Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 84900 |
|---|---|
| ensemblid | ENSG00000135119.15 |
| hgncid | 25905 |
| symbol | RNFT2 |
| name | ring finger protein, transmembrane 2 |
| refseq_nuc | NM_001382266.1 |
| refseq_prot | NP_001369195.1 |
| ensembl_nuc | ENST00000257575.9 |
| ensembl_prot | ENSP00000257575.4 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 116738315 |
| end | 116853631 |
| strand | + |
| ver | v1.2 |
| region | chr12:116738315-116853631 |
| region5000 | chr12:116733315-116858631 |
| regionname0 | RNFT2_chr12_116738315_116853631 |
| regionname5000 | RNFT2_chr12_116733315_116858631 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 444 | 264 | 92 | 42 | 89 | 2 | 37 | 60 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0002 | 0/0 | 444 | 3 | 0 | 0 | 3 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0003 | 0/0 | 444 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 1335 | 146 | 27 | 26 | 63 | 1 | 28 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| c0002 | 0/0 | 1335 | 50 | 25 | 10 | 15 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| c0003 | 1/0 | 1335 | 17 | 8 | 2 | 3 | 1 | 2 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| c0004 | 0/0 | 1335 | 9 | 3 | 0 | 3 | 0 | 3 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| c0005 | 0/0 | 1335 | 7 | 7 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| c0006 | 0/0 | 1335 | 6 | 3 | 1 | 0 | 0 | 2 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| c0007 | 0/0 | 1335 | 6 | 5 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| c0008 | 0/0 | 1335 | 4 | 0 | 0 | 4 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| c0009 | 0/0 | 1335 | 4 | 4 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| c0010 | 0/0 | 1335 | 3 | 0 | 0 | 3 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| c0011 | 0/0 | 1335 | 3 | 3 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| c0012 | 0/0 | 1335 | 3 | 0 | 1 | 0 | 0 | 2 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| c0013 | 0/0 | 1335 | 3 | 3 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| c0014 | 0/0 | 1335 | 2 | 1 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| c0015 | 0/0 | 1335 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| c0016 | 0/0 | 1335 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| c0017 | 0/0 | 1335 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| c0018 | 0/0 | 1335 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| c0019 | 0/0 | 1335 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 4414 | 64 | 3 | 21 | 31 | 0 | 8 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| t0002 | 0/0 | 4403 | 36 | 17 | 4 | 15 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| t0003 | 0/0 | 4407 | 16 | 0 | 0 | 14 | 0 | 2 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| t0004 | 0/0 | 4393 | 14 | 4 | 0 | 4 | 0 | 6 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| t0005 | 0/0 | 4408 | 12 | 11 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| t0006 | 1/0 | 4393 | 9 | 0 | 1 | 1 | 1 | 5 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| t0007 | 0/0 | 4393 | 7 | 0 | 0 | 5 | 0 | 2 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| t0008 | 0/0 | 4380 | 5 | 5 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| t0009 | 0/0 | 4407 | 5 | 0 | 2 | 0 | 0 | 3 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| t0010 | 0/0 | 4402 | 5 | 2 | 0 | 3 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| t0011 | 0/0 | 4403 | 5 | 5 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| t0012 | 0/0 | 4415 | 4 | 0 | 3 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| t0013 | 0/0 | 4406 | 4 | 4 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| t0014 | 0/0 | 4404 | 4 | 3 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| t0015 | 0/0 | 4413 | 3 | 0 | 0 | 2 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| t0016 | 0/0 | 4409 | 3 | 2 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| t0017 | 0/0 | 4414 | 3 | 0 | 0 | 3 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| t0018 | 0/0 | 4390 | 3 | 2 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| t0019 | 0/0 | 4412 | 3 | 1 | 1 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| t0020 | 0/0 | 4402 | 2 | 2 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| t0021 | 0/0 | 4407 | 2 | 2 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| t0022 | 0/0 | 4415 | 2 | 0 | 1 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| t0023 | 0/0 | 4410 | 2 | 2 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| t0024 | 0/0 | 4415 | 2 | 0 | 0 | 1 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| t0025 | 0/0 | 4390 | 2 | 2 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| t0026 | 0/0 | 4394 | 2 | 0 | 0 | 0 | 0 | 2 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| t0027 | 0/0 | 4406 | 2 | 1 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| t0028 | 0/0 | 4407 | 2 | 0 | 0 | 2 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| t0029 | 0/0 | 4408 | 2 | 0 | 0 | 1 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| t0030 | 0/0 | 4406 | 2 | 2 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| t0031 | 0/0 | 4403 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| t0032 | 0/0 | 4403 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| t0033 | 0/0 | 4407 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| t0034 | 0/0 | 4408 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| t0035 | 0/0 | 4408 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| t0036 | 0/0 | 4408 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| t0037 | 0/0 | 4409 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| t0038 | 0/0 | 4414 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| t0039 | 0/0 | 4411 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| t0040 | 0/0 | 4410 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| t0041 | 0/0 | 4392 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| t0042 | 0/0 | 4394 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| t0043 | 0/0 | 4394 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| t0044 | 0/0 | 4401 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| t0045 | 0/0 | 4380 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| t0046 | 0/0 | 4389 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| t0047 | 0/0 | 4393 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| t0048 | 0/0 | 4393 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| t0049 | 0/0 | 4393 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| t0050 | 0/0 | 4391 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| t0051 | 0/0 | 4391 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| t0052 | 0/0 | 4398 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| t0053 | 0/0 | 4400 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| t0054 | 0/0 | 4406 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| t0055 | 0/0 | 4407 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| t0056 | 0/0 | 4410 | 1 | 0 | 0 | 0 | 1 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| t0057 | 0/0 | 4414 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| t0058 | 0/0 | 4407 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| t0059 | 0/0 | 4406 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| t0060 | 0/0 | 4407 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| t0061 | 0/0 | 4407 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| t0062 | 0/0 | 4402 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| t0063 | 0/0 | 4402 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| t0064 | 0/0 | 4402 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| t0065 | 0/0 | 4402 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| t0066 | 0/0 | 4404 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| t0067 | 0/0 | 4405 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| t0068 | 0/0 | 4404 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| t0069 | 0/0 | 4404 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| t0070 | 0/0 | 4396 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| t0071 | 0/0 | 4403 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0058 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0197 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1335 | 146 | 27 | 26 | 63 | 1 | 28 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0002 | 0/0 | 1335 | 50 | 25 | 10 | 15 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0003 | 1/0 | 1335 | 17 | 8 | 2 | 3 | 1 | 2 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0004 | 0/0 | 1335 | 9 | 3 | 0 | 3 | 0 | 3 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0005 | 0/0 | 1335 | 7 | 7 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0006 | 0/0 | 1335 | 6 | 3 | 1 | 0 | 0 | 2 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0007 | 0/0 | 1335 | 6 | 5 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0008 | 0/0 | 1335 | 4 | 0 | 0 | 4 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0009 | 0/0 | 1335 | 4 | 4 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0011 | 0/0 | 1335 | 3 | 3 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0012 | 0/0 | 1335 | 3 | 0 | 1 | 0 | 0 | 2 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0013 | 0/0 | 1335 | 3 | 3 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0014 | 0/0 | 1335 | 2 | 1 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0015 | 0/0 | 1335 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0016 | 0/0 | 1335 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0018 | 0/0 | 1335 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0019 | 0/0 | 1335 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0002c0010 | 0/0 | 1335 | 3 | 0 | 0 | 3 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0003c0017 | 0/0 | 1335 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 5748 | 45 | 2 | 17 | 19 | 0 | 6 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0001t0002 | 0/0 | 5737 | 18 | 8 | 2 | 8 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0001t0003 | 0/0 | 5741 | 14 | 0 | 0 | 12 | 0 | 2 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0001t0004 | 0/0 | 5727 | 12 | 2 | 0 | 4 | 0 | 6 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0001t0005 | 0/0 | 5742 | 3 | 3 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0001t0006 | 0/0 | 5727 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0001t0007 | 0/0 | 5727 | 7 | 0 | 0 | 5 | 0 | 2 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0001t0008 | 0/0 | 5714 | 4 | 4 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0001t0009 | 0/0 | 5741 | 5 | 0 | 2 | 0 | 0 | 3 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0001t0010 | 0/0 | 5736 | 2 | 0 | 0 | 2 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0001t0011 | 0/0 | 5737 | 3 | 3 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0001t0012 | 0/0 | 5749 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0001t0014 | 0/0 | 5738 | 3 | 2 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0001t0015 | 0/0 | 5747 | 2 | 0 | 0 | 1 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0001t0017 | 0/0 | 5748 | 3 | 0 | 0 | 3 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0001t0019 | 0/0 | 5746 | 3 | 1 | 1 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0001t0022 | 0/0 | 5749 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0001t0024 | 0/0 | 5749 | 2 | 0 | 0 | 1 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0001t0026 | 0/0 | 5728 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0001t0027 | 0/0 | 5740 | 2 | 1 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0001t0029 | 0/0 | 5742 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0001t0038 | 0/0 | 5748 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0001t0040 | 0/0 | 5744 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0001t0044 | 0/0 | 5735 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0001t0045 | 0/0 | 5714 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0001t0047 | 0/0 | 5727 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0001t0048 | 0/0 | 5727 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0001t0056 | 0/0 | 5744 | 1 | 0 | 0 | 0 | 1 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0001t0057 | 0/0 | 5748 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0001t0058 | 0/0 | 5741 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0001t0060 | 0/0 | 5741 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0001t0061 | 0/0 | 5741 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0001t0069 | 0/0 | 5738 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0001t0071 | 0/0 | 5737 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0002t0001 | 0/0 | 5748 | 13 | 1 | 3 | 9 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0002t0002 | 0/0 | 5737 | 7 | 4 | 0 | 3 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0002t0003 | 0/0 | 5741 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0002t0004 | 0/0 | 5727 | 2 | 2 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0002t0005 | 0/0 | 5742 | 5 | 4 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0002t0008 | 0/0 | 5714 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0002t0010 | 0/0 | 5736 | 2 | 1 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0002t0011 | 0/0 | 5737 | 2 | 2 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0002t0012 | 0/0 | 5749 | 2 | 0 | 2 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0002t0015 | 0/0 | 5747 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0002t0016 | 0/0 | 5743 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0002t0018 | 0/0 | 5724 | 2 | 2 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0002t0021 | 0/0 | 5741 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0002t0022 | 0/0 | 5749 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0002t0033 | 0/0 | 5741 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0002t0041 | 0/0 | 5726 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0002t0049 | 0/0 | 5727 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0002t0062 | 0/0 | 5736 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0002t0063 | 0/0 | 5736 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0002t0064 | 0/0 | 5736 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0002t0065 | 0/0 | 5736 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0002t0066 | 0/0 | 5738 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0002t0067 | 0/0 | 5739 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0003t0002 | 0/0 | 5737 | 4 | 2 | 2 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0003t0005 | 0/0 | 5742 | 2 | 2 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0003t0006 | 1/0 | 5727 | 5 | 0 | 0 | 1 | 1 | 2 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0003t0014 | 0/0 | 5738 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0003t0016 | 0/0 | 5743 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0003t0021 | 0/0 | 5741 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0003t0035 | 0/0 | 5742 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0003t0042 | 0/0 | 5728 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0003t0043 | 0/0 | 5728 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0004t0001 | 0/0 | 5748 | 3 | 0 | 0 | 3 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0004t0002 | 0/0 | 5737 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0004t0012 | 0/0 | 5749 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0004t0026 | 0/0 | 5728 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0004t0029 | 0/0 | 5742 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0004t0052 | 0/0 | 5732 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0004t0068 | 0/0 | 5738 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0005t0013 | 0/0 | 5740 | 2 | 2 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0005t0020 | 0/0 | 5736 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0005t0030 | 0/0 | 5740 | 2 | 2 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0005t0054 | 0/0 | 5740 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0005t0070 | 0/0 | 5730 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0006t0005 | 0/0 | 5742 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0006t0006 | 0/0 | 5727 | 2 | 0 | 0 | 0 | 0 | 2 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0006t0031 | 0/0 | 5737 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0006t0036 | 0/0 | 5742 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0006t0050 | 0/0 | 5725 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0007t0005 | 0/0 | 5742 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0007t0016 | 0/0 | 5743 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0007t0025 | 0/0 | 5724 | 2 | 2 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0007t0034 | 0/0 | 5742 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0007t0046 | 0/0 | 5723 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0008t0003 | 0/0 | 5741 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0008t0028 | 0/0 | 5741 | 2 | 0 | 0 | 2 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0008t0059 | 0/0 | 5740 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0009t0010 | 0/0 | 5736 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0009t0023 | 0/0 | 5744 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0009t0037 | 0/0 | 5743 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0009t0051 | 0/0 | 5725 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0011t0023 | 0/0 | 5744 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0011t0039 | 0/0 | 5745 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0011t0053 | 0/0 | 5734 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0012t0001 | 0/0 | 5748 | 3 | 0 | 1 | 0 | 0 | 2 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0013t0013 | 0/0 | 5740 | 2 | 2 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0013t0020 | 0/0 | 5736 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0014t0002 | 0/0 | 5737 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0014t0018 | 0/0 | 5724 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0015t0002 | 0/0 | 5737 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0016t0032 | 0/0 | 5737 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0018t0055 | 0/0 | 5741 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0001c0019t0002 | 0/0 | 5737 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0002c0010t0002 | 0/0 | 5737 | 3 | 0 | 0 | 3 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| a0003c0017t0006 | 0/0 | 5727 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | copy fasta | chr12 | 116733315 | 116858631 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0001g0197 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0002g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0003g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0003g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0003g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0004g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0004g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0004g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0004g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0004g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0004g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0004g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0004g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0004g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0004g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0004g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0004g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0005g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0005g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0005g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0006g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0007g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0007g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0007g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0007g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0007g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0007g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0007g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0008g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0008g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0008g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0008g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0009g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0009g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0009g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0009g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0009g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0010g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0010g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0011g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0011g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0011g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0012g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0014g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0014g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0014g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0015g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0015g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0017g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0017g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0017g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0019g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0019g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0019g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0022g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0024g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0024g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0026g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0027g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0027g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0029g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0038g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0040g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0044g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0045g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0047g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0048g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0056g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0057g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0058g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0060g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0061g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0069g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0001t0071g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0002t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0002t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0002t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0002t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0002t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0002t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0002t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0002t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0002t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0002t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0002t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0002t0003g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0002t0004g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0002t0004g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0002t0005g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0002t0005g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0002t0005g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0002t0005g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0002t0005g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0002t0008g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0002t0010g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0002t0010g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0002t0011g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0002t0011g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0002t0012g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0002t0012g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0002t0015g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0002t0016g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0002t0018g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0002t0018g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0002t0021g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0002t0022g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0002t0033g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0002t0041g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0002t0049g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0002t0062g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0002t0063g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0002t0064g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0002t0065g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0002t0066g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0002t0067g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0003t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0003t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0003t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0003t0002g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0003t0005g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0003t0005g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0003t0006g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0003t0006g0058 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0003t0006g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0003t0006g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0003t0006g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0003t0014g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0003t0016g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0003t0021g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0003t0035g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0003t0042g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0003t0043g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0004t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0004t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0004t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0004t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0004t0012g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0004t0026g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0004t0029g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0004t0052g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0004t0068g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0005t0013g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0005t0013g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0005t0020g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0005t0030g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0005t0030g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0005t0054g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0005t0070g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0006t0005g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0006t0006g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0006t0006g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0006t0031g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0006t0036g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0006t0050g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0007t0005g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0007t0016g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0007t0025g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0007t0025g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0007t0034g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0007t0046g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0008t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0008t0028g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0008t0028g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0008t0059g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0009t0010g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0009t0023g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0009t0037g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0009t0051g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0011t0023g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0011t0039g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0011t0053g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0012t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0012t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0012t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0013t0013g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0013t0013g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0013t0020g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0014t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0014t0018g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0015t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0016t0032g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0018t0055g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0001c0019t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0002c0010t0002g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0002c0010t0002g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0002c0010t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| a0003c0017t0006g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0056 | g0220 | EUR | GBR | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG00140 | hp2 | a0001 | c0003 | t0006 | g0054 | EUR | GBR | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | CHS | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0133 | EAS | CHS | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG00423 | hp1 | a0001 | c0002 | t0001 | g0076 | EAS | CHS | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG00423 | hp2 | a0001 | c0001 | t0003 | g0242 | EAS | CHS | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0209 | EAS | CHS | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0189 | EAS | CHS | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG00544 | hp1 | a0001 | c0001 | t0007 | g0071 | EAS | CHS | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | CHS | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG00609 | hp1 | a0001 | c0001 | t0060 | g0090 | EAS | CHS | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | CHS | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG00621 | hp1 | a0001 | c0004 | t0001 | g0091 | EAS | CHS | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG00621 | hp2 | a0001 | c0001 | t0003 | g0157 | EAS | CHS | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG00673 | hp1 | a0001 | c0001 | t0015 | g0112 | EAS | CHS | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG00673 | hp2 | a0001 | c0001 | t0004 | g0128 | EAS | CHS | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG00741 | hp1 | a0001 | c0006 | t0050 | g0013 | AMR | PUR | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG01074 | hp1 | a0001 | c0002 | t0012 | g0089 | AMR | PUR | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG01074 | hp2 | a0001 | c0003 | t0002 | g0101 | AMR | PUR | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0249 | AMR | PUR | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG01099 | hp2 | a0001 | c0002 | t0001 | g0078 | AMR | PUR | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG01106 | hp1 | a0001 | c0014 | t0018 | g0019 | AMR | PUR | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG01109 | hp1 | a0001 | c0001 | t0069 | g0068 | AMR | PUR | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG01109 | hp2 | a0001 | c0001 | t0009 | g0116 | AMR | PUR | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG01169 | hp1 | a0001 | c0001 | t0038 | g0219 | AMR | PUR | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG01169 | hp2 | a0001 | c0002 | t0062 | g0185 | AMR | PUR | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG01175 | hp1 | a0001 | c0012 | t0001 | g0123 | AMR | PUR | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG01175 | hp2 | a0001 | c0002 | t0005 | g0003 | AMR | PUR | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG01192 | hp1 | a0001 | c0001 | t0012 | g0261 | AMR | PUR | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0023 | AMR | PUR | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG01243 | hp1 | a0001 | c0007 | t0016 | g0061 | AMR | PUR | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG01243 | hp2 | a0001 | c0002 | t0049 | g0004 | AMR | PUR | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0262 | AMR | CLM | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0235 | AMR | CLM | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | CLM | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG01258 | hp2 | a0001 | c0001 | t0009 | g0130 | AMR | CLM | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0236 | AMR | CLM | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG01261 | hp2 | a0001 | c0001 | t0019 | g0187 | AMR | CLM | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG01358 | hp1 | a0001 | c0003 | t0002 | g0247 | AMR | CLM | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0237 | AMR | CLM | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG01361 | hp1 | a0001 | c0002 | t0012 | g0014 | AMR | CLM | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | CLM | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG01884 | hp1 | a0001 | c0002 | t0065 | g0093 | AFR | ACB | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG01884 | hp2 | a0001 | c0007 | t0025 | g0009 | AFR | ACB | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG01891 | hp1 | a0001 | c0005 | t0030 | g0052 | AFR | ACB | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG01891 | hp2 | a0001 | c0013 | t0013 | g0046 | AFR | ACB | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG01975 | hp1 | a0001 | c0002 | t0066 | g0010 | AMR | PEL | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | PEL | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0260 | AMR | PEL | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG01978 | hp2 | a0001 | c0001 | t0006 | g0115 | AMR | PEL | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | PEL | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | PEL | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG02040 | hp1 | a0002 | c0010 | t0002 | g0254 | EAS | KHV | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG02040 | hp2 | a0001 | c0001 | t0003 | g0191 | EAS | KHV | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG02055 | hp1 | a0001 | c0004 | t0068 | g0024 | AFR | ACB | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG02055 | hp2 | a0001 | c0001 | t0019 | g0124 | AFR | ACB | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG02071 | hp1 | a0001 | c0002 | t0002 | g0159 | EAS | KHV | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG02071 | hp2 | a0001 | c0001 | t0003 | g0106 | EAS | KHV | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG02074 | hp1 | a0001 | c0001 | t0047 | g0241 | EAS | KHV | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | KHV | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | KHV | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | KHV | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG02132 | hp1 | a0001 | c0004 | t0001 | g0113 | EAS | KHV | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG02132 | hp2 | a0002 | c0010 | t0002 | g0002 | EAS | KHV | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG02135 | hp1 | a0001 | c0002 | t0001 | g0077 | EAS | KHV | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG02135 | hp2 | a0002 | c0010 | t0002 | g0001 | EAS | KHV | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG02145 | hp1 | a0001 | c0007 | t0025 | g0056 | AFR | ACB | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG02145 | hp2 | a0001 | c0001 | t0005 | g0245 | AFR | ACB | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0258 | AMR | PEL | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG02148 | hp2 | a0001 | c0002 | t0001 | g0111 | AMR | PEL | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG02155 | hp1 | a0001 | c0001 | t0004 | g0145 | EAS | CDX | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG02155 | hp2 | a0001 | c0001 | t0003 | g0155 | EAS | CDX | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG02257 | hp1 | a0001 | c0002 | t0018 | g0022 | AFR | ACB | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0032 | AFR | ACB | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG02258 | hp1 | a0001 | c0002 | t0002 | g0129 | AFR | ACB | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG02258 | hp2 | a0001 | c0002 | t0001 | g0066 | AFR | ACB | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | PEL | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0256 | AMR | PEL | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG02280 | hp1 | a0001 | c0001 | t0005 | g0105 | AFR | ACB | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG02280 | hp2 | a0001 | c0003 | t0002 | g0100 | AFR | ACB | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG02293 | hp1 | a0001 | c0002 | t0022 | g0252 | AMR | PEL | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PEL | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG02300 | hp1 | a0001 | c0002 | t0001 | g0080 | AMR | PEL | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | PEL | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG02451 | hp1 | a0001 | c0001 | t0027 | g0125 | AFR | ACB | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG02451 | hp2 | a0001 | c0006 | t0031 | g0067 | AFR | ACB | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG02523 | hp1 | a0001 | c0001 | t0003 | g0127 | EAS | KHV | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG02523 | hp2 | a0001 | c0001 | t0007 | g0171 | EAS | KHV | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG02572 | hp1 | a0001 | c0009 | t0037 | g0043 | AFR | GWD | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG02572 | hp2 | a0001 | c0001 | t0008 | g0040 | AFR | GWD | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0103 | AFR | GWD | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG02615 | hp2 | a0001 | c0006 | t0036 | g0018 | AFR | GWD | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG02622 | hp1 | a0001 | c0002 | t0004 | g0005 | AFR | GWD | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0104 | AFR | GWD | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG02630 | hp1 | a0001 | c0016 | t0032 | g0044 | AFR | GWD | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG02630 | hp2 | a0001 | c0009 | t0023 | g0026 | AFR | GWD | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG02647 | hp1 | a0001 | c0014 | t0002 | g0137 | AFR | GWD | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG02647 | hp2 | a0001 | c0001 | t0004 | g0096 | AFR | GWD | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG02683 | hp1 | a0001 | c0001 | t0009 | g0118 | SAS | PJL | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG02683 | hp2 | a0001 | c0001 | t0004 | g0168 | SAS | PJL | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG02735 | hp1 | a0001 | c0001 | t0019 | g0163 | SAS | PJL | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG02735 | hp2 | a0001 | c0001 | t0027 | g0121 | SAS | PJL | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG02738 | hp1 | a0001 | c0003 | t0006 | g0165 | SAS | PJL | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG02738 | hp2 | a0001 | c0004 | t0029 | g0055 | SAS | PJL | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG02809 | hp1 | a0001 | c0011 | t0053 | g0011 | AFR | GWD | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG02809 | hp2 | a0001 | c0002 | t0011 | g0107 | AFR | GWD | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG02818 | hp1 | a0001 | c0002 | t0063 | g0263 | AFR | GWD | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG02818 | hp2 | a0001 | c0003 | t0035 | g0088 | AFR | GWD | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0253 | AFR | GWD | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG02886 | hp2 | a0001 | c0002 | t0005 | g0064 | AFR | GWD | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG02895 | hp1 | a0001 | c0002 | t0002 | g0142 | AFR | GWD | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG02895 | hp2 | a0001 | c0001 | t0011 | g0099 | AFR | GWD | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG02896 | hp1 | a0001 | c0002 | t0067 | g0042 | AFR | GWD | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG02896 | hp2 | a0001 | c0001 | t0008 | g0028 | AFR | GWD | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG02897 | hp1 | a0001 | c0001 | t0008 | g0029 | AFR | GWD | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG02897 | hp2 | a0001 | c0002 | t0011 | g0097 | AFR | GWD | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG02922 | hp1 | a0001 | c0005 | t0054 | g0021 | AFR | ESN | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG02922 | hp2 | a0001 | c0002 | t0033 | g0150 | AFR | ESN | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG02965 | hp1 | a0001 | c0005 | t0070 | g0050 | AFR | ESN | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG02965 | hp2 | a0001 | c0003 | t0021 | g0038 | AFR | ESN | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG02970 | hp1 | a0001 | c0007 | t0005 | g0062 | AFR | ESN | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG02970 | hp2 | a0001 | c0005 | t0020 | g0162 | AFR | ESN | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0048 | AFR | ESN | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG02976 | hp2 | a0001 | c0009 | t0051 | g0016 | AFR | ESN | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG03017 | hp1 | a0001 | c0001 | t0003 | g0117 | SAS | PJL | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG03017 | hp2 | a0001 | c0012 | t0001 | g0239 | SAS | PJL | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG03041 | hp1 | a0001 | c0001 | t0005 | g0246 | AFR | GWD | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG03041 | hp2 | a0001 | c0001 | t0008 | g0041 | AFR | GWD | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG03130 | hp1 | a0001 | c0003 | t0005 | g0036 | AFR | ESN | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG03130 | hp2 | a0001 | c0001 | t0045 | g0114 | AFR | ESN | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG03139 | hp1 | a0001 | c0004 | t0002 | g0025 | AFR | ESN | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG03139 | hp2 | a0001 | c0007 | t0034 | g0063 | AFR | ESN | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG03195 | hp1 | a0001 | c0011 | t0023 | g0007 | AFR | ESN | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG03195 | hp2 | a0001 | c0003 | t0016 | g0039 | AFR | ESN | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG03209 | hp1 | a0001 | c0003 | t0014 | g0065 | AFR | MSL | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG03209 | hp2 | a0001 | c0001 | t0014 | g0037 | AFR | MSL | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG03225 | hp1 | a0001 | c0002 | t0064 | g0152 | AFR | MSL | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG03225 | hp2 | a0001 | c0001 | t0004 | g0095 | AFR | MSL | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0248 | SAS | PJL | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0169 | SAS | PJL | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG03453 | hp1 | a0001 | c0004 | t0052 | g0015 | AFR | MSL | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG03453 | hp2 | a0001 | c0018 | t0055 | g0059 | AFR | MSL | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG03486 | hp1 | a0001 | c0002 | t0004 | g0268 | AFR | MSL | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG03486 | hp2 | a0001 | c0001 | t0011 | g0033 | AFR | MSL | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG03490 | hp1 | a0001 | c0003 | t0006 | g0208 | SAS | PJL | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG03490 | hp2 | a0001 | c0001 | t0009 | g0153 | SAS | PJL | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG03491 | hp1 | a0001 | c0001 | t0007 | g0179 | SAS | PJL | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG03491 | hp2 | a0001 | c0001 | t0044 | g0255 | SAS | PJL | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG03492 | hp1 | a0001 | c0001 | t0009 | g0161 | SAS | PJL | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG03492 | hp2 | a0001 | c0001 | t0007 | g0180 | SAS | PJL | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG03516 | hp1 | a0001 | c0009 | t0010 | g0049 | AFR | ESN | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG03516 | hp2 | a0001 | c0015 | t0002 | g0020 | AFR | ESN | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG03540 | hp1 | a0001 | c0001 | t0014 | g0027 | AFR | GWD | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0031 | AFR | GWD | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG03579 | hp1 | a0001 | c0005 | t0013 | g0154 | AFR | MSL | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG03579 | hp2 | a0001 | c0001 | t0011 | g0160 | AFR | MSL | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG03654 | hp1 | a0001 | c0001 | t0057 | g0188 | SAS | PJL | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG03654 | hp2 | a0001 | c0006 | t0006 | g0218 | SAS | PJL | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG03688 | hp1 | a0001 | c0001 | t0004 | g0177 | SAS | STU | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG03688 | hp2 | a0001 | c0001 | t0024 | g0147 | SAS | STU | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG03704 | hp1 | a0001 | c0001 | t0015 | g0186 | SAS | PJL | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG03704 | hp2 | a0001 | c0001 | t0004 | g0176 | SAS | PJL | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG03710 | hp1 | a0001 | c0001 | t0071 | g0119 | SAS | PJL | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0259 | SAS | PJL | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG03831 | hp1 | a0001 | c0001 | t0004 | g0172 | SAS | BEB | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG03831 | hp2 | a0001 | c0004 | t0012 | g0134 | SAS | BEB | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0224 | SAS | BEB | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG03834 | hp2 | a0001 | c0006 | t0006 | g0057 | SAS | BEB | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG03942 | hp1 | a0001 | c0001 | t0004 | g0110 | SAS | BEB | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0203 | SAS | BEB | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG04184 | hp1 | a0001 | c0001 | t0026 | g0181 | SAS | BEB | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG04184 | hp2 | a0001 | c0001 | t0022 | g0223 | SAS | BEB | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG04199 | hp1 | a0001 | c0001 | t0004 | g0170 | SAS | STU | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0243 | SAS | STU | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG04228 | hp1 | a0001 | c0004 | t0026 | g0201 | SAS | STU | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG04228 | hp2 | a0001 | c0001 | t0003 | g0240 | SAS | STU | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| NA18522 | hp1 | a0001 | c0002 | t0005 | g0183 | AFR | YRI | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| NA18522 | hp2 | a0001 | c0003 | t0005 | g0035 | AFR | YRI | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | CHB | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| NA18747 | hp2 | a0001 | c0002 | t0001 | g0264 | EAS | CHB | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| NA18906 | hp1 | a0001 | c0003 | t0002 | g0102 | AFR | YRI | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| NA18906 | hp2 | a0001 | c0013 | t0013 | g0158 | AFR | YRI | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| NA18941 | hp1 | a0001 | c0001 | t0003 | g0199 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| NA18945 | hp1 | a0001 | c0001 | t0017 | g0200 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| NA18945 | hp2 | a0001 | c0002 | t0002 | g0265 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| NA18948 | hp1 | a0001 | c0008 | t0028 | g0214 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| NA18948 | hp2 | a0001 | c0001 | t0007 | g0087 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| NA18950 | hp2 | a0001 | c0008 | t0028 | g0138 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| NA18954 | hp1 | a0001 | c0001 | t0003 | g0212 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| NA18954 | hp2 | a0001 | c0001 | t0017 | g0167 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| NA18956 | hp1 | a0001 | c0001 | t0040 | g0143 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| NA18956 | hp2 | a0001 | c0003 | t0043 | g0228 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| NA18957 | hp1 | a0001 | c0002 | t0003 | g0008 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| NA18960 | hp1 | a0001 | c0001 | t0007 | g0070 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| NA18960 | hp2 | a0001 | c0008 | t0059 | g0084 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| NA18962 | hp1 | a0001 | c0001 | t0010 | g0222 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| NA18971 | hp1 | a0001 | c0002 | t0010 | g0266 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| NA18971 | hp2 | a0001 | c0004 | t0001 | g0083 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| NA18974 | hp2 | a0001 | c0001 | t0007 | g0231 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| NA18975 | hp1 | a0001 | c0001 | t0003 | g0144 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| NA18975 | hp2 | a0001 | c0003 | t0006 | g0230 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| NA18977 | hp1 | a0001 | c0001 | t0017 | g0213 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| NA18977 | hp2 | a0001 | c0001 | t0048 | g0182 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| NA18980 | hp1 | a0001 | c0001 | t0061 | g0148 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| NA18980 | hp2 | a0001 | c0003 | t0042 | g0229 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| NA18984 | hp1 | a0001 | c0002 | t0001 | g0250 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| NA18993 | hp1 | a0001 | c0001 | t0058 | g0109 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| NA18993 | hp2 | a0001 | c0001 | t0024 | g0126 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| NA18994 | hp1 | a0001 | c0002 | t0015 | g0082 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| NA18994 | hp2 | a0001 | c0002 | t0001 | g0081 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| NA18999 | hp1 | a0001 | c0001 | t0003 | g0085 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| NA18999 | hp2 | a0001 | c0008 | t0003 | g0206 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| NA19001 | hp2 | a0001 | c0019 | t0002 | g0267 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| NA19005 | hp1 | a0001 | c0001 | t0003 | g0131 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| NA19005 | hp2 | a0001 | c0002 | t0001 | g0251 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| NA19012 | hp1 | a0001 | c0001 | t0029 | g0225 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| NA19012 | hp2 | a0001 | c0001 | t0004 | g0226 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| NA19043 | hp1 | a0001 | c0013 | t0020 | g0098 | AFR | LWK | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| NA19043 | hp2 | a0001 | c0002 | t0021 | g0139 | AFR | LWK | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| NA19054 | hp2 | a0001 | c0002 | t0002 | g0174 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| NA19057 | hp2 | a0001 | c0001 | t0010 | g0233 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| NA19062 | hp2 | a0001 | c0001 | t0014 | g0156 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| NA19065 | hp2 | a0001 | c0002 | t0001 | g0079 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| NA19068 | hp1 | a0001 | c0001 | t0003 | g0164 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| NA19068 | hp2 | a0001 | c0002 | t0001 | g0073 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| NA19082 | hp2 | a0001 | c0001 | t0004 | g0173 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| NA19090 | hp1 | a0001 | c0002 | t0001 | g0074 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0234 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| NA19240 | hp1 | a0001 | c0002 | t0008 | g0140 | AFR | YRI | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0045 | AFR | YRI | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| NA20129 | hp1 | a0001 | c0005 | t0030 | g0051 | AFR | ASW | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| NA20129 | hp2 | a0001 | c0002 | t0005 | g0149 | AFR | ASW | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| NA20905 | hp1 | a0001 | c0012 | t0001 | g0238 | SAS | GIH | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| NA20905 | hp2 | a0003 | c0017 | t0006 | g0060 | SAS | GIH | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG02109 | hp1 | a0001 | c0002 | t0016 | g0136 | AFR | ACB | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG02109 | hp2 | a0001 | c0002 | t0018 | g0047 | AFR | ACB | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG02486 | hp1 | a0001 | c0011 | t0039 | g0012 | AFR | ACB | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG02486 | hp2 | a0001 | c0006 | t0005 | g0017 | AFR | ACB | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG02559 | hp1 | a0001 | c0002 | t0002 | g0030 | AFR | ACB | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG02559 | hp2 | a0001 | c0002 | t0010 | g0132 | AFR | ACB | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG03471 | hp1 | a0001 | c0007 | t0046 | g0053 | AFR | MSL | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG03471 | hp2 | a0001 | c0002 | t0002 | g0108 | AFR | MSL | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG06807 | hp1 | a0001 | c0005 | t0013 | g0006 | AFR | USA | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | USA | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0257 | AFR | USA | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0034 | AFR | USA | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| NA21309 | hp1 | a0001 | c0002 | t0041 | g0075 | AFR | LWK | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| NA21309 | hp2 | a0001 | c0002 | t0005 | g0151 | AFR | LWK | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0197 | REF | REF | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| homoSapiens_grch38 | hp1 | a0001 | c0003 | t0006 | g0058 | REF | REF | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:116750145
|
G | A | 1 | a0002 | 3 | HG02040.hp1 HG02132.hp2 HG02135.hp2 |
missense_variant | MODERATE | c.388G>A | p.Val130Met | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/11 | 597/5727 | 388/1335 | 130/444 | chr12 | 116750145 | ||
| chr12:116833847
|
C | T | 1 | a0003 | 1 | NA20905.hp2 | missense_variant | MODERATE | c.938C>T | p.Pro313Leu | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 8/11 | 1147/5727 | 938/1335 | 313/444 | chr12 | 116833847 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:116749865
|
C | T | 1 | a0001c0019 | 1 | NA19001.hp2 | synonymous_variant | LOW | c.108C>T | p.Ser36Ser | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/11 | 317/5727 | 108/1335 | 36/444 | chr12 | 116749865 | ||
| chr12:116750102
|
T | C | 12 | a0001c0002a0001c0004a0001c0005others(9): Show | 89 | HG00423.hp1 HG00621.hp1 HG00741.hp1 others(86): Show |
synonymous_variant | LOW | c.345T>C | p.His115His | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/11 | 554/5727 | 345/1335 | 115/444 | chr12 | 116750102 | ||
| chr12:116750114
|
C | T | 3 | a0001c0004a0001c0007a0001c0018 | 16 | HG00621.hp1 HG01243.hp1 HG01884.hp2 others(13): Show |
synonymous_variant | LOW | c.357C>T | p.Gly119Gly | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/11 | 566/5727 | 357/1335 | 119/444 | chr12 | 116750114 | ||
| chr12:116766861
|
G | A | 1 | a0001c0012 | 3 | HG01175.hp1 HG03017.hp2 NA20905.hp1 |
synonymous_variant | LOW | c.675G>A | p.Ala225Ala | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/11 | 884/5727 | 675/1335 | 225/444 | chr12 | 116766861 | ||
| chr12:116779336
|
T | C | 13 | a0001c0001a0001c0002a0001c0004others(10): Show | 235 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(232): Show |
synonymous_variant | LOW | c.870T>C | p.Ala290Ala | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/11 | 1079/5727 | 870/1335 | 290/444 | chr12 | 116779336 | ||
| chr12:116833881
|
C | T | 3 | a0001c0009a0001c0011a0001c0014 | 9 | HG01106.hp1 HG02486.hp1 HG02572.hp1 others(6): Show |
synonymous_variant | LOW | c.972C>T | p.Asp324Asp | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 8/11 | 1181/5727 | 972/1335 | 324/444 | chr12 | 116833881 | ||
| chr12:116849347
|
C | T | 1 | a0001c0015 | 1 | HG03516.hp2 | synonymous_variant | LOW | c.1234C>T | p.Leu412Leu | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 1443/5727 | 1234/1335 | 412/444 | chr12 | 116849347 | ||
| chr12:116849385
|
C | T | 4 | a0001c0005a0001c0013a0001c0016others(1): Show | 12 | HG01891.hp1 HG01891.hp2 HG02630.hp1 others(9): Show |
synonymous_variant | LOW | c.1272C>T | p.Val424Val | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 1481/5727 | 1272/1335 | 424/444 | chr12 | 116849385 | ||
| chr12:116849415
|
C | T | 1 | a0001c0008 | 4 | NA18948.hp1 NA18950.hp2 NA18960.hp2 others(1): Show |
synonymous_variant | LOW | c.1302C>T | p.Asp434Asp | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 1511/5727 | 1302/1335 | 434/444 | chr12 | 116849415 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:116740392
