G | A | 1 | a0001c0001t0003g0188 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.802+621G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19827758 | |||||||
| chr16:19827908 | C | T | 1 | a0001c0001t0001g0100 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.802+771C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19827908 | |||||||
| chr16:19827973 | T | C | 61 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0013 others(58): Show |
61 | HG00609.hp2 HG00733.hp1 HG00735.hp2 others(58): Show |
intron_variant | MODIFIER | c.802+836T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19827973 | |||||||
| chr16:19827995 | C | T | 1 | a0001c0001t0012g0243 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.802+858C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19827995 | |||||||
| chr16:19828203 | C | T | 1 | a0002c0002t0001g0208 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.802+1066C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19828203 | |||||||
| chr16:19828204 | G | A | 2 | a0002c0002t0001g0183 a0002c0002t0001g0230 |
2 | HG03704.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.802+1067G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19828204 | |||||||
| chr16:19828216 | C | T | 70 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0013 others(67): Show |
70 | HG00609.hp2 HG00733.hp1 HG00735.hp2 others(67): Show |
intron_variant | MODIFIER | c.802+1079C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19828216 | |||||||
| chr16:19828231 | C | CT | 9 | a0001c0001t0002g0006 a0001c0001t0002g0069 a0001c0001t0002g0093 others(6): Show |
9 | HG00639.hp2 HG01175.hp2 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.802+1114dupT | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 19828231 | ||||||
| chr16:19828231 | CT | C | 20 | a0001c0001t0001g0075 a0001c0001t0001g0134 a0001c0001t0001g0152 others(17): Show |
20 | HG00733.hp1 HG01109.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.802+1114delT | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 19828231 | ||||||
| chr16:19828231 | CTT | C | 23 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0007g0163 others(20): Show |
23 | HG01255.hp1 HG01433.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.802+1113_802+1114d others(4): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 19828231 | ||||||
| chr16:19828231 | CTTT | C | 36 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0013 others(33): Show |
36 | HG00609.hp2 HG00735.hp2 HG01433.hp1 others(33): Show |
intron_variant | MODIFIER | c.802+1112_802+1114d others(5): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 19828231 | ||||||
| chr16:19828272 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.802+1135C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19828272 | |||||||
| chr16:19828527 | C | T | 1 | a0001c0001t0001g0056 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.802+1390C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19828527 | |||||||
| chr16:19828634 | C | T | 6 | a0001c0001t0007g0163 a0001c0001t0007g0165 a0001c0001t0007g0166 others(3): Show |
6 | HG01884.hp1 HG02257.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.802+1497C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19828634 | |||||||
| chr16:19828653 | G | A | 3 | a0001c0001t0009g0239 a0002c0002t0009g0194 a0002c0002t0009g0195 |
3 | HG02486.hp2 HG02895.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.802+1516G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19828653 | |||||||
| chr16:19828689 | C | A | 10 | a0001c0001t0002g0006 a0001c0001t0002g0034 a0001c0001t0002g0035 others(7): Show |
10 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(7): Show |
intron_variant | MODIFIER | c.802+1552C>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19828689 | |||||||
| chr16:19828744 | G | A | 9 | a0001c0001t0004g0005 a0001c0001t0004g0012 a0001c0001t0004g0022 others(6): Show |
9 | HG01109.hp2 HG01884.hp2 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.802+1607G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19828744 | |||||||
| chr16:19828834 | C | T | 3 | a0001c0001t0005g0033 a0001c0001t0005g0043 a0001c0001t0005g0044 |
3 | HG02055.hp2 HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.802+1697C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19828834 | |||||||
| chr16:19828845 | C | T | 7 | a0001c0001t0007g0163 a0001c0001t0007g0165 a0001c0001t0007g0166 others(4): Show |
7 | HG01884.hp1 HG02257.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.802+1708C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19828845 | |||||||
| chr16:19828846 | G | A | 1 | a0002c0002t0001g0221 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.802+1709G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19828846 | |||||||
| chr16:19828857 | AATATATA others(7): Show |
A | 8 | a0001c0001t0005g0019 a0001c0001t0005g0020 a0001c0001t0005g0033 others(5): Show |
8 | HG02055.hp2 HG02145.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.802+1722_802+1735d others(16): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 19828857 | ||||||
| chr16:19828859 | T | A | 171 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(168): Show |
171 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(168): Show |
intron_variant | MODIFIER | c.802+1722T>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19828859 | |||||||
| chr16:19828861 | T | A | 1 | a0001c0001t0001g0098 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.802+1724T>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19828861 | |||||||
| chr16:19828895 | TA | T | 11 | a0001c0001t0003g0045 a0001c0001t0003g0120 a0001c0001t0003g0123 others(8): Show |
11 | HG02055.hp2 HG02145.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.802+1759delA | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19828895 | |||||||
| chr16:19828916 | T | A | 1 | a0001c0001t0001g0134 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.802+1779T>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19828916 | |||||||
| chr16:19829052 | GA | G | 61 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0013 others(58): Show |
61 | HG00609.hp2 HG00733.hp1 HG00735.hp2 others(58): Show |
intron_variant | MODIFIER | c.802+1918delA | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 19829052 | ||||||
| chr16:19829137 | G | A | 1 | a0001c0001t0012g0243 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.802+2000G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19829137 | |||||||
| chr16:19829196 | G | A | 2 | a0002c0002t0001g0219 a0002c0002t0001g0220 |
2 | NA18983.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.802+2059G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19829196 | |||||||
| chr16:19829227 | A | C | 1 | a0001c0001t0006g0073 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.802+2090A>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19829227 | |||||||
| chr16:19829398 | G | T | 7 | a0001c0001t0007g0163 a0001c0001t0007g0165 a0001c0001t0007g0166 others(4): Show |
7 | HG01884.hp1 HG02257.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.802+2261G>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19829398 | |||||||
| chr16:19829460 | C | T | 3 | a0001c0001t0009g0239 a0002c0002t0009g0194 a0002c0002t0009g0195 |
3 | HG02486.hp2 HG02895.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.802+2323C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19829460 | |||||||
| chr16:19829518 | G | T | 1 | a0001c0001t0010g0147 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.802+2381G>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19829518 | |||||||
| chr16:19829703 | T | G | 1 | a0002c0002t0003g0235 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.802+2566T>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19829703 | |||||||
