Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 154661 |
| ensemblid | ENSG00000105784.16 |
| hgncid | 30286 |
| symbol | RUNDC3B |
| name | RUN domain containing 3B |
| refseq_nuc | NM_001134405.2 |
| refseq_prot | NP_001127877.1 |
| ensembl_nuc | ENST00000394654.4 |
| ensembl_prot | ENSP00000378149.3 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 87628398 |
| end | 87832296 |
| strand | + |
| ver | v1.2 |
| region | chr7:87628398-87832296 |
| region5000 | chr7:87623398-87837296 |
| regionname0 | RUNDC3B_chr7_87628398_87832296 |
| regionname5000 | RUNDC3B_chr7_87623398_87837296 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 456 | 199 | 62 | 42 | 65 | 8 | 20 | 47 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | MASRS others(451): Show |
chr7 | 87623398 | 87837296 |
| a0002 | 0/0 | 456 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | MASRS others(451): Show |
chr7 | 87623398 | 87837296 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1368 | 198 | 62 | 42 | 65 | 8 | 19 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | ATGGC others(1363): Show |
chr7 | 87623398 | 87837296 | ||
| a0001c0003 | 0/0 | 1368 | 1 | 0 | 0 | 0 | 0 | 1 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | ATGGC others(1363): Show |
chr7 | 87623398 | 87837296 | ||
| a0002c0002 | 0/0 | 1368 | 3 | 0 | 0 | 3 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | ATGGC others(1363): Show |
chr7 | 87623398 | 87837296 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4053 | 23 | 1 | 6 | 10 | 3 | 3 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | GCCGC others(4048): Show |
chr7 | 87623398 | 87837296 |
| a0001c0001t0002 | 0/0 | 4059 | 10 | 7 | 2 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | GCCGC others(4054): Show |
chr7 | 87623398 | 87837296 |
| a0001c0001t0003 | 0/0 | 4055 | 11 | 1 | 4 | 5 | 0 | 1 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | GCCGC others(4050): Show |
chr7 | 87623398 | 87837296 |
| a0001c0001t0004 | 0/0 | 4059 | 10 | 3 | 3 | 3 | 0 | 1 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | GCCGC others(4054): Show |
chr7 | 87623398 | 87837296 |
| a0001c0001t0005 | 0/0 | 4061 | 10 | 1 | 2 | 5 | 1 | 1 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | GCCGC others(4056): Show |
chr7 | 87623398 | 87837296 |
| a0001c0001t0006 | 0/0 | 4057 | 8 | 1 | 0 | 5 | 1 | 1 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | GCCGC others(4052): Show |
chr7 | 87623398 | 87837296 |
| a0001c0001t0007 | 1/0 | 4063 | 7 | 1 | 1 | 4 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | GCCGC others(4058): Show |
chr7 | 87623398 | 87837296 |
| a0001c0001t0008 | 0/1 | 4065 | 7 | 4 | 1 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | GCCGC others(4060): Show |
chr7 | 87623398 | 87837296 |
| a0001c0001t0009 | 0/0 | 4057 | 5 | 0 | 4 | 0 | 1 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | GCCGC others(4052): Show |
chr7 | 87623398 | 87837296 |
| a0001c0001t0010 | 0/0 | 4055 | 4 | 4 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | GCCGC others(4050): Show |
chr7 | 87623398 | 87837296 |
| a0001c0001t0011 | 0/0 | 4057 | 4 | 0 | 1 | 0 | 1 | 2 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | GCCGC others(4052): Show |
chr7 | 87623398 | 87837296 |
| a0001c0001t0012 | 0/0 | 4063 | 4 | 3 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | GCCGC others(4058): Show |
chr7 | 87623398 | 87837296 |
| a0001c0001t0013 | 0/0 | 4059 | 3 | 0 | 2 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | GCCGC others(4054): Show |
chr7 | 87623398 | 87837296 |
| a0001c0001t0014 | 0/0 | 4068 | 3 | 0 | 0 | 3 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | GCCGC others(4063): Show |
chr7 | 87623398 | 87837296 |
| a0001c0001t0015 | 0/0 | 4064 | 3 | 0 | 0 | 3 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | GCCGC others(4059): Show |
chr7 | 87623398 | 87837296 |
| a0001c0001t0016 | 0/0 | 4054 | 3 | 3 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | GCCGC others(4049): Show |
chr7 | 87623398 | 87837296 |
| a0001c0001t0017 | 0/0 | 4059 | 3 | 0 | 3 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | GCCGC others(4054): Show |
chr7 | 87623398 | 87837296 |
| a0001c0001t0018 | 0/0 | 4061 | 2 | 2 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | GCCGC others(4056): Show |
chr7 | 87623398 | 87837296 |
| a0001c0001t0019 | 0/0 | 4065 | 3 | 0 | 2 | 0 | 0 | 1 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | GCCGC others(4060): Show |
chr7 | 87623398 | 87837296 |
| a0001c0001t0020 | 0/0 | 4059 | 2 | 0 | 0 | 2 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | GCCGC others(4054): Show |
chr7 | 87623398 | 87837296 |
| a0001c0001t0021 | 0/0 | 4061 | 2 | 0 | 0 | 2 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | GCCGC others(4056): Show |
chr7 | 87623398 | 87837296 |
| a0001c0001t0022 | 0/0 | 4061 | 2 | 1 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | GCCGC others(4056): Show |
chr7 | 87623398 | 87837296 |
| a0001c0001t0023 | 0/0 | 4062 | 2 | 0 | 0 | 2 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | GCCGC others(4057): Show |
chr7 | 87623398 | 87837296 |
| a0001c0001t0024 | 0/0 | 4061 | 2 | 2 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | GCCGC others(4056): Show |
chr7 | 87623398 | 87837296 |
| a0001c0001t0025 | 0/0 | 4060 | 2 | 1 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | GCCGC others(4055): Show |
chr7 | 87623398 | 87837296 |
| a0001c0001t0026 | 0/0 | 4051 | 2 | 0 | 0 | 1 | 0 | 1 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | GCCGC others(4046): Show |
chr7 | 87623398 | 87837296 |
| a0001c0001t0027 | 0/0 | 4057 | 2 | 1 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | GCCGC others(4052): Show |
chr7 | 87623398 | 87837296 |
| a0001c0001t0028 | 0/0 | 4056 | 2 | 0 | 2 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | GCCGC others(4051): Show |
chr7 | 87623398 | 87837296 |
| a0001c0001t0029 | 0/0 | 4058 | 2 | 1 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | GCCGC others(4053): Show |
chr7 | 87623398 | 87837296 |
| a0001c0001t0030 | 0/0 | 4059 | 2 | 0 | 0 | 0 | 0 | 2 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | GCCGC others(4054): Show |
chr7 | 87623398 | 87837296 |
| a0001c0001t0031 | 0/0 | 4061 | 2 | 1 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | GCCGC others(4056): Show |
chr7 | 87623398 | 87837296 |
| a0001c0001t0032 | 0/0 | 4060 | 2 | 2 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | GCCGC others(4055): Show |
chr7 | 87623398 | 87837296 |
| a0001c0001t0033 | 0/0 | 4064 | 2 | 0 | 0 | 2 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | GCCGC others(4059): Show |
chr7 | 87623398 | 87837296 |
| a0001c0001t0034 | 0/0 | 4063 | 2 | 0 | 1 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | GCCGC others(4058): Show |
chr7 | 87623398 | 87837296 |
| a0001c0001t0035 | 0/0 | 4059 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | GCCGC others(4054): Show |
chr7 | 87623398 | 87837296 |
| a0001c0001t0036 | 0/0 | 4059 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | GCCGC others(4054): Show |
chr7 | 87623398 | 87837296 |
| a0001c0001t0037 | 0/0 | 4061 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | GCCGC others(4056): Show |
chr7 | 87623398 | 87837296 |
| a0001c0001t0038 | 0/0 | 4057 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | GCCGC others(4052): Show |
chr7 | 87623398 | 87837296 |
| a0001c0001t0039 | 0/0 | 4060 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | GCCGC others(4055): Show |
chr7 | 87623398 | 87837296 |
| a0001c0001t0040 | 0/0 | 4059 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | GCCGC others(4054): Show |
chr7 | 87623398 | 87837296 |
| a0001c0001t0041 | 0/0 | 4058 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | GCCGC others(4053): Show |
chr7 | 87623398 | 87837296 |
| a0001c0001t0042 | 0/0 | 4058 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | GCCGC others(4053): Show |
chr7 | 87623398 | 87837296 |
| a0001c0001t0043 | 0/0 | 4061 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | GCCGC others(4056): Show |
chr7 | 87623398 | 87837296 |
| a0001c0001t0044 | 0/0 | 4066 | 1 | 0 | 0 | 0 | 0 | 1 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | GCCGC others(4061): Show |
chr7 | 87623398 | 87837296 |
| a0001c0001t0045 | 0/0 | 4067 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | GCCGC others(4062): Show |
chr7 | 87623398 | 87837296 |
| a0001c0001t0046 | 0/0 | 4062 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | GCCGC others(4057): Show |
chr7 | 87623398 | 87837296 |
| a0001c0001t0047 | 0/0 | 4063 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | GCCGC others(4058): Show |
chr7 | 87623398 | 87837296 |
| a0001c0001t0048 | 0/0 | 4064 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | GCCGC others(4059): Show |
chr7 | 87623398 | 87837296 |
| a0001c0001t0049 | 0/0 | 4050 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | GCCGC others(4045): Show |
chr7 | 87623398 | 87837296 |
| a0001c0001t0050 | 0/0 | 4054 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | GCCGC others(4049): Show |
chr7 | 87623398 | 87837296 |
| a0001c0001t0051 | 0/0 | 4053 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | GCCGC others(4048): Show |
chr7 | 87623398 | 87837296 |
| a0001c0001t0052 | 0/0 | 4053 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | GCCGC others(4048): Show |
chr7 | 87623398 | 87837296 |
| a0001c0001t0053 | 0/0 | 4053 | 1 | 0 | 0 | 0 | 0 | 1 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | GCCGC others(4048): Show |
chr7 | 87623398 | 87837296 |
| a0001c0001t0054 | 0/0 | 4053 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | GCCGC others(4048): Show |
chr7 | 87623398 | 87837296 |
| a0001c0001t0055 | 0/0 | 4059 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | GCCGC others(4054): Show |
chr7 | 87623398 | 87837296 |
| a0001c0001t0056 | 0/0 | 4058 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | GCCGC others(4053): Show |
chr7 | 87623398 | 87837296 |
| a0001c0001t0057 | 0/0 | 4059 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | GCCGC others(4054): Show |
chr7 | 87623398 | 87837296 |
| a0001c0001t0058 | 0/0 | 4057 | 1 | 0 | 0 | 0 | 0 | 1 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | GCCGC others(4052): Show |
chr7 | 87623398 | 87837296 |
| a0001c0001t0059 | 0/0 | 4057 | 1 | 0 | 0 | 0 | 0 | 1 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | GCCGC others(4052): Show |
chr7 | 87623398 | 87837296 |
| a0001c0001t0060 | 0/0 | 4056 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | GCCGC others(4051): Show |
chr7 | 87623398 | 87837296 |
| a0001c0001t0061 | 0/0 | 4056 | 1 | 0 | 0 | 0 | 0 | 1 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | GCCGC others(4051): Show |
chr7 | 87623398 | 87837296 |
| a0001c0001t0062 | 0/0 | 4052 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | GCCGC others(4047): Show |
chr7 | 87623398 | 87837296 |
| a0001c0001t0063 | 0/0 | 4060 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | GCCGC others(4055): Show |
chr7 | 87623398 | 87837296 |
| a0001c0001t0064 | 0/0 | 4059 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | GCCGC others(4054): Show |
chr7 | 87623398 | 87837296 |
| a0001c0001t0065 | 0/0 | 4059 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | GCCGC others(4054): Show |
chr7 | 87623398 | 87837296 |
| a0001c0001t0066 | 0/0 | 4059 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | GCCGC others(4054): Show |
chr7 | 87623398 | 87837296 |
| a0001c0001t0067 | 0/0 | 4058 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | GCCGC others(4053): Show |
chr7 | 87623398 | 87837296 |
| a0001c0001t0068 | 0/0 | 4057 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | GCCGC others(4052): Show |
chr7 | 87623398 | 87837296 |
| a0001c0001t0069 | 0/0 | 4056 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | GCCGC others(4051): Show |
chr7 | 87623398 | 87837296 |
| a0001c0001t0070 | 0/0 | 4065 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | GCCGC others(4060): Show |
chr7 | 87623398 | 87837296 |
| a0001c0001t0071 | 0/0 | 4063 | 1 | 0 | 0 | 0 | 1 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | GCCGC others(4058): Show |
chr7 | 87623398 | 87837296 |
| a0001c0001t0072 | 0/0 | 4063 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | GCCGC others(4058): Show |
chr7 | 87623398 | 87837296 |
| a0001c0001t0073 | 0/0 | 4063 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | GCCGC others(4058): Show |
chr7 | 87623398 | 87837296 |
| a0001c0001t0074 | 0/0 | 4065 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | GCCGC others(4060): Show |
chr7 | 87623398 | 87837296 |
| a0001c0001t0075 | 0/0 | 4065 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | GCCGC others(4060): Show |
chr7 | 87623398 | 87837296 |
| a0001c0001t0076 | 0/0 | 4064 | 1 | 0 | 0 | 0 | 0 | 1 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | GCCGC others(4059): Show |
chr7 | 87623398 | 87837296 |
| a0001c0001t0077 | 0/0 | 4067 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | GCCGC others(4062): Show |
chr7 | 87623398 | 87837296 |
| a0001c0001t0078 | 0/0 | 4067 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | GCCGC others(4062): Show |
chr7 | 87623398 | 87837296 |
| a0001c0001t0079 | 0/0 | 4055 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | GCCGC others(4050): Show |
chr7 | 87623398 | 87837296 |
| a0001c0003t0001 | 0/0 | 4053 | 1 | 0 | 0 | 0 | 0 | 1 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | GCCGC others(4048): Show |
chr7 | 87623398 | 87837296 |
| a0002c0002t0002 | 0/0 | 4059 | 2 | 0 | 0 | 2 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | GCCGC others(4054): Show |
chr7 | 87623398 | 87837296 |
| a0002c0002t0018 | 0/0 | 4061 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | GCCGC others(4056): Show |
chr7 | 87623398 | 87837296 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0003g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0003g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0003g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0003g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0003g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0004g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0004g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0004g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0004g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0004g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0004g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0004g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0004g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0004g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0004g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0005g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0005g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0005g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0005g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0005g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0005g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0005g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0005g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0005g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0005g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0006g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0006g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0006g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0006g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0006g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0006g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0006g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0006g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0007g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0007g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0007g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0007g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0007g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0007g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0007g0147 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0008g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0008g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0008g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0008g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0008g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0008g0126 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0008g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0009g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0009g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0009g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0009g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0009g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0010g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0010g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0010g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0010g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0011g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0011g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0011g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0011g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0012g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0012g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0012g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0012g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0013g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0013g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0013g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0014g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0014g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0014g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0015g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0015g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0015g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0016g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0016g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0016g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0017g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0017g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0017g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0018g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0018g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0019g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0019g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0019g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0020g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0020g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0021g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0021g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0022g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0022g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0023g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0023g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0024g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0024g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0025g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0025g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0026g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0026g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0027g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0027g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0028g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0028g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0029g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0029g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0030g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0030g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0031g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0031g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0032g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0032g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0033g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0033g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0034g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0034g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0035g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0036g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0037g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0038g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0039g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0040g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0041g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0042g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0043g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0044g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0045g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0046g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0047g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0048g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0049g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0050g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0051g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0052g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0053g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0054g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0055g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0056g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0057g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0058g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0059g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0060g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0061g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0062g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0063g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0064g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0065g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0066g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0067g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0068g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0069g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0070g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0071g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0072g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0073g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0074g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0075g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0076g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0077g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0078g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0079g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0003t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0002c0002t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0002c0002t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0002c0002t0018g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0001 | t0005 | g0128 | EUR | FIN | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG00280 | hp2 | a0001 | c0001 | t0011 | g0195 | EUR | FIN | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG00323 | hp1 | a0001 | c0001 | t0006 | g0088 | EUR | FIN | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG00323 | hp2 | a0001 | c0001 | t0071 | g0078 | EUR | FIN | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG00423 | hp1 | a0001 | c0001 | t0015 | g0154 | EAS | CHS | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG00423 | hp2 | a0001 | c0001 | t0007 | g0122 | EAS | CHS | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG00438 | hp1 | a0001 | c0001 | t0003 | g0082 | EAS | CHS | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG00438 | hp2 | a0001 | c0001 | t0031 | g0044 | EAS | CHS | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG00558 | hp1 | a0001 | c0001 | t0029 | g0061 | EAS | CHS | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | CHS | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG00621 | hp1 | a0001 | c0001 | t0077 | g0081 | EAS | CHS | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | CHS | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG00639 | hp1 | a0001 | c0001 | t0042 | g0050 | AMR | PUR | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG00639 | hp2 | a0001 | c0001 | t0037 | g0006 | AMR | PUR | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG00735 | hp2 | a0001 | c0001 | t0008 | g0121 | AMR | PUR | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG00738 | hp1 | a0001 | c0001 | t0017 | g0085 | AMR | PUR | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG00738 | hp2 | a0001 | c0001 | t0004 | g0109 | AMR | PUR | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0075 | AMR | PUR | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG00741 | hp2 | a0001 | c0001 | t0034 | g0079 | AMR | PUR | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG01069 | hp1 | a0001 | c0001 | t0062 | g0145 | AMR | PUR | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG01069 | hp2 | a0001 | c0001 | t0009 | g0197 | AMR | PUR | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG01071 | hp1 | a0001 | c0001 | t0005 | g0127 | AMR | PUR | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG01071 | hp2 | a0001 | c0001 | t0009 | g0002 | AMR | PUR | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0057 | AMR | PUR | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG01074 | hp2 | a0001 | c0001 | t0028 | g0002 | AMR | PUR | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG01081 | hp1 | a0001 | c0001 | t0007 | g0146 | AMR | PUR | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG01081 | hp2 | a0001 | c0001 | t0013 | g0149 | AMR | PUR | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG01099 | hp2 | a0001 | c0001 | t0025 | g0091 | AMR | PUR | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG01167 | hp1 | a0001 | c0001 | t0009 | g0190 | AMR | PUR | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG01169 | hp1 | a0001 | c0001 | t0028 | g0192 | AMR | PUR | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0056 | AMR | PUR | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG01192 | hp1 | a0001 | c0001 | t0047 | g0172 | AMR | PUR | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG01261 | hp1 | a0001 | c0001 | t0004 | g0139 | AMR | CLM | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG01261 | hp2 | a0001 | c0001 | t0017 | g0065 | AMR | CLM | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG01346 | hp1 | a0001 | c0001 | t0011 | g0194 | AMR | CLM | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG01346 | hp2 | a0001 | c0001 | t0005 | g0124 | AMR | CLM | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG01358 | hp1 | a0001 | c0001 | t0013 | g0001 | AMR | CLM | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG01358 | hp2 | a0001 | c0001 | t0003 | g0076 | AMR | CLM | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG01433 | hp1 | a0001 | c0001 | t0017 | g0112 | AMR | CLM | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG01433 | hp2 | a0001 | c0001 | t0009 | g0193 | AMR | CLM | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG01496 | hp1 | a0001 | c0001 | t0041 | g0001 | AMR | CLM | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | CLM | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG01952 | hp1 | a0001 | c0001 | t0004 | g0083 | AMR | PEL | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0137 | AMR | PEL | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG01978 | hp1 | a0001 | c0001 | t0019 | g0043 | AMR | PEL | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0030 | AMR | PEL | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG01981 | hp1 | a0001 | c0001 | t0012 | g0031 | AMR | PEL | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG01981 | hp2 | a0001 | c0001 | t0019 | g0108 | AMR | PEL | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG02040 | hp1 | a0001 | c0001 | t0043 | g0106 | EAS | KHV | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG02040 | hp2 | a0001 | c0001 | t0006 | g0117 | EAS | KHV | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG02055 | hp1 | a0001 | c0001 | t0040 | g0013 | AFR | ACB | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG02055 | hp2 | a0001 | c0001 | t0008 | g0123 | AFR | ACB | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG02129 | hp1 | a0001 | c0001 | t0020 | g0035 | EAS | KHV | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG02129 | hp2 | a0001 | c0001 | t0006 | g0116 | EAS | KHV | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG02132 | hp1 | a0001 | c0001 | t0003 | g0135 | EAS | KHV | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG02132 | hp2 | a0001 | c0001 | t0054 | g0138 | EAS | KHV | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG02135 | hp1 | a0001 | c0001 | t0008 | g0069 | EAS | KHV | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG02135 | hp2 | a0001 | c0001 | t0003 | g0066 | EAS | KHV | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG02165 | hp1 | a0001 | c0001 | t0007 | g0118 | EAS | CDX | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | CDX | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG02258 | hp1 | a0001 | c0001 | t0004 | g0110 | AFR | ACB | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG02258 | hp2 | a0001 | c0001 | t0074 | g0170 | AFR | ACB | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | ACB | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG02280 | hp2 | a0001 | c0001 | t0010 | g0012 | AFR | ACB | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG02572 | hp1 | a0001 | c0001 | t0065 | g0003 | AFR | GWD | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG02572 | hp2 | a0001 | c0001 | t0070 | g0014 | AFR | GWD | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG02622 | hp1 | a0001 | c0001 | t0052 | g0196 | AFR | GWD | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG02622 | hp2 | a0001 | c0001 | t0018 | g0175 | AFR | GWD | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG02630 | hp1 | a0001 | c0001 | t0057 | g0017 | AFR | GWD | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG02630 | hp2 | a0001 | c0001 | t0031 | g0107 | AFR | GWD | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG02647 | hp1 | a0001 | c0001 | t0024 | g0102 | AFR | GWD | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG02647 | hp2 | a0001 | c0001 | t0010 | g0008 | AFR | GWD | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG02717 | hp1 | a0001 | c0001 | t0022 | g0181 | AFR | GWD | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG02717 | hp2 | a0001 | c0001 | t0056 | g0016 | AFR | GWD | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG02723 | hp1 | a0001 | c0001 | t0039 | g0148 | AFR | GWD | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG02723 | hp2 | a0001 | c0001 | t0075 | g0007 | AFR | GWD | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG02818 | hp1 | a0001 | c0001 | t0012 | g0177 | AFR | GWD | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG02818 | hp2 | a0001 | c0001 | t0008 | g0131 | AFR | GWD | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG02895 | hp1 | a0001 | c0001 | t0068 | g0143 | AFR | GWD | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0162 | AFR | GWD | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG02896 | hp1 | a0001 | c0001 | t0067 | g0018 | AFR | GWD | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG02896 | hp2 | a0001 | c0001 | t0004 | g0047 | AFR | GWD | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG02897 | hp1 | a0001 | c0001 | t0066 | g0019 | AFR | GWD | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG02897 | hp2 | a0001 | c0001 | t0069 | g0144 | AFR | GWD | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0168 | AFR | ESN | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG02965 | hp2 | a0001 | c0001 | t0079 | g0024 | AFR | ESN | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG02970 | hp1 | a0001 | c0001 | t0078 | g0133 | AFR | ESN | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG02970 | hp2 | a0001 | c0001 | t0012 | g0176 | AFR | ESN | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG02976 | hp1 | a0001 | c0001 | t0004 | g0022 | AFR | ESN | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG02976 | hp2 | a0001 | c0001 | t0025 | g0005 | AFR | ESN | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG03017 | hp1 | a0001 | c0001 | t0061 | g0185 | SAS | PJL | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG03017 | hp2 | a0001 | c0001 | t0026 | g0120 | SAS | PJL | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG03041 | hp1 | a0001 | c0001 | t0005 | g0052 | AFR | GWD | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG03041 | hp2 | a0001 | c0001 | t0073 | g0053 | AFR | GWD | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0114 | AFR | MSL | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG03098 | hp2 | a0001 | c0001 | t0036 | g0159 | AFR | MSL | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG03130 | hp1 | a0001 | c0001 | t0008 | g0021 | AFR | ESN | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0166 | AFR | ESN | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG03139 | hp1 | a0001 | c0001 | t0024 | g0004 | AFR | ESN | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG03139 | hp2 | a0001 | c0001 | t0007 | g0132 | AFR | ESN | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG03209 | hp1 | a0001 | c0001 | t0018 | g0171 | AFR | MSL | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG03209 | hp2 | a0001 | c0001 | t0063 | g0015 | AFR | MSL | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0178 | AFR | MSL | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG03225 | hp2 | a0001 | c0001 | t0006 | g0186 | AFR | MSL | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG03239 | hp1 | a0001 | c0001 | t0005 | g0062 | SAS | PJL | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG03239 | hp2 | a0001 | c0001 | t0053 | g0063 | SAS | PJL | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG03453 | hp1 | a0001 | c0001 | t0049 | g0038 | AFR | MSL | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG03453 | hp2 | a0001 | c0001 | t0008 | g0103 | AFR | MSL | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG03491 | hp1 | a0001 | c0001 | t0030 | g0187 | SAS | PJL | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0045 | SAS | PJL | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG03492 | hp1 | a0001 | c0001 | t0030 | g0188 | SAS | PJL | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG03492 | hp2 | a0001 | c0001 | t0019 | g0026 | SAS | PJL | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG03579 | hp1 | a0001 | c0001 | t0010 | g0010 | AFR | MSL | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG03579 | hp2 | a0001 | c0001 | t0032 | g0051 | AFR | MSL | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG03654 | hp1 | a0001 | c0001 | t0076 | g0179 | SAS | PJL | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG03654 | hp2 | a0001 | c0001 | t0059 | g0073 | SAS | PJL | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG03704 | hp1 | a0001 | c0001 | t0003 | g0105 | SAS | PJL | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG03704 | hp2 | a0001 | c0001 | t0011 | g0198 | SAS | PJL | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG03831 | hp1 | a0001 | c0001 | t0004 | g0067 | SAS | BEB | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0042 | SAS | BEB | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG04184 | hp1 | a0001 | c0001 | t0058 | g0184 | SAS | BEB | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0070 | SAS | BEB | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG04199 | hp1 | a0001 | c0001 | t0044 | g0169 | SAS | STU | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG04199 | hp2 | a0001 | c0003 | t0001 | g0025 | SAS | STU | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG04228 | hp1 | a0001 | c0001 | t0011 | g0189 | SAS | STU | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG04228 | hp2 | a0001 | c0001 | t0006 | g0142 | SAS | STU | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA18522 | hp1 | a0001 | c0001 | t0010 | g0011 | AFR | YRI | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0164 | AFR | YRI | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0163 | AFR | YRI | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA18906 | hp2 | a0001 | c0001 | t0016 | g0072 | AFR | YRI | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA18952 | hp1 | a0001 | c0001 | t0048 | g0153 | EAS | JPT | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA18963 | hp1 | a0001 | c0001 | t0023 | g0039 | EAS | JPT | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA18968 | hp2 | a0001 | c0001 | t0007 | g0130 | EAS | JPT | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA18970 | hp1 | a0001 | c0001 | t0003 | g0141 | EAS | JPT | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA18970 | hp2 | a0001 | c0001 | t0015 | g0150 | EAS | JPT | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA18973 | hp1 | a0001 | c0001 | t0006 | g0086 | EAS | JPT | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA18973 | hp2 | a0002 | c0002 | t0002 | g0029 | EAS | JPT | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA18974 | hp1 | a0001 | c0001 | t0027 | g0180 | EAS | JPT | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA18974 | hp2 | a0001 | c0001 | t0005 | g0125 | EAS | JPT | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA18975 | hp1 | a0001 | c0001 | t0022 | g0182 | EAS | JPT | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA18975 | hp2 | a0001 | c0001 | t0005 | g0113 | EAS | JPT | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA18977 | hp1 | a0001 | c0001 | t0005 | g0068 | EAS | JPT | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA18977 | hp2 | a0001 | c0001 | t0038 | g0183 | EAS | JPT | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA18979 | hp1 | a0002 | c0002 | t0002 | g0036 | EAS | JPT | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA18979 | hp2 | a0001 | c0001 | t0005 | g0077 | EAS | JPT | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA18988 | hp1 | a0001 | c0001 | t0005 | g0129 | EAS | JPT | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA18988 | hp2 | a0001 | c0001 | t0014 | g0158 | EAS | JPT | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA18990 | hp1 | a0001 | c0001 | t0026 | g0040 | EAS | JPT | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA18990 | hp2 | a0001 | c0001 | t0014 | g0155 | EAS | JPT | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA18992 | hp1 | a0001 | c0001 | t0060 | g0100 | EAS | JPT | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA18992 | hp2 | a0001 | c0001 | t0045 | g0160 | EAS | JPT | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA18994 | hp1 | a0001 | c0001 | t0003 | g0094 | EAS | JPT | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA18994 | hp2 | a0001 | c0001 | t0013 | g0173 | EAS | JPT | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA18998 | hp1 | a0001 | c0001 | t0014 | g0152 | EAS | JPT | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA18998 | hp2 | a0001 | c0001 | t0007 | g0059 | EAS | JPT | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA19001 | hp2 | a0002 | c0002 | t0018 | g0140 | EAS | JPT | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA19005 | hp1 | a0001 | c0001 | t0050 | g0027 | EAS | JPT | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA19005 | hp2 | a0001 | c0001 | t0021 | g0028 | EAS | JPT | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA19010 | hp1 | a0001 | c0001 | t0006 | g0111 | EAS | JPT | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA19010 | hp2 | a0001 | c0001 | t0004 | g0058 | EAS | JPT | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA19030 | hp1 | a0001 | c0001 | t0064 | g0046 | AFR | LWK | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA19030 | hp2 | a0001 | c0001 | t0027 | g0165 | AFR | LWK | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA19043 | hp1 | a0001 | c0001 | t0016 | g0074 | AFR | LWK | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA19043 | hp2 | a0001 | c0001 | t0055 | g0020 | AFR | LWK | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA19056 | hp1 | a0001 | c0001 | t0020 | g0033 | EAS | JPT | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA19056 | hp2 | a0001 | c0001 | t0004 | g0084 | EAS | JPT | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA19060 | hp1 | a0001 | c0001 | t0004 | g0055 | EAS | JPT | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA19060 | hp2 | a0001 | c0001 | t0023 | g0156 | EAS | JPT | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA19062 | hp1 | a0001 | c0001 | t0033 | g0157 | EAS | JPT | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA19062 | hp2 | a0001 | c0001 | t0034 | g0199 | EAS | JPT | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA19063 | hp2 | a0001 | c0001 | t0021 | g0032 | EAS | JPT | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA19082 | hp2 | a0001 | c0001 | t0015 | g0151 | EAS | JPT | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA19083 | hp1 | a0001 | c0001 | t0035 | g0034 | EAS | JPT | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA19083 | hp2 | a0001 | c0001 | t0051 | g0090 | EAS | JPT | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA19087 | hp1 | a0001 | c0001 | t0033 | g0037 | EAS | JPT | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA19087 | hp2 | a0001 | c0001 | t0006 | g0115 | EAS | JPT | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA20129 | hp1 | a0001 | c0001 | t0012 | g0174 | AFR | ASW | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA20129 | hp2 | a0001 | c0001 | t0016 | g0023 | AFR | ASW | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0136 | EUR | TSI | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0099 | EUR | TSI | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0104 | EUR | TSI | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA20805 | hp2 | a0001 | c0001 | t0009 | g0191 | EUR | TSI | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG01123 | hp1 | a0001 | c0001 | t0046 | g0161 | AMR | CLM | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | CLM | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG02559 | hp1 | a0001 | c0001 | t0032 | g0049 | AFR | ACB | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0167 | AFR | ACB | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG03471 | hp1 | a0001 | c0001 | t0029 | g0048 | AFR | MSL | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG03471 | hp2 | a0001 | c0001 | t0072 | g0009 | AFR | MSL | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0008 | g0126 | REF | REF | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0007 | g0147 | REF | REF | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:87739793 | G | T | 1 | a0002 | 3 | NA18973.hp2 NA18979.hp1 NA19001.hp2 |
missense_variant&splice_region_variant | MODERATE | c.461G>T | p.Arg154Ile | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 5/11 | 887/4063 | 461/1371 | 154/456 | chr7 | 87739793 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:87777887 | T | C | 1 | a0001c0003 | 1 | HG04199.hp2 | synonymous_variant | LOW | c.888T>C | p.Asp296Asp | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/11 | 1314/4063 | 888/1371 | 296/456 | chr7 | 87777887 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:87628549 | G | C | 3 | a0001c0001t0020 a0001c0001t0021 a0001c0001t0035 |
5 | HG02129.hp1 NA19005.hp2 NA19056.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-275G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/11 | 275 | chr7 | 87628549 | ||||||
| chr7:87628552 | G | A | 1 | a0001c0001t0036 | 1 | HG03098.hp2 | 5_prime_UTR_variant | MODIFIER | c.-272G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/11 | 272 | chr7 | 87628552 | ||||||
| chr7:87628572 | G | GGTGC | 3 | a0001c0001t0014 a0001c0001t0044 a0001c0001t0045 |
5 | HG04199.hp1 NA18988.hp2 NA18990.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-240_-237dupCGTG | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/11 | 236 | INFO_REALIGN_3_PRIME | chr7 | 87628572 | |||||
| chr7:87628584 | C | CGT | 5 | a0001c0001t0008 a0001c0001t0019 a0001c0001t0074 others(2): Show |
12 | HG00735.hp2 HG01978.hp1 HG01981.hp2 others(9): Show |
5_prime_UTR_variant | MODIFIER | c.-200_-199dupTG | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/11 | 198 | INFO_REALIGN_3_PRIME | chr7 | 87628584 | |||||
| chr7:87628584 | C | CGTGT | 2 | a0001c0001t0077 a0001c0001t0078 |
2 | HG00621.hp1 HG02970.hp1 |
5_prime_UTR_variant | MODIFIER | c.-202_-199dupTGTG | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/11 | 198 | INFO_REALIGN_3_PRIME | chr7 | 87628584 | |||||
| chr7:87628584 | CGT | C | 14 | a0001c0001t0005 a0001c0001t0018 a0001c0001t0021 others(11): Show |
31 | HG00280.hp1 HG00438.hp2 HG00639.hp2 others(28): Show |
5_prime_UTR_variant | MODIFIER | c.-200_-199delTG | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/11 | 199 | INFO_REALIGN_3_PRIME | chr7 | 87628584 | |||||
| chr7:87628584 | CGTGT | C | 19 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0013 others(16): Show |
45 | HG00558.hp1 HG00639.hp1 HG00738.hp1 others(42): Show |
5_prime_UTR_variant | MODIFIER | c.-202_-199delTGTG | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/11 | 199 | INFO_REALIGN_3_PRIME | chr7 | 87628584 | |||||
| chr7:87628584 | CGTGTGT | C | 14 | a0001c0001t0006 a0001c0001t0009 a0001c0001t0011 others(11): Show |
30 | HG00280.hp2 HG00323.hp1 HG01069.hp1 others(27): Show |
5_prime_UTR_variant | MODIFIER | c.-204_-199delTGTGTG | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/11 | 199 | INFO_REALIGN_3_PRIME | chr7 | 87628584 | |||||
| chr7:87628584 | CGTGTGTG others(1): Show |
C | 4 | a0001c0001t0003 a0001c0001t0010 a0001c0001t0016 others(1): Show |
19 | HG00438.hp1 HG00741.hp1 HG01074.hp1 others(16): Show |
5_prime_UTR_variant | MODIFIER | c.-206_-199delTGTGTG others(2): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/11 | 199 | INFO_REALIGN_3_PRIME | chr7 | 87628584 | |||||
| chr7:87628584 | CGTGTGTG others(3): Show |
C | 7 | a0001c0001t0001 a0001c0001t0050 a0001c0001t0051 others(4): Show |
29 | HG00558.hp2 HG00621.hp2 HG00735.hp1 others(26): Show |
5_prime_UTR_variant | MODIFIER | c.-208_-199delTGTGTG others(4): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/11 | 199 | INFO_REALIGN_3_PRIME | chr7 | 87628584 | |||||
| chr7:87628584 | CGTGTGTG others(5): Show |
C | 2 | a0001c0001t0026 a0001c0001t0049 |
3 | HG03017.hp2 HG03453.hp1 NA18990.hp1 |
5_prime_UTR_variant | MODIFIER | c.-210_-199delTGTGTG others(6): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/11 | 199 | INFO_REALIGN_3_PRIME | chr7 | 87628584 | |||||
| chr7:87628586 | T | TGC | 5 | a0001c0001t0012 a0001c0001t0015 a0001c0001t0033 others(2): Show |
8 | HG00423.hp1 HG01123.hp1 HG01981.hp1 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-237_-236insCG | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/11 | 236 | INFO_REALIGN_3_PRIME | chr7 | 87628586 | |||||
| chr7:87628588 | T | C | 4 | a0001c0001t0007 a0001c0001t0047 a0001c0001t0048 others(1): Show |
5 | HG01081.hp1 HG01192.hp1 HG02572.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-236T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/11 | 236 | chr7 | 87628588 | ||||||
| chr7:87628590 | T | C | 8 | a0001c0001t0015 a0001c0001t0022 a0001c0001t0023 others(5): Show |
14 | HG00423.hp1 HG00639.hp2 HG01099.hp2 others(11): Show |
5_prime_UTR_variant | MODIFIER | c.-234T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/11 | 234 | chr7 | 87628590 | ||||||
| chr7:87628592 | T | C | 7 | a0001c0001t0013 a0001c0001t0039 a0001c0001t0040 others(4): Show |
9 | HG00639.hp1 HG01081.hp2 HG01192.hp1 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-232T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/11 | 232 | chr7 | 87628592 | ||||||
| chr7:87628594 | T | C | 2 | a0001c0001t0037 a0001c0001t0038 |
2 | HG00639.hp2 NA18977.hp2 |
5_prime_UTR_variant | MODIFIER | c.-230T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/11 | 230 | chr7 | 87628594 | ||||||
| chr7:87628621 | G | T | 1 | a0001c0001t0079 | 1 | HG02965.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-203G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/11 | chr7 | 87628621 | |||||||
| chr7:87628711 | C | T | 3 | a0001c0001t0009 a0001c0001t0028 a0001c0001t0030 |
9 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-113C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/11 | 113 | chr7 | 87628711 | ||||||
| chr7:87830440 | C | CA | 31 | a0001c0001t0002 a0001c0001t0009 a0001c0001t0011 others(28): Show |
65 | HG00280.hp2 HG00423.hp1 HG01069.hp2 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*429dupA | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 11/11 | 430 | INFO_REALIGN_3_PRIME | chr7 | 87830440 | |||||
| chr7:87830440 | CA | C | 9 | a0001c0001t0016 a0001c0001t0025 a0001c0001t0029 others(6): Show |
14 | HG00558.hp1 HG00639.hp1 HG01069.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*429delA | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 11/11 | 429 | INFO_REALIGN_3_PRIME | chr7 | 87830440 | |||||
| chr7:87830518 | T | C | 1 | a0001c0001t0055 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*488T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 11/11 | 488 | chr7 | 87830518 | ||||||
| chr7:87830636 | C | T | 47 | a0001c0001t0002 a0001c0001t0009 a0001c0001t0010 others(44): Show |
85 | HG00280.hp2 HG00423.hp1 HG01069.hp2 others(82): Show |
3_prime_UTR_variant | MODIFIER | c.*606C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 11/11 | 606 | chr7 | 87830636 | ||||||
| chr7:87830715 | C | A | 1 | a0001c0001t0040 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*685C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 11/11 | 685 | chr7 | 87830715 | ||||||
| chr7:87830715 | C | T | 40 | a0001c0001t0002 a0001c0001t0009 a0001c0001t0011 others(37): Show |
75 | HG00280.hp2 HG00423.hp1 HG01069.hp2 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*685C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 11/11 | 685 | chr7 | 87830715 | ||||||