|
C | T | 1 | a0001c0001t0071 | 1 | HG03710.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-106C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 2/11 | chr12 | 116740392 | ||||||
| chr12:116740393
|
G | A | 1 | a0001c0006t0031 | 1 | HG02451.hp2 | 5_prime_UTR_variant | MODIFIER | c.-105G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 2/11 | 105 | chr12 | 116740393 | |||||
| chr12:116849467
|
C | T | 2 | a0001c0005t0030a0001c0005t0070 | 3 | HG01891.hp1 HG02965.hp1 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*19C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 19 | chr12 | 116849467 | |||||
| chr12:116849648
|
C | T | 37 | a0001c0001t0002a0001c0001t0003a0001c0001t0009others(34): Show | 91 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(88): Show |
3_prime_UTR_variant | MODIFIER | c.*200C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 200 | chr12 | 116849648 | |||||
| chr12:116849702
|
G | A | 3 | a0001c0005t0020a0001c0013t0020a0001c0016t0032 | 3 | HG02630.hp1 HG02970.hp2 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*254G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 254 | chr12 | 116849702 | |||||
| chr12:116849826
|
C | T | 3 | a0001c0001t0019a0001c0001t0056a0001c0001t0057 | 5 | HG00140.hp1 HG01261.hp2 HG02055.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*378C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 378 | chr12 | 116849826 | |||||
| chr12:116849845
|
C | CTTCCTTC others(8): Show |
2 | a0001c0001t0027a0001c0008t0059 | 3 | HG02451.hp1 HG02735.hp2 NA18960.hp2 |
3_prime_UTR_variant | MODIFIER | c.*399_*400insCCTTCC others(9): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 400 | INFO_REALIGN_3_PRIME | chr12 | 116849845 | ||||
| chr12:116849845
|
C | CTTCCTTC others(9): Show |
10 | a0001c0001t0003a0001c0001t0009a0001c0001t0029others(7): Show | 28 | HG00423.hp2 HG00609.hp1 HG00621.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*399_*400insCCTTCC others(10): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 400 | INFO_REALIGN_3_PRIME | chr12 | 116849845 | ||||
| chr12:116849845
|
C | CTTCCTTT others(4): Show |
7 | a0001c0001t0010a0001c0002t0010a0001c0002t0033others(4): Show | 9 | HG01169.hp2 HG02559.hp2 HG02818.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*399_*400insCCTTTT others(5): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 400 | INFO_REALIGN_3_PRIME | chr12 | 116849845 | ||||
| chr12:116849845
|
C | CTTCCTTT others(5): Show |
33 | a0001c0001t0002a0001c0001t0005a0001c0001t0011others(30): Show | 74 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*399_*400insCCTTTT others(6): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 400 | INFO_REALIGN_3_PRIME | chr12 | 116849845 | ||||
| chr12:116849845
|
C | CTTCCTTT others(6): Show |
15 | a0001c0001t0001a0001c0001t0012a0001c0001t0017others(12): Show | 78 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*399_*400insCCTTTT others(7): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 400 | INFO_REALIGN_3_PRIME | chr12 | 116849845 | ||||
| chr12:116849845
|
C | CTTCCTTT others(7): Show |
3 | a0001c0001t0024a0001c0001t0040a0001c0011t0039 | 4 | HG02486.hp1 HG03688.hp2 NA18956.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*399_*400insCCTTTT others(8): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 400 | INFO_REALIGN_3_PRIME | chr12 | 116849845 | ||||
| chr12:116849845
|
C | CTTTTTTT others(1): Show |
5 | a0001c0001t0019a0001c0001t0056a0001c0001t0057others(2): Show | 7 | HG00140.hp1 HG01261.hp2 HG02055.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*406_*413dupTTTTTT others(2): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 414 | INFO_REALIGN_3_PRIME | chr12 | 116849845 | ||||
| chr12:116849845
|
C | CTTTTTTT others(3): Show |
6 | a0001c0005t0013a0001c0005t0020a0001c0005t0030others(3): Show | 9 | HG01891.hp1 HG01891.hp2 HG02922.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*404_*413dupTTTTTT others(4): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 414 | INFO_REALIGN_3_PRIME | chr12 | 116849845 | ||||
| chr12:116849845
|
C | CTTTTTTT others(4): Show |
2 | a0001c0016t0032a0001c0018t0055 | 2 | HG02630.hp1 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*403_*413dupTTTTTT others(5): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 414 | INFO_REALIGN_3_PRIME | chr12 | 116849845 | ||||
| chr12:116849861
|
T | A | 1 | a0001c0001t0058 | 1 | NA18993.hp1 | 3_prime_UTR_variant | MODIFIER | c.*413T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 413 | chr12 | 116849861 | |||||
| chr12:116849862
|
A | T | 1 | a0001c0009t0051 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*414A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 414 | chr12 | 116849862 | |||||
| chr12:116849868
|
A | G | 102 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(99): Show | 256 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(253): Show |
3_prime_UTR_variant | MODIFIER | c.*420A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 420 | chr12 | 116849868 | |||||
| chr12:116850046
|
T | C | 1 | a0001c0009t0051 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*598T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 598 | chr12 | 116850046 | |||||
| chr12:116850113
|
G | A | 1 | a0001c0006t0036 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*665G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 665 | chr12 | 116850113 | |||||
| chr12:116850148
|
C | CT | 5 | a0001c0001t0026a0001c0003t0042a0001c0003t0043others(2): Show | 5 | HG00741.hp1 HG04184.hp1 HG04228.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*724dupT | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 725 | INFO_REALIGN_3_PRIME | chr12 | 116850148 | ||||
| chr12:116850148
|
CTT | C | 6 | a0001c0001t0057a0001c0002t0016a0001c0003t0016others(3): Show | 6 | HG01243.hp1 HG02109.hp1 HG02572.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*723_*724delTT | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 723 | INFO_REALIGN_3_PRIME | chr12 | 116850148 | ||||
| chr12:116850148
|
CTTT | C | 27 | a0001c0001t0005a0001c0001t0014a0001c0001t0019others(24): Show | 41 | HG01175.hp2 HG01261.hp2 HG01891.hp1 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*722_*724delTTT | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 722 | INFO_REALIGN_3_PRIME | chr12 | 116850148 | ||||
| chr12:116850148
|
CTTTT | C | 51 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(48): Show | 171 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(168): Show |
3_prime_UTR_variant | MODIFIER | c.*721_*724delTTTT | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 721 | INFO_REALIGN_3_PRIME | chr12 | 116850148 | ||||
| chr12:116850181
|
G | T | 2 | a0001c0004t0052a0001c0011t0053 | 2 | HG02809.hp1 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*733G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 733 | chr12 | 116850181 | |||||
| chr12:116850266
|
C | T | 1 | a0001c0003t0035 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*818C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 818 | chr12 | 116850266 | |||||
| chr12:116850295
|
C | T | 2 | a0001c0001t0009a0001c0001t0027 | 7 | HG01109.hp2 HG01258.hp2 HG02451.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*847C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 847 | chr12 | 116850295 | |||||
| chr12:116850321
|
AT | A | 84 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(81): Show | 215 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(212): Show |
3_prime_UTR_variant | MODIFIER | c.*888delT | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 888 | INFO_REALIGN_3_PRIME | chr12 | 116850321 | ||||
| chr12:116850502
|
T | C | 2 | a0001c0002t0062a0001c0004t0068 | 2 | HG01169.hp2 HG02055.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1054T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 1054 | chr12 | 116850502 | |||||
| chr12:116850565
|
A | G | 1 | a0001c0009t0051 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1117A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 1117 | chr12 | 116850565 | |||||
| chr12:116850613
|
T | TTATTTTC | 69 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(66): Show | 197 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(194): Show |
3_prime_UTR_variant | MODIFIER | c.*1166_*1167insATTT others(3): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 1167 | INFO_REALIGN_3_PRIME | chr12 | 116850613 | ||||
| chr12:116850615
|
C | A | 33 | a0001c0001t0004a0001c0001t0007a0001c0001t0008others(30): Show | 59 | HG00140.hp1 HG00544.hp1 HG00673.hp2 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*1167C>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 1167 | chr12 | 116850615 | |||||
| chr12:116850615
|
C | T | 69 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(66): Show | 197 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(194): Show |
3_prime_UTR_variant | MODIFIER | c.*1167C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 1167 | chr12 | 116850615 | |||||
| chr12:116850620
|
C | CTTTTTTC others(1): Show |
7 | a0001c0001t0012a0001c0002t0012a0001c0002t0067others(4): Show | 8 | HG01074.hp1 HG01192.hp1 HG01361.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1178_*1179insCTTT others(4): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 1179 | INFO_REALIGN_3_PRIME | chr12 | 116850620 | ||||
| chr12:116850620
|
C | CTTTTTTC others(7): Show |
1 | a0001c0001t0056 | 1 | HG00140.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1178_*1179insCTTT others(10): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 1179 | INFO_REALIGN_3_PRIME | chr12 | 116850620 | ||||
| chr12:116850620
|
C | CTTTTTTC others(8): Show |
1 | a0001c0001t0019 | 3 | HG01261.hp2 HG02055.hp2 HG02735.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1178_*1179insCTTT others(11): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 1179 | INFO_REALIGN_3_PRIME | chr12 | 116850620 | ||||
| chr12:116850620
|
C | CTTTTTTC others(9): Show |
1 | a0001c0001t0057 | 1 | HG03654.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1178_*1179insCTTT others(12): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 1179 | INFO_REALIGN_3_PRIME | chr12 | 116850620 | ||||
| chr12:116850625
|
T | TTCTTTTT others(1): Show |
3 | a0001c0001t0008a0001c0001t0045a0001c0002t0008 | 6 | HG02572.hp2 HG02896.hp2 HG02897.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1178_*1179insCTTT others(4): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 1179 | INFO_REALIGN_3_PRIME | chr12 | 116850625 | ||||
| chr12:116850625
|
T | TTCTTTTT others(7): Show |
5 | a0001c0002t0018a0001c0006t0050a0001c0007t0025others(2): Show | 7 | HG00741.hp1 HG01106.hp1 HG01884.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1178_*1179insCTTT others(10): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 1179 | INFO_REALIGN_3_PRIME | chr12 | 116850625 | ||||
| chr12:116850629
|
T | G | 1 | a0001c0001t0007 | 7 | HG00544.hp1 HG02523.hp2 HG03491.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1181T>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 1181 | chr12 | 116850629 | |||||
| chr12:116850632
|
T | G | 7 | a0001c0001t0004a0001c0001t0007a0001c0001t0026others(4): Show | 25 | HG00544.hp1 HG00673.hp2 HG02074.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*1184T>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 1184 | chr12 | 116850632 | |||||
| chr12:116850635
|
T | G | 19 | a0001c0001t0004a0001c0001t0007a0001c0001t0026others(16): Show | 40 | HG00544.hp1 HG00673.hp2 HG01243.hp2 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*1187T>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 1187 | chr12 | 116850635 | |||||
| chr12:116850720
|
C | T | 8 | a0001c0001t0008a0001c0001t0045a0001c0002t0008others(5): Show | 13 | HG00741.hp1 HG01106.hp1 HG01884.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1272C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 1272 | chr12 | 116850720 | |||||
| chr12:116850753
|
G | A | 1 | a0001c0001t0060 | 1 | HG00609.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1305G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 1305 | chr12 | 116850753 | |||||
| chr12:116850794
|
AT | A | 12 | a0001c0001t0008a0001c0001t0045a0001c0002t0008others(9): Show | 17 | HG00741.hp1 HG01106.hp1 HG01884.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1356delT | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 1356 | INFO_REALIGN_3_PRIME | chr12 | 116850794 | ||||
| chr12:116850814
|
G | A | 3 | a0001c0005t0020a0001c0013t0020a0001c0016t0032 | 3 | HG02630.hp1 HG02970.hp2 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1366G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 1366 | chr12 | 116850814 | |||||
| chr12:116850833
|
ACGTTGGC others(9): Show |
A | 8 | a0001c0001t0008a0001c0001t0045a0001c0002t0008others(5): Show | 13 | HG00741.hp1 HG01106.hp1 HG01884.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1387_*1402delGTTG others(12): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 1387 | INFO_REALIGN_3_PRIME | chr12 | 116850833 | ||||
| chr12:116850890
|
C | T | 1 | a0001c0001t0038 | 1 | HG01169.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1442C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 1442 | chr12 | 116850890 | |||||
| chr12:116850937
|
G | A | 1 | a0001c0008t0028 | 2 | NA18948.hp1 NA18950.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1489G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 1489 | chr12 | 116850937 | |||||
| chr12:116851024
|
G | C | 9 | a0001c0001t0008a0001c0001t0045a0001c0002t0008others(6): Show | 14 | HG00741.hp1 HG01106.hp1 HG01884.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1576G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 1576 | chr12 | 116851024 | |||||
| chr12:116851137
|
C | T | 8 | a0001c0001t0004a0001c0001t0007a0001c0001t0026others(5): Show | 26 | HG00544.hp1 HG00673.hp2 HG01243.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*1689C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 1689 | chr12 | 116851137 | |||||
| chr12:116851138
|
G | A | 1 | a0001c0003t0042 | 1 | NA18980.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1690G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 1690 | chr12 | 116851138 | |||||
| chr12:116851173
|
G | A | 2 | a0001c0001t0011a0001c0002t0011 | 5 | HG02809.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1725G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 1725 | chr12 | 116851173 | |||||
| chr12:116851229
|
A | T | 1 | a0001c0001t0048 | 1 | NA18977.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1781A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 1781 | chr12 | 116851229 | |||||
| chr12:116851230
|
T | A | 100 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(97): Show | 254 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(251): Show |
3_prime_UTR_variant | MODIFIER | c.*1782T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 1782 | chr12 | 116851230 | |||||
| chr12:116851298
|
T | C | 1 | a0001c0009t0051 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1850T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 1850 | chr12 | 116851298 | |||||
| chr12:116851387
|
G | A | 2 | a0001c0002t0063a0001c0002t0065 | 2 | HG01884.hp1 HG02818.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1939G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 1939 | chr12 | 116851387 | |||||
| chr12:116851389
|
A | T | 1 | a0001c0001t0017 | 3 | NA18945.hp1 NA18954.hp2 NA18977.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1941A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 1941 | chr12 | 116851389 | |||||
| chr12:116851435
|
G | A | 3 | a0001c0005t0020a0001c0013t0020a0001c0016t0032 | 3 | HG02630.hp1 HG02970.hp2 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1987G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 1987 | chr12 | 116851435 | |||||
| chr12:116851603
|
G | T | 1 | a0001c0005t0054 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2155G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 2155 | chr12 | 116851603 | |||||
| chr12:116851608
|
C | T | 1 | a0001c0001t0045 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2160C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 2160 | chr12 | 116851608 | |||||
| chr12:116851609
|
G | A | 37 | a0001c0001t0002a0001c0001t0003a0001c0001t0009others(34): Show | 91 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(88): Show |
3_prime_UTR_variant | MODIFIER | c.*2161G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 2161 | chr12 | 116851609 | |||||
| chr12:116851613
|
G | A | 6 | a0001c0001t0008a0001c0001t0045a0001c0002t0008others(3): Show | 10 | HG00741.hp1 HG01106.hp1 HG02109.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2165G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 2165 | chr12 | 116851613 | |||||
| chr12:116851645
|
C | T | 6 | a0001c0005t0013a0001c0005t0030a0001c0005t0054others(3): Show | 9 | HG01891.hp1 HG01891.hp2 HG02922.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2197C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 2197 | chr12 | 116851645 | |||||
| chr12:116851794
|
GGAAA | G | 37 | a0001c0001t0002a0001c0001t0003a0001c0001t0009others(34): Show | 91 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(88): Show |
3_prime_UTR_variant | MODIFIER | c.*2356_*2359delAAAG | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 2356 | INFO_REALIGN_3_PRIME | chr12 | 116851794 | ||||
| chr12:116851808
|
G | C | 16 | a0001c0001t0001a0001c0001t0012a0001c0001t0015others(13): Show | 81 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*2360G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 2360 | chr12 | 116851808 | |||||
| chr12:116851916
|
C | G | 1 | a0001c0009t0037 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2468C>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 2468 | chr12 | 116851916 | |||||
| chr12:116852198
|
G | A | 9 | a0001c0001t0008a0001c0001t0045a0001c0002t0008others(6): Show | 14 | HG00741.hp1 HG01106.hp1 HG01884.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*2750G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 2750 | chr12 | 116852198 | |||||
| chr12:116852291
|
G | C | 84 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(81): Show | 215 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(212): Show |
3_prime_UTR_variant | MODIFIER | c.*2843G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 2843 | chr12 | 116852291 | |||||
| chr12:116852350
|
T | C | 102 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(99): Show | 256 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(253): Show |
3_prime_UTR_variant | MODIFIER | c.*2902T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 2902 | chr12 | 116852350 | |||||
| chr12:116852377
|
T | TTTCCCC | 16 | a0001c0001t0001a0001c0001t0012a0001c0001t0015others(13): Show | 81 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*2932_*2937dupCCCC others(2): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 2938 | INFO_REALIGN_3_PRIME | chr12 | 116852377 | ||||
| chr12:116852551
|
A | G | 3 | a0001c0005t0020a0001c0013t0020a0001c0016t0032 | 3 | HG02630.hp1 HG02970.hp2 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3103A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 3103 | chr12 | 116852551 | |||||
| chr12:116852628
|
G | A | 11 | a0001c0001t0008a0001c0001t0019a0001c0001t0045others(8): Show | 18 | HG00140.hp1 HG00741.hp1 HG01106.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*3180G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 3180 | chr12 | 116852628 | |||||
| chr12:116852729
|
G | T | 3 | a0001c0005t0020a0001c0013t0020a0001c0016t0032 | 3 | HG02630.hp1 HG02970.hp2 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3281G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 3281 | chr12 | 116852729 | |||||
| chr12:116852764
|
C | T | 8 | a0001c0001t0008a0001c0001t0045a0001c0002t0008others(5): Show | 13 | HG00741.hp1 HG01106.hp1 HG01884.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*3316C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 3316 | chr12 | 116852764 | |||||
| chr12:116852796
|
T | C | 84 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(81): Show | 215 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(212): Show |
3_prime_UTR_variant | MODIFIER | c.*3348T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 3348 | chr12 | 116852796 | |||||
| chr12:116853120
|
G | A | 1 | a0001c0001t0061 | 1 | NA18980.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3672G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 3672 | chr12 | 116853120 | |||||
| chr12:116853330
|
C | T | 1 | a0001c0001t0047 | 1 | HG02074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3882C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 3882 | chr12 | 116853330 | |||||
| chr12:116853334
|
G | A | 39 | a0001c0001t0002a0001c0001t0003a0001c0001t0009others(36): Show | 93 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(90): Show |
3_prime_UTR_variant | MODIFIER | c.*3886G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 3886 | chr12 | 116853334 | |||||
| chr12:116853334
|
G | C | 3 | a0001c0001t0019a0001c0001t0056a0001c0001t0057 | 5 | HG00140.hp1 HG01261.hp2 HG02055.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3886G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 3886 | chr12 | 116853334 | |||||
| chr12:116853348
|
A | T | 8 | a0001c0001t0008a0001c0001t0045a0001c0002t0008others(5): Show | 13 | HG00741.hp1 HG01106.hp1 HG01884.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*3900A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 3900 | chr12 | 116853348 | |||||
| chr12:116853438
|
C | T | 1 | a0001c0009t0051 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3990C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 3990 | chr12 | 116853438 | |||||
| chr12:116853479
|
G | A | 1 | a0001c0001t0047 | 1 | HG02074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4031G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 4031 | chr12 | 116853479 | |||||
| chr12:116853540
|
T | C | 1 | a0001c0002t0063 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4092T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 4092 | chr12 | 116853540 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:116738387
|
A | AT | 181 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0120others(178): Show | 181 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(178): Show |
intron_variant | MODIFIER | c.-154+26dupT | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 116738387 | |||||
| chr12:116738509
|
A | T | 1 | a0001c0002t0004g0268 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-154+139A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 1/10 | chr12 | 116738509 | ||||||
| chr12:116738576
|
A | G | 22 | a0001c0001t0001g0072a0001c0001t0001g0086a0001c0001t0003g0085others(19): Show | 22 | HG00423.hp1 HG00544.hp1 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.-154+206A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 1/10 | chr12 | 116738576 | ||||||
| chr12:116738619
|
A | G | 1 | a0001c0002t0063g0263 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-154+249A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 1/10 | chr12 | 116738619 | ||||||
| chr12:116738708
|
T | A | 2 | a0002c0010t0002g0001a0002c0010t0002g0002 | 2 | HG02132.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.-154+338T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 1/10 | chr12 | 116738708 | ||||||
| chr12:116738747
|
G | A | 43 | a0001c0001t0001g0072a0001c0001t0001g0086a0001c0001t0003g0085others(40): Show | 43 | HG00423.hp1 HG00544.hp1 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.-154+377G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 1/10 | chr12 | 116738747 | ||||||
| chr12:116738784
|
G | C | 2 | a0001c0005t0054g0021a0001c0015t0002g0020 | 2 | HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-154+414G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 1/10 | chr12 | 116738784 | ||||||
| chr12:116738900
|
G | A | 25 | a0001c0001t0001g0072a0001c0001t0007g0070a0001c0001t0007g0071others(22): Show | 25 | HG00423.hp1 HG00544.hp1 HG01099.hp2 others(22): Show |
intron_variant | MODIFIER | c.-154+530G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 1/10 | chr12 | 116738900 | ||||||
| chr12:116738918
|
A | G | 3 | a0001c0006t0005g0017a0001c0006t0036g0018a0001c0014t0018g0019 | 3 | HG01106.hp1 HG02486.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.-154+548A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 1/10 | chr12 | 116738918 | ||||||
| chr12:116738942
|
A | G | 1 | a0001c0001t0001g0069 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-154+572A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 1/10 | chr12 | 116738942 | ||||||
| chr12:116738986
|
G | C | 2 | a0001c0006t0005g0017a0001c0006t0036g0018 | 2 | HG02486.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.-154+616G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 1/10 | chr12 | 116738986 | ||||||
| chr12:116739021
|
C | T | 8 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0258others(5): Show | 8 | HG01192.hp1 HG01257.hp1 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.-154+651C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 1/10 | chr12 | 116739021 | ||||||
| chr12:116739034
|
T | C | 1 | a0001c0001t0060g0090 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-154+664T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 1/10 | chr12 | 116739034 | ||||||
| chr12:116739122
|
C | A | 2 | a0002c0010t0002g0001a0002c0010t0002g0002 | 2 | HG02132.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.-154+752C>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 1/10 | chr12 | 116739122 | ||||||
| chr12:116739206
|
A | G | 3 | a0002c0010t0002g0001a0002c0010t0002g0002a0002c0010t0002g0254 | 3 | HG02040.hp1 HG02132.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.-154+836A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 1/10 | chr12 | 116739206 | ||||||
| chr12:116739291
|
G | A | 11 | a0001c0001t0002g0023a0001c0002t0012g0014a0001c0002t0012g0089others(8): Show | 11 | HG00741.hp1 HG01074.hp1 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.-154+921G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 1/10 | chr12 | 116739291 | ||||||
| chr12:116739322
|
A | C | 4 | a0001c0006t0036g0018a0002c0010t0002g0001a0002c0010t0002g0002others(1): Show | 4 | HG02040.hp1 HG02132.hp2 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.-154+952A>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 1/10 | chr12 | 116739322 | ||||||
| chr12:116739413
|
A | G | 1 | a0001c0001t0002g0253 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-153-932A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 1/10 | chr12 | 116739413 | ||||||
| chr12:116739530
|
C | T | 3 | a0002c0010t0002g0001a0002c0010t0002g0002a0002c0010t0002g0254 | 3 | HG02040.hp1 HG02132.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.-153-815C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 1/10 | chr12 | 116739530 | ||||||
| chr12:116739573
|
C | T | 20 | a0001c0002t0001g0073a0001c0002t0001g0074a0001c0002t0001g0076others(17): Show | 20 | HG00423.hp1 HG01099.hp2 HG02135.hp1 others(17): Show |
intron_variant | MODIFIER | c.-153-772C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 1/10 | chr12 | 116739573 | ||||||
| chr12:116739574
|
G | A | 2 | a0001c0004t0002g0025a0001c0004t0068g0024 | 2 | HG02055.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-153-771G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 1/10 | chr12 | 116739574 | ||||||
| chr12:116739606
|
A | G | 1 | a0001c0001t0069g0068 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-153-739A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 1/10 | chr12 | 116739606 | ||||||
| chr12:116739616
|
G | C | 1 | a0001c0004t0001g0091 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-153-729G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 1/10 | chr12 | 116739616 | ||||||
| chr12:116739887
|
A | G | 1 | a0001c0004t0001g0083 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-153-458A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 1/10 | chr12 | 116739887 | ||||||
| chr12:116740059
|
G | A | 243 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(240): Show | 243 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(240): Show |
intron_variant | MODIFIER | c.-153-286G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 1/10 | chr12 | 116740059 | ||||||
| chr12:116740061
|
G | T | 2 | a0001c0001t0005g0245a0001c0001t0005g0246 | 2 | HG02145.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-153-284G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 1/10 | chr12 | 116740061 | ||||||
| chr12:116740168
|
C | T | 1 | a0001c0001t0001g0244 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-153-177C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 1/10 | chr12 | 116740168 | ||||||
| chr12:116740284
|
G | A | 1 | a0001c0001t0001g0092 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.-153-61G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 1/10 | chr12 | 116740284 | ||||||
| chr12:116740307
|
C | T | 4 | a0001c0001t0002g0023a0002c0010t0002g0001a0002c0010t0002g0002others(1): Show | 4 | HG01192.hp2 HG02040.hp1 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.-153-38C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 1/10 | chr12 | 116740307 | ||||||
| chr12:116740706
|
T | C | 1 | a0001c0002t0065g0093 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.24+185T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 2/10 | chr12 | 116740706 | ||||||
| chr12:116740914
|
C | A | 1 | a0001c0001t0001g0094 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.25-122C>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 2/10 | chr12 | 116740914 | ||||||
| chr12:116741530
|
G | A | 2 | a0002c0010t0002g0001a0002c0010t0002g0254 | 2 | HG02040.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.83+436G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116741530 | ||||||
| chr12:116741636
|
A | G | 2 | a0001c0001t0001g0072a0001c0001t0007g0071 | 2 | HG00544.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.83+542A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116741636 | ||||||
| chr12:116741840
|
G | A | 227 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(224): Show | 227 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(224): Show |
intron_variant | MODIFIER | c.83+746G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116741840 | ||||||
| chr12:116741951
|
T | C | 2 | a0001c0001t0004g0095a0001c0001t0004g0096 | 2 | HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.83+857T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116741951 | ||||||
| chr12:116742030
|
T | C | 5 | a0001c0001t0002g0023a0001c0006t0005g0017a0002c0010t0002g0001others(2): Show | 5 | HG01192.hp2 HG02040.hp1 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.83+936T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116742030 | ||||||
| chr12:116742265
|
C | CT | 11 | a0001c0001t0001g0243a0001c0001t0002g0048a0001c0001t0003g0240others(8): Show | 11 | HG00423.hp2 HG00741.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.83+1191dupT | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 116742265 | |||||
| chr12:116742265
|
CT | C | 5 | a0001c0001t0007g0070a0001c0001t0044g0255a0001c0002t0001g0250others(2): Show | 5 | HG02897.hp2 HG03491.hp2 NA18960.hp1 others(2): Show |
intron_variant | MODIFIER | c.83+1191delT | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 116742265 | |||||
| chr12:116742429
|
C | T | 1 | a0001c0001t0002g0023 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.83+1335C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116742429 | ||||||
| chr12:116742505
|
G | T | 2 | a0001c0012t0001g0238a0001c0012t0001g0239 | 2 | HG03017.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.83+1411G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116742505 | ||||||
| chr12:116742511
|
T | C | 25 | a0001c0001t0002g0031a0001c0001t0002g0032a0001c0001t0002g0034others(22): Show | 25 | HG01074.hp2 HG01106.hp1 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.83+1417T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116742511 | ||||||
| chr12:116742548
|
A | G | 5 | a0001c0001t0002g0023a0001c0006t0005g0017a0002c0010t0002g0001others(2): Show | 5 | HG01192.hp2 HG02040.hp1 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.83+1454A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116742548 | ||||||
| chr12:116742596
|
G | A | 2 | a0001c0001t0004g0095a0001c0001t0004g0096 | 2 | HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.83+1502G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116742596 | ||||||
| chr12:116742900
|
T | C | 6 | a0001c0002t0018g0022a0001c0002t0066g0010a0001c0006t0050g0013others(3): Show | 6 | HG00741.hp1 HG01884.hp2 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.83+1806T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116742900 | ||||||
| chr12:116743039
|
C | T | 2 | a0001c0001t0001g0237a0001c0001t0002g0236 | 2 | HG01261.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.83+1945C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116743039 | ||||||
| chr12:116743080
|
C | CA | 7 | a0001c0002t0018g0022a0001c0003t0002g0247a0001c0003t0006g0054others(4): Show | 7 | HG00140.hp2 HG00741.hp1 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.83+2012dupA | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 116743080 | |||||
| chr12:116743080
|
CAA | C | 17 | a0001c0001t0003g0106a0001c0001t0004g0110a0001c0001t0005g0246others(14): Show | 17 | HG01175.hp2 HG01891.hp1 HG02071.hp2 others(14): Show |
intron_variant | MODIFIER | c.83+2011_83+2012del others(2): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 116743080 | |||||
| chr12:116743080
|
CAAA | C | 143 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0120others(140): Show | 143 | HG00408.hp2 HG00423.hp1 HG00609.hp2 others(140): Show |
intron_variant | MODIFIER | c.83+2010_83+2012del others(3): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 116743080 | |||||
| chr12:116743080
|
CAAAA | C | 69 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(66): Show | 69 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.83+2009_83+2012del others(4): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 116743080 | |||||
| chr12:116743080
|
CAAAAA | C | 6 | a0001c0001t0001g0232a0001c0001t0001g0235a0001c0001t0001g0262others(3): Show | 6 | HG01257.hp1 HG01257.hp2 NA18974.hp2 others(3): Show |
intron_variant | MODIFIER | c.83+2008_83+2012del others(5): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 116743080 | |||||
| chr12:116743136
|
G | C | 1 | a0001c0004t0029g0055 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.83+2042G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116743136 | ||||||
| chr12:116743173
|
G | A | 1 | a0001c0002t0001g0251 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.83+2079G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116743173 | ||||||
| chr12:116743197
|
G | A | 1 | a0001c0002t0001g0111 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.83+2103G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116743197 | ||||||
| chr12:116743213
|
T | TAAAAAAA others(3): Show |
8 | a0001c0001t0002g0045a0001c0001t0002g0048a0001c0002t0004g0268others(5): Show | 8 | HG01884.hp1 HG02630.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.83+2141_83+2150dup others(10): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 116743213 | |||||
| chr12:116743213
|
T | TAAAAAAA others(4): Show |
6 | a0001c0001t0024g0147a0001c0001t0038g0219a0001c0001t0056g0220others(3): Show | 6 | HG00140.hp1 HG01169.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.83+2140_83+2150dup others(11): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 116743213 | |||||
| chr12:116743213
|
T | TAAAAAAA others(5): Show |
20 | a0001c0001t0001g0069a0001c0001t0001g0146a0001c0001t0001g0215others(17): Show | 20 | HG01192.hp1 HG01257.hp1 HG01257.hp2 others(17): Show |
intron_variant | MODIFIER | c.83+2139_83+2150dup others(12): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 116743213 | |||||
| chr12:116743213
|
T | TAAAAAAA others(6): Show |
36 | a0001c0001t0001g0072a0001c0001t0001g0086a0001c0001t0001g0135others(33): Show | 36 | HG00408.hp1 HG00438.hp1 HG01258.hp1 others(33): Show |
intron_variant | MODIFIER | c.83+2138_83+2150dup others(13): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 116743213 | |||||
| chr12:116743213
|
T | TAAAAAAA others(7): Show |
15 | a0001c0001t0001g0198a0001c0001t0001g0244a0001c0001t0002g0023others(12): Show | 15 | HG00408.hp2 HG00673.hp2 HG01192.hp2 others(12): Show |
intron_variant | MODIFIER | c.83+2137_83+2150dup others(14): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 116743213 | |||||
| chr12:116743213
|
T | TAAAAAAA others(8): Show |
9 | a0001c0001t0001g0094a0001c0001t0001g0197a0001c0001t0001g0256others(6): Show | 9 | HG00544.hp1 HG02055.hp2 HG02273.hp2 others(6): Show |
intron_variant | MODIFIER | c.83+2136_83+2150dup others(15): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 116743213 | |||||
| chr12:116743213
|
T | TAAAAAAA others(9): Show |
9 | a0001c0001t0001g0120a0001c0001t0001g0122a0001c0001t0001g0194others(6): Show | 9 | HG00544.hp2 HG00609.hp2 HG00741.hp2 others(6): Show |
intron_variant | MODIFIER | c.83+2135_83+2150dup others(16): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 116743213 | |||||
| chr12:116743213
|
T | TAAAAAAA others(10): Show |
9 | a0001c0001t0001g0193a0001c0001t0002g0192a0001c0001t0003g0117others(6): Show | 9 | HG01109.hp2 HG01361.hp2 HG01978.hp2 others(6): Show |
intron_variant | MODIFIER | c.83+2134_83+2150dup others(17): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 116743213 | |||||
| chr12:116743213
|
T | TAAAAAAA others(11): Show |
6 | a0001c0001t0001g0190a0001c0001t0003g0242a0001c0001t0008g0041others(3): Show | 6 | HG00423.hp2 HG01975.hp2 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.83+2133_83+2150dup others(18): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 116743213 | |||||
| chr12:116743213
|
T | TAAAAAAA others(12): Show |
1 | a0001c0001t0002g0189 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.83+2132_83+2150dup others(19): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 116743213 | |||||
| chr12:116743213
|
T | TAAAAAAA others(13): Show |
1 | a0001c0001t0015g0112 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.83+2131_83+2150dup others(20): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 116743213 | |||||
| chr12:116743213
|
T | TAAAAAAA others(14): Show |
1 | a0001c0001t0003g0106 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.83+2130_83+2150dup others(21): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 116743213 | |||||
| chr12:116743213
|
T | TAAAAAAA others(16): Show |
1 | a0001c0001t0057g0188 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.83+2128_83+2150dup others(23): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 116743213 | |||||
| chr12:116743213
|
T | TAAAAAAA others(17): Show |
1 | a0001c0001t0019g0187 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.83+2127_83+2150dup others(24): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 116743213 | |||||
| chr12:116743229
|
AAAAAAAA others(9): Show |
A | 1 | a0001c0006t0031g0067 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.83+2136_83+2151del others(16): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116743229 | ||||||
| chr12:116743231
|
AAAAAAAA others(7): Show |
A | 1 | a0001c0006t0036g0018 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.83+2138_83+2151del others(14): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116743231 | ||||||
| chr12:116743232
|
AAAAAAAA others(6): Show |
A | 3 | a0001c0003t0006g0230a0001c0003t0042g0229a0001c0006t0005g0017 | 3 | HG02486.hp2 NA18975.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.83+2139_83+2151del others(13): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116743232 | ||||||
| chr12:116743233
|
AAAAAAAA others(5): Show |
A | 1 | a0001c0003t0043g0228 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.83+2140_83+2151del others(12): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116743233 | ||||||
| chr12:116743237
|
AAAAAAAA others(1): Show |
A | 6 | a0001c0001t0001g0227a0001c0001t0002g0184a0001c0001t0015g0186others(3): Show | 6 | HG00609.hp1 HG01169.hp2 HG02074.hp2 others(3): Show |
intron_variant | MODIFIER | c.83+2144_83+2151del others(8): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116743237 | ||||||
| chr12:116743238
|
AAAAAAAC | A | 14 | a0001c0001t0001g0178a0001c0001t0002g0175a0001c0001t0004g0110others(11): Show | 14 | HG00621.hp1 HG02074.hp1 HG03491.hp1 others(11): Show |
intron_variant | MODIFIER | c.83+2145_83+2151del others(7): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116743238 | ||||||
| chr12:116743239
|
AAAAAAC | A | 29 | a0001c0001t0001g0166a0001c0001t0001g0169a0001c0001t0002g0031others(26): Show | 29 | HG01074.hp2 HG01106.hp1 HG02004.hp2 others(26): Show |
intron_variant | MODIFIER | c.83+2146_83+2151del others(6): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116743239 | ||||||
| chr12:116743240
|
AAAAAC | A | 16 | a0001c0001t0003g0164a0001c0001t0004g0226a0001c0001t0011g0099others(13): Show | 16 | HG01891.hp1 HG01891.hp2 HG02040.hp1 others(13): Show |
intron_variant | MODIFIER | c.83+2147_83+2151del others(5): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116743240 | ||||||
| chr12:116743241
|
AAAAC | A | 6 | a0001c0001t0001g0092a0001c0001t0009g0161a0001c0001t0011g0160others(3): Show | 6 | HG01109.hp1 HG02630.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.83+2148_83+2151del others(4): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116743241 | ||||||
| chr12:116743242
|
AAAC | A | 21 | a0001c0001t0001g0224a0001c0001t0003g0157a0001c0002t0001g0077others(18): Show | 21 | HG00621.hp2 HG01074.hp1 HG01099.hp2 others(18): Show |
intron_variant | MODIFIER | c.83+2149_83+2151del others(3): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116743242 | ||||||
| chr12:116743243
|
AAC | A | 24 | a0001c0001t0001g0249a0001c0001t0010g0222a0001c0001t0014g0156others(21): Show | 24 | HG00140.hp2 HG00423.hp1 HG01099.hp1 others(21): Show |
intron_variant | MODIFIER | c.83+2150_83+2151del others(2): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116743243 | ||||||
| chr12:116743244
|
AC | A | 7 | a0001c0001t0001g0248a0001c0001t0003g0155a0001c0002t0001g0073others(4): Show | 7 | HG01358.hp1 HG02145.hp1 HG02155.hp2 others(4): Show |
intron_variant | MODIFIER | c.83+2152delC | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 116743244 | |||||
| chr12:116743245
|
C | A | 138 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(135): Show | 138 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.83+2151C>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116743245 | ||||||
| chr12:116743247
|
G | A | 267 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(264): Show | 267 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(264): Show |
intron_variant | MODIFIER | c.83+2153G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116743247 | ||||||
| chr12:116743406
|
A | G | 1 | a0001c0006t0006g0218 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.83+2312A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116743406 | ||||||
| chr12:116743414
|
G | A | 1 | a0001c0004t0052g0015 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.83+2320G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116743414 | ||||||
| chr12:116743424
|
G | A | 3 | a0001c0005t0030g0051a0001c0005t0030g0052a0001c0005t0070g0050 | 3 | HG01891.hp1 HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.83+2330G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116743424 | ||||||
| chr12:116743452
|
G | A | 1 | a0001c0008t0059g0084 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.83+2358G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116743452 | ||||||
| chr12:116743721
|
G | A | 1 | a0001c0003t0002g0247 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.83+2627G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116743721 | ||||||
| chr12:116743760
|
C | T | 1 | a0001c0001t0002g0133 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.83+2666C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116743760 | ||||||
| chr12:116743874
|
A | C | 7 | a0001c0002t0002g0108a0001c0002t0002g0142a0001c0002t0010g0132others(4): Show | 7 | HG02109.hp2 HG02559.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.83+2780A>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116743874 | ||||||
| chr12:116743885
|
C | T | 3 | a0001c0005t0030g0051a0001c0005t0030g0052a0001c0005t0070g0050 | 3 | HG01891.hp1 HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.83+2791C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116743885 | ||||||
| chr12:116743903
|
C | T | 233 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(230): Show | 233 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(230): Show |
intron_variant | MODIFIER | c.83+2809C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116743903 | ||||||
| chr12:116743986
|
C | T | 3 | a0001c0001t0004g0173a0001c0001t0047g0241a0001c0001t0048g0182 | 3 | HG02074.hp1 NA18977.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.83+2892C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116743986 | ||||||
| chr12:116744184
|
C | A | 1 | a0001c0012t0001g0239 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.83+3090C>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116744184 | ||||||
| chr12:116744225
|
C | CA | 135 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(132): Show | 135 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.83+3149dupA | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 116744225 | |||||
| chr12:116744225
|
C | CAA | 7 | a0001c0001t0001g0237a0001c0001t0001g0244a0001c0001t0002g0236others(4): Show | 7 | HG01261.hp1 HG01358.hp2 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.83+3148_83+3149dup others(2): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 116744225 | |||||
| chr12:116744239
|
A | C | 2 | a0001c0002t0012g0014a0001c0002t0012g0089 | 2 | HG01074.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.83+3145A>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116744239 | ||||||
| chr12:116744249
|
G | A | 4 | a0001c0001t0002g0023a0002c0010t0002g0001a0002c0010t0002g0002others(1): Show | 4 | HG01192.hp2 HG02040.hp1 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.83+3155G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116744249 | ||||||
| chr12:116744415
|
G | T | 1 | a0001c0001t0001g0217 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.83+3321G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116744415 | ||||||
| chr12:116744737
|
G | T | 6 | a0001c0002t0018g0022a0001c0002t0066g0010a0001c0006t0050g0013others(3): Show | 6 | HG00741.hp1 HG01884.hp2 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.83+3643G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116744737 | ||||||
| chr12:116745013
|
T | C | 3 | a0002c0010t0002g0001a0002c0010t0002g0002a0002c0010t0002g0254 | 3 | HG02040.hp1 HG02132.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.83+3919T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116745013 | ||||||
| chr12:116745062
|
T | C | 6 | a0001c0002t0018g0022a0001c0002t0066g0010a0001c0006t0050g0013others(3): Show | 6 | HG00741.hp1 HG01884.hp2 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.83+3968T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116745062 | ||||||
| chr12:116745087
|
C | T | 2 | a0002c0010t0002g0001a0002c0010t0002g0254 | 2 | HG02040.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.83+3993C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116745087 | ||||||
| chr12:116745118
|
G | T | 1 | a0001c0001t0001g0216 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.83+4024G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116745118 | ||||||
| chr12:116745136
|
G | C | 1 | a0001c0006t0036g0018 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.83+4042G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116745136 | ||||||
| chr12:116745163
|
A | C | 1 | a0001c0001t0001g0224 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.83+4069A>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116745163 | ||||||
| chr12:116745173
|
A | AT | 16 | a0001c0001t0001g0202a0001c0001t0002g0023a0001c0001t0008g0028others(13): Show | 16 | HG01074.hp1 HG01192.hp2 HG01361.hp1 others(13): Show |
intron_variant | MODIFIER | c.83+4098dupT | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 116745173 | |||||
| chr12:116745173
|
A | ATT | 215 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(212): Show | 215 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(212): Show |
intron_variant | MODIFIER | c.83+4097_83+4098dup others(2): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 116745173 | |||||
| chr12:116745173
|
A | ATTT | 9 | a0001c0001t0001g0193a0001c0001t0001g0237a0001c0001t0002g0234others(6): Show | 9 | HG01106.hp1 HG01175.hp1 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.83+4096_83+4098dup others(3): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 116745173 | |||||
| chr12:116745277
|
C | T | 1 | a0001c0001t0002g0023 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.83+4183C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116745277 | ||||||
| chr12:116745529
|
G | A | 3 | a0002c0010t0002g0001a0002c0010t0002g0002a0002c0010t0002g0254 | 3 | HG02040.hp1 HG02132.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.84-4312G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116745529 | ||||||
| chr12:116745552
|
T | C | 233 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(230): Show | 233 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(230): Show |
intron_variant | MODIFIER | c.84-4289T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116745552 | ||||||
| chr12:116745882
|
T | C | 3 | a0001c0001t0014g0027a0001c0001t0069g0068a0001c0009t0023g0026 | 3 | HG01109.hp1 HG02630.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.84-3959T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116745882 | ||||||
| chr12:116745903
|
A | G | 1 | a0001c0001t0001g0211 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.84-3938A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116745903 | ||||||
| chr12:116746013
|
G | A | 232 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(229): Show | 232 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(229): Show |
intron_variant | MODIFIER | c.84-3828G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116746013 | ||||||
| chr12:116746028
|
G | A | 1 | a0001c0001t0003g0127 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.84-3813G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116746028 | ||||||
| chr12:116746186
|
G | A | 142 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(139): Show | 142 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.84-3655G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116746186 | ||||||
| chr12:116746193
|
C | T | 232 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(229): Show | 232 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(229): Show |
intron_variant | MODIFIER | c.84-3648C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116746193 | ||||||
| chr12:116746374
|
A | G | 2 | a0001c0001t0004g0172a0001c0001t0026g0181 | 2 | HG03831.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.84-3467A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116746374 | ||||||
| chr12:116746530
|
G | A | 3 | a0001c0001t0001g0237a0001c0001t0002g0236a0001c0001t0024g0147 | 3 | HG01261.hp1 HG01358.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.84-3311G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116746530 | ||||||
| chr12:116746587
|
C | G | 1 | a0001c0003t0035g0088 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.84-3254C>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116746587 | ||||||
| chr12:116746679
|
A | G | 232 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(229): Show | 232 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(229): Show |
intron_variant | MODIFIER | c.84-3162A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116746679 | ||||||
| chr12:116746775
|
G | A | 232 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(229): Show | 232 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(229): Show |
intron_variant | MODIFIER | c.84-3066G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116746775 | ||||||
| chr12:116746818
|
G | A | 2 | a0001c0005t0054g0021a0001c0015t0002g0020 | 2 | HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.84-3023G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116746818 | ||||||
| chr12:116746994
|
C | T | 3 | a0001c0001t0001g0122a0001c0001t0001g0166a0001c0002t0001g0111 | 3 | HG02004.hp2 HG02148.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.84-2847C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116746994 | ||||||
| chr12:116747145
|
C | T | 1 | a0001c0006t0036g0018 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.84-2696C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116747145 | ||||||
| chr12:116747482
|
T | G | 232 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(229): Show | 232 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(229): Show |
intron_variant | MODIFIER | c.84-2359T>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116747482 | ||||||
| chr12:116747624
|
G | A | 5 | a0001c0002t0066g0010a0001c0006t0050g0013a0001c0007t0025g0009others(2): Show | 5 | HG00741.hp1 HG01884.hp2 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.84-2217G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116747624 | ||||||
| chr12:116747764
|
C | T | 1 | a0001c0001t0056g0220 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.84-2077C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116747764 | ||||||
| chr12:116747842
|
G | A | 232 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(229): Show | 232 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(229): Show |
intron_variant | MODIFIER | c.84-1999G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116747842 | ||||||
| chr12:116747918
|
C | T | 1 | a0001c0009t0023g0026 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.84-1923C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116747918 | ||||||
| chr12:116747983
|
G | C | 5 | a0001c0002t0066g0010a0001c0006t0050g0013a0001c0007t0025g0009others(2): Show | 5 | HG00741.hp1 HG01884.hp2 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.84-1858G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116747983 | ||||||
| chr12:116748008
|
C | T | 231 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(228): Show | 231 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(228): Show |
intron_variant | MODIFIER | c.84-1833C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116748008 | ||||||
| chr12:116748104
|
C | T | 1 | a0001c0003t0006g0230 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.84-1737C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116748104 | ||||||
| chr12:116748171
|
C | T | 1 | a0001c0001t0056g0220 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.84-1670C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116748171 | ||||||
| chr12:116748207
|
A | G | 224 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(221): Show | 224 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(221): Show |
intron_variant | MODIFIER | c.84-1634A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116748207 | ||||||
| chr12:116748225
|
G | A | 230 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(227): Show | 230 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(227): Show |
intron_variant | MODIFIER | c.84-1616G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116748225 | ||||||
| chr12:116748311
|
G | A | 2 | a0002c0010t0002g0001a0002c0010t0002g0254 | 2 | HG02040.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.84-1530G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116748311 | ||||||
| chr12:116748428
|
A | G | 1 | a0001c0006t0005g0017 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.84-1413A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116748428 | ||||||
| chr12:116748444
|
A | G | 1 | a0001c0002t0005g0183 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.84-1397A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116748444 | ||||||
| chr12:116748511
|
A | G | 236 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(233): Show | 236 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(233): Show |
intron_variant | MODIFIER | c.84-1330A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116748511 | ||||||
| chr12:116748646
|
G | A | 1 | a0001c0001t0001g0069 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.84-1195G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116748646 | ||||||
| chr12:116748895
|
C | T | 1 | a0001c0006t0036g0018 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.84-946C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116748895 | ||||||
| chr12:116748923
|
C | T | 1 | a0001c0001t0007g0087 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.84-918C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116748923 | ||||||
| chr12:116748969
|
G | A | 1 | a0001c0009t0051g0016 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.84-872G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116748969 | ||||||
| chr12:116749253
|
T | C | 2 | a0001c0009t0010g0049a0001c0013t0013g0046 | 2 | HG01891.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.84-588T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116749253 | ||||||
| chr12:116749259
|
T | G | 8 | a0001c0001t0056g0220a0001c0004t0052g0015a0001c0005t0030g0051others(5): Show | 8 | HG00140.hp1 HG01891.hp1 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.84-582T>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116749259 | ||||||
| chr12:116749279
|
TCC | T | 30 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0002t0005g0064others(27): Show | 30 | HG00621.hp1 HG00741.hp1 HG01099.hp1 others(27): Show |