| chr16:19829762 | G | A | 1 | a0001c0001t0010g0032 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.802+2625G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19829762 | |||||||
| chr16:19830014 | C | CGAAT | 7 | a0001c0001t0001g0157 a0001c0001t0001g0161 a0001c0001t0002g0054 others(4): Show |
7 | HG02258.hp2 HG02559.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.802+2911_802+2914d others(6): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 19830014 | ||||||
| chr16:19830014 | CGAAT | C | 33 | a0001c0001t0001g0040 a0001c0001t0001g0121 a0001c0001t0001g0122 others(30): Show |
33 | HG00099.hp1 HG00733.hp2 HG01175.hp1 others(30): Show |
intron_variant | MODIFIER | c.802+2911_802+2914d others(6): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 19830014 | ||||||
| chr16:19830014 | CGAATGAA others(1): Show |
C | 69 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0013 others(66): Show |
69 | HG00609.hp2 HG00733.hp1 HG00735.hp2 others(66): Show |
intron_variant | MODIFIER | c.802+2907_802+2914d others(10): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 19830014 | ||||||
| chr16:19830026 | T | C | 57 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0013 others(54): Show |
57 | HG00609.hp2 HG00733.hp1 HG00735.hp2 others(54): Show |
intron_variant | MODIFIER | c.802+2889T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19830026 | |||||||
| chr16:19830554 | G | C | 13 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0015g0179 others(10): Show |
13 | HG00733.hp1 HG01255.hp1 HG01433.hp2 others(10): Show |
intron_variant | MODIFIER | c.802+3417G>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19830554 | |||||||
| chr16:19830751 | G | A | 1 | a0002c0002t0017g0212 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.802+3614G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19830751 | |||||||
| chr16:19830810 | A | G | 13 | a0001c0001t0001g0011 a0001c0001t0001g0067 a0001c0001t0001g0070 others(10): Show |
13 | HG01433.hp1 HG01928.hp1 HG01934.hp1 others(10): Show |
intron_variant | MODIFIER | c.802+3673A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19830810 | |||||||
| chr16:19830820 | A | C | 1 | a0001c0001t0001g0008 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.802+3683A>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19830820 | |||||||
| chr16:19830857 | G | T | 1 | a0001c0001t0001g0065 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.802+3720G>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19830857 | |||||||
| chr16:19831369 | G | A | 6 | a0001c0001t0007g0163 a0001c0001t0007g0165 a0001c0001t0007g0166 others(3): Show |
6 | HG01884.hp1 HG02257.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.802+4232G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19831369 | |||||||
| chr16:19831413 | C | A | 45 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0003g0096 others(42): Show |
45 | HG00099.hp2 HG00597.hp2 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.802+4276C>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19831413 | |||||||
| chr16:19831440 | C | A | 3 | a0001c0001t0009g0239 a0002c0002t0009g0194 a0002c0002t0009g0195 |
3 | HG02486.hp2 HG02895.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.802+4303C>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19831440 | |||||||
| chr16:19831537 | G | C | 1 | a0002c0002t0001g0222 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.802+4400G>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19831537 | |||||||
| chr16:19831625 | G | A | 27 | a0001c0001t0001g0003 a0001c0001t0001g0048 a0001c0001t0001g0051 others(24): Show |
27 | HG00140.hp1 HG00597.hp1 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.802+4488G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19831625 | |||||||
| chr16:19831637 | G | A | 1 | a0002c0002t0001g0223 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.802+4500G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19831637 | |||||||
| chr16:19831659 | TA | T | 7 | a0001c0001t0001g0134 a0001c0001t0001g0142 a0001c0001t0001g0143 others(4): Show |
7 | HG02717.hp2 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.802+4535delA | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 19831659 | ||||||
| chr16:19831695 | G | A | 1 | a0001c0001t0010g0124 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.802+4558G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19831695 | |||||||
| chr16:19831744 | C | T | 1 | a0003c0004t0013g0240 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.802+4607C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19831744 | |||||||
| chr16:19831906 | A | G | 1 | a0001c0001t0004g0024 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.802+4769A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19831906 | |||||||
| chr16:19831951 | C | G | 3 | a0001c0001t0009g0239 a0002c0002t0009g0194 a0002c0002t0009g0195 |
3 | HG02486.hp2 HG02895.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.802+4814C>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19831951 | |||||||
| chr16:19832014 | T | C | 4 | a0002c0002t0001g0177 a0002c0002t0001g0187 a0002c0002t0001g0204 others(1): Show |
4 | HG00597.hp2 HG02083.hp2 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.802+4877T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19832014 | |||||||
| chr16:19832195 | T | C | 13 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0015g0179 others(10): Show |
13 | HG00733.hp1 HG01255.hp1 HG01433.hp2 others(10): Show |
intron_variant | MODIFIER | c.802+5058T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19832195 | |||||||
| chr16:19832222 | C | A | 61 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0013 others(58): Show |
61 | HG00609.hp2 HG00733.hp1 HG00735.hp2 others(58): Show |
intron_variant | MODIFIER | c.802+5085C>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19832222 | |||||||
| chr16:19832382 | T | TGGAG | 70 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0013 others(67): Show |
70 | HG00609.hp2 HG00733.hp1 HG00735.hp2 others(67): Show |
intron_variant | MODIFIER | c.802+5246_802+5249d others(6): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 19832382 | ||||||
| chr16:19832465 | G | A | 1 | a0003c0004t0013g0240 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.802+5328G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19832465 | |||||||
| chr16:19832526 | G | T | 1 | a0001c0001t0001g0127 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.802+5389G>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19832526 | |||||||
| chr16:19832922 | C | T | 1 | a0002c0002t0003g0196 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.802+5785C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19832922 | |||||||
| chr16:19832966 | A | G | 3 | a0001c0001t0009g0239 a0002c0002t0009g0194 a0002c0002t0009g0195 |
3 | HG02486.hp2 HG02895.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.802+5829A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19832966 | |||||||
| chr16:19833017 | G | A | 3 | a0001c0001t0009g0239 a0002c0002t0009g0194 a0002c0002t0009g0195 |
3 | HG02486.hp2 HG02895.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.802+5880G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19833017 | |||||||
| chr16:19833079 | G | T | 3 | a0001c0001t0001g0057 a0001c0001t0001g0060 a0001c0001t0001g0061 |
3 | NA18983.hp2 NA18993.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.802+5942G>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19833079 | |||||||
| chr16:19833276 | T | C | 1 | a0001c0001t0001g0090 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.802+6139T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19833276 | |||||||