| chr7:87830898 | ATAGT | A | 3 | a0001c0001t0062 a0001c0001t0068 a0001c0001t0069 |
3 | HG01069.hp1 HG02895.hp1 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*871_*874delGTTA | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 11/11 | 871 | INFO_REALIGN_3_PRIME | chr7 | 87830898 | |||||
| chr7:87830901 | G | T | 6 | a0001c0001t0009 a0001c0001t0011 a0001c0001t0028 others(3): Show |
15 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*871G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 11/11 | 871 | chr7 | 87830901 | ||||||
| chr7:87830991 | A | G | 1 | a0001c0001t0071 | 1 | HG00323.hp2 | 3_prime_UTR_variant | MODIFIER | c.*961A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 11/11 | 961 | chr7 | 87830991 | ||||||
| chr7:87831011 | C | G | 1 | a0001c0001t0071 | 1 | HG00323.hp2 | 3_prime_UTR_variant | MODIFIER | c.*981C>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 11/11 | 981 | chr7 | 87831011 | ||||||
| chr7:87831058 | T | TA | 6 | a0001c0001t0039 a0001c0001t0055 a0001c0001t0057 others(3): Show |
6 | HG02572.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1029dupA | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 11/11 | 1030 | INFO_REALIGN_3_PRIME | chr7 | 87831058 | |||||
| chr7:87831060 | T | C | 8 | a0001c0001t0017 a0001c0001t0019 a0001c0001t0031 others(5): Show |
14 | HG00438.hp2 HG00621.hp1 HG00738.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1030T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 11/11 | 1030 | chr7 | 87831060 | ||||||
| chr7:87831076 | GT | G | 27 | a0001c0001t0002 a0001c0001t0009 a0001c0001t0011 others(24): Show |
56 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*1059delT | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 11/11 | 1059 | INFO_REALIGN_3_PRIME | chr7 | 87831076 | |||||
| chr7:87831105 | AC | A | 2 | a0001c0001t0066 a0001c0001t0067 |
2 | HG02896.hp1 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1076delC | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 11/11 | 1076 | chr7 | 87831105 | ||||||
| chr7:87831106 | CT | C | 6 | a0001c0001t0036 a0001c0001t0039 a0001c0001t0055 others(3): Show |
6 | HG02572.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1088delT | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 11/11 | 1088 | INFO_REALIGN_3_PRIME | chr7 | 87831106 | |||||
| chr7:87831107 | T | A | 2 | a0001c0001t0066 a0001c0001t0067 |
2 | HG02896.hp1 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1077T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 11/11 | 1077 | chr7 | 87831107 | ||||||
| chr7:87831179 | G | A | 1 | a0001c0001t0054 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1149G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 11/11 | 1149 | chr7 | 87831179 | ||||||
| chr7:87831398 | A | G | 7 | a0001c0001t0009 a0001c0001t0011 a0001c0001t0028 others(4): Show |
16 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1368A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 11/11 | 1368 | chr7 | 87831398 | ||||||
| chr7:87831560 | C | T | 1 | a0001c0001t0048 | 1 | NA18952.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1530C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 11/11 | 1530 | chr7 | 87831560 | ||||||
| chr7:87832004 | C | T | 2 | a0001c0001t0058 a0001c0001t0061 |
2 | HG03017.hp1 HG04184.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1974C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 11/11 | 1974 | chr7 | 87832004 | ||||||
| chr7:87832092 | G | A | 6 | a0001c0001t0009 a0001c0001t0011 a0001c0001t0028 others(3): Show |
15 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*2062G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 11/11 | 2062 | chr7 | 87832092 | ||||||
| chr7:87832253 | G | A | 1 | a0001c0001t0064 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2223G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 11/11 | 2223 | chr7 | 87832253 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:87628975 | C | T | 1 | a0001c0001t0002g0200 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.122+30C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87628975 | |||||||
| chr7:87629088 | G | A | 11 | a0001c0001t0010g0008 a0001c0001t0010g0010 a0001c0001t0010g0011 others(8): Show |
11 | HG00639.hp2 HG02055.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.122+143G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87629088 | |||||||
| chr7:87629284 | C | T | 1 | a0001c0001t0040g0013 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.122+339C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87629284 | |||||||
| chr7:87629410 | T | C | 1 | a0001c0001t0070g0014 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.122+465T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87629410 | |||||||
| chr7:87629642 | A | T | 1 | a0001c0001t0034g0199 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.122+697A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87629642 | |||||||
| chr7:87629719 | G | C | 1 | a0001c0001t0065g0003 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.122+774G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87629719 | |||||||
| chr7:87629794 | C | T | 17 | a0001c0001t0006g0186 a0001c0001t0009g0002 a0001c0001t0009g0190 others(14): Show |
17 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.122+849C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87629794 | |||||||
| chr7:87629845 | G | A | 2 | a0001c0001t0056g0016 a0001c0001t0063g0015 |
2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.122+900G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87629845 | |||||||
| chr7:87629908 | G | C | 5 | a0001c0001t0055g0020 a0001c0001t0057g0017 a0001c0001t0066g0019 others(2): Show |
5 | HG02572.hp2 HG02630.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.122+963G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87629908 | |||||||
| chr7:87629920 | C | CA | 7 | a0001c0001t0004g0022 a0001c0001t0008g0021 a0001c0001t0016g0023 others(4): Show |
7 | HG00639.hp2 HG02572.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.122+990dupA | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 87629920 | ||||||
| chr7:87629920 | CA | C | 57 | a0001c0001t0002g0162 a0001c0001t0002g0163 a0001c0001t0002g0164 others(54): Show |
57 | HG00280.hp2 HG00423.hp1 HG01069.hp2 others(54): Show |
intron_variant | MODIFIER | c.122+990delA | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 87629920 | ||||||
| chr7:87630069 | G | A | 199 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0045 others(196): Show |
199 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.122+1124G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87630069 | |||||||
| chr7:87630074 | T | A | 2 | a0001c0001t0058g0184 a0001c0001t0061g0185 |
2 | HG03017.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.122+1129T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87630074 | |||||||
| chr7:87630154 | T | A | 1 | a0001c0001t0039g0148 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.122+1209T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87630154 | |||||||
| chr7:87630533 | C | T | 3 | a0001c0001t0011g0198 a0001c0001t0058g0184 a0001c0001t0061g0185 |
3 | HG03017.hp1 HG03704.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.122+1588C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87630533 | |||||||
| chr7:87630688 | C | CT | 5 | a0001c0001t0003g0141 a0001c0001t0006g0142 a0001c0001t0062g0145 others(2): Show |
5 | HG01069.hp1 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.122+1756dupT | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 87630688 | ||||||
| chr7:87630688 | CT | C | 7 | a0001c0001t0006g0186 a0001c0001t0013g0149 a0001c0001t0055g0020 others(4): Show |
7 | HG01081.hp2 HG02572.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.122+1756delT | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 87630688 | ||||||
| chr7:87630830 | T | C | 17 | a0001c0001t0006g0186 a0001c0001t0009g0002 a0001c0001t0009g0190 others(14): Show |
17 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.122+1885T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87630830 | |||||||
| chr7:87630926 | G | A | 17 | a0001c0001t0006g0186 a0001c0001t0009g0002 a0001c0001t0009g0190 others(14): Show |
17 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.122+1981G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87630926 | |||||||
| chr7:87631296 | A | G | 1 | a0002c0002t0018g0140 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.122+2351A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87631296 | |||||||
| chr7:87631547 | C | T | 1 | a0001c0001t0010g0012 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.122+2602C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87631547 | |||||||
| chr7:87631574 | T | C | 2 | a0001c0001t0030g0187 a0001c0001t0030g0188 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.122+2629T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87631574 | |||||||
| chr7:87631628 | C | T | 1 | a0001c0001t0004g0139 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.122+2683C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87631628 | |||||||
| chr7:87631644 | C | T | 1 | a0001c0001t0054g0138 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.122+2699C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87631644 | |||||||
| chr7:87631861 | A | T | 1 | a0001c0001t0002g0137 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.122+2916A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87631861 | |||||||
| chr7:87631873 | G | C | 1 | a0001c0001t0019g0026 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.122+2928G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87631873 | |||||||
| chr7:87632112 | C | CA | 15 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0200 others(12): Show |
15 | HG01358.hp1 HG01496.hp1 HG01952.hp2 others(12): Show |
intron_variant | MODIFIER | c.122+3180dupA | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 87632112 | ||||||
| chr7:87632264 | A | G | 38 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(35): Show |
38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.122+3319A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87632264 | |||||||
| chr7:87632420 | T | C | 88 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(85): Show |
88 | HG00280.hp2 HG00423.hp1 HG00639.hp2 others(85): Show |
intron_variant | MODIFIER | c.122+3475T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87632420 | |||||||
| chr7:87632644 | G | A | 3 | a0001c0001t0024g0004 a0001c0001t0025g0005 a0001c0001t0037g0006 |
3 | HG00639.hp2 HG02976.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.122+3699G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87632644 | |||||||
| chr7:87633070 | T | G | 38 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(35): Show |
38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.122+4125T>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87633070 | |||||||
| chr7:87633252 | T | C | 1 | a0001c0001t0026g0040 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.122+4307T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87633252 | |||||||
| chr7:87633258 | C | T | 2 | a0001c0001t0010g0010 a0001c0001t0010g0011 |
2 | HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.122+4313C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87633258 | |||||||
| chr7:87633263 | A | G | 1 | a0001c0001t0023g0039 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.122+4318A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87633263 | |||||||
| chr7:87633265 | G | A | 88 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(85): Show |
88 | HG00280.hp2 HG00423.hp1 HG00639.hp2 others(85): Show |
intron_variant | MODIFIER | c.122+4320G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87633265 | |||||||
| chr7:87633407 | A | G | 17 | a0001c0001t0006g0186 a0001c0001t0009g0002 a0001c0001t0009g0190 others(14): Show |
17 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.122+4462A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87633407 | |||||||
| chr7:87633627 | G | A | 38 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(35): Show |
38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.122+4682G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87633627 | |||||||
| chr7:87633668 | AT | A | 16 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0014g0152 others(13): Show |
16 | HG00423.hp1 HG02165.hp2 HG03098.hp2 others(13): Show |
intron_variant | MODIFIER | c.122+4736delT | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 87633668 | ||||||
| chr7:87634244 | T | G | 2 | a0001c0001t0019g0043 a0001c0001t0034g0199 |
2 | HG01978.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.122+5299T>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87634244 | |||||||
| chr7:87634379 | T | C | 1 | a0001c0001t0046g0161 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.122+5434T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87634379 | |||||||
| chr7:87634425 | C | A | 1 | a0001c0001t0003g0141 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.122+5480C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87634425 | |||||||
| chr7:87634487 | T | G | 1 | a0001c0001t0011g0198 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.122+5542T>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87634487 | |||||||
| chr7:87634494 | T | TG | 26 | a0001c0001t0003g0082 a0001c0001t0003g0114 a0001c0001t0004g0055 others(23): Show |
26 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(23): Show |
intron_variant | MODIFIER | c.122+5560dupG | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 87634494 | ||||||
| chr7:87634494 | TG | T | 81 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0045 others(78): Show |
81 | HG00423.hp1 HG01074.hp1 HG01081.hp2 others(78): Show |
intron_variant | MODIFIER | c.122+5560delG | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 87634494 | ||||||
| chr7:87634559 | C | T | 2 | a0001c0001t0036g0159 a0001c0001t0045g0160 |
2 | HG03098.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.122+5614C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87634559 | |||||||
| chr7:87634784 | T | C | 3 | a0001c0001t0019g0043 a0001c0001t0031g0044 a0001c0001t0034g0199 |
3 | HG00438.hp2 HG01978.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.122+5839T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87634784 | |||||||
| chr7:87634831 | C | G | 1 | a0001c0001t0040g0013 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.122+5886C>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87634831 | |||||||
| chr7:87635425 | G | C | 1 | a0001c0001t0001g0045 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.122+6480G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87635425 | |||||||
| chr7:87635508 | A | G | 1 | a0001c0001t0001g0136 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.122+6563A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87635508 | |||||||
| chr7:87635614 | T | C | 38 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(35): Show |
38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.122+6669T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87635614 | |||||||
| chr7:87635621 | T | A | 2 | a0001c0001t0015g0150 a0001c0001t0015g0151 |
2 | NA18970.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.122+6676T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87635621 | |||||||
| chr7:87636734 | G | A | 1 | a0001c0001t0036g0159 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.122+7789G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87636734 | |||||||
| chr7:87637088 | T | C | 2 | a0001c0001t0055g0020 a0001c0001t0070g0014 |
2 | HG02572.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.122+8143T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87637088 | |||||||
| chr7:87637199 | C | T | 1 | a0001c0001t0036g0159 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.122+8254C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87637199 | |||||||
| chr7:87637393 | C | A | 11 | a0001c0001t0010g0008 a0001c0001t0010g0010 a0001c0001t0010g0011 others(8): Show |
11 | HG00639.hp2 HG02055.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.122+8448C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87637393 | |||||||
| chr7:87637495 | C | T | 1 | a0001c0001t0003g0135 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.122+8550C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87637495 | |||||||
| chr7:87637513 | C | A | 1 | a0001c0001t0049g0038 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.122+8568C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87637513 | |||||||
| chr7:87637797 | C | T | 1 | a0001c0001t0036g0159 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.122+8852C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87637797 | |||||||
| chr7:87637805 | T | G | 1 | a0001c0001t0040g0013 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.122+8860T>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87637805 | |||||||
| chr7:87638077 | A | C | 3 | a0001c0001t0009g0002 a0001c0001t0009g0197 a0001c0001t0028g0002 |
3 | HG01069.hp2 HG01071.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.122+9132A>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87638077 | |||||||
| chr7:87638345 | T | TTG | 78 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0045 others(75): Show |
78 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.122+9434_122+9435d others(4): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 87638345 | ||||||
| chr7:87638345 | T | TTGTG | 15 | a0001c0001t0001g0054 a0001c0001t0001g0060 a0001c0001t0003g0056 others(12): Show |
15 | HG00558.hp1 HG00558.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.122+9432_122+9435d others(6): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 87638345 | ||||||
| chr7:87638345 | T | TTGTGTG | 10 | a0001c0001t0004g0047 a0001c0001t0024g0004 a0001c0001t0025g0005 others(7): Show |
10 | HG00639.hp1 HG00639.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.122+9430_122+9435d others(8): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 87638345 | ||||||
| chr7:87638345 | T | TTGTGTGT others(1): Show |
3 | a0001c0001t0014g0158 a0001c0001t0066g0019 a0001c0001t0067g0018 |
3 | HG02896.hp1 HG02897.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.122+9428_122+9435d others(10): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 87638345 | ||||||
| chr7:87638345 | T | TTGTGTGT others(3): Show |
2 | a0001c0001t0010g0010 a0001c0001t0010g0011 |
2 | HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.122+9426_122+9435d others(12): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 87638345 | ||||||
| chr7:87638345 | T | TTGTGTGT others(5): Show |
7 | a0001c0001t0010g0008 a0001c0001t0014g0155 a0001c0001t0015g0154 others(4): Show |
7 | HG00423.hp1 HG02647.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.122+9424_122+9435d others(14): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 87638345 | ||||||
| chr7:87638345 | T | TTGTGTGT others(7): Show |
8 | a0001c0001t0010g0012 a0001c0001t0014g0152 a0001c0001t0033g0037 others(5): Show |
8 | HG02055.hp1 HG02280.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.122+9422_122+9435d others(16): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 87638345 | ||||||
| chr7:87638345 | T | TTGTGTGT others(9): Show |
3 | a0001c0001t0015g0150 a0001c0001t0015g0151 a0001c0001t0023g0039 |
3 | NA18963.hp1 NA18970.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.122+9420_122+9435d others(18): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 87638345 | ||||||
| chr7:87638345 | TTG | T | 8 | a0001c0001t0001g0134 a0001c0001t0002g0163 a0001c0001t0002g0164 others(5): Show |
8 | HG01192.hp2 HG02559.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.122+9434_122+9435d others(4): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 87638345 | ||||||
| chr7:87638345 | TTGTG | T | 30 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0178 others(27): Show |
30 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(27): Show |
intron_variant | MODIFIER | c.122+9432_122+9435d others(6): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 87638345 | ||||||
| chr7:87638371 | G | GTGTGTA | 17 | a0001c0001t0006g0186 a0001c0001t0009g0002 a0001c0001t0009g0190 others(14): Show |
17 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.122+9431_122+9432i others(8): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 87638371 | ||||||
| chr7:87638460 | C | T | 2 | a0001c0001t0001g0119 a0001c0001t0026g0120 |
2 | HG01099.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.122+9515C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87638460 | |||||||
| chr7:87638488 | G | A | 2 | a0001c0001t0058g0184 a0001c0001t0061g0185 |
2 | HG03017.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.122+9543G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87638488 | |||||||
| chr7:87638503 | C | T | 1 | a0001c0001t0007g0118 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.122+9558C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87638503 | |||||||
| chr7:87638957 | C | A | 1 | a0001c0001t0010g0010 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.122+10012C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87638957 | |||||||
| chr7:87638979 | C | T | 1 | a0001c0001t0052g0196 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.122+10034C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87638979 | |||||||
| chr7:87639077 | C | T | 1 | a0001c0001t0049g0038 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.122+10132C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87639077 | |||||||
| chr7:87639078 | G | A | 1 | a0001c0001t0001g0064 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.122+10133G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87639078 | |||||||
| chr7:87639140 | T | C | 88 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(85): Show |
88 | HG00280.hp2 HG00423.hp1 HG00639.hp2 others(85): Show |
intron_variant | MODIFIER | c.122+10195T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87639140 | |||||||
| chr7:87639153 | C | CA | 135 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0045 others(132): Show |
135 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.122+10231dupA | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 87639153 | ||||||
| chr7:87639153 | C | CAA | 32 | a0001c0001t0001g0054 a0001c0001t0001g0064 a0001c0001t0001g0070 others(29): Show |
32 | HG00423.hp2 HG00735.hp1 HG00735.hp2 others(29): Show |
intron_variant | MODIFIER | c.122+10230_122+1023 others(6): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 87639153 | ||||||
| chr7:87639153 | C | CAAA | 7 | a0001c0001t0017g0065 a0001c0001t0021g0028 a0001c0001t0033g0037 others(4): Show |
7 | HG01261.hp2 HG02630.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.122+10229_122+1023 others(7): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 87639153 | ||||||
| chr7:87639277 | T | G | 1 | a0001c0001t0003g0066 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.122+10332T>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87639277 | |||||||
| chr7:87639934 | T | C | 1 | a0001c0001t0015g0154 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.123-10888T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87639934 | |||||||
| chr7:87640072 | C | T | 2 | a0001c0001t0055g0020 a0001c0001t0070g0014 |
2 | HG02572.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.123-10750C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87640072 | |||||||
| chr7:87640181 | T | C | 62 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(59): Show |
62 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(59): Show |
intron_variant | MODIFIER | c.123-10641T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87640181 | |||||||
| chr7:87640192 | G | GTA | 7 | a0001c0001t0049g0038 a0001c0001t0054g0138 a0001c0001t0055g0020 others(4): Show |
7 | HG02132.hp2 HG02572.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.123-10614_123-1061 others(6): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 87640192 | ||||||
| chr7:87640192 | GTA | G | 2 | a0001c0001t0056g0016 a0001c0001t0063g0015 |
2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.123-10614_123-1061 others(6): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 87640192 | ||||||
| chr7:87640266 | A | T | 38 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(35): Show |
38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.123-10556A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87640266 | |||||||
| chr7:87640376 | G | T | 1 | a0001c0001t0011g0195 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.123-10446G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87640376 | |||||||
| chr7:87640503 | C | A | 17 | a0001c0001t0006g0186 a0001c0001t0009g0002 a0001c0001t0009g0190 others(14): Show |
17 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.123-10319C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87640503 | |||||||
| chr7:87640708 | T | C | 1 | a0001c0001t0049g0038 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.123-10114T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87640708 | |||||||
| chr7:87640951 | G | A | 11 | a0001c0001t0010g0008 a0001c0001t0010g0010 a0001c0001t0010g0011 others(8): Show |
11 | HG00639.hp2 HG02055.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.123-9871G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87640951 | |||||||
| chr7:87640955 | G | A | 1 | a0001c0001t0016g0074 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.123-9867G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87640955 | |||||||
| chr7:87641011 | A | G | 1 | a0001c0001t0010g0012 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.123-9811A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87641011 | |||||||
| chr7:87641184 | T | A | 88 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(85): Show |
88 | HG00280.hp2 HG00423.hp1 HG00639.hp2 others(85): Show |
intron_variant | MODIFIER | c.123-9638T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87641184 | |||||||
| chr7:87641531 | C | T | 1 | a0001c0001t0072g0009 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.123-9291C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87641531 | |||||||
| chr7:87641667 | T | A | 1 | a0001c0001t0004g0067 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.123-9155T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87641667 | |||||||
| chr7:87641974 | A | G | 5 | a0001c0001t0055g0020 a0001c0001t0057g0017 a0001c0001t0066g0019 others(2): Show |
5 | HG02572.hp2 HG02630.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.123-8848A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87641974 | |||||||
| chr7:87642026 | G | A | 1 | a0001c0001t0004g0139 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.123-8796G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87642026 | |||||||
| chr7:87642075 | C | T | 1 | a0001c0001t0005g0124 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.123-8747C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87642075 | |||||||
| chr7:87642348 | G | A | 1 | a0001c0001t0019g0043 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.123-8474G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87642348 | |||||||
| chr7:87642522 | A | G | 41 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(38): Show |
41 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(38): Show |
intron_variant | MODIFIER | c.123-8300A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87642522 | |||||||
| chr7:87642659 | C | G | 1 | a0001c0001t0003g0114 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.123-8163C>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87642659 | |||||||
| chr7:87642736 | C | T | 2 | a0001c0001t0056g0016 a0001c0001t0063g0015 |
2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.123-8086C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87642736 | |||||||
| chr7:87643195 | C | T | 1 | a0001c0001t0039g0148 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.123-7627C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87643195 | |||||||
| chr7:87643687 | A | AT | 6 | a0001c0001t0039g0148 a0001c0001t0055g0020 a0001c0001t0057g0017 others(3): Show |
6 | HG02572.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.123-7123dupT | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 87643687 | ||||||
| chr7:87643818 | C | T | 17 | a0001c0001t0006g0186 a0001c0001t0009g0002 a0001c0001t0009g0190 others(14): Show |
17 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.123-7004C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87643818 | |||||||
| chr7:87643889 | C | T | 1 | a0001c0001t0032g0051 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.123-6933C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87643889 | |||||||
| chr7:87643969 | C | T | 1 | a0001c0001t0039g0148 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.123-6853C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87643969 | |||||||
| chr7:87643999 | C | T | 1 | a0001c0001t0013g0173 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.123-6823C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87643999 | |||||||
| chr7:87644123 | T | C | 37 | a0001c0001t0002g0030 a0001c0001t0002g0162 a0001c0001t0002g0163 others(34): Show |
37 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(34): Show |
intron_variant | MODIFIER | c.123-6699T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87644123 | |||||||
| chr7:87644407 | A | C | 1 | a0001c0001t0036g0159 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.123-6415A>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87644407 | |||||||
| chr7:87644517 | G | T | 1 | a0001c0001t0054g0138 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.123-6305G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87644517 | |||||||
| chr7:87644676 | A | G | 17 | a0001c0001t0006g0186 a0001c0001t0009g0002 a0001c0001t0009g0190 others(14): Show |
17 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.123-6146A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87644676 | |||||||
| chr7:87644704 | T | C | 1 | a0001c0001t0036g0159 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.123-6118T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87644704 | |||||||
| chr7:87644764 | G | GAT | 2 | a0001c0001t0003g0075 a0001c0001t0004g0067 |
2 | HG00741.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.123-6047_123-6046d others(4): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 87644764 | ||||||
| chr7:87644788 | A | G | 1 | a0001c0001t0014g0158 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.123-6034A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87644788 | |||||||
| chr7:87645002 | C | G | 1 | a0001c0001t0039g0148 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.123-5820C>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87645002 | |||||||
| chr7:87645081 | C | CT | 23 | a0001c0001t0005g0113 a0001c0001t0009g0002 a0001c0001t0009g0190 others(20): Show |
23 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.123-5723dupT | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 87645081 | ||||||
| chr7:87645206 | T | C | 7 | a0001c0001t0010g0008 a0001c0001t0010g0010 a0001c0001t0010g0011 others(4): Show |
7 | HG02055.hp1 HG02280.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.123-5616T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87645206 | |||||||
| chr7:87645791 | C | T | 38 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(35): Show |
38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.123-5031C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87645791 | |||||||
| chr7:87645819 | A | T | 1 | a0001c0001t0006g0111 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.123-5003A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87645819 | |||||||
| chr7:87645832 | G | C | 17 | a0001c0001t0006g0186 a0001c0001t0009g0002 a0001c0001t0009g0190 others(14): Show |
17 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.123-4990G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87645832 | |||||||
| chr7:87645855 | ACT | A | 7 | a0001c0001t0010g0008 a0001c0001t0010g0010 a0001c0001t0010g0011 others(4): Show |
7 | HG02055.hp1 HG02280.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.123-4964_123-4963d others(4): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 87645855 | ||||||
| chr7:87646073 | G | A | 1 | a0001c0001t0003g0076 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.123-4749G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87646073 | |||||||
| chr7:87646225 | C | T | 3 | a0001c0001t0019g0043 a0001c0001t0031g0044 a0001c0001t0034g0199 |
3 | HG00438.hp2 HG01978.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.123-4597C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87646225 | |||||||
| chr7:87646325 | A | G | 185 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0045 others(182): Show |
185 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(182): Show |
intron_variant | MODIFIER | c.123-4497A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87646325 | |||||||
| chr7:87646341 | T | C | 1 | a0001c0001t0049g0038 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.123-4481T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87646341 | |||||||
| chr7:87646732 | G | A | 1 | a0001c0001t0004g0055 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.123-4090G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87646732 | |||||||
| chr7:87646737 | CCAGGGAT others(6): Show |
C | 17 | a0001c0001t0006g0186 a0001c0001t0009g0002 a0001c0001t0009g0190 others(14): Show |
17 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.123-4082_123-4070d others(15): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 87646737 | ||||||
| chr7:87646759 | TTG | T | 2 | a0001c0001t0017g0112 a0001c0001t0034g0079 |
2 | HG00741.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.123-4059_123-4058d others(4): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 87646759 | ||||||
| chr7:87646796 | G | T | 1 | a0001c0001t0005g0124 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.123-4026G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87646796 | |||||||
| chr7:87647137 | G | A | 2 | a0001c0001t0003g0056 a0001c0001t0003g0057 |
2 | HG01074.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.123-3685G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87647137 | |||||||
| chr7:87647218 | C | G | 17 | a0001c0001t0006g0186 a0001c0001t0009g0002 a0001c0001t0009g0190 others(14): Show |
17 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.123-3604C>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87647218 | |||||||
| chr7:87647295 | CT | C | 6 | a0001c0001t0039g0148 a0001c0001t0055g0020 a0001c0001t0057g0017 others(3): Show |
6 | HG02572.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.123-3523delT | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 87647295 | ||||||
| chr7:87647509 | A | G | 16 | a0001c0001t0006g0186 a0001c0001t0009g0002 a0001c0001t0009g0190 others(13): Show |
16 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.123-3313A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87647509 | |||||||
| chr7:87647535 | T | C | 1 | a0001c0001t0001g0080 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.123-3287T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87647535 | |||||||
| chr7:87647575 | T | C | 1 | a0001c0001t0008g0121 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.123-3247T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87647575 | |||||||
| chr7:87647760 | ACAT | A | 17 | a0001c0001t0006g0186 a0001c0001t0009g0002 a0001c0001t0009g0190 others(14): Show |
17 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.123-3058_123-3056d others(5): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 87647760 | ||||||
| chr7:87647925 | C | G | 2 | a0001c0001t0007g0122 a0001c0001t0007g0130 |
2 | HG00423.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.123-2897C>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87647925 | |||||||
| chr7:87647958 | G | A | 1 | a0001c0001t0077g0081 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.123-2864G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87647958 | |||||||
| chr7:87648109 | G | A | 1 | a0001c0001t0001g0080 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.123-2713G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87648109 | |||||||
| chr7:87648115 | G | GCATA | 12 | a0001c0001t0014g0152 a0001c0001t0014g0155 a0001c0001t0014g0158 others(9): Show |
12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.123-2706_123-2703d others(6): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 87648115 | ||||||
| chr7:87648184 | C | CA | 46 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(43): Show |
46 | HG00438.hp1 HG01081.hp2 HG01123.hp1 others(43): Show |
intron_variant | MODIFIER | c.123-2621dupA | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 87648184 | ||||||
| chr7:87648410 | G | A | 1 | a0001c0001t0065g0003 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.123-2412G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87648410 | |||||||
| chr7:87648532 | CA | C | 86 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(83): Show |
86 | HG00280.hp2 HG00423.hp1 HG00639.hp2 others(83): Show |
intron_variant | MODIFIER | c.123-2279delA | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 87648532 | ||||||
| chr7:87648708 | G | T | 1 | a0001c0001t0065g0003 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.123-2114G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87648708 | |||||||
| chr7:87648711 | A | G | 1 | a0001c0001t0036g0159 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.123-2111A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87648711 | |||||||
| chr7:87648797 | A | G | 3 | a0001c0001t0057g0017 a0001c0001t0066g0019 a0001c0001t0067g0018 |
3 | HG02630.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.123-2025A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87648797 | |||||||
| chr7:87649096 | C | T | 1 | a0001c0001t0070g0014 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.123-1726C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87649096 | |||||||
| chr7:87649121 | TC | T | 13 | a0001c0001t0014g0152 a0001c0001t0014g0155 a0001c0001t0014g0158 others(10): Show |
13 | HG00423.hp1 HG03453.hp1 NA18952.hp1 others(10): Show |
intron_variant | MODIFIER | c.123-1699delC | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 87649121 | ||||||
| chr7:87649444 | G | A | 179 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0045 others(176): Show |
179 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(176): Show |
intron_variant | MODIFIER | c.123-1378G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87649444 | |||||||
| chr7:87649527 | G | A | 1 | a0001c0001t0072g0009 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.123-1295G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87649527 | |||||||
| chr7:87649539 | T | C | 5 | a0001c0001t0004g0022 a0001c0001t0004g0047 a0001c0001t0005g0052 others(2): Show |
5 | HG02896.hp2 HG02976.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.123-1283T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87649539 | |||||||
| chr7:87649629 | A | G | 5 | a0001c0001t0055g0020 a0001c0001t0057g0017 a0001c0001t0066g0019 others(2): Show |
5 | HG02572.hp2 HG02630.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.123-1193A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87649629 | |||||||
| chr7:87649645 | A | G | 17 | a0001c0001t0006g0186 a0001c0001t0009g0002 a0001c0001t0009g0190 others(14): Show |
17 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.123-1177A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87649645 | |||||||
| chr7:87650082 | G | A | 1 | a0001c0001t0034g0079 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.123-740G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87650082 | |||||||
| chr7:87650301 | A | G | 1 | a0001c0001t0003g0057 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.123-521A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87650301 | |||||||
| chr7:87650436 | C | T | 1 | a0001c0001t0070g0014 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.123-386C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87650436 | |||||||
| chr7:87650476 | A | G | 1 | a0001c0001t0006g0186 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.123-346A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87650476 | |||||||
| chr7:87650492 | T | C | 1 | a0001c0001t0010g0010 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.123-330T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87650492 | |||||||
| chr7:87650540 | C | T | 88 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(85): Show |
88 | HG00280.hp2 HG00423.hp1 HG00639.hp2 others(85): Show |
intron_variant | MODIFIER | c.123-282C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87650540 | |||||||
| chr7:87651212 | G | A | 1 | a0001c0001t0077g0081 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.238+275G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87651212 | |||||||
| chr7:87651517 | A | G | 1 | a0001c0001t0036g0159 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.238+580A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87651517 | |||||||
| chr7:87651699 | T | C | 1 | a0001c0001t0017g0085 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.238+762T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87651699 | |||||||
| chr7:87651715 | C | T | 1 | a0001c0001t0001g0054 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.238+778C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87651715 | |||||||
| chr7:87651768 | G | A | 12 | a0001c0001t0014g0152 a0001c0001t0014g0155 a0001c0001t0014g0158 others(9): Show |
12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.238+831G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87651768 | |||||||
| chr7:87651843 | G | A | 2 | a0001c0001t0056g0016 a0001c0001t0063g0015 |
2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.238+906G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87651843 | |||||||
| chr7:87651947 | G | GT | 4 | a0001c0001t0005g0129 a0001c0001t0016g0023 a0001c0001t0036g0159 others(1): Show |
4 | HG03098.hp2 NA18988.hp1 NA19001.hp2 others(1): Show |
intron_variant | MODIFIER | c.238+1018dupT | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 87651947 | ||||||
| chr7:87652011 | T | A | 1 | a0001c0001t0036g0159 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.238+1074T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87652011 | |||||||
| chr7:87652023 | A | C | 1 | a0001c0001t0002g0137 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.238+1086A>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87652023 | |||||||
| chr7:87652136 | A | G | 1 | a0001c0001t0004g0022 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.238+1199A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87652136 | |||||||
| chr7:87652357 | C | T | 1 | a0001c0001t0026g0120 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.238+1420C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87652357 | |||||||
| chr7:87652359 | C | T | 2 | a0001c0001t0007g0122 a0001c0001t0007g0130 |
2 | HG00423.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.238+1422C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87652359 | |||||||
| chr7:87652621 | G | GAGATATA others(11): Show |
1 | a0001c0001t0012g0174 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.238+1685_238+1686i others(20): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 87652621 | ||||||
| chr7:87652621 | G | GAGATATA others(13): Show |
5 | a0001c0001t0012g0176 a0001c0001t0012g0177 a0001c0001t0013g0149 others(2): Show |
5 | HG01081.hp2 HG02258.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.238+1685_238+1686i others(22): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 87652621 | ||||||
| chr7:87652621 | G | GAT | 13 | a0001c0001t0003g0105 a0001c0001t0004g0047 a0001c0001t0004g0055 others(10): Show |
13 | HG00639.hp1 HG02040.hp1 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.238+1708_238+1709d others(4): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 87652621 | ||||||
| chr7:87652621 | G | GATAT | 11 | a0001c0001t0004g0067 a0001c0001t0016g0023 a0001c0001t0017g0065 others(8): Show |
11 | HG00438.hp2 HG00738.hp1 HG00741.hp2 others(8): Show |
intron_variant | MODIFIER | c.238+1706_238+1709d others(6): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 87652621 | ||||||
| chr7:87652621 | G | GATATAT | 2 | a0001c0001t0019g0043 a0001c0001t0059g0073 |
2 | HG01978.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.238+1704_238+1709d others(8): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 87652621 | ||||||
| chr7:87652621 | G | GATATATA others(1): Show |
17 | a0001c0001t0009g0002 a0001c0001t0009g0190 a0001c0001t0009g0191 others(14): Show |
17 | HG00423.hp1 HG00621.hp1 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.238+1702_238+1709d others(10): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 87652621 | ||||||
| chr7:87652621 | G | GATATATA others(3): Show |
9 | a0001c0001t0009g0193 a0001c0001t0011g0198 a0001c0001t0014g0152 others(6): Show |
9 | HG01433.hp2 HG02896.hp1 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.238+1700_238+1709d others(12): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 87652621 | ||||||
| chr7:87652621 | G | GATATATA others(5): Show |
2 | a0001c0001t0037g0006 a0001c0001t0048g0153 |
2 | HG00639.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.238+1698_238+1709d others(14): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 87652621 | ||||||
| chr7:87652621 | G | GATATATA others(7): Show |
3 | a0001c0001t0011g0189 a0001c0001t0015g0150 a0001c0001t0015g0151 |
3 | HG04228.hp1 NA18970.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.238+1696_238+1709d others(16): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 87652621 | ||||||
| chr7:87652621 | G | GATATATA others(9): Show |
4 | a0001c0001t0011g0195 a0001c0001t0036g0159 a0001c0001t0052g0196 others(1): Show |
4 | HG00280.hp2 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.238+1694_238+1709d others(18): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 87652621 | ||||||
| chr7:87652621 | G | GATATATA others(11): Show |
3 | a0001c0001t0002g0137 a0001c0001t0011g0194 a0001c0001t0065g0003 |
3 | HG01346.hp1 HG01952.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.238+1692_238+1709d others(20): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 87652621 | ||||||
| chr7:87652621 | G | GATATATA others(13): Show |
6 | a0001c0001t0002g0163 a0001c0001t0002g0178 a0001c0001t0018g0171 others(3): Show |
6 | HG02572.hp2 HG03209.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.238+1690_238+1709d others(22): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 87652621 | ||||||
| chr7:87652621 | G | GATATATA others(15): Show |
9 | a0001c0001t0002g0030 a0001c0001t0002g0162 a0001c0001t0002g0164 others(6): Show |
9 | HG01358.hp1 HG01496.hp1 HG01978.hp2 others(6): Show |
intron_variant | MODIFIER | c.238+1688_238+1709d others(24): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 87652621 | ||||||
| chr7:87652621 | G | GATATATA others(17): Show |
11 | a0001c0001t0002g0166 a0001c0001t0002g0167 a0001c0001t0002g0168 others(8): Show |
11 | HG01981.hp1 HG02280.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.238+1686_238+1709d others(26): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 87652621 | ||||||
| chr7:87652621 | G | GATATATA others(19): Show |
9 | a0001c0001t0006g0186 a0001c0001t0010g0008 a0001c0001t0010g0010 others(6): Show |
9 | HG01123.hp1 HG01192.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.238+1709_238+1710i others(28): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 87652621 | ||||||
| chr7:87652621 | G | GATATATA others(21): Show |
4 | a0001c0001t0013g0173 a0001c0001t0020g0035 a0001c0001t0021g0032 others(1): Show |
4 | HG02129.hp1 NA18975.hp1 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.238+1709_238+1710i others(30): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 87652621 | ||||||
| chr7:87652621 | G | GATATATA others(23): Show |
3 | a0001c0001t0040g0013 a0001c0001t0044g0169 a0001c0001t0055g0020 |
3 | HG02055.hp1 HG04199.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.238+1709_238+1710i others(32): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 87652621 | ||||||
| chr7:87652621 | G | GATATATA others(25): Show |
1 | a0001c0001t0038g0183 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.238+1709_238+1710i others(34): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 87652621 | ||||||
| chr7:87652621 | G | GATATATA others(39): Show |
1 | a0002c0002t0002g0036 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.238+1709_238+1710i others(48): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 87652621 | ||||||
| chr7:87652813 | T | C | 17 | a0001c0001t0006g0186 a0001c0001t0009g0002 a0001c0001t0009g0190 others(14): Show |
17 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.238+1876T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87652813 | |||||||
| chr7:87652888 | C | T | 1 | a0001c0001t0010g0008 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.238+1951C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87652888 | |||||||
| chr7:87653609 | T | C | 1 | a0001c0001t0039g0148 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.238+2672T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87653609 | |||||||
| chr7:87653734 | T | C | 1 | a0001c0001t0007g0118 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.238+2797T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87653734 | |||||||
| chr7:87653850 | T | C | 1 | a0001c0001t0036g0159 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.238+2913T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87653850 | |||||||
| chr7:87654163 | C | T | 12 | a0001c0001t0014g0152 a0001c0001t0014g0155 a0001c0001t0014g0158 others(9): Show |
12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.238+3226C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87654163 | |||||||
| chr7:87654172 | C | T | 12 | a0001c0001t0014g0152 a0001c0001t0014g0155 a0001c0001t0014g0158 others(9): Show |
12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.238+3235C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87654172 | |||||||