intron_variant | MODIFIER | c.84-555_84-554delCC | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 116749279 | |||||
| chr12:116749287
|
CA | C | 188 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(185): Show | 188 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(185): Show |
intron_variant | MODIFIER | c.84-553delA | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116749287 | ||||||
| chr12:116749288
|
A | C | 39 | a0001c0001t0001g0235a0001c0001t0002g0023a0001c0001t0002g0236others(36): Show | 39 | HG00423.hp1 HG01099.hp2 HG01169.hp1 others(36): Show |
intron_variant | MODIFIER | c.84-553A>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116749288 | ||||||
| chr12:116749334
|
G | A | 1 | a0001c0002t0018g0022 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.84-507G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116749334 | ||||||
| chr12:116749366
|
C | T | 227 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(224): Show | 227 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(224): Show |
intron_variant | MODIFIER | c.84-475C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116749366 | ||||||
| chr12:116749378
|
A | G | 13 | a0001c0001t0001g0141a0001c0001t0001g0190a0001c0001t0001g0193others(10): Show | 13 | HG00438.hp1 HG01257.hp2 HG01258.hp1 others(10): Show |
intron_variant | MODIFIER | c.84-463A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116749378 | ||||||
| chr12:116750390
|
T | C | 1 | a0001c0003t0035g0088 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.550+83T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116750390 | ||||||
| chr12:116750634
|
C | T | 1 | a0001c0001t0001g0190 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.550+327C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116750634 | ||||||
| chr12:116750660
|
C | T | 205 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(202): Show | 205 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(202): Show |
intron_variant | MODIFIER | c.550+353C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116750660 | ||||||
| chr12:116750754
|
C | G | 227 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(224): Show | 227 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(224): Show |
intron_variant | MODIFIER | c.550+447C>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116750754 | ||||||
| chr12:116750768
|
AAC | A | 9 | a0001c0001t0019g0124a0001c0001t0019g0163a0001c0001t0019g0187others(6): Show | 9 | HG00140.hp1 HG00741.hp1 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.550+465_550+466del others(2): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116750768 | |||||
| chr12:116750785
|
ATATG | A | 3 | a0001c0005t0030g0051a0001c0005t0030g0052a0001c0005t0070g0050 | 3 | HG01891.hp1 HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.550+480_550+483del others(4): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116750785 | |||||
| chr12:116750797
|
G | GTA | 4 | a0001c0001t0019g0124a0001c0001t0019g0163a0001c0001t0056g0220others(1): Show | 4 | HG00140.hp1 HG02055.hp2 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.550+501_550+502dup others(2): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116750797 | |||||
| chr12:116750797
|
G | GTATATAT others(99): Show |
4 | a0001c0001t0002g0031a0001c0001t0002g0032a0001c0001t0011g0033others(1): Show | 4 | HG02257.hp2 HG02559.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.550+522_550+523ins others(106): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116750797 | |||||
| chr12:116750799
|
A | ATATATAT others(140): Show |
1 | a0001c0004t0052g0015 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.550+500_550+501ins others(147): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116750799 | |||||
| chr12:116750799
|
A | ATATATAT others(119): Show |
3 | a0001c0001t0008g0028a0001c0001t0008g0029a0001c0001t0008g0040 | 3 | HG02572.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.550+522_550+523ins others(126): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116750799 | |||||
| chr12:116750808
|
TA | T | 9 | a0001c0001t0001g0146a0001c0001t0002g0234a0001c0001t0010g0233others(6): Show | 9 | HG01106.hp1 HG01243.hp1 HG02293.hp2 others(6): Show |
intron_variant | MODIFIER | c.550+503delA | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116750808 | |||||
| chr12:116750810
|
A | T | 13 | a0001c0001t0019g0124a0001c0001t0019g0163a0001c0001t0056g0220others(10): Show | 13 | HG00140.hp1 HG01074.hp2 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.550+503A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116750810 | ||||||
| chr12:116750811
|
TATATATA others(11): Show |
T | 2 | a0001c0001t0002g0045a0001c0001t0002g0048 | 2 | HG02976.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.550+513_550+530del others(18): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116750811 | |||||
| chr12:116750813
|
T | C | 2 | a0001c0006t0005g0017a0001c0006t0036g0018 | 2 | HG02486.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.550+506T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116750813 | ||||||
| chr12:116750813
|
TATATATT others(21): Show |
T | 4 | a0001c0005t0013g0006a0001c0007t0005g0062a0001c0007t0016g0061others(1): Show | 4 | HG01243.hp1 HG02970.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.550+507_550+534del others(28): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116750813 | ||||||
| chr12:116750819
|
T | A | 1 | a0001c0004t0052g0015 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.550+512T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116750819 | ||||||
| chr12:116750819
|
T | TTA | 6 | a0001c0003t0042g0229a0001c0003t0043g0228a0001c0007t0046g0053others(3): Show | 6 | HG02040.hp1 HG02132.hp2 HG02135.hp2 others(3): Show |
intron_variant | MODIFIER | c.550+521_550+522dup others(2): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116750819 | |||||
| chr12:116750819
|
T | TTATATAT others(59): Show |
1 | a0001c0006t0031g0067 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.550+522_550+523ins others(66): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116750819 | |||||
| chr12:116750819
|
T | TTATATAT others(83): Show |
2 | a0001c0002t0004g0005a0001c0002t0049g0004 | 2 | HG01243.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.550+522_550+523ins others(90): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116750819 | |||||
| chr12:116750819
|
T | TTATATAT others(109): Show |
1 | a0001c0016t0032g0044 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.550+522_550+523ins others(116): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116750819 | |||||
| chr12:116750820
|
T | A | 16 | a0001c0001t0019g0124a0001c0001t0019g0163a0001c0001t0040g0143others(13): Show | 16 | HG00140.hp1 HG01074.hp2 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.550+513T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116750820 | ||||||
| chr12:116750822
|
TATATATA | T | 8 | a0001c0001t0001g0260a0001c0001t0004g0095a0001c0001t0004g0096others(5): Show | 8 | HG01978.hp1 HG02155.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.550+523_550+529del others(7): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116750822 | |||||
| chr12:116750824
|
TATATA | T | 13 | a0001c0001t0001g0086a0001c0001t0001g0202a0001c0001t0001g0211others(10): Show | 13 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(10): Show |
intron_variant | MODIFIER | c.550+523_550+527del others(5): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116750824 | |||||
| chr12:116750824
|
TATATAAT others(20): Show |
T | 18 | a0001c0001t0001g0169a0001c0001t0001g0178a0001c0001t0002g0023others(15): Show | 18 | HG01192.hp2 HG02074.hp1 HG02523.hp2 others(15): Show |
intron_variant | MODIFIER | c.550+523_550+549del others(27): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116750824 | |||||
| chr12:116750826
|
TATA | T | 126 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0092others(123): Show | 126 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.550+523_550+525del others(3): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116750826 | |||||
| chr12:116750826
|
TATAATAT others(18): Show |
T | 10 | a0001c0001t0002g0236a0001c0002t0004g0268a0001c0002t0012g0014others(7): Show | 10 | HG01074.hp1 HG01169.hp2 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.550+523_550+547del others(25): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116750826 | |||||
| chr12:116750828
|
TA | T | 3 | a0001c0001t0024g0126a0001c0002t0015g0082a0001c0004t0012g0134 | 3 | HG03831.hp2 NA18993.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.550+523delA | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116750828 | |||||
| chr12:116750829
|
A | AT | 4 | a0001c0003t0014g0065a0001c0005t0030g0051a0001c0005t0030g0052others(1): Show | 4 | HG01891.hp1 HG02965.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.550+522_550+523ins others(1): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116750829 | ||||||
| chr12:116750829
|
A | G | 2 | a0001c0006t0005g0017a0001c0006t0036g0018 | 2 | HG02486.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.550+522A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116750829 | ||||||
| chr12:116750829
|
A | T | 13 | a0001c0001t0019g0124a0001c0001t0019g0163a0001c0001t0056g0220others(10): Show | 13 | HG00140.hp1 HG01074.hp2 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.550+522A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116750829 | ||||||
| chr12:116750829
|
AAT | A | 4 | a0001c0002t0018g0022a0001c0005t0054g0021a0001c0006t0050g0013others(1): Show | 4 | HG00741.hp1 HG02257.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.550+531_550+532del others(2): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116750829 | |||||
| chr12:116750830
|
A | T | 2 | a0001c0006t0005g0017a0001c0006t0036g0018 | 2 | HG02486.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.550+523A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116750830 | ||||||
| chr12:116750831
|
T | A | 2 | a0001c0006t0005g0017a0001c0006t0036g0018 | 2 | HG02486.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.550+524T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116750831 | ||||||
| chr12:116750831
|
T | C | 9 | a0001c0002t0005g0003a0001c0002t0005g0064a0001c0002t0008g0140others(6): Show | 9 | HG01074.hp2 HG01175.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.550+524T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116750831 | ||||||
| chr12:116750831
|
T | TA | 4 | a0001c0003t0014g0065a0001c0005t0030g0051a0001c0005t0030g0052others(1): Show | 4 | HG01891.hp1 HG02965.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.550+525dupA | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116750831 | |||||
| chr12:116750837
|
TATTATAT others(3): Show |
T | 23 | a0001c0001t0001g0141a0001c0001t0001g0190a0001c0001t0001g0193others(20): Show | 23 | HG00423.hp1 HG01099.hp2 HG01257.hp2 others(20): Show |
intron_variant | MODIFIER | c.550+531_550+540del others(10): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116750837 | ||||||
| chr12:116750839
|
T | A | 1 | a0001c0004t0052g0015 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.550+532T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116750839 | ||||||
| chr12:116750839
|
TTA | T | 4 | a0001c0001t0019g0124a0001c0001t0019g0163a0001c0001t0056g0220others(1): Show | 4 | HG00140.hp1 HG02055.hp2 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.550+543_550+544del others(2): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116750839 | |||||
| chr12:116750841
|
A | T | 2 | a0001c0001t0001g0260a0001c0001t0060g0090 | 2 | HG00609.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.550+534A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116750841 | ||||||
| chr12:116750841
|
ATATATAT others(2): Show |
A | 147 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(144): Show | 147 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(144): Show |
intron_variant | MODIFIER | c.550+535_550+543del others(9): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116750841 | ||||||
| chr12:116750842
|
T | C | 7 | a0001c0001t0038g0219a0001c0002t0018g0022a0001c0005t0054g0021others(4): Show | 7 | HG00741.hp1 HG01169.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.550+535T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116750842 | ||||||
| chr12:116750847
|
A | G | 11 | a0001c0002t0005g0003a0001c0002t0005g0064a0001c0002t0008g0140others(8): Show | 11 | HG01074.hp2 HG01175.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.550+540A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116750847 | ||||||
| chr12:116750848
|
TATA | T | 3 | a0001c0001t0002g0045a0001c0001t0002g0048a0001c0001t0002g0103 | 3 | HG02615.hp1 HG02976.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.550+545_550+547del others(3): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116750848 | |||||
| chr12:116750849
|
AT | A | 23 | a0001c0001t0001g0141a0001c0001t0001g0190a0001c0001t0001g0193others(20): Show | 23 | HG00423.hp1 HG01099.hp2 HG01257.hp2 others(20): Show |
intron_variant | MODIFIER | c.550+543delT | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116750849 | ||||||
| chr12:116750850
|
T | A | 3 | a0001c0005t0030g0051a0001c0005t0030g0052a0001c0005t0070g0050 | 3 | HG01891.hp1 HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.550+543T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116750850 | ||||||
| chr12:116750851
|
A | AAT | 7 | a0001c0002t0002g0030a0001c0002t0004g0005a0001c0002t0049g0004others(4): Show | 7 | HG01243.hp2 HG02040.hp1 HG02132.hp2 others(4): Show |
intron_variant | MODIFIER | c.550+551_550+552dup others(2): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116750851 | |||||
| chr12:116750851
|
A | AATATATA others(77): Show |
3 | a0001c0007t0025g0056a0001c0007t0046g0053a0001c0018t0055g0059 | 3 | HG02145.hp1 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.550+562_550+563ins others(84): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116750851 | |||||
| chr12:116750851
|
A | ATAAT | 7 | a0001c0001t0002g0031a0001c0001t0002g0032a0001c0001t0008g0028others(4): Show | 7 | HG02257.hp2 HG02572.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.550+544_550+545ins others(4): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116750851 | ||||||
| chr12:116750851
|
A | ATATATAT others(76): Show |
1 | a0001c0004t0001g0083 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.550+544_550+545ins others(83): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116750851 | ||||||
| chr12:116750851
|
A | C | 172 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(169): Show | 172 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(169): Show |
intron_variant | MODIFIER | c.550+544A>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116750851 | ||||||
| chr12:116750851
|
A | T | 8 | a0001c0001t0038g0219a0001c0002t0018g0022a0001c0005t0030g0051others(5): Show | 8 | HG00741.hp1 HG01169.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.550+544A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116750851 | ||||||
| chr12:116750852
|
ATATATAT others(22): Show |
A | 4 | a0001c0002t0018g0022a0001c0005t0054g0021a0001c0006t0050g0013others(1): Show | 4 | HG00741.hp1 HG02257.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.550+553_550+581del others(29): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116750852 | |||||
| chr12:116750858
|
A | G | 1 | a0001c0001t0038g0219 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.550+551A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116750858 | ||||||
| chr12:116750859
|
T | TATTATAT others(41): Show |
1 | a0001c0003t0014g0065 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.550+552_550+553ins others(48): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116750859 | ||||||
| chr12:116750859
|
TTATATAT others(25): Show |
T | 6 | a0001c0002t0005g0003a0001c0002t0005g0064a0001c0002t0008g0140others(3): Show | 6 | HG01175.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.550+553_550+584del others(32): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116750859 | ||||||
| chr12:116750860
|
T | A | 1 | a0001c0001t0038g0219 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.550+553T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116750860 | ||||||
| chr12:116750860
|
T | G | 2 | a0001c0006t0005g0017a0001c0006t0036g0018 | 2 | HG02486.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.550+553T>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116750860 | ||||||
| chr12:116750861
|
A | T | 3 | a0001c0001t0038g0219a0001c0006t0005g0017a0001c0006t0036g0018 | 3 | HG01169.hp1 HG02486.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.550+554A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116750861 | ||||||
| chr12:116750862
|
T | A | 3 | a0001c0001t0038g0219a0001c0006t0005g0017a0001c0006t0036g0018 | 3 | HG01169.hp1 HG02486.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.550+555T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116750862 | ||||||
| chr12:116750862
|
T | C | 40 | a0001c0001t0001g0169a0001c0001t0001g0178a0001c0001t0002g0023others(37): Show | 40 | HG00140.hp1 HG01074.hp1 HG01169.hp2 others(37): Show |
intron_variant | MODIFIER | c.550+555T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116750862 | ||||||
| chr12:116750867
|
A | G | 173 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(170): Show | 173 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(170): Show |
intron_variant | MODIFIER | c.550+560A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116750867 | ||||||
| chr12:116750870
|
TA | T | 3 | a0001c0001t0038g0219a0001c0003t0002g0100a0001c0003t0002g0101 | 3 | HG01074.hp2 HG01169.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.550+565delA | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116750870 | |||||
| chr12:116750871
|
A | T | 42 | a0001c0001t0001g0169a0001c0001t0001g0178a0001c0001t0002g0023others(39): Show | 42 | HG00140.hp1 HG01074.hp1 HG01169.hp2 others(39): Show |
intron_variant | MODIFIER | c.550+564A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116750871 | ||||||
| chr12:116750874
|
ATATATAT | A | 3 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0007g0231 | 3 | HG00741.hp2 HG01106.hp2 NA18974.hp2 |
intron_variant | MODIFIER | c.550+575_550+581del others(7): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116750874 | |||||
| chr12:116750875
|
TATATATT others(9): Show |
T | 3 | a0001c0001t0001g0235a0001c0001t0003g0242a0001c0002t0067g0042 | 3 | HG00423.hp2 HG01257.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.550+575_550+590del others(16): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116750875 | |||||
| chr12:116750876
|
ATATAT | A | 7 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0203others(4): Show | 7 | HG00438.hp1 HG02080.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.550+575_550+579del others(5): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116750876 | |||||
| chr12:116750877
|
TATATTAT others(7): Show |
T | 91 | a0001c0001t0001g0092a0001c0001t0001g0120a0001c0001t0001g0135others(88): Show | 91 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(88): Show |
intron_variant | MODIFIER | c.550+575_550+588del others(14): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116750877 | |||||
| chr12:116750878
|
A | G | 42 | a0001c0001t0001g0169a0001c0001t0001g0178a0001c0001t0002g0023others(39): Show | 42 | HG00140.hp1 HG01074.hp1 HG01074.hp2 others(39): Show |
intron_variant | MODIFIER | c.550+571A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116750878 | ||||||
| chr12:116750878
|
ATAT | A | 3 | a0001c0001t0004g0095a0001c0001t0004g0145a0001c0012t0001g0123 | 3 | HG01175.hp1 HG02155.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.550+575_550+577del others(3): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116750878 | |||||
| chr12:116750879
|
TATTATAT others(5): Show |
T | 6 | a0001c0001t0002g0133a0001c0001t0003g0127a0001c0001t0003g0155others(3): Show | 6 | HG00408.hp2 HG02155.hp2 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.550+575_550+586del others(12): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116750879 | |||||
| chr12:116750881
|
T | A | 2 | a0001c0006t0005g0017a0001c0006t0036g0018 | 2 | HG02486.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.550+574T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116750881 | ||||||
| chr12:116750881
|
T | TTA | 5 | a0001c0004t0001g0083a0001c0006t0031g0067a0001c0007t0025g0056others(2): Show | 5 | HG02145.hp1 HG02451.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.550+583_550+584dup others(2): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116750881 | |||||
| chr12:116750881
|
T | TTATA | 15 | a0001c0001t0002g0031a0001c0001t0002g0032a0001c0001t0008g0028others(12): Show | 15 | HG01243.hp2 HG01891.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.550+581_550+584dup others(4): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116750881 | |||||
| chr12:116750881
|
T | TTATATAT others(79): Show |
2 | a0001c0002t0001g0066a0003c0017t0006g0060 | 2 | HG02258.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.550+594_550+595ins others(86): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116750881 | |||||
| chr12:116750881
|
T | TTATATAT others(101): Show |
1 | a0001c0004t0001g0091 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.550+584_550+585ins others(108): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116750881 | |||||
| chr12:116750881
|
T | TTATATAT others(81): Show |
4 | a0001c0003t0006g0054a0001c0004t0026g0201a0001c0004t0029g0055others(1): Show | 4 | HG00140.hp2 HG02738.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.550+584_550+585ins others(88): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116750881 | |||||
| chr12:116750881
|
T | TTATATAT others(61): Show |
3 | a0001c0003t0006g0230a0001c0003t0042g0229a0001c0003t0043g0228 | 3 | NA18956.hp2 NA18975.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.550+584_550+585ins others(68): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116750881 | |||||
| chr12:116750881
|
T | TTATATAT others(83): Show |
1 | a0001c0006t0006g0218 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.550+584_550+585ins others(90): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116750881 | |||||
| chr12:116750881
|
T | TTATATAT others(143): Show |
2 | a0002c0010t0002g0001a0002c0010t0002g0254 | 2 | HG02040.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.550+584_550+585ins others(150): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116750881 | |||||
| chr12:116750881
|
T | TTATATAT others(116): Show |
1 | a0002c0010t0002g0002 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.550+584_550+585ins others(123): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116750881 | |||||
| chr12:116750881
|
T | TTATATAT others(79): Show |
2 | a0001c0004t0002g0025a0001c0004t0068g0024 | 2 | HG02055.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.550+584_550+585ins others(86): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116750881 | |||||
| chr12:116750881
|
T | TTATATAT others(79): Show |
1 | a0001c0007t0025g0009 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.550+584_550+585ins others(86): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116750881 | |||||
| chr12:116750881
|
T | TTATATAT others(114): Show |
1 | a0001c0003t0002g0247 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.550+584_550+585ins others(121): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116750881 | |||||
| chr12:116750881
|
T | TTATATAT others(112): Show |
1 | a0001c0004t0001g0113 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.550+584_550+585ins others(119): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116750881 | |||||
| chr12:116750881
|
TTATATAT others(3): Show |
T | 60 | a0001c0001t0001g0086a0001c0001t0001g0094a0001c0001t0001g0122others(57): Show | 60 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(57): Show |
intron_variant | MODIFIER | c.550+575_550+584del others(10): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116750881 | ||||||
| chr12:116750882
|
T | A | 37 | a0001c0001t0001g0169a0001c0001t0001g0178a0001c0001t0002g0023others(34): Show | 37 | HG01074.hp1 HG01074.hp2 HG01169.hp2 others(34): Show |
intron_variant | MODIFIER | c.550+575T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116750882 | ||||||
| chr12:116750887
|
A | G | 4 | a0001c0002t0018g0022a0001c0005t0054g0021a0001c0006t0050g0013others(1): Show | 4 | HG00741.hp1 HG02257.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.550+580A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116750887 | ||||||
| chr12:116750888
|
TATA | T | 11 | a0001c0001t0002g0103a0001c0001t0002g0236a0001c0001t0007g0171others(8): Show | 11 | HG01074.hp1 HG01243.hp1 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.550+585_550+587del others(3): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116750888 | |||||
| chr12:116750890
|
TA | T | 40 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0169others(37): Show | 40 | HG00438.hp1 HG00741.hp2 HG01074.hp2 others(37): Show |
intron_variant | MODIFIER | c.550+585delA | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116750890 | |||||
| chr12:116750891
|
A | AT | 7 | a0001c0001t0019g0124a0001c0001t0019g0163a0001c0001t0019g0187others(4): Show | 7 | HG00140.hp1 HG01261.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.550+584_550+585ins others(1): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116750891 | ||||||
| chr12:116750899
|
TA | T | 12 | a0001c0001t0001g0141a0001c0001t0001g0190a0001c0001t0001g0193others(9): Show | 12 | HG00140.hp1 HG01099.hp2 HG01258.hp1 others(9): Show |
intron_variant | MODIFIER | c.550+593delA | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116750899 | ||||||
| chr12:116750900
|
A | T | 4 | a0001c0005t0013g0006a0001c0007t0005g0062a0001c0007t0016g0061others(1): Show | 4 | HG01243.hp1 HG02970.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.550+593A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116750900 | ||||||
| chr12:116750901
|
TA | T | 15 | a0001c0002t0001g0074a0001c0002t0001g0076a0001c0002t0001g0077others(12): Show | 15 | HG00423.hp1 HG01074.hp2 HG02071.hp1 others(12): Show |
intron_variant | MODIFIER | c.550+595delA | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116750901 | ||||||
| chr12:116750902
|
A | T | 23 | a0001c0001t0001g0141a0001c0001t0001g0190a0001c0001t0001g0193others(20): Show | 23 | HG00140.hp1 HG01099.hp2 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.550+595A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116750902 | ||||||
| chr12:116750903
|
TA | T | 3 | a0001c0002t0001g0073a0001c0002t0062g0185a0001c0003t0021g0038 | 3 | HG01169.hp2 HG02965.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.550+597delA | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116750903 | ||||||
| chr12:116750904
|
A | AT | 4 | a0001c0001t0001g0256a0001c0001t0002g0192a0001c0001t0002g0210others(1): Show | 4 | HG02273.hp2 NA18955.hp2 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.550+598dupT | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116750904 | |||||
| chr12:116750904
|
A | T | 41 | a0001c0001t0001g0141a0001c0001t0001g0190a0001c0001t0001g0193others(38): Show | 41 | HG00140.hp1 HG00423.hp1 HG01074.hp2 others(38): Show |
intron_variant | MODIFIER | c.550+597A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116750904 | ||||||
| chr12:116750905
|
TA | T | 28 | a0001c0001t0002g0034a0001c0001t0002g0045a0001c0001t0002g0048others(25): Show | 28 | HG00438.hp1 HG01884.hp1 HG02148.hp2 others(25): Show |
intron_variant | MODIFIER | c.550+599delA | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116750905 | ||||||
| chr12:116750906
|
A | AT | 22 | a0001c0001t0001g0122a0001c0001t0001g0146a0001c0001t0001g0194others(19): Show | 22 | HG00544.hp2 HG00609.hp1 HG00673.hp2 others(19): Show |
intron_variant | MODIFIER | c.550+600dupT | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116750906 | |||||
| chr12:116750906
|
A | T | 52 | a0001c0001t0001g0141a0001c0001t0001g0190a0001c0001t0001g0193others(49): Show | 52 | HG00140.hp1 HG00423.hp1 HG00741.hp2 others(49): Show |
intron_variant | MODIFIER | c.550+599A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116750906 | ||||||
| chr12:116750907
|
TA | T | 62 | a0001c0001t0001g0072a0001c0001t0001g0092a0001c0001t0001g0120others(59): Show | 62 | HG00408.hp2 HG00609.hp2 HG00673.hp1 others(59): Show |
intron_variant | MODIFIER | c.550+601delA | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116750907 | ||||||
| chr12:116750908
|
A | AT | 27 | a0001c0001t0001g0086a0001c0001t0001g0094a0001c0001t0001g0198others(24): Show | 27 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(24): Show |
intron_variant | MODIFIER | c.550+610dupT | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116750908 | |||||
| chr12:116750908
|
A | T | 112 | a0001c0001t0001g0122a0001c0001t0001g0141a0001c0001t0001g0146others(109): Show | 112 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.550+601A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116750908 | ||||||
| chr12:116750908
|
AT | A | 10 | a0001c0001t0001g0069a0001c0001t0002g0236a0001c0001t0003g0106others(7): Show | 10 | HG00621.hp2 HG01106.hp1 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.550+610delT | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116750908 | |||||
| chr12:116750908
|
ATTT | A | 22 | a0001c0001t0001g0169a0001c0001t0001g0178a0001c0001t0002g0023others(19): Show | 22 | HG01192.hp2 HG02074.hp1 HG02155.hp1 others(19): Show |
intron_variant | MODIFIER | c.550+608_550+610del others(3): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116750908 | |||||
| chr12:116750926
|
G | T | 3 | a0001c0005t0030g0051a0001c0005t0030g0052a0001c0005t0070g0050 | 3 | HG01891.hp1 HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.550+619G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116750926 | ||||||
| chr12:116751004
|
C | T | 3 | a0001c0003t0002g0100a0001c0003t0002g0101a0001c0003t0002g0102 | 3 | HG01074.hp2 HG02280.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.550+697C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116751004 | ||||||
| chr12:116751018
|
T | G | 228 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(225): Show | 228 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(225): Show |
intron_variant | MODIFIER | c.550+711T>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116751018 | ||||||
| chr12:116751075
|
C | T | 3 | a0001c0003t0002g0100a0001c0003t0002g0101a0001c0003t0002g0102 | 3 | HG01074.hp2 HG02280.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.550+768C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116751075 | ||||||
| chr12:116751131
|
G | T | 7 | a0001c0002t0004g0005a0001c0002t0049g0004a0001c0003t0014g0065others(4): Show | 7 | HG01243.hp2 HG01891.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.550+824G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116751131 | ||||||
| chr12:116751223
|
T | C | 1 | a0001c0016t0032g0044 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.550+916T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116751223 | ||||||
| chr12:116751408
|
G | A | 1 | a0001c0003t0035g0088 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.550+1101G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116751408 | ||||||
| chr12:116751421
|
G | A | 3 | a0001c0005t0030g0051a0001c0005t0030g0052a0001c0005t0070g0050 | 3 | HG01891.hp1 HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.550+1114G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116751421 | ||||||
| chr12:116751466
|
C | T | 2 | a0001c0001t0004g0168a0001c0001t0004g0170 | 2 | HG02683.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.550+1159C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116751466 | ||||||
| chr12:116751593
|
C | T | 1 | a0001c0001t0004g0110 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.550+1286C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116751593 | ||||||
| chr12:116751648
|
G | A | 24 | a0001c0001t0001g0169a0001c0001t0001g0178a0001c0001t0002g0023others(21): Show | 24 | HG01192.hp2 HG02074.hp1 HG02155.hp1 others(21): Show |
intron_variant | MODIFIER | c.550+1341G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116751648 | ||||||
| chr12:116751681
|
G | A | 228 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(225): Show | 228 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(225): Show |
intron_variant | MODIFIER | c.550+1374G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116751681 | ||||||
| chr12:116751836
|
G | A | 68 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(65): Show | 68 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.550+1529G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116751836 | ||||||
| chr12:116751846
|
A | G | 1 | a0001c0001t0040g0143 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.550+1539A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116751846 | ||||||
| chr12:116751927
|
T | C | 228 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(225): Show | 228 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(225): Show |
intron_variant | MODIFIER | c.550+1620T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116751927 | ||||||
| chr12:116752045
|
A | C | 17 | a0001c0002t0005g0003a0001c0002t0005g0064a0001c0002t0008g0140others(14): Show | 17 | HG00741.hp1 HG01074.hp2 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.550+1738A>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116752045 | ||||||
| chr12:116752051
|
T | C | 4 | a0001c0005t0013g0006a0001c0007t0005g0062a0001c0007t0016g0061others(1): Show | 4 | HG01243.hp1 HG02970.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.550+1744T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116752051 | ||||||
| chr12:116752079
|
G | A | 5 | a0001c0001t0019g0124a0001c0001t0019g0163a0001c0001t0019g0187others(2): Show | 5 | HG00140.hp1 HG01261.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.550+1772G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116752079 | ||||||
| chr12:116752137
|
G | T | 3 | a0002c0010t0002g0001a0002c0010t0002g0002a0002c0010t0002g0254 | 3 | HG02040.hp1 HG02132.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.550+1830G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116752137 | ||||||
| chr12:116752196
|
AAG | A | 228 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(225): Show | 228 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(225): Show |
intron_variant | MODIFIER | c.551-1776_551-1775d others(4): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116752196 | |||||
| chr12:116752217
|
G | A | 1 | a0001c0002t0002g0129 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.551-1767G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116752217 | ||||||
| chr12:116752359
|
T | C | 1 | a0001c0003t0035g0088 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.551-1625T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116752359 | ||||||
| chr12:116752445
|
G | A | 27 | a0001c0001t0001g0169a0001c0001t0001g0178a0001c0001t0002g0023others(24): Show | 27 | HG01192.hp2 HG02074.hp1 HG02155.hp1 others(24): Show |
intron_variant | MODIFIER | c.551-1539G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116752445 | ||||||
| chr12:116752455
|
T | G | 2 | a0001c0001t0001g0146a0001c0001t0001g0217 | 2 | HG02293.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.551-1529T>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116752455 | ||||||
| chr12:116752595
|
C | A | 225 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(222): Show | 225 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(222): Show |
intron_variant | MODIFIER | c.551-1389C>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116752595 | ||||||
| chr12:116752652
|
C | T | 27 | a0001c0001t0001g0169a0001c0001t0001g0178a0001c0001t0002g0023others(24): Show | 27 | HG01192.hp2 HG02074.hp1 HG02155.hp1 others(24): Show |
intron_variant | MODIFIER | c.551-1332C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116752652 | ||||||
| chr12:116752808
|
G | C | 6 | a0001c0001t0001g0169a0001c0001t0004g0110a0001c0001t0004g0168others(3): Show | 6 | HG02683.hp2 HG03239.hp2 HG03688.hp1 others(3): Show |
intron_variant | MODIFIER | c.551-1176G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116752808 | ||||||
| chr12:116753104
|
T | A | 1 | a0001c0009t0023g0026 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.551-880T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116753104 | ||||||
| chr12:116753110
|
A | ATGGCGTT others(1): Show |
3 | a0002c0010t0002g0001a0002c0010t0002g0002a0002c0010t0002g0254 | 3 | HG02040.hp1 HG02132.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.551-872_551-865dup others(8): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116753110 | |||||
| chr12:116753124
|
T | G | 10 | a0001c0001t0002g0034a0001c0001t0002g0103a0001c0001t0002g0104others(7): Show | 10 | HG01891.hp2 HG02280.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.551-860T>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116753124 | ||||||
| chr12:116753142
|
CTTTTTCT others(5): Show |
C | 2 | a0001c0002t0005g0064a0001c0011t0039g0012 | 2 | HG02486.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.551-836_551-825del others(12): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116753142 | |||||
| chr12:116753148
|
C | CT | 144 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(141): Show | 144 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(141): Show |
intron_variant | MODIFIER | c.551-816dupT | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116753148 | |||||
| chr12:116753148
|
C | CTT | 29 | a0001c0001t0002g0236a0001c0001t0004g0095a0001c0001t0004g0096others(26): Show | 29 | HG00741.hp1 HG01074.hp1 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.551-817_551-816dup others(2): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116753148 | |||||
| chr12:116753148
|
CTTTTTTT others(4): Show |
C | 3 | a0001c0003t0002g0100a0001c0003t0002g0101a0001c0003t0002g0102 | 3 | HG01074.hp2 HG02280.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.551-826_551-816del others(11): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116753148 | |||||
| chr12:116753152
|
T | TTC | 25 | a0001c0001t0001g0092a0001c0001t0001g0135a0001c0001t0001g0166others(22): Show | 25 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.551-831_551-830ins others(2): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116753152 | |||||
| chr12:116753153
|
T | TC | 12 | a0001c0001t0001g0207a0001c0001t0002g0133a0001c0001t0002g0175others(9): Show | 12 | HG00408.hp2 HG02155.hp2 HG02523.hp1 others(9): Show |
intron_variant | MODIFIER | c.551-831_551-830ins others(1): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116753153 | ||||||
| chr12:116753182
|
G | A | 2 | a0001c0001t0002g0236a0001c0002t0012g0014 | 2 | HG01261.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.551-802G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116753182 | ||||||
| chr12:116753220
|
A | G | 4 | a0001c0005t0013g0006a0001c0007t0005g0062a0001c0007t0016g0061others(1): Show | 4 | HG01243.hp1 HG02970.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.551-764A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116753220 | ||||||
| chr12:116753293
|
G | A | 1 | a0001c0002t0018g0022 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.551-691G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116753293 | ||||||
| chr12:116753403
|
G | A | 3 | a0001c0001t0004g0095a0001c0001t0004g0096a0001c0001t0004g0145 | 3 | HG02155.hp1 HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.551-581G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116753403 | ||||||
| chr12:116753408
|
C | T | 3 | a0001c0003t0002g0100a0001c0003t0002g0101a0001c0003t0002g0102 | 3 | HG01074.hp2 HG02280.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.551-576C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116753408 | ||||||
| chr12:116753414
|
G | A | 26 | a0001c0001t0001g0169a0001c0001t0002g0023a0001c0001t0004g0095others(23): Show | 26 | HG01192.hp2 HG02074.hp1 HG02155.hp1 others(23): Show |
intron_variant | MODIFIER | c.551-570G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116753414 | ||||||
| chr12:116753477
|
T | C | 4 | a0001c0005t0013g0006a0001c0007t0005g0062a0001c0007t0016g0061others(1): Show | 4 | HG01243.hp1 HG02970.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.551-507T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116753477 | ||||||
| chr12:116753654
|
G | A | 247 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(244): Show | 247 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(244): Show |
intron_variant | MODIFIER | c.551-330G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116753654 | ||||||
| chr12:116753657
|
G | A | 2 | a0001c0002t0062g0185a0001c0002t0063g0263 | 2 | HG01169.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.551-327G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116753657 | ||||||
| chr12:116753862
|
T | A | 7 | a0001c0001t0002g0031a0001c0001t0002g0032a0001c0001t0008g0028others(4): Show | 7 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.551-122T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116753862 | ||||||
| chr12:116753888
|
G | A | 1 | a0001c0001t0024g0147 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.551-96G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116753888 | ||||||
| chr12:116754308
|
T | G | 1 | a0001c0001t0008g0041 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.627+248T>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116754308 | ||||||
| chr12:116754322
|
C | T | 219 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(216): Show | 219 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(216): Show |
intron_variant | MODIFIER | c.627+262C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116754322 | ||||||
| chr12:116754339
|
A | G | 1 | a0001c0001t0002g0045 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.627+279A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116754339 | ||||||
| chr12:116754572
|
C | G | 1 | a0001c0001t0001g0092 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.627+512C>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116754572 | ||||||
| chr12:116754916
|
T | C | 2 | a0001c0002t0005g0064a0001c0011t0039g0012 | 2 | HG02486.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.627+856T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116754916 | ||||||
| chr12:116755245
|
T | C | 219 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(216): Show | 219 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(216): Show |
intron_variant | MODIFIER | c.627+1185T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116755245 | ||||||
| chr12:116755284
|
T | C | 1 | a0001c0001t0019g0163 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.627+1224T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116755284 | ||||||
| chr12:116755334
|
A | G | 1 | a0001c0001t0045g0114 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.627+1274A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116755334 | ||||||
| chr12:116755369
|
T | TA | 3 | a0001c0001t0001g0205a0001c0006t0005g0017a0001c0006t0050g0013 | 3 | HG00741.hp1 HG02486.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.627+1309_627+1310i others(3): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116755369 | ||||||
| chr12:116755370
|
T | A | 233 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(230): Show | 233 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(230): Show |
intron_variant | MODIFIER | c.627+1310T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116755370 | ||||||
| chr12:116755371
|
T | A | 3 | a0001c0001t0004g0095a0001c0001t0004g0096a0001c0001t0004g0145 | 3 | HG02155.hp1 HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.627+1311T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116755371 | ||||||
| chr12:116755408
|
C | T | 219 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(216): Show | 219 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(216): Show |
intron_variant | MODIFIER | c.627+1348C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116755408 | ||||||
| chr12:116755518
|
C | G | 220 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(217): Show | 220 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(217): Show |
intron_variant | MODIFIER | c.627+1458C>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116755518 | ||||||
| chr12:116755946
|
C | T | 3 | a0001c0001t0008g0041a0001c0001t0045g0114a0001c0009t0051g0016 | 3 | HG02976.hp2 HG03041.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.627+1886C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116755946 | ||||||
| chr12:116756054
|
T | C | 5 | a0001c0001t0019g0124a0001c0001t0019g0163a0001c0001t0019g0187others(2): Show | 5 | HG00140.hp1 HG01261.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.627+1994T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116756054 | ||||||
| chr12:116756284
|
C | T | 8 | a0001c0002t0005g0003a0001c0002t0005g0064a0001c0003t0002g0100others(5): Show | 8 | HG01074.hp2 HG01175.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.627+2224C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116756284 | ||||||
| chr12:116756285
|
G | A | 4 | a0001c0001t0009g0116a0001c0001t0009g0130a0001c0001t0009g0153others(1): Show | 4 | HG01109.hp2 HG01258.hp2 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.627+2225G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116756285 | ||||||
| chr12:116756306
|
G | GT | 8 | a0001c0003t0006g0165a0001c0005t0013g0006a0001c0005t0030g0051others(5): Show | 8 | HG01243.hp1 HG01891.hp1 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.627+2255dupT | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 116756306 | |||||
| chr12:116756306
|
GT | G | 5 | a0001c0001t0019g0124a0001c0001t0019g0163a0001c0001t0019g0187others(2): Show | 5 | HG00140.hp1 HG01261.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.627+2255delT | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 116756306 | |||||
| chr12:116756309
|
T | TTTTTTTG | 23 | a0001c0001t0001g0141a0001c0001t0001g0190a0001c0001t0001g0193others(20): Show | 23 | HG00423.hp1 HG00423.hp2 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.627+2268_627+2274d others(9): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 116756309 | |||||
| chr12:116756311
|
T | A | 5 | a0001c0001t0019g0124a0001c0001t0019g0163a0001c0001t0019g0187others(2): Show | 5 | HG00140.hp1 HG01261.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.627+2251T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116756311 | ||||||
| chr12:116756366
|
T | C | 3 | a0002c0010t0002g0001a0002c0010t0002g0002a0002c0010t0002g0254 | 3 | HG02040.hp1 HG02132.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.627+2306T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116756366 | ||||||
| chr12:116756385
|
G | A | 13 | a0001c0001t0019g0124a0001c0001t0019g0163a0001c0001t0019g0187others(10): Show | 13 | HG00140.hp1 HG00741.hp1 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.627+2325G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116756385 | ||||||
| chr12:116756492
|
A | T | 1 | a0001c0001t0004g0168 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.627+2432A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116756492 | ||||||
| chr12:116756520
|
G | A | 4 | a0001c0005t0013g0006a0001c0007t0005g0062a0001c0007t0016g0061others(1): Show | 4 | HG01243.hp1 HG02970.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.627+2460G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116756520 | ||||||
| chr12:116756539
|
G | C | 11 | a0001c0001t0002g0034a0001c0001t0002g0103a0001c0001t0002g0104others(8): Show | 11 | HG01106.hp1 HG01891.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.627+2479G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116756539 | ||||||
| chr12:116756713
|
T | C | 5 | a0001c0001t0019g0124a0001c0001t0019g0163a0001c0001t0019g0187others(2): Show | 5 | HG00140.hp1 HG01261.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.627+2653T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116756713 | ||||||
| chr12:116756722
|
C | T | 221 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(218): Show | 221 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(218): Show |
intron_variant | MODIFIER | c.627+2662C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116756722 | ||||||
| chr12:116756833
|
C | A | 1 | a0001c0003t0035g0088 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.627+2773C>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116756833 | ||||||
| chr12:116756847
|
T | C | 5 | a0001c0002t0005g0003a0001c0002t0005g0064a0001c0011t0023g0007others(2): Show | 5 | HG01175.hp2 HG02486.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.627+2787T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116756847 | ||||||
| chr12:116756870
|
T | C | 3 | a0001c0003t0002g0100a0001c0003t0002g0101a0001c0003t0002g0102 | 3 | HG01074.hp2 HG02280.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.627+2810T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116756870 | ||||||
| chr12:116756981
|
A | T | 246 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(243): Show | 246 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(243): Show |
intron_variant | MODIFIER | c.627+2921A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116756981 | ||||||
| chr12:116757091
|
A | G | 3 | a0001c0001t0001g0072a0001c0001t0001g0224a0001c0001t0010g0222 | 3 | HG03834.hp1 NA18955.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.627+3031A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116757091 | ||||||
| chr12:116757392
|
A | G | 221 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(218): Show | 221 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(218): Show |
intron_variant | MODIFIER | c.627+3332A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116757392 | ||||||
| chr12:116757402
|
G | A | 3 | a0001c0003t0002g0100a0001c0003t0002g0101a0001c0003t0002g0102 | 3 | HG01074.hp2 HG02280.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.627+3342G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116757402 | ||||||
| chr12:116757413
|
G | A | 221 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(218): Show | 221 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(218): Show |
intron_variant | MODIFIER | c.627+3353G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116757413 | ||||||
| chr12:116757579
|
T | C | 221 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(218): Show | 221 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(218): Show |
intron_variant | MODIFIER | c.627+3519T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116757579 | ||||||
| chr12:116757583
|
A | G | 27 | a0001c0001t0001g0169a0001c0001t0001g0178a0001c0001t0002g0023others(24): Show | 27 | HG01192.hp2 HG02074.hp1 HG02155.hp1 others(24): Show |
intron_variant | MODIFIER | c.627+3523A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116757583 | ||||||
| chr12:116757838
|
C | T | 1 | a0001c0002t0018g0022 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.627+3778C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116757838 | ||||||
| chr12:116757995
|
G | A | 5 | a0001c0001t0019g0124a0001c0001t0019g0163a0001c0001t0019g0187others(2): Show | 5 | HG00140.hp1 HG01261.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.627+3935G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116757995 | ||||||
| chr12:116758083
|
C | T | 1 | a0001c0001t0001g0197 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.627+4023C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116758083 | ||||||
| chr12:116758293
|
A | C | 27 | a0001c0001t0001g0169a0001c0001t0001g0178a0001c0001t0002g0023others(24): Show | 27 | HG01192.hp2 HG02074.hp1 HG02155.hp1 others(24): Show |
intron_variant | MODIFIER | c.627+4233A>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116758293 | ||||||
| chr12:116758300
|
C | T | 1 | a0001c0006t0005g0017 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.627+4240C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116758300 | ||||||
| chr12:116758314
|
A | G | 181 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(178): Show | 181 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(178): Show |
intron_variant | MODIFIER | c.627+4254A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116758314 | ||||||
| chr12:116758570
|
C | T | 4 | a0001c0001t0002g0031a0001c0001t0002g0032a0001c0001t0011g0033others(1): Show | 4 | HG02257.hp2 HG02559.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.627+4510C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116758570 | ||||||
| chr12:116758700
|
A | G | 1 | a0001c0001t0002g0133 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.627+4640A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116758700 | ||||||
| chr12:116758701
|
G | A | 8 | a0001c0002t0002g0129a0001c0002t0005g0149a0001c0002t0005g0151others(5): Show | 8 | HG02109.hp1 HG02258.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.627+4641G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116758701 | ||||||
| chr12:116758716
|
G | C | 221 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(218): Show | 221 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(218): Show |
intron_variant | MODIFIER | c.627+4656G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116758716 | ||||||
| chr12:116758774
|
G | T | 221 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(218): Show | 221 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(218): Show |
intron_variant | MODIFIER | c.627+4714G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116758774 | ||||||
| chr12:116758780
|
C | T | 1 | a0001c0014t0018g0019 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.627+4720C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116758780 | ||||||
| chr12:116758937
|
T | A | 27 | a0001c0001t0001g0169a0001c0001t0001g0178a0001c0001t0002g0023others(24): Show | 27 | HG01192.hp2 HG02074.hp1 HG02155.hp1 others(24): Show |
intron_variant | MODIFIER | c.627+4877T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116758937 | ||||||
| chr12:116759096
|
A | G | 14 | a0001c0001t0019g0124a0001c0001t0019g0163a0001c0001t0019g0187others(11): Show | 14 | HG00140.hp1 HG00741.hp1 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.627+5036A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116759096 | ||||||
| chr12:116759153
|
G | C | 3 | a0001c0003t0002g0100a0001c0003t0002g0101a0001c0003t0002g0102 | 3 | HG01074.hp2 HG02280.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.627+5093G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116759153 | ||||||
| chr12:116759284
|
C | T | 1 | a0001c0001t0004g0095 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.627+5224C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116759284 | ||||||
| chr12:116759414
|
T | A | 14 | a0001c0001t0019g0124a0001c0001t0019g0163a0001c0001t0019g0187others(11): Show | 14 | HG00140.hp1 HG00741.hp1 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.627+5354T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116759414 | ||||||
| chr12:116759499
|
C | T | 27 | a0001c0001t0001g0169a0001c0001t0001g0178a0001c0001t0002g0023others(24): Show | 27 | HG01192.hp2 HG02074.hp1 HG02155.hp1 others(24): Show |
intron_variant | MODIFIER | c.627+5439C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116759499 | ||||||
| chr12:116759732
|
C | T | 1 | a0001c0002t0002g0174 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.627+5672C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116759732 | ||||||
| chr12:116759756
|
A | G | 243 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(240): Show | 243 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(240): Show |
intron_variant | MODIFIER | c.627+5696A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116759756 | ||||||
| chr12:116759797
|
T | C | 2 | a0001c0006t0005g0017a0001c0014t0018g0019 | 2 | HG01106.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.627+5737T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116759797 | ||||||
| chr12:116759892
|
G | A | 1 | a0001c0001t0001g0094 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.627+5832G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116759892 | ||||||
| chr12:116759921
|
T | A | 1 | a0001c0001t0002g0023 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.627+5861T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116759921 | ||||||
| chr12:116759941
|
C | T | 1 | a0001c0001t0071g0119 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.627+5881C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116759941 | ||||||
| chr12:116760011
|
C | T | 1 | a0001c0005t0020g0162 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.627+5951C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116760011 | ||||||
| chr12:116760044
|
A | G | 246 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(243): Show | 246 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(243): Show |
intron_variant | MODIFIER | c.627+5984A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116760044 | ||||||
| chr12:116760164
|
C | T | 2 | a0001c0001t0001g0146a0001c0001t0001g0217 | 2 | HG02293.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.627+6104C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116760164 | ||||||
| chr12:116760332
|
G | C | 1 | a0001c0004t0052g0015 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.627+6272G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116760332 | ||||||
| chr12:116760421
|
G | A | 1 | a0001c0002t0004g0268 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.627+6361G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116760421 | ||||||
| chr12:116760449
|
T | C | 1 | a0001c0001t0008g0041 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.628-6365T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116760449 | ||||||
| chr12:116760495
|
G | T | 4 | a0001c0002t0005g0003a0001c0002t0005g0064a0001c0011t0023g0007others(1): Show | 4 | HG01175.hp2 HG02486.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.628-6319G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116760495 | ||||||