| chr16:19833347 | G | A | 10 | a0001c0001t0002g0006 a0001c0001t0002g0034 a0001c0001t0002g0035 others(7): Show |
10 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(7): Show |
intron_variant | MODIFIER | c.802+6210G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19833347 | |||||||
| chr16:19833468 | C | G | 120 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0013 others(117): Show |
120 | HG00609.hp2 HG00733.hp1 HG00733.hp2 others(117): Show |
intron_variant | MODIFIER | c.802+6331C>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19833468 | |||||||
| chr16:19833543 | G | T | 13 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0015g0179 others(10): Show |
13 | HG00733.hp1 HG01255.hp1 HG01433.hp2 others(10): Show |
intron_variant | MODIFIER | c.802+6406G>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19833543 | |||||||
| chr16:19833816 | A | C | 1 | a0001c0001t0001g0030 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.802+6679A>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19833816 | |||||||
| chr16:19834081 | C | T | 3 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0113 |
3 | HG01928.hp2 HG01975.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.802+6944C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19834081 | |||||||
| chr16:19834088 | G | A | 3 | a0001c0001t0009g0239 a0002c0002t0009g0194 a0002c0002t0009g0195 |
3 | HG02486.hp2 HG02895.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.802+6951G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19834088 | |||||||
| chr16:19834101 | C | A | 80 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0013 others(77): Show |
80 | HG00609.hp2 HG00733.hp1 HG00735.hp2 others(77): Show |
intron_variant | MODIFIER | c.802+6964C>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19834101 | |||||||
| chr16:19834204 | G | A | 10 | a0001c0001t0003g0045 a0001c0001t0003g0120 a0001c0001t0005g0019 others(7): Show |
10 | HG02055.hp2 HG02145.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.802+7067G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19834204 | |||||||
| chr16:19834822 | G | A | 1 | a0002c0002t0001g0232 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.802+7685G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19834822 | |||||||
| chr16:19835002 | T | C | 69 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0013 others(66): Show |
69 | HG00609.hp2 HG00733.hp1 HG00735.hp2 others(66): Show |
intron_variant | MODIFIER | c.802+7865T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19835002 | |||||||
| chr16:19835040 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.802+7903G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19835040 | |||||||
| chr16:19835298 | G | A | 1 | a0001c0001t0006g0041 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.802+8161G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19835298 | |||||||
| chr16:19835346 | T | C | 69 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0013 others(66): Show |
69 | HG00609.hp2 HG00733.hp1 HG00735.hp2 others(66): Show |
intron_variant | MODIFIER | c.802+8209T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19835346 | |||||||
| chr16:19835493 | G | A | 2 | a0001c0001t0005g0019 a0001c0001t0005g0020 |
2 | HG02258.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.802+8356G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19835493 | |||||||
| chr16:19835587 | C | CT | 41 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0013 others(38): Show |
41 | HG00609.hp2 HG00735.hp2 HG01433.hp1 others(38): Show |
intron_variant | MODIFIER | c.802+8465dupT | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 19835587 | ||||||
| chr16:19835587 | C | CTTT | 9 | a0001c0001t0004g0005 a0001c0001t0004g0012 a0001c0001t0004g0022 others(6): Show |
9 | HG01109.hp2 HG01884.hp2 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.802+8463_802+8465d others(5): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 19835587 | ||||||
| chr16:19835615 | T | C | 69 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0013 others(66): Show |
69 | HG00609.hp2 HG00733.hp1 HG00735.hp2 others(66): Show |
intron_variant | MODIFIER | c.802+8478T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19835615 | |||||||
| chr16:19835633 | G | A | 3 | a0001c0001t0009g0239 a0002c0002t0009g0194 a0002c0002t0009g0195 |
3 | HG02486.hp2 HG02895.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.802+8496G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19835633 | |||||||
| chr16:19835770 | A | T | 13 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0015g0179 others(10): Show |
13 | HG00733.hp1 HG01255.hp1 HG01433.hp2 others(10): Show |
intron_variant | MODIFIER | c.802+8633A>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19835770 | |||||||
| chr16:19835773 | C | T | 3 | a0001c0001t0009g0239 a0002c0002t0009g0194 a0002c0002t0009g0195 |
3 | HG02486.hp2 HG02895.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.802+8636C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19835773 | |||||||
| chr16:19835865 | G | A | 7 | a0001c0001t0007g0163 a0001c0001t0007g0165 a0001c0001t0007g0166 others(4): Show |
7 | HG01884.hp1 HG02257.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.802+8728G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19835865 | |||||||
| chr16:19835896 | C | T | 3 | a0001c0001t0009g0239 a0002c0002t0009g0194 a0002c0002t0009g0195 |
3 | HG02486.hp2 HG02895.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.802+8759C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19835896 | |||||||
| chr16:19835903 | A | G | 35 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0013 others(32): Show |
35 | HG00609.hp2 HG00735.hp2 HG01433.hp1 others(32): Show |
intron_variant | MODIFIER | c.802+8766A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19835903 | |||||||
| chr16:19836044 | A | G | 69 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0013 others(66): Show |
69 | HG00609.hp2 HG00733.hp1 HG00735.hp2 others(66): Show |
intron_variant | MODIFIER | c.802+8907A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19836044 | |||||||
| chr16:19836248 | A | C | 68 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0013 others(65): Show |
68 | HG00609.hp2 HG00733.hp1 HG00735.hp2 others(65): Show |
intron_variant | MODIFIER | c.802+9111A>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19836248 | |||||||
| chr16:19836661 | A | G | 1 | a0001c0001t0002g0004 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.802+9524A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19836661 | |||||||
| chr16:19836662 | C | T | 2 | a0001c0001t0002g0004 a0002c0002t0001g0220 |
2 | NA18612.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.802+9525C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19836662 | |||||||
| chr16:19836704 | G | A | 1 | a0001c0001t0001g0064 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.802+9567G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19836704 | |||||||
| chr16:19836726 | A | C | 1 | a0001c0001t0006g0118 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.802+9589A>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19836726 | |||||||
| chr16:19836729 | C | G | 3 | a0001c0001t0007g0163 a0001c0001t0007g0170 a0001c0001t0018g0164 |
3 | HG02258.hp1 HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.802+9592C>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19836729 | |||||||
| chr16:19836794 | T | G | 1 | a0001c0001t0002g0094 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.802+9657T>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19836794 | |||||||
| chr16:19836802 | G | A | 1 | a0001c0001t0002g0085 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.802+9665G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19836802 | |||||||