| chr7:87654206 | T | C | 1 | a0001c0001t0006g0086 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.238+3269T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87654206 | |||||||
| chr7:87654346 | ATT | A | 4 | a0001c0001t0044g0169 a0001c0001t0046g0161 a0001c0001t0047g0172 others(1): Show |
4 | HG01123.hp1 HG01192.hp1 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.238+3410_238+3411d others(4): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87654346 | |||||||
| chr7:87654640 | G | T | 3 | a0001c0001t0005g0127 a0001c0001t0005g0128 a0001c0001t0071g0078 |
3 | HG00280.hp1 HG00323.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.238+3703G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87654640 | |||||||
| chr7:87654782 | G | A | 5 | a0001c0001t0001g0087 a0001c0001t0001g0119 a0001c0001t0001g0134 others(2): Show |
5 | HG01099.hp1 HG01123.hp2 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.238+3845G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87654782 | |||||||
| chr7:87655104 | A | G | 1 | a0001c0001t0023g0039 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.238+4167A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87655104 | |||||||
| chr7:87655339 | A | G | 1 | a0001c0001t0079g0024 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.238+4402A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87655339 | |||||||
| chr7:87655342 | C | T | 2 | a0001c0001t0056g0016 a0001c0001t0063g0015 |
2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.238+4405C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87655342 | |||||||
| chr7:87655344 | A | AT | 2 | a0001c0001t0004g0055 a0001c0001t0005g0068 |
2 | NA18977.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.238+4408dupT | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 87655344 | ||||||
| chr7:87655439 | G | A | 6 | a0001c0001t0039g0148 a0001c0001t0055g0020 a0001c0001t0057g0017 others(3): Show |
6 | HG02572.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.238+4502G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87655439 | |||||||
| chr7:87655790 | C | A | 1 | a0001c0001t0059g0073 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.238+4853C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87655790 | |||||||
| chr7:87655801 | C | G | 38 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(35): Show |
38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.238+4864C>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87655801 | |||||||
| chr7:87655818 | G | C | 3 | a0001c0001t0024g0004 a0001c0001t0025g0005 a0001c0001t0037g0006 |
3 | HG00639.hp2 HG02976.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.238+4881G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87655818 | |||||||
| chr7:87656259 | T | A | 38 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(35): Show |
38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.238+5322T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87656259 | |||||||
| chr7:87656439 | G | C | 1 | a0001c0001t0006g0088 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.238+5502G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87656439 | |||||||
| chr7:87656614 | G | A | 12 | a0001c0001t0014g0152 a0001c0001t0014g0155 a0001c0001t0014g0158 others(9): Show |
12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.238+5677G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87656614 | |||||||
| chr7:87656703 | A | C | 4 | a0001c0001t0024g0004 a0001c0001t0025g0005 a0001c0001t0037g0006 others(1): Show |
4 | HG00639.hp2 HG02976.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.238+5766A>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87656703 | |||||||
| chr7:87657062 | C | T | 38 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(35): Show |
38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.238+6125C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87657062 | |||||||
| chr7:87657130 | T | C | 2 | a0001c0001t0003g0114 a0001c0001t0006g0088 |
2 | HG00323.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.238+6193T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87657130 | |||||||
| chr7:87657131 | G | A | 1 | a0001c0001t0049g0038 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.238+6194G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87657131 | |||||||
| chr7:87657165 | A | G | 1 | a0001c0001t0004g0139 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.238+6228A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87657165 | |||||||
| chr7:87657381 | C | T | 2 | a0001c0001t0056g0016 a0001c0001t0063g0015 |
2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.238+6444C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87657381 | |||||||
| chr7:87657491 | C | T | 1 | a0001c0001t0003g0141 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.238+6554C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87657491 | |||||||
| chr7:87657516 | C | T | 1 | a0001c0001t0005g0062 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.238+6579C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87657516 | |||||||
| chr7:87657608 | G | A | 2 | a0001c0001t0068g0143 a0001c0001t0069g0144 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.238+6671G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87657608 | |||||||
| chr7:87657704 | G | C | 2 | a0001c0001t0003g0082 a0001c0001t0008g0069 |
2 | HG00438.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.238+6767G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87657704 | |||||||
| chr7:87657975 | T | C | 1 | a0001c0001t0006g0186 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.238+7038T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87657975 | |||||||
| chr7:87658024 | C | A | 2 | a0001c0001t0020g0033 a0001c0001t0035g0034 |
2 | NA19056.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.238+7087C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87658024 | |||||||
| chr7:87658078 | C | T | 55 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(52): Show |
55 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(52): Show |
intron_variant | MODIFIER | c.238+7141C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87658078 | |||||||
| chr7:87658564 | A | G | 38 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(35): Show |
38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.238+7627A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87658564 | |||||||
| chr7:87658879 | A | G | 1 | a0001c0001t0007g0130 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.238+7942A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87658879 | |||||||
| chr7:87658898 | G | C | 1 | a0001c0001t0039g0148 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.238+7961G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87658898 | |||||||
| chr7:87658927 | G | A | 1 | a0001c0001t0036g0159 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.238+7990G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87658927 | |||||||
| chr7:87659008 | T | C | 88 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(85): Show |
88 | HG00280.hp2 HG00423.hp1 HG00639.hp2 others(85): Show |
intron_variant | MODIFIER | c.238+8071T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87659008 | |||||||
| chr7:87659111 | G | T | 1 | a0001c0001t0044g0169 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.238+8174G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87659111 | |||||||
| chr7:87659289 | T | G | 3 | a0001c0001t0057g0017 a0001c0001t0066g0019 a0001c0001t0067g0018 |
3 | HG02630.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.238+8352T>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87659289 | |||||||
| chr7:87659367 | T | A | 2 | a0001c0001t0056g0016 a0001c0001t0063g0015 |
2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.238+8430T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87659367 | |||||||
| chr7:87659410 | A | G | 1 | a0001c0001t0065g0003 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.238+8473A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87659410 | |||||||
| chr7:87659429 | G | T | 1 | a0001c0001t0010g0012 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.238+8492G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87659429 | |||||||
| chr7:87659781 | G | T | 1 | a0001c0001t0018g0171 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.238+8844G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87659781 | |||||||
| chr7:87659936 | C | T | 3 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0104 |
3 | HG01496.hp2 HG04184.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.238+8999C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87659936 | |||||||
| chr7:87660323 | A | T | 1 | a0001c0001t0054g0138 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.238+9386A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87660323 | |||||||
| chr7:87660358 | C | G | 1 | a0001c0001t0040g0013 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.238+9421C>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87660358 | |||||||
| chr7:87660526 | C | T | 1 | a0001c0001t0026g0040 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.238+9589C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87660526 | |||||||
| chr7:87660611 | T | C | 1 | a0001c0001t0049g0038 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.238+9674T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87660611 | |||||||
| chr7:87660650 | C | G | 2 | a0001c0001t0056g0016 a0001c0001t0063g0015 |
2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.238+9713C>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87660650 | |||||||
| chr7:87660903 | A | G | 1 | a0001c0001t0015g0151 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.238+9966A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87660903 | |||||||
| chr7:87660991 | C | T | 1 | a0001c0001t0049g0038 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.238+10054C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87660991 | |||||||
| chr7:87661117 | T | A | 1 | a0001c0001t0017g0065 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.238+10180T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87661117 | |||||||
| chr7:87661359 | TTCTA | T | 12 | a0001c0001t0014g0152 a0001c0001t0014g0155 a0001c0001t0014g0158 others(9): Show |
12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.238+10427_238+1043 others(8): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 87661359 | ||||||
| chr7:87661424 | C | T | 3 | a0001c0001t0062g0145 a0001c0001t0068g0143 a0001c0001t0069g0144 |
3 | HG01069.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.238+10487C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87661424 | |||||||
| chr7:87661496 | C | G | 1 | a0001c0001t0073g0053 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.238+10559C>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87661496 | |||||||
| chr7:87661549 | T | C | 75 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(72): Show |
75 | HG00280.hp2 HG00423.hp1 HG01069.hp2 others(72): Show |
intron_variant | MODIFIER | c.238+10612T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87661549 | |||||||
| chr7:87661964 | A | G | 1 | a0001c0001t0001g0087 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.238+11027A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87661964 | |||||||
| chr7:87662084 | A | T | 2 | a0001c0001t0004g0047 a0001c0001t0064g0046 |
2 | HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.238+11147A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87662084 | |||||||
| chr7:87662169 | AG | A | 38 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(35): Show |
38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.238+11233delG | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87662169 | |||||||
| chr7:87662243 | C | G | 3 | a0001c0001t0029g0048 a0001c0001t0032g0049 a0001c0001t0032g0051 |
3 | HG02559.hp1 HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.238+11306C>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87662243 | |||||||
| chr7:87662272 | C | T | 2 | a0001c0001t0003g0075 a0001c0001t0004g0067 |
2 | HG00741.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.238+11335C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87662272 | |||||||
| chr7:87662449 | C | T | 13 | a0001c0001t0014g0152 a0001c0001t0014g0155 a0001c0001t0014g0158 others(10): Show |
13 | HG00423.hp1 HG03453.hp1 NA18952.hp1 others(10): Show |
intron_variant | MODIFIER | c.238+11512C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87662449 | |||||||
| chr7:87662510 | G | A | 2 | a0001c0001t0040g0013 a0001c0001t0065g0003 |
2 | HG02055.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.238+11573G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87662510 | |||||||
| chr7:87662715 | A | G | 1 | a0001c0001t0001g0042 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.238+11778A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87662715 | |||||||
| chr7:87662729 | T | C | 3 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0104 |
3 | HG01496.hp2 HG04184.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.238+11792T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87662729 | |||||||
| chr7:87662846 | A | G | 1 | a0001c0001t0031g0107 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.238+11909A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87662846 | |||||||
| chr7:87663007 | T | G | 1 | a0001c0001t0049g0038 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.238+12070T>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87663007 | |||||||
| chr7:87663147 | C | A | 1 | a0001c0001t0011g0198 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.238+12210C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87663147 | |||||||
| chr7:87663195 | A | G | 1 | a0001c0001t0036g0159 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.238+12258A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87663195 | |||||||
| chr7:87663199 | G | A | 38 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(35): Show |
38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.238+12262G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87663199 | |||||||
| chr7:87663334 | G | A | 5 | a0001c0001t0055g0020 a0001c0001t0057g0017 a0001c0001t0066g0019 others(2): Show |
5 | HG02572.hp2 HG02630.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.238+12397G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87663334 | |||||||
| chr7:87663367 | C | T | 16 | a0001c0001t0006g0186 a0001c0001t0009g0002 a0001c0001t0009g0190 others(13): Show |
16 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.238+12430C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87663367 | |||||||
| chr7:87663369 | G | A | 38 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(35): Show |
38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.238+12432G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87663369 | |||||||
| chr7:87663907 | A | T | 75 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(72): Show |
75 | HG00280.hp2 HG00423.hp1 HG01069.hp2 others(72): Show |
intron_variant | MODIFIER | c.238+12970A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87663907 | |||||||
| chr7:87664177 | G | A | 61 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(58): Show |
61 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(58): Show |
intron_variant | MODIFIER | c.238+13240G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87664177 | |||||||
| chr7:87664388 | A | C | 1 | a0001c0001t0049g0038 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.238+13451A>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87664388 | |||||||
| chr7:87664661 | G | A | 1 | a0001c0001t0040g0013 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.238+13724G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87664661 | |||||||
| chr7:87664825 | G | C | 1 | a0001c0001t0059g0073 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.238+13888G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87664825 | |||||||
| chr7:87664980 | G | C | 1 | a0001c0001t0049g0038 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.238+14043G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87664980 | |||||||
| chr7:87665433 | TAG | T | 12 | a0001c0001t0014g0152 a0001c0001t0014g0155 a0001c0001t0014g0158 others(9): Show |
12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.238+14498_238+1449 others(6): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 87665433 | ||||||
| chr7:87665469 | C | T | 1 | a0001c0001t0049g0038 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.238+14532C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87665469 | |||||||
| chr7:87665470 | A | T | 1 | a0001c0001t0054g0138 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.238+14533A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87665470 | |||||||
| chr7:87665677 | C | G | 4 | a0001c0001t0010g0010 a0001c0001t0010g0011 a0001c0001t0010g0012 others(1): Show |
4 | HG02280.hp2 HG02723.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.238+14740C>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87665677 | |||||||
| chr7:87665902 | A | G | 1 | a0001c0001t0019g0043 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.238+14965A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87665902 | |||||||
| chr7:87665960 | C | T | 12 | a0001c0001t0014g0152 a0001c0001t0014g0155 a0001c0001t0014g0158 others(9): Show |
12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.238+15023C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87665960 | |||||||
| chr7:87666082 | C | G | 1 | a0001c0001t0005g0068 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.238+15145C>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87666082 | |||||||
| chr7:87666472 | G | T | 1 | a0001c0001t0036g0159 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.238+15535G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87666472 | |||||||
| chr7:87666581 | G | A | 1 | a0001c0001t0059g0073 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.238+15644G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87666581 | |||||||
| chr7:87666647 | T | C | 1 | a0001c0001t0040g0013 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.238+15710T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87666647 | |||||||
| chr7:87666805 | T | C | 1 | a0001c0001t0065g0003 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.238+15868T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87666805 | |||||||
| chr7:87666900 | A | G | 1 | a0001c0001t0049g0038 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.238+15963A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87666900 | |||||||
| chr7:87667015 | A | G | 1 | a0001c0001t0031g0044 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.238+16078A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87667015 | |||||||
| chr7:87667199 | C | T | 1 | a0001c0001t0039g0148 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.238+16262C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87667199 | |||||||
| chr7:87667279 | T | C | 38 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(35): Show |
38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.238+16342T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87667279 | |||||||
| chr7:87667433 | C | G | 1 | a0001c0001t0007g0130 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.238+16496C>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87667433 | |||||||
| chr7:87667842 | A | G | 1 | a0001c0001t0008g0103 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.238+16905A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87667842 | |||||||
| chr7:87668153 | T | G | 55 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(52): Show |
55 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(52): Show |
intron_variant | MODIFIER | c.238+17216T>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87668153 | |||||||
| chr7:87668252 | A | C | 1 | a0001c0001t0070g0014 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.238+17315A>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87668252 | |||||||
| chr7:87668317 | G | A | 1 | a0001c0001t0049g0038 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.238+17380G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87668317 | |||||||
| chr7:87668444 | A | G | 2 | a0001c0001t0056g0016 a0001c0001t0063g0015 |
2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.238+17507A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87668444 | |||||||
| chr7:87668848 | G | A | 3 | a0001c0001t0057g0017 a0001c0001t0066g0019 a0001c0001t0067g0018 |
3 | HG02630.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.238+17911G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87668848 | |||||||
| chr7:87668972 | C | T | 1 | a0001c0001t0049g0038 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.238+18035C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87668972 | |||||||
| chr7:87669423 | T | C | 12 | a0001c0001t0014g0152 a0001c0001t0014g0155 a0001c0001t0014g0158 others(9): Show |
12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.238+18486T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87669423 | |||||||
| chr7:87669552 | A | G | 179 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0045 others(176): Show |
179 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(176): Show |
intron_variant | MODIFIER | c.238+18615A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87669552 | |||||||
| chr7:87669697 | T | C | 1 | a0001c0001t0039g0148 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.238+18760T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87669697 | |||||||
| chr7:87669931 | G | A | 1 | a0001c0001t0057g0017 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.238+18994G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87669931 | |||||||
| chr7:87669938 | A | G | 1 | a0001c0001t0004g0139 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.238+19001A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87669938 | |||||||
| chr7:87670024 | C | T | 1 | a0001c0001t0070g0014 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.238+19087C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87670024 | |||||||
| chr7:87670604 | G | A | 7 | a0001c0001t0039g0148 a0001c0001t0049g0038 a0001c0001t0055g0020 others(4): Show |
7 | HG02572.hp2 HG02630.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.238+19667G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87670604 | |||||||
| chr7:87670685 | G | T | 1 | a0001c0001t0049g0038 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.238+19748G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87670685 | |||||||
| chr7:87670877 | G | T | 1 | a0001c0001t0011g0195 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.238+19940G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87670877 | |||||||
| chr7:87670940 | T | C | 1 | a0001c0001t0001g0089 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.238+20003T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87670940 | |||||||
| chr7:87670970 | TCA | T | 4 | a0001c0001t0024g0004 a0001c0001t0025g0005 a0001c0001t0037g0006 others(1): Show |
4 | HG00639.hp2 HG02976.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.238+20034_238+2003 others(6): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87670970 | |||||||
| chr7:87671038 | A | C | 1 | a0001c0001t0039g0148 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.238+20101A>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87671038 | |||||||
| chr7:87671063 | G | A | 1 | a0001c0001t0039g0148 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.238+20126G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87671063 | |||||||
| chr7:87671165 | C | T | 38 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(35): Show |
38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.238+20228C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87671165 | |||||||
| chr7:87671251 | C | T | 1 | a0001c0001t0039g0148 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.238+20314C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87671251 | |||||||
| chr7:87671284 | G | A | 6 | a0001c0001t0039g0148 a0001c0001t0055g0020 a0001c0001t0057g0017 others(3): Show |
6 | HG02572.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.238+20347G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87671284 | |||||||
| chr7:87671430 | TGAG | T | 2 | a0001c0001t0066g0019 a0001c0001t0067g0018 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.238+20497_238+2049 others(7): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 87671430 | ||||||
| chr7:87671691 | G | C | 12 | a0001c0001t0014g0152 a0001c0001t0014g0155 a0001c0001t0014g0158 others(9): Show |
12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.238+20754G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87671691 | |||||||
| chr7:87671718 | C | T | 1 | a0001c0001t0031g0044 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.238+20781C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87671718 | |||||||
| chr7:87671938 | T | C | 1 | a0001c0001t0046g0161 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.238+21001T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87671938 | |||||||
| chr7:87672229 | A | G | 1 | a0001c0001t0057g0017 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.238+21292A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87672229 | |||||||
| chr7:87672308 | C | T | 3 | a0001c0001t0019g0043 a0001c0001t0031g0044 a0001c0001t0034g0199 |
3 | HG00438.hp2 HG01978.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.238+21371C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87672308 | |||||||
| chr7:87672480 | G | A | 1 | a0001c0001t0036g0159 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.238+21543G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87672480 | |||||||
| chr7:87672607 | A | G | 1 | a0001c0001t0010g0011 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.238+21670A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87672607 | |||||||
| chr7:87672683 | C | T | 1 | a0001c0001t0049g0038 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.238+21746C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87672683 | |||||||
| chr7:87672766 | A | G | 1 | a0001c0001t0054g0138 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.238+21829A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87672766 | |||||||
| chr7:87672824 | A | G | 75 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(72): Show |
75 | HG00280.hp2 HG00423.hp1 HG01069.hp2 others(72): Show |
intron_variant | MODIFIER | c.238+21887A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87672824 | |||||||
| chr7:87672869 | A | G | 17 | a0001c0001t0006g0186 a0001c0001t0009g0002 a0001c0001t0009g0190 others(14): Show |
17 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.238+21932A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87672869 | |||||||
| chr7:87672893 | A | C | 1 | a0001c0001t0001g0080 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.238+21956A>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87672893 | |||||||
| chr7:87673099 | G | A | 1 | a0001c0001t0057g0017 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.238+22162G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87673099 | |||||||
| chr7:87673189 | T | C | 4 | a0001c0001t0024g0004 a0001c0001t0025g0005 a0001c0001t0037g0006 others(1): Show |
4 | HG00639.hp2 HG02976.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.238+22252T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87673189 | |||||||
| chr7:87673499 | G | A | 1 | a0001c0001t0036g0159 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.238+22562G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87673499 | |||||||
| chr7:87673519 | T | C | 62 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(59): Show |
62 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(59): Show |
intron_variant | MODIFIER | c.238+22582T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87673519 | |||||||
| chr7:87673625 | C | T | 2 | a0001c0001t0010g0010 a0001c0001t0010g0011 |
2 | HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.238+22688C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87673625 | |||||||
| chr7:87673702 | A | G | 4 | a0001c0001t0003g0066 a0001c0001t0006g0115 a0001c0001t0006g0116 others(1): Show |
4 | HG02040.hp2 HG02129.hp2 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.238+22765A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87673702 | |||||||
| chr7:87673767 | G | T | 1 | a0001c0001t0024g0102 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.238+22830G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87673767 | |||||||
| chr7:87674137 | C | T | 1 | a0001c0001t0001g0041 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.238+23200C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87674137 | |||||||
| chr7:87674138 | G | A | 7 | a0001c0001t0039g0148 a0001c0001t0049g0038 a0001c0001t0055g0020 others(4): Show |
7 | HG02572.hp2 HG02630.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.238+23201G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87674138 | |||||||
| chr7:87674215 | G | A | 3 | a0001c0001t0005g0077 a0001c0001t0005g0125 a0001c0001t0005g0129 |
3 | NA18974.hp2 NA18979.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.238+23278G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87674215 | |||||||
| chr7:87674301 | G | A | 1 | a0001c0001t0039g0148 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.238+23364G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87674301 | |||||||
| chr7:87674913 | G | A | 12 | a0001c0001t0014g0152 a0001c0001t0014g0155 a0001c0001t0014g0158 others(9): Show |
12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.238+23976G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87674913 | |||||||
| chr7:87675466 | T | A | 1 | a0001c0001t0049g0038 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.238+24529T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87675466 | |||||||
| chr7:87675653 | C | CA | 10 | a0001c0001t0001g0134 a0001c0001t0004g0109 a0001c0001t0004g0110 others(7): Show |
10 | HG00738.hp2 HG01192.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.238+24735dupA | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 87675653 | ||||||
| chr7:87675653 | CA | C | 31 | a0001c0001t0001g0101 a0001c0001t0006g0186 a0001c0001t0009g0002 others(28): Show |
31 | HG00280.hp2 HG00639.hp2 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.238+24735delA | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 87675653 | ||||||
| chr7:87675653 | CAA | C | 39 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(36): Show |
39 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(36): Show |
intron_variant | MODIFIER | c.238+24734_238+2473 others(6): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 87675653 | ||||||
| chr7:87675653 | CAAAAAAA others(1): Show |
C | 12 | a0001c0001t0017g0065 a0001c0001t0017g0085 a0001c0001t0019g0026 others(9): Show |
12 | HG00438.hp2 HG00621.hp1 HG00738.hp1 others(9): Show |
intron_variant | MODIFIER | c.238+24728_238+2473 others(12): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 87675653 | ||||||
| chr7:87676283 | A | C | 2 | a0001c0001t0017g0065 a0001c0001t0017g0085 |
2 | HG00738.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.239-24138A>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87676283 | |||||||
| chr7:87676378 | AAAC | A | 38 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(35): Show |
38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.239-24023_239-2402 others(7): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 87676378 | ||||||
| chr7:87676419 | G | A | 1 | a0001c0001t0006g0186 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.239-24002G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87676419 | |||||||
| chr7:87676703 | C | CA | 12 | a0001c0001t0001g0064 a0001c0001t0001g0134 a0001c0001t0005g0077 others(9): Show |
12 | HG00735.hp1 HG00735.hp2 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.239-23692dupA | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 87676703 | ||||||
| chr7:87676703 | CA | C | 44 | a0001c0001t0002g0168 a0001c0001t0004g0022 a0001c0001t0004g0047 others(41): Show |
44 | HG00423.hp1 HG00438.hp2 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.239-23692delA | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 87676703 | ||||||
| chr7:87676926 | A | G | 1 | a0001c0001t0038g0183 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.239-23495A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87676926 | |||||||
| chr7:87676957 | A | G | 1 | a0001c0001t0001g0099 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.239-23464A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87676957 | |||||||
| chr7:87677053 | T | C | 17 | a0001c0001t0006g0186 a0001c0001t0009g0002 a0001c0001t0009g0190 others(14): Show |
17 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.239-23368T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87677053 | |||||||
| chr7:87677215 | A | T | 1 | a0001c0001t0038g0183 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.239-23206A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87677215 | |||||||
| chr7:87677255 | A | G | 1 | a0001c0001t0001g0064 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.239-23166A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87677255 | |||||||
| chr7:87677274 | A | AAC | 28 | a0001c0001t0001g0119 a0001c0001t0001g0134 a0001c0001t0001g0136 others(25): Show |
28 | HG00423.hp1 HG00639.hp2 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.239-23112_239-2311 others(6): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 87677274 | ||||||
| chr7:87677274 | A | AACAC | 2 | a0001c0001t0001g0064 a0001c0001t0057g0017 |
2 | HG00735.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.239-23114_239-2311 others(8): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 87677274 | ||||||
| chr7:87677274 | AAC | A | 43 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0163 others(40): Show |
43 | HG00323.hp1 HG00735.hp2 HG01081.hp2 others(40): Show |
intron_variant | MODIFIER | c.239-23112_239-2311 others(6): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 87677274 | ||||||
| chr7:87677274 | AACAC | A | 5 | a0001c0001t0001g0098 a0001c0001t0012g0177 a0001c0001t0016g0023 others(2): Show |
5 | HG01167.hp2 HG02818.hp1 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.239-23114_239-2311 others(8): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 87677274 | ||||||
| chr7:87677335 | T | TA | 45 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(42): Show |
45 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(42): Show |
intron_variant | MODIFIER | c.239-23071dupA | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 87677335 | ||||||
| chr7:87677335 | TA | T | 7 | a0001c0001t0001g0045 a0001c0001t0005g0129 a0001c0001t0016g0023 others(4): Show |
7 | HG00639.hp1 HG03098.hp2 HG03491.hp2 others(4): Show |
intron_variant | MODIFIER | c.239-23071delA | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 87677335 | ||||||
| chr7:87677504 | G | T | 3 | a0001c0001t0029g0048 a0001c0001t0032g0049 a0001c0001t0032g0051 |
3 | HG02559.hp1 HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.239-22917G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87677504 | |||||||
| chr7:87677809 | T | C | 1 | a0001c0001t0002g0162 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.239-22612T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87677809 | |||||||
| chr7:87678193 | A | G | 1 | a0001c0001t0036g0159 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.239-22228A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87678193 | |||||||
| chr7:87678405 | T | C | 3 | a0001c0001t0009g0002 a0001c0001t0009g0197 a0001c0001t0028g0002 |
3 | HG01069.hp2 HG01071.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.239-22016T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87678405 | |||||||
| chr7:87678594 | C | A | 17 | a0001c0001t0006g0186 a0001c0001t0009g0002 a0001c0001t0009g0190 others(14): Show |
17 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.239-21827C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87678594 | |||||||
| chr7:87678759 | GA | G | 7 | a0001c0001t0010g0008 a0001c0001t0010g0010 a0001c0001t0010g0011 others(4): Show |
7 | HG02055.hp1 HG02280.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.239-21655delA | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 87678759 | ||||||
| chr7:87678817 | C | T | 7 | a0001c0001t0010g0008 a0001c0001t0010g0010 a0001c0001t0010g0011 others(4): Show |
7 | HG02055.hp1 HG02280.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.239-21604C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87678817 | |||||||
| chr7:87679017 | AGAAAATT others(2762): Show |
A | 38 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(35): Show |
38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.239-21401_239-1863 others(4): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 87679017 | ||||||
| chr7:87679087 | CT | C | 137 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0045 others(134): Show |
137 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.239-21311delT | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 87679087 | ||||||
| chr7:87679087 | CTT | C | 18 | a0001c0001t0003g0076 a0001c0001t0006g0186 a0001c0001t0009g0002 others(15): Show |
18 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.239-21312_239-2131 others(6): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 87679087 | ||||||
| chr7:87679389 | G | A | 1 | a0001c0001t0042g0050 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.239-21032G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87679389 | |||||||
| chr7:87679473 | C | A | 2 | a0001c0001t0055g0020 a0001c0001t0070g0014 |
2 | HG02572.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.239-20948C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87679473 | |||||||
| chr7:87679525 | G | A | 1 | a0001c0001t0077g0081 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.239-20896G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87679525 | |||||||
| chr7:87679668 | G | A | 1 | a0001c0001t0006g0186 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.239-20753G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87679668 | |||||||
| chr7:87679794 | T | C | 1 | a0001c0001t0036g0159 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.239-20627T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87679794 | |||||||
| chr7:87679832 | T | C | 1 | a0001c0001t0036g0159 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.239-20589T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87679832 | |||||||
| chr7:87679852 | A | G | 1 | a0001c0001t0070g0014 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.239-20569A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87679852 | |||||||
| chr7:87680097 | A | G | 1 | a0001c0001t0049g0038 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.239-20324A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87680097 | |||||||
| chr7:87680563 | C | T | 1 | a0001c0001t0010g0008 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.239-19858C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87680563 | |||||||
| chr7:87680750 | G | A | 2 | a0001c0001t0004g0109 a0001c0001t0004g0110 |
2 | HG00738.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.239-19671G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87680750 | |||||||
| chr7:87681004 | A | G | 1 | a0001c0001t0040g0013 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.239-19417A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87681004 | |||||||
| chr7:87681058 | T | C | 50 | a0001c0001t0006g0186 a0001c0001t0009g0002 a0001c0001t0009g0190 others(47): Show |
50 | HG00280.hp2 HG00423.hp1 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.239-19363T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87681058 | |||||||
| chr7:87681127 | A | G | 2 | a0001c0001t0017g0065 a0001c0001t0017g0085 |
2 | HG00738.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.239-19294A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87681127 | |||||||
| chr7:87681634 | G | A | 1 | a0001c0001t0043g0106 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.239-18787G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87681634 | |||||||
| chr7:87681934 | C | T | 6 | a0001c0001t0039g0148 a0001c0001t0055g0020 a0001c0001t0057g0017 others(3): Show |
6 | HG02572.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.239-18487C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87681934 | |||||||
| chr7:87682204 | G | A | 1 | a0001c0001t0053g0063 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.239-18217G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87682204 | |||||||
| chr7:87682364 | C | T | 3 | a0001c0001t0056g0016 a0001c0001t0063g0015 a0001c0001t0070g0014 |
3 | HG02572.hp2 HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.239-18057C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87682364 | |||||||
| chr7:87682561 | T | C | 1 | a0001c0001t0003g0056 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.239-17860T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87682561 | |||||||
| chr7:87682648 | A | G | 1 | a0001c0001t0026g0040 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.239-17773A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87682648 | |||||||
| chr7:87682781 | T | G | 1 | a0001c0001t0001g0041 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.239-17640T>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87682781 | |||||||
| chr7:87682868 | G | A | 12 | a0001c0001t0014g0152 a0001c0001t0014g0155 a0001c0001t0014g0158 others(9): Show |
12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.239-17553G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87682868 | |||||||
| chr7:87683142 | C | T | 1 | a0001c0001t0002g0162 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.239-17279C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87683142 | |||||||
| chr7:87683277 | G | C | 1 | a0001c0001t0077g0081 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.239-17144G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87683277 | |||||||
| chr7:87683726 | G | A | 1 | a0001c0001t0075g0007 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.239-16695G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87683726 | |||||||
| chr7:87683799 | G | A | 4 | a0001c0001t0024g0004 a0001c0001t0025g0005 a0001c0001t0037g0006 others(1): Show |
4 | HG00639.hp2 HG02976.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.239-16622G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87683799 | |||||||
| chr7:87684330 | T | G | 2 | a0001c0001t0022g0182 a0001c0001t0027g0180 |
2 | NA18974.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.239-16091T>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87684330 | |||||||
| chr7:87684370 | A | G | 7 | a0001c0001t0010g0008 a0001c0001t0010g0010 a0001c0001t0010g0011 others(4): Show |
7 | HG02055.hp1 HG02280.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.239-16051A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87684370 | |||||||
| chr7:87684746 | C | CA | 8 | a0001c0001t0004g0055 a0001c0001t0007g0059 a0001c0001t0007g0122 others(5): Show |
8 | HG00423.hp2 HG00621.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.239-15648dupA | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 87684746 | ||||||
| chr7:87684746 | C | CAA | 10 | a0001c0001t0014g0155 a0001c0001t0014g0158 a0001c0001t0015g0150 others(7): Show |
10 | HG00423.hp1 HG03098.hp2 NA18952.hp1 others(7): Show |
intron_variant | MODIFIER | c.239-15649_239-1564 others(6): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 87684746 | ||||||
| chr7:87684746 | C | CAAAA | 44 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(41): Show |
44 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(41): Show |
intron_variant | MODIFIER | c.239-15651_239-1564 others(8): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 87684746 | ||||||
| chr7:87684746 | C | CAAAAA | 10 | a0001c0001t0002g0166 a0001c0001t0002g0200 a0001c0001t0012g0176 others(7): Show |
10 | HG02622.hp2 HG02970.hp2 HG03130.hp2 others(7): Show |
intron_variant | MODIFIER | c.239-15652_239-1564 others(9): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 87684746 | ||||||
| chr7:87684746 | CA | C | 40 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0045 others(37): Show |
40 | HG00735.hp1 HG00741.hp1 HG01074.hp1 others(37): Show |
intron_variant | MODIFIER | c.239-15648delA | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 87684746 | ||||||
| chr7:87684746 | CAA | C | 5 | a0001c0001t0039g0148 a0001c0001t0057g0017 a0001c0001t0060g0100 others(2): Show |
5 | HG02630.hp1 HG02723.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.239-15649_239-1564 others(6): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 87684746 | ||||||
| chr7:87684815 | A | G | 2 | a0001c0001t0003g0075 a0001c0001t0004g0067 |
2 | HG00741.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.239-15606A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87684815 | |||||||
| chr7:87685472 | G | T | 4 | a0001c0001t0044g0169 a0001c0001t0046g0161 a0001c0001t0047g0172 others(1): Show |
4 | HG01123.hp1 HG01192.hp1 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.239-14949G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87685472 | |||||||
| chr7:87685494 | C | T | 17 | a0001c0001t0006g0186 a0001c0001t0009g0002 a0001c0001t0009g0190 others(14): Show |
17 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.239-14927C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87685494 | |||||||
| chr7:87685509 | G | GA | 13 | a0001c0001t0017g0065 a0001c0001t0017g0085 a0001c0001t0017g0112 others(10): Show |
13 | HG00621.hp1 HG00738.hp1 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.239-14904dupA | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 87685509 | ||||||
| chr7:87685593 | G | A | 1 | a0001c0001t0036g0159 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.239-14828G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87685593 | |||||||
| chr7:87685942 | A | G | 1 | a0001c0001t0004g0083 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.239-14479A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87685942 | |||||||
| chr7:87685958 | A | G | 4 | a0001c0001t0024g0004 a0001c0001t0025g0005 a0001c0001t0037g0006 others(1): Show |
4 | HG00639.hp2 HG02976.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.239-14463A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87685958 | |||||||
| chr7:87685996 | C | A | 12 | a0001c0001t0014g0152 a0001c0001t0014g0155 a0001c0001t0014g0158 others(9): Show |
12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.239-14425C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87685996 | |||||||
| chr7:87686323 | A | G | 4 | a0001c0001t0044g0169 a0001c0001t0046g0161 a0001c0001t0047g0172 others(1): Show |
4 | HG01123.hp1 HG01192.hp1 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.239-14098A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87686323 | |||||||
| chr7:87686429 | G | A | 1 | a0001c0001t0043g0106 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.239-13992G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87686429 | |||||||
| chr7:87686505 | C | A | 2 | a0001c0001t0058g0184 a0001c0001t0061g0185 |
2 | HG03017.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.239-13916C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87686505 | |||||||
| chr7:87686565 | G | A | 38 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(35): Show |
38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.239-13856G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87686565 | |||||||
| chr7:87686570 | A | C | 1 | a0001c0001t0049g0038 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.239-13851A>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87686570 | |||||||
| chr7:87686606 | A | C | 1 | a0001c0001t0001g0119 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.239-13815A>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87686606 | |||||||
| chr7:87686727 | C | A | 1 | a0001c0001t0036g0159 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.239-13694C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87686727 | |||||||
| chr7:87686769 | G | A | 1 | a0001c0001t0010g0008 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.239-13652G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87686769 | |||||||
| chr7:87686776 | G | GA | 5 | a0001c0001t0001g0042 a0001c0001t0001g0098 a0001c0001t0049g0038 others(2): Show |
5 | HG01167.hp2 HG02572.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.239-13629dupA | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 87686776 | ||||||
| chr7:87686812 | G | A | 2 | a0001c0001t0008g0123 a0001c0001t0008g0131 |
2 | HG02055.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.239-13609G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87686812 | |||||||
| chr7:87686848 | G | A | 1 | a0001c0001t0006g0142 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.239-13573G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87686848 | |||||||
| chr7:87686935 | G | T | 1 | a0001c0001t0040g0013 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.239-13486G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87686935 | |||||||
| chr7:87687304 | A | C | 1 | a0001c0001t0036g0159 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.239-13117A>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87687304 | |||||||
| chr7:87687323 | T | C | 1 | a0001c0001t0072g0009 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.239-13098T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87687323 | |||||||
| chr7:87687324 | G | C | 1 | a0001c0001t0072g0009 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.239-13097G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87687324 | |||||||
| chr7:87687325 | G | A | 1 | a0001c0001t0072g0009 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.239-13096G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87687325 | |||||||
| chr7:87687744 | A | C | 1 | a0001c0001t0065g0003 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.239-12677A>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87687744 | |||||||