| chr12:116760846
|
C | T | 1 | a0001c0011t0053g0011 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.628-5968C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116760846 | ||||||
| chr12:116760966
|
A | G | 1 | a0001c0001t0045g0114 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.628-5848A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116760966 | ||||||
| chr12:116760998
|
C | T | 3 | a0001c0007t0025g0056a0001c0007t0046g0053a0001c0018t0055g0059 | 3 | HG02145.hp1 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.628-5816C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116760998 | ||||||
| chr12:116761020
|
G | A | 4 | a0001c0001t0008g0041a0001c0001t0045g0114a0001c0002t0008g0140others(1): Show | 4 | HG02976.hp2 HG03041.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.628-5794G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116761020 | ||||||
| chr12:116761106
|
C | A | 10 | a0001c0001t0002g0031a0001c0001t0002g0032a0001c0001t0008g0028others(7): Show | 10 | HG01891.hp1 HG02257.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.628-5708C>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116761106 | ||||||
| chr12:116761114
|
G | A | 30 | a0001c0001t0001g0169a0001c0001t0001g0178a0001c0001t0004g0095others(27): Show | 30 | HG01243.hp1 HG02074.hp1 HG02155.hp1 others(27): Show |
intron_variant | MODIFIER | c.628-5700G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116761114 | ||||||
| chr12:116761263
|
C | T | 4 | a0001c0005t0013g0006a0001c0007t0005g0062a0001c0007t0016g0061others(1): Show | 4 | HG01243.hp1 HG02970.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.628-5551C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116761263 | ||||||
| chr12:116761401
|
G | T | 5 | a0001c0006t0005g0017a0001c0006t0036g0018a0001c0006t0050g0013others(2): Show | 5 | HG00741.hp1 HG01106.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.628-5413G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116761401 | ||||||
| chr12:116761452
|
T | C | 1 | a0001c0002t0018g0022 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.628-5362T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116761452 | ||||||
| chr12:116761609
|
G | T | 30 | a0001c0001t0001g0169a0001c0001t0001g0178a0001c0001t0004g0095others(27): Show | 30 | HG01243.hp1 HG02074.hp1 HG02155.hp1 others(27): Show |
intron_variant | MODIFIER | c.628-5205G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116761609 | ||||||
| chr12:116761761
|
C | T | 1 | a0001c0001t0007g0231 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.628-5053C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116761761 | ||||||
| chr12:116761922
|
C | T | 5 | a0001c0001t0019g0124a0001c0001t0019g0163a0001c0001t0019g0187others(2): Show | 5 | HG00140.hp1 HG01261.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.628-4892C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116761922 | ||||||
| chr12:116761930
|
G | A | 6 | a0001c0001t0002g0034a0001c0001t0002g0103a0001c0001t0002g0104others(3): Show | 6 | HG02280.hp1 HG02615.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.628-4884G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116761930 | ||||||
| chr12:116762064
|
C | CA | 108 | a0001c0001t0001g0072a0001c0001t0001g0086a0001c0001t0001g0092others(105): Show | 108 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.628-4734dupA | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 116762064 | |||||
| chr12:116762064
|
CA | C | 23 | a0001c0001t0002g0031a0001c0001t0002g0032a0001c0001t0002g0034others(20): Show | 23 | HG00140.hp1 HG01074.hp2 HG01261.hp2 others(20): Show |
intron_variant | MODIFIER | c.628-4734delA | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 116762064 | |||||
| chr12:116762064
|
CAA | C | 29 | a0001c0001t0001g0169a0001c0001t0001g0178a0001c0001t0004g0095others(26): Show | 29 | HG01243.hp1 HG02074.hp1 HG02155.hp1 others(26): Show |
intron_variant | MODIFIER | c.628-4735_628-4734d others(4): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 116762064 | |||||
| chr12:116762107
|
T | G | 35 | a0001c0001t0001g0169a0001c0001t0001g0178a0001c0001t0004g0095others(32): Show | 35 | HG00140.hp1 HG01243.hp1 HG01261.hp2 others(32): Show |
intron_variant | MODIFIER | c.628-4707T>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116762107 | ||||||
| chr12:116762403
|
C | CA | 184 | a0001c0001t0001g0072a0001c0001t0001g0086a0001c0001t0001g0092others(181): Show | 184 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(181): Show |
intron_variant | MODIFIER | c.628-4399dupA | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 116762403 | |||||
| chr12:116762403
|
C | CAA | 8 | a0001c0001t0001g0069a0001c0001t0001g0120a0001c0001t0001g0227others(5): Show | 8 | HG00609.hp1 HG00609.hp2 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.628-4400_628-4399d others(4): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 116762403 | |||||
| chr12:116762416
|
C | G | 4 | a0001c0005t0013g0006a0001c0007t0005g0062a0001c0007t0016g0061others(1): Show | 4 | HG01243.hp1 HG02970.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.628-4398C>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116762416 | ||||||
| chr12:116762580
|
A | AT | 19 | a0001c0001t0001g0092a0001c0001t0001g0194a0001c0001t0001g0232others(16): Show | 19 | HG00544.hp1 HG00544.hp2 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.628-4217dupT | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 116762580 | |||||
| chr12:116762580
|
A | ATT | 25 | a0001c0001t0001g0178a0001c0001t0004g0095a0001c0001t0004g0096others(22): Show | 25 | HG01243.hp1 HG02074.hp1 HG02155.hp1 others(22): Show |
intron_variant | MODIFIER | c.628-4218_628-4217d others(4): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 116762580 | |||||
| chr12:116762580
|
A | ATTT | 8 | a0001c0001t0001g0169a0001c0001t0004g0168a0001c0001t0004g0170others(5): Show | 8 | HG00140.hp1 HG01261.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.628-4219_628-4217d others(5): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 116762580 | |||||
| chr12:116762580
|
AT | A | 8 | a0001c0001t0001g0190a0001c0001t0001g0221a0001c0001t0008g0028others(5): Show | 8 | HG01074.hp2 HG01975.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.628-4217delT | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 116762580 | |||||
| chr12:116762639
|
G | C | 2 | a0001c0002t0001g0251a0001c0002t0002g0174 | 2 | NA19005.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.628-4175G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116762639 | ||||||
| chr12:116762802
|
G | C | 1 | a0001c0011t0053g0011 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.628-4012G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116762802 | ||||||
| chr12:116762854
|
C | T | 5 | a0001c0001t0019g0124a0001c0001t0019g0163a0001c0001t0019g0187others(2): Show | 5 | HG00140.hp1 HG01261.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.628-3960C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116762854 | ||||||
| chr12:116762934
|
T | G | 5 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0258others(2): Show | 5 | HG01192.hp1 HG01257.hp1 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.628-3880T>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116762934 | ||||||
| chr12:116762978
|
A | C | 1 | a0001c0006t0031g0067 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.628-3836A>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116762978 | ||||||
| chr12:116763003
|
T | C | 2 | a0001c0001t0001g0122a0001c0001t0001g0237 | 2 | HG01358.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.628-3811T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116763003 | ||||||
| chr12:116763046
|
C | T | 4 | a0001c0001t0002g0045a0001c0001t0002g0048a0001c0002t0004g0268others(1): Show | 4 | HG02572.hp1 HG02976.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.628-3768C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116763046 | ||||||
| chr12:116763176
|
GA | G | 220 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(217): Show | 220 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(217): Show |
intron_variant | MODIFIER | c.628-3624delA | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 116763176 | |||||
| chr12:116763195
|
A | C | 3 | a0001c0001t0002g0236a0001c0002t0012g0014a0001c0002t0012g0089 | 3 | HG01074.hp1 HG01261.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.628-3619A>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116763195 | ||||||
| chr12:116763605
|
AAAAAAAA others(7): Show |
A | 3 | a0001c0001t0001g0190a0001c0001t0001g0193a0001c0001t0001g0215 | 3 | HG01361.hp2 HG01975.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.628-3197_628-3184d others(16): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 116763605 | |||||
| chr12:116763619
|
C | CA | 201 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(198): Show | 201 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.628-3185dupA | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 116763619 | |||||
| chr12:116763651
|
C | T | 1 | a0001c0013t0013g0158 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.628-3163C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116763651 | ||||||
| chr12:116763652
|
G | A | 1 | a0001c0002t0001g0081 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.628-3162G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116763652 | ||||||
| chr12:116763766
|
G | A | 8 | a0001c0003t0005g0035a0001c0003t0005g0036a0001c0003t0016g0039others(5): Show | 8 | HG01243.hp1 HG02965.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.628-3048G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116763766 | ||||||
| chr12:116763783
|
A | G | 16 | a0001c0001t0002g0031a0001c0001t0002g0032a0001c0001t0008g0028others(13): Show | 16 | HG01891.hp1 HG02040.hp1 HG02132.hp2 others(13): Show |
intron_variant | MODIFIER | c.628-3031A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116763783 | ||||||
| chr12:116763784
|
A | C | 3 | a0001c0002t0062g0185a0001c0002t0063g0263a0001c0002t0065g0093 | 3 | HG01169.hp2 HG01884.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.628-3030A>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116763784 | ||||||
| chr12:116763785
|
A | T | 3 | a0001c0003t0002g0100a0001c0003t0002g0101a0001c0003t0002g0102 | 3 | HG01074.hp2 HG02280.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.628-3029A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116763785 | ||||||
| chr12:116763794
|
C | A | 18 | a0001c0001t0001g0178a0001c0001t0004g0110a0001c0001t0004g0168others(15): Show | 18 | HG02074.hp1 HG02523.hp2 HG02683.hp2 others(15): Show |
intron_variant | MODIFIER | c.628-3020C>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116763794 | ||||||
| chr12:116763794
|
C | CG | 18 | a0001c0001t0001g0203a0001c0001t0001g0217a0001c0001t0001g0258others(15): Show | 18 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(15): Show |
intron_variant | MODIFIER | c.628-3012dupG | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 116763794 | |||||
| chr12:116763794
|
C | G | 1 | a0001c0019t0002g0267 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.628-3020C>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116763794 | ||||||
| chr12:116763794
|
CG | C | 45 | a0001c0001t0001g0072a0001c0001t0001g0141a0001c0001t0001g0190others(42): Show | 45 | HG01074.hp2 HG01169.hp2 HG01243.hp1 others(42): Show |
intron_variant | MODIFIER | c.628-3012delG | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 116763794 | |||||
| chr12:116763795
|
G | C | 1 | a0001c0019t0002g0267 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.628-3019G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116763795 | ||||||
| chr12:116763802
|
GA | G | 15 | a0001c0001t0002g0031a0001c0001t0002g0032a0001c0001t0008g0028others(12): Show | 15 | HG01891.hp1 HG02040.hp1 HG02132.hp2 others(12): Show |
intron_variant | MODIFIER | c.628-3009delA | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 116763802 | |||||
| chr12:116763899
|
A | C | 21 | a0001c0001t0001g0141a0001c0001t0001g0190a0001c0001t0001g0193others(18): Show | 21 | HG01099.hp2 HG01257.hp2 HG01258.hp1 others(18): Show |
intron_variant | MODIFIER | c.628-2915A>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116763899 | ||||||
| chr12:116763950
|
C | T | 1 | a0001c0006t0031g0067 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.628-2864C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116763950 | ||||||
| chr12:116763970
|
T | C | 48 | a0001c0001t0002g0031a0001c0001t0002g0032a0001c0001t0008g0028others(45): Show | 48 | HG00140.hp1 HG01074.hp2 HG01106.hp1 others(45): Show |
intron_variant | MODIFIER | c.628-2844T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116763970 | ||||||
| chr12:116764059
|
A | G | 1 | a0001c0014t0018g0019 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.628-2755A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116764059 | ||||||
| chr12:116764062
|
G | T | 1 | a0001c0001t0056g0220 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.628-2752G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116764062 | ||||||
| chr12:116764279
|
G | A | 5 | a0001c0001t0019g0124a0001c0001t0019g0163a0001c0001t0019g0187others(2): Show | 5 | HG00140.hp1 HG01261.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.628-2535G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116764279 | ||||||
| chr12:116764340
|
C | T | 1 | a0001c0011t0053g0011 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.628-2474C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116764340 | ||||||
| chr12:116764352
|
A | AT | 14 | a0001c0002t0018g0022a0001c0003t0002g0100a0001c0003t0002g0101others(11): Show | 14 | HG01074.hp2 HG01891.hp1 HG02040.hp1 others(11): Show |
intron_variant | MODIFIER | c.628-2452dupT | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 116764352 | |||||
| chr12:116764518
|
G | A | 3 | a0001c0005t0030g0051a0001c0005t0030g0052a0001c0005t0070g0050 | 3 | HG01891.hp1 HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.628-2296G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116764518 | ||||||
| chr12:116764644
|
C | T | 18 | a0001c0001t0002g0031a0001c0001t0002g0032a0001c0001t0008g0028others(15): Show | 18 | HG01884.hp2 HG02055.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.628-2170C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116764644 | ||||||
| chr12:116764686
|
G | A | 7 | a0001c0001t0002g0031a0001c0001t0002g0032a0001c0001t0008g0028others(4): Show | 7 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.628-2128G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116764686 | ||||||
| chr12:116764753
|
A | G | 7 | a0001c0001t0002g0031a0001c0001t0002g0032a0001c0001t0008g0028others(4): Show | 7 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.628-2061A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116764753 | ||||||
| chr12:116764758
|
G | C | 1 | a0001c0001t0007g0231 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.628-2056G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116764758 | ||||||
| chr12:116764764
|
C | T | 4 | a0001c0001t0002g0045a0001c0001t0002g0048a0001c0002t0004g0268others(1): Show | 4 | HG02572.hp1 HG02976.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.628-2050C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116764764 | ||||||
| chr12:116764781
|
A | G | 69 | a0001c0001t0001g0178a0001c0001t0002g0031a0001c0001t0002g0032others(66): Show | 69 | HG01074.hp2 HG01106.hp1 HG01243.hp1 others(66): Show |
intron_variant | MODIFIER | c.628-2033A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116764781 | ||||||
| chr12:116764823
|
C | T | 105 | a0001c0001t0001g0141a0001c0001t0001g0178a0001c0001t0001g0190others(102): Show | 105 | HG00140.hp1 HG00438.hp2 HG00741.hp1 others(102): Show |
intron_variant | MODIFIER | c.628-1991C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116764823 | ||||||
| chr12:116764888
|
G | A | 2 | a0001c0012t0001g0123a0001c0012t0001g0239 | 2 | HG01175.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.628-1926G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116764888 | ||||||
| chr12:116765016
|
C | T | 3 | a0001c0003t0002g0100a0001c0003t0002g0101a0001c0003t0002g0102 | 3 | HG01074.hp2 HG02280.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.628-1798C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116765016 | ||||||
| chr12:116765017
|
G | A | 1 | a0001c0001t0008g0041 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.628-1797G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116765017 | ||||||
| chr12:116765418
|
C | T | 1 | a0001c0006t0050g0013 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.628-1396C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116765418 | ||||||
| chr12:116765840
|
G | A | 2 | a0001c0001t0003g0117a0001c0001t0003g0240 | 2 | HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.628-974G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116765840 | ||||||
| chr12:116766010
|
G | A | 31 | a0001c0001t0001g0178a0001c0001t0004g0095a0001c0001t0004g0096others(28): Show | 31 | HG01243.hp2 HG02074.hp1 HG02155.hp1 others(28): Show |
intron_variant | MODIFIER | c.628-804G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116766010 | ||||||
| chr12:116766091
|
G | A | 1 | a0001c0001t0001g0122 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.628-723G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116766091 | ||||||
| chr12:116766116
|
T | TA | 48 | a0001c0001t0001g0178a0001c0001t0002g0031a0001c0001t0002g0032others(45): Show | 48 | HG00140.hp1 HG01175.hp2 HG01243.hp2 others(45): Show |
intron_variant | MODIFIER | c.628-693dupA | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 116766116 | |||||
| chr12:116766121
|
A | T | 3 | a0001c0001t0001g0166a0001c0001t0001g0169a0001c0014t0018g0019 | 3 | HG01106.hp1 HG02004.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.628-693A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116766121 | ||||||
| chr12:116766122
|
T | A | 40 | a0001c0001t0001g0178a0001c0001t0001g0216a0001c0001t0001g0260others(37): Show | 40 | HG01243.hp2 HG01884.hp2 HG01978.hp1 others(37): Show |
intron_variant | MODIFIER | c.628-692T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116766122 | ||||||
| chr12:116766123
|
T | A | 31 | a0001c0001t0001g0178a0001c0001t0004g0095a0001c0001t0004g0096others(28): Show | 31 | HG01243.hp2 HG02074.hp1 HG02155.hp1 others(28): Show |
intron_variant | MODIFIER | c.628-691T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116766123 | ||||||
| chr12:116766125
|
T | G | 7 | a0001c0003t0005g0035a0001c0003t0005g0036a0001c0003t0016g0039others(4): Show | 7 | HG01243.hp1 HG02965.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.628-689T>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116766125 | ||||||
| chr12:116766275
|
T | A | 8 | a0001c0001t0002g0034a0001c0001t0002g0103a0001c0001t0002g0104others(5): Show | 8 | HG02615.hp1 HG02622.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.628-539T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116766275 | ||||||
| chr12:116766477
|
A | G | 31 | a0001c0001t0001g0178a0001c0001t0004g0095a0001c0001t0004g0096others(28): Show | 31 | HG01243.hp2 HG02074.hp1 HG02155.hp1 others(28): Show |
intron_variant | MODIFIER | c.628-337A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116766477 | ||||||
| chr12:116766600
|
T | C | 2 | a0001c0006t0005g0017a0001c0014t0018g0019 | 2 | HG01106.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.628-214T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116766600 | ||||||
| chr12:116766753
|
C | T | 1 | a0001c0001t0061g0148 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.628-61C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116766753 | ||||||
| chr12:116767053
|
T | TTA | 5 | a0001c0001t0019g0124a0001c0001t0019g0163a0001c0001t0019g0187others(2): Show | 5 | HG00140.hp1 HG01261.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.728+147_728+148dup others(2): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 116767053 | |||||
| chr12:116767130
|
T | G | 2 | a0001c0005t0030g0051a0001c0005t0030g0052 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.728+216T>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116767130 | ||||||
| chr12:116767169
|
T | C | 1 | a0001c0001t0001g0224 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.728+255T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116767169 | ||||||
| chr12:116767339
|
T | C | 253 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(250): Show | 253 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(250): Show |
intron_variant | MODIFIER | c.728+425T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116767339 | ||||||
| chr12:116767380
|
G | A | 24 | a0001c0001t0001g0178a0001c0001t0004g0095a0001c0001t0004g0096others(21): Show | 24 | HG01243.hp2 HG02074.hp1 HG02155.hp1 others(21): Show |
intron_variant | MODIFIER | c.728+466G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116767380 | ||||||
| chr12:116767476
|
C | T | 3 | a0001c0003t0002g0100a0001c0003t0002g0101a0001c0003t0002g0102 | 3 | HG01074.hp2 HG02280.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.728+562C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116767476 | ||||||
| chr12:116767552
|
G | A | 5 | a0001c0001t0019g0124a0001c0001t0019g0163a0001c0001t0019g0187others(2): Show | 5 | HG00140.hp1 HG01261.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.728+638G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116767552 | ||||||
| chr12:116767565
|
T | TG | 8 | a0001c0001t0002g0031a0001c0001t0002g0032a0001c0001t0008g0028others(5): Show | 8 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.728+652dupG | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 116767565 | |||||
| chr12:116767567
|
T | G | 4 | a0001c0002t0005g0003a0001c0002t0005g0064a0001c0011t0023g0007others(1): Show | 4 | HG01175.hp2 HG02486.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.728+653T>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116767567 | ||||||
| chr12:116767568
|
T | G | 243 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(240): Show | 243 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(240): Show |
intron_variant | MODIFIER | c.728+654T>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116767568 | ||||||
| chr12:116767569
|
T | G | 40 | a0001c0001t0001g0141a0001c0001t0001g0190a0001c0001t0001g0193others(37): Show | 40 | HG00140.hp1 HG00438.hp2 HG01099.hp2 others(37): Show |
intron_variant | MODIFIER | c.728+655T>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116767569 | ||||||
| chr12:116767665
|
C | T | 1 | a0001c0001t0001g0224 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.728+751C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116767665 | ||||||
| chr12:116767813
|
C | T | 12 | a0001c0001t0002g0031a0001c0001t0002g0032a0001c0001t0008g0028others(9): Show | 12 | HG01175.hp2 HG02257.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.728+899C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116767813 | ||||||
| chr12:116767814
|
G | A | 1 | a0001c0006t0005g0017 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.728+900G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116767814 | ||||||
| chr12:116767894
|
C | T | 1 | a0001c0016t0032g0044 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.728+980C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116767894 | ||||||
| chr12:116767930
|
G | A | 5 | a0001c0001t0019g0124a0001c0001t0019g0163a0001c0001t0019g0187others(2): Show | 5 | HG00140.hp1 HG01261.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.728+1016G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116767930 | ||||||
| chr12:116767986
|
T | A | 1 | a0001c0011t0053g0011 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.728+1072T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116767986 | ||||||
| chr12:116768099
|
C | CT | 64 | a0001c0001t0001g0178a0001c0001t0001g0207a0001c0001t0002g0031others(61): Show | 64 | HG00140.hp1 HG00741.hp1 HG01074.hp2 others(61): Show |
intron_variant | MODIFIER | c.728+1201dupT | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 116768099 | |||||
| chr12:116768099
|
C | CTT | 6 | a0001c0001t0004g0095a0001c0001t0004g0096a0001c0001t0007g0179others(3): Show | 6 | HG02055.hp2 HG02647.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.728+1200_728+1201d others(4): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 116768099 | |||||
| chr12:116768145
|
G | A | 31 | a0001c0001t0001g0178a0001c0001t0004g0095a0001c0001t0004g0096others(28): Show | 31 | HG01243.hp2 HG02074.hp1 HG02155.hp1 others(28): Show |
intron_variant | MODIFIER | c.728+1231G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116768145 | ||||||
| chr12:116768223
|
C | T | 1 | a0001c0001t0003g0155 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.728+1309C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116768223 | ||||||
| chr12:116768247
|
C | T | 1 | a0001c0016t0032g0044 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.728+1333C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116768247 | ||||||
| chr12:116768305
|
T | A | 1 | a0001c0001t0004g0170 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.728+1391T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116768305 | ||||||
| chr12:116768321
|
G | A | 12 | a0001c0001t0002g0031a0001c0001t0002g0032a0001c0001t0008g0028others(9): Show | 12 | HG01175.hp2 HG02257.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.728+1407G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116768321 | ||||||
| chr12:116768454
|
C | T | 31 | a0001c0001t0001g0178a0001c0001t0004g0095a0001c0001t0004g0096others(28): Show | 31 | HG01243.hp2 HG02074.hp1 HG02155.hp1 others(28): Show |
intron_variant | MODIFIER | c.728+1540C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116768454 | ||||||
| chr12:116768713
|
A | AT | 12 | a0001c0001t0002g0031a0001c0001t0002g0032a0001c0001t0008g0028others(9): Show | 12 | HG01175.hp2 HG02257.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.728+1809dupT | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 116768713 | |||||
| chr12:116768728
|
T | TTCTC | 16 | a0001c0001t0002g0031a0001c0001t0002g0032a0001c0001t0008g0028others(13): Show | 16 | HG00140.hp1 HG01175.hp2 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.728+1820_728+1823d others(6): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 116768728 | |||||
| chr12:116768736
|
C | CTCTT | 30 | a0001c0001t0001g0178a0001c0001t0004g0095a0001c0001t0004g0096others(27): Show | 30 | HG01243.hp2 HG02074.hp1 HG02155.hp1 others(27): Show |
intron_variant | MODIFIER | c.728+1823_728+1824i others(6): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 116768736 | |||||
| chr12:116768738
|
T | C | 1 | a0001c0011t0053g0011 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.728+1824T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116768738 | ||||||
| chr12:116768753
|
C | T | 1 | a0001c0001t0002g0192 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.728+1839C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116768753 | ||||||
| chr12:116768770
|
G | A | 1 | a0001c0001t0002g0192 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.728+1856G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116768770 | ||||||
| chr12:116768857
|
A | C | 12 | a0001c0001t0002g0031a0001c0001t0002g0032a0001c0001t0008g0028others(9): Show | 12 | HG01175.hp2 HG02257.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.728+1943A>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116768857 | ||||||
| chr12:116768951
|
A | G | 48 | a0001c0001t0001g0178a0001c0001t0002g0031a0001c0001t0002g0032others(45): Show | 48 | HG00140.hp1 HG01175.hp2 HG01243.hp2 others(45): Show |
intron_variant | MODIFIER | c.728+2037A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116768951 | ||||||
| chr12:116768982
|
C | T | 150 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(147): Show | 150 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(147): Show |
intron_variant | MODIFIER | c.728+2068C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116768982 | ||||||
| chr12:116769082
|
G | A | 4 | a0001c0002t0005g0003a0001c0002t0005g0064a0001c0011t0023g0007others(1): Show | 4 | HG01175.hp2 HG02486.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.728+2168G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116769082 | ||||||
| chr12:116769149
|
G | A | 31 | a0001c0001t0001g0178a0001c0001t0004g0095a0001c0001t0004g0096others(28): Show | 31 | HG01243.hp2 HG02074.hp1 HG02155.hp1 others(28): Show |
intron_variant | MODIFIER | c.728+2235G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116769149 | ||||||
| chr12:116769197
|
A | G | 5 | a0001c0001t0001g0086a0001c0001t0001g0205a0001c0001t0001g0211others(2): Show | 5 | HG00408.hp1 HG02080.hp2 NA18950.hp1 others(2): Show |
intron_variant | MODIFIER | c.728+2283A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116769197 | ||||||
| chr12:116769225
|
A | G | 74 | a0001c0001t0001g0141a0001c0001t0001g0178a0001c0001t0001g0190others(71): Show | 74 | HG00140.hp1 HG00438.hp2 HG01099.hp2 others(71): Show |
intron_variant | MODIFIER | c.728+2311A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116769225 | ||||||
| chr12:116769283
|
G | A | 1 | a0001c0001t0001g0094 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.728+2369G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116769283 | ||||||
| chr12:116769345
|
G | A | 1 | a0001c0003t0014g0065 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.728+2431G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116769345 | ||||||
| chr12:116769349
|
T | C | 253 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(250): Show | 253 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(250): Show |
intron_variant | MODIFIER | c.728+2435T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116769349 | ||||||
| chr12:116769403
|
A | G | 253 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(250): Show | 253 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(250): Show |
intron_variant | MODIFIER | c.728+2489A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116769403 | ||||||
| chr12:116769611
|
C | T | 7 | a0001c0001t0002g0031a0001c0001t0002g0032a0001c0001t0008g0028others(4): Show | 7 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.728+2697C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116769611 | ||||||
| chr12:116769754
|
G | A | 34 | a0001c0001t0001g0141a0001c0001t0001g0190a0001c0001t0001g0193others(31): Show | 34 | HG00438.hp2 HG01099.hp2 HG01257.hp2 others(31): Show |
intron_variant | MODIFIER | c.728+2840G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116769754 | ||||||
| chr12:116769774
|
G | A | 1 | a0001c0001t0001g0243 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.728+2860G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116769774 | ||||||
| chr12:116769782
|
A | G | 1 | a0001c0001t0003g0157 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.728+2868A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116769782 | ||||||
| chr12:116769943
|
G | T | 5 | a0001c0001t0004g0095a0001c0001t0004g0096a0001c0001t0004g0145others(2): Show | 5 | HG01243.hp2 HG02155.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.728+3029G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116769943 | ||||||
| chr12:116770101
|
A | G | 1 | a0001c0006t0036g0018 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.728+3187A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116770101 | ||||||
| chr12:116770263
|
C | T | 2 | a0001c0007t0025g0056a0001c0007t0046g0053 | 2 | HG02145.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.728+3349C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116770263 | ||||||
| chr12:116770294
|
A | G | 1 | a0001c0003t0035g0088 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.728+3380A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116770294 | ||||||
| chr12:116770394
|
A | C | 3 | a0001c0003t0002g0100a0001c0003t0002g0101a0001c0003t0002g0102 | 3 | HG01074.hp2 HG02280.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.728+3480A>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116770394 | ||||||
| chr12:116770547
|
T | C | 4 | a0001c0002t0005g0003a0001c0002t0005g0064a0001c0011t0023g0007others(1): Show | 4 | HG01175.hp2 HG02486.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.728+3633T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116770547 | ||||||
| chr12:116770633
|
C | T | 7 | a0001c0001t0002g0031a0001c0001t0002g0032a0001c0001t0008g0028others(4): Show | 7 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.728+3719C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116770633 | ||||||
| chr12:116770644
|
A | G | 4 | a0001c0002t0005g0003a0001c0002t0005g0064a0001c0011t0023g0007others(1): Show | 4 | HG01175.hp2 HG02486.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.728+3730A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116770644 | ||||||
| chr12:116770703
|
G | A | 3 | a0001c0003t0002g0100a0001c0003t0002g0101a0001c0003t0002g0102 | 3 | HG01074.hp2 HG02280.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.728+3789G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116770703 | ||||||
| chr12:116770759
|
A | G | 1 | a0001c0006t0036g0018 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.728+3845A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116770759 | ||||||
| chr12:116770937
|
G | A | 2 | a0001c0005t0020g0162a0001c0013t0020g0098 | 2 | HG02970.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.728+4023G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116770937 | ||||||
| chr12:116771033
|
G | A | 9 | a0001c0001t0019g0124a0001c0001t0019g0163a0001c0001t0019g0187others(6): Show | 9 | HG00140.hp1 HG01175.hp2 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.728+4119G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116771033 | ||||||
| chr12:116771071
|
A | G | 1 | a0001c0003t0016g0039 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.728+4157A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116771071 | ||||||
| chr12:116771180
|
T | G | 253 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(250): Show | 253 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(250): Show |
intron_variant | MODIFIER | c.728+4266T>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116771180 | ||||||
| chr12:116771199
|
G | A | 1 | a0001c0004t0052g0015 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.728+4285G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116771199 | ||||||
| chr12:116771340
|
G | A | 1 | a0001c0006t0050g0013 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.728+4426G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116771340 | ||||||
| chr12:116771430
|
G | A | 32 | a0001c0001t0001g0178a0001c0001t0004g0095a0001c0001t0004g0096others(29): Show | 32 | HG01243.hp2 HG02055.hp1 HG02074.hp1 others(29): Show |
intron_variant | MODIFIER | c.728+4516G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116771430 | ||||||
| chr12:116771457
|
C | T | 1 | a0001c0001t0002g0023 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.728+4543C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116771457 | ||||||
| chr12:116771460
|
TA | T | 93 | a0001c0001t0001g0094a0001c0001t0001g0120a0001c0001t0001g0122others(90): Show | 93 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.728+4581delA | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 116771460 | |||||
| chr12:116771460
|
TAAA | T | 10 | a0001c0001t0011g0160a0001c0002t0011g0107a0001c0003t0005g0036others(7): Show | 10 | HG02486.hp2 HG02630.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.728+4579_728+4581d others(5): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 116771460 | |||||
| chr12:116771460
|
TAAAA | T | 14 | a0001c0001t0002g0031a0001c0001t0002g0045a0001c0001t0002g0048others(11): Show | 14 | HG02572.hp1 HG02615.hp1 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.728+4578_728+4581d others(6): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 116771460 | |||||
| chr12:116771460
|
TAAAAAAA others(1): Show |
T | 25 | a0001c0001t0001g0178a0001c0001t0003g0106a0001c0001t0004g0110others(22): Show | 25 | HG02071.hp2 HG02074.hp1 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.728+4574_728+4581d others(10): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 116771460 | |||||
| chr12:116771460
|
TAAAAAAA others(2): Show |
T | 8 | a0001c0001t0001g0262a0001c0001t0002g0210a0001c0001t0004g0095others(5): Show | 8 | HG01243.hp2 HG01257.hp1 HG02155.hp1 others(5): Show |
intron_variant | MODIFIER | c.728+4573_728+4581d others(11): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 116771460 | |||||
| chr12:116771460
|
TAAAAAAA others(3): Show |
T | 9 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0258others(6): Show | 9 | HG01175.hp2 HG01192.hp1 HG02148.hp1 others(6): Show |
intron_variant | MODIFIER | c.728+4572_728+4581d others(12): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 116771460 | |||||
| chr12:116771460
|
TAAAAAAA others(4): Show |
T | 30 | a0001c0001t0001g0141a0001c0001t0001g0190a0001c0001t0001g0193others(27): Show | 30 | HG00438.hp2 HG01099.hp2 HG01257.hp2 others(27): Show |
intron_variant | MODIFIER | c.728+4571_728+4581d others(13): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 116771460 | |||||
| chr12:116771460
|
TAAAAAAA others(8): Show |
T | 5 | a0001c0001t0019g0124a0001c0001t0019g0163a0001c0001t0019g0187others(2): Show | 5 | HG00140.hp1 HG01261.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.728+4567_728+4581d others(17): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 116771460 | |||||
| chr12:116771460
|
TAAAAAAA others(12): Show |
T | 1 | a0001c0016t0032g0044 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.728+4563_728+4581d others(21): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 116771460 | |||||
| chr12:116771480
|
A | T | 1 | a0001c0004t0001g0083 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.728+4566A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116771480 | ||||||
| chr12:116771482
|
A | T | 6 | a0001c0003t0002g0100a0001c0003t0002g0101a0001c0003t0002g0102others(3): Show | 6 | HG01074.hp2 HG02132.hp2 HG02135.hp2 others(3): Show |
intron_variant | MODIFIER | c.728+4568A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116771482 | ||||||
| chr12:116771484
|
A | T | 12 | a0001c0001t0001g0249a0001c0002t0002g0108a0001c0002t0005g0151others(9): Show | 12 | HG01074.hp2 HG01099.hp1 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.728+4570A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116771484 | ||||||
| chr12:116771486
|
A | T | 52 | a0001c0001t0001g0069a0001c0001t0001g0092a0001c0001t0001g0194others(49): Show | 52 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.728+4572A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116771486 | ||||||
| chr12:116771488
|
A | AT | 5 | a0001c0001t0001g0086a0001c0001t0001g0146a0001c0001t0001g0217others(2): Show | 5 | HG02293.hp2 HG02300.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.728+4574_728+4575i others(3): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116771488 | ||||||
| chr12:116771488
|
A | T | 131 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0092others(128): Show | 131 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.728+4574A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116771488 | ||||||
| chr12:116771490
|
A | T | 156 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(153): Show | 156 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(153): Show |
intron_variant | MODIFIER | c.728+4576A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116771490 | ||||||
| chr12:116771492
|
A | T | 173 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(170): Show | 173 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(170): Show |
intron_variant | MODIFIER | c.728+4578A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116771492 | ||||||
| chr12:116771494
|
A | T | 250 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(247): Show | 250 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(247): Show |
intron_variant | MODIFIER | c.728+4580A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116771494 | ||||||
| chr12:116771496
|
T | A | 1 | a0001c0014t0002g0137 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.728+4582T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116771496 | ||||||
| chr12:116771497
|
ACG | A | 25 | a0001c0001t0001g0092a0001c0001t0001g0204a0001c0001t0001g0216others(22): Show | 25 | HG01074.hp2 HG01099.hp1 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.728+4584_728+4585d others(4): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116771497 | ||||||
| chr12:116771498
|
C | T | 153 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(150): Show | 153 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.728+4584C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116771498 | ||||||
| chr12:116771499
|
G | A | 153 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(150): Show | 153 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.728+4585G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116771499 | ||||||
| chr12:116771697
|
A | G | 1 | a0001c0001t0003g0242 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.728+4783A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116771697 | ||||||
| chr12:116771740
|
C | T | 33 | a0001c0001t0001g0141a0001c0001t0001g0190a0001c0001t0001g0193others(30): Show | 33 | HG00438.hp2 HG01099.hp2 HG01257.hp2 others(30): Show |
intron_variant | MODIFIER | c.728+4826C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116771740 | ||||||
| chr12:116771751
|
G | A | 3 | a0001c0001t0008g0028a0001c0001t0008g0029a0001c0001t0008g0040 | 3 | HG02572.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.728+4837G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116771751 | ||||||
| chr12:116771860
|
G | A | 253 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(250): Show | 253 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(250): Show |
intron_variant | MODIFIER | c.728+4946G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116771860 | ||||||
| chr12:116772009
|
A | G | 253 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(250): Show | 253 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(250): Show |
intron_variant | MODIFIER | c.728+5095A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116772009 | ||||||
| chr12:116772066
|
A | G | 253 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(250): Show | 253 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(250): Show |
intron_variant | MODIFIER | c.728+5152A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116772066 | ||||||
| chr12:116772082
|
T | A | 1 | a0001c0001t0002g0032 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.728+5168T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116772082 | ||||||
| chr12:116772094
|
AT | A | 253 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(250): Show | 253 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(250): Show |
intron_variant | MODIFIER | c.728+5189delT | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 116772094 | |||||
| chr12:116772260
|
G | A | 178 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(175): Show | 178 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(175): Show |
intron_variant | MODIFIER | c.728+5346G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116772260 | ||||||
| chr12:116772293
|
A | G | 1 | a0001c0003t0035g0088 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.728+5379A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116772293 | ||||||
| chr12:116772468
|
G | A | 187 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(184): Show | 187 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(184): Show |
intron_variant | MODIFIER | c.728+5554G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116772468 | ||||||
| chr12:116772557
|
G | A | 66 | a0001c0001t0001g0141a0001c0001t0001g0178a0001c0001t0001g0190others(63): Show | 66 | HG00438.hp2 HG01099.hp2 HG01243.hp2 others(63): Show |
intron_variant | MODIFIER | c.728+5643G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116772557 | ||||||
| chr12:116772625
|
T | C | 27 | a0001c0001t0001g0141a0001c0001t0001g0190a0001c0001t0001g0193others(24): Show | 27 | HG00438.hp2 HG01099.hp2 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.728+5711T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116772625 | ||||||
| chr12:116772834
|
C | G | 5 | a0001c0006t0031g0067a0001c0007t0025g0009a0001c0007t0025g0056others(2): Show | 5 | HG01884.hp2 HG02145.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.728+5920C>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116772834 | ||||||
| chr12:116772976
|
A | G | 1 | a0001c0001t0003g0157 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.728+6062A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116772976 | ||||||
| chr12:116772987
|
T | C | 254 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(251): Show | 254 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(251): Show |
intron_variant | MODIFIER | c.728+6073T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116772987 | ||||||
| chr12:116773003
|
A | G | 9 | a0001c0001t0019g0124a0001c0001t0019g0163a0001c0001t0019g0187others(6): Show | 9 | HG00140.hp1 HG01175.hp2 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.728+6089A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116773003 | ||||||
| chr12:116773078
|
C | T | 1 | a0001c0003t0042g0229 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.729-6117C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116773078 | ||||||
| chr12:116773214
|
G | A | 4 | a0001c0007t0025g0009a0001c0007t0025g0056a0001c0007t0046g0053others(1): Show | 4 | HG01884.hp2 HG02145.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.729-5981G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116773214 | ||||||
| chr12:116773300
|
A | G | 33 | a0001c0001t0001g0178a0001c0001t0004g0095a0001c0001t0004g0096others(30): Show | 33 | HG01243.hp2 HG02055.hp1 HG02074.hp1 others(30): Show |
intron_variant | MODIFIER | c.729-5895A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116773300 | ||||||
| chr12:116773688
|
A | G | 6 | a0001c0001t0002g0032a0001c0001t0008g0028a0001c0001t0008g0029others(3): Show | 6 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.729-5507A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116773688 | ||||||
| chr12:116774099
|
G | A | 188 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(185): Show | 188 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(185): Show |
intron_variant | MODIFIER | c.729-5096G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116774099 | ||||||
| chr12:116774208
|
G | A | 1 | a0001c0001t0011g0099 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.729-4987G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116774208 | ||||||
| chr12:116774209
|
T | A | 1 | a0001c0001t0011g0099 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.729-4986T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116774209 | ||||||
| chr12:116774210
|
G | A | 1 | a0001c0001t0011g0099 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.729-4985G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116774210 | ||||||
| chr12:116774211
|
G | A | 1 | a0001c0001t0011g0099 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.729-4984G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116774211 | ||||||
| chr12:116774212
|
T | G | 1 | a0001c0001t0011g0099 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.729-4983T>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116774212 | ||||||
| chr12:116774213
|
T | C | 1 | a0001c0001t0011g0099 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.729-4982T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116774213 | ||||||
| chr12:116774214
|
G | A | 1 | a0001c0001t0011g0099 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.729-4981G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116774214 | ||||||
| chr12:116774217
|
T | A | 1 | a0001c0001t0011g0099 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.729-4978T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116774217 | ||||||
| chr12:116774219
|
G | C | 1 | a0001c0001t0011g0099 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.729-4976G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116774219 | ||||||
| chr12:116774220
|
T | A | 1 | a0001c0001t0011g0099 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.729-4975T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116774220 | ||||||
| chr12:116774229
|
T | G | 1 | a0001c0001t0011g0099 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.729-4966T>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116774229 | ||||||
| chr12:116774230
|
T | A | 1 | a0001c0001t0011g0099 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.729-4965T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116774230 | ||||||
| chr12:116774232
|
T | A | 1 | a0001c0001t0011g0099 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.729-4963T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116774232 | ||||||
| chr12:116774233
|
G | A | 1 | a0001c0001t0011g0099 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.729-4962G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116774233 | ||||||
| chr12:116774242
|
T | G | 1 | a0001c0001t0011g0099 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.729-4953T>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116774242 | ||||||
| chr12:116774248
|
T | C | 1 | a0001c0001t0011g0099 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.729-4947T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116774248 | ||||||
| chr12:116774249
|
A | C | 1 | a0001c0001t0011g0099 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.729-4946A>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116774249 | ||||||
| chr12:116774252
|
T | C | 1 | a0001c0001t0011g0099 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.729-4943T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116774252 | ||||||
| chr12:116774257
|
T | C | 1 | a0001c0001t0011g0099 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.729-4938T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116774257 | ||||||
| chr12:116774258
|
C | A | 1 | a0001c0001t0011g0099 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.729-4937C>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116774258 | ||||||
| chr12:116774259
|
A | C | 1 | a0001c0001t0011g0099 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.729-4936A>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116774259 | ||||||
| chr12:116774260
|
T | A | 1 | a0001c0001t0011g0099 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.729-4935T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116774260 | ||||||
| chr12:116774261
|
T | C | 1 | a0001c0001t0011g0099 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.729-4934T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116774261 | ||||||
| chr12:116774266
|
T | A | 1 | a0001c0001t0011g0099 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.729-4929T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116774266 | ||||||
| chr12:116774268
|
T | G | 1 | a0001c0001t0011g0099 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.729-4927T>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116774268 | ||||||
| chr12:116774270
|
C | A | 1 | a0001c0001t0011g0099 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.729-4925C>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116774270 | ||||||
| chr12:116774271
|
G | A | 253 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(250): Show | 253 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(250): Show |
intron_variant | MODIFIER | c.729-4924G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116774271 | ||||||
| chr12:116774276
|
A | C | 1 | a0001c0001t0011g0099 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.729-4919A>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116774276 | ||||||
| chr12:116774511
|
T | G | 27 | a0001c0001t0001g0141a0001c0001t0001g0190a0001c0001t0001g0193others(24): Show | 27 | HG00438.hp2 HG01099.hp2 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.729-4684T>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116774511 | ||||||
| chr12:116774512
|
A | G | 1 | a0001c0004t0052g0015 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.729-4683A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116774512 | ||||||
| chr12:116774738
|
G | A | 188 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(185): Show | 188 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(185): Show |
intron_variant | MODIFIER | c.729-4457G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116774738 | ||||||
| chr12:116774770
|
C | CGGGTGGA | 5 | a0001c0001t0004g0095a0001c0001t0004g0096a0001c0001t0004g0145others(2): Show | 5 | HG01243.hp2 HG02155.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.729-4407_729-4401d others(9): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 116774770 | |||||
| chr12:116774770
|
C | CGGGTGGA others(7): Show |
61 | a0001c0001t0001g0141a0001c0001t0001g0178a0001c0001t0001g0190others(58): Show | 61 | HG00438.hp2 HG01099.hp2 HG01257.hp2 others(58): Show |
intron_variant | MODIFIER | c.729-4414_729-4401d others(16): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 116774770 | |||||
| chr12:116774773
|
GTGGAGGG others(16): Show |
G | 1 | a0001c0006t0031g0067 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.729-4408_729-4386d others(25): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 116774773 | |||||
| chr12:116774824
|
A | T | 1 | a0001c0003t0014g0065 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.729-4371A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116774824 | ||||||
| chr12:116774871
|
A | T | 3 | a0001c0001t0002g0031a0001c0001t0002g0045a0001c0001t0002g0048 | 3 | HG02976.hp1 HG03540.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.729-4324A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116774871 | ||||||
| chr12:116774934
|
A | AAG | 5 | a0001c0001t0019g0124a0001c0001t0019g0163a0001c0001t0019g0187others(2): Show | 5 | HG00140.hp1 HG01261.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.729-4237_729-4236d others(4): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 116774934 | |||||
| chr12:116774934
|
A | AAGAG | 3 | a0001c0002t0005g0003a0001c0002t0005g0064a0001c0011t0039g0012 | 3 | HG01175.hp2 HG02486.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.729-4239_729-4236d others(6): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 116774934 | |||||
| chr12:116774934
|
AAGAGAG | A | 8 | a0001c0003t0005g0035a0001c0003t0005g0036a0001c0003t0016g0039others(5): Show | 8 | HG01243.hp1 HG02486.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.729-4241_729-4236d others(8): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 116774934 | |||||
| chr12:116774984
|
A | G | 5 | a0001c0001t0019g0124a0001c0001t0019g0163a0001c0001t0019g0187others(2): Show | 5 | HG00140.hp1 HG01261.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.729-4211A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116774984 | ||||||
| chr12:116774997
|
C | T | 4 | a0001c0001t0009g0116a0001c0001t0009g0130a0001c0001t0009g0153others(1): Show | 4 | HG01109.hp2 HG01258.hp2 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.729-4198C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116774997 | ||||||
| chr12:116774999
|
C | T | 1 | a0001c0002t0018g0022 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.729-4196C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116774999 | ||||||
| chr12:116775261
|
C | CA | 151 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(148): Show | 151 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(148): Show |
intron_variant | MODIFIER | c.729-3916dupA | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 116775261 | |||||
| chr12:116775278
|
A | G | 6 | a0001c0001t0002g0032a0001c0001t0008g0028a0001c0001t0008g0029others(3): Show | 6 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.729-3917A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116775278 | ||||||
| chr12:116775279
|
AGAG | A | 9 | a0001c0002t0005g0183a0001c0003t0005g0035a0001c0003t0005g0036others(6): Show | 9 | HG01243.hp1 HG02486.hp2 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.729-3915_729-3913d others(5): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116775279 | ||||||
| chr12:116775294
|
C | T | 1 | a0001c0001t0044g0255 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.729-3901C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116775294 | ||||||
| chr12:116775320
|
TGAAGTCA others(3): Show |
T | 251 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(248): Show | 251 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(248): Show |
intron_variant | MODIFIER | c.729-3863_729-3854d others(12): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 116775320 | |||||
| chr12:116775462
|
C | T | 1 | a0001c0003t0014g0065 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.729-3733C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116775462 | ||||||
| chr12:116775713
|
C | T | 33 | a0001c0001t0001g0141a0001c0001t0001g0190a0001c0001t0001g0193others(30): Show | 33 | HG00438.hp2 HG01099.hp2 HG01257.hp2 others(30): Show |
intron_variant | MODIFIER | c.729-3482C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116775713 | ||||||
| chr12:116775722
|
C | T | 1 | a0001c0002t0001g0080 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.729-3473C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116775722 | ||||||
| chr12:116775795
|
C | T | 33 | a0001c0001t0001g0141a0001c0001t0001g0190a0001c0001t0001g0193others(30): Show | 33 | HG00438.hp2 HG01099.hp2 HG01257.hp2 others(30): Show |
intron_variant | MODIFIER | c.729-3400C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116775795 | ||||||
| chr12:116775863
|
C | T | 1 | a0001c0002t0001g0073 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.729-3332C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116775863 | ||||||