| chr16:19836860 | C | T | 3 | a0001c0001t0009g0239 a0002c0002t0009g0194 a0002c0002t0009g0195 |
3 | HG02486.hp2 HG02895.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.802+9723C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19836860 | |||||||
| chr16:19836906 | A | T | 1 | a0002c0002t0001g0227 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.802+9769A>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19836906 | |||||||
| chr16:19837042 | G | A | 1 | a0001c0001t0002g0088 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.802+9905G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19837042 | |||||||
| chr16:19837184 | C | T | 34 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0013 others(31): Show |
34 | HG00609.hp2 HG00735.hp2 HG01433.hp1 others(31): Show |
intron_variant | MODIFIER | c.802+10047C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19837184 | |||||||
| chr16:19837200 | C | T | 2 | a0001c0001t0007g0163 a0001c0001t0018g0164 |
2 | HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.802+10063C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19837200 | |||||||
| chr16:19837296 | G | T | 1 | a0001c0001t0001g0040 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.802+10159G>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19837296 | |||||||
| chr16:19837350 | A | G | 3 | a0001c0001t0009g0239 a0002c0002t0009g0194 a0002c0002t0009g0195 |
3 | HG02486.hp2 HG02895.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.802+10213A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19837350 | |||||||
| chr16:19837957 | AGTTCCTG others(3): Show |
A | 3 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0100 |
3 | HG00597.hp1 HG02074.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.802+10822_802+1083 others(14): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 19837957 | ||||||
| chr16:19838424 | G | A | 2 | a0001c0001t0001g0135 a0001c0001t0003g0136 |
2 | HG02451.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.802+11287G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19838424 | |||||||
| chr16:19838611 | G | T | 1 | a0001c0001t0002g0119 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.802+11474G>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19838611 | |||||||
| chr16:19838710 | C | T | 1 | a0001c0001t0001g0106 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.802+11573C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19838710 | |||||||
| chr16:19838866 | A | G | 2 | a0001c0001t0002g0119 a0001c0001t0002g0242 |
2 | HG02622.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.802+11729A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19838866 | |||||||
| chr16:19838932 | T | C | 9 | a0001c0001t0004g0005 a0001c0001t0004g0012 a0001c0001t0004g0022 others(6): Show |
9 | HG01109.hp2 HG01884.hp2 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.802+11795T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19838932 | |||||||
| chr16:19839018 | C | CA | 20 | a0001c0001t0001g0040 a0001c0001t0001g0061 a0001c0001t0001g0063 others(17): Show |
20 | HG00735.hp1 HG01175.hp1 HG01928.hp2 others(17): Show |
intron_variant | MODIFIER | c.802+11905dupA | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 19839018 | ||||||
| chr16:19839018 | CA | C | 20 | a0001c0001t0001g0126 a0001c0001t0001g0156 a0001c0001t0001g0157 others(17): Show |
20 | HG00733.hp1 HG01255.hp1 HG01433.hp2 others(17): Show |
intron_variant | MODIFIER | c.802+11905delA | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 19839018 | ||||||
| chr16:19839018 | CAA | C | 28 | a0001c0001t0001g0013 a0001c0001t0001g0018 a0001c0001t0001g0066 others(25): Show |
28 | HG00597.hp2 HG00639.hp1 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.802+11904_802+1190 others(6): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 19839018 | ||||||
| chr16:19839018 | CAAA | C | 68 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0014 others(65): Show |
68 | HG00099.hp2 HG00609.hp1 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.802+11903_802+1190 others(7): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 19839018 | ||||||
| chr16:19839106 | C | T | 80 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0013 others(77): Show |
80 | HG00099.hp2 HG00597.hp2 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.802+11969C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19839106 | |||||||
| chr16:19839144 | AATTT | A | 114 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0013 others(111): Show |
114 | HG00099.hp2 HG00597.hp2 HG00609.hp1 others(111): Show |
intron_variant | MODIFIER | c.802+12036_802+1203 others(8): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 19839144 | ||||||
| chr16:19839214 | G | A | 9 | a0001c0001t0004g0005 a0001c0001t0004g0012 a0001c0001t0004g0022 others(6): Show |
9 | HG01109.hp2 HG01884.hp2 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.802+12077G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19839214 | |||||||
| chr16:19839216 | A | C | 1 | a0001c0001t0001g0082 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.802+12079A>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19839216 | |||||||
| chr16:19839228 | T | G | 9 | a0001c0001t0004g0005 a0001c0001t0004g0012 a0001c0001t0004g0022 others(6): Show |
9 | HG01109.hp2 HG01884.hp2 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.802+12091T>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19839228 | |||||||
| chr16:19839230 | G | T | 3 | a0001c0001t0002g0006 a0001c0001t0002g0081 a0001c0001t0002g0093 |
3 | HG00639.hp2 HG01175.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.802+12093G>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19839230 | |||||||
| chr16:19839310 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.802+12173G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19839310 | |||||||
| chr16:19839324 | C | T | 1 | a0001c0001t0002g0050 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.802+12187C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19839324 | |||||||
| chr16:19839404 | A | T | 111 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0013 others(108): Show |
111 | HG00099.hp2 HG00597.hp2 HG00609.hp1 others(108): Show |
intron_variant | MODIFIER | c.802+12267A>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19839404 | |||||||
| chr16:19839439 | G | T | 1 | a0001c0001t0001g0017 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.802+12302G>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19839439 | |||||||
| chr16:19839748 | C | A | 4 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0133 others(1): Show |
4 | HG02622.hp1 HG02630.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.802+12611C>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19839748 | |||||||
| chr16:19839851 | T | C | 1 | a0002c0002t0003g0203 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.802+12714T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19839851 | |||||||
| chr16:19840031 | C | CA | 8 | a0001c0001t0001g0127 a0001c0001t0001g0148 a0001c0001t0001g0151 others(5): Show |
8 | HG00733.hp2 HG01081.hp1 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.802+12908dupA | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 19840031 | ||||||
| chr16:19840031 | C | CAA | 9 | a0001c0001t0004g0005 a0001c0001t0004g0012 a0001c0001t0004g0022 others(6): Show |
9 | HG01109.hp2 HG01884.hp2 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.802+12907_802+1290 others(6): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 19840031 | ||||||
| chr16:19840076 | T | C | 46 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0003g0096 others(43): Show |