| chr7:87687778 | C | T | 2 | a0001c0001t0056g0016 a0001c0001t0063g0015 |
2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.239-12643C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87687778 | |||||||
| chr7:87687926 | C | G | 1 | a0001c0001t0026g0120 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.239-12495C>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87687926 | |||||||
| chr7:87687949 | C | T | 1 | a0001c0001t0006g0186 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.239-12472C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87687949 | |||||||
| chr7:87688080 | A | G | 1 | a0001c0001t0036g0159 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.239-12341A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87688080 | |||||||
| chr7:87688154 | G | C | 1 | a0001c0001t0006g0115 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.239-12267G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87688154 | |||||||
| chr7:87688220 | G | A | 1 | a0001c0001t0052g0196 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.239-12201G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87688220 | |||||||
| chr7:87688444 | T | A | 1 | a0001c0001t0055g0020 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.239-11977T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87688444 | |||||||
| chr7:87688643 | G | A | 2 | a0001c0001t0004g0109 a0001c0001t0004g0110 |
2 | HG00738.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.239-11778G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87688643 | |||||||
| chr7:87688742 | A | G | 1 | a0001c0001t0006g0111 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.239-11679A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87688742 | |||||||
| chr7:87688855 | A | G | 1 | a0001c0001t0001g0098 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.239-11566A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87688855 | |||||||
| chr7:87688971 | C | G | 1 | a0001c0001t0004g0058 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.239-11450C>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87688971 | |||||||
| chr7:87689133 | T | C | 2 | a0001c0001t0056g0016 a0001c0001t0063g0015 |
2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.239-11288T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87689133 | |||||||
| chr7:87689492 | G | A | 1 | a0001c0001t0049g0038 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.239-10929G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87689492 | |||||||
| chr7:87689689 | A | G | 4 | a0001c0001t0044g0169 a0001c0001t0046g0161 a0001c0001t0047g0172 others(1): Show |
4 | HG01123.hp1 HG01192.hp1 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.239-10732A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87689689 | |||||||
| chr7:87689991 | T | A | 58 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(55): Show |
58 | HG00423.hp1 HG00639.hp2 HG01081.hp2 others(55): Show |
intron_variant | MODIFIER | c.239-10430T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87689991 | |||||||
| chr7:87689997 | T | A | 3 | a0001c0001t0057g0017 a0001c0001t0066g0019 a0001c0001t0067g0018 |
3 | HG02630.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.239-10424T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87689997 | |||||||
| chr7:87690286 | G | T | 3 | a0001c0001t0057g0017 a0001c0001t0066g0019 a0001c0001t0067g0018 |
3 | HG02630.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.239-10135G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87690286 | |||||||
| chr7:87690483 | C | T | 1 | a0001c0001t0055g0020 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.239-9938C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87690483 | |||||||
| chr7:87690928 | T | C | 2 | a0001c0001t0066g0019 a0001c0001t0067g0018 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.239-9493T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87690928 | |||||||
| chr7:87691037 | A | G | 12 | a0001c0001t0014g0152 a0001c0001t0014g0155 a0001c0001t0014g0158 others(9): Show |
12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.239-9384A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87691037 | |||||||
| chr7:87691397 | A | G | 1 | a0001c0001t0070g0014 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.239-9024A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87691397 | |||||||
| chr7:87691734 | T | A | 1 | a0001c0001t0049g0038 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.239-8687T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87691734 | |||||||
| chr7:87691762 | T | G | 1 | a0001c0001t0049g0038 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.239-8659T>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87691762 | |||||||
| chr7:87691803 | G | A | 12 | a0001c0001t0014g0152 a0001c0001t0014g0155 a0001c0001t0014g0158 others(9): Show |
12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.239-8618G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87691803 | |||||||
| chr7:87691832 | G | A | 17 | a0001c0001t0006g0186 a0001c0001t0009g0002 a0001c0001t0009g0190 others(14): Show |
17 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.239-8589G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87691832 | |||||||
| chr7:87691858 | C | A | 1 | a0001c0001t0025g0091 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.239-8563C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87691858 | |||||||
| chr7:87692155 | A | G | 2 | a0001c0001t0056g0016 a0001c0001t0063g0015 |
2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.239-8266A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87692155 | |||||||
| chr7:87692255 | A | G | 1 | a0001c0001t0008g0069 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.239-8166A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87692255 | |||||||
| chr7:87692666 | A | G | 1 | a0001c0001t0003g0076 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.239-7755A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87692666 | |||||||
| chr7:87692706 | T | C | 1 | a0001c0001t0057g0017 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.239-7715T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87692706 | |||||||
| chr7:87692729 | A | T | 2 | a0001c0001t0020g0033 a0001c0001t0035g0034 |
2 | NA19056.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.239-7692A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87692729 | |||||||
| chr7:87693028 | A | G | 1 | a0001c0001t0021g0028 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.239-7393A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87693028 | |||||||
| chr7:87693034 | G | A | 1 | a0001c0001t0052g0196 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.239-7387G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87693034 | |||||||
| chr7:87693070 | A | G | 17 | a0001c0001t0006g0186 a0001c0001t0009g0002 a0001c0001t0009g0190 others(14): Show |
17 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.239-7351A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87693070 | |||||||
| chr7:87693123 | T | C | 1 | a0001c0001t0002g0030 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.239-7298T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87693123 | |||||||
| chr7:87693180 | G | GA | 17 | a0001c0001t0006g0186 a0001c0001t0009g0002 a0001c0001t0009g0190 others(14): Show |
17 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.239-7236dupA | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 87693180 | ||||||
| chr7:87693385 | T | A | 4 | a0001c0001t0004g0022 a0001c0001t0004g0047 a0001c0001t0008g0021 others(1): Show |
4 | HG02896.hp2 HG02976.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.239-7036T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87693385 | |||||||
| chr7:87693503 | A | T | 1 | a0001c0001t0003g0114 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.239-6918A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87693503 | |||||||
| chr7:87693507 | T | C | 2 | a0001c0001t0056g0016 a0001c0001t0063g0015 |
2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.239-6914T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87693507 | |||||||
| chr7:87693588 | C | A | 2 | a0001c0001t0055g0020 a0001c0001t0070g0014 |
2 | HG02572.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.239-6833C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87693588 | |||||||
| chr7:87693613 | G | A | 1 | a0001c0001t0001g0060 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.239-6808G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87693613 | |||||||
| chr7:87693695 | T | A | 1 | a0001c0001t0049g0038 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.239-6726T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87693695 | |||||||
| chr7:87693829 | C | T | 16 | a0001c0001t0006g0186 a0001c0001t0009g0002 a0001c0001t0009g0190 others(13): Show |
16 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.239-6592C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87693829 | |||||||
| chr7:87694100 | GT | G | 70 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(67): Show |
70 | HG00423.hp1 HG00639.hp2 HG01081.hp2 others(67): Show |
intron_variant | MODIFIER | c.239-6309delT | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 87694100 | ||||||
| chr7:87694100 | GTT | G | 16 | a0001c0001t0006g0186 a0001c0001t0009g0002 a0001c0001t0009g0190 others(13): Show |
16 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.239-6310_239-6309d others(4): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 87694100 | ||||||
| chr7:87694271 | T | A | 1 | a0001c0001t0004g0047 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.239-6150T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87694271 | |||||||
| chr7:87694418 | A | G | 14 | a0001c0001t0002g0162 a0001c0001t0002g0163 a0001c0001t0002g0164 others(11): Show |
14 | HG01081.hp2 HG02258.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.239-6003A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87694418 | |||||||
| chr7:87694702 | T | A | 2 | a0001c0001t0030g0187 a0001c0001t0030g0188 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.239-5719T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87694702 | |||||||
| chr7:87694712 | C | A | 1 | a0001c0001t0074g0170 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.239-5709C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87694712 | |||||||
| chr7:87695053 | G | A | 1 | a0001c0001t0018g0175 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.239-5368G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87695053 | |||||||
| chr7:87695070 | G | A | 38 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(35): Show |
38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.239-5351G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87695070 | |||||||
| chr7:87695823 | C | T | 2 | a0001c0001t0004g0047 a0001c0001t0064g0046 |
2 | HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.239-4598C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87695823 | |||||||
| chr7:87695862 | T | C | 3 | a0001c0001t0057g0017 a0001c0001t0066g0019 a0001c0001t0067g0018 |
3 | HG02630.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.239-4559T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87695862 | |||||||
| chr7:87696418 | A | T | 1 | a0001c0001t0054g0138 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.239-4003A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87696418 | |||||||
| chr7:87696630 | T | C | 1 | a0001c0001t0002g0200 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.239-3791T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87696630 | |||||||
| chr7:87696809 | T | G | 13 | a0001c0001t0014g0152 a0001c0001t0014g0155 a0001c0001t0014g0158 others(10): Show |
13 | HG00423.hp1 HG02723.hp1 NA18952.hp1 others(10): Show |
intron_variant | MODIFIER | c.239-3612T>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87696809 | |||||||
| chr7:87696816 | G | C | 3 | a0001c0001t0004g0055 a0001c0001t0004g0058 a0001c0001t0005g0068 |
3 | NA18977.hp1 NA19010.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.239-3605G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87696816 | |||||||
| chr7:87697018 | C | T | 2 | a0001c0001t0001g0134 a0001c0001t0001g0136 |
2 | HG01192.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.239-3403C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87697018 | |||||||
| chr7:87697146 | G | A | 1 | a0001c0001t0057g0017 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.239-3275G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87697146 | |||||||
| chr7:87697259 | G | C | 1 | a0001c0001t0023g0156 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.239-3162G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87697259 | |||||||
| chr7:87697273 | C | T | 1 | a0001c0001t0049g0038 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.239-3148C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87697273 | |||||||
| chr7:87697772 | C | T | 1 | a0001c0001t0039g0148 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.239-2649C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87697772 | |||||||
| chr7:87697886 | T | C | 1 | a0001c0001t0061g0185 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.239-2535T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87697886 | |||||||
| chr7:87697924 | G | A | 1 | a0001c0001t0046g0161 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.239-2497G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87697924 | |||||||
| chr7:87698383 | C | T | 2 | a0001c0001t0056g0016 a0001c0001t0063g0015 |
2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.239-2038C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87698383 | |||||||
| chr7:87698687 | T | C | 88 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(85): Show |
88 | HG00280.hp2 HG00423.hp1 HG00639.hp2 others(85): Show |
intron_variant | MODIFIER | c.239-1734T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87698687 | |||||||
| chr7:87699099 | C | T | 2 | a0001c0001t0055g0020 a0001c0001t0070g0014 |
2 | HG02572.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.239-1322C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87699099 | |||||||
| chr7:87699415 | C | CT | 5 | a0001c0001t0001g0071 a0001c0001t0001g0104 a0001c0001t0055g0020 others(2): Show |
5 | HG01496.hp2 HG02572.hp2 NA19001.hp2 others(2): Show |
intron_variant | MODIFIER | c.239-997dupT | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 87699415 | ||||||
| chr7:87699870 | G | T | 1 | a0001c0001t0049g0038 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.239-551G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87699870 | |||||||
| chr7:87700342 | G | C | 1 | a0001c0001t0001g0092 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.239-79G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87700342 | |||||||
| chr7:87700706 | A | AAT | 17 | a0001c0001t0006g0186 a0001c0001t0009g0002 a0001c0001t0009g0190 others(14): Show |
17 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.372+153_372+154dup others(2): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr7 | 87700706 | ||||||
| chr7:87700785 | A | T | 63 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(60): Show |
63 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(60): Show |
intron_variant | MODIFIER | c.372+231A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87700785 | |||||||
| chr7:87701107 | G | A | 62 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(59): Show |
62 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(59): Show |
intron_variant | MODIFIER | c.372+553G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87701107 | |||||||
| chr7:87701872 | G | A | 8 | a0001c0001t0010g0008 a0001c0001t0010g0010 a0001c0001t0010g0011 others(5): Show |
8 | HG02055.hp1 HG02280.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.372+1318G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87701872 | |||||||
| chr7:87701959 | T | C | 62 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(59): Show |
62 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(59): Show |
intron_variant | MODIFIER | c.372+1405T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87701959 | |||||||
| chr7:87702000 | A | G | 88 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(85): Show |
88 | HG00280.hp2 HG00423.hp1 HG00639.hp2 others(85): Show |
intron_variant | MODIFIER | c.372+1446A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87702000 | |||||||
| chr7:87702060 | G | A | 1 | a0001c0001t0065g0003 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.372+1506G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87702060 | |||||||
| chr7:87702100 | G | A | 12 | a0001c0001t0014g0152 a0001c0001t0014g0155 a0001c0001t0014g0158 others(9): Show |
12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.372+1546G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87702100 | |||||||
| chr7:87702142 | C | CA | 49 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0054 others(46): Show |
49 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(46): Show |
intron_variant | MODIFIER | c.372+1618dupA | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr7 | 87702142 | ||||||
| chr7:87702142 | C | CAA | 23 | a0001c0001t0001g0064 a0001c0001t0003g0082 a0001c0001t0004g0110 others(20): Show |
23 | HG00423.hp2 HG00438.hp1 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.372+1617_372+1618d others(4): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr7 | 87702142 | ||||||
| chr7:87702142 | C | CAAA | 6 | a0001c0001t0004g0109 a0001c0001t0006g0186 a0001c0001t0008g0123 others(3): Show |
6 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(3): Show |
intron_variant | MODIFIER | c.372+1616_372+1618d others(5): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr7 | 87702142 | ||||||
| chr7:87702142 | C | CAAAA | 14 | a0001c0001t0009g0191 a0001c0001t0009g0193 a0001c0001t0010g0008 others(11): Show |
14 | HG01123.hp1 HG01346.hp1 HG01358.hp1 others(11): Show |
intron_variant | MODIFIER | c.372+1615_372+1618d others(6): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr7 | 87702142 | ||||||
| chr7:87702142 | C | CAAAAA | 19 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(16): Show |
19 | HG01081.hp2 HG01192.hp1 HG01952.hp2 others(16): Show |
intron_variant | MODIFIER | c.372+1614_372+1618d others(7): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr7 | 87702142 | ||||||
| chr7:87702142 | C | CAAAAAA | 16 | a0001c0001t0002g0163 a0001c0001t0002g0164 a0001c0001t0002g0167 others(13): Show |
16 | HG02258.hp2 HG02559.hp2 HG02622.hp2 others(13): Show |
intron_variant | MODIFIER | c.372+1613_372+1618d others(8): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr7 | 87702142 | ||||||
| chr7:87702142 | C | CAAAAAAA | 6 | a0001c0001t0002g0168 a0001c0001t0012g0177 a0001c0001t0022g0181 others(3): Show |
6 | HG02622.hp1 HG02630.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.372+1612_372+1618d others(9): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr7 | 87702142 | ||||||
| chr7:87702142 | C | CAAAAAAA others(1): Show |
5 | a0001c0001t0015g0150 a0001c0001t0023g0039 a0001c0001t0045g0160 others(2): Show |
5 | HG02572.hp1 HG03209.hp2 NA18963.hp1 others(2): Show |
intron_variant | MODIFIER | c.372+1611_372+1618d others(10): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr7 | 87702142 | ||||||
| chr7:87702142 | C | CAAAAAAA others(2): Show |
5 | a0001c0001t0014g0152 a0001c0001t0014g0155 a0001c0001t0014g0158 others(2): Show |
5 | NA18952.hp1 NA18988.hp2 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.372+1610_372+1618d others(11): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr7 | 87702142 | ||||||
| chr7:87702142 | C | CAAAAAAA others(3): Show |
3 | a0001c0001t0015g0154 a0001c0001t0033g0037 a0001c0001t0033g0157 |
3 | HG00423.hp1 NA19062.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.372+1609_372+1618d others(12): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr7 | 87702142 | ||||||
| chr7:87702142 | C | CAAAAAAA others(4): Show |
1 | a0001c0001t0023g0156 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.372+1608_372+1618d others(13): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr7 | 87702142 | ||||||
| chr7:87702142 | CAAAAAAA others(9): Show |
C | 3 | a0002c0002t0002g0029 a0002c0002t0002g0036 a0002c0002t0018g0140 |
3 | NA18973.hp2 NA18979.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.372+1603_372+1618d others(18): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr7 | 87702142 | ||||||
| chr7:87702168 | A | AAAAAAAA others(3): Show |
1 | a0001c0001t0039g0148 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.372+1618_372+1619i others(12): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr7 | 87702168 | ||||||
| chr7:87702175 | G | C | 1 | a0001c0001t0001g0099 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.372+1621G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87702175 | |||||||
| chr7:87702297 | G | A | 1 | a0001c0001t0010g0008 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.372+1743G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87702297 | |||||||
| chr7:87702391 | A | G | 2 | a0001c0001t0039g0148 a0001c0001t0049g0038 |
2 | HG02723.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.372+1837A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87702391 | |||||||
| chr7:87702540 | G | T | 1 | a0001c0001t0055g0020 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.372+1986G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87702540 | |||||||
| chr7:87702649 | T | C | 40 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(37): Show |
40 | HG01081.hp2 HG01099.hp2 HG01123.hp1 others(37): Show |
intron_variant | MODIFIER | c.372+2095T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87702649 | |||||||
| chr7:87702696 | T | G | 3 | a0001c0001t0057g0017 a0001c0001t0066g0019 a0001c0001t0067g0018 |
3 | HG02630.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.372+2142T>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87702696 | |||||||
| chr7:87703121 | G | A | 1 | a0001c0001t0010g0008 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.372+2567G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87703121 | |||||||
| chr7:87703122 | A | G | 38 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(35): Show |
38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.372+2568A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87703122 | |||||||
| chr7:87703143 | C | T | 2 | a0001c0001t0010g0010 a0001c0001t0010g0011 |
2 | HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.372+2589C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87703143 | |||||||
| chr7:87703155 | T | A | 39 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(36): Show |
39 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(36): Show |
intron_variant | MODIFIER | c.372+2601T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87703155 | |||||||
| chr7:87703381 | C | G | 12 | a0001c0001t0014g0152 a0001c0001t0014g0155 a0001c0001t0014g0158 others(9): Show |
12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.372+2827C>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87703381 | |||||||
| chr7:87703457 | G | A | 2 | a0001c0001t0055g0020 a0001c0001t0070g0014 |
2 | HG02572.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.372+2903G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87703457 | |||||||
| chr7:87703523 | C | A | 1 | a0001c0001t0007g0132 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.372+2969C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87703523 | |||||||
| chr7:87703680 | AT | A | 6 | a0001c0001t0039g0148 a0001c0001t0055g0020 a0001c0001t0057g0017 others(3): Show |
6 | HG02572.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.372+3131delT | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr7 | 87703680 | ||||||
| chr7:87703731 | C | T | 1 | a0001c0001t0011g0198 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.372+3177C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87703731 | |||||||
| chr7:87703755 | T | C | 2 | a0001c0001t0055g0020 a0001c0001t0070g0014 |
2 | HG02572.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.372+3201T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87703755 | |||||||
| chr7:87703885 | CT | C | 15 | a0001c0001t0001g0042 a0001c0001t0001g0045 a0001c0001t0003g0066 others(12): Show |
15 | HG00323.hp1 HG00323.hp2 HG02135.hp2 others(12): Show |
intron_variant | MODIFIER | c.372+3358delT | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr7 | 87703885 | ||||||
| chr7:87703885 | CTTTTTTT others(22): Show |
C | 3 | a0001c0001t0001g0098 a0001c0001t0062g0145 a0001c0001t0068g0143 |
3 | HG01069.hp1 HG01167.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.372+3358_372+3386d others(31): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr7 | 87703885 | ||||||
| chr7:87703885 | CTTTTTTT others(23): Show |
C | 2 | a0001c0001t0035g0034 a0001c0001t0042g0050 |
2 | HG00639.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.372+3357_372+3386d others(32): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr7 | 87703885 | ||||||
| chr7:87703885 | CTTTTTTT others(24): Show |
C | 40 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(37): Show |
40 | HG00423.hp1 HG01081.hp2 HG01123.hp1 others(37): Show |
intron_variant | MODIFIER | c.372+3356_372+3386d others(33): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr7 | 87703885 | ||||||
| chr7:87703885 | CTTTTTTT others(25): Show |
C | 27 | a0001c0001t0001g0054 a0001c0001t0009g0002 a0001c0001t0009g0190 others(24): Show |
27 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(24): Show |
intron_variant | MODIFIER | c.372+3355_372+3386d others(34): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr7 | 87703885 | ||||||
| chr7:87703885 | CTTTTTTT others(26): Show |
C | 1 | a0001c0001t0030g0187 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.372+3354_372+3386d others(35): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr7 | 87703885 | ||||||
| chr7:87703886 | TTTTTTTT others(21): Show |
T | 1 | a0001c0001t0069g0144 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.372+3360_372+3387d others(30): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr7 | 87703886 | ||||||
| chr7:87703896 | T | C | 1 | a0001c0001t0001g0089 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.372+3342T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87703896 | |||||||
| chr7:87703897 | T | C | 1 | a0001c0001t0001g0097 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.372+3343T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87703897 | |||||||
| chr7:87703911 | TTG | T | 42 | a0001c0001t0001g0041 a0001c0001t0001g0060 a0001c0001t0001g0070 others(39): Show |
42 | HG00558.hp2 HG01074.hp1 HG01081.hp1 others(39): Show |
intron_variant | MODIFIER | c.372+3358_372+3359d others(4): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87703911 | |||||||
| chr7:87703912 | T | G | 5 | a0001c0001t0003g0076 a0001c0001t0008g0021 a0001c0001t0008g0123 others(2): Show |
5 | HG01358.hp2 HG02055.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.372+3358T>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87703912 | |||||||
| chr7:87703914 | G | T | 5 | a0001c0001t0003g0076 a0001c0001t0008g0021 a0001c0001t0008g0123 others(2): Show |
5 | HG01358.hp2 HG02055.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.372+3360G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87703914 | |||||||
| chr7:87703914 | GT | G | 18 | a0001c0001t0001g0092 a0001c0001t0001g0097 a0001c0001t0001g0134 others(15): Show |
18 | HG00621.hp1 HG00621.hp2 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.372+3386delT | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr7 | 87703914 | ||||||
| chr7:87703915 | T | G | 51 | a0001c0001t0001g0041 a0001c0001t0001g0060 a0001c0001t0001g0070 others(48): Show |
51 | HG00558.hp2 HG01074.hp1 HG01081.hp1 others(48): Show |
intron_variant | MODIFIER | c.372+3361T>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87703915 | |||||||
| chr7:87703919 | T | G | 2 | a0001c0001t0004g0047 a0001c0001t0064g0046 |
2 | HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.372+3365T>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87703919 | |||||||
| chr7:87703922 | T | G | 1 | a0001c0001t0072g0009 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.372+3368T>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87703922 | |||||||
| chr7:87703991 | G | T | 1 | a0001c0001t0010g0011 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.372+3437G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87703991 | |||||||
| chr7:87704010 | T | A | 1 | a0001c0001t0001g0119 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.372+3456T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87704010 | |||||||
| chr7:87704291 | C | T | 1 | a0001c0001t0036g0159 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.372+3737C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87704291 | |||||||
| chr7:87704681 | C | T | 1 | a0001c0001t0010g0012 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.372+4127C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87704681 | |||||||
| chr7:87705068 | A | G | 63 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(60): Show |
63 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(60): Show |
intron_variant | MODIFIER | c.372+4514A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87705068 | |||||||
| chr7:87705295 | G | A | 3 | a0001c0001t0057g0017 a0001c0001t0066g0019 a0001c0001t0067g0018 |
3 | HG02630.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.372+4741G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87705295 | |||||||
| chr7:87705318 | T | C | 84 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(81): Show |
84 | HG00280.hp2 HG00423.hp1 HG01069.hp2 others(81): Show |
intron_variant | MODIFIER | c.372+4764T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87705318 | |||||||
| chr7:87705441 | C | T | 38 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(35): Show |
38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.372+4887C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87705441 | |||||||
| chr7:87705453 | A | C | 1 | a0001c0001t0016g0072 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.372+4899A>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87705453 | |||||||
| chr7:87705525 | T | C | 12 | a0001c0001t0014g0152 a0001c0001t0014g0155 a0001c0001t0014g0158 others(9): Show |
12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.372+4971T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87705525 | |||||||
| chr7:87705988 | G | T | 2 | a0001c0001t0066g0019 a0001c0001t0067g0018 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.373-4582G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87705988 | |||||||
| chr7:87706139 | A | G | 12 | a0001c0001t0014g0152 a0001c0001t0014g0155 a0001c0001t0014g0158 others(9): Show |
12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.373-4431A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87706139 | |||||||
| chr7:87706441 | A | G | 2 | a0001c0001t0017g0065 a0001c0001t0017g0085 |
2 | HG00738.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.373-4129A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87706441 | |||||||
| chr7:87706707 | G | A | 1 | a0001c0001t0004g0067 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.373-3863G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87706707 | |||||||
| chr7:87707165 | C | A | 2 | a0001c0001t0001g0042 a0001c0001t0001g0098 |
2 | HG01167.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.373-3405C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87707165 | |||||||
| chr7:87707401 | C | T | 38 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(35): Show |
38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.373-3169C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87707401 | |||||||
| chr7:87707402 | G | A | 1 | a0001c0001t0034g0199 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.373-3168G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87707402 | |||||||
| chr7:87707417 | T | C | 1 | a0001c0001t0005g0062 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.373-3153T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87707417 | |||||||
| chr7:87707679 | AAAATAAA others(6): Show |
A | 1 | a0002c0002t0002g0036 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.373-2878_373-2866d others(15): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr7 | 87707679 | ||||||
| chr7:87707912 | G | T | 11 | a0001c0001t0003g0082 a0001c0001t0004g0055 a0001c0001t0004g0058 others(8): Show |
11 | HG00438.hp1 HG00558.hp1 HG01952.hp1 others(8): Show |
intron_variant | MODIFIER | c.373-2658G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87707912 | |||||||
| chr7:87708196 | C | A | 2 | a0001c0001t0001g0119 a0001c0001t0024g0102 |
2 | HG01099.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.373-2374C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87708196 | |||||||
| chr7:87708317 | A | T | 16 | a0001c0001t0009g0002 a0001c0001t0009g0190 a0001c0001t0009g0191 others(13): Show |
16 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.373-2253A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87708317 | |||||||
| chr7:87708443 | G | A | 74 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(71): Show |
74 | HG00280.hp2 HG00423.hp1 HG01069.hp2 others(71): Show |
intron_variant | MODIFIER | c.373-2127G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87708443 | |||||||
| chr7:87708463 | G | A | 74 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(71): Show |
74 | HG00280.hp2 HG00423.hp1 HG01069.hp2 others(71): Show |
intron_variant | MODIFIER | c.373-2107G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87708463 | |||||||
| chr7:87708511 | T | A | 2 | a0001c0001t0056g0016 a0001c0001t0063g0015 |
2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.373-2059T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87708511 | |||||||
| chr7:87708727 | G | A | 1 | a0001c0001t0004g0055 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.373-1843G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87708727 | |||||||
| chr7:87708753 | G | A | 1 | a0001c0001t0036g0159 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.373-1817G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87708753 | |||||||
| chr7:87708792 | G | T | 1 | a0001c0001t0049g0038 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.373-1778G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87708792 | |||||||
| chr7:87708793 | C | T | 1 | a0001c0001t0049g0038 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.373-1777C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87708793 | |||||||
| chr7:87708937 | A | C | 1 | a0001c0001t0011g0194 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.373-1633A>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87708937 | |||||||
| chr7:87708978 | A | T | 1 | a0001c0001t0003g0141 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.373-1592A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87708978 | |||||||
| chr7:87709298 | T | C | 16 | a0001c0001t0009g0002 a0001c0001t0009g0190 a0001c0001t0009g0191 others(13): Show |
16 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.373-1272T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87709298 | |||||||
| chr7:87709323 | G | A | 1 | a0001c0001t0049g0038 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.373-1247G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87709323 | |||||||
| chr7:87709506 | T | C | 1 | a0001c0001t0055g0020 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.373-1064T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87709506 | |||||||
| chr7:87709756 | A | C | 1 | a0001c0001t0002g0200 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.373-814A>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87709756 | |||||||
| chr7:87709758 | T | A | 1 | a0001c0001t0002g0200 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.373-812T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87709758 | |||||||
| chr7:87709760 | T | A | 1 | a0001c0001t0002g0200 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.373-810T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87709760 | |||||||
| chr7:87709762 | T | A | 1 | a0001c0001t0002g0200 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.373-808T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87709762 | |||||||
| chr7:87709763 | A | T | 1 | a0001c0001t0002g0200 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.373-807A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87709763 | |||||||
| chr7:87709764 | T | A | 1 | a0001c0001t0002g0200 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.373-806T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87709764 | |||||||
| chr7:87709767 | A | G | 1 | a0001c0001t0002g0200 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.373-803A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87709767 | |||||||
| chr7:87709768 | T | A | 1 | a0001c0001t0002g0200 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.373-802T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87709768 | |||||||
| chr7:87709770 | T | G | 1 | a0001c0001t0002g0200 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.373-800T>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87709770 | |||||||
| chr7:87709771 | A | T | 1 | a0001c0001t0002g0200 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.373-799A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87709771 | |||||||
| chr7:87709772 | G | T | 1 | a0001c0001t0002g0200 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.373-798G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87709772 | |||||||
| chr7:87710531 | T | A | 1 | a0001c0001t0049g0038 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.373-39T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87710531 | |||||||
| chr7:87711067 | C | T | 2 | a0001c0001t0004g0109 a0001c0001t0004g0110 |
2 | HG00738.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.458+412C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87711067 | |||||||
| chr7:87711165 | C | A | 61 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(58): Show |
61 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(58): Show |
intron_variant | MODIFIER | c.458+510C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87711165 | |||||||
| chr7:87711219 | G | A | 21 | a0001c0001t0016g0023 a0001c0001t0016g0072 a0001c0001t0016g0074 others(18): Show |
21 | HG00438.hp2 HG00621.hp1 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.458+564G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87711219 | |||||||
| chr7:87711264 | T | C | 5 | a0001c0001t0055g0020 a0001c0001t0057g0017 a0001c0001t0066g0019 others(2): Show |
5 | HG02572.hp2 HG02630.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.458+609T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87711264 | |||||||
| chr7:87711277 | GATTGAGC others(1): Show |
G | 6 | a0001c0001t0039g0148 a0001c0001t0055g0020 a0001c0001t0057g0017 others(3): Show |
6 | HG02572.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.458+627_458+634del others(8): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87711277 | ||||||
| chr7:87711293 | C | T | 2 | a0001c0001t0066g0019 a0001c0001t0067g0018 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.458+638C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87711293 | |||||||
| chr7:87711550 | T | C | 2 | a0001c0001t0056g0016 a0001c0001t0063g0015 |
2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.458+895T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87711550 | |||||||
| chr7:87712006 | G | A | 3 | a0001c0001t0062g0145 a0001c0001t0068g0143 a0001c0001t0069g0144 |
3 | HG01069.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.458+1351G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87712006 | |||||||
| chr7:87712545 | A | G | 1 | a0001c0001t0001g0119 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.458+1890A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87712545 | |||||||
| chr7:87712695 | C | G | 16 | a0001c0001t0009g0002 a0001c0001t0009g0190 a0001c0001t0009g0191 others(13): Show |
16 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.458+2040C>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87712695 | |||||||
| chr7:87712834 | G | T | 1 | a0001c0001t0007g0118 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.458+2179G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87712834 | |||||||
| chr7:87713270 | A | G | 12 | a0001c0001t0014g0152 a0001c0001t0014g0155 a0001c0001t0014g0158 others(9): Show |
12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.458+2615A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87713270 | |||||||
| chr7:87713450 | A | G | 38 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(35): Show |
38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.458+2795A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87713450 | |||||||
| chr7:87713488 | G | A | 1 | a0001c0001t0038g0183 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.458+2833G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87713488 | |||||||
| chr7:87713583 | T | G | 12 | a0001c0001t0014g0152 a0001c0001t0014g0155 a0001c0001t0014g0158 others(9): Show |
12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.458+2928T>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87713583 | |||||||
| chr7:87713596 | G | A | 1 | a0001c0003t0001g0025 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.458+2941G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87713596 | |||||||
| chr7:87713663 | A | G | 2 | a0001c0001t0004g0022 a0001c0001t0008g0021 |
2 | HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.458+3008A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87713663 | |||||||
| chr7:87713760 | A | C | 1 | a0001c0001t0008g0103 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.458+3105A>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87713760 | |||||||
| chr7:87714216 | C | T | 1 | a0001c0001t0003g0114 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.458+3561C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87714216 | |||||||
| chr7:87714217 | G | A | 7 | a0001c0001t0016g0023 a0001c0001t0016g0072 a0001c0001t0016g0074 others(4): Show |
7 | HG00639.hp1 HG02559.hp1 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.458+3562G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87714217 | |||||||
| chr7:87714263 | C | A | 1 | a0001c0001t0039g0148 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.458+3608C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87714263 | |||||||
| chr7:87714352 | A | G | 5 | a0001c0001t0055g0020 a0001c0001t0057g0017 a0001c0001t0066g0019 others(2): Show |
5 | HG02572.hp2 HG02630.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.458+3697A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87714352 | |||||||
| chr7:87714385 | G | T | 1 | a0001c0001t0001g0089 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.458+3730G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87714385 | |||||||
| chr7:87714393 | G | A | 1 | a0001c0001t0003g0114 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.458+3738G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87714393 | |||||||
| chr7:87714592 | G | T | 1 | a0001c0001t0003g0135 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.458+3937G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87714592 | |||||||
| chr7:87714706 | T | C | 47 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0045 others(44): Show |
47 | HG00558.hp2 HG00621.hp2 HG00741.hp1 others(44): Show |
intron_variant | MODIFIER | c.458+4051T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87714706 | |||||||
| chr7:87714707 | G | C | 47 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0045 others(44): Show |
47 | HG00558.hp2 HG00621.hp2 HG00741.hp1 others(44): Show |
intron_variant | MODIFIER | c.458+4052G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87714707 | |||||||
| chr7:87714733 | C | T | 38 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(35): Show |
38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.458+4078C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87714733 | |||||||
| chr7:87715034 | G | A | 38 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(35): Show |
38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.458+4379G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87715034 | |||||||
| chr7:87715102 | A | C | 38 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(35): Show |
38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.458+4447A>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87715102 | |||||||
| chr7:87715139 | G | A | 1 | a0001c0001t0011g0189 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.458+4484G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87715139 | |||||||
| chr7:87715202 | A | G | 16 | a0001c0001t0009g0002 a0001c0001t0009g0190 a0001c0001t0009g0191 others(13): Show |
16 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.458+4547A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87715202 | |||||||
| chr7:87715251 | T | TATTATAT others(17): Show |
21 | a0001c0001t0001g0042 a0001c0001t0001g0054 a0001c0001t0001g0089 others(18): Show |
21 | HG00280.hp1 HG00621.hp2 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.458+4701_458+4724d others(26): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87715251 | ||||||
| chr7:87715251 | T | TATTATAT others(41): Show |
3 | a0001c0001t0024g0004 a0001c0001t0025g0005 a0001c0001t0072g0009 |
3 | HG02976.hp2 HG03139.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.458+4677_458+4724d others(50): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87715251 | ||||||
| chr7:87715251 | T | TATTATAT others(89): Show |
1 | a0001c0001t0006g0186 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.458+4629_458+4724d others(98): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87715251 | ||||||
| chr7:87715251 | TATTATAT others(17): Show |
T | 3 | a0001c0001t0057g0017 a0001c0001t0066g0019 a0001c0001t0067g0018 |
3 | HG02630.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.458+4701_458+4724d others(26): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87715251 | ||||||
| chr7:87715251 | TATTATAT others(41): Show |
T | 3 | a0001c0001t0039g0148 a0001c0001t0055g0020 a0001c0001t0070g0014 |
3 | HG02572.hp2 HG02723.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.458+4677_458+4724d others(50): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87715251 | ||||||
| chr7:87715274 | T | A | 1 | a0001c0001t0005g0052 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.458+4619T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87715274 | |||||||
| chr7:87715292 | T | G | 38 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(35): Show |
38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.458+4637T>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87715292 | |||||||
| chr7:87715321 | A | ATAATTAT others(17): Show |
1 | a0001c0001t0049g0038 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.458+4689_458+4690i others(26): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87715321 | ||||||
| chr7:87715321 | A | T | 39 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(36): Show |
39 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(36): Show |
intron_variant | MODIFIER | c.458+4666A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87715321 | |||||||
| chr7:87715331 | ATAAT | A | 2 | a0001c0001t0036g0159 a0001c0001t0073g0053 |
2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.458+4682_458+4685d others(6): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87715331 | ||||||
| chr7:87715331 | ATAATTAA others(47): Show |
A | 38 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(35): Show |
38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.458+4677_458+4730d others(56): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87715331 | |||||||
| chr7:87715341 | TATAATAA others(20): Show |
T | 12 | a0001c0001t0014g0152 a0001c0001t0014g0155 a0001c0001t0014g0158 others(9): Show |
12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.458+4692_458+4718d others(29): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87715341 | ||||||
| chr7:87715345 | A | T | 1 | a0001c0001t0049g0038 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.458+4690A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87715345 | |||||||
| chr7:87715369 | A | ATAATTAT others(17): Show |
3 | a0001c0001t0009g0193 a0001c0001t0011g0194 a0001c0001t0061g0185 |
3 | HG01346.hp1 HG01433.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.458+4724_458+4725i others(26): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87715369 | ||||||
| chr7:87715369 | A | T | 20 | a0001c0001t0009g0002 a0001c0001t0009g0190 a0001c0001t0009g0191 others(17): Show |
20 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.458+4714A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87715369 | |||||||
| chr7:87715382 | CAATAT | C | 16 | a0001c0001t0009g0002 a0001c0001t0009g0190 a0001c0001t0009g0191 others(13): Show |
16 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.458+4739_458+4743d others(7): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87715382 | ||||||
| chr7:87715387 | T | TC | 38 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(35): Show |
38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.458+4732_458+4733i others(3): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87715387 | |||||||
| chr7:87715421 | TTAATATA others(14): Show |
T | 12 | a0001c0001t0014g0152 a0001c0001t0014g0155 a0001c0001t0014g0158 others(9): Show |
12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.458+4785_458+4805d others(23): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87715421 | ||||||
| chr7:87715473 | TTAA | T | 38 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(35): Show |
38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.458+4821_458+4823d others(5): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87715473 | ||||||
| chr7:87715516 | TTA | T | 38 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(35): Show |
38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.458+4870_458+4871d others(4): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87715516 | ||||||