| chr12:116775903
|
C | T | 3 | a0001c0002t0005g0149a0001c0002t0005g0151a0001c0002t0033g0150 | 3 | HG02922.hp2 NA20129.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.729-3292C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116775903 | ||||||
| chr12:116776022
|
A | G | 254 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(251): Show | 254 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(251): Show |
intron_variant | MODIFIER | c.729-3173A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116776022 | ||||||
| chr12:116776048
|
A | C | 1 | a0001c0016t0032g0044 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.729-3147A>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116776048 | ||||||
| chr12:116776343
|
G | C | 2 | a0001c0007t0025g0056a0001c0007t0046g0053 | 2 | HG02145.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.729-2852G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116776343 | ||||||
| chr12:116776463
|
C | T | 15 | a0001c0002t0018g0022a0001c0003t0005g0035a0001c0003t0005g0036others(12): Show | 15 | HG01243.hp1 HG01891.hp1 HG02132.hp2 others(12): Show |
intron_variant | MODIFIER | c.729-2732C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116776463 | ||||||
| chr12:116776487
|
C | A | 1 | a0001c0006t0050g0013 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.729-2708C>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116776487 | ||||||
| chr12:116776710
|
A | G | 6 | a0001c0001t0002g0032a0001c0001t0008g0028a0001c0001t0008g0029others(3): Show | 6 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.729-2485A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116776710 | ||||||
| chr12:116776812
|
G | A | 152 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(149): Show | 152 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.729-2383G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116776812 | ||||||
| chr12:116776916
|
A | AT | 30 | a0001c0001t0001g0141a0001c0001t0001g0190a0001c0001t0001g0215others(27): Show | 30 | HG00438.hp2 HG01099.hp2 HG01257.hp2 others(27): Show |
intron_variant | MODIFIER | c.729-2260dupT | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 116776916 | |||||
| chr12:116776916
|
A | ATT | 118 | a0001c0001t0001g0069a0001c0001t0001g0086a0001c0001t0001g0092others(115): Show | 118 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.729-2261_729-2260d others(4): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 116776916 | |||||
| chr12:116776916
|
A | ATTT | 33 | a0001c0001t0001g0072a0001c0001t0001g0122a0001c0001t0001g0166others(30): Show | 33 | HG01109.hp2 HG01258.hp2 HG01261.hp1 others(30): Show |
intron_variant | MODIFIER | c.729-2262_729-2260d others(5): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 116776916 | |||||
| chr12:116776986
|
C | T | 34 | a0001c0001t0001g0178a0001c0001t0004g0095a0001c0001t0004g0096others(31): Show | 34 | HG01175.hp2 HG01243.hp2 HG02055.hp1 others(31): Show |
intron_variant | MODIFIER | c.729-2209C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116776986 | ||||||
| chr12:116777090
|
G | A | 205 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(202): Show | 205 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(202): Show |
intron_variant | MODIFIER | c.729-2105G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116777090 | ||||||
| chr12:116777127
|
G | A | 5 | a0001c0001t0004g0095a0001c0001t0004g0096a0001c0001t0004g0145others(2): Show | 5 | HG01243.hp2 HG02155.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.729-2068G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116777127 | ||||||
| chr12:116777202
|
G | A | 1 | a0001c0006t0050g0013 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.729-1993G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116777202 | ||||||
| chr12:116777278
|
A | G | 1 | a0001c0005t0020g0162 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.729-1917A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116777278 | ||||||
| chr12:116777369
|
A | G | 4 | a0001c0002t0005g0003a0001c0002t0005g0064a0001c0011t0023g0007others(1): Show | 4 | HG01175.hp2 HG02486.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.729-1826A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116777369 | ||||||
| chr12:116777543
|
T | G | 1 | a0001c0001t0019g0187 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.729-1652T>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116777543 | ||||||
| chr12:116777647
|
G | C | 3 | a0001c0004t0001g0083a0002c0010t0002g0001a0002c0010t0002g0002 | 3 | HG02132.hp2 HG02135.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.729-1548G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116777647 | ||||||
| chr12:116777700
|
C | T | 5 | a0001c0001t0019g0124a0001c0001t0019g0163a0001c0001t0019g0187others(2): Show | 5 | HG00140.hp1 HG01261.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.729-1495C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116777700 | ||||||
| chr12:116777715
|
C | G | 1 | a0001c0002t0001g0076 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.729-1480C>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116777715 | ||||||
| chr12:116777715
|
C | T | 1 | a0001c0001t0040g0143 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.729-1480C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116777715 | ||||||
| chr12:116777792
|
G | T | 1 | a0001c0001t0011g0160 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.729-1403G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116777792 | ||||||
| chr12:116778131
|
CTCCTTTC others(5): Show |
C | 1 | a0001c0011t0053g0011 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.729-1058_729-1047d others(14): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 116778131 | |||||
| chr12:116778328
|
C | T | 9 | a0001c0001t0008g0041a0001c0001t0045g0114a0001c0002t0002g0129others(6): Show | 9 | HG02055.hp1 HG02258.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.729-867C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116778328 | ||||||
| chr12:116778421
|
A | G | 4 | a0001c0002t0005g0003a0001c0002t0005g0064a0001c0011t0023g0007others(1): Show | 4 | HG01175.hp2 HG02486.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.729-774A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116778421 | ||||||
| chr12:116778498
|
C | G | 4 | a0001c0004t0001g0083a0001c0004t0052g0015a0002c0010t0002g0001others(1): Show | 4 | HG02132.hp2 HG02135.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.729-697C>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116778498 | ||||||
| chr12:116778798
|
C | T | 1 | a0001c0002t0018g0022 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.729-397C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116778798 | ||||||
| chr12:116779407
|
A | C | 15 | a0001c0001t0002g0032a0001c0001t0008g0028a0001c0001t0008g0029others(12): Show | 15 | HG00140.hp1 HG01261.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.882+59A>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116779407 | ||||||
| chr12:116779543
|
C | T | 1 | a0001c0001t0002g0032 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.882+195C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116779543 | ||||||
| chr12:116779667
|
G | A | 2 | a0001c0001t0001g0141a0001c0001t0001g0235 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.882+319G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116779667 | ||||||
| chr12:116779913
|
G | A | 37 | a0001c0001t0001g0178a0001c0001t0004g0095a0001c0001t0004g0096others(34): Show | 37 | HG01243.hp2 HG01891.hp1 HG02055.hp1 others(34): Show |
intron_variant | MODIFIER | c.882+565G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116779913 | ||||||
| chr12:116779915
|
C | T | 37 | a0001c0001t0001g0178a0001c0001t0004g0095a0001c0001t0004g0096others(34): Show | 37 | HG01243.hp2 HG01891.hp1 HG02055.hp1 others(34): Show |
intron_variant | MODIFIER | c.882+567C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116779915 | ||||||
| chr12:116779928
|
AGACAAGG others(1716): Show |
A | 1 | a0001c0003t0006g0208 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.882+581_882+2303de others(1): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116779928 | ||||||
| chr12:116780040
|
C | T | 6 | a0001c0001t0002g0032a0001c0001t0008g0028a0001c0001t0008g0029others(3): Show | 6 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.882+692C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116780040 | ||||||
| chr12:116780068
|
G | C | 1 | a0001c0006t0031g0067 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.882+720G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116780068 | ||||||
| chr12:116780083
|
A | T | 1 | a0001c0001t0038g0219 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.882+735A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116780083 | ||||||
| chr12:116780168
|
A | C | 4 | a0001c0002t0005g0003a0001c0002t0005g0064a0001c0011t0023g0007others(1): Show | 4 | HG01175.hp2 HG02486.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.882+820A>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116780168 | ||||||
| chr12:116780276
|
T | C | 14 | a0001c0003t0005g0035a0001c0003t0005g0036a0001c0003t0016g0039others(11): Show | 14 | HG01243.hp1 HG01884.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.882+928T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116780276 | ||||||
| chr12:116780317
|
G | A | 2 | a0001c0001t0003g0144a0001c0001t0061g0148 | 2 | NA18975.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.882+969G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116780317 | ||||||
| chr12:116780326
|
C | A | 1 | a0001c0002t0005g0183 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.882+978C>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116780326 | ||||||
| chr12:116780364
|
G | A | 253 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(250): Show | 253 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(250): Show |
intron_variant | MODIFIER | c.882+1016G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116780364 | ||||||
| chr12:116780472
|
G | A | 179 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(176): Show | 179 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(176): Show |
intron_variant | MODIFIER | c.882+1124G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116780472 | ||||||
| chr12:116780593
|
C | T | 4 | a0001c0002t0005g0003a0001c0002t0005g0064a0001c0011t0023g0007others(1): Show | 4 | HG01175.hp2 HG02486.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.882+1245C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116780593 | ||||||
| chr12:116780670
|
CA | C | 45 | a0001c0001t0001g0178a0001c0001t0004g0095a0001c0001t0004g0096others(42): Show | 45 | HG01169.hp2 HG01243.hp1 HG01243.hp2 others(42): Show |
intron_variant | MODIFIER | c.882+1336delA | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116780670 | |||||
| chr12:116780686
|
A | G | 45 | a0001c0001t0001g0178a0001c0001t0004g0095a0001c0001t0004g0096others(42): Show | 45 | HG01243.hp1 HG01243.hp2 HG01891.hp1 others(42): Show |
intron_variant | MODIFIER | c.882+1338A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116780686 | ||||||
| chr12:116780694
|
A | G | 45 | a0001c0001t0001g0178a0001c0001t0004g0095a0001c0001t0004g0096others(42): Show | 45 | HG01243.hp1 HG01243.hp2 HG01891.hp1 others(42): Show |
intron_variant | MODIFIER | c.882+1346A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116780694 | ||||||
| chr12:116780723
|
C | T | 1 | a0001c0001t0003g0155 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.882+1375C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116780723 | ||||||
| chr12:116780731
|
A | G | 1 | a0001c0001t0006g0115 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.882+1383A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116780731 | ||||||
| chr12:116780908
|
C | G | 4 | a0001c0004t0001g0083a0001c0004t0052g0015a0002c0010t0002g0001others(1): Show | 4 | HG02132.hp2 HG02135.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.882+1560C>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116780908 | ||||||
| chr12:116780909
|
CA | C | 4 | a0001c0004t0001g0083a0001c0004t0052g0015a0002c0010t0002g0001others(1): Show | 4 | HG02132.hp2 HG02135.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.882+1562delA | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116780909 | ||||||
| chr12:116781057
|
C | T | 200 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(197): Show | 200 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(197): Show |
intron_variant | MODIFIER | c.882+1709C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116781057 | ||||||
| chr12:116781267
|
C | G | 6 | a0001c0001t0002g0032a0001c0001t0008g0028a0001c0001t0008g0029others(3): Show | 6 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.882+1919C>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116781267 | ||||||
| chr12:116781279
|
G | C | 1 | a0001c0001t0056g0220 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.882+1931G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116781279 | ||||||
| chr12:116781553
|
C | T | 152 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(149): Show | 152 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.882+2205C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116781553 | ||||||
| chr12:116781554
|
G | A | 9 | a0001c0003t0005g0035a0001c0003t0005g0036a0001c0003t0016g0039others(6): Show | 9 | HG01243.hp1 HG02486.hp2 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.882+2206G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116781554 | ||||||
| chr12:116781577
|
G | A | 4 | a0001c0007t0025g0009a0001c0007t0025g0056a0001c0007t0046g0053others(1): Show | 4 | HG01884.hp2 HG02145.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.882+2229G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116781577 | ||||||
| chr12:116781627
|
G | A | 2 | a0001c0007t0025g0056a0001c0007t0046g0053 | 2 | HG02145.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.882+2279G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116781627 | ||||||
| chr12:116781642
|
C | T | 2 | a0001c0001t0004g0172a0001c0001t0026g0181 | 2 | HG03831.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.882+2294C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116781642 | ||||||
| chr12:116781653
|
C | A | 1 | a0001c0003t0006g0208 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.882+2305C>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116781653 | ||||||
| chr12:116781654
|
T | G | 1 | a0001c0003t0006g0208 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.882+2306T>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116781654 | ||||||
| chr12:116781847
|
C | T | 185 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(182): Show | 185 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(182): Show |
intron_variant | MODIFIER | c.882+2499C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116781847 | ||||||
| chr12:116781927
|
A | G | 1 | a0001c0009t0037g0043 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.882+2579A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116781927 | ||||||
| chr12:116781934
|
C | G | 4 | a0001c0002t0005g0003a0001c0002t0005g0064a0001c0011t0023g0007others(1): Show | 4 | HG01175.hp2 HG02486.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.882+2586C>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116781934 | ||||||
| chr12:116781935
|
T | G | 4 | a0001c0002t0005g0003a0001c0002t0005g0064a0001c0011t0023g0007others(1): Show | 4 | HG01175.hp2 HG02486.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.882+2587T>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116781935 | ||||||
| chr12:116781948
|
A | G | 45 | a0001c0001t0001g0178a0001c0001t0004g0095a0001c0001t0004g0096others(42): Show | 45 | HG01243.hp1 HG01243.hp2 HG01891.hp1 others(42): Show |
intron_variant | MODIFIER | c.882+2600A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116781948 | ||||||
| chr12:116781951
|
C | T | 1 | a0001c0004t0001g0113 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.882+2603C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116781951 | ||||||
| chr12:116782047
|
C | A | 3 | a0001c0001t0001g0120a0001c0001t0001g0227a0002c0010t0002g0254 | 3 | HG00609.hp2 HG02040.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.882+2699C>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116782047 | ||||||
| chr12:116782056
|
G | T | 1 | a0001c0001t0071g0119 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.882+2708G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116782056 | ||||||
| chr12:116782066
|
G | A | 4 | a0001c0004t0001g0083a0001c0004t0052g0015a0002c0010t0002g0001others(1): Show | 4 | HG02132.hp2 HG02135.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.882+2718G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116782066 | ||||||
| chr12:116782073
|
C | T | 27 | a0001c0001t0001g0141a0001c0001t0001g0190a0001c0001t0001g0193others(24): Show | 27 | HG00438.hp2 HG01099.hp2 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.882+2725C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116782073 | ||||||
| chr12:116782074
|
G | A | 1 | a0001c0001t0003g0106 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.882+2726G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116782074 | ||||||
| chr12:116782079
|
C | CAAAAAAA | 13 | a0001c0001t0001g0202a0001c0002t0018g0022a0001c0003t0005g0035others(10): Show | 13 | HG01243.hp1 HG01891.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.882+2740_882+2746d others(9): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116782079 | |||||
| chr12:116782079
|
C | CAAAAAAA others(1): Show |
6 | a0001c0001t0004g0168a0001c0001t0008g0028a0001c0001t0008g0029others(3): Show | 6 | HG02559.hp1 HG02572.hp2 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.882+2739_882+2746d others(10): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116782079 | |||||
| chr12:116782079
|
C | CAAAAAAA others(2): Show |
29 | a0001c0001t0001g0178a0001c0001t0002g0032a0001c0001t0004g0095others(26): Show | 29 | HG01243.hp2 HG02055.hp1 HG02074.hp1 others(26): Show |
intron_variant | MODIFIER | c.882+2738_882+2746d others(11): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116782079 | |||||
| chr12:116782079
|
C | CAAAAAAA others(3): Show |
8 | a0001c0001t0007g0180a0001c0002t0001g0079a0001c0002t0004g0005others(5): Show | 8 | HG02486.hp1 HG02622.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.882+2737_882+2746d others(12): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116782079 | |||||
| chr12:116782079
|
C | CAAAAAAA others(4): Show |
2 | a0001c0002t0005g0003a0001c0002t0067g0042 | 2 | HG01175.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.882+2736_882+2746d others(13): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116782079 | |||||
| chr12:116782079
|
C | CAAAAAAA others(8): Show |
3 | a0001c0002t0001g0078a0001c0004t0001g0083a0002c0010t0002g0002 | 3 | HG01099.hp2 HG02132.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.882+2732_882+2746d others(17): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116782079 | |||||
| chr12:116782079
|
C | CAAAAAAA others(9): Show |
17 | a0001c0001t0001g0141a0001c0001t0001g0190a0001c0001t0001g0215others(14): Show | 17 | HG01258.hp1 HG01975.hp2 HG02004.hp1 others(14): Show |
intron_variant | MODIFIER | c.882+2746_882+2747i others(18): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116782079 | |||||
| chr12:116782079
|
C | CAAAAAAA others(10): Show |
10 | a0001c0001t0001g0193a0001c0001t0001g0235a0001c0001t0002g0189others(7): Show | 10 | HG00438.hp2 HG01257.hp2 HG01361.hp2 others(7): Show |
intron_variant | MODIFIER | c.882+2746_882+2747i others(19): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116782079 | |||||
| chr12:116782079
|
C | CAAAAAAA others(11): Show |
1 | a0001c0004t0052g0015 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.882+2746_882+2747i others(20): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116782079 | |||||
| chr12:116782079
|
C | CAAAAAAA others(12): Show |
5 | a0001c0001t0001g0211a0001c0001t0007g0087a0001c0001t0038g0219others(2): Show | 5 | HG00408.hp1 HG00423.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.882+2746_882+2747i others(21): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116782079 | |||||
| chr12:116782079
|
C | CAAAAAAA others(13): Show |
31 | a0001c0001t0001g0072a0001c0001t0001g0086a0001c0001t0001g0092others(28): Show | 31 | HG00609.hp1 HG01261.hp1 HG02155.hp2 others(28): Show |
intron_variant | MODIFIER | c.882+2746_882+2747i others(22): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116782079 | |||||
| chr12:116782079
|
C | CAAAAAAA others(14): Show |
67 | a0001c0001t0001g0069a0001c0001t0001g0120a0001c0001t0001g0135others(64): Show | 67 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.882+2746_882+2747i others(23): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116782079 | |||||
| chr12:116782079
|
C | CAAAAAAA others(15): Show |
31 | a0001c0001t0001g0094a0001c0001t0001g0196a0001c0001t0001g0197others(28): Show | 31 | HG00741.hp2 HG01109.hp2 HG01192.hp1 others(28): Show |
intron_variant | MODIFIER | c.882+2746_882+2747i others(24): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116782079 | |||||
| chr12:116782079
|
C | CAAAAAAA others(16): Show |
16 | a0001c0001t0001g0195a0001c0001t0001g0257a0001c0001t0001g0260others(13): Show | 16 | HG01106.hp2 HG01891.hp2 HG01978.hp1 others(13): Show |
intron_variant | MODIFIER | c.882+2746_882+2747i others(25): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116782079 | |||||
| chr12:116782079
|
C | CAAAAAAA others(17): Show |
3 | a0001c0001t0001g0205a0001c0001t0019g0124a0001c0001t0056g0220 | 3 | HG00140.hp1 HG02055.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.882+2746_882+2747i others(26): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116782079 | |||||
| chr12:116782079
|
C | CAAAAAAA others(18): Show |
1 | a0001c0003t0002g0101 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.882+2746_882+2747i others(27): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116782079 | |||||
| chr12:116782079
|
C | CAAAAAAA others(19): Show |
2 | a0001c0003t0002g0100a0001c0003t0002g0102 | 2 | HG02280.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.882+2746_882+2747i others(28): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116782079 | |||||
| chr12:116782079
|
C | CAAAAAAA others(24): Show |
2 | a0001c0001t0019g0163a0001c0016t0032g0044 | 2 | HG02630.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.882+2746_882+2747i others(33): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116782079 | |||||
| chr12:116782079
|
C | CAAAAAAA others(27): Show |
2 | a0001c0001t0019g0187a0001c0001t0057g0188 | 2 | HG01261.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.882+2746_882+2747i others(36): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116782079 | |||||
| chr12:116782079
|
C | CAAAAAAA others(30): Show |
1 | a0001c0006t0031g0067 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.882+2746_882+2747i others(39): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116782079 | |||||
| chr12:116782081
|
A | AAAAAAAA others(14): Show |
1 | a0001c0001t0001g0227 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.882+2746_882+2747i others(23): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116782081 | |||||
| chr12:116782142
|
G | A | 152 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(149): Show | 152 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.882+2794G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116782142 | ||||||
| chr12:116782148
|
G | A | 6 | a0001c0006t0031g0067a0001c0007t0025g0009a0001c0007t0025g0056others(3): Show | 6 | HG01884.hp2 HG02145.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.882+2800G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116782148 | ||||||
| chr12:116782184
|
A | G | 4 | a0001c0002t0005g0003a0001c0002t0005g0064a0001c0011t0023g0007others(1): Show | 4 | HG01175.hp2 HG02486.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.882+2836A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116782184 | ||||||
| chr12:116782252
|
C | T | 27 | a0001c0001t0001g0141a0001c0001t0001g0190a0001c0001t0001g0193others(24): Show | 27 | HG00438.hp2 HG01099.hp2 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.882+2904C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116782252 | ||||||
| chr12:116782343
|
G | A | 2 | a0001c0001t0004g0173a0001c0001t0047g0241 | 2 | HG02074.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.882+2995G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116782343 | ||||||
| chr12:116782431
|
A | C | 1 | a0001c0006t0006g0218 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.882+3083A>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116782431 | ||||||
| chr12:116782454
|
G | C | 179 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(176): Show | 179 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(176): Show |
intron_variant | MODIFIER | c.882+3106G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116782454 | ||||||
| chr12:116782601
|
C | T | 45 | a0001c0001t0001g0178a0001c0001t0004g0095a0001c0001t0004g0096others(42): Show | 45 | HG01243.hp1 HG01243.hp2 HG01891.hp1 others(42): Show |
intron_variant | MODIFIER | c.882+3253C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116782601 | ||||||
| chr12:116782716
|
G | A | 4 | a0001c0007t0025g0009a0001c0007t0025g0056a0001c0007t0046g0053others(1): Show | 4 | HG01884.hp2 HG02145.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.882+3368G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116782716 | ||||||
| chr12:116782762
|
A | T | 1 | a0001c0006t0036g0018 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.882+3414A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116782762 | ||||||
| chr12:116782798
|
T | C | 2 | a0001c0001t0001g0169a0001c0004t0012g0134 | 2 | HG03239.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.882+3450T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116782798 | ||||||
| chr12:116782971
|
A | G | 3 | a0001c0004t0001g0083a0002c0010t0002g0001a0002c0010t0002g0002 | 3 | HG02132.hp2 HG02135.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.882+3623A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116782971 | ||||||
| chr12:116783033
|
T | A | 1 | a0001c0002t0012g0014 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.882+3685T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116783033 | ||||||
| chr12:116783043
|
A | G | 45 | a0001c0001t0001g0178a0001c0001t0004g0095a0001c0001t0004g0096others(42): Show | 45 | HG01243.hp1 HG01243.hp2 HG01891.hp1 others(42): Show |
intron_variant | MODIFIER | c.882+3695A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116783043 | ||||||
| chr12:116783055
|
T | C | 12 | a0001c0001t0001g0166a0001c0001t0002g0236a0001c0001t0006g0115others(9): Show | 12 | HG01109.hp2 HG01258.hp2 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.882+3707T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116783055 | ||||||
| chr12:116783121
|
G | A | 6 | a0001c0001t0005g0105a0001c0005t0013g0006a0001c0005t0013g0154others(3): Show | 6 | HG01891.hp2 HG02280.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.882+3773G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116783121 | ||||||
| chr12:116783179
|
T | A | 1 | a0001c0001t0048g0182 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.882+3831T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116783179 | ||||||
| chr12:116783187
|
T | C | 5 | a0001c0001t0019g0124a0001c0001t0019g0163a0001c0001t0019g0187others(2): Show | 5 | HG00140.hp1 HG01261.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.882+3839T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116783187 | ||||||
| chr12:116783323
|
C | T | 2 | a0001c0001t0001g0141a0001c0001t0001g0235 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.882+3975C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116783323 | ||||||
| chr12:116783453
|
G | A | 1 | a0001c0001t0014g0156 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.882+4105G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116783453 | ||||||
| chr12:116783692
|
T | C | 1 | a0001c0009t0010g0049 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.882+4344T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116783692 | ||||||
| chr12:116783839
|
G | T | 6 | a0001c0001t0002g0032a0001c0001t0008g0028a0001c0001t0008g0029others(3): Show | 6 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.882+4491G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116783839 | ||||||
| chr12:116783947
|
G | A | 4 | a0001c0002t0005g0003a0001c0002t0005g0064a0001c0011t0023g0007others(1): Show | 4 | HG01175.hp2 HG02486.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.882+4599G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116783947 | ||||||
| chr12:116783980
|
G | A | 27 | a0001c0001t0001g0141a0001c0001t0001g0190a0001c0001t0001g0193others(24): Show | 27 | HG00438.hp2 HG01099.hp2 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.882+4632G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116783980 | ||||||
| chr12:116783984
|
T | C | 1 | a0001c0006t0006g0218 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.882+4636T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116783984 | ||||||
| chr12:116784173
|
G | C | 1 | a0001c0001t0002g0192 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.882+4825G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116784173 | ||||||
| chr12:116784323
|
C | T | 2 | a0001c0001t0001g0237a0001c0002t0012g0089 | 2 | HG01074.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.882+4975C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116784323 | ||||||
| chr12:116784335
|
C | T | 7 | a0001c0003t0002g0100a0001c0003t0002g0101a0001c0003t0002g0102others(4): Show | 7 | HG00741.hp1 HG01074.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.882+4987C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116784335 | ||||||
| chr12:116784360
|
G | A | 1 | a0001c0016t0032g0044 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.882+5012G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116784360 | ||||||
| chr12:116784485
|
A | G | 2 | a0001c0001t0019g0187a0001c0001t0057g0188 | 2 | HG01261.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.882+5137A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116784485 | ||||||
| chr12:116784493
|
T | G | 5 | a0001c0001t0019g0124a0001c0001t0019g0163a0001c0001t0019g0187others(2): Show | 5 | HG00140.hp1 HG01261.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.882+5145T>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116784493 | ||||||
| chr12:116784651
|
C | T | 4 | a0001c0002t0005g0003a0001c0002t0005g0064a0001c0011t0023g0007others(1): Show | 4 | HG01175.hp2 HG02486.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.882+5303C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116784651 | ||||||
| chr12:116784673
|
T | C | 1 | a0001c0001t0010g0233 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.882+5325T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116784673 | ||||||
| chr12:116784752
|
A | G | 1 | a0001c0001t0048g0182 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.882+5404A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116784752 | ||||||
| chr12:116785130
|
A | G | 1 | a0001c0004t0002g0025 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.882+5782A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116785130 | ||||||
| chr12:116785249
|
C | CTGTG | 3 | a0001c0001t0001g0216a0001c0001t0003g0131a0001c0008t0003g0206 | 3 | HG02273.hp1 NA18999.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.882+5924_882+5927d others(6): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116785249 | |||||
| chr12:116785249
|
C | CTGTGTG | 6 | a0001c0001t0002g0032a0001c0001t0003g0085a0001c0001t0008g0028others(3): Show | 6 | HG02257.hp2 HG02559.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.882+5922_882+5927d others(8): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116785249 | |||||
| chr12:116785249
|
C | CTGTGTGT others(1): Show |
126 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(123): Show | 126 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.882+5920_882+5927d others(10): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116785249 | |||||
| chr12:116785249
|
C | CTGTGTGT others(3): Show |
23 | a0001c0001t0001g0169a0001c0001t0001g0203a0001c0001t0001g0249others(20): Show | 23 | HG00673.hp1 HG01099.hp1 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.882+5918_882+5927d others(12): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116785249 | |||||
| chr12:116785249
|
C | CTGTGTGT others(5): Show |
2 | a0001c0001t0027g0125a0001c0002t0005g0003 | 2 | HG01175.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.882+5916_882+5927d others(14): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116785249 | |||||
| chr12:116785249
|
C | CTGTGTGT others(7): Show |
2 | a0001c0001t0002g0031a0001c0002t0062g0185 | 2 | HG01169.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.882+5914_882+5927d others(16): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116785249 | |||||
| chr12:116785249
|
C | CTGTGTGT others(9): Show |
3 | a0001c0002t0005g0064a0001c0011t0023g0007a0001c0011t0039g0012 | 3 | HG02486.hp1 HG02886.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.882+5912_882+5927d others(18): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116785249 | |||||
| chr12:116785249
|
C | CTGTGTGT others(13): Show |
1 | a0001c0004t0052g0015 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.882+5908_882+5927d others(22): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116785249 | |||||
| chr12:116785249
|
C | CTGTGTGT others(15): Show |
1 | a0001c0007t0034g0063 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.882+5906_882+5927d others(24): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116785249 | |||||
| chr12:116785249
|
C | CTGTGTGT others(17): Show |
1 | a0001c0016t0032g0044 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.882+5904_882+5927d others(26): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116785249 | |||||
| chr12:116785249
|
C | CTGTGTGT others(19): Show |
1 | a0001c0006t0036g0018 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.882+5902_882+5927d others(28): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116785249 | |||||
| chr12:116785249
|
C | CTGTGTGT others(23): Show |
1 | a0001c0006t0031g0067 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.882+5927_882+5928i others(32): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116785249 | |||||
| chr12:116785249
|
CTG | C | 4 | a0001c0003t0002g0100a0001c0003t0002g0101a0001c0003t0002g0102others(1): Show | 4 | HG01074.hp2 HG02280.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.882+5926_882+5927d others(4): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116785249 | |||||
| chr12:116785249
|
CTGTG | C | 5 | a0001c0003t0035g0088a0001c0007t0025g0009a0001c0007t0025g0056others(2): Show | 5 | HG01884.hp2 HG02145.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.882+5924_882+5927d others(6): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116785249 | |||||
| chr12:116785275
|
G | GTGTGTGT others(2): Show |
34 | a0001c0001t0001g0141a0001c0001t0001g0190a0001c0001t0001g0193others(31): Show | 34 | HG00438.hp2 HG01099.hp2 HG01257.hp2 others(31): Show |
intron_variant | MODIFIER | c.882+5927_882+5928i others(11): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116785275 | ||||||
| chr12:116785275
|
G | GTGTGTGT others(4): Show |
17 | a0001c0001t0001g0178a0001c0001t0004g0110a0001c0001t0004g0168others(14): Show | 17 | HG02074.hp1 HG02257.hp1 HG02300.hp1 others(14): Show |
intron_variant | MODIFIER | c.882+5927_882+5928i others(13): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116785275 | ||||||
| chr12:116785275
|
G | GTGTGTGT others(6): Show |
4 | a0001c0001t0004g0095a0001c0001t0004g0173a0001c0001t0004g0177others(1): Show | 4 | HG02965.hp1 HG03225.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.882+5927_882+5928i others(15): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116785275 | ||||||
| chr12:116785275
|
G | GTGTGTGT others(8): Show |
6 | a0001c0001t0004g0145a0001c0003t0005g0035a0001c0003t0005g0036others(3): Show | 6 | HG00741.hp1 HG02155.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.882+5927_882+5928i others(17): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116785275 | ||||||
| chr12:116785275
|
G | GTGTGTGT others(10): Show |
5 | a0001c0001t0002g0175a0001c0001t0002g0184a0001c0002t0049g0004others(2): Show | 5 | HG01243.hp1 HG01243.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.882+5927_882+5928i others(19): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116785275 | ||||||
| chr12:116785275
|
G | GTGTGTGT others(12): Show |
5 | a0001c0001t0004g0096a0001c0002t0004g0005a0001c0005t0020g0162others(2): Show | 5 | HG02486.hp2 HG02622.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.882+5927_882+5928i others(21): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116785275 | ||||||
| chr12:116785275
|
G | GTGTGTGT others(14): Show |
1 | a0001c0001t0019g0163 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.882+5927_882+5928i others(23): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116785275 | ||||||
| chr12:116785275
|
G | GTGTGTGT others(16): Show |
1 | a0001c0001t0056g0220 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.882+5927_882+5928i others(25): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116785275 | ||||||
| chr12:116785275
|
G | GTGTGTGT others(18): Show |
2 | a0001c0001t0019g0187a0001c0001t0057g0188 | 2 | HG01261.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.882+5927_882+5928i others(27): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116785275 | ||||||
| chr12:116785275
|
G | GTGTGTGT others(20): Show |
1 | a0001c0001t0019g0124 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.882+5927_882+5928i others(29): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116785275 | ||||||
| chr12:116785277
|
C | G | 77 | a0001c0001t0001g0141a0001c0001t0001g0178a0001c0001t0001g0190others(74): Show | 77 | HG00140.hp1 HG00438.hp2 HG00741.hp1 others(74): Show |
intron_variant | MODIFIER | c.882+5929C>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116785277 | ||||||
| chr12:116785278
|
G | C | 77 | a0001c0001t0001g0141a0001c0001t0001g0178a0001c0001t0001g0190others(74): Show | 77 | HG00140.hp1 HG00438.hp2 HG00741.hp1 others(74): Show |
intron_variant | MODIFIER | c.882+5930G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116785278 | ||||||
| chr12:116785286
|
G | T | 1 | a0001c0007t0034g0063 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.882+5938G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116785286 | ||||||
| chr12:116785293
|
G | GTTTGTTT others(3): Show |
71 | a0001c0001t0001g0141a0001c0001t0001g0178a0001c0001t0001g0190others(68): Show | 71 | HG00438.hp2 HG01099.hp2 HG01243.hp1 others(68): Show |
intron_variant | MODIFIER | c.882+5953_882+5962d others(12): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116785293 | |||||
| chr12:116785293
|
G | GTTTGTTT others(13): Show |
4 | a0001c0002t0005g0003a0001c0002t0005g0064a0001c0011t0023g0007others(1): Show | 4 | HG01175.hp2 HG02486.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.882+5962_882+5963i others(22): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116785293 | |||||
| chr12:116785504
|
T | C | 4 | a0001c0002t0005g0003a0001c0002t0005g0064a0001c0011t0023g0007others(1): Show | 4 | HG01175.hp2 HG02486.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.882+6156T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116785504 | ||||||
| chr12:116785551
|
C | A | 1 | a0001c0002t0002g0159 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.882+6203C>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116785551 | ||||||
| chr12:116785567
|
T | C | 1 | a0001c0003t0014g0065 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.882+6219T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116785567 | ||||||
| chr12:116785751
|
G | A | 4 | a0001c0003t0002g0100a0001c0003t0002g0101a0001c0003t0002g0102others(1): Show | 4 | HG01074.hp2 HG02280.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.882+6403G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116785751 | ||||||
| chr12:116785836
|
T | C | 257 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(254): Show | 257 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(254): Show |
intron_variant | MODIFIER | c.882+6488T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116785836 | ||||||
| chr12:116785843
|
G | A | 2 | a0001c0001t0007g0070a0001c0001t0007g0171 | 2 | HG02523.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.882+6495G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116785843 | ||||||
| chr12:116785851
|
C | T | 6 | a0001c0001t0002g0032a0001c0001t0008g0028a0001c0001t0008g0029others(3): Show | 6 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.882+6503C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116785851 | ||||||
| chr12:116785910
|
T | C | 3 | a0001c0003t0002g0100a0001c0003t0002g0101a0001c0003t0002g0102 | 3 | HG01074.hp2 HG02280.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.882+6562T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116785910 | ||||||
| chr12:116785972
|
A | C | 1 | a0001c0003t0035g0088 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.882+6624A>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116785972 | ||||||
| chr12:116786032
|
A | G | 1 | a0001c0011t0023g0007 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.882+6684A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116786032 | ||||||
| chr12:116786122
|
C | CT | 30 | a0001c0001t0001g0178a0001c0001t0001g0202a0001c0001t0001g0243others(27): Show | 30 | HG01884.hp2 HG02074.hp1 HG02132.hp2 others(27): Show |
intron_variant | MODIFIER | c.882+6790dupT | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116786122 | |||||
| chr12:116786268
|
C | T | 45 | a0001c0001t0001g0178a0001c0001t0004g0095a0001c0001t0004g0096others(42): Show | 45 | HG01243.hp1 HG01243.hp2 HG01891.hp1 others(42): Show |
intron_variant | MODIFIER | c.882+6920C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116786268 | ||||||
| chr12:116786286
|
TA | T | 4 | a0001c0002t0005g0003a0001c0002t0005g0064a0001c0011t0023g0007others(1): Show | 4 | HG01175.hp2 HG02486.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.882+6940delA | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116786286 | |||||
| chr12:116786331
|
G | A | 1 | a0001c0003t0002g0247 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.882+6983G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116786331 | ||||||
| chr12:116786352
|
C | G | 45 | a0001c0001t0001g0178a0001c0001t0004g0095a0001c0001t0004g0096others(42): Show | 45 | HG01243.hp1 HG01243.hp2 HG01891.hp1 others(42): Show |
intron_variant | MODIFIER | c.882+7004C>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116786352 | ||||||
| chr12:116786362
|
C | T | 5 | a0001c0001t0002g0031a0001c0001t0002g0045a0001c0001t0002g0048others(2): Show | 5 | HG02572.hp1 HG02976.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.882+7014C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116786362 | ||||||
| chr12:116786388
|
G | T | 4 | a0001c0002t0005g0003a0001c0002t0005g0064a0001c0011t0023g0007others(1): Show | 4 | HG01175.hp2 HG02486.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.882+7040G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116786388 | ||||||
| chr12:116786544
|
A | AT | 49 | a0001c0001t0001g0178a0001c0001t0004g0095a0001c0001t0004g0096others(46): Show | 49 | HG01175.hp2 HG01243.hp1 HG01243.hp2 others(46): Show |
intron_variant | MODIFIER | c.882+7196_882+7197i others(3): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116786544 | ||||||
| chr12:116786548
|
T | G | 49 | a0001c0001t0001g0178a0001c0001t0004g0095a0001c0001t0004g0096others(46): Show | 49 | HG01175.hp2 HG01243.hp1 HG01243.hp2 others(46): Show |
intron_variant | MODIFIER | c.882+7200T>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116786548 | ||||||
| chr12:116786563
|
G | A | 28 | a0001c0001t0001g0141a0001c0001t0001g0190a0001c0001t0001g0193others(25): Show | 28 | HG00438.hp2 HG01099.hp2 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.882+7215G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116786563 | ||||||
| chr12:116786575
|
C | A | 1 | a0001c0001t0003g0164 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.882+7227C>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116786575 | ||||||
| chr12:116786693
|
C | T | 1 | a0001c0009t0051g0016 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.882+7345C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116786693 | ||||||
| chr12:116786754
|
G | T | 153 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(150): Show | 153 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.882+7406G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116786754 | ||||||
| chr12:116786811
|
C | T | 3 | a0001c0004t0001g0083a0002c0010t0002g0001a0002c0010t0002g0002 | 3 | HG02132.hp2 HG02135.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.882+7463C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116786811 | ||||||
| chr12:116786984
|
G | A | 2 | a0001c0001t0001g0092a0001c0001t0001g0232 | 2 | NA18941.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.882+7636G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116786984 | ||||||
| chr12:116787035
|
G | A | 45 | a0001c0001t0001g0178a0001c0001t0004g0095a0001c0001t0004g0096others(42): Show | 45 | HG01243.hp1 HG01243.hp2 HG01891.hp1 others(42): Show |
intron_variant | MODIFIER | c.882+7687G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116787035 | ||||||
| chr12:116787054
|
G | A | 9 | a0001c0001t0008g0041a0001c0001t0045g0114a0001c0002t0002g0129others(6): Show | 9 | HG02055.hp1 HG02258.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.882+7706G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116787054 | ||||||
| chr12:116787078
|
T | C | 1 | a0001c0002t0021g0139 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.882+7730T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116787078 | ||||||
| chr12:116787118
|
G | A | 255 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(252): Show | 255 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(252): Show |
intron_variant | MODIFIER | c.882+7770G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116787118 | ||||||
| chr12:116787273
|
C | T | 71 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(68): Show | 71 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.882+7925C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116787273 | ||||||
| chr12:116787394
|
G | A | 45 | a0001c0001t0001g0178a0001c0001t0004g0095a0001c0001t0004g0096others(42): Show | 45 | HG01243.hp1 HG01243.hp2 HG01891.hp1 others(42): Show |
intron_variant | MODIFIER | c.882+8046G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116787394 | ||||||
| chr12:116787686
|
C | T | 33 | a0001c0001t0001g0178a0001c0001t0004g0095a0001c0001t0004g0096others(30): Show | 33 | HG01243.hp2 HG02055.hp1 HG02074.hp1 others(30): Show |
intron_variant | MODIFIER | c.882+8338C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116787686 | ||||||
| chr12:116787718
|
GA | G | 184 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(181): Show | 184 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(181): Show |
intron_variant | MODIFIER | c.882+8385delA | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116787718 | |||||
| chr12:116787718
|
GAA | G | 44 | a0001c0001t0001g0141a0001c0001t0001g0190a0001c0001t0001g0193others(41): Show | 44 | HG00140.hp1 HG00438.hp2 HG01099.hp2 others(41): Show |
intron_variant | MODIFIER | c.882+8384_882+8385d others(4): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116787718 | |||||
| chr12:116787838
|
T | A | 3 | a0001c0001t0017g0167a0001c0001t0017g0200a0001c0001t0017g0213 | 3 | NA18945.hp1 NA18954.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.882+8490T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116787838 | ||||||
| chr12:116787914
|
C | T | 7 | a0001c0003t0002g0100a0001c0003t0002g0101a0001c0003t0002g0102others(4): Show | 7 | HG00741.hp1 HG01074.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.882+8566C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116787914 | ||||||
| chr12:116787984
|
A | G | 152 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(149): Show | 152 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.882+8636A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116787984 | ||||||
| chr12:116788133
|
G | A | 2 | a0001c0007t0025g0056a0001c0007t0046g0053 | 2 | HG02145.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.882+8785G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116788133 | ||||||
| chr12:116788223
|
A | G | 49 | a0001c0001t0001g0178a0001c0001t0004g0095a0001c0001t0004g0096others(46): Show | 49 | HG01175.hp2 HG01243.hp1 HG01243.hp2 others(46): Show |
intron_variant | MODIFIER | c.882+8875A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116788223 | ||||||
| chr12:116788254
|
C | T | 27 | a0001c0001t0001g0141a0001c0001t0001g0190a0001c0001t0001g0193others(24): Show | 27 | HG00438.hp2 HG01099.hp2 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.882+8906C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116788254 | ||||||
| chr12:116788255
|
G | A | 6 | a0001c0006t0031g0067a0001c0007t0025g0009a0001c0007t0025g0056others(3): Show | 6 | HG01884.hp2 HG02145.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.882+8907G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116788255 | ||||||
| chr12:116788528
|
C | T | 2 | a0001c0001t0001g0069a0001c0002t0001g0251 | 2 | HG02080.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.882+9180C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116788528 | ||||||
| chr12:116788666
|
G | C | 1 | a0001c0003t0002g0101 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.882+9318G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116788666 | ||||||
| chr12:116788767
|
A | G | 4 | a0001c0002t0005g0003a0001c0002t0005g0064a0001c0011t0023g0007others(1): Show | 4 | HG01175.hp2 HG02486.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.882+9419A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116788767 | ||||||
| chr12:116788796
|
T | C | 49 | a0001c0001t0001g0178a0001c0001t0004g0095a0001c0001t0004g0096others(46): Show | 49 | HG01175.hp2 HG01243.hp1 HG01243.hp2 others(46): Show |
intron_variant | MODIFIER | c.882+9448T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116788796 | ||||||
| chr12:116788810
|
T | TGGTGGAT others(17): Show |
1 | a0001c0016t0032g0044 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.882+9464_882+9487d others(26): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116788810 | |||||
| chr12:116788826
|
A | AGATGGAT others(5): Show |
30 | a0001c0001t0001g0178a0001c0001t0004g0095a0001c0001t0004g0096others(27): Show | 30 | HG01243.hp2 HG02055.hp1 HG02074.hp1 others(27): Show |
intron_variant | MODIFIER | c.882+9490_882+9501d others(14): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116788826 | |||||
| chr12:116788826
|
A | AGATGGAT others(9): Show |
11 | a0001c0001t0008g0041a0001c0001t0045g0114a0001c0002t0008g0140others(8): Show | 11 | HG01243.hp1 HG02486.hp2 HG02965.hp2 others(8): Show |
intron_variant | MODIFIER | c.882+9486_882+9501d others(18): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116788826 | |||||
| chr12:116788826
|
A | AGATGGAT others(13): Show |
4 | a0001c0002t0018g0022a0001c0005t0030g0051a0001c0005t0030g0052others(1): Show | 4 | HG01891.hp1 HG02257.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.882+9482_882+9501d others(22): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116788826 | |||||
| chr12:116788826
|
AGATG | A | 152 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(149): Show | 152 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.882+9498_882+9501d others(6): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116788826 | |||||
| chr12:116788955
|
GGGAT | G | 199 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(196): Show | 199 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(196): Show |
intron_variant | MODIFIER | c.882+9634_882+9637d others(6): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116788955 | |||||
| chr12:116788955
|
GGGATGGA others(1): Show |
G | 7 | a0001c0001t0017g0167a0001c0001t0017g0200a0001c0001t0017g0213others(4): Show | 7 | HG02132.hp2 HG02135.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.882+9630_882+9637d others(10): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116788955 | |||||
| chr12:116788955
|
GGGATGGA others(5): Show |
G | 45 | a0001c0001t0001g0178a0001c0001t0004g0095a0001c0001t0004g0096others(42): Show | 45 | HG01243.hp1 HG01243.hp2 HG01891.hp1 others(42): Show |
intron_variant | MODIFIER | c.882+9626_882+9637d others(14): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116788955 | |||||
| chr12:116788955
|
GGGATGGA others(9): Show |
G | 2 | a0001c0001t0015g0112a0001c0001t0024g0126 | 2 | HG00673.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.882+9622_882+9637d others(18): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116788955 | |||||
| chr12:116788968
|
GGATGGAT others(32): Show |
G | 1 | a0001c0001t0002g0192 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.882+9634_882+9672d others(41): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116788968 | |||||
| chr12:116789106
|
G | A | 49 | a0001c0001t0001g0178a0001c0001t0004g0095a0001c0001t0004g0096others(46): Show | 49 | HG01175.hp2 HG01243.hp1 HG01243.hp2 others(46): Show |
intron_variant | MODIFIER | c.882+9758G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116789106 | ||||||
| chr12:116789163
|
A | AGATGGGT others(69): Show |
4 | a0001c0004t0001g0083a0001c0004t0052g0015a0002c0010t0002g0001others(1): Show | 4 | HG02132.hp2 HG02135.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.882+9837_882+9912d others(78): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116789163 | |||||
| chr12:116789228
|
G | A | 4 | a0001c0002t0005g0003a0001c0002t0005g0064a0001c0011t0023g0007others(1): Show | 4 | HG01175.hp2 HG02486.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.882+9880G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116789228 | ||||||
| chr12:116789247
|
G | A | 1 | a0001c0006t0050g0013 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.882+9899G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116789247 | ||||||
| chr12:116789311
|
G | A | 1 | a0001c0002t0005g0151 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.882+9963G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116789311 | ||||||
| chr12:116789369
|
G | A | 1 | a0001c0001t0001g0122 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.882+10021G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116789369 | ||||||
| chr12:116789389
|
A | G | 4 | a0001c0002t0005g0003a0001c0002t0005g0064a0001c0011t0023g0007others(1): Show | 4 | HG01175.hp2 HG02486.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.882+10041A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116789389 | ||||||
| chr12:116789438
|
GTAGA | G | 8 | a0001c0003t0005g0035a0001c0003t0005g0036a0001c0003t0016g0039others(5): Show | 8 | HG01243.hp1 HG02486.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.882+10092_882+1009 others(8): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116789438 | |||||
| chr12:116789440
|
A | AGATG | 25 | a0001c0001t0001g0141a0001c0001t0001g0190a0001c0001t0001g0193others(22): Show | 25 | HG00438.hp2 HG01099.hp2 HG01257.hp2 others(22): Show |
intron_variant | MODIFIER | c.882+10114_882+1011 others(8): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116789440 | |||||
| chr12:116789458
|
ATGGATGG others(24): Show |
A | 1 | a0001c0001t0004g0173 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.882+10175_882+1020 others(35): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116789458 | |||||
| chr12:116789635
|
G | GTGGA | 8 | a0001c0001t0002g0236a0001c0001t0004g0170a0001c0001t0007g0179others(5): Show | 8 | HG01074.hp2 HG01261.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.882+10317_882+1032 others(8): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116789635 | |||||
| chr12:116789635
|
G | GTGGATGG others(1): Show |
10 | a0001c0001t0004g0110a0001c0001t0004g0145a0001c0002t0018g0022others(7): Show | 10 | HG01243.hp1 HG01891.hp1 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.882+10313_882+1032 others(12): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116789635 | |||||
| chr12:116789635
|
G | GTGGATGG others(5): Show |
30 | a0001c0001t0001g0178a0001c0001t0004g0096a0001c0001t0004g0168others(27): Show | 30 | HG01243.hp2 HG02055.hp1 HG02074.hp1 others(27): Show |
intron_variant | MODIFIER | c.882+10309_882+1032 others(16): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116789635 | |||||
| chr12:116789635
|
G | GTGGATGG others(9): Show |
2 | a0001c0001t0004g0095a0001c0002t0001g0079 | 2 | HG03225.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.882+10305_882+1032 others(20): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116789635 | |||||
| chr12:116789635
|
GTGGA | G | 15 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0258others(12): Show | 15 | HG00140.hp1 HG01175.hp2 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.882+10317_882+1032 others(8): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116789635 | |||||
| chr12:116789722
|
T | C | 1 | a0001c0011t0053g0011 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.882+10374T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116789722 | ||||||
| chr12:116789772
|
ATGGATGG others(16): Show |
A | 1 | a0001c0001t0001g0194 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.882+10457_882+1047 others(27): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116789772 | |||||
| chr12:116789824
|
G | A | 1 | a0001c0001t0003g0240 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.882+10476G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116789824 | ||||||
| chr12:116789876
|