46 | HG00099.hp2 HG00597.hp2 HG00609.hp1 others(43): Show |
intron_variant | MODIFIER | c.802+12939T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19840076 | |||||||
| chr16:19840127 | T | A | 9 | a0001c0001t0004g0005 a0001c0001t0004g0012 a0001c0001t0004g0022 others(6): Show |
9 | HG01109.hp2 HG01884.hp2 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.802+12990T>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19840127 | |||||||
| chr16:19840351 | G | A | 111 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0013 others(108): Show |
111 | HG00099.hp2 HG00597.hp2 HG00609.hp1 others(108): Show |
intron_variant | MODIFIER | c.802+13214G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19840351 | |||||||
| chr16:19840388 | G | A | 3 | a0001c0001t0009g0239 a0002c0002t0009g0194 a0002c0002t0009g0195 |
3 | HG02486.hp2 HG02895.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.802+13251G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19840388 | |||||||
| chr16:19840418 | T | C | 1 | a0001c0001t0003g0123 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.802+13281T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19840418 | |||||||
| chr16:19840538 | A | G | 3 | a0001c0001t0009g0239 a0002c0002t0009g0194 a0002c0002t0009g0195 |
3 | HG02486.hp2 HG02895.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.802+13401A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19840538 | |||||||
| chr16:19840775 | C | T | 2 | a0001c0001t0002g0001 a0001c0001t0002g0029 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.802+13638C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19840775 | |||||||
| chr16:19841003 | T | A | 2 | a0001c0001t0001g0014 a0001c0001t0001g0146 |
2 | HG02280.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.802+13866T>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19841003 | |||||||
| chr16:19841191 | A | C | 1 | a0001c0001t0001g0105 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.802+14054A>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19841191 | |||||||
| chr16:19841336 | A | T | 1 | a0002c0002t0001g0182 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.802+14199A>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19841336 | |||||||
| chr16:19841473 | G | T | 1 | a0001c0001t0001g0141 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.802+14336G>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19841473 | |||||||
| chr16:19841492 | C | A | 114 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0013 others(111): Show |
114 | HG00099.hp2 HG00597.hp2 HG00609.hp1 others(111): Show |
intron_variant | MODIFIER | c.802+14355C>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19841492 | |||||||
| chr16:19841570 | A | G | 3 | a0001c0001t0009g0239 a0002c0002t0009g0194 a0002c0002t0009g0195 |
3 | HG02486.hp2 HG02895.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.802+14433A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19841570 | |||||||
| chr16:19841684 | T | A | 6 | a0001c0001t0001g0003 a0001c0001t0001g0082 a0001c0001t0001g0083 others(3): Show |
6 | HG01167.hp2 HG01255.hp2 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.802+14547T>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19841684 | |||||||
| chr16:19841847 | CT | C | 114 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0013 others(111): Show |
114 | HG00099.hp2 HG00323.hp1 HG00597.hp2 others(111): Show |
intron_variant | MODIFIER | c.803-14625delT | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 19841847 | ||||||
| chr16:19841867 | C | T | 111 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0013 others(108): Show |
111 | HG00099.hp2 HG00597.hp2 HG00609.hp1 others(108): Show |
intron_variant | MODIFIER | c.803-14620C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19841867 | |||||||
| chr16:19842455 | T | G | 46 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0003g0096 others(43): Show |
46 | HG00099.hp2 HG00597.hp2 HG00609.hp1 others(43): Show |
intron_variant | MODIFIER | c.803-14032T>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19842455 | |||||||
| chr16:19842902 | T | C | 239 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(236): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.803-13585T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19842902 | |||||||
| chr16:19842937 | A | T | 102 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0013 others(99): Show |
102 | HG00099.hp2 HG00597.hp2 HG00609.hp1 others(99): Show |
intron_variant | MODIFIER | c.803-13550A>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19842937 | |||||||
| chr16:19843072 | CT | C | 45 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0003g0096 others(42): Show |
45 | HG00099.hp2 HG00597.hp2 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.803-13413delT | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 19843072 | ||||||
| chr16:19843333 | G | A | 114 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0013 others(111): Show |
114 | HG00099.hp2 HG00597.hp2 HG00609.hp1 others(111): Show |
intron_variant | MODIFIER | c.803-13154G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19843333 | |||||||
| chr16:19843536 | G | A | 1 | a0001c0001t0001g0162 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.803-12951G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19843536 | |||||||
| chr16:19843605 | A | T | 114 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0013 others(111): Show |
114 | HG00099.hp2 HG00597.hp2 HG00609.hp1 others(111): Show |
intron_variant | MODIFIER | c.803-12882A>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19843605 | |||||||
| chr16:19843711 | G | A | 3 | a0001c0001t0002g0002 a0001c0001t0002g0031 a0001c0001t0002g0107 |
3 | NA18946.hp2 NA19009.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.803-12776G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19843711 | |||||||
| chr16:19844010 | C | T | 1 | a0001c0001t0006g0099 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.803-12477C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19844010 | |||||||
| chr16:19844075 | T | C | 1 | a0001c0001t0001g0126 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.803-12412T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19844075 | |||||||
| chr16:19844081 | C | CT | 16 | a0001c0001t0001g0075 a0001c0001t0001g0129 a0001c0001t0001g0131 others(13): Show |
16 | HG01081.hp1 HG01109.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.803-12390dupT | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 19844081 | ||||||
| chr16:19844142 | C | T | 7 | a0001c0001t0007g0163 a0001c0001t0007g0165 a0001c0001t0007g0166 others(4): Show |
7 | HG01884.hp1 HG02257.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.803-12345C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19844142 | |||||||
| chr16:19844240 | C | T | 111 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0013 others(108): Show |
111 | HG00099.hp2 HG00597.hp2 HG00609.hp1 others(108): Show |
intron_variant | MODIFIER | c.803-12247C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19844240 | |||||||
| chr16:19844340 | A | G | 1 | a0002c0002t0003g0192 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.803-12147A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19844340 | |||||||
| chr16:19844544 | C | T | 114 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0013 others(111): Show |
114 | HG00099.hp2 HG00597.hp2 HG00609.hp1 others(111): Show |
intron_variant | MODIFIER | c.803-11943C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19844544 | |||||||
| chr16:19844630 | T | A | 1 | a0002c0002t0003g0198 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.803-11857T>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19844630 | |||||||