| chr7:87715648 | T | G | 1 | a0001c0001t0001g0045 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.458+4993T>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87715648 | |||||||
| chr7:87715665 | A | G | 1 | a0001c0001t0007g0059 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.458+5010A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87715665 | |||||||
| chr7:87715808 | G | T | 2 | a0001c0001t0056g0016 a0001c0001t0063g0015 |
2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.458+5153G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87715808 | |||||||
| chr7:87715892 | C | T | 1 | a0001c0001t0003g0135 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.458+5237C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87715892 | |||||||
| chr7:87715937 | C | T | 1 | a0001c0001t0043g0106 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.458+5282C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87715937 | |||||||
| chr7:87716090 | T | A | 1 | a0001c0001t0010g0008 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.458+5435T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87716090 | |||||||
| chr7:87716091 | A | T | 38 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(35): Show |
38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.458+5436A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87716091 | |||||||
| chr7:87716133 | T | C | 1 | a0001c0001t0072g0009 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.458+5478T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87716133 | |||||||
| chr7:87716202 | A | C | 7 | a0001c0001t0039g0148 a0001c0001t0049g0038 a0001c0001t0055g0020 others(4): Show |
7 | HG02572.hp2 HG02630.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.458+5547A>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87716202 | |||||||
| chr7:87716875 | C | T | 1 | a0001c0001t0004g0022 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.458+6220C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87716875 | |||||||
| chr7:87717024 | C | T | 12 | a0001c0001t0014g0152 a0001c0001t0014g0155 a0001c0001t0014g0158 others(9): Show |
12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.458+6369C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87717024 | |||||||
| chr7:87717344 | TAAAG | T | 12 | a0001c0001t0014g0152 a0001c0001t0014g0155 a0001c0001t0014g0158 others(9): Show |
12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.458+6690_458+6693d others(6): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87717344 | |||||||
| chr7:87717464 | A | G | 1 | a0001c0001t0065g0003 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.458+6809A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87717464 | |||||||
| chr7:87717485 | G | A | 1 | a0001c0001t0040g0013 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.458+6830G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87717485 | |||||||
| chr7:87717503 | G | T | 2 | a0001c0001t0001g0089 a0001c0001t0001g0097 |
2 | NA18952.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.458+6848G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87717503 | |||||||
| chr7:87718072 | A | C | 39 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(36): Show |
39 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(36): Show |
intron_variant | MODIFIER | c.458+7417A>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87718072 | |||||||
| chr7:87718213 | T | C | 2 | a0001c0001t0022g0182 a0001c0001t0027g0180 |
2 | NA18974.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.458+7558T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87718213 | |||||||
| chr7:87718269 | A | G | 3 | a0001c0001t0057g0017 a0001c0001t0066g0019 a0001c0001t0067g0018 |
3 | HG02630.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.458+7614A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87718269 | |||||||
| chr7:87718269 | A | T | 1 | a0001c0001t0001g0045 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.458+7614A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87718269 | |||||||
| chr7:87718695 | A | C | 2 | a0001c0001t0066g0019 a0001c0001t0067g0018 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.458+8040A>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87718695 | |||||||
| chr7:87718916 | A | G | 1 | a0001c0001t0065g0003 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.458+8261A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87718916 | |||||||
| chr7:87719329 | T | G | 38 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(35): Show |
38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.458+8674T>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87719329 | |||||||
| chr7:87719458 | A | G | 16 | a0001c0001t0009g0002 a0001c0001t0009g0190 a0001c0001t0009g0191 others(13): Show |
16 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.458+8803A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87719458 | |||||||
| chr7:87719465 | C | T | 2 | a0001c0001t0004g0084 a0001c0001t0029g0061 |
2 | HG00558.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.458+8810C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87719465 | |||||||
| chr7:87719665 | G | T | 1 | a0001c0001t0004g0055 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.458+9010G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87719665 | |||||||
| chr7:87719680 | A | G | 15 | a0001c0001t0001g0099 a0001c0001t0017g0065 a0001c0001t0017g0085 others(12): Show |
15 | HG00438.hp2 HG00621.hp1 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.458+9025A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87719680 | |||||||
| chr7:87719703 | A | G | 16 | a0001c0001t0009g0002 a0001c0001t0009g0190 a0001c0001t0009g0191 others(13): Show |
16 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.458+9048A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87719703 | |||||||
| chr7:87719911 | C | T | 1 | a0001c0001t0049g0038 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.458+9256C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87719911 | |||||||
| chr7:87719990 | C | CA | 11 | a0001c0001t0001g0119 a0001c0001t0004g0022 a0001c0001t0004g0047 others(8): Show |
11 | HG00639.hp2 HG01099.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.458+9351dupA | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87719990 | ||||||
| chr7:87719990 | CA | C | 47 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0054 others(44): Show |
47 | HG00558.hp2 HG00621.hp2 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.458+9351delA | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87719990 | ||||||
| chr7:87720002 | A | AAAGAAAG | 6 | a0001c0001t0020g0033 a0001c0001t0020g0035 a0001c0001t0021g0028 others(3): Show |
6 | HG02129.hp1 HG02258.hp2 NA19005.hp2 others(3): Show |
intron_variant | MODIFIER | c.458+9349_458+9350i others(9): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87720002 | ||||||
| chr7:87720002 | A | AAGAAAG | 55 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(52): Show |
55 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(52): Show |
intron_variant | MODIFIER | c.458+9348_458+9349i others(8): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87720002 | ||||||
| chr7:87720055 | A | G | 1 | a0001c0001t0008g0103 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.458+9400A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87720055 | |||||||
| chr7:87720131 | G | A | 1 | a0001c0001t0001g0104 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.458+9476G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87720131 | |||||||
| chr7:87720362 | C | T | 1 | a0001c0001t0072g0009 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.458+9707C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87720362 | |||||||
| chr7:87720394 | A | G | 1 | a0001c0001t0039g0148 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.458+9739A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87720394 | |||||||
| chr7:87720540 | A | ATG | 2 | a0001c0001t0055g0020 a0001c0001t0070g0014 |
2 | HG02572.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.458+9886_458+9887i others(4): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87720540 | ||||||
| chr7:87720542 | A | ATG | 2 | a0001c0001t0016g0074 a0001c0001t0017g0065 |
2 | HG01261.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.458+9919_458+9920d others(4): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87720542 | ||||||
| chr7:87720542 | A | ATGTG | 10 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0012g0031 others(7): Show |
10 | HG01358.hp1 HG01496.hp1 HG01952.hp2 others(7): Show |
intron_variant | MODIFIER | c.458+9917_458+9920d others(6): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87720542 | ||||||
| chr7:87720542 | A | ATGTGTG | 33 | a0001c0001t0002g0162 a0001c0001t0002g0163 a0001c0001t0002g0164 others(30): Show |
33 | HG00280.hp2 HG00423.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.458+9915_458+9920d others(8): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87720542 | ||||||
| chr7:87720542 | A | ATGTGTGT others(1): Show |
23 | a0001c0001t0002g0200 a0001c0001t0011g0198 a0001c0001t0012g0174 others(20): Show |
23 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.458+9913_458+9920d others(10): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87720542 | ||||||
| chr7:87720542 | A | ATGTGTGT others(3): Show |
2 | a0001c0001t0014g0152 a0001c0001t0033g0037 |
2 | NA18998.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.458+9911_458+9920d others(12): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87720542 | ||||||
| chr7:87720542 | A | ATGTGTGT others(5): Show |
1 | a0002c0002t0018g0140 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.458+9909_458+9920d others(14): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87720542 | ||||||
| chr7:87720542 | A | G | 4 | a0001c0001t0055g0020 a0001c0001t0066g0019 a0001c0001t0067g0018 others(1): Show |
4 | HG02572.hp2 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.458+9887A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87720542 | |||||||
| chr7:87720542 | ATG | A | 88 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0045 others(85): Show |
88 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.458+9919_458+9920d others(4): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87720542 | ||||||
| chr7:87720542 | ATGTGTG | A | 2 | a0001c0001t0018g0171 a0001c0001t0036g0159 |
2 | HG03098.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.458+9915_458+9920d others(8): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87720542 | ||||||
| chr7:87720624 | CAG | C | 12 | a0001c0001t0014g0152 a0001c0001t0014g0155 a0001c0001t0014g0158 others(9): Show |
12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.458+9972_458+9973d others(4): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87720624 | ||||||
| chr7:87720683 | C | T | 12 | a0001c0001t0014g0152 a0001c0001t0014g0155 a0001c0001t0014g0158 others(9): Show |
12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.458+10028C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87720683 | |||||||
| chr7:87720747 | C | T | 1 | a0001c0001t0024g0102 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.458+10092C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87720747 | |||||||
| chr7:87720758 | G | A | 2 | a0001c0001t0056g0016 a0001c0001t0063g0015 |
2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.458+10103G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87720758 | |||||||
| chr7:87720776 | A | G | 5 | a0001c0001t0001g0119 a0001c0001t0024g0004 a0001c0001t0024g0102 others(2): Show |
5 | HG00639.hp2 HG01099.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.458+10121A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87720776 | |||||||
| chr7:87720857 | C | G | 6 | a0001c0001t0039g0148 a0001c0001t0055g0020 a0001c0001t0057g0017 others(3): Show |
6 | HG02572.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.458+10202C>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87720857 | |||||||
| chr7:87720919 | A | G | 2 | a0001c0001t0001g0119 a0001c0001t0065g0003 |
2 | HG01099.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.458+10264A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87720919 | |||||||
| chr7:87721744 | A | G | 16 | a0001c0001t0009g0002 a0001c0001t0009g0190 a0001c0001t0009g0191 others(13): Show |
16 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.458+11089A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87721744 | |||||||
| chr7:87721862 | C | T | 12 | a0001c0001t0014g0152 a0001c0001t0014g0155 a0001c0001t0014g0158 others(9): Show |
12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.458+11207C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87721862 | |||||||
| chr7:87721951 | G | A | 2 | a0001c0001t0039g0148 a0001c0001t0049g0038 |
2 | HG02723.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.458+11296G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87721951 | |||||||
| chr7:87722007 | G | A | 3 | a0001c0001t0009g0002 a0001c0001t0009g0197 a0001c0001t0028g0002 |
3 | HG01069.hp2 HG01071.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.458+11352G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87722007 | |||||||
| chr7:87722270 | T | C | 2 | a0001c0001t0017g0112 a0001c0001t0034g0079 |
2 | HG00741.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.458+11615T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87722270 | |||||||
| chr7:87722881 | C | T | 1 | a0001c0001t0039g0148 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.458+12226C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87722881 | |||||||
| chr7:87722958 | G | A | 1 | a0001c0001t0054g0138 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.458+12303G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87722958 | |||||||
| chr7:87722975 | G | A | 38 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(35): Show |
38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.458+12320G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87722975 | |||||||
| chr7:87723033 | T | C | 85 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(82): Show |
85 | HG00280.hp2 HG00423.hp1 HG01069.hp2 others(82): Show |
intron_variant | MODIFIER | c.458+12378T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87723033 | |||||||
| chr7:87723328 | C | T | 12 | a0001c0001t0014g0152 a0001c0001t0014g0155 a0001c0001t0014g0158 others(9): Show |
12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.458+12673C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87723328 | |||||||
| chr7:87723412 | G | A | 2 | a0001c0001t0001g0042 a0001c0001t0001g0098 |
2 | HG01167.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.458+12757G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87723412 | |||||||
| chr7:87723527 | C | T | 8 | a0001c0001t0010g0008 a0001c0001t0010g0010 a0001c0001t0010g0011 others(5): Show |
8 | HG02055.hp1 HG02280.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.458+12872C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87723527 | |||||||
| chr7:87723632 | T | C | 61 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(58): Show |
61 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(58): Show |
intron_variant | MODIFIER | c.458+12977T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87723632 | |||||||
| chr7:87723760 | C | T | 4 | a0001c0001t0044g0169 a0001c0001t0046g0161 a0001c0001t0047g0172 others(1): Show |
4 | HG01123.hp1 HG01192.hp1 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.458+13105C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87723760 | |||||||
| chr7:87723904 | G | A | 1 | a0001c0001t0006g0142 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.458+13249G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87723904 | |||||||
| chr7:87723907 | C | T | 2 | a0001c0001t0010g0010 a0001c0001t0010g0011 |
2 | HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.458+13252C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87723907 | |||||||
| chr7:87724234 | T | C | 2 | a0001c0001t0025g0091 a0001c0001t0026g0120 |
2 | HG01099.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.458+13579T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87724234 | |||||||
| chr7:87724607 | A | G | 4 | a0001c0001t0044g0169 a0001c0001t0046g0161 a0001c0001t0047g0172 others(1): Show |
4 | HG01123.hp1 HG01192.hp1 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.458+13952A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87724607 | |||||||
| chr7:87724887 | T | C | 1 | a0001c0001t0003g0105 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.458+14232T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87724887 | |||||||
| chr7:87724888 | A | G | 1 | a0001c0001t0072g0009 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.458+14233A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87724888 | |||||||
| chr7:87724976 | A | G | 5 | a0001c0001t0055g0020 a0001c0001t0057g0017 a0001c0001t0066g0019 others(2): Show |
5 | HG02572.hp2 HG02630.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.458+14321A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87724976 | |||||||
| chr7:87725264 | C | T | 1 | a0001c0001t0039g0148 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.459-14527C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87725264 | |||||||
| chr7:87725294 | A | G | 38 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(35): Show |
38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.459-14497A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87725294 | |||||||
| chr7:87725337 | G | A | 2 | a0001c0001t0003g0114 a0001c0001t0006g0115 |
2 | HG03098.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.459-14454G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87725337 | |||||||
| chr7:87725501 | T | G | 2 | a0001c0001t0010g0010 a0001c0001t0010g0011 |
2 | HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.459-14290T>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87725501 | |||||||
| chr7:87725660 | T | C | 1 | a0001c0001t0072g0009 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.459-14131T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87725660 | |||||||
| chr7:87725778 | C | A | 1 | a0001c0001t0039g0148 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.459-14013C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87725778 | |||||||
| chr7:87725922 | A | C | 1 | a0001c0001t0049g0038 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.459-13869A>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87725922 | |||||||
| chr7:87726059 | A | G | 2 | a0001c0001t0066g0019 a0001c0001t0067g0018 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.459-13732A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87726059 | |||||||
| chr7:87726147 | T | C | 1 | a0001c0001t0075g0007 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.459-13644T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87726147 | |||||||
| chr7:87726357 | C | T | 2 | a0001c0001t0036g0159 a0001c0001t0073g0053 |
2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.459-13434C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87726357 | |||||||
| chr7:87726382 | G | A | 1 | a0001c0001t0010g0012 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.459-13409G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87726382 | |||||||
| chr7:87726528 | T | G | 85 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(82): Show |
85 | HG00280.hp2 HG00423.hp1 HG01069.hp2 others(82): Show |
intron_variant | MODIFIER | c.459-13263T>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87726528 | |||||||
| chr7:87726589 | C | G | 8 | a0001c0001t0010g0008 a0001c0001t0010g0010 a0001c0001t0010g0011 others(5): Show |
8 | HG02055.hp1 HG02280.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.459-13202C>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87726589 | |||||||
| chr7:87726614 | T | C | 16 | a0001c0001t0009g0002 a0001c0001t0009g0190 a0001c0001t0009g0191 others(13): Show |
16 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.459-13177T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87726614 | |||||||
| chr7:87726620 | T | G | 1 | a0001c0001t0007g0118 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.459-13171T>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87726620 | |||||||
| chr7:87726690 | C | T | 8 | a0001c0001t0010g0008 a0001c0001t0010g0010 a0001c0001t0010g0011 others(5): Show |
8 | HG02055.hp1 HG02280.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.459-13101C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87726690 | |||||||
| chr7:87726816 | T | C | 3 | a0001c0001t0004g0083 a0001c0001t0005g0113 a0001c0001t0007g0059 |
3 | HG01952.hp1 NA18975.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.459-12975T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87726816 | |||||||
| chr7:87726826 | A | G | 2 | a0001c0001t0017g0065 a0001c0001t0017g0085 |
2 | HG00738.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.459-12965A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87726826 | |||||||
| chr7:87726914 | T | C | 2 | a0001c0001t0010g0010 a0001c0001t0010g0011 |
2 | HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.459-12877T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87726914 | |||||||
| chr7:87726926 | C | G | 1 | a0001c0001t0072g0009 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.459-12865C>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87726926 | |||||||
| chr7:87726942 | C | A | 1 | a0001c0001t0072g0009 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.459-12849C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87726942 | |||||||
| chr7:87727110 | A | G | 7 | a0001c0001t0001g0119 a0001c0001t0004g0022 a0001c0001t0004g0047 others(4): Show |
7 | HG01099.hp1 HG01261.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.459-12681A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87727110 | |||||||
| chr7:87727286 | G | C | 1 | a0001c0001t0057g0017 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.459-12505G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87727286 | |||||||
| chr7:87727587 | AT | A | 85 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(82): Show |
85 | HG00280.hp2 HG00423.hp1 HG01069.hp2 others(82): Show |
intron_variant | MODIFIER | c.459-12197delT | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87727587 | ||||||
| chr7:87727675 | C | T | 1 | a0001c0001t0039g0148 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.459-12116C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87727675 | |||||||
| chr7:87727723 | T | C | 1 | a0001c0001t0022g0181 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.459-12068T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87727723 | |||||||
| chr7:87728096 | A | G | 3 | a0001c0001t0057g0017 a0001c0001t0066g0019 a0001c0001t0067g0018 |
3 | HG02630.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.459-11695A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87728096 | |||||||
| chr7:87728411 | G | C | 6 | a0001c0001t0002g0163 a0001c0001t0002g0164 a0001c0001t0002g0166 others(3): Show |
6 | HG02559.hp2 HG02965.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.459-11380G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87728411 | |||||||
| chr7:87728474 | C | T | 2 | a0001c0001t0019g0043 a0001c0001t0034g0199 |
2 | HG01978.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.459-11317C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87728474 | |||||||
| chr7:87728487 | T | G | 1 | a0001c0001t0039g0148 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.459-11304T>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87728487 | |||||||
| chr7:87728550 | T | A | 54 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(51): Show |
54 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(51): Show |
intron_variant | MODIFIER | c.459-11241T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87728550 | |||||||
| chr7:87728830 | G | A | 38 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(35): Show |
38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.459-10961G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87728830 | |||||||
| chr7:87729048 | ATCTG | A | 5 | a0001c0001t0055g0020 a0001c0001t0057g0017 a0001c0001t0066g0019 others(2): Show |
5 | HG02572.hp2 HG02630.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.459-10739_459-1073 others(8): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87729048 | ||||||
| chr7:87729170 | G | A | 2 | a0001c0001t0004g0084 a0001c0001t0029g0061 |
2 | HG00558.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.459-10621G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87729170 | |||||||
| chr7:87729176 | A | G | 2 | a0001c0001t0003g0056 a0001c0001t0003g0057 |
2 | HG01074.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.459-10615A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87729176 | |||||||
| chr7:87729202 | T | C | 38 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(35): Show |
38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.459-10589T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87729202 | |||||||
| chr7:87729460 | G | A | 2 | a0001c0001t0056g0016 a0001c0001t0063g0015 |
2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.459-10331G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87729460 | |||||||
| chr7:87729674 | G | A | 1 | a0001c0001t0075g0007 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.459-10117G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87729674 | |||||||
| chr7:87729712 | C | T | 11 | a0001c0001t0003g0082 a0001c0001t0004g0055 a0001c0001t0004g0058 others(8): Show |
11 | HG00438.hp1 HG00558.hp1 HG01952.hp1 others(8): Show |
intron_variant | MODIFIER | c.459-10079C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87729712 | |||||||
| chr7:87729770 | C | T | 1 | a0001c0001t0053g0063 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.459-10021C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87729770 | |||||||
| chr7:87730015 | G | T | 1 | a0001c0001t0001g0104 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.459-9776G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87730015 | |||||||
| chr7:87730189 | G | A | 38 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(35): Show |
38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.459-9602G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87730189 | |||||||
| chr7:87730525 | G | C | 2 | a0001c0001t0056g0016 a0001c0001t0063g0015 |
2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.459-9266G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87730525 | |||||||
| chr7:87730582 | C | T | 5 | a0001c0001t0003g0141 a0001c0001t0006g0086 a0001c0001t0006g0111 others(2): Show |
5 | HG02132.hp2 NA18970.hp1 NA18973.hp1 others(2): Show |
intron_variant | MODIFIER | c.459-9209C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87730582 | |||||||
| chr7:87730851 | G | A | 2 | a0001c0001t0001g0134 a0001c0001t0001g0136 |
2 | HG01192.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.459-8940G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87730851 | |||||||
| chr7:87731008 | G | A | 1 | a0001c0001t0060g0100 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.459-8783G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87731008 | |||||||
| chr7:87731310 | T | A | 38 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(35): Show |
38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.459-8481T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87731310 | |||||||
| chr7:87731512 | C | A | 1 | a0001c0001t0001g0087 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.459-8279C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87731512 | |||||||
| chr7:87731612 | G | T | 8 | a0001c0001t0003g0082 a0001c0001t0004g0055 a0001c0001t0004g0058 others(5): Show |
8 | HG00438.hp1 HG01952.hp1 HG02135.hp1 others(5): Show |
intron_variant | MODIFIER | c.459-8179G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87731612 | |||||||
| chr7:87731729 | T | C | 7 | a0001c0001t0010g0008 a0001c0001t0010g0010 a0001c0001t0010g0011 others(4): Show |
7 | HG02055.hp1 HG02280.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.459-8062T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87731729 | |||||||
| chr7:87731823 | G | A | 2 | a0001c0001t0056g0016 a0001c0001t0063g0015 |
2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.459-7968G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87731823 | |||||||
| chr7:87731887 | C | T | 5 | a0001c0001t0055g0020 a0001c0001t0057g0017 a0001c0001t0066g0019 others(2): Show |
5 | HG02572.hp2 HG02630.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.459-7904C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87731887 | |||||||
| chr7:87731940 | A | G | 2 | a0001c0001t0039g0148 a0001c0001t0049g0038 |
2 | HG02723.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.459-7851A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87731940 | |||||||
| chr7:87732053 | A | G | 1 | a0001c0001t0004g0022 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.459-7738A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87732053 | |||||||
| chr7:87732202 | C | A | 3 | a0001c0001t0024g0004 a0001c0001t0025g0005 a0001c0001t0037g0006 |
3 | HG00639.hp2 HG02976.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.459-7589C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87732202 | |||||||
| chr7:87732227 | C | T | 54 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(51): Show |
54 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(51): Show |
intron_variant | MODIFIER | c.459-7564C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87732227 | |||||||
| chr7:87732249 | C | A | 7 | a0001c0001t0039g0148 a0001c0001t0049g0038 a0001c0001t0055g0020 others(4): Show |
7 | HG02572.hp2 HG02630.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.459-7542C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87732249 | |||||||
| chr7:87732322 | A | G | 1 | a0001c0001t0029g0061 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.459-7469A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87732322 | |||||||
| chr7:87732385 | G | GAAAGAAA others(272): Show |
2 | a0001c0001t0004g0047 a0001c0001t0064g0046 |
2 | HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.459-7397_459-7396i others(281): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87732385 | ||||||
| chr7:87732932 | A | G | 3 | a0001c0001t0029g0048 a0001c0001t0032g0049 a0001c0001t0032g0051 |
3 | HG02559.hp1 HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.459-6859A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87732932 | |||||||
| chr7:87733132 | GC | G | 14 | a0001c0001t0017g0065 a0001c0001t0017g0085 a0001c0001t0017g0112 others(11): Show |
14 | HG00438.hp2 HG00621.hp1 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.459-6652delC | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87733132 | ||||||
| chr7:87733376 | T | G | 9 | a0001c0001t0009g0002 a0001c0001t0009g0190 a0001c0001t0009g0191 others(6): Show |
9 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.459-6415T>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87733376 | |||||||
| chr7:87733392 | T | C | 1 | a0001c0001t0001g0060 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.459-6399T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87733392 | |||||||
| chr7:87733568 | G | A | 1 | a0001c0001t0039g0148 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.459-6223G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87733568 | |||||||
| chr7:87733627 | C | T | 1 | a0001c0001t0059g0073 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.459-6164C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87733627 | |||||||
| chr7:87733711 | A | G | 1 | a0001c0001t0001g0054 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.459-6080A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87733711 | |||||||
| chr7:87733791 | C | G | 1 | a0001c0001t0001g0093 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.459-6000C>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87733791 | |||||||
| chr7:87733901 | C | T | 1 | a0001c0001t0005g0128 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.459-5890C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87733901 | |||||||
| chr7:87733902 | G | A | 2 | a0001c0001t0001g0042 a0001c0001t0001g0098 |
2 | HG01167.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.459-5889G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87733902 | |||||||
| chr7:87733940 | T | C | 2 | a0001c0001t0013g0001 a0001c0001t0041g0001 |
2 | HG01358.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.459-5851T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87733940 | |||||||
| chr7:87734011 | G | C | 2 | a0001c0001t0001g0042 a0001c0001t0001g0098 |
2 | HG01167.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.459-5780G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87734011 | |||||||
| chr7:87734526 | A | G | 2 | a0001c0001t0036g0159 a0001c0001t0073g0053 |
2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.459-5265A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87734526 | |||||||
| chr7:87734662 | T | C | 2 | a0001c0001t0036g0159 a0001c0001t0073g0053 |
2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.459-5129T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87734662 | |||||||
| chr7:87734738 | A | G | 3 | a0001c0001t0024g0004 a0001c0001t0025g0005 a0001c0001t0037g0006 |
3 | HG00639.hp2 HG02976.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.459-5053A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87734738 | |||||||
| chr7:87734781 | T | C | 85 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(82): Show |
85 | HG00280.hp2 HG00423.hp1 HG01069.hp2 others(82): Show |
intron_variant | MODIFIER | c.459-5010T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87734781 | |||||||
| chr7:87734787 | ACTCCAT | A | 2 | a0001c0001t0019g0108 a0001c0001t0053g0063 |
2 | HG01981.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.459-4999_459-4994d others(8): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87734787 | ||||||
| chr7:87734874 | A | C | 12 | a0001c0001t0014g0152 a0001c0001t0014g0155 a0001c0001t0014g0158 others(9): Show |
12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.459-4917A>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87734874 | |||||||
| chr7:87734891 | G | A | 7 | a0001c0001t0010g0008 a0001c0001t0010g0010 a0001c0001t0010g0011 others(4): Show |
7 | HG02055.hp1 HG02280.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.459-4900G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87734891 | |||||||
| chr7:87735106 | T | G | 16 | a0001c0001t0009g0002 a0001c0001t0009g0190 a0001c0001t0009g0191 others(13): Show |
16 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.459-4685T>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87735106 | |||||||
| chr7:87735325 | C | A | 2 | a0001c0001t0055g0020 a0001c0001t0070g0014 |
2 | HG02572.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.459-4466C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87735325 | |||||||
| chr7:87735846 | G | C | 12 | a0001c0001t0014g0152 a0001c0001t0014g0155 a0001c0001t0014g0158 others(9): Show |
12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.459-3945G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87735846 | |||||||
| chr7:87735932 | C | T | 38 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(35): Show |
38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.459-3859C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87735932 | |||||||
| chr7:87735933 | G | A | 1 | a0001c0001t0011g0189 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.459-3858G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87735933 | |||||||
| chr7:87735949 | A | G | 1 | a0001c0001t0049g0038 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.459-3842A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87735949 | |||||||
| chr7:87735966 | A | T | 61 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(58): Show |
61 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(58): Show |
intron_variant | MODIFIER | c.459-3825A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87735966 | |||||||
| chr7:87736102 | T | C | 1 | a0001c0001t0004g0022 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.459-3689T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87736102 | |||||||
| chr7:87736226 | T | C | 2 | a0001c0001t0056g0016 a0001c0001t0063g0015 |
2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.459-3565T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87736226 | |||||||
| chr7:87736296 | A | G | 2 | a0001c0001t0066g0019 a0001c0001t0067g0018 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.459-3495A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87736296 | |||||||
| chr7:87736441 | A | G | 1 | a0001c0001t0025g0005 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.459-3350A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87736441 | |||||||
| chr7:87736450 | A | G | 1 | a0001c0001t0006g0115 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.459-3341A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87736450 | |||||||
| chr7:87736548 | C | T | 2 | a0001c0001t0017g0065 a0001c0001t0017g0085 |
2 | HG00738.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.459-3243C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87736548 | |||||||
| chr7:87736750 | G | A | 1 | a0001c0001t0001g0136 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.459-3041G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87736750 | |||||||
| chr7:87736804 | ATATATT | A | 2 | a0001c0001t0036g0159 a0001c0001t0073g0053 |
2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.459-2975_459-2970d others(8): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87736804 | ||||||
| chr7:87736808 | A | T | 1 | a0001c0001t0004g0084 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.459-2983A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87736808 | |||||||
| chr7:87736855 | C | CTA | 3 | a0001c0001t0004g0109 a0001c0001t0017g0085 a0001c0001t0031g0044 |
3 | HG00438.hp2 HG00738.hp1 HG00738.hp2 |
intron_variant | MODIFIER | c.459-2902_459-2901d others(4): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87736855 | ||||||
| chr7:87736855 | CTA | C | 7 | a0001c0001t0003g0076 a0001c0001t0006g0088 a0001c0001t0006g0142 others(4): Show |
7 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(4): Show |
intron_variant | MODIFIER | c.459-2902_459-2901d others(4): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87736855 | ||||||
| chr7:87736855 | CTATA | C | 5 | a0001c0001t0001g0045 a0001c0001t0001g0087 a0001c0001t0003g0094 others(2): Show |
5 | HG01123.hp2 HG03098.hp1 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.459-2904_459-2901d others(6): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87736855 | ||||||
| chr7:87736855 | CTATATAT others(7): Show |
C | 6 | a0001c0001t0010g0008 a0001c0001t0010g0012 a0001c0001t0040g0013 others(3): Show |
6 | HG02055.hp1 HG02280.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.459-2914_459-2901d others(16): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87736855 | ||||||
| chr7:87736855 | CTATATAT others(9): Show |
C | 9 | a0001c0001t0014g0152 a0001c0001t0014g0155 a0001c0001t0014g0158 others(6): Show |
9 | NA18963.hp1 NA18970.hp2 NA18988.hp2 others(6): Show |
intron_variant | MODIFIER | c.459-2916_459-2901d others(18): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87736855 | ||||||
| chr7:87736869 | ATATATAT others(16): Show |
A | 1 | a0001c0001t0039g0148 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.459-2920_459-2898d others(25): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87736869 | ||||||
| chr7:87736869 | ATATATAT others(20): Show |
A | 1 | a0001c0001t0070g0014 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.459-2920_459-2894d others(29): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87736869 | ||||||
| chr7:87736870 | TATATATA others(10): Show |
T | 1 | a0001c0001t0045g0160 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.459-2920_459-2904d others(19): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87736870 | |||||||
| chr7:87736871 | ATATATAT others(15): Show |
A | 22 | a0001c0001t0002g0030 a0001c0001t0002g0162 a0001c0001t0002g0163 others(19): Show |
22 | HG01123.hp1 HG01358.hp1 HG01978.hp2 others(19): Show |
intron_variant | MODIFIER | c.459-2918_459-2897d others(24): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87736871 | ||||||
| chr7:87736871 | ATATATAT others(16): Show |
A | 5 | a0001c0001t0002g0137 a0001c0001t0002g0168 a0001c0001t0012g0174 others(2): Show |
5 | HG01496.hp1 HG01952.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.459-2918_459-2896d others(25): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87736871 | ||||||
| chr7:87736871 | ATATATAT others(18): Show |
A | 1 | a0001c0001t0055g0020 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.459-2918_459-2894d others(27): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87736871 | ||||||
| chr7:87736872 | TATATATA others(8): Show |
T | 2 | a0001c0001t0010g0010 a0001c0001t0015g0154 |
2 | HG00423.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.459-2918_459-2904d others(17): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87736872 | |||||||
| chr7:87736873 | ATATATAT others(13): Show |
A | 1 | a0001c0001t0052g0196 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.459-2916_459-2897d others(22): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87736873 | ||||||
| chr7:87736873 | ATATATAT others(14): Show |
A | 1 | a0001c0001t0013g0149 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.459-2916_459-2896d others(23): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87736873 | ||||||
| chr7:87736873 | ATATATAT others(15): Show |
A | 11 | a0001c0001t0020g0033 a0001c0001t0020g0035 a0001c0001t0021g0028 others(8): Show |
11 | HG01192.hp1 HG02129.hp1 HG03453.hp1 others(8): Show |
intron_variant | MODIFIER | c.459-2916_459-2895d others(24): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87736873 | ||||||
| chr7:87736873 | ATATATAT others(18): Show |
A | 1 | a0001c0001t0057g0017 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.459-2916_459-2892d others(27): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87736873 | ||||||
| chr7:87736874 | TATATATA others(6): Show |
T | 1 | a0001c0001t0010g0011 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.459-2916_459-2904d others(15): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87736874 | |||||||
| chr7:87736875 | ATATATAT others(13): Show |
A | 12 | a0001c0001t0009g0002 a0001c0001t0009g0191 a0001c0001t0009g0193 others(9): Show |
12 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.459-2914_459-2895d others(22): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87736875 | ||||||
| chr7:87736875 | ATATATAT others(14): Show |
A | 2 | a0001c0001t0009g0190 a0001c0001t0028g0192 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.459-2914_459-2894d others(23): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87736875 | ||||||
| chr7:87736876 | TATATATA others(6): Show |
T | 1 | a0001c0001t0072g0009 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.459-2914_459-2902d others(15): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87736876 | |||||||
| chr7:87736877 | ATATATAT others(15): Show |
A | 1 | a0001c0001t0066g0019 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.459-2912_459-2891d others(24): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87736877 | ||||||
| chr7:87736877 | ATATATAT others(16): Show |
A | 1 | a0001c0001t0067g0018 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.459-2912_459-2890d others(25): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87736877 | ||||||
| chr7:87736879 | ATATATAT others(5): Show |
A | 1 | a0001c0001t0004g0139 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.459-2910_459-2899d others(14): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87736879 | ||||||
| chr7:87736879 | ATATATAT others(13): Show |
A | 1 | a0001c0001t0011g0198 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.459-2910_459-2891d others(22): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87736879 | ||||||
| chr7:87736881 | ATATATAT others(3): Show |
A | 2 | a0001c0001t0001g0119 a0001c0001t0073g0053 |
2 | HG01099.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.459-2908_459-2899d others(12): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87736881 | ||||||
| chr7:87736881 | ATATATAT others(5): Show |
A | 1 | a0001c0001t0036g0159 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.459-2908_459-2897d others(14): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87736881 | ||||||
| chr7:87736882 | TATA | T | 3 | a0001c0001t0004g0055 a0001c0001t0004g0058 a0001c0001t0005g0068 |
3 | NA18977.hp1 NA19010.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.459-2908_459-2906d others(5): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87736882 | |||||||
| chr7:87736883 | ATATATAT others(3): Show |
A | 1 | a0001c0001t0037g0006 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.459-2906_459-2897d others(12): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87736883 | ||||||
| chr7:87736883 | ATATATAT others(4): Show |
A | 4 | a0001c0001t0024g0004 a0001c0001t0025g0005 a0001c0001t0056g0016 others(1): Show |
4 | HG02717.hp2 HG02976.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.459-2906_459-2896d others(13): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87736883 | ||||||
| chr7:87736884 | TATA | T | 4 | a0001c0001t0007g0132 a0001c0001t0008g0123 a0001c0001t0008g0131 others(1): Show |
4 | HG02055.hp2 HG02818.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.459-2906_459-2904d others(5): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87736884 | |||||||
| chr7:87736885 | A | T | 2 | a0001c0001t0005g0052 a0001c0001t0065g0003 |
2 | HG02572.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.459-2906A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87736885 | |||||||
| chr7:87736886 | TA | T | 2 | a0001c0001t0005g0125 a0001c0001t0005g0129 |
2 | NA18974.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.459-2904delA | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87736886 | |||||||
| chr7:87736886 | TATA | T | 7 | a0001c0001t0001g0054 a0001c0001t0001g0060 a0001c0001t0001g0080 others(4): Show |
7 | HG00558.hp2 HG02132.hp1 NA18940.hp2 others(4): Show |
intron_variant | MODIFIER | c.459-2904_459-2902d others(5): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87736886 | |||||||
| chr7:87736887 | A | T | 17 | a0001c0001t0004g0055 a0001c0001t0004g0058 a0001c0001t0005g0052 others(14): Show |
17 | HG00280.hp1 HG02055.hp1 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.459-2904A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87736887 | |||||||
| chr7:87736887 | ATAT | A | 9 | a0001c0001t0001g0041 a0001c0001t0001g0070 a0001c0001t0001g0095 others(6): Show |
9 | HG02165.hp2 HG02965.hp2 HG04184.hp2 others(6): Show |
intron_variant | MODIFIER | c.459-2902_459-2900d others(5): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87736887 | ||||||
| chr7:87736888 | TA | T | 3 | a0001c0001t0001g0064 a0001c0001t0006g0117 a0001c0001t0050g0027 |
3 | HG00735.hp1 HG02040.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.459-2902delA | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87736888 | |||||||
| chr7:87736889 | A | T | 38 | a0001c0001t0001g0045 a0001c0001t0003g0094 a0001c0001t0003g0114 others(35): Show |
38 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(35): Show |
intron_variant | MODIFIER | c.459-2902A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87736889 | |||||||
| chr7:87736889 | AT | A | 13 | a0001c0001t0001g0071 a0001c0001t0001g0099 a0001c0001t0003g0066 others(10): Show |
13 | HG01081.hp1 HG01496.hp2 HG01978.hp1 others(10): Show |
intron_variant | MODIFIER | c.459-2876delT | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87736889 | ||||||
| chr7:87736889 | ATT | A | 6 | a0001c0001t0003g0082 a0001c0001t0004g0083 a0001c0001t0004g0084 others(3): Show |
6 | HG00438.hp1 HG00558.hp1 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.459-2877_459-2876d others(4): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87736889 | ||||||
| chr7:87736890 | T | TA | 9 | a0001c0001t0001g0042 a0001c0001t0001g0134 a0001c0001t0001g0136 others(6): Show |
9 | HG00423.hp2 HG00741.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.459-2901_459-2900i others(3): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87736890 | |||||||
| chr7:87736890 | T | TATATA | 3 | a0001c0001t0017g0112 a0001c0001t0031g0107 a0001c0001t0043g0106 |
3 | HG01433.hp1 HG02040.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.459-2901_459-2900i others(7): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87736890 | |||||||
| chr7:87736891 | T | A | 9 | a0001c0001t0001g0092 a0001c0001t0001g0104 a0001c0001t0003g0056 others(6): Show |
9 | HG00438.hp2 HG00621.hp2 HG00738.hp1 others(6): Show |
intron_variant | MODIFIER | c.459-2900T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87736891 | |||||||
| chr7:87736892 | T | A | 15 | a0001c0001t0001g0071 a0001c0001t0001g0099 a0001c0001t0005g0113 others(12): Show |
15 | HG00741.hp2 HG01099.hp2 HG01433.hp1 others(12): Show |
intron_variant | MODIFIER | c.459-2899T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87736892 | |||||||
| chr7:87736893 | T | A | 3 | a0001c0001t0003g0056 a0001c0001t0003g0057 a0001c0001t0017g0085 |
3 | HG00738.hp1 HG01074.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.459-2898T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87736893 | |||||||
| chr7:87736894 | T | A | 5 | a0001c0001t0017g0112 a0001c0001t0019g0108 a0001c0001t0034g0079 others(2): Show |
5 | HG00741.hp2 HG01433.hp1 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.459-2897T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87736894 | |||||||
| chr7:87736916 | G | T | 1 | a0001c0001t0003g0056 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.459-2875G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87736916 | |||||||
| chr7:87737055 | G | A | 38 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(35): Show |
38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.459-2736G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87737055 | |||||||