G | T | 1 | a0001c0006t0036g0018 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.882+10528G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116789876 | ||||||
| chr12:116789938
|
T | C | 45 | a0001c0001t0001g0178a0001c0001t0004g0095a0001c0001t0004g0096others(42): Show | 45 | HG01243.hp1 HG01243.hp2 HG01891.hp1 others(42): Show |
intron_variant | MODIFIER | c.882+10590T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116789938 | ||||||
| chr12:116789960
|
G | GTGGA | 39 | a0001c0001t0001g0141a0001c0001t0001g0190a0001c0001t0001g0215others(36): Show | 39 | HG00438.hp2 HG01175.hp2 HG01257.hp2 others(36): Show |
intron_variant | MODIFIER | c.882+10642_882+1064 others(8): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116789960 | |||||
| chr12:116789960
|
G | GTGGATGG others(1): Show |
149 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(146): Show | 149 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(146): Show |
intron_variant | MODIFIER | c.882+10638_882+1064 others(12): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116789960 | |||||
| chr12:116789960
|
G | GTGGATGG others(5): Show |
43 | a0001c0001t0001g0178a0001c0001t0001g0216a0001c0001t0001g0217others(40): Show | 43 | HG01109.hp2 HG01169.hp1 HG01243.hp2 others(40): Show |
intron_variant | MODIFIER | c.882+10634_882+1064 others(16): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116789960 | |||||
| chr12:116789960
|
G | GTGGATGG others(9): Show |
1 | a0001c0001t0001g0260 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.882+10630_882+1064 others(20): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116789960 | |||||
| chr12:116790171
|
T | C | 1 | a0001c0002t0001g0079 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.882+10823T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116790171 | ||||||
| chr12:116790334
|
A | G | 1 | a0001c0003t0035g0088 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.882+10986A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116790334 | ||||||
| chr12:116790373
|
T | TG | 49 | a0001c0001t0001g0178a0001c0001t0004g0095a0001c0001t0004g0096others(46): Show | 49 | HG01175.hp2 HG01243.hp1 HG01243.hp2 others(46): Show |
intron_variant | MODIFIER | c.882+11026dupG | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116790373 | |||||
| chr12:116790376
|
G | A | 2 | a0001c0001t0014g0027a0001c0009t0023g0026 | 2 | HG02630.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.882+11028G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116790376 | ||||||
| chr12:116790538
|
G | A | 1 | a0001c0001t0061g0148 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.882+11190G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116790538 | ||||||
| chr12:116790653
|
C | T | 1 | a0001c0006t0036g0018 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.882+11305C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116790653 | ||||||
| chr12:116790654
|
G | A | 3 | a0001c0003t0002g0100a0001c0003t0002g0101a0001c0003t0002g0102 | 3 | HG01074.hp2 HG02280.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.882+11306G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116790654 | ||||||
| chr12:116790681
|
G | C | 1 | a0001c0019t0002g0267 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.882+11333G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116790681 | ||||||
| chr12:116790748
|
G | C | 2 | a0001c0001t0001g0216a0001c0001t0001g0260 | 2 | HG01978.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.882+11400G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116790748 | ||||||
| chr12:116790756
|
A | G | 1 | a0001c0003t0014g0065 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.882+11408A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116790756 | ||||||
| chr12:116790771
|
A | G | 1 | a0001c0016t0032g0044 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.882+11423A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116790771 | ||||||
| chr12:116790799
|
T | C | 1 | a0001c0003t0035g0088 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.882+11451T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116790799 | ||||||
| chr12:116790814
|
G | A | 45 | a0001c0001t0001g0178a0001c0001t0004g0095a0001c0001t0004g0096others(42): Show | 45 | HG01243.hp1 HG01243.hp2 HG01891.hp1 others(42): Show |
intron_variant | MODIFIER | c.882+11466G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116790814 | ||||||
| chr12:116791334
|
G | A | 1 | a0001c0013t0013g0158 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.882+11986G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116791334 | ||||||
| chr12:116791529
|
G | C | 45 | a0001c0001t0001g0178a0001c0001t0004g0095a0001c0001t0004g0096others(42): Show | 45 | HG01243.hp1 HG01243.hp2 HG01891.hp1 others(42): Show |
intron_variant | MODIFIER | c.882+12181G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116791529 | ||||||
| chr12:116791734
|
G | A | 246 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(243): Show | 246 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(243): Show |
intron_variant | MODIFIER | c.882+12386G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116791734 | ||||||
| chr12:116791786
|
A | G | 6 | a0001c0001t0002g0032a0001c0001t0008g0028a0001c0001t0008g0029others(3): Show | 6 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.882+12438A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116791786 | ||||||
| chr12:116791793
|
G | T | 246 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(243): Show | 246 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(243): Show |
intron_variant | MODIFIER | c.882+12445G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116791793 | ||||||
| chr12:116791814
|
A | AATCCTAT others(13): Show |
1 | a0001c0011t0023g0007 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.882+12468_882+1248 others(24): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116791814 | |||||
| chr12:116791839
|
A | T | 27 | a0001c0001t0001g0141a0001c0001t0001g0190a0001c0001t0001g0193others(24): Show | 27 | HG00438.hp2 HG01099.hp2 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.882+12491A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116791839 | ||||||
| chr12:116791972
|
A | G | 1 | a0001c0003t0014g0065 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.882+12624A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116791972 | ||||||
| chr12:116792015
|
G | A | 1 | a0001c0006t0050g0013 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.882+12667G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116792015 | ||||||
| chr12:116792179
|
A | G | 3 | a0001c0003t0002g0100a0001c0003t0002g0101a0001c0003t0002g0102 | 3 | HG01074.hp2 HG02280.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.882+12831A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116792179 | ||||||
| chr12:116792236
|
GACGGGGT others(48): Show |
G | 1 | a0001c0011t0023g0007 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.882+12889_882+1294 others(59): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116792236 | ||||||
| chr12:116792238
|
C | A | 3 | a0001c0002t0005g0003a0001c0002t0005g0064a0001c0011t0039g0012 | 3 | HG01175.hp2 HG02486.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.882+12890C>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116792238 | ||||||
| chr12:116792262
|
C | G | 45 | a0001c0001t0001g0178a0001c0001t0004g0095a0001c0001t0004g0096others(42): Show | 45 | HG01243.hp1 HG01243.hp2 HG01891.hp1 others(42): Show |
intron_variant | MODIFIER | c.882+12914C>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116792262 | ||||||
| chr12:116792308
|
C | T | 4 | a0001c0002t0018g0022a0001c0005t0030g0051a0001c0005t0030g0052others(1): Show | 4 | HG01891.hp1 HG02257.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.882+12960C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116792308 | ||||||
| chr12:116792342
|
G | A | 45 | a0001c0001t0001g0178a0001c0001t0004g0095a0001c0001t0004g0096others(42): Show | 45 | HG01243.hp1 HG01243.hp2 HG01891.hp1 others(42): Show |
intron_variant | MODIFIER | c.882+12994G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116792342 | ||||||
| chr12:116792525
|
A | G | 252 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(249): Show | 252 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(249): Show |
intron_variant | MODIFIER | c.882+13177A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116792525 | ||||||
| chr12:116792550
|
A | T | 1 | a0001c0001t0045g0114 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.882+13202A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116792550 | ||||||
| chr12:116792589
|
C | T | 1 | a0001c0001t0019g0124 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.882+13241C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116792589 | ||||||
| chr12:116792614
|
C | T | 33 | a0001c0001t0001g0178a0001c0001t0004g0095a0001c0001t0004g0096others(30): Show | 33 | HG01243.hp2 HG02055.hp1 HG02074.hp1 others(30): Show |
intron_variant | MODIFIER | c.882+13266C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116792614 | ||||||
| chr12:116792846
|
C | T | 1 | a0001c0006t0050g0013 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.882+13498C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116792846 | ||||||
| chr12:116793071
|
G | C | 4 | a0001c0007t0025g0009a0001c0007t0025g0056a0001c0007t0046g0053others(1): Show | 4 | HG01884.hp2 HG02145.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.882+13723G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116793071 | ||||||
| chr12:116793210
|
C | CT | 148 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(145): Show | 148 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(145): Show |
intron_variant | MODIFIER | c.882+13881dupT | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116793210 | |||||
| chr12:116793210
|
C | CTT | 14 | a0001c0001t0001g0194a0001c0001t0017g0213a0001c0001t0022g0223others(11): Show | 14 | HG00544.hp2 HG00609.hp1 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.882+13880_882+1388 others(6): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116793210 | |||||
| chr12:116793210
|
CT | C | 25 | a0001c0001t0002g0032a0001c0001t0007g0171a0001c0001t0008g0028others(22): Show | 25 | HG00140.hp1 HG01243.hp1 HG01261.hp2 others(22): Show |
intron_variant | MODIFIER | c.882+13881delT | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116793210 | |||||
| chr12:116793210
|
CTT | C | 26 | a0001c0001t0001g0141a0001c0001t0001g0190a0001c0001t0001g0193others(23): Show | 26 | HG00438.hp2 HG01099.hp2 HG01257.hp2 others(23): Show |
intron_variant | MODIFIER | c.882+13880_882+1388 others(6): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116793210 | |||||
| chr12:116793248
|
C | A | 1 | a0001c0014t0018g0019 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.882+13900C>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116793248 | ||||||
| chr12:116793442
|
C | T | 1 | a0001c0002t0001g0066 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.882+14094C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116793442 | ||||||
| chr12:116793468
|
G | A | 54 | a0001c0001t0001g0178a0001c0001t0002g0031a0001c0001t0002g0045others(51): Show | 54 | HG01175.hp2 HG01243.hp1 HG01243.hp2 others(51): Show |
intron_variant | MODIFIER | c.882+14120G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116793468 | ||||||
| chr12:116793636
|
G | A | 51 | a0001c0001t0001g0178a0001c0001t0002g0209a0001c0001t0004g0095others(48): Show | 51 | HG00438.hp1 HG00544.hp1 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.882+14288G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116793636 | ||||||
| chr12:116793640
|
T | G | 1 | a0001c0001t0001g0195 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.882+14292T>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116793640 | ||||||
| chr12:116793800
|
C | G | 1 | a0001c0001t0001g0211 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.882+14452C>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116793800 | ||||||
| chr12:116794041
|
G | A | 3 | a0001c0002t0005g0003a0001c0011t0023g0007a0001c0011t0039g0012 | 3 | HG01175.hp2 HG02486.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.882+14693G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116794041 | ||||||
| chr12:116794130
|
T | G | 20 | a0001c0001t0001g0178a0001c0001t0004g0110a0001c0001t0004g0168others(17): Show | 20 | HG00544.hp1 HG02074.hp1 HG02523.hp2 others(17): Show |
intron_variant | MODIFIER | c.882+14782T>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116794130 | ||||||
| chr12:116794338
|
TTGTAATC others(801): Show |
T | 2 | a0001c0006t0031g0067a0001c0016t0032g0044 | 2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.882+15019_882+1582 others(4): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116794338 | |||||
| chr12:116794489
|
G | A | 118 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(115): Show | 118 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.882+15141G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116794489 | ||||||
| chr12:116794490
|
C | T | 6 | a0001c0001t0002g0209a0001c0004t0001g0083a0001c0006t0050g0013others(3): Show | 6 | HG00438.hp1 HG00741.hp1 HG02040.hp1 others(3): Show |
intron_variant | MODIFIER | c.882+15142C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116794490 | ||||||
| chr12:116794495
|
G | A | 2 | a0001c0001t0001g0169a0001c0001t0015g0186 | 2 | HG03239.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.882+15147G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116794495 | ||||||
| chr12:116794521
|
C | A | 6 | a0001c0001t0002g0209a0001c0004t0001g0083a0001c0006t0050g0013others(3): Show | 6 | HG00438.hp1 HG00741.hp1 HG02040.hp1 others(3): Show |
intron_variant | MODIFIER | c.882+15173C>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116794521 | ||||||
| chr12:116794523
|
G | A | 1 | a0001c0001t0071g0119 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.882+15175G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116794523 | ||||||
| chr12:116794542
|
G | A | 1 | a0001c0001t0045g0114 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.882+15194G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116794542 | ||||||
| chr12:116794547
|
G | A | 2 | a0001c0002t0004g0005a0001c0002t0049g0004 | 2 | HG01243.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.882+15199G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116794547 | ||||||
| chr12:116794587
|
G | T | 1 | a0001c0001t0003g0127 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.882+15239G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116794587 | ||||||
| chr12:116794646
|
A | AGAAG | 5 | a0001c0001t0019g0124a0001c0001t0019g0163a0001c0001t0019g0187others(2): Show | 5 | HG00140.hp1 HG01261.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.882+15312_882+1531 others(8): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116794646 | |||||
| chr12:116794646
|
A | AGGAGGGA others(17): Show |
2 | a0001c0004t0001g0083a0001c0006t0050g0013 | 2 | HG00741.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.882+15299_882+1530 others(28): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116794646 | |||||
| chr12:116794646
|
A | AGGAGGGA others(17): Show |
1 | a0002c0010t0002g0254 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.882+15299_882+1530 others(28): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116794646 | |||||
| chr12:116794646
|
A | AGGAGGGA others(21): Show |
3 | a0001c0001t0002g0209a0002c0010t0002g0001a0002c0010t0002g0002 | 3 | HG00438.hp1 HG02132.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.882+15299_882+1530 others(32): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116794646 | |||||
| chr12:116794646
|
AGAAG | A | 4 | a0001c0002t0005g0003a0001c0009t0023g0026a0001c0011t0023g0007others(1): Show | 4 | HG01175.hp2 HG02486.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.882+15312_882+1531 others(8): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116794646 | |||||
| chr12:116794648
|
A | G | 1 | a0001c0014t0002g0137 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.882+15300A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116794648 | ||||||
| chr12:116794652
|
A | G | 4 | a0001c0002t0005g0003a0001c0009t0023g0026a0001c0011t0023g0007others(1): Show | 4 | HG01175.hp2 HG02486.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.882+15304A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116794652 | ||||||
| chr12:116794656
|
A | AAGGGAGG others(13): Show |
1 | a0001c0001t0014g0156 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.882+15311_882+1531 others(24): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116794656 | |||||
| chr12:116794656
|
A | AAGGGAGG others(9): Show |
6 | a0001c0001t0002g0032a0001c0001t0008g0028a0001c0001t0008g0029others(3): Show | 6 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.882+15311_882+1531 others(20): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116794656 | |||||
| chr12:116794656
|
A | AAGGGAGG others(13): Show |
2 | a0001c0005t0013g0006a0001c0013t0013g0046 | 2 | HG01891.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.882+15311_882+1531 others(24): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116794656 | |||||
| chr12:116794656
|
A | AAGGGAGG others(17): Show |
3 | a0001c0005t0013g0154a0001c0013t0013g0158a0001c0018t0055g0059 | 3 | HG03453.hp2 HG03579.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.882+15311_882+1531 others(28): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116794656 | |||||
| chr12:116794656
|
AAGGAAGG others(13): Show |
A | 1 | a0001c0014t0002g0137 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.882+15312_882+1533 others(24): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116794656 | |||||
| chr12:116794660
|
A | G | 13 | a0001c0001t0002g0032a0001c0001t0008g0028a0001c0001t0008g0029others(10): Show | 13 | HG01891.hp2 HG02257.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.882+15312A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116794660 | ||||||
| chr12:116794664
|
G | A | 6 | a0001c0001t0002g0209a0001c0004t0001g0083a0001c0006t0050g0013others(3): Show | 6 | HG00438.hp1 HG00741.hp1 HG02040.hp1 others(3): Show |
intron_variant | MODIFIER | c.882+15316G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116794664 | ||||||
| chr12:116794668
|
A | AAGGGAGG others(9): Show |
1 | a0001c0002t0015g0082 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.882+15323_882+1532 others(20): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116794668 | |||||
| chr12:116794668
|
A | AAGGGAGG others(13): Show |
112 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(109): Show | 112 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.882+15323_882+1532 others(24): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116794668 | |||||
| chr12:116794668
|
A | AAGGGAGG others(17): Show |
3 | a0001c0001t0001g0146a0001c0001t0001g0217a0001c0001t0003g0131 | 3 | HG02293.hp2 HG02300.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.882+15323_882+1532 others(28): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116794668 | |||||
| chr12:116794668
|
A | AAGGGAGG others(5): Show |
1 | a0001c0003t0035g0088 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.882+15323_882+1532 others(16): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116794668 | |||||
| chr12:116794668
|
A | AAGGGAGG others(9): Show |
5 | a0001c0003t0014g0065a0001c0005t0030g0051a0001c0005t0030g0052others(2): Show | 5 | HG01891.hp1 HG02965.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.882+15323_882+1532 others(20): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116794668 | |||||
| chr12:116794668
|
A | AAGGGAGG others(13): Show |
9 | a0001c0001t0002g0031a0001c0001t0002g0045a0001c0001t0002g0048others(6): Show | 9 | HG01884.hp2 HG02257.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.882+15323_882+1532 others(24): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116794668 | |||||
| chr12:116794668
|
A | AAGGGAGG others(21): Show |
2 | a0001c0007t0025g0056a0001c0007t0046g0053 | 2 | HG02145.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.882+15323_882+1532 others(32): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116794668 | |||||
| chr12:116794668
|
A | G | 21 | a0001c0001t0002g0032a0001c0001t0008g0028a0001c0001t0008g0029others(18): Show | 21 | HG00140.hp1 HG01175.hp2 HG01261.hp2 others(18): Show |
intron_variant | MODIFIER | c.882+15320A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116794668 | ||||||
| chr12:116794672
|
A | AAGGGAGG others(5): Show |
4 | a0001c0001t0004g0170a0001c0001t0004g0172a0001c0001t0026g0181others(1): Show | 4 | HG02809.hp1 HG03831.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.882+15334_882+1534 others(16): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116794672 | |||||
| chr12:116794672
|
A | AAGGGAGG others(9): Show |
20 | a0001c0001t0008g0041a0001c0001t0045g0114a0001c0002t0002g0129others(17): Show | 20 | HG00140.hp2 HG01106.hp1 HG01358.hp1 others(17): Show |
intron_variant | MODIFIER | c.882+15330_882+1534 others(20): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116794672 | |||||
| chr12:116794672
|
A | AAGGGAGG others(13): Show |
51 | a0001c0001t0001g0141a0001c0001t0001g0190a0001c0001t0001g0193others(48): Show | 51 | HG00408.hp2 HG00438.hp2 HG01074.hp2 others(48): Show |
intron_variant | MODIFIER | c.882+15326_882+1534 others(24): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116794672 | |||||
| chr12:116794672
|
A | AAGGGAGG others(17): Show |
12 | a0001c0001t0005g0105a0001c0002t0004g0005a0001c0002t0005g0064others(9): Show | 12 | HG01243.hp1 HG01243.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.882+15345_882+1534 others(28): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116794672 | |||||
| chr12:116794672
|
A | AAGGGAGG others(21): Show |
11 | a0001c0001t0001g0178a0001c0001t0004g0110a0001c0001t0004g0168others(8): Show | 11 | HG02074.hp1 HG02683.hp2 HG03491.hp1 others(8): Show |
intron_variant | MODIFIER | c.882+15345_882+1534 others(32): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116794672 | |||||
| chr12:116794672
|
A | AAGGGAGG others(25): Show |
4 | a0001c0001t0007g0070a0001c0001t0007g0071a0001c0001t0007g0087others(1): Show | 4 | HG00544.hp1 HG02523.hp2 NA18948.hp2 others(1): Show |
intron_variant | MODIFIER | c.882+15345_882+1534 others(36): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116794672 | |||||
| chr12:116794672
|
A | G | 154 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(151): Show | 154 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(151): Show |
intron_variant | MODIFIER | c.882+15324A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116794672 | ||||||
| chr12:116794674
|
G | GGAA | 6 | a0001c0001t0002g0209a0001c0004t0001g0083a0001c0006t0050g0013others(3): Show | 6 | HG00438.hp1 HG00741.hp1 HG02040.hp1 others(3): Show |
intron_variant | MODIFIER | c.882+15327_882+1532 others(7): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116794674 | |||||
| chr12:116794674
|
G | GGGAGGGA others(19): Show |
1 | a0001c0001t0007g0231 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.882+15345_882+1534 others(30): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116794674 | |||||
| chr12:116794678
|
G | A | 6 | a0001c0001t0002g0209a0001c0004t0001g0083a0001c0006t0050g0013others(3): Show | 6 | HG00438.hp1 HG00741.hp1 HG02040.hp1 others(3): Show |
intron_variant | MODIFIER | c.882+15330G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116794678 | ||||||
| chr12:116794682
|
G | A | 6 | a0001c0001t0002g0209a0001c0004t0001g0083a0001c0006t0050g0013others(3): Show | 6 | HG00438.hp1 HG00741.hp1 HG02040.hp1 others(3): Show |
intron_variant | MODIFIER | c.882+15334G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116794682 | ||||||
| chr12:116794686
|
G | A | 6 | a0001c0001t0002g0209a0001c0004t0001g0083a0001c0006t0050g0013others(3): Show | 6 | HG00438.hp1 HG00741.hp1 HG02040.hp1 others(3): Show |
intron_variant | MODIFIER | c.882+15338G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116794686 | ||||||
| chr12:116794690
|
G | A | 6 | a0001c0001t0002g0209a0001c0004t0001g0083a0001c0006t0050g0013others(3): Show | 6 | HG00438.hp1 HG00741.hp1 HG02040.hp1 others(3): Show |
intron_variant | MODIFIER | c.882+15342G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116794690 | ||||||
| chr12:116794697
|
G | A | 6 | a0001c0001t0002g0209a0001c0004t0001g0083a0001c0006t0050g0013others(3): Show | 6 | HG00438.hp1 HG00741.hp1 HG02040.hp1 others(3): Show |
intron_variant | MODIFIER | c.882+15349G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116794697 | ||||||
| chr12:116794698
|
AAGGG | A | 5 | a0001c0002t0005g0003a0001c0009t0023g0026a0001c0011t0023g0007others(2): Show | 5 | HG01175.hp2 HG02486.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.882+15354_882+1535 others(8): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116794698 | |||||
| chr12:116794699
|
A | G | 6 | a0001c0001t0002g0209a0001c0004t0001g0083a0001c0006t0050g0013others(3): Show | 6 | HG00438.hp1 HG00741.hp1 HG02040.hp1 others(3): Show |
intron_variant | MODIFIER | c.882+15351A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116794699 | ||||||
| chr12:116794702
|
G | A | 6 | a0001c0001t0002g0209a0001c0004t0001g0083a0001c0006t0050g0013others(3): Show | 6 | HG00438.hp1 HG00741.hp1 HG02040.hp1 others(3): Show |
intron_variant | MODIFIER | c.882+15354G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116794702 | ||||||
| chr12:116794708
|
A | G | 11 | a0001c0001t0002g0209a0001c0002t0005g0003a0001c0004t0001g0083others(8): Show | 11 | HG00438.hp1 HG00741.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.882+15360A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116794708 | ||||||
| chr12:116794806
|
C | T | 1 | a0001c0014t0002g0137 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.882+15458C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116794806 | ||||||
| chr12:116794853
|
G | T | 2 | a0001c0005t0030g0051a0001c0005t0030g0052 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.882+15505G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116794853 | ||||||
| chr12:116794961
|
A | C | 1 | a0001c0001t0007g0231 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.882+15613A>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116794961 | ||||||
| chr12:116795009
|
A | T | 1 | a0001c0001t0007g0231 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.882+15661A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116795009 | ||||||
| chr12:116795029
|
A | G | 7 | a0001c0001t0003g0085a0001c0001t0003g0144a0001c0001t0003g0191others(4): Show | 7 | HG02040.hp2 NA18954.hp1 NA18957.hp1 others(4): Show |
intron_variant | MODIFIER | c.882+15681A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116795029 | ||||||
| chr12:116795115
|
G | GA | 4 | a0001c0002t0005g0003a0001c0009t0023g0026a0001c0011t0023g0007others(1): Show | 4 | HG01175.hp2 HG02486.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.882+15771dupA | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116795115 | |||||
| chr12:116795302
|
A | G | 35 | a0001c0001t0001g0178a0001c0001t0004g0095a0001c0001t0004g0096others(32): Show | 35 | HG00544.hp1 HG01243.hp1 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.882+15954A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116795302 | ||||||
| chr12:116795387
|
G | A | 1 | a0001c0001t0060g0090 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.882+16039G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116795387 | ||||||
| chr12:116795410
|
G | GA | 21 | a0001c0001t0001g0178a0001c0001t0004g0110a0001c0001t0004g0168others(18): Show | 21 | HG00544.hp1 HG02074.hp1 HG02523.hp2 others(18): Show |
intron_variant | MODIFIER | c.882+16075dupA | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116795410 | |||||
| chr12:116795484
|
T | C | 11 | a0001c0001t0002g0209a0001c0002t0005g0003a0001c0004t0001g0083others(8): Show | 11 | HG00438.hp1 HG00741.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.882+16136T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116795484 | ||||||
| chr12:116795564
|
G | A | 1 | a0001c0001t0004g0110 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.882+16216G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116795564 | ||||||
| chr12:116795711
|
T | C | 5 | a0001c0001t0019g0124a0001c0001t0019g0163a0001c0001t0019g0187others(2): Show | 5 | HG00140.hp1 HG01261.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.882+16363T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116795711 | ||||||
| chr12:116795740
|
A | G | 2 | a0001c0003t0035g0088a0001c0011t0053g0011 | 2 | HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.882+16392A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116795740 | ||||||
| chr12:116795785
|
G | A | 11 | a0001c0001t0002g0209a0001c0002t0005g0003a0001c0004t0001g0083others(8): Show | 11 | HG00438.hp1 HG00741.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.882+16437G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116795785 | ||||||
| chr12:116796053
|
C | T | 1 | a0001c0002t0002g0108 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.882+16705C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116796053 | ||||||
| chr12:116796095
|
G | GT | 5 | a0001c0001t0002g0209a0001c0004t0001g0083a0002c0010t0002g0001others(2): Show | 5 | HG00438.hp1 HG02040.hp1 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.882+16747_882+1674 others(5): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116796095 | ||||||
| chr12:116796125
|
T | C | 1 | a0001c0014t0002g0137 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.882+16777T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116796125 | ||||||
| chr12:116796136
|
C | T | 7 | a0001c0001t0002g0209a0001c0001t0004g0110a0001c0004t0001g0083others(4): Show | 7 | HG00438.hp1 HG00741.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.882+16788C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116796136 | ||||||
| chr12:116796268
|
A | G | 1 | a0001c0009t0037g0043 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.882+16920A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116796268 | ||||||
| chr12:116796501
|
A | G | 2 | a0001c0006t0031g0067a0001c0016t0032g0044 | 2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.882+17153A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116796501 | ||||||
| chr12:116796687
|
C | T | 20 | a0001c0001t0001g0178a0001c0001t0004g0110a0001c0001t0004g0168others(17): Show | 20 | HG00544.hp1 HG02074.hp1 HG02523.hp2 others(17): Show |
intron_variant | MODIFIER | c.882+17339C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116796687 | ||||||
| chr12:116796719
|
G | A | 1 | a0001c0001t0047g0241 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.882+17371G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116796719 | ||||||
| chr12:116796719
|
G | T | 140 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(137): Show | 140 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.882+17371G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116796719 | ||||||
| chr12:116796785
|
T | G | 25 | a0001c0001t0001g0178a0001c0001t0004g0095a0001c0001t0004g0096others(22): Show | 25 | HG00544.hp1 HG01243.hp2 HG02074.hp1 others(22): Show |
intron_variant | MODIFIER | c.882+17437T>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116796785 | ||||||
| chr12:116796851
|
G | A | 1 | a0001c0014t0002g0137 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.882+17503G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116796851 | ||||||
| chr12:116796871
|
G | T | 250 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(247): Show | 250 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(247): Show |
intron_variant | MODIFIER | c.882+17523G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116796871 | ||||||
| chr12:116796894
|
G | C | 5 | a0001c0001t0002g0031a0001c0001t0002g0045a0001c0001t0002g0048others(2): Show | 5 | HG02572.hp1 HG02976.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.882+17546G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116796894 | ||||||
| chr12:116796985
|
C | T | 140 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(137): Show | 140 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.882+17637C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116796985 | ||||||
| chr12:116797048
|
T | C | 11 | a0001c0001t0002g0209a0001c0002t0005g0003a0001c0004t0001g0083others(8): Show | 11 | HG00438.hp1 HG00741.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.882+17700T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116797048 | ||||||
| chr12:116797053
|
T | A | 3 | a0001c0003t0014g0065a0001c0005t0020g0162a0001c0013t0020g0098 | 3 | HG02970.hp2 HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.882+17705T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116797053 | ||||||
| chr12:116797218
|
G | A | 1 | a0001c0003t0035g0088 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.882+17870G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116797218 | ||||||
| chr12:116797224
|
C | T | 1 | a0001c0009t0010g0049 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.882+17876C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116797224 | ||||||
| chr12:116797266
|
G | T | 5 | a0001c0002t0005g0003a0001c0009t0023g0026a0001c0011t0023g0007others(2): Show | 5 | HG01175.hp2 HG02486.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.882+17918G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116797266 | ||||||
| chr12:116797297
|
T | C | 11 | a0001c0001t0002g0209a0001c0002t0005g0003a0001c0004t0001g0083others(8): Show | 11 | HG00438.hp1 HG00741.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.882+17949T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116797297 | ||||||
| chr12:116797357
|
C | T | 1 | a0001c0006t0050g0013 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.882+18009C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116797357 | ||||||
| chr12:116797428
|
C | T | 25 | a0001c0001t0001g0178a0001c0001t0004g0095a0001c0001t0004g0096others(22): Show | 25 | HG00544.hp1 HG01243.hp2 HG02074.hp1 others(22): Show |
intron_variant | MODIFIER | c.882+18080C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116797428 | ||||||
| chr12:116797454
|
G | A | 3 | a0001c0003t0014g0065a0001c0005t0020g0162a0001c0013t0020g0098 | 3 | HG02970.hp2 HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.882+18106G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116797454 | ||||||
| chr12:116797483
|
C | T | 1 | a0001c0009t0051g0016 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.882+18135C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116797483 | ||||||
| chr12:116797530
|
G | A | 6 | a0001c0001t0002g0032a0001c0001t0008g0028a0001c0001t0008g0029others(3): Show | 6 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.882+18182G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116797530 | ||||||
| chr12:116797535
|
T | G | 85 | a0001c0001t0001g0141a0001c0001t0001g0178a0001c0001t0001g0190others(82): Show | 85 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.882+18187T>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116797535 | ||||||
| chr12:116797538
|
C | CA | 25 | a0001c0001t0002g0209a0001c0001t0005g0105a0001c0001t0019g0124others(22): Show | 25 | HG00140.hp1 HG00438.hp1 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.882+18205dupA | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116797538 | |||||
| chr12:116797538
|
CA | C | 7 | a0001c0001t0001g0262a0001c0001t0007g0171a0001c0001t0027g0121others(4): Show | 7 | HG01257.hp1 HG02523.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.882+18205delA | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116797538 | |||||
| chr12:116797644
|
G | GAA | 11 | a0001c0001t0002g0209a0001c0002t0005g0003a0001c0004t0001g0083others(8): Show | 11 | HG00438.hp1 HG00741.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.882+18297_882+1829 others(6): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116797644 | |||||
| chr12:116797700
|
C | T | 6 | a0001c0001t0002g0209a0001c0004t0001g0083a0001c0006t0050g0013others(3): Show | 6 | HG00438.hp1 HG00741.hp1 HG02040.hp1 others(3): Show |
intron_variant | MODIFIER | c.882+18352C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116797700 | ||||||
| chr12:116797701
|
G | A | 1 | a0001c0004t0001g0113 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.882+18353G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116797701 | ||||||
| chr12:116797729
|
G | A | 5 | a0001c0002t0005g0003a0001c0009t0023g0026a0001c0011t0023g0007others(2): Show | 5 | HG01175.hp2 HG02486.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.882+18381G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116797729 | ||||||
| chr12:116797735
|
ACTC | A | 33 | a0001c0001t0003g0085a0001c0001t0003g0106a0001c0001t0003g0117others(30): Show | 33 | HG00423.hp2 HG00609.hp1 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.882+18390_882+1839 others(7): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116797735 | |||||
| chr12:116797809
|
A | C | 5 | a0001c0002t0005g0003a0001c0009t0023g0026a0001c0011t0023g0007others(2): Show | 5 | HG01175.hp2 HG02486.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.882+18461A>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116797809 | ||||||
| chr12:116797816
|
A | C | 1 | a0001c0003t0035g0088 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.882+18468A>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116797816 | ||||||
| chr12:116797843
|
T | C | 1 | a0001c0001t0001g0244 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.882+18495T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116797843 | ||||||
| chr12:116797872
|
C | CTTTTGGG others(43): Show |
1 | a0001c0011t0023g0007 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.882+18573_882+1857 others(54): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116797872 | |||||
| chr12:116797893
|
G | A | 5 | a0001c0001t0019g0124a0001c0001t0019g0163a0001c0001t0019g0187others(2): Show | 5 | HG00140.hp1 HG01261.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.882+18545G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116797893 | ||||||
| chr12:116797922
|
T | G | 256 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(253): Show | 256 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(253): Show |
intron_variant | MODIFIER | c.882+18574T>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116797922 | ||||||
| chr12:116797955
|
C | T | 24 | a0001c0001t0002g0031a0001c0001t0002g0032a0001c0001t0002g0045others(21): Show | 24 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.882+18607C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116797955 | ||||||
| chr12:116797959
|
T | C | 1 | a0001c0011t0053g0011 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.882+18611T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116797959 | ||||||
| chr12:116798031
|
G | C | 24 | a0001c0001t0002g0031a0001c0001t0002g0032a0001c0001t0002g0045others(21): Show | 24 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.882+18683G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116798031 | ||||||
| chr12:116798064
|
A | G | 1 | a0001c0002t0015g0082 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.882+18716A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116798064 | ||||||
| chr12:116798076
|
C | T | 93 | a0001c0001t0001g0141a0001c0001t0001g0178a0001c0001t0001g0190others(90): Show | 93 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.882+18728C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116798076 | ||||||
| chr12:116798212
|
C | T | 1 | a0001c0007t0025g0009 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.882+18864C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116798212 | ||||||
| chr12:116798225
|
C | CA | 46 | a0001c0001t0001g0178a0001c0001t0002g0031a0001c0001t0002g0032others(43): Show | 46 | HG00544.hp1 HG01884.hp2 HG01891.hp1 others(43): Show |
intron_variant | MODIFIER | c.882+18889dupA | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116798225 | |||||
| chr12:116798225
|
CA | C | 8 | a0001c0001t0008g0041a0001c0001t0045g0114a0001c0002t0002g0129others(5): Show | 8 | HG02055.hp1 HG02258.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.882+18889delA | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116798225 | |||||
| chr12:116798239
|
A | C | 6 | a0001c0001t0007g0070a0001c0002t0005g0003a0001c0009t0023g0026others(3): Show | 6 | HG01175.hp2 HG02486.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.882+18891A>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116798239 | ||||||
| chr12:116798331
|
G | C | 11 | a0001c0001t0002g0209a0001c0002t0005g0003a0001c0004t0001g0083others(8): Show | 11 | HG00438.hp1 HG00741.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.882+18983G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116798331 | ||||||
| chr12:116798360
|
A | T | 6 | a0001c0001t0002g0209a0001c0004t0001g0083a0001c0006t0050g0013others(3): Show | 6 | HG00438.hp1 HG00741.hp1 HG02040.hp1 others(3): Show |
intron_variant | MODIFIER | c.882+19012A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116798360 | ||||||
| chr12:116798548
|
C | G | 1 | a0001c0002t0018g0022 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.882+19200C>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116798548 | ||||||
| chr12:116798585
|
A | T | 11 | a0001c0001t0002g0209a0001c0002t0005g0003a0001c0004t0001g0083others(8): Show | 11 | HG00438.hp1 HG00741.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.882+19237A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116798585 | ||||||
| chr12:116798742
|
A | G | 11 | a0001c0001t0002g0209a0001c0002t0005g0003a0001c0004t0001g0083others(8): Show | 11 | HG00438.hp1 HG00741.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.882+19394A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116798742 | ||||||
| chr12:116798765
|
G | A | 1 | a0001c0002t0002g0108 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.882+19417G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116798765 | ||||||
| chr12:116798777
|
T | C | 1 | a0001c0001t0004g0177 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.882+19429T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116798777 | ||||||
| chr12:116798796
|
G | A | 8 | a0001c0001t0008g0041a0001c0001t0045g0114a0001c0002t0002g0129others(5): Show | 8 | HG02055.hp1 HG02258.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.882+19448G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116798796 | ||||||
| chr12:116798886
|
C | T | 1 | a0001c0001t0001g0243 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.882+19538C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116798886 | ||||||
| chr12:116799099
|
C | T | 11 | a0001c0001t0002g0209a0001c0002t0005g0003a0001c0004t0001g0083others(8): Show | 11 | HG00438.hp1 HG00741.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.882+19751C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116799099 | ||||||
| chr12:116799134
|
C | T | 138 | a0001c0001t0001g0141a0001c0001t0001g0178a0001c0001t0001g0190others(135): Show | 138 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.882+19786C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116799134 | ||||||
| chr12:116799204
|
C | T | 1 | a0001c0009t0010g0049 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.882+19856C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116799204 | ||||||
| chr12:116799209
|
C | A | 2 | a0001c0003t0035g0088a0001c0011t0053g0011 | 2 | HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.882+19861C>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116799209 | ||||||
| chr12:116799326
|
G | A | 49 | a0001c0001t0001g0141a0001c0001t0001g0190a0001c0001t0001g0193others(46): Show | 49 | HG00408.hp2 HG00438.hp2 HG01074.hp2 others(46): Show |
intron_variant | MODIFIER | c.882+19978G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116799326 | ||||||
| chr12:116799503
|
A | G | 1 | a0001c0001t0003g0117 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.882+20155A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116799503 | ||||||
| chr12:116799505
|
C | T | 2 | a0001c0002t0002g0265a0001c0002t0010g0266 | 2 | NA18945.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.882+20157C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116799505 | ||||||
| chr12:116799579
|
G | GT | 44 | a0001c0001t0002g0209a0001c0001t0003g0085a0001c0001t0003g0106others(41): Show | 44 | HG00423.hp2 HG00438.hp1 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.882+20240dupT | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116799579 | |||||
| chr12:116799701
|
C | T | 35 | a0001c0001t0001g0178a0001c0001t0004g0095a0001c0001t0004g0096others(32): Show | 35 | HG00544.hp1 HG01243.hp1 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.882+20353C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116799701 | ||||||
| chr12:116799751
|
C | T | 3 | a0001c0001t0002g0031a0001c0001t0002g0045a0001c0001t0002g0048 | 3 | HG02976.hp1 HG03540.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.882+20403C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116799751 | ||||||
| chr12:116799806
|
A | G | 1 | a0001c0001t0001g0244 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.882+20458A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116799806 | ||||||
| chr12:116799987
|
A | C | 5 | a0001c0001t0019g0124a0001c0001t0019g0163a0001c0001t0019g0187others(2): Show | 5 | HG00140.hp1 HG01261.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.882+20639A>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116799987 | ||||||
| chr12:116800127
|
C | T | 118 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(115): Show | 118 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.882+20779C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116800127 | ||||||
| chr12:116800169
|
C | A | 1 | a0001c0014t0002g0137 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.882+20821C>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116800169 | ||||||
| chr12:116800171
|
A | G | 5 | a0001c0001t0019g0124a0001c0001t0019g0163a0001c0001t0019g0187others(2): Show | 5 | HG00140.hp1 HG01261.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.882+20823A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116800171 | ||||||
| chr12:116800180
|
G | A | 245 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(242): Show | 245 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(242): Show |
intron_variant | MODIFIER | c.882+20832G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116800180 | ||||||
| chr12:116800236
|
C | T | 3 | a0001c0007t0025g0009a0001c0007t0025g0056a0001c0007t0046g0053 | 3 | HG01884.hp2 HG02145.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.882+20888C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116800236 | ||||||
| chr12:116800355
|
G | A | 73 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(70): Show | 73 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.882+21007G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116800355 | ||||||
| chr12:116800526
|
G | A | 49 | a0001c0001t0001g0141a0001c0001t0001g0190a0001c0001t0001g0193others(46): Show | 49 | HG00408.hp2 HG00438.hp2 HG01074.hp2 others(46): Show |
intron_variant | MODIFIER | c.882+21178G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116800526 | ||||||
| chr12:116800583
|
G | A | 1 | a0001c0003t0006g0208 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.882+21235G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116800583 | ||||||
| chr12:116800633
|
C | CA | 6 | a0001c0002t0001g0081a0001c0003t0014g0065a0001c0005t0020g0162others(3): Show | 6 | HG02451.hp2 HG02630.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.882+21297dupA | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116800633 | |||||
| chr12:116800633
|
CA | C | 152 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(149): Show | 152 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(149): Show |
intron_variant | MODIFIER | c.882+21297delA | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116800633 | |||||
| chr12:116800711
|
G | T | 1 | a0001c0002t0001g0076 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.882+21363G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116800711 | ||||||
| chr12:116800738
|
T | C | 18 | a0001c0001t0002g0209a0001c0001t0019g0124a0001c0001t0019g0163others(15): Show | 18 | HG00140.hp1 HG00438.hp1 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.882+21390T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116800738 | ||||||
| chr12:116800773
|
C | T | 1 | a0001c0011t0039g0012 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.882+21425C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116800773 | ||||||
| chr12:116800775
|
T | C | 1 | a0001c0001t0003g0157 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.882+21427T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116800775 | ||||||
| chr12:116800812
|
T | TCAAAATA others(163): Show |
1 | a0001c0009t0023g0026 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.882+21464_882+2146 others(174): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116800812 | ||||||
| chr12:116800812
|
T | TCAAAATA others(233): Show |
1 | a0001c0011t0039g0012 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.882+21464_882+2146 others(244): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116800812 | ||||||
| chr12:116800812
|
T | TTAAAA | 47 | a0001c0001t0001g0069a0001c0001t0001g0092a0001c0001t0001g0122others(44): Show | 47 | HG00140.hp1 HG00423.hp1 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.882+21510_882+2151 others(9): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116800812 | |||||
| chr12:116800812
|
T | TTAAAATA others(3): Show |
53 | a0001c0001t0001g0120a0001c0001t0001g0198a0001c0001t0001g0204others(50): Show | 53 | HG00408.hp1 HG00609.hp1 HG00609.hp2 others(50): Show |
intron_variant | MODIFIER | c.882+21505_882+2151 others(14): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116800812 | |||||
| chr12:116800812
|
T | TTAAAATA others(8): Show |
37 | a0001c0001t0001g0072a0001c0001t0001g0086a0001c0001t0001g0094others(34): Show | 37 | HG00423.hp2 HG00544.hp2 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.882+21500_882+2151 others(19): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116800812 | |||||
| chr12:116800812
|
T | TTAAAATA others(13): Show |
4 | a0001c0001t0001g0195a0001c0001t0002g0236a0001c0001t0022g0223others(1): Show | 4 | HG01106.hp2 HG01261.hp1 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.882+21495_882+2151 others(24): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116800812 | |||||
| chr12:116800812
|
T | TTAAAATA others(18): Show |
3 | a0001c0001t0001g0202a0001c0001t0001g0221a0001c0001t0040g0143 | 3 | NA18956.hp1 NA18962.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.882+21490_882+2151 others(29): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116800812 | |||||
| chr12:116800812
|
TTAAAA | T | 21 | a0001c0001t0002g0034a0001c0001t0014g0037a0001c0001t0045g0114others(18): Show | 21 | HG01358.hp1 HG01891.hp1 HG02922.hp1 others(18): Show |
intron_variant | MODIFIER | c.882+21510_882+2151 others(9): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116800812 | |||||
| chr12:116800812
|
TTAAAATA others(3): Show |
T | 4 | a0001c0001t0004g0145a0001c0002t0002g0129a0001c0014t0018g0019others(1): Show | 4 | HG01106.hp1 HG02155.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.882+21505_882+2151 others(14): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116800812 | |||||
| chr12:116800812
|
TTAAAATA others(8): Show |
T | 4 | a0001c0001t0004g0095a0001c0001t0004g0096a0001c0002t0004g0005others(1): Show | 4 | HG01243.hp2 HG02622.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.882+21500_882+2151 others(19): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116800812 | |||||
| chr12:116800812
|
TTAAAATA others(13): Show |
T | 2 | a0001c0003t0035g0088a0001c0011t0053g0011 | 2 | HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.882+21495_882+2151 others(24): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116800812 | |||||
| chr12:116800813
|
T | C | 8 | a0001c0001t0002g0209a0001c0002t0005g0003a0001c0004t0001g0083others(5): Show | 8 | HG00438.hp1 HG00741.hp1 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.882+21465T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116800813 | ||||||
| chr12:116800853
|
TAAAATAA | T | 4 | a0001c0004t0001g0083a0001c0006t0050g0013a0002c0010t0002g0001others(1): Show | 4 | HG00741.hp1 HG02132.hp2 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.882+21509_882+2151 others(11): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116800853 | |||||
| chr12:116800858
|
T | TAAAATAA others(258): Show |
1 | a0001c0011t0023g0007 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.882+21514_882+2151 others(269): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116800858 | |||||
| chr12:116800860
|
A | AAATAAAA others(6): Show |
1 | a0001c0014t0002g0137 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.882+21514_882+2151 others(17): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116800860 | |||||
| chr12:116800861
|
A | AATAAAAT others(73): Show |
1 | a0001c0002t0005g0003 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.882+21514_882+2151 others(84): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116800861 | |||||
| chr12:116800863
|
A | T | 10 | a0001c0001t0002g0209a0001c0002t0005g0003a0001c0004t0001g0083others(7): Show | 10 | HG00438.hp1 HG00741.hp1 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.882+21515A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116800863 | ||||||
| chr12:116800870
|
A | G | 257 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(254): Show | 257 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(254): Show |
intron_variant | MODIFIER | c.882+21522A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116800870 | ||||||
| chr12:116801084
|
G | T | 3 | a0001c0005t0030g0051a0001c0005t0030g0052a0001c0005t0070g0050 | 3 | HG01891.hp1 HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.882+21736G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116801084 | ||||||
| chr12:116801214
|
T | A | 6 | a0001c0001t0002g0209a0001c0004t0001g0083a0001c0006t0050g0013others(3): Show | 6 | HG00438.hp1 HG00741.hp1 HG02040.hp1 others(3): Show |
intron_variant | MODIFIER | c.882+21866T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116801214 | ||||||
| chr12:116801345
|
C | G | 35 | a0001c0001t0001g0178a0001c0001t0004g0095a0001c0001t0004g0096others(32): Show | 35 | HG00544.hp1 HG01243.hp1 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.882+21997C>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116801345 | ||||||
| chr12:116801429
|
A | C | 5 | a0001c0002t0005g0003a0001c0009t0023g0026a0001c0011t0023g0007others(2): Show | 5 | HG01175.hp2 HG02486.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.882+22081A>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116801429 | ||||||
| chr12:116801481
|
C | T | 1 | a0001c0002t0018g0022 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.882+22133C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116801481 | ||||||
| chr12:116801804
|
T | TTTTG | 8 | a0001c0001t0002g0032a0001c0001t0003g0240a0001c0001t0008g0040others(5): Show | 8 | HG01884.hp2 HG02145.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.882+22484_882+2248 others(8): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116801804 | |||||
| chr12:116801804
|
TTTTG | T | 104 | a0001c0001t0001g0141a0001c0001t0001g0178a0001c0001t0001g0190others(101): Show | 104 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.882+22484_882+2248 others(8): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116801804 | |||||
| chr12:116801804
|
TTTTGTTT others(1): Show |
T | 9 | a0001c0001t0008g0041a0001c0001t0045g0114a0001c0002t0002g0129others(6): Show | 9 | HG02055.hp1 HG02258.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.882+22480_882+2248 others(12): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116801804 | |||||
| chr12:116801836
|
T | G | 22 | a0001c0001t0002g0031a0001c0001t0002g0032a0001c0001t0002g0045others(19): Show | 22 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.882+22488T>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116801836 | ||||||
| chr12:116801907
|
C | T | 5 | a0001c0002t0005g0003a0001c0009t0023g0026a0001c0011t0023g0007others(2): Show | 5 | HG01175.hp2 HG02486.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.882+22559C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116801907 | ||||||
| chr12:116801982
|
C | T | 11 | a0001c0001t0002g0209a0001c0002t0005g0003a0001c0004t0001g0083others(8): Show | 11 | HG00438.hp1 HG00741.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.882+22634C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116801982 | ||||||
| chr12:116802074
|
G | A | 10 | a0001c0001t0005g0105a0001c0002t0005g0064a0001c0003t0005g0035others(7): Show | 10 | HG01243.hp1 HG02280.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.882+22726G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116802074 | ||||||
| chr12:116802110
|
T | C | 11 | a0001c0001t0002g0209a0001c0002t0005g0003a0001c0004t0001g0083others(8): Show | 11 | HG00438.hp1 HG00741.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.882+22762T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116802110 | ||||||
| chr12:116802211
|
A | G | 49 | a0001c0001t0001g0141a0001c0001t0001g0190a0001c0001t0001g0193others(46): Show | 49 | HG00408.hp2 HG00438.hp2 HG01074.hp2 others(46): Show |
intron_variant | MODIFIER | c.882+22863A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116802211 | ||||||
| chr12:116802307
|
G | A | 1 | a0001c0001t0001g0249 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.882+22959G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116802307 | ||||||
| chr12:116802388
|
T | C | 2 | a0001c0001t0001g0205a0001c0001t0001g0244 | 2 | HG02080.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.882+23040T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116802388 | ||||||
| chr12:116802404
|