| chr16:19844663 | G | A | 22 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0007g0163 others(19): Show |
22 | HG00733.hp1 HG01255.hp1 HG01433.hp2 others(19): Show |
intron_variant | MODIFIER | c.803-11824G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19844663 | |||||||
| chr16:19845055 | C | T | 1 | a0001c0001t0002g0035 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.803-11432C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19845055 | |||||||
| chr16:19845312 | A | G | 1 | a0001c0001t0004g0026 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.803-11175A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19845312 | |||||||
| chr16:19845379 | G | T | 1 | a0001c0001t0001g0160 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.803-11108G>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19845379 | |||||||
| chr16:19845730 | A | G | 1 | a0001c0001t0007g0170 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.803-10757A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19845730 | |||||||
| chr16:19845817 | G | A | 1 | a0001c0001t0012g0243 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.803-10670G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19845817 | |||||||
| chr16:19845872 | C | T | 2 | a0001c0001t0001g0167 a0001c0001t0001g0171 |
2 | HG03225.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.803-10615C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19845872 | |||||||
| chr16:19845994 | C | G | 7 | a0001c0001t0007g0163 a0001c0001t0007g0165 a0001c0001t0007g0166 others(4): Show |
7 | HG01884.hp1 HG02257.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.803-10493C>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19845994 | |||||||
| chr16:19846174 | A | G | 2 | a0001c0001t0002g0042 a0001c0001t0002g0052 |
2 | HG00099.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.803-10313A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19846174 | |||||||
| chr16:19846543 | G | A | 44 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0003g0096 others(41): Show |
44 | HG00099.hp2 HG00597.hp2 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.803-9944G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19846543 | |||||||
| chr16:19846544 | C | T | 1 | a0001c0001t0005g0033 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.803-9943C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19846544 | |||||||
| chr16:19846618 | C | T | 1 | a0001c0001t0001g0040 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.803-9869C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19846618 | |||||||
| chr16:19846696 | C | G | 1 | a0001c0001t0019g0238 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.803-9791C>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19846696 | |||||||
| chr16:19846773 | A | T | 1 | a0001c0001t0001g0055 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.803-9714A>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19846773 | |||||||
| chr16:19846801 | G | A | 44 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0003g0096 others(41): Show |
44 | HG00099.hp2 HG00597.hp2 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.803-9686G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19846801 | |||||||
| chr16:19846817 | A | AT | 9 | a0001c0001t0004g0005 a0001c0001t0004g0012 a0001c0001t0004g0022 others(6): Show |
9 | HG01109.hp2 HG01884.hp2 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.803-9660dupT | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 19846817 | ||||||
| chr16:19847247 | G | T | 3 | a0001c0001t0009g0239 a0002c0002t0009g0194 a0002c0002t0009g0195 |
3 | HG02486.hp2 HG02895.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.803-9240G>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19847247 | |||||||
| chr16:19847321 | TC | T | 9 | a0001c0001t0004g0005 a0001c0001t0004g0012 a0001c0001t0004g0022 others(6): Show |
9 | HG01109.hp2 HG01884.hp2 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.803-9164delC | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 19847321 | ||||||
| chr16:19847500 | T | C | 113 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0013 others(110): Show |
113 | HG00099.hp2 HG00597.hp2 HG00609.hp1 others(110): Show |
intron_variant | MODIFIER | c.803-8987T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19847500 | |||||||
| chr16:19847531 | A | G | 11 | a0001c0001t0003g0045 a0001c0001t0003g0120 a0001c0001t0003g0123 others(8): Show |
11 | HG02055.hp2 HG02145.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.803-8956A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19847531 | |||||||
| chr16:19847581 | T | C | 14 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0042 others(11): Show |
14 | HG00099.hp1 HG01074.hp2 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.803-8906T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19847581 | |||||||
| chr16:19847584 | T | C | 13 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0015g0179 others(10): Show |
13 | HG00733.hp1 HG01255.hp1 HG01433.hp2 others(10): Show |
intron_variant | MODIFIER | c.803-8903T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19847584 | |||||||
| chr16:19847598 | C | G | 1 | a0002c0002t0001g0226 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.803-8889C>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19847598 | |||||||
| chr16:19847774 | A | C | 1 | a0002c0002t0001g0204 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.803-8713A>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19847774 | |||||||
| chr16:19847826 | G | T | 6 | a0002c0002t0001g0189 a0002c0002t0001g0201 a0002c0002t0001g0216 others(3): Show |
6 | NA18963.hp2 NA18967.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.803-8661G>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19847826 | |||||||
| chr16:19847855 | T | G | 1 | a0002c0002t0001g0223 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.803-8632T>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19847855 | |||||||
| chr16:19847904 | G | C | 1 | a0001c0001t0002g0086 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.803-8583G>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19847904 | |||||||
| chr16:19848010 | G | A | 22 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0007g0163 others(19): Show |
22 | HG00733.hp1 HG01255.hp1 HG01433.hp2 others(19): Show |
intron_variant | MODIFIER | c.803-8477G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19848010 | |||||||
| chr16:19848084 | G | A | 181 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(178): Show |
181 | HG00099.hp2 HG00140.hp1 HG00597.hp1 others(178): Show |
intron_variant | MODIFIER | c.803-8403G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19848084 | |||||||
| chr16:19848098 | C | T | 1 | a0001c0001t0005g0033 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.803-8389C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19848098 | |||||||
| chr16:19848258 | C | A | 2 | a0002c0002t0001g0183 a0002c0002t0001g0230 |
2 | HG03704.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.803-8229C>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19848258 | |||||||
| chr16:19848281 | T | G | 1 | a0002c0002t0001g0193 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.803-8206T>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19848281 | |||||||
| chr16:19848357 | A | G | 3 | a0001c0001t0002g0001 a0001c0001t0002g0027 a0001c0001t0002g0029 |
3 | HG02895.hp1 HG02897.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.803-8130A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19848357 | |||||||
| chr16:19848398 | C | T | 45 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0003g0096 others(42): Show |