| chr7:87737146 | G | A | 1 | a0001c0001t0072g0009 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.459-2645G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87737146 | |||||||
| chr7:87737342 | T | C | 5 | a0001c0001t0001g0080 a0001c0001t0005g0077 a0001c0001t0005g0125 others(2): Show |
5 | HG00423.hp2 NA18968.hp1 NA18974.hp2 others(2): Show |
intron_variant | MODIFIER | c.459-2449T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87737342 | |||||||
| chr7:87737484 | C | T | 38 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(35): Show |
38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.459-2307C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87737484 | |||||||
| chr7:87737564 | C | A | 1 | a0001c0001t0001g0042 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.459-2227C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87737564 | |||||||
| chr7:87737832 | G | A | 12 | a0001c0001t0014g0152 a0001c0001t0014g0155 a0001c0001t0014g0158 others(9): Show |
12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.459-1959G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87737832 | |||||||
| chr7:87737906 | C | T | 16 | a0001c0001t0009g0002 a0001c0001t0009g0190 a0001c0001t0009g0191 others(13): Show |
16 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.459-1885C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87737906 | |||||||
| chr7:87737961 | G | A | 38 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(35): Show |
38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.459-1830G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87737961 | |||||||
| chr7:87738005 | G | C | 24 | a0001c0001t0010g0008 a0001c0001t0010g0010 a0001c0001t0010g0011 others(21): Show |
24 | HG00423.hp1 HG02055.hp1 HG02280.hp2 others(21): Show |
intron_variant | MODIFIER | c.459-1786G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87738005 | |||||||
| chr7:87738026 | C | T | 2 | a0001c0001t0036g0159 a0001c0001t0073g0053 |
2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.459-1765C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87738026 | |||||||
| chr7:87738165 | A | G | 1 | a0001c0001t0072g0009 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.459-1626A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87738165 | |||||||
| chr7:87738208 | A | T | 3 | a0001c0001t0062g0145 a0001c0001t0068g0143 a0001c0001t0069g0144 |
3 | HG01069.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.459-1583A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87738208 | |||||||
| chr7:87738217 | AG | A | 38 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(35): Show |
38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.459-1570delG | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87738217 | ||||||
| chr7:87738411 | G | A | 1 | a0001c0001t0010g0012 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.459-1380G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87738411 | |||||||
| chr7:87738529 | C | T | 3 | a0001c0001t0024g0004 a0001c0001t0025g0005 a0001c0001t0037g0006 |
3 | HG00639.hp2 HG02976.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.459-1262C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87738529 | |||||||
| chr7:87739026 | T | G | 1 | a0001c0001t0009g0191 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.459-765T>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87739026 | |||||||
| chr7:87739381 | A | G | 1 | a0001c0001t0003g0082 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.459-410A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87739381 | |||||||
| chr7:87739415 | G | A | 75 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(72): Show |
75 | HG00280.hp2 HG00423.hp1 HG01069.hp2 others(72): Show |
intron_variant | MODIFIER | c.459-376G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87739415 | |||||||
| chr7:87739556 | C | A | 1 | a0001c0001t0003g0105 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.459-235C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87739556 | |||||||
| chr7:87739669 | T | A | 1 | a0001c0001t0006g0142 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.459-122T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87739669 | |||||||
| chr7:87739746 | C | T | 5 | a0001c0001t0055g0020 a0001c0001t0057g0017 a0001c0001t0066g0019 others(2): Show |
5 | HG02572.hp2 HG02630.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.459-45C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87739746 | |||||||
| chr7:87740145 | C | T | 6 | a0001c0001t0010g0010 a0001c0001t0010g0011 a0001c0001t0010g0012 others(3): Show |
6 | HG02055.hp1 HG02280.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.548+265C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 5/10 | chr7 | 87740145 | |||||||
| chr7:87740347 | A | T | 1 | a0001c0001t0055g0020 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.548+467A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 5/10 | chr7 | 87740347 | |||||||
| chr7:87740369 | G | A | 75 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(72): Show |
75 | HG00280.hp2 HG00423.hp1 HG01069.hp2 others(72): Show |
intron_variant | MODIFIER | c.548+489G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 5/10 | chr7 | 87740369 | |||||||
| chr7:87740393 | A | G | 1 | a0001c0001t0077g0081 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.548+513A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 5/10 | chr7 | 87740393 | |||||||
| chr7:87740867 | A | G | 14 | a0001c0001t0017g0065 a0001c0001t0017g0085 a0001c0001t0017g0112 others(11): Show |
14 | HG00438.hp2 HG00621.hp1 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.549-632A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 5/10 | chr7 | 87740867 | |||||||
| chr7:87740953 | C | T | 38 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(35): Show |
38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.549-546C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 5/10 | chr7 | 87740953 | |||||||
| chr7:87740955 | A | G | 2 | a0001c0001t0001g0095 a0001c0001t0001g0101 |
2 | NA19063.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.549-544A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 5/10 | chr7 | 87740955 | |||||||
| chr7:87741226 | C | G | 1 | a0001c0001t0026g0040 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.549-273C>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 5/10 | chr7 | 87741226 | |||||||
| chr7:87741300 | A | G | 1 | a0001c0001t0029g0048 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.549-199A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 5/10 | chr7 | 87741300 | |||||||
| chr7:87741344 | G | A | 1 | a0001c0001t0047g0172 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.549-155G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 5/10 | chr7 | 87741344 | |||||||
| chr7:87741848 | TATA | T | 38 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(35): Show |
38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.629+274_629+276del others(3): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 87741848 | ||||||
| chr7:87741915 | G | T | 38 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(35): Show |
38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.629+336G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87741915 | |||||||
| chr7:87742044 | T | C | 5 | a0001c0001t0055g0020 a0001c0001t0057g0017 a0001c0001t0066g0019 others(2): Show |
5 | HG02572.hp2 HG02630.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.629+465T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87742044 | |||||||
| chr7:87742503 | A | G | 2 | a0001c0001t0015g0150 a0001c0001t0015g0151 |
2 | NA18970.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.629+924A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87742503 | |||||||
| chr7:87742575 | A | AATAG | 38 | a0001c0001t0001g0041 a0001c0001t0001g0045 a0001c0001t0001g0060 others(35): Show |
38 | HG00558.hp2 HG01099.hp2 HG01346.hp1 others(35): Show |
intron_variant | MODIFIER | c.629+1040_629+1043d others(6): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 87742575 | ||||||
| chr7:87742575 | A | AATAGATA others(1): Show |
4 | a0001c0001t0001g0042 a0001c0001t0019g0108 a0001c0001t0033g0037 others(1): Show |
4 | HG01981.hp2 HG03239.hp2 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.629+1036_629+1043d others(10): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 87742575 | ||||||
| chr7:87742575 | A | G | 1 | a0001c0001t0054g0138 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.629+996A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87742575 | |||||||
| chr7:87742575 | AATAG | A | 33 | a0001c0001t0001g0092 a0001c0001t0002g0137 a0001c0001t0002g0167 others(30): Show |
33 | HG00621.hp2 HG00639.hp2 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.629+1040_629+1043d others(6): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 87742575 | ||||||
| chr7:87742575 | AATAGATA others(1): Show |
A | 17 | a0001c0001t0002g0030 a0001c0001t0002g0200 a0001c0001t0005g0077 others(14): Show |
17 | HG01192.hp1 HG01358.hp1 HG01496.hp1 others(14): Show |
intron_variant | MODIFIER | c.629+1036_629+1043d others(10): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 87742575 | ||||||
| chr7:87742575 | AATAGATA others(21): Show |
A | 1 | a0001c0001t0049g0038 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.629+1016_629+1043d others(30): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 87742575 | ||||||
| chr7:87742824 | C | T | 1 | a0001c0001t0025g0091 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.629+1245C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87742824 | |||||||
| chr7:87742930 | G | A | 1 | a0001c0001t0040g0013 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.629+1351G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87742930 | |||||||
| chr7:87742962 | A | C | 16 | a0001c0001t0009g0002 a0001c0001t0009g0190 a0001c0001t0009g0191 others(13): Show |
16 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.629+1383A>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87742962 | |||||||
| chr7:87743113 | C | CA | 17 | a0001c0001t0006g0115 a0001c0001t0009g0002 a0001c0001t0009g0191 others(14): Show |
17 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.629+1548dupA | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 87743113 | ||||||
| chr7:87743113 | CA | C | 10 | a0001c0001t0010g0008 a0001c0001t0010g0010 a0001c0001t0010g0011 others(7): Show |
10 | HG02055.hp1 HG02280.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.629+1548delA | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 87743113 | ||||||
| chr7:87743278 | C | T | 6 | a0001c0001t0012g0174 a0001c0001t0012g0176 a0001c0001t0012g0177 others(3): Show |
6 | HG01081.hp2 HG02258.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.629+1699C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87743278 | |||||||
| chr7:87743576 | C | T | 1 | a0001c0001t0007g0059 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.629+1997C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87743576 | |||||||
| chr7:87743666 | GT | G | 3 | a0001c0001t0057g0017 a0001c0001t0066g0019 a0001c0001t0067g0018 |
3 | HG02630.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.629+2094delT | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 87743666 | ||||||
| chr7:87743671 | T | C | 1 | a0001c0001t0065g0003 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.629+2092T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87743671 | |||||||
| chr7:87743811 | G | A | 1 | a0001c0001t0003g0105 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.629+2232G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87743811 | |||||||
| chr7:87743857 | T | C | 3 | a0001c0001t0057g0017 a0001c0001t0066g0019 a0001c0001t0067g0018 |
3 | HG02630.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.629+2278T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87743857 | |||||||
| chr7:87744125 | T | C | 7 | a0001c0001t0010g0008 a0001c0001t0010g0010 a0001c0001t0010g0011 others(4): Show |
7 | HG02055.hp1 HG02280.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.629+2546T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87744125 | |||||||
| chr7:87744169 | A | G | 2 | a0001c0001t0003g0075 a0001c0001t0004g0067 |
2 | HG00741.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.629+2590A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87744169 | |||||||
| chr7:87744219 | A | G | 1 | a0001c0001t0006g0142 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.629+2640A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87744219 | |||||||
| chr7:87744257 | A | G | 6 | a0001c0001t0039g0148 a0001c0001t0055g0020 a0001c0001t0057g0017 others(3): Show |
6 | HG02572.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.629+2678A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87744257 | |||||||
| chr7:87744271 | C | T | 2 | a0001c0001t0056g0016 a0001c0001t0063g0015 |
2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.629+2692C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87744271 | |||||||
| chr7:87744292 | T | C | 6 | a0001c0001t0039g0148 a0001c0001t0055g0020 a0001c0001t0057g0017 others(3): Show |
6 | HG02572.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.629+2713T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87744292 | |||||||
| chr7:87744726 | C | T | 1 | a0001c0001t0001g0119 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.629+3147C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87744726 | |||||||
| chr7:87744791 | C | T | 1 | a0001c0001t0039g0148 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.629+3212C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87744791 | |||||||
| chr7:87744899 | CAGAG | C | 6 | a0001c0001t0039g0148 a0001c0001t0055g0020 a0001c0001t0057g0017 others(3): Show |
6 | HG02572.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.629+3321_629+3324d others(6): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87744899 | |||||||
| chr7:87745025 | G | T | 1 | a0001c0001t0016g0023 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.629+3446G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87745025 | |||||||
| chr7:87745129 | G | A | 1 | a0001c0001t0072g0009 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.629+3550G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87745129 | |||||||
| chr7:87745170 | C | G | 1 | a0001c0001t0071g0078 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.629+3591C>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87745170 | |||||||
| chr7:87745468 | T | A | 14 | a0001c0001t0002g0162 a0001c0001t0002g0163 a0001c0001t0002g0164 others(11): Show |
14 | HG01081.hp2 HG02258.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.629+3889T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87745468 | |||||||
| chr7:87745512 | G | A | 11 | a0001c0001t0003g0082 a0001c0001t0004g0055 a0001c0001t0004g0058 others(8): Show |
11 | HG00438.hp1 HG00558.hp1 HG01952.hp1 others(8): Show |
intron_variant | MODIFIER | c.629+3933G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87745512 | |||||||
| chr7:87745512 | GTA | G | 7 | a0001c0001t0010g0008 a0001c0001t0010g0010 a0001c0001t0010g0011 others(4): Show |
7 | HG02055.hp1 HG02280.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.629+3935_629+3936d others(4): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 87745512 | ||||||
| chr7:87745553 | T | G | 6 | a0001c0001t0004g0022 a0001c0001t0004g0047 a0001c0001t0004g0139 others(3): Show |
6 | HG01261.hp1 HG02896.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.629+3974T>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87745553 | |||||||
| chr7:87745779 | A | AT | 84 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(81): Show |
84 | HG00280.hp2 HG00423.hp1 HG01069.hp2 others(81): Show |
intron_variant | MODIFIER | c.629+4207dupT | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 87745779 | ||||||
| chr7:87745893 | G | A | 2 | a0001c0001t0003g0105 a0001c0001t0026g0040 |
2 | HG03704.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.629+4314G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87745893 | |||||||
| chr7:87745896 | C | T | 2 | a0001c0001t0056g0016 a0001c0001t0063g0015 |
2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.629+4317C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87745896 | |||||||
| chr7:87745946 | A | G | 1 | a0001c0001t0077g0081 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.629+4367A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87745946 | |||||||
| chr7:87746005 | ATTG | A | 4 | a0001c0001t0044g0169 a0001c0001t0046g0161 a0001c0001t0047g0172 others(1): Show |
4 | HG01123.hp1 HG01192.hp1 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.629+4432_629+4434d others(5): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 87746005 | ||||||
| chr7:87746205 | C | T | 1 | a0001c0001t0039g0148 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.629+4626C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87746205 | |||||||
| chr7:87746317 | A | G | 12 | a0001c0001t0014g0152 a0001c0001t0014g0155 a0001c0001t0014g0158 others(9): Show |
12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.629+4738A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87746317 | |||||||
| chr7:87746335 | T | C | 1 | a0001c0001t0004g0139 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.629+4756T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87746335 | |||||||
| chr7:87746506 | C | T | 1 | a0001c0001t0003g0114 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.629+4927C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87746506 | |||||||
| chr7:87746775 | A | G | 7 | a0001c0001t0039g0148 a0001c0001t0049g0038 a0001c0001t0055g0020 others(4): Show |
7 | HG02572.hp2 HG02630.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.629+5196A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87746775 | |||||||
| chr7:87747292 | G | C | 2 | a0001c0001t0056g0016 a0001c0001t0063g0015 |
2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.629+5713G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87747292 | |||||||
| chr7:87747564 | G | C | 1 | a0001c0001t0049g0038 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.629+5985G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87747564 | |||||||
| chr7:87747600 | A | G | 1 | a0001c0001t0004g0055 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.629+6021A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87747600 | |||||||
| chr7:87748314 | G | T | 16 | a0001c0001t0009g0002 a0001c0001t0009g0190 a0001c0001t0009g0191 others(13): Show |
16 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.629+6735G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87748314 | |||||||
| chr7:87748376 | A | C | 1 | a0001c0001t0001g0089 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.629+6797A>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87748376 | |||||||
| chr7:87748549 | G | T | 3 | a0001c0001t0024g0004 a0001c0001t0025g0005 a0001c0001t0037g0006 |
3 | HG00639.hp2 HG02976.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.629+6970G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87748549 | |||||||
| chr7:87748604 | A | G | 1 | a0001c0001t0065g0003 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.629+7025A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87748604 | |||||||
| chr7:87748663 | C | T | 1 | a0001c0001t0075g0007 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.629+7084C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87748663 | |||||||
| chr7:87748832 | G | T | 1 | a0001c0001t0017g0112 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.629+7253G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87748832 | |||||||
| chr7:87749120 | T | C | 38 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(35): Show |
38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.629+7541T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87749120 | |||||||
| chr7:87749334 | C | A | 12 | a0001c0001t0014g0152 a0001c0001t0014g0155 a0001c0001t0014g0158 others(9): Show |
12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.629+7755C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87749334 | |||||||
| chr7:87749518 | T | C | 2 | a0001c0001t0066g0019 a0001c0001t0067g0018 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.629+7939T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87749518 | |||||||
| chr7:87749520 | A | T | 2 | a0001c0001t0066g0019 a0001c0001t0067g0018 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.629+7941A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87749520 | |||||||
| chr7:87749745 | G | A | 3 | a0001c0001t0009g0190 a0001c0001t0028g0192 a0001c0001t0073g0053 |
3 | HG01167.hp1 HG01169.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.629+8166G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87749745 | |||||||
| chr7:87749859 | C | CT | 13 | a0001c0001t0005g0077 a0001c0001t0005g0124 a0001c0001t0005g0125 others(10): Show |
13 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(10): Show |
intron_variant | MODIFIER | c.629+8289dupT | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 87749859 | ||||||
| chr7:87749868 | T | A | 1 | a0001c0001t0008g0103 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.629+8289T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87749868 | |||||||
| chr7:87749907 | T | C | 16 | a0001c0001t0009g0002 a0001c0001t0009g0190 a0001c0001t0009g0191 others(13): Show |
16 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.629+8328T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87749907 | |||||||
| chr7:87749944 | T | A | 3 | a0001c0001t0057g0017 a0001c0001t0066g0019 a0001c0001t0067g0018 |
3 | HG02630.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.629+8365T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87749944 | |||||||
| chr7:87749972 | C | T | 39 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(36): Show |
39 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(36): Show |
intron_variant | MODIFIER | c.629+8393C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87749972 | |||||||
| chr7:87750117 | G | C | 2 | a0001c0001t0056g0016 a0001c0001t0063g0015 |
2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.629+8538G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87750117 | |||||||
| chr7:87750169 | A | G | 38 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(35): Show |
38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.629+8590A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87750169 | |||||||
| chr7:87750176 | A | G | 1 | a0001c0001t0052g0196 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.629+8597A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87750176 | |||||||
| chr7:87750198 | G | C | 1 | a0001c0001t0005g0052 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.629+8619G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87750198 | |||||||
| chr7:87750226 | T | C | 2 | a0001c0001t0036g0159 a0001c0001t0073g0053 |
2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.629+8647T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87750226 | |||||||
| chr7:87750341 | G | T | 1 | a0001c0001t0001g0119 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.629+8762G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87750341 | |||||||
| chr7:87750362 | A | G | 1 | a0001c0001t0073g0053 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.629+8783A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87750362 | |||||||
| chr7:87750390 | A | G | 1 | a0001c0001t0039g0148 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.629+8811A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87750390 | |||||||
| chr7:87750582 | C | G | 1 | a0001c0001t0040g0013 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.629+9003C>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87750582 | |||||||
| chr7:87750674 | C | G | 1 | a0001c0001t0002g0178 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.629+9095C>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87750674 | |||||||
| chr7:87750718 | A | T | 1 | a0001c0001t0017g0085 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.629+9139A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87750718 | |||||||
| chr7:87750752 | G | T | 1 | a0001c0001t0065g0003 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.629+9173G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87750752 | |||||||
| chr7:87750795 | G | A | 1 | a0001c0001t0039g0148 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.629+9216G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87750795 | |||||||
| chr7:87750862 | G | A | 1 | a0001c0001t0001g0099 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.629+9283G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87750862 | |||||||
| chr7:87750891 | T | C | 15 | a0001c0001t0009g0191 a0001c0001t0017g0065 a0001c0001t0017g0085 others(12): Show |
15 | HG00438.hp2 HG00621.hp1 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.629+9312T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87750891 | |||||||
| chr7:87750992 | C | G | 1 | a0001c0001t0044g0169 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.629+9413C>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87750992 | |||||||
| chr7:87751021 | T | A | 2 | a0001c0001t0001g0119 a0001c0001t0024g0102 |
2 | HG01099.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.629+9442T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87751021 | |||||||
| chr7:87751369 | T | C | 1 | a0001c0001t0001g0095 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.629+9790T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87751369 | |||||||
| chr7:87751406 | A | G | 1 | a0001c0001t0011g0189 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.629+9827A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87751406 | |||||||
| chr7:87751653 | G | C | 2 | a0001c0001t0036g0159 a0001c0001t0073g0053 |
2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.629+10074G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87751653 | |||||||
| chr7:87751683 | TC | T | 12 | a0001c0001t0014g0152 a0001c0001t0014g0155 a0001c0001t0014g0158 others(9): Show |
12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.629+10105delC | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87751683 | |||||||
| chr7:87751686 | G | GTTA | 16 | a0001c0001t0009g0002 a0001c0001t0009g0190 a0001c0001t0009g0191 others(13): Show |
16 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.629+10109_629+1011 others(7): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 87751686 | ||||||
| chr7:87751725 | T | A | 38 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(35): Show |
38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.629+10146T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87751725 | |||||||
| chr7:87752015 | C | T | 16 | a0001c0001t0009g0002 a0001c0001t0009g0190 a0001c0001t0009g0191 others(13): Show |
16 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.629+10436C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87752015 | |||||||
| chr7:87752086 | C | G | 23 | a0001c0001t0009g0002 a0001c0001t0009g0190 a0001c0001t0009g0191 others(20): Show |
23 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.629+10507C>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87752086 | |||||||
| chr7:87752087 | G | A | 13 | a0001c0001t0014g0152 a0001c0001t0014g0155 a0001c0001t0014g0158 others(10): Show |
13 | HG00423.hp1 HG03139.hp1 NA18952.hp1 others(10): Show |
intron_variant | MODIFIER | c.629+10508G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87752087 | |||||||
| chr7:87752199 | C | A | 1 | a0001c0001t0049g0038 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.629+10620C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87752199 | |||||||
| chr7:87752244 | A | C | 1 | a0001c0001t0031g0107 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.629+10665A>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87752244 | |||||||
| chr7:87752270 | T | A | 2 | a0001c0001t0055g0020 a0001c0001t0070g0014 |
2 | HG02572.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.629+10691T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87752270 | |||||||
| chr7:87752292 | G | C | 1 | a0001c0001t0025g0091 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.629+10713G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87752292 | |||||||
| chr7:87752359 | A | G | 85 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(82): Show |
85 | HG00280.hp2 HG00423.hp1 HG01069.hp2 others(82): Show |
intron_variant | MODIFIER | c.629+10780A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87752359 | |||||||
| chr7:87752464 | A | T | 12 | a0001c0001t0014g0152 a0001c0001t0014g0155 a0001c0001t0014g0158 others(9): Show |
12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.629+10885A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87752464 | |||||||
| chr7:87752551 | G | C | 1 | a0001c0001t0049g0038 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.629+10972G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87752551 | |||||||
| chr7:87752555 | C | G | 2 | a0001c0001t0003g0114 a0001c0001t0071g0078 |
2 | HG00323.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.629+10976C>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87752555 | |||||||
| chr7:87752791 | GGTTTATC others(21): Show |
G | 1 | a0001c0001t0008g0103 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.629+11213_629+1124 others(32): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87752791 | |||||||
| chr7:87752794 | T | C | 38 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(35): Show |
38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.629+11215T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87752794 | |||||||
| chr7:87752800 | G | A | 38 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(35): Show |
38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.629+11221G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87752800 | |||||||
| chr7:87752822 | A | T | 1 | a0001c0001t0008g0103 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.629+11243A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87752822 | |||||||
| chr7:87752883 | T | C | 2 | a0001c0001t0056g0016 a0001c0001t0063g0015 |
2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.629+11304T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87752883 | |||||||
| chr7:87752982 | G | T | 12 | a0001c0001t0014g0152 a0001c0001t0014g0155 a0001c0001t0014g0158 others(9): Show |
12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.629+11403G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87752982 | |||||||
| chr7:87753193 | A | T | 1 | a0001c0001t0024g0102 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.629+11614A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87753193 | |||||||
| chr7:87753286 | A | C | 1 | a0001c0001t0039g0148 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.629+11707A>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87753286 | |||||||
| chr7:87753294 | G | C | 2 | a0001c0001t0022g0182 a0001c0001t0027g0180 |
2 | NA18974.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.629+11715G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87753294 | |||||||
| chr7:87753620 | G | A | 61 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(58): Show |
61 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(58): Show |
intron_variant | MODIFIER | c.629+12041G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87753620 | |||||||
| chr7:87753715 | T | C | 1 | a0001c0001t0072g0009 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.629+12136T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87753715 | |||||||
| chr7:87753861 | T | A | 39 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(36): Show |
39 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(36): Show |
intron_variant | MODIFIER | c.629+12282T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87753861 | |||||||
| chr7:87754066 | G | C | 1 | a0001c0001t0005g0125 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.629+12487G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87754066 | |||||||
| chr7:87754086 | C | A | 16 | a0001c0001t0009g0002 a0001c0001t0009g0190 a0001c0001t0009g0191 others(13): Show |
16 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.629+12507C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87754086 | |||||||
| chr7:87754312 | G | A | 1 | a0001c0001t0032g0051 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.629+12733G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87754312 | |||||||
| chr7:87754352 | A | C | 7 | a0001c0001t0039g0148 a0001c0001t0049g0038 a0001c0001t0055g0020 others(4): Show |
7 | HG02572.hp2 HG02630.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.629+12773A>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87754352 | |||||||
| chr7:87754416 | G | T | 1 | a0001c0001t0007g0118 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.629+12837G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87754416 | |||||||
| chr7:87754487 | A | T | 12 | a0001c0001t0014g0152 a0001c0001t0014g0155 a0001c0001t0014g0158 others(9): Show |
12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.629+12908A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87754487 | |||||||
| chr7:87754599 | A | C | 16 | a0001c0001t0009g0002 a0001c0001t0009g0190 a0001c0001t0009g0191 others(13): Show |
16 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.629+13020A>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87754599 | |||||||
| chr7:87754854 | T | G | 1 | a0001c0001t0003g0056 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.629+13275T>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87754854 | |||||||
| chr7:87754857 | C | T | 38 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(35): Show |
38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.629+13278C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87754857 | |||||||
| chr7:87754905 | A | C | 38 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(35): Show |
38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.629+13326A>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87754905 | |||||||
| chr7:87754943 | C | CA | 25 | a0001c0001t0001g0064 a0001c0001t0001g0080 a0001c0001t0001g0092 others(22): Show |
25 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(22): Show |
intron_variant | MODIFIER | c.629+13382dupA | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 87754943 | ||||||
| chr7:87754943 | CA | C | 14 | a0001c0001t0003g0056 a0001c0001t0004g0022 a0001c0001t0008g0021 others(11): Show |
14 | HG00639.hp1 HG01169.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.629+13382delA | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 87754943 | ||||||
| chr7:87754996 | C | T | 12 | a0001c0001t0014g0152 a0001c0001t0014g0155 a0001c0001t0014g0158 others(9): Show |
12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.629+13417C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87754996 | |||||||
| chr7:87755027 | C | CT | 39 | a0001c0001t0001g0093 a0001c0001t0002g0030 a0001c0001t0002g0137 others(36): Show |
39 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(36): Show |
intron_variant | MODIFIER | c.629+13461dupT | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 87755027 | ||||||
| chr7:87755116 | G | A | 1 | a0001c0001t0039g0148 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.629+13537G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87755116 | |||||||
| chr7:87755148 | G | A | 1 | a0001c0001t0029g0061 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.629+13569G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87755148 | |||||||
| chr7:87755295 | A | G | 4 | a0001c0001t0003g0066 a0001c0001t0006g0115 a0001c0001t0006g0116 others(1): Show |
4 | HG02040.hp2 HG02129.hp2 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.629+13716A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87755295 | |||||||
| chr7:87755851 | G | A | 2 | a0001c0001t0001g0080 a0001c0001t0007g0122 |
2 | HG00423.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.629+14272G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87755851 | |||||||
| chr7:87756051 | C | T | 12 | a0001c0001t0014g0152 a0001c0001t0014g0155 a0001c0001t0014g0158 others(9): Show |
12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.629+14472C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87756051 | |||||||
| chr7:87756279 | C | T | 1 | a0001c0001t0010g0012 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.630-14302C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87756279 | |||||||
| chr7:87756627 | C | T | 85 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(82): Show |
85 | HG00280.hp2 HG00423.hp1 HG01069.hp2 others(82): Show |
intron_variant | MODIFIER | c.630-13954C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87756627 | |||||||
| chr7:87756770 | G | T | 38 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(35): Show |
38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.630-13811G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87756770 | |||||||
| chr7:87756796 | T | C | 16 | a0001c0001t0009g0002 a0001c0001t0009g0190 a0001c0001t0009g0191 others(13): Show |
16 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.630-13785T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87756796 | |||||||
| chr7:87757153 | C | T | 2 | a0001c0001t0022g0182 a0001c0001t0027g0180 |
2 | NA18974.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.630-13428C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87757153 | |||||||
| chr7:87757288 | A | T | 63 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(60): Show |
63 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(60): Show |
intron_variant | MODIFIER | c.630-13293A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87757288 | |||||||
| chr7:87757353 | T | G | 55 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(52): Show |
55 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(52): Show |
intron_variant | MODIFIER | c.630-13228T>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87757353 | |||||||
| chr7:87757678 | G | A | 1 | a0001c0001t0008g0121 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.630-12903G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87757678 | |||||||
| chr7:87757802 | A | C | 1 | a0001c0001t0020g0035 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.630-12779A>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87757802 | |||||||
| chr7:87758024 | A | C | 1 | a0001c0001t0070g0014 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.630-12557A>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87758024 | |||||||
| chr7:87758082 | G | T | 14 | a0001c0001t0017g0065 a0001c0001t0017g0085 a0001c0001t0017g0112 others(11): Show |
14 | HG00438.hp2 HG00621.hp1 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.630-12499G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87758082 | |||||||
| chr7:87758358 | C | T | 14 | a0001c0001t0002g0162 a0001c0001t0002g0163 a0001c0001t0002g0164 others(11): Show |
14 | HG01081.hp2 HG02258.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.630-12223C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87758358 | |||||||
| chr7:87758803 | T | C | 1 | a0001c0001t0079g0024 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.630-11778T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87758803 | |||||||
| chr7:87759233 | A | C | 5 | a0001c0001t0055g0020 a0001c0001t0057g0017 a0001c0001t0066g0019 others(2): Show |
5 | HG02572.hp2 HG02630.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.630-11348A>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87759233 | |||||||
| chr7:87759236 | A | G | 16 | a0001c0001t0009g0002 a0001c0001t0009g0190 a0001c0001t0009g0191 others(13): Show |
16 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.630-11345A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87759236 | |||||||
| chr7:87759325 | C | T | 1 | a0001c0001t0001g0098 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.630-11256C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87759325 | |||||||
| chr7:87759443 | A | G | 7 | a0001c0001t0010g0008 a0001c0001t0010g0010 a0001c0001t0010g0011 others(4): Show |
7 | HG02055.hp1 HG02280.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.630-11138A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87759443 | |||||||
| chr7:87759466 | C | A | 1 | a0001c0001t0036g0159 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.630-11115C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87759466 | |||||||
| chr7:87759605 | T | G | 1 | a0001c0001t0004g0139 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.630-10976T>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87759605 | |||||||
| chr7:87759658 | T | A | 12 | a0001c0001t0014g0152 a0001c0001t0014g0155 a0001c0001t0014g0158 others(9): Show |
12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.630-10923T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87759658 | |||||||
| chr7:87759735 | C | CTACA | 85 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(82): Show |
85 | HG00280.hp2 HG00423.hp1 HG01069.hp2 others(82): Show |
intron_variant | MODIFIER | c.630-10846_630-1084 others(8): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87759735 | |||||||
| chr7:87759736 | A | G | 85 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(82): Show |
85 | HG00280.hp2 HG00423.hp1 HG01069.hp2 others(82): Show |
intron_variant | MODIFIER | c.630-10845A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87759736 | |||||||
| chr7:87759793 | C | CA | 13 | a0001c0001t0014g0152 a0001c0001t0014g0155 a0001c0001t0015g0150 others(10): Show |
13 | HG00423.hp1 HG02559.hp1 HG03471.hp1 others(10): Show |
intron_variant | MODIFIER | c.630-10774dupA | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 87759793 | ||||||
| chr7:87760069 | G | T | 1 | a0001c0001t0005g0128 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.630-10512G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87760069 | |||||||
| chr7:87760069 | GT | G | 61 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(58): Show |
61 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(58): Show |
intron_variant | MODIFIER | c.630-10500delT | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 87760069 | ||||||
| chr7:87760135 | C | T | 2 | a0001c0001t0055g0020 a0001c0001t0070g0014 |
2 | HG02572.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.630-10446C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87760135 | |||||||
| chr7:87760866 | A | C | 2 | a0001c0001t0001g0134 a0001c0001t0001g0136 |
2 | HG01192.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.630-9715A>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87760866 | |||||||
| chr7:87761014 | A | G | 63 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(60): Show |
63 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(60): Show |
intron_variant | MODIFIER | c.630-9567A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87761014 | |||||||
| chr7:87761148 | G | A | 61 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(58): Show |
61 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(58): Show |
intron_variant | MODIFIER | c.630-9433G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87761148 | |||||||
| chr7:87761506 | G | A | 38 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(35): Show |
38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.630-9075G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87761506 | |||||||
| chr7:87761593 | A | G | 39 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(36): Show |
39 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(36): Show |
intron_variant | MODIFIER | c.630-8988A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87761593 | |||||||
| chr7:87761845 | G | C | 15 | a0001c0001t0001g0064 a0001c0001t0001g0080 a0001c0001t0005g0077 others(12): Show |
15 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(12): Show |
intron_variant | MODIFIER | c.630-8736G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87761845 | |||||||
| chr7:87761990 | G | T | 1 | a0001c0001t0003g0114 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.630-8591G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87761990 | |||||||
| chr7:87762300 | T | C | 85 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(82): Show |
85 | HG00280.hp2 HG00423.hp1 HG01069.hp2 others(82): Show |
intron_variant | MODIFIER | c.630-8281T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87762300 | |||||||
| chr7:87762330 | G | A | 1 | a0001c0001t0031g0107 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.630-8251G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87762330 | |||||||
| chr7:87762418 | A | G | 16 | a0001c0001t0009g0002 a0001c0001t0009g0190 a0001c0001t0009g0191 others(13): Show |
16 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.630-8163A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87762418 | |||||||
| chr7:87762445 | A | G | 153 | a0001c0001t0001g0064 a0001c0001t0001g0080 a0001c0001t0001g0097 others(150): Show |
153 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.630-8136A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87762445 | |||||||
| chr7:87762583 | T | C | 4 | a0001c0001t0003g0066 a0001c0001t0006g0115 a0001c0001t0006g0116 others(1): Show |
4 | HG02040.hp2 HG02129.hp2 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.630-7998T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87762583 | |||||||
| chr7:87762693 | G | A | 5 | a0001c0001t0055g0020 a0001c0001t0057g0017 a0001c0001t0066g0019 others(2): Show |
5 | HG02572.hp2 HG02630.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.630-7888G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87762693 | |||||||
| chr7:87762728 | A | T | 1 | a0001c0001t0007g0059 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.630-7853A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87762728 | |||||||
| chr7:87762878 | TA | T | 61 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(58): Show |
61 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(58): Show |
intron_variant | MODIFIER | c.630-7694delA | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 87762878 | ||||||
| chr7:87762894 | C | T | 14 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0200 others(11): Show |
14 | HG01358.hp1 HG01496.hp1 HG01952.hp2 others(11): Show |
intron_variant | MODIFIER | c.630-7687C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87762894 | |||||||
| chr7:87762896 | G | A | 2 | a0001c0001t0055g0020 a0001c0001t0070g0014 |
2 | HG02572.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.630-7685G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87762896 | |||||||
| chr7:87762979 | TACTTATC others(5): Show |
T | 39 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(36): Show |
39 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(36): Show |
intron_variant | MODIFIER | c.630-7597_630-7586d others(14): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 87762979 | ||||||
| chr7:87763203 | T | C | 2 | a0001c0001t0010g0010 a0001c0001t0010g0011 |
2 | HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.630-7378T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87763203 | |||||||
| chr7:87763627 | A | G | 11 | a0001c0001t0003g0082 a0001c0001t0004g0055 a0001c0001t0004g0058 others(8): Show |
11 | HG00438.hp1 HG00558.hp1 HG01952.hp1 others(8): Show |
intron_variant | MODIFIER | c.630-6954A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87763627 | |||||||
| chr7:87763821 | C | A | 85 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(82): Show |
85 | HG00280.hp2 HG00423.hp1 HG01069.hp2 others(82): Show |
intron_variant | MODIFIER | c.630-6760C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87763821 | |||||||
| chr7:87764203 | A | G | 3 | a0001c0001t0024g0004 a0001c0001t0025g0005 a0001c0001t0037g0006 |
3 | HG00639.hp2 HG02976.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.630-6378A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87764203 | |||||||
| chr7:87764355 | T | G | 12 | a0001c0001t0014g0152 a0001c0001t0014g0155 a0001c0001t0014g0158 others(9): Show |
12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.630-6226T>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87764355 | |||||||
| chr7:87764434 | G | C | 2 | a0001c0001t0022g0182 a0001c0001t0027g0180 |
2 | NA18974.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.630-6147G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87764434 | |||||||
| chr7:87764447 | A | G | 5 | a0001c0001t0003g0082 a0001c0001t0004g0083 a0001c0001t0005g0113 others(2): Show |
5 | HG00438.hp1 HG01952.hp1 HG02135.hp1 others(2): Show |
intron_variant | MODIFIER | c.630-6134A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87764447 | |||||||
| chr7:87764459 | G | C | 199 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0045 others(196): Show |
199 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.630-6122G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87764459 | |||||||
| chr7:87765019 | C | T | 2 | a0001c0001t0056g0016 a0001c0001t0063g0015 |
2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.630-5562C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87765019 | |||||||
| chr7:87765037 | G | C | 54 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(51): Show |
54 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(51): Show |
intron_variant | MODIFIER | c.630-5544G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87765037 | |||||||
| chr7:87765230 | C | T | 1 | a0001c0001t0001g0098 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.630-5351C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87765230 | |||||||
| chr7:87765274 | AT | A | 38 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(35): Show |
38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.630-5298delT | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 87765274 | ||||||
| chr7:87765337 | C | G | 38 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(35): Show |
38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.630-5244C>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87765337 | |||||||
| chr7:87765435 | T | G | 1 | a0001c0001t0049g0038 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.630-5146T>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87765435 | |||||||