C | T | 11 | a0001c0001t0002g0209a0001c0002t0005g0003a0001c0004t0001g0083others(8): Show | 11 | HG00438.hp1 HG00741.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.882+23056C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116802404 | ||||||
| chr12:116802552
|
A | C | 11 | a0001c0001t0002g0209a0001c0002t0005g0003a0001c0004t0001g0083others(8): Show | 11 | HG00438.hp1 HG00741.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.882+23204A>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116802552 | ||||||
| chr12:116802603
|
G | C | 2 | a0001c0001t0002g0209a0002c0010t0002g0254 | 2 | HG00438.hp1 HG02040.hp1 |
intron_variant | MODIFIER | c.882+23255G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116802603 | ||||||
| chr12:116802821
|
G | A | 5 | a0001c0001t0019g0124a0001c0001t0019g0163a0001c0001t0019g0187others(2): Show | 5 | HG00140.hp1 HG01261.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.882+23473G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116802821 | ||||||
| chr12:116802872
|
A | T | 5 | a0001c0002t0005g0003a0001c0009t0023g0026a0001c0011t0023g0007others(2): Show | 5 | HG01175.hp2 HG02486.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.882+23524A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116802872 | ||||||
| chr12:116802910
|
C | G | 1 | a0001c0001t0040g0143 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.882+23562C>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116802910 | ||||||
| chr12:116802932
|
C | CA | 54 | a0001c0001t0001g0141a0001c0001t0001g0190a0001c0001t0001g0193others(51): Show | 54 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.882+23597dupA | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116802932 | |||||
| chr12:116802958
|
G | A | 49 | a0001c0001t0001g0141a0001c0001t0001g0190a0001c0001t0001g0193others(46): Show | 49 | HG00408.hp2 HG00438.hp2 HG01074.hp2 others(46): Show |
intron_variant | MODIFIER | c.882+23610G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116802958 | ||||||
| chr12:116803006
|
A | G | 116 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(113): Show | 116 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.882+23658A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116803006 | ||||||
| chr12:116803075
|
A | T | 2 | a0001c0002t0004g0005a0001c0002t0049g0004 | 2 | HG01243.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.882+23727A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116803075 | ||||||
| chr12:116803076
|
C | T | 2 | a0001c0002t0004g0005a0001c0002t0049g0004 | 2 | HG01243.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.882+23728C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116803076 | ||||||
| chr12:116803077
|
A | T | 2 | a0001c0002t0004g0005a0001c0002t0049g0004 | 2 | HG01243.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.882+23729A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116803077 | ||||||
| chr12:116803078
|
G | A | 2 | a0001c0002t0004g0005a0001c0002t0049g0004 | 2 | HG01243.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.882+23730G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116803078 | ||||||
| chr12:116803094
|
TA | T | 157 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(154): Show | 157 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(154): Show |
intron_variant | MODIFIER | c.882+23757delA | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116803094 | |||||
| chr12:116803177
|
G | A | 1 | a0001c0006t0036g0018 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.882+23829G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116803177 | ||||||
| chr12:116803229
|
G | A | 3 | a0001c0003t0035g0088a0001c0009t0051g0016a0001c0011t0053g0011 | 3 | HG02809.hp1 HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.882+23881G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116803229 | ||||||
| chr12:116803253
|
C | T | 3 | a0001c0001t0056g0220a0001c0007t0025g0056a0001c0007t0046g0053 | 3 | HG00140.hp1 HG02145.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.882+23905C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116803253 | ||||||
| chr12:116803411
|
T | C | 248 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(245): Show | 248 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(245): Show |
intron_variant | MODIFIER | c.882+24063T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116803411 | ||||||
| chr12:116803707
|
C | A | 6 | a0001c0001t0002g0209a0001c0004t0001g0083a0001c0006t0050g0013others(3): Show | 6 | HG00438.hp1 HG00741.hp1 HG02040.hp1 others(3): Show |
intron_variant | MODIFIER | c.882+24359C>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116803707 | ||||||
| chr12:116803709
|
C | T | 6 | a0001c0001t0002g0209a0001c0004t0001g0083a0001c0006t0050g0013others(3): Show | 6 | HG00438.hp1 HG00741.hp1 HG02040.hp1 others(3): Show |
intron_variant | MODIFIER | c.882+24361C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116803709 | ||||||
| chr12:116803752
|
A | G | 1 | a0001c0003t0014g0065 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.882+24404A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116803752 | ||||||
| chr12:116803980
|
G | C | 1 | a0001c0004t0001g0091 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.882+24632G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116803980 | ||||||
| chr12:116804073
|
C | G | 256 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(253): Show | 256 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(253): Show |
intron_variant | MODIFIER | c.882+24725C>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116804073 | ||||||
| chr12:116804084
|
G | A | 1 | a0001c0001t0004g0095 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.882+24736G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116804084 | ||||||
| chr12:116804260
|
A | G | 11 | a0001c0001t0002g0209a0001c0002t0005g0003a0001c0004t0001g0083others(8): Show | 11 | HG00438.hp1 HG00741.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.882+24912A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116804260 | ||||||
| chr12:116804478
|
T | C | 11 | a0001c0001t0002g0209a0001c0002t0005g0003a0001c0004t0001g0083others(8): Show | 11 | HG00438.hp1 HG00741.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.882+25130T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116804478 | ||||||
| chr12:116804598
|
A | G | 1 | a0002c0010t0002g0001 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.882+25250A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116804598 | ||||||
| chr12:116804868
|
G | A | 25 | a0001c0001t0001g0178a0001c0001t0004g0095a0001c0001t0004g0096others(22): Show | 25 | HG00544.hp1 HG01243.hp2 HG02074.hp1 others(22): Show |
intron_variant | MODIFIER | c.882+25520G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116804868 | ||||||
| chr12:116804926
|
C | T | 12 | a0001c0001t0011g0099a0001c0001t0011g0160a0001c0001t0014g0037others(9): Show | 12 | HG01074.hp2 HG01109.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.882+25578C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116804926 | ||||||
| chr12:116805005
|
A | G | 3 | a0001c0001t0003g0127a0001c0001t0003g0155a0001c0001t0003g0242 | 3 | HG00423.hp2 HG02155.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.882+25657A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116805005 | ||||||
| chr12:116805121
|
C | CT | 144 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(141): Show | 144 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.882+25789dupT | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116805121 | |||||
| chr12:116805121
|
C | CTT | 92 | a0001c0001t0001g0141a0001c0001t0001g0178a0001c0001t0001g0190others(89): Show | 92 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.882+25788_882+2578 others(6): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116805121 | |||||
| chr12:116805121
|
C | CTTT | 7 | a0001c0001t0002g0209a0001c0004t0001g0083a0001c0006t0050g0013others(4): Show | 7 | HG00438.hp1 HG00741.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.882+25787_882+2578 others(7): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116805121 | |||||
| chr12:116805245
|
A | G | 1 | a0001c0004t0068g0024 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.882+25897A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116805245 | ||||||
| chr12:116805418
|
A | C | 5 | a0001c0002t0005g0003a0001c0009t0023g0026a0001c0011t0023g0007others(2): Show | 5 | HG01175.hp2 HG02486.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.882+26070A>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116805418 | ||||||
| chr12:116805464
|
A | G | 6 | a0001c0001t0002g0209a0001c0004t0001g0083a0001c0006t0050g0013others(3): Show | 6 | HG00438.hp1 HG00741.hp1 HG02040.hp1 others(3): Show |
intron_variant | MODIFIER | c.882+26116A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116805464 | ||||||
| chr12:116805489
|
T | G | 2 | a0001c0001t0001g0146a0001c0001t0001g0217 | 2 | HG02293.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.882+26141T>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116805489 | ||||||
| chr12:116805501
|
G | A | 1 | a0001c0001t0001g0207 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.882+26153G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116805501 | ||||||
| chr12:116805531
|
G | A | 208 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(205): Show | 208 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(205): Show |
intron_variant | MODIFIER | c.882+26183G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116805531 | ||||||
| chr12:116805582
|
C | T | 5 | a0001c0002t0005g0003a0001c0009t0023g0026a0001c0011t0023g0007others(2): Show | 5 | HG01175.hp2 HG02486.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.882+26234C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116805582 | ||||||
| chr12:116805870
|
G | C | 1 | a0001c0002t0033g0150 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.882+26522G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116805870 | ||||||
| chr12:116805932
|
A | G | 5 | a0001c0002t0005g0003a0001c0009t0023g0026a0001c0011t0023g0007others(2): Show | 5 | HG01175.hp2 HG02486.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.882+26584A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116805932 | ||||||
| chr12:116805938
|
A | G | 205 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(202): Show | 205 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(202): Show |
intron_variant | MODIFIER | c.882+26590A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116805938 | ||||||
| chr12:116806003
|
C | T | 8 | a0001c0001t0002g0031a0001c0001t0002g0045a0001c0001t0002g0048others(5): Show | 8 | HG01884.hp2 HG02145.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.882+26655C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116806003 | ||||||
| chr12:116806022
|
T | G | 5 | a0001c0001t0019g0124a0001c0001t0019g0163a0001c0001t0019g0187others(2): Show | 5 | HG00140.hp1 HG01261.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.882+26674T>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116806022 | ||||||
| chr12:116806047
|
C | T | 2 | a0001c0001t0003g0199a0001c0004t0029g0055 | 2 | HG02738.hp2 NA18941.hp1 |
intron_variant | MODIFIER | c.882+26699C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116806047 | ||||||
| chr12:116806094
|
A | G | 1 | a0001c0012t0001g0239 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.882+26746A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116806094 | ||||||
| chr12:116806147
|
G | A | 36 | a0001c0001t0001g0178a0001c0001t0004g0095a0001c0001t0004g0096others(33): Show | 36 | HG00544.hp1 HG01243.hp1 HG01243.hp2 others(33): Show |
intron_variant | MODIFIER | c.882+26799G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116806147 | ||||||
| chr12:116806237
|
G | A | 3 | a0001c0003t0014g0065a0001c0005t0020g0162a0001c0013t0020g0098 | 3 | HG02970.hp2 HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.882+26889G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116806237 | ||||||
| chr12:116806367
|
CA | C | 57 | a0001c0001t0001g0122a0001c0001t0001g0166a0001c0001t0001g0169others(54): Show | 57 | HG00609.hp1 HG00621.hp1 HG00673.hp2 others(54): Show |
intron_variant | MODIFIER | c.882+27034delA | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116806367 | |||||
| chr12:116806367
|
CAA | C | 7 | a0001c0001t0001g0216a0001c0001t0019g0187a0001c0001t0056g0220others(4): Show | 7 | HG00140.hp1 HG01261.hp2 HG02273.hp1 others(4): Show |
intron_variant | MODIFIER | c.882+27033_882+2703 others(6): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116806367 | |||||
| chr12:116806367
|
CAAA | C | 13 | a0001c0001t0004g0095a0001c0001t0004g0110a0001c0001t0004g0170others(10): Show | 13 | HG01175.hp2 HG02074.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.882+27032_882+2703 others(7): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116806367 | |||||
| chr12:116806367
|
CAAAAA | C | 9 | a0001c0001t0001g0195a0001c0001t0001g0203a0001c0001t0001g0204others(6): Show | 9 | HG01106.hp2 HG01192.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.882+27030_882+2703 others(9): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116806367 | |||||
| chr12:116806376
|
AAAAAAAT others(6): Show |
A | 2 | a0001c0001t0001g0207a0001c0001t0015g0112 | 2 | HG00673.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.882+27030_882+2704 others(17): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116806376 | |||||
| chr12:116806377
|
A | AT | 7 | a0001c0001t0001g0120a0001c0001t0001g0194a0001c0001t0001g0202others(4): Show | 7 | HG00544.hp2 HG00609.hp2 HG03831.hp2 others(4): Show |
intron_variant | MODIFIER | c.882+27029_882+2703 others(5): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116806377 | ||||||
| chr12:116806377
|
A | ATAT | 34 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(31): Show | 34 | HG00408.hp1 HG00423.hp1 HG01074.hp1 others(31): Show |
intron_variant | MODIFIER | c.882+27029_882+2703 others(7): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116806377 | ||||||
| chr12:116806377
|
A | T | 1 | a0001c0001t0002g0023 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.882+27029A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116806377 | ||||||
| chr12:116806378
|
AAAAATAT | A | 7 | a0001c0001t0001g0178a0001c0001t0004g0173a0001c0001t0007g0070others(4): Show | 7 | HG02523.hp2 NA18948.hp2 NA18960.hp1 others(4): Show |
intron_variant | MODIFIER | c.882+27032_882+2703 others(11): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116806378 | |||||
| chr12:116806379
|
A | AT | 6 | a0001c0001t0003g0106a0001c0001t0004g0145a0001c0001t0004g0168others(3): Show | 6 | HG02071.hp2 HG02155.hp1 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.882+27031_882+2703 others(5): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116806379 | ||||||
| chr12:116806379
|
A | ATAT | 14 | a0001c0001t0002g0103a0001c0001t0002g0104a0001c0001t0002g0253others(11): Show | 14 | HG00423.hp2 HG00621.hp2 HG02132.hp1 others(11): Show |
intron_variant | MODIFIER | c.882+27031_882+2703 others(7): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116806379 | ||||||
| chr12:116806379
|
A | T | 57 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(54): Show | 57 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.882+27031A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116806379 | ||||||
| chr12:116806381
|
A | AAAT | 11 | a0001c0001t0008g0028a0001c0001t0008g0029a0001c0001t0008g0040others(8): Show | 11 | HG02145.hp1 HG02572.hp2 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.882+27034_882+2703 others(7): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116806381 | |||||
| chr12:116806381
|
A | AATAT | 6 | a0001c0002t0041g0075a0001c0003t0006g0208a0001c0003t0006g0230others(3): Show | 6 | HG03490.hp1 HG03654.hp2 NA18975.hp2 others(3): Show |
intron_variant | MODIFIER | c.882+27049_882+2705 others(8): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116806381 | |||||
| chr12:116806381
|
A | AT | 9 | a0001c0001t0001g0141a0001c0001t0001g0235a0001c0001t0002g0133others(6): Show | 9 | HG00408.hp2 HG00438.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.882+27033_882+2703 others(5): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116806381 | ||||||
| chr12:116806381
|
A | ATAT | 25 | a0001c0001t0001g0190a0001c0001t0001g0193a0001c0001t0001g0215others(22): Show | 25 | HG00438.hp2 HG01074.hp2 HG01099.hp2 others(22): Show |
intron_variant | MODIFIER | c.882+27033_882+2703 others(7): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116806381 | ||||||
| chr12:116806381
|
A | G | 1 | a0001c0001t0001g0224 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.882+27033A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116806381 | ||||||
| chr12:116806381
|
A | T | 109 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(106): Show | 109 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.882+27033A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116806381 | ||||||
| chr12:116806382
|
AT | A | 6 | a0001c0001t0005g0105a0001c0003t0005g0036a0001c0006t0005g0017others(3): Show | 6 | HG01243.hp1 HG01891.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.882+27035delT | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116806382 | ||||||
| chr12:116806383
|
T | A | 4 | a0001c0001t0008g0041a0001c0002t0008g0140a0001c0005t0030g0051others(1): Show | 4 | HG02965.hp1 HG03041.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.882+27035T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116806383 | ||||||
| chr12:116806385
|
T | G | 4 | a0001c0001t0001g0224a0001c0001t0001g0259a0001c0001t0004g0096others(1): Show | 4 | HG02647.hp2 HG03710.hp2 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.882+27037T>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116806385 | ||||||
| chr12:116806389
|
T | G | 69 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(66): Show | 69 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.882+27041T>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116806389 | ||||||
| chr12:116806389
|
T | TAG | 3 | a0001c0001t0002g0023a0001c0001t0019g0124a0001c0016t0032g0044 | 3 | HG01192.hp2 HG02055.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.882+27042_882+2704 others(6): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116806389 | |||||
| chr12:116806389
|
T | TAGATAG | 9 | a0001c0001t0002g0133a0001c0001t0010g0233a0001c0001t0011g0099others(6): Show | 9 | HG00408.hp2 HG02109.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.882+27042_882+2704 others(10): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116806389 | |||||
| chr12:116806389
|
T | TAGATAGA others(3): Show |
2 | a0001c0001t0001g0194a0001c0004t0012g0134 | 2 | HG00544.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.882+27042_882+2704 others(14): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116806389 | |||||
| chr12:116806393
|
T | G | 160 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(157): Show | 160 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(157): Show |
intron_variant | MODIFIER | c.882+27045T>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116806393 | ||||||
| chr12:116806393
|
T | TAG | 3 | a0001c0005t0013g0006a0001c0006t0050g0013a0001c0007t0025g0009 | 3 | HG00741.hp1 HG01884.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.882+27046_882+2704 others(6): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116806393 | |||||
| chr12:116806393
|
T | TAGATAG | 10 | a0001c0001t0001g0120a0001c0001t0001g0141a0001c0001t0001g0202others(7): Show | 10 | HG00438.hp1 HG00609.hp2 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.882+27046_882+2704 others(10): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116806393 | |||||
| chr12:116806393
|
T | TAGATAGA others(3): Show |
1 | a0001c0001t0002g0032 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.882+27046_882+2704 others(14): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116806393 | |||||
| chr12:116806395
|
TATATAG | T | 3 | a0001c0001t0008g0041a0001c0001t0045g0114a0001c0002t0008g0140 | 3 | HG03041.hp2 HG03130.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.882+27051_882+2705 others(10): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116806395 | |||||
| chr12:116806397
|
T | G | 234 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(231): Show | 234 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(231): Show |
intron_variant | MODIFIER | c.882+27049T>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116806397 | ||||||
| chr12:116806397
|
T | TATAGATA others(1): Show |
4 | a0001c0001t0002g0031a0001c0001t0002g0048a0001c0005t0030g0051others(1): Show | 4 | HG02965.hp1 HG02976.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.882+27076_882+2708 others(12): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116806397 | |||||
| chr12:116806397
|
T | TATAGATA others(5): Show |
2 | a0001c0001t0002g0045a0001c0009t0037g0043 | 2 | HG02572.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.882+27072_882+2708 others(16): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116806397 | |||||
| chr12:116806401
|
G | T | 4 | a0001c0001t0001g0207a0001c0001t0015g0112a0001c0003t0006g0054others(1): Show | 4 | HG00140.hp2 HG00673.hp1 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.882+27053G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116806401 | ||||||
| chr12:116806588
|
A | G | 1 | a0001c0001t0004g0128 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.883-27204A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116806588 | ||||||
| chr12:116806671
|
A | G | 240 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(237): Show | 240 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(237): Show |
intron_variant | MODIFIER | c.883-27121A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116806671 | ||||||
| chr12:116806741
|
C | G | 54 | a0001c0001t0001g0141a0001c0001t0001g0190a0001c0001t0001g0193others(51): Show | 54 | HG00408.hp2 HG00438.hp2 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.883-27051C>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116806741 | ||||||
| chr12:116806745
|
C | CA | 61 | a0001c0001t0001g0141a0001c0001t0001g0146a0001c0001t0001g0190others(58): Show | 61 | HG00408.hp2 HG00438.hp2 HG01074.hp2 others(58): Show |
intron_variant | MODIFIER | c.883-27030dupA | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116806745 | |||||
| chr12:116806745
|
CA | C | 11 | a0001c0001t0001g0202a0001c0001t0002g0048a0001c0001t0008g0041others(8): Show | 11 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.883-27030delA | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116806745 | |||||
| chr12:116807153
|
C | T | 11 | a0001c0001t0002g0209a0001c0001t0019g0124a0001c0001t0019g0163others(8): Show | 11 | HG00140.hp1 HG00438.hp1 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.883-26639C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116807153 | ||||||
| chr12:116807229
|
G | A | 2 | a0001c0006t0031g0067a0001c0016t0032g0044 | 2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.883-26563G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116807229 | ||||||
| chr12:116807341
|
G | A | 205 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(202): Show | 205 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(202): Show |
intron_variant | MODIFIER | c.883-26451G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116807341 | ||||||
| chr12:116807368
|
G | A | 49 | a0001c0001t0001g0141a0001c0001t0001g0190a0001c0001t0001g0193others(46): Show | 49 | HG00408.hp2 HG00438.hp2 HG01074.hp2 others(46): Show |
intron_variant | MODIFIER | c.883-26424G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116807368 | ||||||
| chr12:116807520
|
C | T | 5 | a0001c0002t0002g0129a0001c0004t0002g0025a0001c0004t0068g0024others(2): Show | 5 | HG02055.hp1 HG02258.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.883-26272C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116807520 | ||||||
| chr12:116807567
|
A | T | 5 | a0001c0002t0002g0129a0001c0004t0002g0025a0001c0004t0068g0024others(2): Show | 5 | HG02055.hp1 HG02258.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.883-26225A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116807567 | ||||||
| chr12:116807657
|
T | A | 54 | a0001c0001t0001g0141a0001c0001t0001g0190a0001c0001t0001g0193others(51): Show | 54 | HG00408.hp2 HG00438.hp2 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.883-26135T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116807657 | ||||||
| chr12:116807828
|
G | C | 3 | a0001c0003t0002g0100a0001c0003t0002g0101a0001c0003t0002g0102 | 3 | HG01074.hp2 HG02280.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.883-25964G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116807828 | ||||||
| chr12:116807855
|
GT | G | 49 | a0001c0001t0001g0141a0001c0001t0001g0190a0001c0001t0001g0193others(46): Show | 49 | HG00408.hp2 HG00438.hp2 HG01074.hp2 others(46): Show |
intron_variant | MODIFIER | c.883-25936delT | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116807855 | ||||||
| chr12:116807906
|
C | T | 5 | a0001c0001t0019g0124a0001c0001t0019g0163a0001c0001t0019g0187others(2): Show | 5 | HG00140.hp1 HG01261.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.883-25886C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116807906 | ||||||
| chr12:116807999
|
G | A | 1 | a0001c0003t0016g0039 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.883-25793G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116807999 | ||||||
| chr12:116808019
|
A | T | 5 | a0001c0001t0019g0124a0001c0001t0019g0163a0001c0001t0019g0187others(2): Show | 5 | HG00140.hp1 HG01261.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.883-25773A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116808019 | ||||||
| chr12:116808021
|
G | T | 54 | a0001c0001t0001g0141a0001c0001t0001g0190a0001c0001t0001g0193others(51): Show | 54 | HG00408.hp2 HG00438.hp2 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.883-25771G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116808021 | ||||||
| chr12:116808031
|
C | T | 49 | a0001c0001t0001g0141a0001c0001t0001g0190a0001c0001t0001g0193others(46): Show | 49 | HG00408.hp2 HG00438.hp2 HG01074.hp2 others(46): Show |
intron_variant | MODIFIER | c.883-25761C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116808031 | ||||||
| chr12:116808049
|
C | T | 11 | a0001c0001t0002g0032a0001c0001t0008g0028a0001c0001t0008g0029others(8): Show | 11 | HG01891.hp2 HG02257.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.883-25743C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116808049 | ||||||
| chr12:116808050
|
G | A | 3 | a0001c0003t0014g0065a0001c0005t0020g0162a0001c0013t0020g0098 | 3 | HG02970.hp2 HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.883-25742G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116808050 | ||||||
| chr12:116808228
|
G | A | 5 | a0001c0002t0005g0003a0001c0009t0023g0026a0001c0011t0023g0007others(2): Show | 5 | HG01175.hp2 HG02486.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.883-25564G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116808228 | ||||||
| chr12:116808234
|
G | A | 49 | a0001c0001t0001g0141a0001c0001t0001g0190a0001c0001t0001g0193others(46): Show | 49 | HG00408.hp2 HG00438.hp2 HG01074.hp2 others(46): Show |
intron_variant | MODIFIER | c.883-25558G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116808234 | ||||||
| chr12:116808236
|
A | G | 251 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(248): Show | 251 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(248): Show |
intron_variant | MODIFIER | c.883-25556A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116808236 | ||||||
| chr12:116808586
|
G | C | 205 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(202): Show | 205 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(202): Show |
intron_variant | MODIFIER | c.883-25206G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116808586 | ||||||
| chr12:116808608
|
C | A | 5 | a0001c0001t0019g0124a0001c0001t0019g0163a0001c0001t0019g0187others(2): Show | 5 | HG00140.hp1 HG01261.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.883-25184C>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116808608 | ||||||
| chr12:116808636
|
A | G | 3 | a0001c0003t0014g0065a0001c0005t0020g0162a0001c0013t0020g0098 | 3 | HG02970.hp2 HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.883-25156A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116808636 | ||||||
| chr12:116808718
|
A | G | 1 | a0001c0002t0066g0010 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.883-25074A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116808718 | ||||||
| chr12:116808831
|
G | C | 54 | a0001c0001t0001g0141a0001c0001t0001g0190a0001c0001t0001g0193others(51): Show | 54 | HG00408.hp2 HG00438.hp2 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.883-24961G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116808831 | ||||||
| chr12:116809051
|
A | G | 3 | a0001c0001t0003g0085a0001c0001t0003g0212a0001c0001t0029g0225 | 3 | NA18954.hp1 NA18999.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.883-24741A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116809051 | ||||||
| chr12:116809187
|
GTTCA | G | 69 | a0001c0001t0001g0141a0001c0001t0001g0190a0001c0001t0001g0193others(66): Show | 69 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.883-24571_883-2456 others(8): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116809187 | |||||
| chr12:116809187
|
GTTCATTC others(1): Show |
G | 179 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(176): Show | 179 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(176): Show |
intron_variant | MODIFIER | c.883-24575_883-2456 others(12): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116809187 | |||||
| chr12:116809231
|
G | A | 5 | a0001c0002t0005g0003a0001c0009t0023g0026a0001c0011t0023g0007others(2): Show | 5 | HG01175.hp2 HG02486.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.883-24561G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116809231 | ||||||
| chr12:116809337
|
G | A | 11 | a0001c0001t0002g0209a0001c0001t0019g0124a0001c0001t0019g0163others(8): Show | 11 | HG00140.hp1 HG00438.hp1 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.883-24455G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116809337 | ||||||
| chr12:116809369
|
G | A | 5 | a0001c0001t0019g0124a0001c0001t0019g0163a0001c0001t0019g0187others(2): Show | 5 | HG00140.hp1 HG01261.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.883-24423G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116809369 | ||||||
| chr12:116809377
|
C | T | 5 | a0001c0001t0002g0031a0001c0001t0002g0045a0001c0001t0002g0048others(2): Show | 5 | HG02572.hp1 HG02976.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.883-24415C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116809377 | ||||||
| chr12:116809584
|
C | T | 7 | a0001c0001t0008g0041a0001c0002t0002g0129a0001c0002t0008g0140others(4): Show | 7 | HG02055.hp1 HG02258.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.883-24208C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116809584 | ||||||
| chr12:116809619
|
A | G | 2 | a0001c0006t0031g0067a0001c0016t0032g0044 | 2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.883-24173A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116809619 | ||||||
| chr12:116809656
|
C | T | 6 | a0001c0001t0002g0209a0001c0004t0001g0083a0001c0006t0050g0013others(3): Show | 6 | HG00438.hp1 HG00741.hp1 HG02040.hp1 others(3): Show |
intron_variant | MODIFIER | c.883-24136C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116809656 | ||||||
| chr12:116809750
|
G | A | 5 | a0001c0001t0019g0124a0001c0001t0019g0163a0001c0001t0019g0187others(2): Show | 5 | HG00140.hp1 HG01261.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.883-24042G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116809750 | ||||||
| chr12:116809803
|
G | C | 1 | a0001c0003t0035g0088 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.883-23989G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116809803 | ||||||
| chr12:116809858
|
A | G | 9 | a0001c0001t0005g0245a0001c0001t0005g0246a0001c0002t0005g0149others(6): Show | 9 | HG02109.hp1 HG02145.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.883-23934A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116809858 | ||||||
| chr12:116809981
|
G | T | 118 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(115): Show | 118 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.883-23811G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116809981 | ||||||
| chr12:116809987
|
C | T | 2 | a0001c0001t0008g0041a0001c0002t0008g0140 | 2 | HG03041.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.883-23805C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116809987 | ||||||
| chr12:116810318
|
C | G | 1 | a0001c0011t0053g0011 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.883-23474C>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116810318 | ||||||
| chr12:116810322
|
A | G | 1 | a0001c0003t0006g0208 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.883-23470A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116810322 | ||||||
| chr12:116810388
|
C | T | 3 | a0001c0003t0014g0065a0001c0005t0020g0162a0001c0013t0020g0098 | 3 | HG02970.hp2 HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.883-23404C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116810388 | ||||||
| chr12:116810555
|
G | A | 1 | a0001c0006t0050g0013 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.883-23237G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116810555 | ||||||
| chr12:116810828
|
G | C | 3 | a0001c0001t0001g0166a0001c0002t0001g0111a0001c0002t0012g0014 | 3 | HG01361.hp1 HG02004.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.883-22964G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116810828 | ||||||
| chr12:116810831
|
G | A | 3 | a0001c0003t0014g0065a0001c0005t0020g0162a0001c0013t0020g0098 | 3 | HG02970.hp2 HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.883-22961G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116810831 | ||||||
| chr12:116810934
|
G | A | 35 | a0001c0001t0001g0178a0001c0001t0004g0095a0001c0001t0004g0096others(32): Show | 35 | HG00544.hp1 HG01243.hp1 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.883-22858G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116810934 | ||||||
| chr12:116810985
|
T | C | 6 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0258others(3): Show | 6 | HG01192.hp1 HG01257.hp1 HG02148.hp1 others(3): Show |
intron_variant | MODIFIER | c.883-22807T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116810985 | ||||||
| chr12:116811074
|
A | G | 249 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(246): Show | 249 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(246): Show |
intron_variant | MODIFIER | c.883-22718A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116811074 | ||||||
| chr12:116811132
|
G | A | 1 | a0001c0009t0051g0016 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.883-22660G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116811132 | ||||||
| chr12:116811196
|
A | C | 1 | a0001c0005t0020g0162 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.883-22596A>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116811196 | ||||||
| chr12:116811373
|
A | AT | 185 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(182): Show | 185 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(182): Show |
intron_variant | MODIFIER | c.883-22408dupT | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116811373 | |||||
| chr12:116811373
|
A | ATT | 46 | a0001c0001t0001g0141a0001c0001t0001g0190a0001c0001t0001g0193others(43): Show | 46 | HG00408.hp2 HG00438.hp2 HG01074.hp2 others(43): Show |
intron_variant | MODIFIER | c.883-22409_883-2240 others(6): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116811373 | |||||
| chr12:116811435
|
G | A | 1 | a0001c0014t0002g0137 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.883-22357G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116811435 | ||||||
| chr12:116811444
|
C | T | 49 | a0001c0001t0001g0141a0001c0001t0001g0190a0001c0001t0001g0193others(46): Show | 49 | HG00408.hp2 HG00438.hp2 HG01074.hp2 others(46): Show |
intron_variant | MODIFIER | c.883-22348C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116811444 | ||||||
| chr12:116811573
|
G | A | 5 | a0001c0001t0005g0245a0001c0002t0005g0003a0001c0009t0023g0026others(2): Show | 5 | HG01175.hp2 HG02145.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.883-22219G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116811573 | ||||||
| chr12:116811623
|
G | T | 2 | a0001c0001t0008g0041a0001c0002t0008g0140 | 2 | HG03041.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.883-22169G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116811623 | ||||||
| chr12:116811650
|
A | G | 25 | a0001c0001t0001g0178a0001c0001t0004g0095a0001c0001t0004g0096others(22): Show | 25 | HG00544.hp1 HG01243.hp2 HG02074.hp1 others(22): Show |
intron_variant | MODIFIER | c.883-22142A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116811650 | ||||||
| chr12:116811679
|
G | A | 3 | a0001c0001t0001g0122a0001c0001t0001g0237a0001c0002t0012g0089 | 3 | HG01074.hp1 HG01358.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.883-22113G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116811679 | ||||||
| chr12:116811687
|
G | A | 5 | a0001c0002t0005g0003a0001c0009t0023g0026a0001c0011t0023g0007others(2): Show | 5 | HG01175.hp2 HG02486.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.883-22105G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116811687 | ||||||
| chr12:116811759
|
T | C | 11 | a0001c0001t0002g0209a0001c0001t0019g0124a0001c0001t0019g0163others(8): Show | 11 | HG00140.hp1 HG00438.hp1 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.883-22033T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116811759 | ||||||
| chr12:116811813
|
G | A | 50 | a0001c0001t0001g0141a0001c0001t0001g0190a0001c0001t0001g0193others(47): Show | 50 | HG00408.hp2 HG00438.hp2 HG01074.hp2 others(47): Show |
intron_variant | MODIFIER | c.883-21979G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116811813 | ||||||
| chr12:116811874
|
A | G | 5 | a0001c0002t0005g0003a0001c0009t0023g0026a0001c0011t0023g0007others(2): Show | 5 | HG01175.hp2 HG02486.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.883-21918A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116811874 | ||||||
| chr12:116812076
|
G | A | 3 | a0001c0007t0025g0009a0001c0007t0025g0056a0001c0007t0046g0053 | 3 | HG01884.hp2 HG02145.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.883-21716G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116812076 | ||||||
| chr12:116812229
|
C | T | 195 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(192): Show | 195 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(192): Show |
intron_variant | MODIFIER | c.883-21563C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116812229 | ||||||
| chr12:116812478
|
A | G | 50 | a0001c0001t0001g0141a0001c0001t0001g0190a0001c0001t0001g0193others(47): Show | 50 | HG00408.hp2 HG00438.hp2 HG01074.hp2 others(47): Show |
intron_variant | MODIFIER | c.883-21314A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116812478 | ||||||
| chr12:116812596
|
G | A | 5 | a0001c0002t0005g0003a0001c0009t0023g0026a0001c0011t0023g0007others(2): Show | 5 | HG01175.hp2 HG02486.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.883-21196G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116812596 | ||||||
| chr12:116812604
|
A | G | 196 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(193): Show | 196 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(193): Show |
intron_variant | MODIFIER | c.883-21188A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116812604 | ||||||
| chr12:116812647
|
G | A | 1 | a0001c0002t0018g0022 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.883-21145G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116812647 | ||||||
| chr12:116812670
|
G | A | 1 | a0001c0002t0066g0010 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.883-21122G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116812670 | ||||||
| chr12:116812825
|
C | T | 3 | a0001c0003t0014g0065a0001c0005t0020g0162a0001c0013t0020g0098 | 3 | HG02970.hp2 HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.883-20967C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116812825 | ||||||
| chr12:116812883
|
G | A | 195 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(192): Show | 195 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(192): Show |
intron_variant | MODIFIER | c.883-20909G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116812883 | ||||||
| chr12:116812893
|
C | T | 20 | a0001c0001t0001g0178a0001c0001t0004g0110a0001c0001t0004g0168others(17): Show | 20 | HG00544.hp1 HG02074.hp1 HG02523.hp2 others(17): Show |
intron_variant | MODIFIER | c.883-20899C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116812893 | ||||||
| chr12:116812929
|
T | C | 1 | a0001c0002t0018g0022 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.883-20863T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116812929 | ||||||
| chr12:116812979
|
A | G | 35 | a0001c0001t0001g0178a0001c0001t0004g0095a0001c0001t0004g0096others(32): Show | 35 | HG00544.hp1 HG01243.hp1 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.883-20813A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116812979 | ||||||
| chr12:116813024
|
C | T | 4 | a0001c0002t0005g0003a0001c0009t0023g0026a0001c0011t0023g0007others(1): Show | 4 | HG01175.hp2 HG02486.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.883-20768C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116813024 | ||||||
| chr12:116813037
|
C | G | 5 | a0001c0002t0005g0003a0001c0009t0023g0026a0001c0011t0023g0007others(2): Show | 5 | HG01175.hp2 HG02486.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.883-20755C>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116813037 | ||||||
| chr12:116813125
|
T | G | 1 | a0001c0009t0051g0016 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.883-20667T>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116813125 | ||||||
| chr12:116813147
|
C | T | 49 | a0001c0001t0001g0141a0001c0001t0001g0190a0001c0001t0001g0193others(46): Show | 49 | HG00408.hp2 HG00438.hp2 HG01074.hp2 others(46): Show |
intron_variant | MODIFIER | c.883-20645C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116813147 | ||||||
| chr12:116813728
|
G | A | 50 | a0001c0001t0001g0141a0001c0001t0001g0190a0001c0001t0001g0193others(47): Show | 50 | HG00408.hp2 HG00438.hp2 HG01074.hp2 others(47): Show |
intron_variant | MODIFIER | c.883-20064G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116813728 | ||||||
| chr12:116813805
|
C | T | 249 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(246): Show | 249 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(246): Show |
intron_variant | MODIFIER | c.883-19987C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116813805 | ||||||
| chr12:116814080
|
C | T | 1 | a0001c0009t0051g0016 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.883-19712C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116814080 | ||||||
| chr12:116814081
|
G | A | 1 | a0001c0001t0004g0145 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.883-19711G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116814081 | ||||||
| chr12:116814083
|
G | T | 1 | a0001c0014t0002g0137 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.883-19709G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116814083 | ||||||
| chr12:116814126
|
C | T | 1 | a0001c0001t0024g0147 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.883-19666C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116814126 | ||||||
| chr12:116814185
|
C | A | 6 | a0001c0001t0002g0034a0001c0001t0002g0103a0001c0001t0002g0104others(3): Show | 6 | HG02615.hp1 HG02622.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.883-19607C>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116814185 | ||||||
| chr12:116814248
|
C | T | 7 | a0001c0001t0001g0178a0001c0001t0007g0070a0001c0001t0007g0071others(4): Show | 7 | HG00544.hp1 HG02523.hp2 NA18948.hp2 others(4): Show |
intron_variant | MODIFIER | c.883-19544C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116814248 | ||||||
| chr12:116814249
|
A | C | 3 | a0001c0005t0030g0051a0001c0005t0030g0052a0001c0005t0070g0050 | 3 | HG01891.hp1 HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.883-19543A>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116814249 | ||||||
| chr12:116814683
|
T | A | 50 | a0001c0001t0001g0141a0001c0001t0001g0190a0001c0001t0001g0193others(47): Show | 50 | HG00408.hp2 HG00438.hp2 HG01074.hp2 others(47): Show |
intron_variant | MODIFIER | c.883-19109T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116814683 | ||||||
| chr12:116814688
|
T | C | 3 | a0001c0003t0014g0065a0001c0005t0020g0162a0001c0013t0020g0098 | 3 | HG02970.hp2 HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.883-19104T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116814688 | ||||||
| chr12:116814694
|
G | A | 5 | a0001c0001t0003g0106a0001c0001t0003g0131a0001c0001t0004g0128others(2): Show | 5 | HG00673.hp2 HG02071.hp2 NA18993.hp2 others(2): Show |
intron_variant | MODIFIER | c.883-19098G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116814694 | ||||||
| chr12:116814747
|
C | T | 34 | a0001c0001t0003g0085a0001c0001t0003g0106a0001c0001t0003g0117others(31): Show | 34 | HG00423.hp2 HG00609.hp1 HG00621.hp2 others(31): Show |
intron_variant | MODIFIER | c.883-19045C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116814747 | ||||||
| chr12:116814823
|
C | A | 1 | a0001c0001t0001g0259 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.883-18969C>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116814823 | ||||||
| chr12:116814835
|
T | C | 199 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(196): Show | 199 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(196): Show |
intron_variant | MODIFIER | c.883-18957T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116814835 | ||||||
| chr12:116814950
|
G | A | 6 | a0001c0001t0001g0195a0001c0002t0005g0003a0001c0009t0023g0026others(3): Show | 6 | HG01106.hp2 HG01175.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.883-18842G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116814950 | ||||||
| chr12:116815306
|
G | A | 7 | a0001c0001t0006g0115a0001c0001t0009g0116a0001c0001t0009g0118others(4): Show | 7 | HG01109.hp2 HG01258.hp2 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.883-18486G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116815306 | ||||||
| chr12:116815395
|
C | T | 1 | a0001c0006t0050g0013 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.883-18397C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116815395 | ||||||
| chr12:116815447
|
G | C | 2 | a0001c0001t0001g0141a0001c0001t0001g0235 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.883-18345G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116815447 | ||||||
| chr12:116815554
|
T | C | 8 | a0001c0001t0008g0041a0001c0001t0045g0114a0001c0002t0002g0129others(5): Show | 8 | HG02055.hp1 HG02258.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.883-18238T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116815554 | ||||||
| chr12:116815648
|
C | T | 5 | a0001c0002t0005g0003a0001c0009t0023g0026a0001c0011t0023g0007others(2): Show | 5 | HG01175.hp2 HG02486.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.883-18144C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116815648 | ||||||
| chr12:116815859
|
CCAGCAGG others(1): Show |
C | 8 | a0001c0001t0008g0041a0001c0001t0045g0114a0001c0002t0002g0129others(5): Show | 8 | HG02055.hp1 HG02258.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.883-17929_883-1792 others(12): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116815859 | |||||
| chr12:116815915
|
T | C | 1 | a0001c0001t0001g0224 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.883-17877T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116815915 | ||||||
| chr12:116816066
|
T | A | 200 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(197): Show | 200 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(197): Show |
intron_variant | MODIFIER | c.883-17726T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116816066 | ||||||
| chr12:116816174
|
C | G | 134 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(131): Show | 134 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.883-17618C>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116816174 | ||||||
| chr12:116816366
|
C | A | 49 | a0001c0001t0001g0141a0001c0001t0001g0190a0001c0001t0001g0193others(46): Show | 49 | HG00408.hp2 HG00438.hp2 HG01074.hp2 others(46): Show |
intron_variant | MODIFIER | c.883-17426C>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116816366 | ||||||
| chr12:116816436
|
A | G | 14 | a0001c0001t0002g0032a0001c0001t0008g0028a0001c0001t0008g0029others(11): Show | 14 | HG01891.hp1 HG01891.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.883-17356A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116816436 | ||||||
| chr12:116816447
|
C | T | 5 | a0001c0001t0019g0124a0001c0001t0019g0163a0001c0001t0019g0187others(2): Show | 5 | HG00140.hp1 HG01261.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.883-17345C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116816447 | ||||||
| chr12:116816448
|
G | A | 1 | a0001c0009t0051g0016 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.883-17344G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116816448 | ||||||
| chr12:116816469
|
G | A | 5 | a0001c0002t0005g0003a0001c0009t0023g0026a0001c0011t0023g0007others(2): Show | 5 | HG01175.hp2 HG02486.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.883-17323G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116816469 | ||||||
| chr12:116816643
|
A | C | 11 | a0001c0001t0002g0209a0001c0001t0019g0124a0001c0001t0019g0163others(8): Show | 11 | HG00140.hp1 HG00438.hp1 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.883-17149A>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116816643 | ||||||
| chr12:116816669
|
A | G | 20 | a0001c0001t0001g0178a0001c0001t0004g0110a0001c0001t0004g0168others(17): Show | 20 | HG00544.hp1 HG02074.hp1 HG02523.hp2 others(17): Show |
intron_variant | MODIFIER | c.883-17123A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116816669 | ||||||
| chr12:116816672
|
T | C | 1 | a0001c0009t0051g0016 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.883-17120T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116816672 | ||||||
| chr12:116816675
|
T | G | 50 | a0001c0001t0001g0141a0001c0001t0001g0190a0001c0001t0001g0193others(47): Show | 50 | HG00408.hp2 HG00438.hp2 HG01074.hp2 others(47): Show |
intron_variant | MODIFIER | c.883-17117T>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116816675 | ||||||
| chr12:116816836
|
TAAC | T | 5 | a0001c0002t0005g0003a0001c0009t0023g0026a0001c0011t0023g0007others(2): Show | 5 | HG01175.hp2 HG02486.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.883-16953_883-1695 others(7): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116816836 | |||||
| chr12:116816860
|
T | A | 3 | a0001c0001t0008g0028a0001c0001t0008g0029a0001c0001t0008g0040 | 3 | HG02572.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.883-16932T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116816860 | ||||||
| chr12:116817115
|
C | T | 1 | a0001c0004t0052g0015 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.883-16677C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116817115 | ||||||
| chr12:116817159
|
C | T | 134 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(131): Show | 134 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.883-16633C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116817159 | ||||||
| chr12:116817276
|
G | C | 1 | a0001c0001t0001g0069 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.883-16516G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116817276 | ||||||
| chr12:116817495
|
G | A | 2 | a0001c0002t0004g0005a0001c0002t0049g0004 | 2 | HG01243.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.883-16297G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116817495 | ||||||
| chr12:116817633
|
T | A | 11 | a0001c0001t0002g0209a0001c0001t0019g0124a0001c0001t0019g0163others(8): Show | 11 | HG00140.hp1 HG00438.hp1 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.883-16159T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116817633 | ||||||
| chr12:116817710
|
T | C | 35 | a0001c0001t0001g0178a0001c0001t0004g0095a0001c0001t0004g0096others(32): Show | 35 | HG00544.hp1 HG01243.hp1 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.883-16082T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116817710 | ||||||
| chr12:116817850
|
C | G | 134 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(131): Show | 134 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.883-15942C>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116817850 | ||||||
| chr12:116817896
|
C | A | 2 | a0001c0002t0004g0005a0001c0002t0049g0004 | 2 | HG01243.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.883-15896C>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116817896 | ||||||
| chr12:116817992
|
G | A | 50 | a0001c0001t0001g0141a0001c0001t0001g0190a0001c0001t0001g0193others(47): Show | 50 | HG00408.hp2 HG00438.hp2 HG01074.hp2 others(47): Show |
intron_variant | MODIFIER | c.883-15800G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116817992 | ||||||
| chr12:116818228
|
G | C | 1 | a0001c0001t0010g0222 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.883-15564G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116818228 | ||||||
| chr12:116818298
|
G | C | 5 | a0001c0001t0002g0031a0001c0001t0002g0045a0001c0001t0002g0048others(2): Show | 5 | HG02572.hp1 HG02976.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.883-15494G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116818298 | ||||||
| chr12:116818320
|
C | CA | 187 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(184): Show | 187 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(184): Show |
intron_variant | MODIFIER | c.883-15456dupA | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116818320 | |||||
| chr12:116818320
|
C | CAA | 22 | a0001c0001t0001g0190a0001c0001t0001g0193a0001c0001t0001g0195others(19): Show | 22 | HG00140.hp1 HG00544.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.883-15457_883-1545 others(6): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116818320 | |||||
| chr12:116818320
|
C | CAAA | 44 | a0001c0001t0001g0141a0001c0001t0001g0235a0001c0001t0002g0133others(41): Show | 44 | HG00408.hp2 HG00438.hp2 HG01074.hp2 others(41): Show |
intron_variant | MODIFIER | c.883-15458_883-1545 others(7): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116818320 | |||||
| chr12:116818363
|
C | T | 1 | a0001c0003t0035g0088 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.883-15429C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116818363 | ||||||
| chr12:116818553
|
G | A | 35 | a0001c0001t0001g0178a0001c0001t0004g0095a0001c0001t0004g0096others(32): Show | 35 | HG00544.hp1 HG01243.hp1 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.883-15239G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116818553 | ||||||
| chr12:116818557
|
G | C | 1 | a0001c0001t0002g0236 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.883-15235G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116818557 | ||||||
| chr12:116818893
|
A | C | 200 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(197): Show | 200 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(197): Show |
intron_variant | MODIFIER | c.883-14899A>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116818893 | ||||||
| chr12:116818895
|
A | G | 1 | a0001c0001t0001g0237 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.883-14897A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116818895 | ||||||
| chr12:116819160
|
G | T | 3 | a0001c0005t0013g0154a0001c0013t0013g0158a0001c0018t0055g0059 | 3 | HG03453.hp2 HG03579.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.883-14632G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116819160 | ||||||
| chr12:116819207
|
G | T | 1 | a0001c0001t0001g0256 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.883-14585G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116819207 | ||||||
| chr12:116819214
|
C | T | 50 | a0001c0001t0001g0141a0001c0001t0001g0190a0001c0001t0001g0193others(47): Show | 50 | HG00408.hp2 HG00438.hp2 HG01074.hp2 others(47): Show |
intron_variant | MODIFIER | c.883-14578C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116819214 | ||||||
| chr12:116819372
|
C | G | 2 | a0001c0006t0031g0067a0001c0016t0032g0044 | 2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.883-14420C>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116819372 | ||||||
| chr12:116819381
|
C | A | 1 | a0001c0004t0052g0015 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.883-14411C>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116819381 | ||||||
| chr12:116819393
|
C | A | 5 | a0001c0002t0005g0003a0001c0009t0023g0026a0001c0011t0023g0007others(2): Show | 5 | HG01175.hp2 HG02486.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.883-14399C>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116819393 | ||||||
| chr12:116819430
|
C | G | 1 | a0001c0002t0041g0075 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.883-14362C>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116819430 | ||||||
| chr12:116819448
|
G | T | 1 | a0001c0002t0005g0003 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.883-14344G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116819448 | ||||||
| chr12:116819664
|
C | G | 1 | a0001c0004t0052g0015 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.883-14128C>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116819664 | ||||||
| chr12:116819737
|
C | A | 2 | a0001c0001t0003g0144a0001c0001t0061g0148 | 2 | NA18975.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.883-14055C>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116819737 | ||||||