45 | HG00099.hp2 HG00597.hp2 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.803-8089C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19848398 | |||||||
| chr16:19848511 | A | G | 3 | a0001c0001t0003g0045 a0001c0001t0003g0120 a0001c0001t0003g0123 |
3 | HG03225.hp1 HG03453.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.803-7976A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19848511 | |||||||
| chr16:19848529 | T | C | 13 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0015g0179 others(10): Show |
13 | HG00733.hp1 HG01255.hp1 HG01433.hp2 others(10): Show |
intron_variant | MODIFIER | c.803-7958T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19848529 | |||||||
| chr16:19848764 | A | C | 3 | a0001c0001t0007g0166 a0001c0001t0007g0168 a0001c0001t0007g0169 |
3 | HG01884.hp1 HG02257.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.803-7723A>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19848764 | |||||||
| chr16:19848787 | A | T | 3 | a0001c0001t0002g0069 a0001c0001t0002g0079 a0001c0001t0002g0085 |
3 | HG01167.hp1 HG02738.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.803-7700A>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19848787 | |||||||
| chr16:19848999 | G | A | 1 | a0001c0001t0002g0042 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.803-7488G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19848999 | |||||||
| chr16:19849067 | A | G | 1 | a0002c0002t0001g0189 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.803-7420A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19849067 | |||||||
| chr16:19849075 | G | C | 1 | a0001c0001t0001g0075 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.803-7412G>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19849075 | |||||||
| chr16:19849261 | G | GT | 53 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(50): Show |
53 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(50): Show |
intron_variant | MODIFIER | c.803-7212dupT | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 19849261 | ||||||
| chr16:19849261 | G | GTT | 24 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0066 others(21): Show |
24 | HG00609.hp2 HG00733.hp1 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.803-7213_803-7212d others(4): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 19849261 | ||||||
| chr16:19849275 | T | A | 1 | a0002c0002t0001g0201 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.803-7212T>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19849275 | |||||||
| chr16:19849309 | A | G | 7 | a0001c0001t0007g0163 a0001c0001t0007g0165 a0001c0001t0007g0166 others(4): Show |
7 | HG01884.hp1 HG02257.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.803-7178A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19849309 | |||||||
| chr16:19849514 | C | T | 3 | a0001c0001t0009g0239 a0002c0002t0009g0194 a0002c0002t0009g0195 |
3 | HG02486.hp2 HG02895.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.803-6973C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19849514 | |||||||
| chr16:19849724 | G | C | 3 | a0001c0001t0009g0239 a0002c0002t0009g0194 a0002c0002t0009g0195 |
3 | HG02486.hp2 HG02895.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.803-6763G>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19849724 | |||||||
| chr16:19849762 | G | GA | 8 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0050 others(5): Show |
8 | HG01928.hp2 HG01975.hp2 HG02300.hp1 others(5): Show |
intron_variant | MODIFIER | c.803-6714dupA | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 19849762 | ||||||
| chr16:19849983 | T | C | 190 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(187): Show |
190 | HG00099.hp2 HG00140.hp1 HG00597.hp1 others(187): Show |
intron_variant | MODIFIER | c.803-6504T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19849983 | |||||||
| chr16:19849989 | G | A | 1 | a0002c0002t0003g0199 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.803-6498G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19849989 | |||||||
| chr16:19850235 | G | A | 46 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0003g0096 others(43): Show |
46 | HG00099.hp2 HG00597.hp2 HG00609.hp1 others(43): Show |
intron_variant | MODIFIER | c.803-6252G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19850235 | |||||||
| chr16:19850285 | A | G | 35 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0013 others(32): Show |
35 | HG00609.hp2 HG00735.hp2 HG01433.hp1 others(32): Show |
intron_variant | MODIFIER | c.803-6202A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19850285 | |||||||
| chr16:19850355 | G | A | 1 | a0002c0002t0001g0230 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.803-6132G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19850355 | |||||||
| chr16:19850525 | G | A | 1 | a0002c0002t0009g0194 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.803-5962G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19850525 | |||||||
| chr16:19850940 | T | C | 3 | a0001c0001t0009g0239 a0002c0002t0009g0194 a0002c0002t0009g0195 |
3 | HG02486.hp2 HG02895.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.803-5547T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19850940 | |||||||
| chr16:19851017 | T | C | 2 | a0001c0001t0005g0019 a0001c0001t0005g0020 |
2 | HG02258.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.803-5470T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19851017 | |||||||
| chr16:19851034 | C | T | 89 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0013 others(86): Show |
89 | HG00099.hp2 HG00597.hp2 HG00609.hp1 others(86): Show |
intron_variant | MODIFIER | c.803-5453C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19851034 | |||||||
| chr16:19851515 | G | A | 1 | a0002c0002t0001g0183 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.803-4972G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19851515 | |||||||
| chr16:19851645 | G | A | 1 | a0002c0002t0001g0177 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.803-4842G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19851645 | |||||||
| chr16:19851663 | C | T | 1 | a0003c0004t0013g0240 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.803-4824C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19851663 | |||||||
| chr16:19851708 | C | T | 1 | a0001c0001t0006g0041 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.803-4779C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19851708 | |||||||
| chr16:19851792 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.803-4695C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19851792 | |||||||
| chr16:19851843 | C | G | 3 | a0001c0001t0003g0045 a0001c0001t0003g0120 a0001c0001t0003g0123 |
3 | HG03225.hp1 HG03453.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.803-4644C>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19851843 | |||||||
| chr16:19851942 | C | T | 4 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0090 others(1): Show |
4 | HG01167.hp2 HG01255.hp2 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.803-4545C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19851942 | |||||||
| chr16:19852355 | C | A | 1 | a0001c0001t0003g0096 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.803-4132C>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19852355 | |||||||
| chr16:19852407 | TAACAAAC others(1): Show |
T | 37 | a0001c0001t0001g0003 a0001c0001t0001g0048 a0001c0001t0001g0051 others(34): Show |
37 | HG00140.hp1 HG00597.hp1 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.803-4059_803-4052d others(10): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 19852407 | ||||||
| chr16:19852463 | T | TC | 7 | a0001c0001t0001g0134 a0001c0001t0001g0142 a0001c0001t0001g0143 others(4): Show |