| chr7:87765451 | C | A | 2 | a0001c0001t0017g0112 a0001c0001t0034g0079 |
2 | HG00741.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.630-5130C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87765451 | |||||||
| chr7:87765890 | A | G | 85 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(82): Show |
85 | HG00280.hp2 HG00423.hp1 HG01069.hp2 others(82): Show |
intron_variant | MODIFIER | c.630-4691A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87765890 | |||||||
| chr7:87765926 | T | A | 1 | a0001c0001t0070g0014 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.630-4655T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87765926 | |||||||
| chr7:87766086 | G | C | 15 | a0001c0001t0009g0002 a0001c0001t0009g0190 a0001c0001t0009g0191 others(12): Show |
15 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.630-4495G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87766086 | |||||||
| chr7:87766206 | G | A | 12 | a0001c0001t0014g0152 a0001c0001t0014g0155 a0001c0001t0014g0158 others(9): Show |
12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.630-4375G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87766206 | |||||||
| chr7:87766439 | C | T | 1 | a0001c0001t0005g0124 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.630-4142C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87766439 | |||||||
| chr7:87766710 | T | C | 2 | a0001c0001t0013g0173 a0001c0001t0038g0183 |
2 | NA18977.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.630-3871T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87766710 | |||||||
| chr7:87766871 | A | C | 39 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(36): Show |
39 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(36): Show |
intron_variant | MODIFIER | c.630-3710A>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87766871 | |||||||
| chr7:87766877 | G | A | 1 | a0001c0001t0009g0191 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.630-3704G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87766877 | |||||||
| chr7:87766936 | A | T | 1 | a0001c0001t0039g0148 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.630-3645A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87766936 | |||||||
| chr7:87767025 | A | T | 16 | a0001c0001t0009g0002 a0001c0001t0009g0190 a0001c0001t0009g0191 others(13): Show |
16 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.630-3556A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87767025 | |||||||
| chr7:87767086 | G | A | 2 | a0001c0001t0003g0075 a0001c0001t0004g0067 |
2 | HG00741.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.630-3495G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87767086 | |||||||
| chr7:87767130 | G | A | 75 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(72): Show |
75 | HG00280.hp2 HG00423.hp1 HG01069.hp2 others(72): Show |
intron_variant | MODIFIER | c.630-3451G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87767130 | |||||||
| chr7:87767296 | A | G | 1 | a0001c0001t0001g0097 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.630-3285A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87767296 | |||||||
| chr7:87767302 | C | T | 1 | a0001c0001t0004g0083 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.630-3279C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87767302 | |||||||
| chr7:87767730 | C | T | 1 | a0001c0001t0079g0024 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.630-2851C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87767730 | |||||||
| chr7:87767816 | G | A | 16 | a0001c0001t0009g0002 a0001c0001t0009g0190 a0001c0001t0009g0191 others(13): Show |
16 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.630-2765G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87767816 | |||||||
| chr7:87768029 | T | C | 85 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(82): Show |
85 | HG00280.hp2 HG00423.hp1 HG01069.hp2 others(82): Show |
intron_variant | MODIFIER | c.630-2552T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87768029 | |||||||
| chr7:87768284 | G | C | 1 | a0001c0001t0057g0017 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.630-2297G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87768284 | |||||||
| chr7:87768472 | G | A | 12 | a0001c0001t0014g0152 a0001c0001t0014g0155 a0001c0001t0014g0158 others(9): Show |
12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.630-2109G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87768472 | |||||||
| chr7:87768540 | C | T | 2 | a0001c0001t0055g0020 a0001c0001t0070g0014 |
2 | HG02572.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.630-2041C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87768540 | |||||||
| chr7:87768704 | C | T | 4 | a0001c0001t0005g0127 a0001c0001t0005g0128 a0001c0001t0006g0088 others(1): Show |
4 | HG00280.hp1 HG00323.hp1 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.630-1877C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87768704 | |||||||
| chr7:87768862 | G | A | 1 | a0001c0001t0001g0099 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.630-1719G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87768862 | |||||||
| chr7:87769026 | G | A | 1 | a0001c0001t0010g0008 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.630-1555G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87769026 | |||||||
| chr7:87769157 | C | T | 38 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(35): Show |
38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.630-1424C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87769157 | |||||||
| chr7:87769210 | C | T | 1 | a0001c0001t0040g0013 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.630-1371C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87769210 | |||||||
| chr7:87769211 | A | G | 2 | a0001c0001t0002g0162 a0001c0001t0002g0178 |
2 | HG02895.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.630-1370A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87769211 | |||||||
| chr7:87769330 | C | A | 1 | a0001c0001t0019g0026 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.630-1251C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87769330 | |||||||
| chr7:87769386 | G | A | 1 | a0001c0001t0008g0103 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.630-1195G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87769386 | |||||||
| chr7:87769601 | T | C | 1 | a0001c0001t0044g0169 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.630-980T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87769601 | |||||||
| chr7:87769640 | T | C | 1 | a0001c0001t0001g0041 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.630-941T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87769640 | |||||||
| chr7:87769826 | C | T | 1 | a0001c0001t0057g0017 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.630-755C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87769826 | |||||||
| chr7:87769942 | T | C | 1 | a0001c0001t0003g0082 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.630-639T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87769942 | |||||||
| chr7:87770038 | C | G | 3 | a0001c0001t0057g0017 a0001c0001t0066g0019 a0001c0001t0067g0018 |
3 | HG02630.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.630-543C>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87770038 | |||||||
| chr7:87770081 | C | T | 16 | a0001c0001t0009g0002 a0001c0001t0009g0190 a0001c0001t0009g0191 others(13): Show |
16 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.630-500C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87770081 | |||||||
| chr7:87770121 | A | T | 6 | a0001c0001t0039g0148 a0001c0001t0055g0020 a0001c0001t0057g0017 others(3): Show |
6 | HG02572.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.630-460A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87770121 | |||||||
| chr7:87770318 | G | C | 1 | a0001c0001t0071g0078 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.630-263G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87770318 | |||||||
| chr7:87770455 | A | G | 3 | a0002c0002t0002g0029 a0002c0002t0002g0036 a0002c0002t0018g0140 |
3 | NA18973.hp2 NA18979.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.630-126A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87770455 | |||||||
| chr7:87770572 | T | C | 3 | a0001c0001t0057g0017 a0001c0001t0066g0019 a0001c0001t0067g0018 |
3 | HG02630.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.630-9T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87770572 | |||||||
| chr7:87771286 | C | G | 2 | a0001c0001t0036g0159 a0001c0001t0073g0053 |
2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.798+537C>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | chr7 | 87771286 | |||||||
| chr7:87771295 | T | C | 2 | a0001c0001t0036g0159 a0001c0001t0073g0053 |
2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.798+546T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | chr7 | 87771295 | |||||||
| chr7:87771339 | T | A | 16 | a0001c0001t0009g0002 a0001c0001t0009g0190 a0001c0001t0009g0191 others(13): Show |
16 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.798+590T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | chr7 | 87771339 | |||||||
| chr7:87771782 | A | G | 1 | a0001c0001t0055g0020 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.798+1033A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | chr7 | 87771782 | |||||||
| chr7:87772460 | G | A | 1 | a0001c0001t0034g0199 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.798+1711G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | chr7 | 87772460 | |||||||
| chr7:87772762 | A | G | 3 | a0001c0001t0016g0023 a0001c0001t0016g0072 a0001c0001t0016g0074 |
3 | NA18906.hp2 NA19043.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.798+2013A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | chr7 | 87772762 | |||||||
| chr7:87772870 | G | A | 2 | a0001c0001t0058g0184 a0001c0001t0061g0185 |
2 | HG03017.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.798+2121G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | chr7 | 87772870 | |||||||
| chr7:87772995 | T | TAAGACTA others(321): Show |
2 | a0001c0001t0036g0159 a0001c0001t0073g0053 |
2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.798+2260_798+2261i others(330): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr7 | 87772995 | ||||||
| chr7:87773031 | A | T | 1 | a0001c0001t0001g0101 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.798+2282A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | chr7 | 87773031 | |||||||
| chr7:87773051 | T | C | 85 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(82): Show |
85 | HG00280.hp2 HG00423.hp1 HG01069.hp2 others(82): Show |
intron_variant | MODIFIER | c.798+2302T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | chr7 | 87773051 | |||||||
| chr7:87773180 | G | A | 2 | a0001c0001t0036g0159 a0001c0001t0073g0053 |
2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.798+2431G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | chr7 | 87773180 | |||||||
| chr7:87773220 | A | G | 152 | a0001c0001t0001g0064 a0001c0001t0001g0080 a0001c0001t0001g0119 others(149): Show |
152 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.798+2471A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | chr7 | 87773220 | |||||||
| chr7:87773317 | C | T | 1 | a0001c0001t0007g0059 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.798+2568C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | chr7 | 87773317 | |||||||
| chr7:87773322 | C | CA | 8 | a0001c0001t0002g0200 a0001c0001t0006g0088 a0001c0001t0008g0121 others(5): Show |
8 | HG00323.hp1 HG00735.hp2 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.798+2594dupA | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr7 | 87773322 | ||||||
| chr7:87773322 | CA | C | 23 | a0001c0001t0005g0124 a0001c0001t0009g0002 a0001c0001t0009g0190 others(20): Show |
23 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.798+2594delA | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr7 | 87773322 | ||||||
| chr7:87773526 | G | A | 1 | a0001c0001t0070g0014 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.798+2777G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | chr7 | 87773526 | |||||||
| chr7:87773630 | TGTTTG | T | 6 | a0001c0001t0010g0008 a0001c0001t0010g0012 a0001c0001t0040g0013 others(3): Show |
6 | HG02055.hp1 HG02280.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.798+2887_798+2891d others(7): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr7 | 87773630 | ||||||
| chr7:87773636 | G | T | 2 | a0001c0001t0010g0010 a0001c0001t0010g0011 |
2 | HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.798+2887G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | chr7 | 87773636 | |||||||
| chr7:87773645 | G | T | 2 | a0001c0001t0010g0010 a0001c0001t0010g0011 |
2 | HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.798+2896G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | chr7 | 87773645 | |||||||
| chr7:87773646 | T | G | 2 | a0001c0001t0010g0010 a0001c0001t0010g0011 |
2 | HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.798+2897T>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | chr7 | 87773646 | |||||||
| chr7:87773648 | T | C | 2 | a0001c0001t0010g0010 a0001c0001t0010g0011 |
2 | HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.798+2899T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | chr7 | 87773648 | |||||||
| chr7:87773658 | C | CTTGTT | 89 | a0001c0001t0001g0064 a0001c0001t0001g0119 a0001c0001t0002g0030 others(86): Show |
89 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.798+2943_798+2947d others(7): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr7 | 87773658 | ||||||
| chr7:87773658 | C | CTTGTTTT others(3): Show |
30 | a0001c0001t0002g0166 a0001c0001t0003g0114 a0001c0001t0004g0055 others(27): Show |
30 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(27): Show |
intron_variant | MODIFIER | c.798+2938_798+2947d others(12): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr7 | 87773658 | ||||||
| chr7:87773658 | C | T | 5 | a0001c0001t0010g0010 a0001c0001t0010g0011 a0001c0001t0057g0017 others(2): Show |
5 | HG02630.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.798+2909C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | chr7 | 87773658 | |||||||
| chr7:87773658 | CTTGTT | C | 15 | a0001c0001t0009g0002 a0001c0001t0009g0190 a0001c0001t0009g0191 others(12): Show |
15 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.798+2943_798+2947d others(7): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr7 | 87773658 | ||||||
| chr7:87773658 | CTTGTTTT others(3): Show |
C | 4 | a0001c0001t0029g0048 a0001c0001t0032g0049 a0001c0001t0032g0051 others(1): Show |
4 | HG00639.hp1 HG02559.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.798+2938_798+2947d others(12): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr7 | 87773658 | ||||||
| chr7:87773768 | C | T | 16 | a0001c0001t0009g0002 a0001c0001t0009g0190 a0001c0001t0009g0191 others(13): Show |
16 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.798+3019C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | chr7 | 87773768 | |||||||
| chr7:87773849 | T | C | 3 | a0001c0001t0004g0055 a0001c0001t0004g0058 a0001c0001t0005g0068 |
3 | NA18977.hp1 NA19010.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.798+3100T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | chr7 | 87773849 | |||||||
| chr7:87773876 | C | T | 1 | a0001c0001t0001g0095 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.798+3127C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | chr7 | 87773876 | |||||||
| chr7:87773877 | G | A | 1 | a0001c0001t0004g0139 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.798+3128G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | chr7 | 87773877 | |||||||
| chr7:87774029 | A | G | 1 | a0001c0001t0010g0008 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.798+3280A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | chr7 | 87774029 | |||||||
| chr7:87774104 | T | A | 2 | a0001c0001t0055g0020 a0001c0001t0070g0014 |
2 | HG02572.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.798+3355T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | chr7 | 87774104 | |||||||
| chr7:87774329 | T | A | 1 | a0001c0001t0003g0094 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.799-3469T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | chr7 | 87774329 | |||||||
| chr7:87774418 | A | G | 1 | a0001c0001t0070g0014 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.799-3380A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | chr7 | 87774418 | |||||||
| chr7:87774426 | C | G | 1 | a0001c0001t0076g0179 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.799-3372C>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | chr7 | 87774426 | |||||||
| chr7:87775309 | A | G | 1 | a0001c0001t0026g0040 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.799-2489A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | chr7 | 87775309 | |||||||
| chr7:87775360 | A | G | 1 | a0001c0001t0057g0017 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.799-2438A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | chr7 | 87775360 | |||||||
| chr7:87775516 | A | G | 2 | a0001c0001t0004g0109 a0001c0001t0004g0110 |
2 | HG00738.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.799-2282A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | chr7 | 87775516 | |||||||
| chr7:87775635 | T | C | 1 | a0001c0001t0074g0170 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.799-2163T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | chr7 | 87775635 | |||||||
| chr7:87775761 | C | T | 16 | a0001c0001t0009g0002 a0001c0001t0009g0190 a0001c0001t0009g0191 others(13): Show |
16 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.799-2037C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | chr7 | 87775761 | |||||||
| chr7:87775810 | T | C | 12 | a0001c0001t0014g0152 a0001c0001t0014g0155 a0001c0001t0014g0158 others(9): Show |
12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.799-1988T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | chr7 | 87775810 | |||||||
| chr7:87775905 | G | T | 1 | a0001c0001t0050g0027 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.799-1893G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | chr7 | 87775905 | |||||||
| chr7:87776035 | A | C | 75 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(72): Show |
75 | HG00280.hp2 HG00423.hp1 HG01069.hp2 others(72): Show |
intron_variant | MODIFIER | c.799-1763A>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | chr7 | 87776035 | |||||||
| chr7:87776075 | A | G | 1 | a0001c0001t0018g0175 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.799-1723A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | chr7 | 87776075 | |||||||
| chr7:87776147 | A | T | 1 | a0001c0003t0001g0025 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.799-1651A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | chr7 | 87776147 | |||||||
| chr7:87776325 | A | G | 1 | a0001c0001t0072g0009 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.799-1473A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | chr7 | 87776325 | |||||||
| chr7:87776574 | G | T | 1 | a0001c0001t0072g0009 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.799-1224G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | chr7 | 87776574 | |||||||
| chr7:87776717 | A | G | 16 | a0001c0001t0009g0002 a0001c0001t0009g0190 a0001c0001t0009g0191 others(13): Show |
16 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.799-1081A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | chr7 | 87776717 | |||||||
| chr7:87776772 | A | G | 1 | a0001c0001t0008g0103 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.799-1026A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | chr7 | 87776772 | |||||||
| chr7:87776859 | T | C | 1 | a0001c0001t0052g0196 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.799-939T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | chr7 | 87776859 | |||||||
| chr7:87777061 | A | G | 2 | a0001c0001t0056g0016 a0001c0001t0063g0015 |
2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.799-737A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | chr7 | 87777061 | |||||||
| chr7:87777336 | G | A | 1 | a0001c0001t0007g0132 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.799-462G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | chr7 | 87777336 | |||||||
| chr7:87777399 | C | T | 1 | a0001c0001t0001g0104 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.799-399C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | chr7 | 87777399 | |||||||
| chr7:87777400 | TCTCA | T | 3 | a0001c0001t0057g0017 a0001c0001t0066g0019 a0001c0001t0067g0018 |
3 | HG02630.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.799-395_799-392del others(4): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr7 | 87777400 | ||||||
| chr7:87777582 | T | C | 2 | a0001c0001t0055g0020 a0001c0001t0070g0014 |
2 | HG02572.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.799-216T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | chr7 | 87777582 | |||||||
| chr7:87778056 | T | C | 4 | a0001c0001t0029g0048 a0001c0001t0032g0049 a0001c0001t0032g0051 others(1): Show |
4 | HG00639.hp1 HG02559.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.956+101T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87778056 | |||||||
| chr7:87778115 | G | A | 85 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(82): Show |
85 | HG00280.hp2 HG00423.hp1 HG01069.hp2 others(82): Show |
intron_variant | MODIFIER | c.956+160G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87778115 | |||||||
| chr7:87778205 | G | C | 12 | a0001c0001t0014g0152 a0001c0001t0014g0155 a0001c0001t0014g0158 others(9): Show |
12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.956+250G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87778205 | |||||||
| chr7:87778284 | A | G | 2 | a0001c0001t0010g0010 a0001c0001t0010g0011 |
2 | HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.956+329A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87778284 | |||||||
| chr7:87778390 | C | T | 5 | a0001c0001t0055g0020 a0001c0001t0057g0017 a0001c0001t0066g0019 others(2): Show |
5 | HG02572.hp2 HG02630.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.956+435C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87778390 | |||||||
| chr7:87778440 | C | CA | 81 | a0001c0001t0001g0087 a0001c0001t0002g0030 a0001c0001t0002g0137 others(78): Show |
81 | HG00280.hp2 HG00423.hp1 HG01069.hp2 others(78): Show |
intron_variant | MODIFIER | c.956+501dupA | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr7 | 87778440 | ||||||
| chr7:87778465 | A | G | 1 | a0001c0001t0072g0009 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.956+510A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87778465 | |||||||
| chr7:87778694 | A | G | 6 | a0001c0001t0009g0190 a0001c0001t0009g0191 a0001c0001t0009g0193 others(3): Show |
6 | HG01167.hp1 HG01169.hp1 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.956+739A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87778694 | |||||||
| chr7:87778875 | AT | A | 12 | a0001c0001t0014g0152 a0001c0001t0014g0155 a0001c0001t0014g0158 others(9): Show |
12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.956+921delT | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87778875 | |||||||
| chr7:87778928 | C | T | 2 | a0001c0001t0001g0089 a0001c0001t0001g0097 |
2 | NA18952.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.956+973C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87778928 | |||||||
| chr7:87778949 | A | G | 8 | a0001c0001t0010g0008 a0001c0001t0010g0010 a0001c0001t0010g0011 others(5): Show |
8 | HG02055.hp1 HG02280.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.956+994A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87778949 | |||||||
| chr7:87779023 | C | T | 16 | a0001c0001t0009g0002 a0001c0001t0009g0190 a0001c0001t0009g0191 others(13): Show |
16 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.956+1068C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87779023 | |||||||
| chr7:87779030 | A | G | 41 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(38): Show |
41 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(38): Show |
intron_variant | MODIFIER | c.956+1075A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87779030 | |||||||
| chr7:87779145 | T | G | 2 | a0001c0001t0056g0016 a0001c0001t0063g0015 |
2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.956+1190T>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87779145 | |||||||
| chr7:87779167 | G | A | 2 | a0001c0001t0056g0016 a0001c0001t0063g0015 |
2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.956+1212G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87779167 | |||||||
| chr7:87779875 | C | T | 1 | a0001c0001t0039g0148 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.956+1920C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87779875 | |||||||
| chr7:87780142 | T | A | 2 | a0001c0001t0001g0089 a0001c0001t0001g0097 |
2 | NA18952.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.956+2187T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87780142 | |||||||
| chr7:87780209 | T | A | 16 | a0001c0001t0009g0002 a0001c0001t0009g0190 a0001c0001t0009g0191 others(13): Show |
16 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.956+2254T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87780209 | |||||||
| chr7:87780428 | C | T | 42 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(39): Show |
42 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(39): Show |
intron_variant | MODIFIER | c.956+2473C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87780428 | |||||||
| chr7:87780449 | GTTAT | G | 2 | a0001c0001t0056g0016 a0001c0001t0063g0015 |
2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.956+2497_956+2500d others(6): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr7 | 87780449 | ||||||
| chr7:87780775 | AAGATAAG others(17): Show |
A | 1 | a0001c0001t0077g0081 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.956+2823_956+2846d others(26): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr7 | 87780775 | ||||||
| chr7:87781019 | T | C | 1 | a0001c0001t0004g0084 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.956+3064T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87781019 | |||||||
| chr7:87781292 | G | A | 2 | a0001c0001t0001g0134 a0001c0001t0001g0136 |
2 | HG01192.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.956+3337G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87781292 | |||||||
| chr7:87781304 | T | TAGAAGTA others(313): Show |
16 | a0001c0001t0009g0002 a0001c0001t0009g0190 a0001c0001t0009g0191 others(13): Show |
16 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.956+3368_956+3369i others(322): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr7 | 87781304 | ||||||
| chr7:87781421 | C | A | 3 | a0001c0001t0057g0017 a0001c0001t0066g0019 a0001c0001t0067g0018 |
3 | HG02630.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.956+3466C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87781421 | |||||||
| chr7:87781579 | T | A | 2 | a0001c0001t0036g0159 a0001c0001t0073g0053 |
2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.956+3624T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87781579 | |||||||
| chr7:87781676 | G | A | 2 | a0001c0001t0011g0194 a0001c0001t0011g0195 |
2 | HG00280.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.956+3721G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87781676 | |||||||
| chr7:87782214 | C | T | 2 | a0001c0001t0055g0020 a0001c0001t0070g0014 |
2 | HG02572.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.956+4259C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87782214 | |||||||
| chr7:87782267 | C | G | 2 | a0001c0001t0003g0075 a0001c0001t0004g0067 |
2 | HG00741.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.956+4312C>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87782267 | |||||||
| chr7:87782534 | T | C | 1 | a0001c0001t0043g0106 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.956+4579T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87782534 | |||||||
| chr7:87783007 | T | A | 6 | a0001c0001t0039g0148 a0001c0001t0055g0020 a0001c0001t0057g0017 others(3): Show |
6 | HG02572.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.956+5052T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87783007 | |||||||
| chr7:87783053 | G | A | 1 | a0001c0001t0020g0035 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.956+5098G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87783053 | |||||||
| chr7:87783100 | C | G | 1 | a0001c0001t0039g0148 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.956+5145C>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87783100 | |||||||
| chr7:87783173 | T | G | 88 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(85): Show |
88 | HG00280.hp2 HG00423.hp1 HG01069.hp2 others(85): Show |
intron_variant | MODIFIER | c.956+5218T>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87783173 | |||||||
| chr7:87783197 | A | G | 12 | a0001c0001t0014g0152 a0001c0001t0014g0155 a0001c0001t0014g0158 others(9): Show |
12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.956+5242A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87783197 | |||||||
| chr7:87783238 | A | G | 1 | a0001c0001t0016g0072 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.956+5283A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87783238 | |||||||
| chr7:87783242 | T | C | 1 | a0001c0001t0073g0053 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.956+5287T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87783242 | |||||||
| chr7:87783337 | T | C | 1 | a0001c0001t0001g0042 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.956+5382T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87783337 | |||||||
| chr7:87783395 | C | T | 16 | a0001c0001t0009g0002 a0001c0001t0009g0190 a0001c0001t0009g0191 others(13): Show |
16 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.956+5440C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87783395 | |||||||
| chr7:87783500 | C | T | 1 | a0001c0001t0004g0139 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.956+5545C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87783500 | |||||||
| chr7:87783595 | C | T | 1 | a0001c0001t0005g0068 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.956+5640C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87783595 | |||||||
| chr7:87783647 | A | G | 1 | a0001c0001t0055g0020 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.956+5692A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87783647 | |||||||
| chr7:87783764 | G | A | 78 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(75): Show |
78 | HG00280.hp2 HG00423.hp1 HG01069.hp2 others(75): Show |
intron_variant | MODIFIER | c.956+5809G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87783764 | |||||||
| chr7:87783956 | C | A | 78 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(75): Show |
78 | HG00280.hp2 HG00423.hp1 HG01069.hp2 others(75): Show |
intron_variant | MODIFIER | c.956+6001C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87783956 | |||||||
| chr7:87784593 | T | C | 14 | a0001c0001t0017g0065 a0001c0001t0017g0085 a0001c0001t0017g0112 others(11): Show |
14 | HG00438.hp2 HG00621.hp1 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.956+6638T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87784593 | |||||||
| chr7:87784795 | G | A | 1 | a0001c0001t0046g0161 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.956+6840G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87784795 | |||||||
| chr7:87784811 | T | C | 1 | a0001c0001t0004g0139 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.956+6856T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87784811 | |||||||
| chr7:87785071 | G | A | 1 | a0001c0001t0071g0078 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.956+7116G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87785071 | |||||||
| chr7:87785130 | G | A | 41 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(38): Show |
41 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(38): Show |
intron_variant | MODIFIER | c.956+7175G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87785130 | |||||||
| chr7:87785309 | G | C | 1 | a0001c0001t0075g0007 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.956+7354G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87785309 | |||||||
| chr7:87785709 | G | T | 1 | a0001c0001t0010g0012 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.956+7754G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87785709 | |||||||
| chr7:87785777 | C | T | 6 | a0001c0001t0002g0163 a0001c0001t0002g0164 a0001c0001t0002g0166 others(3): Show |
6 | HG02559.hp2 HG02965.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.956+7822C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87785777 | |||||||
| chr7:87785887 | T | C | 1 | a0001c0001t0037g0006 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.956+7932T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87785887 | |||||||
| chr7:87785922 | G | A | 2 | a0001c0001t0004g0047 a0001c0001t0064g0046 |
2 | HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.956+7967G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87785922 | |||||||
| chr7:87786407 | A | T | 16 | a0001c0001t0009g0002 a0001c0001t0009g0190 a0001c0001t0009g0191 others(13): Show |
16 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.956+8452A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87786407 | |||||||
| chr7:87786454 | A | G | 7 | a0001c0001t0039g0148 a0001c0001t0049g0038 a0001c0001t0055g0020 others(4): Show |
7 | HG02572.hp2 HG02630.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.956+8499A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87786454 | |||||||
| chr7:87786668 | A | T | 4 | a0001c0001t0044g0169 a0001c0001t0046g0161 a0001c0001t0047g0172 others(1): Show |
4 | HG01123.hp1 HG01192.hp1 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.956+8713A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87786668 | |||||||
| chr7:87786835 | G | A | 5 | a0001c0001t0055g0020 a0001c0001t0057g0017 a0001c0001t0066g0019 others(2): Show |
5 | HG02572.hp2 HG02630.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.956+8880G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87786835 | |||||||
| chr7:87786985 | T | C | 1 | a0001c0001t0001g0064 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.956+9030T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87786985 | |||||||
| chr7:87787010 | G | A | 12 | a0001c0001t0014g0152 a0001c0001t0014g0155 a0001c0001t0014g0158 others(9): Show |
12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.956+9055G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87787010 | |||||||
| chr7:87787022 | T | C | 1 | a0001c0001t0052g0196 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.956+9067T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87787022 | |||||||
| chr7:87787066 | G | C | 3 | a0001c0001t0057g0017 a0001c0001t0066g0019 a0001c0001t0067g0018 |
3 | HG02630.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.956+9111G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87787066 | |||||||
| chr7:87787524 | C | T | 153 | a0001c0001t0001g0064 a0001c0001t0001g0080 a0001c0001t0001g0119 others(150): Show |
153 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.956+9569C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87787524 | |||||||
| chr7:87787560 | T | C | 1 | a0001c0001t0007g0118 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.956+9605T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87787560 | |||||||
| chr7:87787891 | T | C | 2 | a0001c0001t0036g0159 a0001c0001t0073g0053 |
2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.956+9936T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87787891 | |||||||
| chr7:87788058 | A | G | 1 | a0001c0001t0052g0196 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.956+10103A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87788058 | |||||||
| chr7:87788060 | T | C | 2 | a0001c0001t0010g0010 a0001c0001t0010g0011 |
2 | HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.956+10105T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87788060 | |||||||
| chr7:87788076 | A | G | 1 | a0001c0001t0072g0009 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.956+10121A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87788076 | |||||||
| chr7:87788152 | G | A | 1 | a0001c0001t0040g0013 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.956+10197G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87788152 | |||||||
| chr7:87788378 | A | C | 2 | a0001c0001t0055g0020 a0001c0001t0070g0014 |
2 | HG02572.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.956+10423A>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87788378 | |||||||
| chr7:87788627 | C | T | 2 | a0001c0001t0066g0019 a0001c0001t0067g0018 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.956+10672C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87788627 | |||||||
| chr7:87788647 | A | T | 21 | a0001c0001t0016g0023 a0001c0001t0016g0072 a0001c0001t0016g0074 others(18): Show |
21 | HG00438.hp2 HG00621.hp1 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.956+10692A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87788647 | |||||||
| chr7:87788663 | A | G | 2 | a0001c0001t0001g0080 a0001c0001t0007g0122 |
2 | HG00423.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.956+10708A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87788663 | |||||||
| chr7:87788703 | C | CT | 15 | a0001c0001t0009g0002 a0001c0001t0009g0190 a0001c0001t0009g0191 others(12): Show |
15 | HG00280.hp2 HG01071.hp2 HG01074.hp2 others(12): Show |
intron_variant | MODIFIER | c.956+10765dupT | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr7 | 87788703 | ||||||
| chr7:87788703 | CT | C | 35 | a0001c0001t0001g0093 a0001c0001t0001g0095 a0001c0001t0001g0119 others(32): Show |
35 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(32): Show |
intron_variant | MODIFIER | c.956+10765delT | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr7 | 87788703 | ||||||
| chr7:87788703 | CTT | C | 24 | a0001c0001t0002g0162 a0001c0001t0002g0163 a0001c0001t0002g0164 others(21): Show |
24 | HG01081.hp2 HG02055.hp2 HG02258.hp2 others(21): Show |
intron_variant | MODIFIER | c.956+10764_956+1076 others(6): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr7 | 87788703 | ||||||
| chr7:87788703 | CTTT | C | 24 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0200 others(21): Show |
24 | HG01123.hp1 HG01192.hp1 HG01358.hp1 others(21): Show |
intron_variant | MODIFIER | c.956+10763_956+1076 others(7): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr7 | 87788703 | ||||||
| chr7:87788832 | A | C | 5 | a0001c0001t0055g0020 a0001c0001t0057g0017 a0001c0001t0066g0019 others(2): Show |
5 | HG02572.hp2 HG02630.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.956+10877A>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87788832 | |||||||
| chr7:87789527 | C | T | 4 | a0001c0001t0010g0010 a0001c0001t0010g0011 a0001c0001t0010g0012 others(1): Show |
4 | HG02280.hp2 HG02723.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.956+11572C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87789527 | |||||||
| chr7:87789546 | T | C | 153 | a0001c0001t0001g0064 a0001c0001t0001g0080 a0001c0001t0001g0119 others(150): Show |
153 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.956+11591T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87789546 | |||||||
| chr7:87789572 | T | A | 8 | a0001c0001t0010g0008 a0001c0001t0010g0010 a0001c0001t0010g0011 others(5): Show |
8 | HG02055.hp1 HG02280.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.956+11617T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87789572 | |||||||
| chr7:87790032 | A | G | 40 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(37): Show |
40 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(37): Show |
intron_variant | MODIFIER | c.956+12077A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87790032 | |||||||
| chr7:87790541 | G | T | 2 | a0001c0001t0036g0159 a0001c0001t0073g0053 |
2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.956+12586G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87790541 | |||||||
| chr7:87790652 | AAG | A | 12 | a0001c0001t0014g0152 a0001c0001t0014g0155 a0001c0001t0014g0158 others(9): Show |
12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.956+12700_956+1270 others(6): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr7 | 87790652 | ||||||
| chr7:87790775 | T | C | 2 | a0001c0001t0017g0112 a0001c0001t0034g0079 |
2 | HG00741.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.956+12820T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87790775 | |||||||
| chr7:87791387 | A | G | 12 | a0001c0001t0014g0152 a0001c0001t0014g0155 a0001c0001t0014g0158 others(9): Show |
12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.956+13432A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87791387 | |||||||
| chr7:87791664 | A | G | 16 | a0001c0001t0009g0002 a0001c0001t0009g0190 a0001c0001t0009g0191 others(13): Show |
16 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.956+13709A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87791664 | |||||||
| chr7:87791668 | C | A | 2 | a0001c0001t0066g0019 a0001c0001t0067g0018 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.956+13713C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87791668 | |||||||
| chr7:87791681 | C | T | 1 | a0001c0001t0003g0135 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.956+13726C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87791681 | |||||||
| chr7:87792350 | A | G | 1 | a0001c0001t0057g0017 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.956+14395A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87792350 | |||||||
| chr7:87792635 | G | T | 1 | a0001c0001t0053g0063 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.956+14680G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87792635 | |||||||
| chr7:87793003 | A | G | 2 | a0001c0001t0015g0150 a0001c0001t0015g0151 |
2 | NA18970.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.957-14370A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87793003 | |||||||
| chr7:87793429 | G | A | 2 | a0001c0001t0010g0010 a0001c0001t0010g0011 |
2 | HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.957-13944G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87793429 | |||||||
| chr7:87793509 | G | A | 16 | a0001c0001t0009g0002 a0001c0001t0009g0190 a0001c0001t0009g0191 others(13): Show |
16 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.957-13864G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87793509 | |||||||
| chr7:87793820 | G | A | 2 | a0001c0001t0017g0065 a0001c0001t0017g0085 |
2 | HG00738.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.957-13553G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87793820 | |||||||
| chr7:87794309 | C | T | 1 | a0001c0001t0006g0086 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.957-13064C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87794309 | |||||||
| chr7:87794625 | CA | C | 82 | a0001c0001t0001g0095 a0001c0001t0002g0030 a0001c0001t0002g0137 others(79): Show |
82 | HG00280.hp2 HG00423.hp1 HG01069.hp2 others(79): Show |
intron_variant | MODIFIER | c.957-12734delA | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr7 | 87794625 | ||||||
| chr7:87794633 | A | T | 1 | a0001c0001t0001g0054 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.957-12740A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87794633 | |||||||
| chr7:87794652 | A | G | 1 | a0001c0001t0079g0024 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.957-12721A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87794652 | |||||||
| chr7:87795014 | G | T | 1 | a0001c0001t0003g0135 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.957-12359G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87795014 | |||||||
| chr7:87795231 | T | A | 1 | a0001c0001t0001g0060 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.957-12142T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87795231 | |||||||
| chr7:87795413 | C | A | 1 | a0001c0001t0072g0009 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.957-11960C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87795413 | |||||||
| chr7:87795706 | C | T | 2 | a0001c0001t0036g0159 a0001c0001t0073g0053 |
2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.957-11667C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87795706 | |||||||
| chr7:87795723 | C | CA | 45 | a0001c0001t0001g0101 a0001c0001t0004g0047 a0001c0001t0007g0130 others(42): Show |
45 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(42): Show |
intron_variant | MODIFIER | c.957-11633dupA | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr7 | 87795723 | ||||||
| chr7:87795723 | C | CAAA | 35 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0163 others(32): Show |
35 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(32): Show |
intron_variant | MODIFIER | c.957-11635_957-1163 others(7): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr7 | 87795723 | ||||||
| chr7:87795723 | CA | C | 5 | a0001c0001t0006g0117 a0001c0001t0008g0123 a0001c0001t0040g0013 others(2): Show |
5 | HG02040.hp2 HG02055.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.957-11633delA | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr7 | 87795723 | ||||||
| chr7:87795757 | C | T | 1 | a0001c0001t0011g0195 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.957-11616C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87795757 | |||||||
| chr7:87795847 | G | T | 1 | a0001c0001t0072g0009 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.957-11526G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87795847 | |||||||
| chr7:87796051 | A | G | 2 | a0001c0001t0036g0159 a0001c0001t0073g0053 |
2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.957-11322A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87796051 | |||||||
| chr7:87796183 | G | A | 2 | a0001c0001t0056g0016 a0001c0001t0063g0015 |
2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.957-11190G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87796183 | |||||||
| chr7:87796234 | T | C | 1 | a0001c0001t0039g0148 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.957-11139T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87796234 | |||||||
| chr7:87796347 | G | A | 2 | a0001c0001t0056g0016 a0001c0001t0063g0015 |
2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.957-11026G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87796347 | |||||||
| chr7:87796650 | T | C | 7 | a0001c0001t0010g0008 a0001c0001t0010g0010 a0001c0001t0010g0011 others(4): Show |
7 | HG02055.hp1 HG02280.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.957-10723T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87796650 | |||||||
| chr7:87797538 | C | T | 61 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(58): Show |
61 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(58): Show |
intron_variant | MODIFIER | c.957-9835C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87797538 | |||||||
| chr7:87797730 | T | C | 38 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(35): Show |
38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.957-9643T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87797730 | |||||||
| chr7:87798070 | T | C | 1 | a0001c0001t0015g0154 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.957-9303T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87798070 | |||||||
| chr7:87798376 | A | G | 75 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(72): Show |
75 | HG00280.hp2 HG00423.hp1 HG01069.hp2 others(72): Show |
intron_variant | MODIFIER | c.957-8997A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87798376 | |||||||
| chr7:87798844 | T | C | 2 | a0001c0001t0004g0022 a0001c0001t0024g0004 |
2 | HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.957-8529T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87798844 | |||||||
| chr7:87798963 | T | C | 6 | a0001c0001t0010g0010 a0001c0001t0010g0011 a0001c0001t0010g0012 others(3): Show |
6 | HG02055.hp1 HG02280.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.957-8410T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87798963 | |||||||
| chr7:87799111 | T | A | 1 | a0001c0001t0052g0196 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.957-8262T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87799111 | |||||||
| chr7:87799145 | T | C | 1 | a0001c0001t0003g0075 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.957-8228T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87799145 | |||||||
| chr7:87799348 | C | T | 1 | a0001c0001t0071g0078 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.957-8025C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87799348 | |||||||
| chr7:87799398 | C | G | 2 | a0001c0001t0004g0109 a0001c0001t0004g0110 |
2 | HG00738.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.957-7975C>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87799398 | |||||||
| chr7:87799616 | C | T | 1 | a0001c0001t0010g0010 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.957-7757C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87799616 | |||||||
| chr7:87799817 | C | T | 1 | a0001c0001t0072g0009 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.957-7556C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87799817 | |||||||
| chr7:87799845 | C | T | 1 | a0001c0001t0036g0159 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.957-7528C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87799845 | |||||||
| chr7:87799872 | C | T | 2 | a0001c0001t0055g0020 a0001c0001t0070g0014 |
2 | HG02572.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.957-7501C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87799872 | |||||||
| chr7:87799885 | CA | C | 65 | a0001c0001t0001g0096 a0001c0001t0001g0119 a0001c0001t0002g0030 others(62): Show |
65 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(62): Show |
intron_variant | MODIFIER | c.957-7467delA | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr7 | 87799885 | ||||||
| chr7:87800121 | G | C | 1 | a0001c0001t0023g0039 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.957-7252G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87800121 | |||||||
| chr7:87800653 | C | CT | 15 | a0001c0001t0002g0200 a0001c0001t0004g0022 a0001c0001t0014g0152 others(12): Show |
15 | HG00423.hp1 HG02976.hp1 HG03139.hp1 others(12): Show |
intron_variant | MODIFIER | c.957-6704dupT | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr7 | 87800653 | ||||||
| chr7:87800653 | C | CTT | 16 | a0001c0001t0009g0002 a0001c0001t0009g0190 a0001c0001t0009g0191 others(13): Show |
16 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.957-6705_957-6704d others(4): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr7 | 87800653 | ||||||
| chr7:87800735 | C | T | 1 | a0001c0001t0018g0171 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.957-6638C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87800735 | |||||||
| chr7:87801254 | C | T | 1 | a0001c0001t0005g0052 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.957-6119C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87801254 | |||||||
| chr7:87801354 | G | A | 152 | a0001c0001t0001g0064 a0001c0001t0001g0080 a0001c0001t0001g0119 others(149): Show |
152 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.957-6019G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87801354 | |||||||
| chr7:87801401 | A | G | 1 | a0001c0001t0065g0003 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.957-5972A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87801401 | |||||||
| chr7:87801656 | C | A | 2 | a0001c0001t0004g0047 a0001c0001t0064g0046 |
2 | HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.957-5717C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87801656 | |||||||
| chr7:87801670 | G | T | 1 | a0001c0001t0049g0038 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.957-5703G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87801670 | |||||||
| chr7:87801838 | A | C | 1 | a0001c0001t0055g0020 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.957-5535A>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87801838 | |||||||
| chr7:87802247 | G | T | 6 | a0001c0001t0039g0148 a0001c0001t0055g0020 a0001c0001t0057g0017 others(3): Show |
6 | HG02572.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.957-5126G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87802247 | |||||||
| chr7:87802321 | A | G | 2 | a0001c0001t0025g0091 a0001c0001t0026g0120 |
2 | HG01099.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.957-5052A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87802321 | |||||||
| chr7:87802373 | C | T | 15 | a0001c0001t0009g0002 a0001c0001t0009g0190 a0001c0001t0009g0191 others(12): Show |
15 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.957-5000C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87802373 | |||||||
| chr7:87802493 | T | C | 2 | a0001c0001t0001g0042 a0001c0001t0001g0098 |
2 | HG01167.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.957-4880T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87802493 | |||||||
| chr7:87802543 | A | G | 2 | a0001c0001t0013g0173 a0001c0001t0038g0183 |
2 | NA18977.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.957-4830A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87802543 | |||||||
| chr7:87802762 | T | C | 1 | a0001c0001t0008g0121 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.957-4611T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87802762 | |||||||
| chr7:87802965 | A | G | 1 | a0001c0001t0001g0064 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.957-4408A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87802965 | |||||||
| chr7:87803324 | G | A | 1 | a0001c0001t0005g0113 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.957-4049G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87803324 | |||||||
| chr7:87803383 | C | A | 4 | a0001c0001t0010g0010 a0001c0001t0010g0011 a0001c0001t0010g0012 others(1): Show |
4 | HG02280.hp2 HG02723.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.957-3990C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87803383 | |||||||
| chr7:87803444 | C | T | 3 | a0001c0001t0056g0016 a0001c0001t0063g0015 a0001c0001t0070g0014 |
3 | HG02572.hp2 HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.957-3929C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87803444 | |||||||
| chr7:87803459 | A | C | 12 | a0001c0001t0014g0152 a0001c0001t0014g0155 a0001c0001t0014g0158 others(9): Show |
12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.957-3914A>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87803459 | |||||||
| chr7:87803512 | A | G | 12 | a0001c0001t0014g0152 a0001c0001t0014g0155 a0001c0001t0014g0158 others(9): Show |
12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.957-3861A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87803512 | |||||||
| chr7:87803623 | C | G | 2 | a0001c0001t0010g0010 a0001c0001t0010g0011 |
2 | HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.957-3750C>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87803623 | |||||||
| chr7:87803692 | A | G | 38 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(35): Show |
38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.957-3681A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87803692 | |||||||
| chr7:87803833 | C | A | 1 | a0001c0001t0073g0053 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.957-3540C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87803833 | |||||||
| chr7:87803849 | G | A | 1 | a0001c0001t0016g0023 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.957-3524G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87803849 | |||||||
| chr7:87803870 | A | G | 3 | a0001c0001t0004g0055 a0001c0001t0004g0058 a0001c0001t0005g0068 |
3 | NA18977.hp1 NA19010.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.957-3503A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87803870 | |||||||
| chr7:87804143 | G | C | 38 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(35): Show |
38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.957-3230G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87804143 | |||||||
| chr7:87804569 | A | G | 6 | a0001c0001t0010g0010 a0001c0001t0010g0011 a0001c0001t0010g0012 others(3): Show |
6 | HG02055.hp1 HG02280.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.957-2804A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87804569 | |||||||
| chr7:87805255 | CAACTT | C | 6 | a0001c0001t0039g0148 a0001c0001t0055g0020 a0001c0001t0057g0017 others(3): Show |
6 | HG02572.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.957-2110_957-2106d others(7): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr7 | 87805255 | ||||||
| chr7:87805284 | A | G | 2 | a0001c0001t0009g0190 a0001c0001t0028g0192 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.957-2089A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87805284 | |||||||
| chr7:87805298 | T | C | 6 | a0001c0001t0039g0148 a0001c0001t0055g0020 a0001c0001t0057g0017 others(3): Show |
6 | HG02572.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.957-2075T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87805298 | |||||||
| chr7:87805468 | G | A | 16 | a0001c0001t0009g0002 a0001c0001t0009g0190 a0001c0001t0009g0191 others(13): Show |
16 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.957-1905G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87805468 | |||||||
| chr7:87805944 | T | C | 2 | a0001c0001t0039g0148 a0001c0001t0049g0038 |
2 | HG02723.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.957-1429T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87805944 | |||||||
| chr7:87806293 | G | T | 1 | a0001c0001t0049g0038 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.957-1080G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87806293 | |||||||
| chr7:87806615 | T | C | 2 | a0001c0001t0036g0159 a0001c0001t0073g0053 |
2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.957-758T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87806615 | |||||||
| chr7:87807837 | A | G | 1 | a0001c0001t0049g0038 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1103+318A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | chr7 | 87807837 | |||||||
| chr7:87807867 | A | G | 3 | a0001c0001t0019g0043 a0001c0001t0031g0044 a0001c0001t0034g0199 |
3 | HG00438.hp2 HG01978.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.1103+348A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | chr7 | 87807867 | |||||||
| chr7:87807895 | A | T | 1 | a0001c0001t0017g0065 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1103+376A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | chr7 | 87807895 | |||||||
| chr7:87807896 | T | C | 14 | a0001c0001t0002g0162 a0001c0001t0002g0163 a0001c0001t0002g0164 others(11): Show |
14 | HG01081.hp2 HG02258.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.1103+377T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | chr7 | 87807896 | |||||||
| chr7:87807940 | A | T | 38 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(35): Show |
38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.1103+421A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | chr7 | 87807940 | |||||||
| chr7:87807943 | T | G | 2 | a0001c0001t0066g0019 a0001c0001t0067g0018 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1103+424T>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | chr7 | 87807943 | |||||||
| chr7:87808454 | G | C | 16 | a0001c0001t0009g0002 a0001c0001t0009g0190 a0001c0001t0009g0191 others(13): Show |
16 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.1103+935G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | chr7 | 87808454 | |||||||
| chr7:87808460 | C | T | 2 | a0001c0001t0036g0159 a0001c0001t0073g0053 |
2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1103+941C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | chr7 | 87808460 | |||||||
| chr7:87808766 | C | T | 61 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(58): Show |
61 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(58): Show |
intron_variant | MODIFIER | c.1103+1247C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | chr7 | 87808766 | |||||||
| chr7:87809032 | C | T | 1 | a0001c0001t0057g0017 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1103+1513C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | chr7 | 87809032 | |||||||
| chr7:87809430 | T | TA | 38 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(35): Show |
38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.1103+1912dupA | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr7 | 87809430 | ||||||
| chr7:87809832 | C | T | 1 | a0001c0001t0002g0200 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1103+2313C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | chr7 | 87809832 | |||||||
| chr7:87809943 | G | A | 1 | a0001c0001t0070g0014 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1103+2424G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | chr7 | 87809943 | |||||||
| chr7:87810029 | CCCTATAA others(34): Show |
C | 1 | a0001c0001t0065g0003 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1103+2514_1103+255 others(45): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr7 | 87810029 | ||||||
| chr7:87810060 | A | G | 1 | a0001c0001t0001g0119 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1103+2541A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | chr7 | 87810060 | |||||||
| chr7:87810368 | G | A | 2 | a0001c0001t0004g0047 a0001c0001t0064g0046 |
2 | HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1103+2849G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | chr7 | 87810368 | |||||||
| chr7:87810523 | C | A | 38 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(35): Show |
38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.1103+3004C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | chr7 | 87810523 | |||||||
| chr7:87810711 | G | A | 1 | a0001c0001t0070g0014 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1103+3192G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | chr7 | 87810711 | |||||||
| chr7:87810755 | G | A | 1 | a0001c0001t0052g0196 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1103+3236G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | chr7 | 87810755 | |||||||
| chr7:87810757 | C | A | 1 | a0001c0001t0036g0159 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1103+3238C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | chr7 | 87810757 | |||||||
| chr7:87811068 | T | C | 2 | a0001c0001t0055g0020 a0001c0001t0070g0014 |
2 | HG02572.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1103+3549T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | chr7 | 87811068 | |||||||
| chr7:87811261 | T | A | 4 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0093 others(1): Show |
4 | HG01496.hp2 HG02280.hp1 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.1103+3742T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | chr7 | 87811261 | |||||||
| chr7:87811339 | A | AT | 89 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(86): Show |
89 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.1103+3835dupT | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr7 | 87811339 | ||||||
| chr7:87811539 | T | C | 2 | a0001c0001t0056g0016 a0001c0001t0063g0015 |
2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1103+4020T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | chr7 | 87811539 | |||||||
| chr7:87811548 | G | A | 3 | a0001c0001t0014g0155 a0001c0001t0014g0158 a0001c0001t0045g0160 |
3 | NA18988.hp2 NA18990.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.1103+4029G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | chr7 | 87811548 | |||||||
| chr7:87811640 | G | A | 16 | a0001c0001t0009g0002 a0001c0001t0009g0190 a0001c0001t0009g0191 others(13): Show |
16 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.1103+4121G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | chr7 | 87811640 | |||||||
| chr7:87811706 | T | A | 3 | a0001c0001t0004g0022 a0001c0001t0024g0004 a0001c0001t0037g0006 |
3 | HG00639.hp2 HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1103+4187T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | chr7 | 87811706 | |||||||
| chr7:87811775 | T | G | 12 | a0001c0001t0014g0152 a0001c0001t0014g0155 a0001c0001t0014g0158 others(9): Show |
12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.1103+4256T>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | chr7 | 87811775 | |||||||
| chr7:87812446 | T | C | 1 | a0001c0001t0037g0006 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1104-3695T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | chr7 | 87812446 | |||||||
| chr7:87812619 | G | C | 1 | a0001c0001t0006g0186 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1104-3522G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | chr7 | 87812619 | |||||||
| chr7:87812721 | T | G | 2 | a0001c0001t0056g0016 a0001c0001t0063g0015 |
2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1104-3420T>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | chr7 | 87812721 | |||||||
| chr7:87812923 | G | A | 4 | a0001c0001t0005g0127 a0001c0001t0005g0128 a0001c0001t0006g0088 others(1): Show |
4 | HG00280.hp1 HG00323.hp1 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.1104-3218G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | chr7 | 87812923 | |||||||
| chr7:87813062 | G | A | 2 | a0001c0001t0056g0016 a0001c0001t0063g0015 |
2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1104-3079G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | chr7 | 87813062 | |||||||
| chr7:87813660 | T | C | 12 | a0001c0001t0014g0152 a0001c0001t0014g0155 a0001c0001t0014g0158 others(9): Show |
12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.1104-2481T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | chr7 | 87813660 | |||||||
| chr7:87813849 | C | T | 2 | a0001c0001t0036g0159 a0001c0001t0073g0053 |
2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1104-2292C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | chr7 | 87813849 | |||||||
| chr7:87813850 | A | G | 2 | a0001c0001t0036g0159 a0001c0001t0073g0053 |
2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1104-2291A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | chr7 | 87813850 | |||||||
| chr7:87813949 | C | A | 6 | a0001c0001t0039g0148 a0001c0001t0055g0020 a0001c0001t0057g0017 others(3): Show |
6 | HG02572.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1104-2192C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | chr7 | 87813949 | |||||||
| chr7:87813961 | A | G | 3 | a0001c0001t0062g0145 a0001c0001t0068g0143 a0001c0001t0069g0144 |
3 | HG01069.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1104-2180A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | chr7 | 87813961 | |||||||
| chr7:87813975 | C | T | 12 | a0001c0001t0014g0152 a0001c0001t0014g0155 a0001c0001t0014g0158 others(9): Show |
12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.1104-2166C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | chr7 | 87813975 | |||||||
| chr7:87813980 | C | CA | 14 | a0001c0001t0003g0082 a0001c0001t0004g0055 a0001c0001t0004g0083 others(11): Show |
14 | HG00438.hp1 HG00558.hp1 HG01952.hp1 others(11): Show |
intron_variant | MODIFIER | c.1104-2147dupA | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr7 | 87813980 | ||||||
| chr7:87813995 | G | A | 1 | a0001c0001t0005g0113 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1104-2146G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | chr7 | 87813995 | |||||||
| chr7:87813996 | A | G | 1 | a0001c0001t0005g0113 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1104-2145A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | chr7 | 87813996 | |||||||
| chr7:87813997 | T | A | 1 | a0001c0001t0005g0113 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1104-2144T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | chr7 | 87813997 | |||||||
| chr7:87814101 | C | CT | 20 | a0001c0001t0001g0070 a0001c0001t0014g0152 a0001c0001t0014g0155 others(17): Show |
20 | HG00423.hp1 HG01978.hp1 HG02129.hp1 others(17): Show |
intron_variant | MODIFIER | c.1104-2024dupT | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr7 | 87814101 | ||||||
| chr7:87814257 | C | T | 1 | a0001c0001t0010g0008 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1104-1884C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | chr7 | 87814257 | |||||||
| chr7:87814432 | A | T | 1 | a0001c0001t0001g0087 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1104-1709A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | chr7 | 87814432 | |||||||
| chr7:87814611 | A | G | 1 | a0001c0001t0057g0017 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1104-1530A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | chr7 | 87814611 | |||||||
| chr7:87814626 | G | T | 1 | a0001c0001t0006g0088 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1104-1515G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | chr7 | 87814626 | |||||||
| chr7:87814657 | G | A | 61 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(58): Show |
61 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(58): Show |
intron_variant | MODIFIER | c.1104-1484G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | chr7 | 87814657 | |||||||
| chr7:87814661 | G | T | 2 | a0001c0001t0012g0174 a0001c0001t0012g0176 |
2 | HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1104-1480G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | chr7 | 87814661 | |||||||
| chr7:87814736 | G | A | 2 | a0001c0001t0055g0020 a0001c0001t0070g0014 |
2 | HG02572.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1104-1405G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | chr7 | 87814736 | |||||||
| chr7:87814825 | C | T | 1 | a0001c0001t0031g0044 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1104-1316C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | chr7 | 87814825 | |||||||
| chr7:87814850 | T | G | 1 | a0001c0001t0073g0053 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1104-1291T>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | chr7 | 87814850 | |||||||
| chr7:87815090 | C | G | 39 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(36): Show |
39 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(36): Show |
intron_variant | MODIFIER | c.1104-1051C>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | chr7 | 87815090 | |||||||
| chr7:87815323 | A | G | 16 | a0001c0001t0009g0002 a0001c0001t0009g0190 a0001c0001t0009g0191 others(13): Show |
16 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.1104-818A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | chr7 | 87815323 | |||||||
| chr7:87815556 | G | A | 12 | a0001c0001t0014g0152 a0001c0001t0014g0155 a0001c0001t0014g0158 others(9): Show |
12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.1104-585G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | chr7 | 87815556 | |||||||
| chr7:87815570 | C | G | 2 | a0001c0001t0039g0148 a0001c0001t0049g0038 |
2 | HG02723.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1104-571C>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | chr7 | 87815570 | |||||||
| chr7:87815633 | C | A | 3 | a0001c0001t0057g0017 a0001c0001t0066g0019 a0001c0001t0067g0018 |
3 | HG02630.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1104-508C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | chr7 | 87815633 | |||||||
| chr7:87815915 | C | CT | 8 | a0001c0001t0005g0113 a0001c0001t0039g0148 a0001c0001t0049g0038 others(5): Show |
8 | HG02572.hp2 HG02630.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1104-217dupT | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr7 | 87815915 | ||||||
| chr7:87816312 | A | G | 7 | a0001c0001t0039g0148 a0001c0001t0049g0038 a0001c0001t0055g0020 others(4): Show |
7 | HG02572.hp2 HG02630.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1225+50A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87816312 | |||||||
| chr7:87816376 | T | G | 1 | a0001c0001t0010g0008 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1225+114T>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87816376 | |||||||
| chr7:87816433 | G | T | 130 | a0001c0001t0001g0042 a0001c0001t0001g0064 a0001c0001t0001g0070 others(127): Show |
130 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.1225+171G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87816433 | |||||||
| chr7:87816434 | G | A | 12 | a0001c0001t0014g0152 a0001c0001t0014g0155 a0001c0001t0014g0158 others(9): Show |
12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.1225+172G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87816434 | |||||||
| chr7:87816438 | G | T | 38 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(35): Show |
38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.1225+176G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87816438 | |||||||
| chr7:87816683 | G | A | 1 | a0001c0001t0001g0064 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1225+421G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87816683 | |||||||
| chr7:87816735 | A | T | 1 | a0001c0001t0052g0196 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1225+473A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87816735 | |||||||
| chr7:87816757 | T | C | 1 | a0001c0001t0052g0196 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1225+495T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87816757 | |||||||
| chr7:87816959 | T | C | 1 | a0001c0001t0049g0038 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1225+697T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87816959 | |||||||
| chr7:87817076 | C | A | 1 | a0001c0001t0001g0060 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1225+814C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87817076 | |||||||
| chr7:87817514 | T | C | 16 | a0001c0001t0009g0002 a0001c0001t0009g0190 a0001c0001t0009g0191 others(13): Show |
16 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.1225+1252T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87817514 | |||||||
| chr7:87817614 | C | T | 3 | a0001c0001t0019g0026 a0001c0001t0019g0108 a0001c0001t0053g0063 |
3 | HG01981.hp2 HG03239.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1225+1352C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87817614 | |||||||
| chr7:87817724 | C | A | 2 | a0001c0001t0056g0016 a0001c0001t0063g0015 |
2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1225+1462C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87817724 | |||||||
| chr7:87817825 | G | C | 2 | a0001c0001t0055g0020 a0001c0001t0070g0014 |
2 | HG02572.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1225+1563G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87817825 | |||||||
| chr7:87818202 | T | A | 1 | a0001c0001t0001g0080 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1225+1940T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87818202 | |||||||
| chr7:87818756 | T | C | 1 | a0001c0001t0005g0062 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1225+2494T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87818756 | |||||||
| chr7:87818809 | T | G | 3 | a0001c0001t0004g0022 a0001c0001t0024g0004 a0001c0001t0037g0006 |
3 | HG00639.hp2 HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1225+2547T>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87818809 | |||||||
| chr7:87818998 | G | A | 1 | a0001c0001t0009g0193 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1225+2736G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87818998 | |||||||
| chr7:87819038 | C | T | 1 | a0001c0001t0003g0135 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1225+2776C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87819038 | |||||||
| chr7:87819145 | C | T | 1 | a0001c0001t0077g0081 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1225+2883C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87819145 | |||||||
| chr7:87819529 | A | G | 2 | a0001c0001t0055g0020 a0001c0001t0070g0014 |
2 | HG02572.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1225+3267A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87819529 | |||||||
| chr7:87819724 | C | T | 1 | a0001c0001t0007g0059 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1225+3462C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87819724 | |||||||
| chr7:87819961 | C | T | 3 | a0001c0001t0014g0155 a0001c0001t0014g0158 a0001c0001t0045g0160 |
3 | NA18988.hp2 NA18990.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.1225+3699C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87819961 | |||||||
| chr7:87820134 | C | T | 7 | a0001c0001t0010g0008 a0001c0001t0010g0010 a0001c0001t0010g0011 others(4): Show |
7 | HG02055.hp1 HG02280.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1225+3872C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87820134 | |||||||
| chr7:87820197 | A | C | 39 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(36): Show |
39 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(36): Show |
intron_variant | MODIFIER | c.1225+3935A>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87820197 | |||||||
| chr7:87820215 | G | A | 1 | a0001c0001t0001g0095 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1225+3953G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87820215 | |||||||
| chr7:87820219 | T | C | 1 | a0001c0001t0001g0095 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1225+3957T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87820219 | |||||||
| chr7:87820266 | A | G | 85 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(82): Show |
85 | HG00280.hp2 HG00423.hp1 HG01069.hp2 others(82): Show |
intron_variant | MODIFIER | c.1225+4004A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87820266 | |||||||
| chr7:87820491 | C | A | 1 | a0001c0001t0004g0058 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1225+4229C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87820491 | |||||||
| chr7:87820515 | A | G | 4 | a0001c0001t0019g0026 a0001c0001t0057g0017 a0001c0001t0066g0019 others(1): Show |
4 | HG02630.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1225+4253A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87820515 | |||||||
| chr7:87820521 | C | T | 1 | a0001c0001t0003g0066 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1225+4259C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87820521 | |||||||
| chr7:87820536 | T | C | 21 | a0001c0001t0016g0023 a0001c0001t0016g0072 a0001c0001t0016g0074 others(18): Show |
21 | HG00438.hp2 HG00621.hp1 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.1225+4274T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87820536 | |||||||
| chr7:87820774 | C | A | 1 | a0001c0001t0057g0017 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1225+4512C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87820774 | |||||||
| chr7:87820838 | G | A | 61 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(58): Show |
61 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(58): Show |
intron_variant | MODIFIER | c.1225+4576G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87820838 | |||||||
| chr7:87820962 | C | T | 1 | a0001c0001t0022g0181 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1225+4700C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87820962 | |||||||
| chr7:87821115 | T | A | 3 | a0001c0001t0004g0022 a0001c0001t0024g0004 a0001c0001t0037g0006 |
3 | HG00639.hp2 HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1225+4853T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87821115 | |||||||
| chr7:87821170 | C | T | 16 | a0001c0001t0009g0002 a0001c0001t0009g0190 a0001c0001t0009g0191 others(13): Show |
16 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.1225+4908C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87821170 | |||||||
| chr7:87821173 | A | T | 16 | a0001c0001t0009g0002 a0001c0001t0009g0190 a0001c0001t0009g0191 others(13): Show |
16 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.1225+4911A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87821173 | |||||||
| chr7:87821198 | G | T | 1 | a0001c0001t0008g0121 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1225+4936G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87821198 | |||||||
| chr7:87821263 | G | C | 41 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(38): Show |
41 | HG01074.hp1 HG01081.hp2 HG01123.hp1 others(38): Show |
intron_variant | MODIFIER | c.1225+5001G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87821263 | |||||||
| chr7:87821423 | C | T | 39 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(36): Show |
39 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(36): Show |
intron_variant | MODIFIER | c.1225+5161C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87821423 | |||||||
| chr7:87821492 | C | T | 1 | a0001c0001t0023g0039 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1225+5230C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87821492 | |||||||
| chr7:87821573 | G | A | 1 | a0001c0001t0079g0024 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1225+5311G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87821573 | |||||||
| chr7:87821578 | G | A | 1 | a0001c0001t0065g0003 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1225+5316G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87821578 | |||||||
| chr7:87821622 | G | A | 1 | a0001c0001t0001g0045 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1225+5360G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87821622 | |||||||
| chr7:87821735 | C | T | 1 | a0001c0001t0070g0014 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1225+5473C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87821735 | |||||||
| chr7:87821813 | G | C | 2 | a0001c0001t0036g0159 a0001c0001t0073g0053 |
2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1225+5551G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87821813 | |||||||
| chr7:87821870 | C | G | 12 | a0001c0001t0014g0152 a0001c0001t0014g0155 a0001c0001t0014g0158 others(9): Show |
12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.1225+5608C>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87821870 | |||||||
| chr7:87821881 | A | C | 1 | a0001c0001t0039g0148 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1225+5619A>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87821881 | |||||||
| chr7:87821886 | T | C | 1 | a0001c0001t0007g0146 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1225+5624T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87821886 | |||||||
| chr7:87822041 | G | C | 1 | a0001c0001t0079g0024 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1225+5779G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87822041 | |||||||
| chr7:87822224 | G | A | 1 | a0001c0001t0072g0009 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1225+5962G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87822224 | |||||||
| chr7:87822236 | C | A | 1 | a0001c0001t0039g0148 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1225+5974C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87822236 | |||||||
| chr7:87822321 | G | A | 1 | a0001c0001t0040g0013 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1225+6059G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87822321 | |||||||
| chr7:87822343 | G | A | 1 | a0001c0001t0005g0124 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1225+6081G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87822343 | |||||||
| chr7:87822441 | A | G | 1 | a0001c0001t0039g0148 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1225+6179A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87822441 | |||||||
| chr7:87822678 | C | G | 3 | a0001c0001t0005g0077 a0001c0001t0005g0125 a0001c0001t0005g0129 |
3 | NA18974.hp2 NA18979.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.1225+6416C>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87822678 | |||||||
| chr7:87822814 | C | T | 1 | a0001c0001t0010g0012 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1225+6552C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87822814 | |||||||
| chr7:87822859 | A | C | 2 | a0001c0001t0009g0190 a0001c0001t0028g0192 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1225+6597A>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87822859 | |||||||
| chr7:87822878 | G | C | 39 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(36): Show |
39 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(36): Show |
intron_variant | MODIFIER | c.1225+6616G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87822878 | |||||||
| chr7:87823007 | T | G | 63 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(60): Show |
63 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(60): Show |
intron_variant | MODIFIER | c.1225+6745T>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87823007 | |||||||
| chr7:87823056 | A | T | 64 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(61): Show |
64 | HG00280.hp2 HG00438.hp1 HG01069.hp2 others(61): Show |
intron_variant | MODIFIER | c.1225+6794A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87823056 | |||||||
| chr7:87823070 | C | T | 1 | a0001c0001t0005g0052 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1225+6808C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87823070 | |||||||
| chr7:87823110 | C | A | 1 | a0001c0001t0075g0007 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1226-6775C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87823110 | |||||||
| chr7:87823141 | G | A | 1 | a0001c0001t0075g0007 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1226-6744G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87823141 | |||||||
| chr7:87823264 | G | A | 3 | a0001c0001t0057g0017 a0001c0001t0066g0019 a0001c0001t0067g0018 |
3 | HG02630.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1226-6621G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87823264 | |||||||
| chr7:87823318 | C | T | 2 | a0001c0001t0056g0016 a0001c0001t0063g0015 |
2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1226-6567C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87823318 | |||||||
| chr7:87823380 | TTTAAAA | T | 38 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(35): Show |
38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.1226-6502_1226-649 others(10): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 87823380 | ||||||
| chr7:87823393 | A | T | 2 | a0001c0001t0001g0045 a0001c0001t0008g0121 |
2 | HG00735.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.1226-6492A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87823393 | |||||||
| chr7:87823412 | A | AT | 74 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(71): Show |
74 | HG00280.hp2 HG00423.hp1 HG01069.hp2 others(71): Show |
intron_variant | MODIFIER | c.1226-6465dupT | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 87823412 | ||||||
| chr7:87823783 | C | CAT | 8 | a0001c0001t0010g0008 a0001c0001t0010g0010 a0001c0001t0010g0011 others(5): Show |
8 | HG02055.hp1 HG02280.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1226-6094_1226-609 others(6): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 87823783 | ||||||
| chr7:87823791 | T | C | 6 | a0001c0001t0001g0119 a0001c0001t0004g0139 a0001c0001t0024g0102 others(3): Show |
6 | HG01099.hp1 HG01261.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1226-6094T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87823791 | |||||||
| chr7:87823791 | T | TAC | 10 | a0001c0001t0001g0041 a0001c0001t0001g0060 a0001c0001t0001g0096 others(7): Show |
10 | HG00558.hp2 HG00621.hp1 HG00738.hp1 others(7): Show |
intron_variant | MODIFIER | c.1226-6062_1226-606 others(6): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 87823791 | ||||||
| chr7:87823791 | T | TACAC | 2 | a0001c0001t0001g0134 a0001c0001t0042g0050 |
2 | HG00639.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1226-6064_1226-606 others(8): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 87823791 | ||||||
| chr7:87823791 | TAC | T | 5 | a0001c0001t0003g0141 a0001c0001t0006g0116 a0001c0001t0007g0130 others(2): Show |
5 | HG02129.hp2 HG03041.hp2 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.1226-6062_1226-606 others(6): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 87823791 | ||||||
| chr7:87823791 | TACAC | T | 17 | a0001c0001t0001g0070 a0001c0001t0002g0167 a0001c0001t0005g0124 others(14): Show |
17 | HG00423.hp1 HG01346.hp2 HG02040.hp2 others(14): Show |
intron_variant | MODIFIER | c.1226-6064_1226-606 others(8): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 87823791 | ||||||
| chr7:87823793 | C | T | 60 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(57): Show |
60 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(57): Show |
intron_variant | MODIFIER | c.1226-6092C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87823793 | |||||||
| chr7:87823795 | C | T | 22 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0200 others(19): Show |
22 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.1226-6090C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87823795 | |||||||
| chr7:87823797 | C | T | 15 | a0001c0001t0002g0167 a0001c0001t0014g0152 a0001c0001t0014g0155 others(12): Show |
15 | HG00423.hp1 HG02559.hp2 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.1226-6088C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87823797 | |||||||
| chr7:87823823 | C | CAT | 3 | a0001c0001t0003g0066 a0001c0001t0005g0052 a0001c0001t0006g0115 |
3 | HG02135.hp2 HG03041.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.1226-6052_1226-605 others(6): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 87823823 | ||||||
| chr7:87823823 | C | T | 4 | a0001c0001t0006g0116 a0001c0001t0006g0117 a0001c0001t0066g0019 others(1): Show |
4 | HG02040.hp2 HG02129.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1226-6062C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87823823 | |||||||
| chr7:87823823 | CAT | C | 9 | a0001c0001t0004g0055 a0001c0001t0004g0058 a0001c0001t0004g0083 others(6): Show |
9 | HG00558.hp1 HG01952.hp1 HG02165.hp1 others(6): Show |
intron_variant | MODIFIER | c.1226-6052_1226-605 others(6): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 87823823 | ||||||
| chr7:87823825 | T | C | 3 | a0001c0001t0003g0082 a0001c0001t0008g0069 a0001c0001t0070g0014 |
3 | HG00438.hp1 HG02135.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.1226-6060T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87823825 | |||||||
| chr7:87823827 | T | C | 11 | a0001c0001t0003g0082 a0001c0001t0004g0055 a0001c0001t0004g0058 others(8): Show |
11 | HG00438.hp1 HG00558.hp1 HG01952.hp1 others(8): Show |
intron_variant | MODIFIER | c.1226-6058T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87823827 | |||||||
| chr7:87824084 | T | C | 2 | a0001c0001t0036g0159 a0001c0001t0073g0053 |
2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1226-5801T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87824084 | |||||||
| chr7:87824159 | GCAATTAG others(19): Show |
G | 12 | a0001c0001t0014g0152 a0001c0001t0014g0155 a0001c0001t0014g0158 others(9): Show |
12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.1226-5722_1226-569 others(30): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 87824159 | ||||||
| chr7:87824287 | A | G | 75 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(72): Show |
75 | HG00280.hp2 HG00423.hp1 HG01069.hp2 others(72): Show |
intron_variant | MODIFIER | c.1226-5598A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87824287 | |||||||
| chr7:87824466 | C | CT | 6 | a0001c0001t0039g0148 a0001c0001t0055g0020 a0001c0001t0057g0017 others(3): Show |
6 | HG02572.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1226-5412dupT | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 87824466 | ||||||
| chr7:87824504 | T | C | 1 | a0001c0001t0005g0052 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1226-5381T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87824504 | |||||||
| chr7:87825042 | A | T | 6 | a0001c0001t0039g0148 a0001c0001t0055g0020 a0001c0001t0057g0017 others(3): Show |
6 | HG02572.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1226-4843A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87825042 | |||||||
| chr7:87825063 | C | CA | 12 | a0001c0001t0014g0152 a0001c0001t0014g0155 a0001c0001t0014g0158 others(9): Show |
12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.1226-4813dupA | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 87825063 | ||||||
| chr7:87825139 | G | A | 12 | a0001c0001t0014g0152 a0001c0001t0014g0155 a0001c0001t0014g0158 others(9): Show |
12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.1226-4746G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87825139 | |||||||
| chr7:87825419 | C | T | 11 | a0001c0001t0014g0152 a0001c0001t0014g0155 a0001c0001t0014g0158 others(8): Show |
11 | HG00423.hp1 NA18952.hp1 NA18970.hp2 others(8): Show |
intron_variant | MODIFIER | c.1226-4466C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87825419 | |||||||
| chr7:87825432 | G | A | 2 | a0001c0001t0055g0020 a0001c0001t0070g0014 |
2 | HG02572.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1226-4453G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87825432 | |||||||
| chr7:87825669 | G | A | 2 | a0001c0001t0004g0109 a0001c0001t0004g0110 |
2 | HG00738.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.1226-4216G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87825669 | |||||||
| chr7:87825749 | T | C | 63 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(60): Show |
63 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(60): Show |
intron_variant | MODIFIER | c.1226-4136T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87825749 | |||||||
| chr7:87825840 | C | T | 154 | a0001c0001t0001g0064 a0001c0001t0001g0080 a0001c0001t0001g0119 others(151): Show |
154 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.1226-4045C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87825840 | |||||||
| chr7:87825856 | T | C | 16 | a0001c0001t0009g0002 a0001c0001t0009g0190 a0001c0001t0009g0191 others(13): Show |
16 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.1226-4029T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87825856 | |||||||
| chr7:87825971 | A | C | 1 | a0001c0001t0003g0082 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1226-3914A>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87825971 | |||||||
| chr7:87825973 | A | G | 1 | a0001c0001t0003g0082 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1226-3912A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87825973 | |||||||
| chr7:87826043 | T | G | 1 | a0001c0001t0008g0131 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1226-3842T>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87826043 | |||||||
| chr7:87826046 | G | A | 12 | a0001c0001t0014g0152 a0001c0001t0014g0155 a0001c0001t0014g0158 others(9): Show |
12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.1226-3839G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87826046 | |||||||
| chr7:87826112 | G | T | 1 | a0001c0001t0017g0065 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1226-3773G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87826112 | |||||||
| chr7:87826390 | T | TG | 85 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(82): Show |
85 | HG00280.hp2 HG00423.hp1 HG01069.hp2 others(82): Show |
intron_variant | MODIFIER | c.1226-3494dupG | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 87826390 | ||||||
| chr7:87826404 | A | T | 38 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(35): Show |
38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.1226-3481A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87826404 | |||||||
| chr7:87826415 | T | C | 2 | a0001c0001t0008g0021 a0001c0001t0025g0005 |
2 | HG02976.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1226-3470T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87826415 | |||||||
| chr7:87826451 | T | G | 2 | a0001c0001t0001g0080 a0001c0001t0007g0122 |
2 | HG00423.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.1226-3434T>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87826451 | |||||||
| chr7:87826507 | A | G | 1 | a0001c0001t0031g0107 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1226-3378A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87826507 | |||||||
| chr7:87826523 | C | A | 2 | a0001c0001t0036g0159 a0001c0001t0073g0053 |
2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1226-3362C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87826523 | |||||||
| chr7:87826524 | A | C | 2 | a0001c0001t0036g0159 a0001c0001t0073g0053 |
2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1226-3361A>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87826524 | |||||||
| chr7:87826905 | T | C | 1 | a0001c0001t0006g0086 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1226-2980T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87826905 | |||||||
| chr7:87827377 | C | T | 15 | a0001c0001t0009g0002 a0001c0001t0009g0190 a0001c0001t0009g0191 others(12): Show |
15 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.1226-2508C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87827377 | |||||||
| chr7:87827443 | C | T | 4 | a0001c0001t0001g0101 a0001c0001t0003g0105 a0001c0001t0004g0067 others(1): Show |
4 | HG03704.hp1 HG03831.hp1 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.1226-2442C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87827443 | |||||||
| chr7:87827663 | G | A | 5 | a0001c0001t0001g0087 a0001c0001t0001g0134 a0001c0001t0001g0136 others(2): Show |
5 | HG01099.hp2 HG01123.hp2 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.1226-2222G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87827663 | |||||||
| chr7:87827952 | T | A | 1 | a0001c0001t0003g0094 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1226-1933T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87827952 | |||||||
| chr7:87828030 | A | G | 15 | a0001c0001t0009g0002 a0001c0001t0009g0190 a0001c0001t0009g0191 others(12): Show |
15 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.1226-1855A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87828030 | |||||||
| chr7:87828170 | TTC | T | 38 | a0001c0001t0002g0030 a0001c0001t0002g0137 a0001c0001t0002g0162 others(35): Show |
38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.1226-1713_1226-171 others(6): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 87828170 | ||||||
| chr7:87828209 | G | A | 1 | a0001c0001t0003g0114 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1226-1676G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87828209 | |||||||
| chr7:87828217 | T | A | 1 | a0001c0001t0039g0148 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1226-1668T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87828217 | |||||||
| chr7:87828455 | T | C | 2 | a0001c0001t0001g0096 a0001c0001t0035g0034 |
2 | NA19001.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.1226-1430T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87828455 | |||||||
| chr7:87829080 | G | A | 1 | a0001c0001t0040g0013 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1226-805G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87829080 | |||||||
| chr7:87829117 | T | C | 1 | a0001c0001t0065g0003 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1226-768T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87829117 | |||||||
| chr7:87829207 | A | G | 16 | a0001c0001t0009g0002 a0001c0001t0009g0190 a0001c0001t0009g0191 others(13): Show |
16 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.1226-678A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87829207 | |||||||
| chr7:87829262 | T | C | 1 | a0001c0001t0005g0124 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1226-623T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87829262 | |||||||
| chr7:87829318 | T | A | 1 | a0001c0001t0004g0084 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1226-567T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87829318 | |||||||
| chr7:87829510 | G | A | 4 | a0001c0001t0029g0048 a0001c0001t0032g0049 a0001c0001t0032g0051 others(1): Show |
4 | HG00639.hp1 HG02559.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1226-375G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87829510 | |||||||
| chr7:87829593 | G | A | 2 | a0001c0001t0036g0159 a0001c0001t0073g0053 |
2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1226-292G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87829593 |