7 | HG02717.hp2 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.803-4019dupC | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 19852463 | ||||||
| chr16:19852583 | A | G | 9 | a0001c0001t0004g0005 a0001c0001t0004g0012 a0001c0001t0004g0022 others(6): Show |
9 | HG01109.hp2 HG01884.hp2 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.803-3904A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19852583 | |||||||
| chr16:19852619 | C | CT | 11 | a0001c0001t0001g0011 a0001c0001t0001g0061 a0001c0001t0001g0114 others(8): Show |
11 | HG01928.hp1 HG01934.hp1 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.803-3847dupT | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 19852619 | ||||||
| chr16:19852619 | CT | C | 7 | a0001c0001t0001g0083 a0001c0001t0001g0162 a0001c0001t0002g0009 others(4): Show |
7 | HG01167.hp2 HG01975.hp2 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.803-3847delT | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 19852619 | ||||||
| chr16:19852673 | A | G | 3 | a0001c0001t0009g0239 a0002c0002t0009g0194 a0002c0002t0009g0195 |
3 | HG02486.hp2 HG02895.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.803-3814A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19852673 | |||||||
| chr16:19852772 | G | A | 1 | a0001c0001t0006g0073 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.803-3715G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19852772 | |||||||
| chr16:19852868 | C | T | 2 | a0001c0001t0002g0084 a0002c0002t0002g0218 |
2 | HG02056.hp2 HG02074.hp1 |
intron_variant | MODIFIER | c.803-3619C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19852868 | |||||||
| chr16:19852966 | C | T | 3 | a0001c0001t0009g0239 a0002c0002t0009g0194 a0002c0002t0009g0195 |
3 | HG02486.hp2 HG02895.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.803-3521C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19852966 | |||||||
| chr16:19852999 | G | T | 13 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0015g0179 others(10): Show |
13 | HG00733.hp1 HG01255.hp1 HG01433.hp2 others(10): Show |
intron_variant | MODIFIER | c.803-3488G>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19852999 | |||||||
| chr16:19853236 | G | A | 114 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0013 others(111): Show |
114 | HG00099.hp2 HG00597.hp2 HG00609.hp1 others(111): Show |
intron_variant | MODIFIER | c.803-3251G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19853236 | |||||||
| chr16:19853454 | T | G | 3 | a0001c0001t0002g0069 a0001c0001t0002g0079 a0001c0001t0002g0085 |
3 | HG01167.hp1 HG02738.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.803-3033T>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19853454 | |||||||
| chr16:19853513 | C | T | 14 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0015g0179 others(11): Show |
14 | HG00733.hp1 HG01255.hp1 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.803-2974C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19853513 | |||||||
| chr16:19853593 | T | G | 1 | a0002c0002t0003g0203 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.803-2894T>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19853593 | |||||||
| chr16:19853786 | C | T | 80 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0013 others(77): Show |
80 | HG00099.hp2 HG00597.hp2 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.803-2701C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19853786 | |||||||
| chr16:19853974 | G | A | 3 | a0001c0001t0009g0239 a0002c0002t0009g0194 a0002c0002t0009g0195 |
3 | HG02486.hp2 HG02895.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.803-2513G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19853974 | |||||||
| chr16:19854356 | T | G | 1 | a0001c0001t0019g0238 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.803-2131T>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19854356 | |||||||
| chr16:19854481 | G | A | 28 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0013 others(25): Show |
28 | HG00609.hp2 HG00735.hp2 HG01433.hp1 others(25): Show |
intron_variant | MODIFIER | c.803-2006G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19854481 | |||||||
| chr16:19854608 | TGCACTAG others(24): Show |
T | 1 | a0001c0001t0015g0179 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.803-1877_803-1847d others(33): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 19854608 | ||||||
| chr16:19854818 | C | T | 7 | a0001c0001t0007g0163 a0001c0001t0007g0165 a0001c0001t0007g0166 others(4): Show |
7 | HG01884.hp1 HG02257.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.803-1669C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19854818 | |||||||
| chr16:19854840 | C | T | 1 | a0003c0004t0013g0240 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.803-1647C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19854840 | |||||||
| chr16:19854935 | T | C | 1 | a0001c0001t0001g0083 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.803-1552T>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19854935 | |||||||
| chr16:19855438 | A | C | 22 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0007g0163 others(19): Show |
22 | HG00733.hp1 HG01255.hp1 HG01433.hp2 others(19): Show |
intron_variant | MODIFIER | c.803-1049A>C | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19855438 | |||||||
| chr16:19855605 | A | ATGATGTA others(42): Show |
1 | a0001c0001t0015g0179 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.803-880_803-879ins others(49): Show |
IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 19855605 | ||||||
| chr16:19855611 | T | G | 1 | a0001c0001t0015g0179 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.803-876T>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19855611 | |||||||
| chr16:19855627 | C | G | 1 | a0001c0001t0015g0179 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.803-860C>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19855627 | |||||||
| chr16:19855634 | C | A | 1 | a0001c0001t0015g0179 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.803-853C>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19855634 | |||||||
| chr16:19855648 | T | G | 1 | a0001c0001t0015g0179 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.803-839T>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19855648 | |||||||
| chr16:19855680 | A | T | 1 | a0001c0001t0015g0179 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.803-807A>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19855680 | |||||||
| chr16:19855696 | A | G | 1 | a0001c0001t0015g0179 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.803-791A>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19855696 | |||||||
| chr16:19855699 | C | T | 22 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0007g0163 others(19): Show |
22 | HG00733.hp1 HG01255.hp1 HG01433.hp2 others(19): Show |
intron_variant | MODIFIER | c.803-788C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19855699 | |||||||
| chr16:19856046 | C | T | 46 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0003g0096 others(43): Show |
46 | HG00099.hp2 HG00597.hp2 HG00609.hp1 others(43): Show |
intron_variant | MODIFIER | c.803-441C>T | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19856046 | |||||||
| chr16:19856156 | G | A | 1 | a0003c0004t0013g0240 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.803-331G>A | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19856156 | |||||||
| chr16:19856350 | C | G | 34 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0013 others(31): Show |
34 | HG00609.hp2 HG00735.hp2 HG01433.hp1 others(31): Show |
intron_variant | MODIFIER | c.803-137C>G | IQCK | ENSG00000174628.17 | transcript | ENST00000695302.1 | protein_coding | 8/8 | chr16 | 19856350 |