| chr12:116819739
|
T | G | 50 | a0001c0001t0001g0141a0001c0001t0001g0190a0001c0001t0001g0193others(47): Show | 50 | HG00408.hp2 HG00438.hp2 HG01074.hp2 others(47): Show |
intron_variant | MODIFIER | c.883-14053T>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116819739 | ||||||
| chr12:116819871
|
T | G | 200 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(197): Show | 200 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(197): Show |
intron_variant | MODIFIER | c.883-13921T>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116819871 | ||||||
| chr12:116819927
|
A | G | 50 | a0001c0001t0001g0141a0001c0001t0001g0190a0001c0001t0001g0193others(47): Show | 50 | HG00408.hp2 HG00438.hp2 HG01074.hp2 others(47): Show |
intron_variant | MODIFIER | c.883-13865A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116819927 | ||||||
| chr12:116819947
|
T | C | 1 | a0001c0001t0024g0147 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.883-13845T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116819947 | ||||||
| chr12:116819948
|
A | G | 1 | a0001c0002t0005g0003 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.883-13844A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116819948 | ||||||
| chr12:116820052
|
T | C | 1 | a0001c0004t0052g0015 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.883-13740T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116820052 | ||||||
| chr12:116820240
|
G | A | 1 | a0001c0001t0001g0203 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.883-13552G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116820240 | ||||||
| chr12:116820288
|
C | G | 150 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(147): Show | 150 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(147): Show |
intron_variant | MODIFIER | c.883-13504C>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116820288 | ||||||
| chr12:116820342
|
G | A | 1 | a0001c0001t0001g0086 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.883-13450G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116820342 | ||||||
| chr12:116820373
|
T | C | 249 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(246): Show | 249 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(246): Show |
intron_variant | MODIFIER | c.883-13419T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116820373 | ||||||
| chr12:116820615
|
C | T | 1 | a0001c0002t0018g0022 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.883-13177C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116820615 | ||||||
| chr12:116820631
|
C | T | 1 | a0001c0009t0051g0016 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.883-13161C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116820631 | ||||||
| chr12:116820901
|
A | G | 1 | a0001c0006t0036g0018 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.883-12891A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116820901 | ||||||
| chr12:116821032
|
A | G | 2 | a0001c0002t0004g0268a0001c0009t0037g0043 | 2 | HG02572.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.883-12760A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116821032 | ||||||
| chr12:116821051
|
G | T | 8 | a0001c0001t0008g0041a0001c0001t0045g0114a0001c0002t0002g0129others(5): Show | 8 | HG02055.hp1 HG02258.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.883-12741G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116821051 | ||||||
| chr12:116821058
|
C | T | 3 | a0001c0005t0030g0051a0001c0005t0030g0052a0001c0005t0070g0050 | 3 | HG01891.hp1 HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.883-12734C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116821058 | ||||||
| chr12:116821073
|
G | C | 1 | a0001c0002t0001g0079 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.883-12719G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116821073 | ||||||
| chr12:116821088
|
G | A | 1 | a0001c0004t0052g0015 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.883-12704G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116821088 | ||||||
| chr12:116821175
|
C | G | 29 | a0001c0001t0001g0178a0001c0001t0004g0168a0001c0001t0004g0170others(26): Show | 29 | HG00544.hp1 HG01243.hp1 HG02074.hp1 others(26): Show |
intron_variant | MODIFIER | c.883-12617C>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116821175 | ||||||
| chr12:116821230
|
C | T | 8 | a0001c0001t0008g0041a0001c0001t0045g0114a0001c0002t0002g0129others(5): Show | 8 | HG02055.hp1 HG02258.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.883-12562C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116821230 | ||||||
| chr12:116821319
|
C | T | 5 | a0001c0001t0019g0124a0001c0001t0019g0163a0001c0001t0019g0187others(2): Show | 5 | HG00140.hp1 HG01261.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.883-12473C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116821319 | ||||||
| chr12:116821403
|
G | A | 1 | a0001c0004t0052g0015 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.883-12389G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116821403 | ||||||
| chr12:116821471
|
C | G | 230 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(227): Show | 230 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(227): Show |
intron_variant | MODIFIER | c.883-12321C>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116821471 | ||||||
| chr12:116821540
|
G | A | 4 | a0001c0002t0062g0185a0001c0002t0063g0263a0001c0002t0064g0152others(1): Show | 4 | HG01169.hp2 HG01884.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.883-12252G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116821540 | ||||||
| chr12:116821546
|
T | C | 5 | a0001c0002t0005g0003a0001c0009t0023g0026a0001c0011t0023g0007others(2): Show | 5 | HG01175.hp2 HG02486.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.883-12246T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116821546 | ||||||
| chr12:116821572
|
A | C | 256 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(253): Show | 256 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(253): Show |
intron_variant | MODIFIER | c.883-12220A>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116821572 | ||||||
| chr12:116821639
|
G | A | 5 | a0001c0001t0004g0110a0001c0001t0004g0168a0001c0001t0004g0176others(2): Show | 5 | HG02683.hp2 HG03688.hp1 HG03704.hp2 others(2): Show |
intron_variant | MODIFIER | c.883-12153G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116821639 | ||||||
| chr12:116821671
|
G | A | 1 | a0001c0001t0040g0143 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.883-12121G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116821671 | ||||||
| chr12:116821741
|
C | T | 1 | a0001c0011t0053g0011 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.883-12051C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116821741 | ||||||
| chr12:116821802
|
C | CT | 6 | a0001c0001t0002g0045a0001c0001t0004g0110a0001c0001t0007g0171others(3): Show | 6 | HG01243.hp2 HG02523.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.883-11958dupT | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116821802 | |||||
| chr12:116821802
|
C | CTT | 10 | a0001c0001t0002g0032a0001c0001t0008g0040a0001c0001t0011g0033others(7): Show | 10 | HG00673.hp1 HG01106.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.883-11959_883-1195 others(6): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116821802 | |||||
| chr12:116821802
|
CT | C | 54 | a0001c0001t0001g0069a0001c0001t0001g0197a0001c0001t0001g0203others(51): Show | 54 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.883-11958delT | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116821802 | |||||
| chr12:116821802
|
CTT | C | 106 | a0001c0001t0001g0072a0001c0001t0001g0086a0001c0001t0001g0092others(103): Show | 106 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.883-11959_883-1195 others(6): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116821802 | |||||
| chr12:116821802
|
CTTT | C | 57 | a0001c0001t0002g0034a0001c0001t0002g0103a0001c0001t0002g0104others(54): Show | 57 | HG00140.hp1 HG00438.hp1 HG00609.hp1 others(54): Show |
intron_variant | MODIFIER | c.883-11960_883-1195 others(7): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116821802 | |||||
| chr12:116821802
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0002t0001g0077 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.883-11967_883-1195 others(14): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116821802 | |||||
| chr12:116821863
|
C | CTGGAGTG others(2): Show |
56 | a0001c0001t0001g0141a0001c0001t0001g0190a0001c0001t0001g0193others(53): Show | 56 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.883-11910_883-1190 others(13): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116821863 | |||||
| chr12:116821863
|
CTGGAGTG others(2): Show |
C | 6 | a0001c0001t0002g0236a0001c0002t0005g0003a0001c0009t0023g0026others(3): Show | 6 | HG01175.hp2 HG01261.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.883-11910_883-1190 others(13): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116821863 | |||||
| chr12:116821930
|
G | A | 1 | a0001c0001t0002g0023 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.883-11862G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116821930 | ||||||
| chr12:116822169
|
C | G | 117 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(114): Show | 117 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.883-11623C>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116822169 | ||||||
| chr12:116822332
|
C | G | 1 | a0001c0001t0014g0037 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.883-11460C>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116822332 | ||||||
| chr12:116822467
|
G | A | 2 | a0001c0009t0037g0043a0001c0014t0018g0019 | 2 | HG01106.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.883-11325G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116822467 | ||||||
| chr12:116822707
|
TAGAA | T | 14 | a0001c0001t0002g0032a0001c0001t0008g0028a0001c0001t0008g0029others(11): Show | 14 | HG01106.hp1 HG02257.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.883-11081_883-1107 others(8): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116822707 | |||||
| chr12:116822731
|
G | A | 5 | a0001c0001t0019g0124a0001c0001t0019g0163a0001c0001t0019g0187others(2): Show | 5 | HG00140.hp1 HG01261.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.883-11061G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116822731 | ||||||
| chr12:116822854
|
A | G | 31 | a0001c0001t0002g0032a0001c0001t0002g0209a0001c0001t0008g0028others(28): Show | 31 | HG00140.hp1 HG00438.hp1 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.883-10938A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116822854 | ||||||
| chr12:116822934
|
T | C | 15 | a0001c0001t0002g0032a0001c0001t0008g0028a0001c0001t0008g0029others(12): Show | 15 | HG01106.hp1 HG02257.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.883-10858T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116822934 | ||||||
| chr12:116823041
|
A | G | 11 | a0001c0001t0002g0209a0001c0002t0018g0022a0001c0004t0001g0083others(8): Show | 11 | HG00438.hp1 HG00741.hp1 HG02040.hp1 others(8): Show |
intron_variant | MODIFIER | c.883-10751A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116823041 | ||||||
| chr12:116823192
|
G | C | 9 | a0001c0001t0002g0032a0001c0001t0008g0028a0001c0001t0008g0029others(6): Show | 9 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.883-10600G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116823192 | ||||||
| chr12:116823237
|
C | T | 2 | a0001c0009t0051g0016a0001c0011t0053g0011 | 2 | HG02809.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.883-10555C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116823237 | ||||||
| chr12:116823264
|
C | G | 1 | a0001c0001t0001g0072 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.883-10528C>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116823264 | ||||||
| chr12:116823512
|
T | C | 174 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(171): Show | 174 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(171): Show |
intron_variant | MODIFIER | c.883-10280T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116823512 | ||||||
| chr12:116823687
|
A | T | 1 | a0001c0006t0036g0018 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.883-10105A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116823687 | ||||||
| chr12:116823901
|
AT | A | 4 | a0001c0006t0005g0017a0001c0007t0005g0062a0001c0007t0016g0061others(1): Show | 4 | HG01243.hp1 HG02486.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.883-9887delT | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116823901 | |||||
| chr12:116823912
|
G | A | 2 | a0001c0001t0001g0086a0001c0001t0001g0221 | 2 | NA18950.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.883-9880G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116823912 | ||||||
| chr12:116824319
|
C | T | 14 | a0001c0001t0002g0032a0001c0001t0008g0028a0001c0001t0008g0029others(11): Show | 14 | HG01106.hp1 HG02257.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.883-9473C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116824319 | ||||||
| chr12:116824362
|
G | A | 5 | a0001c0001t0019g0124a0001c0001t0019g0163a0001c0001t0019g0187others(2): Show | 5 | HG00140.hp1 HG01261.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.883-9430G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116824362 | ||||||
| chr12:116824369
|
A | G | 1 | a0001c0011t0053g0011 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.883-9423A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116824369 | ||||||
| chr12:116824476
|
C | T | 3 | a0001c0007t0025g0009a0001c0007t0025g0056a0001c0007t0046g0053 | 3 | HG01884.hp2 HG02145.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.883-9316C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116824476 | ||||||
| chr12:116824482
|
T | G | 5 | a0001c0001t0019g0124a0001c0001t0019g0163a0001c0001t0019g0187others(2): Show | 5 | HG00140.hp1 HG01261.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.883-9310T>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116824482 | ||||||
| chr12:116824564
|
A | C | 9 | a0001c0001t0002g0032a0001c0001t0008g0028a0001c0001t0008g0029others(6): Show | 9 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.883-9228A>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116824564 | ||||||
| chr12:116824655
|
C | T | 3 | a0001c0009t0023g0026a0001c0011t0023g0007a0001c0011t0039g0012 | 3 | HG02486.hp1 HG02630.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.883-9137C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116824655 | ||||||
| chr12:116824741
|
C | T | 1 | a0001c0009t0051g0016 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.883-9051C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116824741 | ||||||
| chr12:116824965
|
A | G | 9 | a0001c0001t0005g0245a0001c0001t0005g0246a0001c0002t0005g0003others(6): Show | 9 | HG01175.hp2 HG02109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.883-8827A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116824965 | ||||||
| chr12:116825008
|
G | A | 1 | a0001c0006t0036g0018 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.883-8784G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116825008 | ||||||
| chr12:116825032
|
A | T | 4 | a0001c0009t0023g0026a0001c0011t0023g0007a0001c0011t0039g0012others(1): Show | 4 | HG02486.hp1 HG02630.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.883-8760A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116825032 | ||||||
| chr12:116825164
|
T | C | 52 | a0001c0001t0001g0178a0001c0001t0002g0209a0001c0001t0004g0095others(49): Show | 52 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.883-8628T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116825164 | ||||||
| chr12:116825208
|
A | G | 1 | a0001c0004t0001g0083 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.883-8584A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116825208 | ||||||
| chr12:116825650
|
C | T | 1 | a0001c0001t0003g0240 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.883-8142C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116825650 | ||||||
| chr12:116825678
|
A | G | 1 | a0001c0003t0002g0247 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.883-8114A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116825678 | ||||||
| chr12:116825755
|
G | A | 68 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(65): Show | 68 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.883-8037G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116825755 | ||||||
| chr12:116825797
|
T | C | 1 | a0001c0013t0013g0158 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.883-7995T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116825797 | ||||||
| chr12:116825880
|
G | A | 1 | a0001c0002t0066g0010 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.883-7912G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116825880 | ||||||
| chr12:116825926
|
G | A | 3 | a0001c0001t0001g0197a0001c0001t0022g0223a0001c0002t0001g0066 | 3 | HG02258.hp2 HG04184.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.883-7866G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116825926 | ||||||
| chr12:116825937
|
A | G | 4 | a0001c0001t0003g0085a0001c0001t0003g0191a0001c0001t0003g0212others(1): Show | 4 | HG02040.hp2 NA18954.hp1 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.883-7855A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116825937 | ||||||
| chr12:116825941
|
G | A | 10 | a0001c0001t0005g0105a0001c0002t0005g0064a0001c0003t0005g0035others(7): Show | 10 | HG01243.hp1 HG02280.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.883-7851G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116825941 | ||||||
| chr12:116826001
|
CTCTG | C | 3 | a0001c0007t0025g0009a0001c0007t0025g0056a0001c0007t0046g0053 | 3 | HG01884.hp2 HG02145.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.883-7785_883-7782d others(6): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116826001 | |||||
| chr12:116826059
|
C | T | 8 | a0001c0001t0002g0032a0001c0001t0008g0028a0001c0001t0008g0029others(5): Show | 8 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.883-7733C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116826059 | ||||||
| chr12:116826126
|
A | C | 1 | a0002c0010t0002g0254 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.883-7666A>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116826126 | ||||||
| chr12:116826132
|
C | T | 1 | a0001c0003t0035g0088 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.883-7660C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116826132 | ||||||
| chr12:116826252
|
C | T | 9 | a0001c0001t0002g0032a0001c0001t0008g0028a0001c0001t0008g0029others(6): Show | 9 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.883-7540C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116826252 | ||||||
| chr12:116826282
|
G | A | 9 | a0001c0001t0002g0209a0001c0002t0018g0022a0001c0004t0001g0083others(6): Show | 9 | HG00438.hp1 HG00741.hp1 HG02040.hp1 others(6): Show |
intron_variant | MODIFIER | c.883-7510G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116826282 | ||||||
| chr12:116826291
|
A | G | 1 | a0003c0017t0006g0060 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.883-7501A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116826291 | ||||||
| chr12:116826299
|
C | G | 3 | a0001c0009t0010g0049a0001c0009t0037g0043a0001c0014t0018g0019 | 3 | HG01106.hp1 HG02572.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.883-7493C>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116826299 | ||||||
| chr12:116826371
|
G | A | 1 | a0002c0010t0002g0001 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.883-7421G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116826371 | ||||||
| chr12:116826377
|
C | T | 11 | a0001c0001t0002g0209a0001c0002t0018g0022a0001c0004t0001g0083others(8): Show | 11 | HG00438.hp1 HG00741.hp1 HG02040.hp1 others(8): Show |
intron_variant | MODIFIER | c.883-7415C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116826377 | ||||||
| chr12:116826514
|
C | G | 1 | a0001c0001t0004g0096 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.883-7278C>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116826514 | ||||||
| chr12:116826551
|
A | C | 2 | a0001c0001t0001g0092a0001c0001t0001g0232 | 2 | NA18941.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.883-7241A>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116826551 | ||||||
| chr12:116826619
|
C | T | 1 | a0001c0009t0010g0049 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.883-7173C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116826619 | ||||||
| chr12:116826804
|
A | G | 6 | a0001c0001t0006g0115a0001c0001t0009g0116a0001c0001t0009g0118others(3): Show | 6 | HG01109.hp2 HG01258.hp2 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.883-6988A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116826804 | ||||||
| chr12:116826810
|
T | C | 1 | a0001c0001t0001g0244 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.883-6982T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116826810 | ||||||
| chr12:116826825
|
A | C | 1 | a0001c0001t0001g0069 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.883-6967A>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116826825 | ||||||
| chr12:116826987
|
G | A | 2 | a0001c0003t0016g0039a0001c0009t0051g0016 | 2 | HG02976.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.883-6805G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116826987 | ||||||
| chr12:116827219
|
C | CA | 16 | a0001c0001t0002g0209a0001c0001t0019g0124a0001c0001t0019g0163others(13): Show | 16 | HG00438.hp1 HG00741.hp1 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.883-6558dupA | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116827219 | |||||
| chr12:116827219
|
C | CAA | 47 | a0001c0001t0001g0178a0001c0001t0002g0032a0001c0001t0004g0095others(44): Show | 47 | HG00544.hp1 HG01243.hp1 HG01243.hp2 others(44): Show |
intron_variant | MODIFIER | c.883-6559_883-6558d others(4): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116827219 | |||||
| chr12:116827228
|
A | G | 4 | a0001c0009t0023g0026a0001c0011t0023g0007a0001c0011t0039g0012others(1): Show | 4 | HG02486.hp1 HG02630.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.883-6564A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116827228 | ||||||
| chr12:116827231
|
A | AGAAAGAA others(141): Show |
1 | a0001c0011t0039g0012 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.883-6561_883-6560i others(150): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116827231 | ||||||
| chr12:116827231
|
A | AGAAAGAA others(131): Show |
1 | a0001c0014t0002g0137 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.883-6561_883-6560i others(140): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116827231 | ||||||
| chr12:116827231
|
A | AGAAAGAA others(137): Show |
1 | a0001c0009t0023g0026 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.883-6561_883-6560i others(146): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116827231 | ||||||
| chr12:116827231
|
A | AGAAAGAA others(137): Show |
1 | a0001c0011t0023g0007 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.883-6561_883-6560i others(146): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116827231 | ||||||
| chr12:116827231
|
A | G | 2 | a0001c0001t0001g0069a0001c0002t0001g0251 | 2 | HG02080.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.883-6561A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116827231 | ||||||
| chr12:116827334
|
C | T | 1 | a0001c0009t0037g0043 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.883-6458C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116827334 | ||||||
| chr12:116827503
|
TC | T | 6 | a0001c0009t0010g0049a0001c0009t0037g0043a0001c0009t0051g0016others(3): Show | 6 | HG01106.hp1 HG02572.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.883-6285delC | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116827503 | |||||
| chr12:116827698
|
C | T | 1 | a0001c0009t0051g0016 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.883-6094C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116827698 | ||||||
| chr12:116828010
|
C | T | 9 | a0001c0001t0002g0209a0001c0002t0018g0022a0001c0004t0001g0083others(6): Show | 9 | HG00438.hp1 HG00741.hp1 HG02040.hp1 others(6): Show |
intron_variant | MODIFIER | c.883-5782C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116828010 | ||||||
| chr12:116828011
|
A | G | 26 | a0001c0001t0001g0178a0001c0001t0004g0095a0001c0001t0004g0096others(23): Show | 26 | HG00544.hp1 HG01243.hp2 HG02074.hp1 others(23): Show |
intron_variant | MODIFIER | c.883-5781A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116828011 | ||||||
| chr12:116828131
|
C | T | 11 | a0001c0001t0002g0209a0001c0002t0018g0022a0001c0004t0001g0083others(8): Show | 11 | HG00438.hp1 HG00741.hp1 HG02040.hp1 others(8): Show |
intron_variant | MODIFIER | c.883-5661C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116828131 | ||||||
| chr12:116828157
|
T | G | 3 | a0001c0005t0013g0154a0001c0013t0013g0158a0001c0018t0055g0059 | 3 | HG03453.hp2 HG03579.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.883-5635T>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116828157 | ||||||
| chr12:116828353
|
G | A | 3 | a0001c0009t0023g0026a0001c0011t0023g0007a0001c0011t0039g0012 | 3 | HG02486.hp1 HG02630.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.883-5439G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116828353 | ||||||
| chr12:116828506
|
A | G | 1 | a0001c0014t0002g0137 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.883-5286A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116828506 | ||||||
| chr12:116828932
|
G | A | 1 | a0001c0006t0050g0013 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.883-4860G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116828932 | ||||||
| chr12:116829005
|
G | GA | 8 | a0001c0001t0002g0175a0001c0001t0069g0068a0001c0002t0005g0003others(5): Show | 8 | HG01109.hp1 HG01175.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.883-4775dupA | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116829005 | |||||
| chr12:116829175
|
A | G | 2 | a0001c0001t0001g0120a0001c0001t0001g0227 | 2 | HG00609.hp2 HG02074.hp2 |
intron_variant | MODIFIER | c.883-4617A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116829175 | ||||||
| chr12:116829252
|
T | G | 1 | a0001c0001t0017g0167 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.883-4540T>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116829252 | ||||||
| chr12:116829376
|
C | T | 5 | a0001c0001t0019g0124a0001c0001t0019g0163a0001c0001t0019g0187others(2): Show | 5 | HG00140.hp1 HG01261.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.883-4416C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116829376 | ||||||
| chr12:116829502
|
G | C | 5 | a0001c0001t0019g0124a0001c0001t0019g0163a0001c0001t0019g0187others(2): Show | 5 | HG00140.hp1 HG01261.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.883-4290G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116829502 | ||||||
| chr12:116829608
|
A | T | 1 | a0001c0001t0001g0122 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.883-4184A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116829608 | ||||||
| chr12:116829617
|
G | C | 1 | a0001c0004t0002g0025 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.883-4175G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116829617 | ||||||
| chr12:116829632
|
C | G | 5 | a0001c0001t0007g0070a0001c0001t0007g0071a0001c0001t0007g0087others(2): Show | 5 | HG00544.hp1 HG02523.hp2 NA18948.hp2 others(2): Show |
intron_variant | MODIFIER | c.883-4160C>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116829632 | ||||||
| chr12:116829741
|
G | A | 5 | a0001c0009t0010g0049a0001c0009t0037g0043a0001c0009t0051g0016others(2): Show | 5 | HG01106.hp1 HG02572.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.883-4051G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116829741 | ||||||
| chr12:116829849
|
G | A | 5 | a0001c0001t0019g0124a0001c0001t0019g0163a0001c0001t0019g0187others(2): Show | 5 | HG00140.hp1 HG01261.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.883-3943G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116829849 | ||||||
| chr12:116829893
|
T | C | 3 | a0001c0009t0023g0026a0001c0011t0023g0007a0001c0011t0039g0012 | 3 | HG02486.hp1 HG02630.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.883-3899T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116829893 | ||||||
| chr12:116829913
|
C | T | 4 | a0001c0009t0023g0026a0001c0011t0023g0007a0001c0011t0039g0012others(1): Show | 4 | HG02486.hp1 HG02630.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.883-3879C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116829913 | ||||||
| chr12:116829962
|
A | AT | 6 | a0001c0001t0002g0209a0001c0004t0001g0083a0001c0006t0036g0018others(3): Show | 6 | HG00438.hp1 HG02040.hp1 HG02132.hp2 others(3): Show |
intron_variant | MODIFIER | c.883-3818dupT | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116829962 | |||||
| chr12:116830046
|
G | T | 9 | a0001c0009t0010g0049a0001c0009t0023g0026a0001c0009t0037g0043others(6): Show | 9 | HG01106.hp1 HG02486.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.883-3746G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116830046 | ||||||
| chr12:116830524
|
G | A | 1 | a0001c0003t0006g0054 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.883-3268G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116830524 | ||||||
| chr12:116830683
|
G | C | 10 | a0001c0001t0005g0105a0001c0002t0005g0064a0001c0003t0005g0035others(7): Show | 10 | HG01243.hp1 HG02280.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.883-3109G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116830683 | ||||||
| chr12:116830853
|
G | A | 1 | a0001c0003t0035g0088 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.883-2939G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116830853 | ||||||
| chr12:116830902
|
C | T | 1 | a0001c0008t0028g0214 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.883-2890C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116830902 | ||||||
| chr12:116830907
|
C | CA | 7 | a0001c0001t0010g0222a0001c0001t0019g0124a0001c0001t0019g0163others(4): Show | 7 | HG00140.hp1 HG00423.hp1 HG01261.hp2 others(4): Show |
intron_variant | MODIFIER | c.883-2872dupA | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116830907 | |||||
| chr12:116831078
|
G | A | 5 | a0001c0001t0019g0124a0001c0001t0019g0163a0001c0001t0019g0187others(2): Show | 5 | HG00140.hp1 HG01261.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.883-2714G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116831078 | ||||||
| chr12:116831095
|
C | G | 3 | a0001c0009t0023g0026a0001c0011t0023g0007a0001c0011t0039g0012 | 3 | HG02486.hp1 HG02630.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.883-2697C>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116831095 | ||||||
| chr12:116831198
|
C | CA | 183 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(180): Show | 183 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(180): Show |
intron_variant | MODIFIER | c.883-2582dupA | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116831198 | |||||
| chr12:116831426
|
C | T | 1 | a0001c0002t0012g0014 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.883-2366C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116831426 | ||||||
| chr12:116831534
|
C | CT | 5 | a0001c0001t0019g0124a0001c0001t0019g0163a0001c0001t0019g0187others(2): Show | 5 | HG00140.hp1 HG01261.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.883-2246dupT | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116831534 | |||||
| chr12:116831574
|
A | G | 1 | a0001c0003t0035g0088 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.883-2218A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116831574 | ||||||
| chr12:116831644
|
TTAGAG | T | 5 | a0001c0001t0002g0209a0001c0004t0001g0083a0002c0010t0002g0001others(2): Show | 5 | HG00438.hp1 HG02040.hp1 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.883-2145_883-2141d others(7): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116831644 | |||||
| chr12:116831784
|
GC | G | 16 | a0001c0001t0002g0209a0001c0001t0019g0124a0001c0001t0019g0163others(13): Show | 16 | HG00140.hp1 HG00438.hp1 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.883-2007delC | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116831784 | ||||||
| chr12:116831819
|
C | T | 1 | a0001c0009t0051g0016 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.883-1973C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116831819 | ||||||
| chr12:116831879
|
A | G | 10 | a0001c0001t0005g0245a0001c0001t0005g0246a0001c0002t0005g0003others(7): Show | 10 | HG01175.hp2 HG02109.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.883-1913A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116831879 | ||||||
| chr12:116832130
|
CAAAAAA | C | 7 | a0001c0001t0019g0124a0001c0001t0019g0163a0001c0001t0019g0187others(4): Show | 7 | HG00140.hp1 HG01261.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.883-1648_883-1643d others(8): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116832130 | |||||
| chr12:116832140
|
A | ATATATAT others(10): Show |
1 | a0001c0005t0020g0162 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.883-1652_883-1651i others(19): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116832140 | ||||||
| chr12:116832140
|
A | ATATATAT others(18): Show |
1 | a0001c0013t0020g0098 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.883-1652_883-1651i others(27): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116832140 | ||||||
| chr12:116832142
|
A | AATATATA others(15): Show |
1 | a0001c0002t0018g0022 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.883-1649_883-1648i others(24): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116832142 | |||||
| chr12:116832142
|
A | T | 3 | a0001c0003t0014g0065a0001c0005t0020g0162a0001c0013t0020g0098 | 3 | HG02970.hp2 HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.883-1650A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116832142 | ||||||
| chr12:116832144
|
A | AAT | 7 | a0001c0001t0002g0034a0001c0001t0002g0103a0001c0001t0002g0104others(4): Show | 7 | HG02615.hp1 HG02622.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.883-1647_883-1646i others(4): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116832144 | |||||
| chr12:116832144
|
A | AATAT | 11 | a0001c0001t0001g0094a0001c0001t0001g0205a0001c0001t0002g0031others(8): Show | 11 | HG00673.hp2 HG02071.hp2 HG02976.hp1 others(8): Show |
intron_variant | MODIFIER | c.883-1647_883-1646i others(6): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116832144 | |||||
| chr12:116832144
|
A | AATATATA others(11): Show |
1 | a0001c0001t0002g0209 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.883-1647_883-1646i others(20): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116832144 | |||||
| chr12:116832144
|
A | AT | 5 | a0001c0001t0011g0099a0001c0001t0011g0160a0001c0001t0048g0182others(2): Show | 5 | HG01109.hp1 HG02809.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.883-1648_883-1647i others(3): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116832144 | ||||||
| chr12:116832144
|
A | ATAT | 5 | a0001c0001t0001g0196a0001c0001t0002g0023a0001c0001t0060g0090others(2): Show | 5 | HG00609.hp1 HG00741.hp2 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.883-1648_883-1647i others(5): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116832144 | ||||||
| chr12:116832144
|
A | ATATAT | 3 | a0001c0001t0001g0216a0001c0001t0001g0243a0001c0001t0015g0112 | 3 | HG00673.hp1 HG02273.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.883-1648_883-1647i others(7): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116832144 | ||||||
| chr12:116832144
|
A | T | 10 | a0001c0002t0002g0108a0001c0002t0011g0097a0001c0002t0018g0022others(7): Show | 10 | HG01169.hp2 HG02055.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.883-1648A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116832144 | ||||||
| chr12:116832146
|
A | AAT | 6 | a0001c0001t0001g0262a0001c0001t0009g0118a0001c0001t0009g0153others(3): Show | 6 | HG01257.hp1 HG02683.hp1 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.883-1645_883-1644i others(4): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116832146 | |||||
| chr12:116832146
|
A | AATATATA others(5): Show |
1 | a0002c0010t0002g0254 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.883-1645_883-1644i others(14): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116832146 | |||||
| chr12:116832146
|
A | AATATATA others(17): Show |
1 | a0002c0010t0002g0002 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.883-1645_883-1644i others(26): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116832146 | |||||
| chr12:116832146
|
A | AATATATA others(23): Show |
1 | a0001c0003t0016g0039 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.883-1645_883-1644i others(32): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116832146 | |||||
| chr12:116832146
|
A | AT | 21 | a0001c0001t0001g0197a0001c0001t0002g0032a0001c0001t0004g0168others(18): Show | 21 | HG01074.hp2 HG01175.hp2 HG02074.hp1 others(18): Show |
intron_variant | MODIFIER | c.883-1646_883-1645i others(3): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116832146 | ||||||
| chr12:116832146
|
A | ATAT | 39 | a0001c0001t0001g0069a0001c0001t0001g0120a0001c0001t0001g0122others(36): Show | 39 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(36): Show |
intron_variant | MODIFIER | c.883-1646_883-1645i others(5): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116832146 | ||||||
| chr12:116832146
|
A | ATATAT | 23 | a0001c0001t0001g0072a0001c0001t0001g0166a0001c0001t0001g0198others(20): Show | 23 | HG00621.hp1 HG01361.hp1 HG01978.hp1 others(20): Show |
intron_variant | MODIFIER | c.883-1646_883-1645i others(7): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116832146 | ||||||
| chr12:116832146
|
A | ATATATAT others(8): Show |
1 | a0001c0002t0065g0093 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.883-1646_883-1645i others(17): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116832146 | ||||||
| chr12:116832146
|
A | T | 51 | a0001c0001t0001g0094a0001c0001t0001g0196a0001c0001t0001g0205others(48): Show | 51 | HG00438.hp1 HG00438.hp2 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.883-1646A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116832146 | ||||||
| chr12:116832148
|
A | AAAAAATA others(15): Show |
1 | a0002c0010t0002g0001 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.883-1643_883-1642i others(24): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116832148 | |||||
| chr12:116832148
|
A | AAAAATAT others(8): Show |
3 | a0001c0002t0063g0263a0001c0007t0005g0062a0001c0007t0016g0061 | 3 | HG01243.hp1 HG02818.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.883-1643_883-1642i others(17): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116832148 | |||||
| chr12:116832148
|
A | AAATATAT others(8): Show |
2 | a0001c0006t0005g0017a0001c0007t0034g0063 | 2 | HG02486.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.883-1643_883-1642i others(17): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116832148 | |||||
| chr12:116832148
|
A | AT | 10 | a0001c0001t0004g0110a0001c0001t0004g0172a0001c0001t0004g0176others(7): Show | 10 | HG03130.hp2 HG03209.hp2 HG03471.hp1 others(7): Show |
intron_variant | MODIFIER | c.883-1644_883-1643i others(3): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116832148 | ||||||
| chr12:116832148
|
A | ATAT | 25 | a0001c0001t0001g0086a0001c0001t0001g0169a0001c0001t0001g0178others(22): Show | 25 | HG01099.hp1 HG01109.hp2 HG01192.hp1 others(22): Show |
intron_variant | MODIFIER | c.883-1644_883-1643i others(5): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116832148 | ||||||
| chr12:116832148
|
A | ATATATAT others(16): Show |
1 | a0001c0004t0001g0083 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.883-1644_883-1643i others(25): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116832148 | ||||||
| chr12:116832148
|
A | ATATATAT others(20): Show |
1 | a0001c0003t0021g0038 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.883-1644_883-1643i others(29): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116832148 | ||||||
| chr12:116832148
|
A | ATATATAT others(22): Show |
2 | a0001c0001t0005g0105a0001c0003t0005g0035 | 2 | HG02280.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.883-1644_883-1643i others(31): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116832148 | ||||||
| chr12:116832148
|
A | ATATATAT others(26): Show |
1 | a0001c0003t0005g0036 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.883-1644_883-1643i others(35): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116832148 | ||||||
| chr12:116832148
|
A | T | 187 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0092others(184): Show | 187 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(184): Show |
intron_variant | MODIFIER | c.883-1644A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116832148 | ||||||
| chr12:116832150
|
T | A | 2 | a0001c0009t0023g0026a0001c0011t0023g0007 | 2 | HG02630.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.883-1642T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116832150 | ||||||
| chr12:116832239
|
C | T | 3 | a0001c0005t0030g0051a0001c0005t0030g0052a0001c0005t0070g0050 | 3 | HG01891.hp1 HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.883-1553C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116832239 | ||||||
| chr12:116832458
|
G | A | 3 | a0001c0009t0010g0049a0001c0009t0037g0043a0001c0014t0018g0019 | 3 | HG01106.hp1 HG02572.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.883-1334G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116832458 | ||||||
| chr12:116832631
|
C | T | 1 | a0001c0009t0010g0049 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.883-1161C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116832631 | ||||||
| chr12:116832867
|
C | T | 1 | a0001c0001t0001g0178 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.883-925C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116832867 | ||||||
| chr12:116832898
|
C | CT | 189 | a0001c0001t0001g0069a0001c0001t0001g0086a0001c0001t0001g0092others(186): Show | 189 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(186): Show |
intron_variant | MODIFIER | c.883-870dupT | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116832898 | |||||
| chr12:116832898
|
C | CTT | 26 | a0001c0001t0001g0072a0001c0001t0001g0094a0001c0001t0001g0146others(23): Show | 26 | HG00140.hp1 HG00438.hp2 HG01175.hp1 others(23): Show |
intron_variant | MODIFIER | c.883-871_883-870dup others(2): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116832898 | |||||
| chr12:116833002
|
C | T | 49 | a0001c0001t0001g0141a0001c0001t0001g0190a0001c0001t0001g0193others(46): Show | 49 | HG00408.hp2 HG00438.hp2 HG01074.hp2 others(46): Show |
intron_variant | MODIFIER | c.883-790C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116833002 | ||||||
| chr12:116833042
|
C | T | 53 | a0001c0001t0001g0178a0001c0001t0002g0209a0001c0001t0004g0095others(50): Show | 53 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.883-750C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116833042 | ||||||
| chr12:116833101
|
T | C | 1 | a0001c0014t0018g0019 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.883-691T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116833101 | ||||||
| chr12:116833296
|
G | A | 1 | a0001c0004t0001g0113 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.883-496G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116833296 | ||||||
| chr12:116833387
|
C | T | 1 | a0001c0003t0035g0088 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.883-405C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116833387 | ||||||
| chr12:116833442
|
C | T | 1 | a0001c0009t0010g0049 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.883-350C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116833442 | ||||||
| chr12:116833498
|
T | C | 1 | a0001c0014t0002g0137 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.883-294T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116833498 | ||||||
| chr12:116833630
|
A | G | 1 | a0001c0001t0007g0231 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.883-162A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116833630 | ||||||
| chr12:116833720
|
C | T | 1 | a0001c0003t0035g0088 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.883-72C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116833720 | ||||||
| chr12:116834187
|
C | T | 4 | a0001c0009t0023g0026a0001c0011t0023g0007a0001c0011t0039g0012others(1): Show | 4 | HG02486.hp1 HG02630.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.1032+246C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 8/10 | chr12 | 116834187 | ||||||
| chr12:116834242
|
A | G | 62 | a0001c0001t0001g0178a0001c0001t0002g0209a0001c0001t0004g0095others(59): Show | 62 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.1032+301A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 8/10 | chr12 | 116834242 | ||||||
| chr12:116834270
|
A | G | 9 | a0001c0009t0010g0049a0001c0009t0023g0026a0001c0009t0037g0043others(6): Show | 9 | HG01106.hp1 HG02486.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1032+329A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 8/10 | chr12 | 116834270 | ||||||
| chr12:116834410
|
C | T | 5 | a0001c0009t0010g0049a0001c0009t0037g0043a0001c0009t0051g0016others(2): Show | 5 | HG01106.hp1 HG02572.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1032+469C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 8/10 | chr12 | 116834410 | ||||||
| chr12:116834441
|
A | G | 1 | a0001c0003t0042g0229 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1032+500A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 8/10 | chr12 | 116834441 | ||||||
| chr12:116834625
|
A | C | 1 | a0001c0003t0035g0088 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1032+684A>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 8/10 | chr12 | 116834625 | ||||||
| chr12:116834678
|
G | A | 1 | a0001c0009t0037g0043 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1032+737G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 8/10 | chr12 | 116834678 | ||||||
| chr12:116834850
|
C | CT | 8 | a0001c0001t0045g0114a0001c0002t0001g0077a0001c0006t0050g0013others(5): Show | 8 | HG00741.hp1 HG01106.hp1 HG02135.hp1 others(5): Show |
intron_variant | MODIFIER | c.1032+927dupT | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 116834850 | |||||
| chr12:116834850
|
CT | C | 42 | a0001c0001t0001g0178a0001c0001t0002g0032a0001c0001t0004g0095others(39): Show | 42 | HG00544.hp1 HG01243.hp1 HG02074.hp1 others(39): Show |
intron_variant | MODIFIER | c.1032+927delT | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 116834850 | |||||
| chr12:116835041
|
T | C | 2 | a0001c0002t0002g0129a0001c0015t0002g0020 | 2 | HG02258.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1033-919T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 8/10 | chr12 | 116835041 | ||||||
| chr12:116835300
|
T | TCTC | 172 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(169): Show | 172 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(169): Show |
intron_variant | MODIFIER | c.1033-658_1033-657i others(5): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 116835300 | |||||
| chr12:116835567
|
T | C | 1 | a0001c0005t0013g0006 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1033-393T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 8/10 | chr12 | 116835567 | ||||||
| chr12:116835763
|
G | A | 1 | a0001c0001t0004g0168 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1033-197G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 8/10 | chr12 | 116835763 | ||||||
| chr12:116836050
|
A | G | 1 | a0001c0001t0003g0240 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1098+25A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 9/10 | chr12 | 116836050 | ||||||
| chr12:116836058
|
C | T | 1 | a0001c0011t0053g0011 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1098+33C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 9/10 | chr12 | 116836058 | ||||||
| chr12:116836130
|
G | A | 1 | a0001c0011t0053g0011 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1099-51G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 9/10 | chr12 | 116836130 | ||||||
| chr12:116836299
|
C | A | 1 | a0001c0009t0037g0043 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1200+17C>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116836299 | ||||||
| chr12:116836358
|
G | A | 1 | a0001c0003t0035g0088 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1200+76G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116836358 | ||||||
| chr12:116836430
|
A | G | 1 | a0001c0002t0005g0003 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1200+148A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116836430 | ||||||
| chr12:116836489
|
G | C | 1 | a0001c0001t0040g0143 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1200+207G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116836489 | ||||||
| chr12:116836523
|
G | A | 6 | a0001c0005t0013g0006a0001c0005t0013g0154a0001c0005t0054g0021others(3): Show | 6 | HG01891.hp2 HG02922.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.1200+241G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116836523 | ||||||
| chr12:116836606
|
C | T | 2 | a0001c0001t0019g0187a0001c0001t0057g0188 | 2 | HG01261.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.1200+324C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116836606 | ||||||
| chr12:116836640
|
A | G | 2 | a0001c0001t0005g0105a0001c0003t0021g0038 | 2 | HG02280.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1200+358A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116836640 | ||||||
| chr12:116836763
|
A | G | 9 | a0001c0005t0013g0006a0001c0005t0013g0154a0001c0005t0030g0051others(6): Show | 9 | HG01891.hp1 HG01891.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.1200+481A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116836763 | ||||||
| chr12:116836841
|
A | T | 2 | a0001c0002t0004g0005a0001c0002t0049g0004 | 2 | HG01243.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.1200+559A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116836841 | ||||||
| chr12:116836938
|
A | C | 1 | a0001c0002t0002g0142 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1200+656A>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116836938 | ||||||
| chr12:116837268
|
C | T | 2 | a0001c0009t0051g0016a0001c0011t0053g0011 | 2 | HG02809.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1200+986C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116837268 | ||||||
| chr12:116837369
|
T | G | 2 | a0001c0001t0002g0133a0001c0001t0002g0189 | 2 | HG00408.hp2 HG00438.hp2 |
intron_variant | MODIFIER | c.1200+1087T>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116837369 | ||||||
| chr12:116837388
|
G | T | 9 | a0001c0001t0002g0032a0001c0001t0008g0028a0001c0001t0008g0029others(6): Show | 9 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.1200+1106G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116837388 | ||||||
| chr12:116837572
|
T | C | 2 | a0001c0006t0031g0067a0001c0016t0032g0044 | 2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1200+1290T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116837572 | ||||||
| chr12:116837628
|
A | G | 1 | a0001c0006t0050g0013 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1200+1346A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116837628 | ||||||
| chr12:116837773
|
A | G | 1 | a0001c0001t0011g0160 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1200+1491A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116837773 | ||||||
| chr12:116837797
|
A | G | 1 | a0001c0002t0018g0047 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1200+1515A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116837797 | ||||||
| chr12:116837932
|
A | G | 1 | a0001c0001t0010g0222 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1200+1650A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116837932 | ||||||
| chr12:116837958
|
G | A | 1 | a0001c0001t0004g0172 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1200+1676G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116837958 | ||||||
| chr12:116838022
|
T | TA | 41 | a0001c0001t0001g0178a0001c0001t0004g0095a0001c0001t0004g0096others(38): Show | 41 | HG00544.hp1 HG01106.hp1 HG01243.hp1 others(38): Show |
intron_variant | MODIFIER | c.1200+1749dupA | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116838022 | |||||
| chr12:116838046
|
C | T | 36 | a0001c0001t0001g0178a0001c0001t0004g0095a0001c0001t0004g0096others(33): Show | 36 | HG00544.hp1 HG01243.hp1 HG01243.hp2 others(33): Show |
intron_variant | MODIFIER | c.1200+1764C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116838046 | ||||||
| chr12:116838106
|
T | C | 1 | a0001c0011t0053g0011 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1200+1824T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116838106 | ||||||
| chr12:116838211
|
G | A | 1 | a0001c0001t0004g0172 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1200+1929G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116838211 | ||||||
| chr12:116838412
|
T | C | 258 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(255): Show | 258 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(255): Show |
intron_variant | MODIFIER | c.1200+2130T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116838412 | ||||||
| chr12:116838420
|
A | C | 62 | a0001c0001t0001g0178a0001c0001t0002g0209a0001c0001t0004g0095others(59): Show | 62 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.1200+2138A>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116838420 | ||||||
| chr12:116838461
|
T | C | 3 | a0001c0009t0023g0026a0001c0011t0023g0007a0001c0011t0039g0012 | 3 | HG02486.hp1 HG02630.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1200+2179T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116838461 | ||||||
| chr12:116838498
|
G | C | 11 | a0001c0001t0002g0209a0001c0002t0018g0022a0001c0004t0001g0083others(8): Show | 11 | HG00438.hp1 HG00741.hp1 HG02040.hp1 others(8): Show |
intron_variant | MODIFIER | c.1200+2216G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116838498 | ||||||
| chr12:116838581
|
A | G | 1 | a0001c0001t0001g0094 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1200+2299A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116838581 | ||||||
| chr12:116838706
|
A | G | 59 | a0001c0001t0001g0178a0001c0001t0002g0209a0001c0001t0004g0095others(56): Show | 59 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.1200+2424A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116838706 | ||||||
| chr12:116839045
|
G | A | 1 | a0001c0014t0018g0019 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1200+2763G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116839045 | ||||||
| chr12:116839105
|
G | A | 7 | a0001c0003t0035g0088a0001c0009t0010g0049a0001c0009t0037g0043others(4): Show | 7 | HG01106.hp1 HG02572.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1200+2823G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116839105 | ||||||
| chr12:116839293
|
T | TTGGA | 2 | a0001c0006t0031g0067a0001c0016t0032g0044 | 2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1200+3028_1200+303 others(8): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116839293 | |||||
| chr12:116839336
|
G | A | 2 | a0001c0001t0069g0068a0001c0002t0010g0132 | 2 | HG01109.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.1200+3054G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116839336 | ||||||
| chr12:116839352
|
G | A | 1 | a0001c0006t0036g0018 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1200+3070G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116839352 | ||||||
| chr12:116839392
|
A | G | 1 | a0001c0006t0036g0018 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1200+3110A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116839392 | ||||||
| chr12:116839413
|
ATGGG | A | 11 | a0001c0001t0002g0209a0001c0002t0005g0183a0001c0002t0018g0022others(8): Show | 11 | HG00438.hp1 HG00741.hp1 HG02040.hp1 others(8): Show |
intron_variant | MODIFIER | c.1200+3143_1200+314 others(8): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116839413 | |||||
| chr12:116839417
|
G | A | 1 | a0001c0009t0051g0016 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1200+3135G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116839417 | ||||||
| chr12:116839421
|
G | GTGGATGG others(5): Show |
1 | a0001c0014t0002g0137 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1200+3142_1200+314 others(16): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116839421 | |||||
| chr12:116839421
|
GTGGGTGG others(1): Show |
G | 14 | a0001c0001t0005g0245a0001c0001t0005g0246a0001c0001t0019g0124others(11): Show | 14 | HG00140.hp1 HG01175.hp2 HG01261.hp2 others(11): Show |
intron_variant | MODIFIER | c.1200+3143_1200+315 others(12): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116839421 | |||||
| chr12:116839421
|
GTGGGTGG others(5): Show |
G | 1 | a0001c0014t0018g0019 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1200+3143_1200+315 others(16): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116839421 | |||||
| chr12:116839425
|
G | A | 7 | a0001c0003t0035g0088a0001c0004t0001g0091a0001c0009t0010g0049others(4): Show | 7 | HG00621.hp1 HG02572.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1200+3143G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116839425 | ||||||
| chr12:116839425
|
GTGGA | G | 170 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(167): Show | 170 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(167): Show |
intron_variant | MODIFIER | c.1200+3178_1200+318 others(8): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116839425 | |||||
| chr12:116839425
|
GTGGATGG others(1): Show |
G | 9 | a0001c0001t0002g0032a0001c0001t0008g0028a0001c0001t0008g0029others(6): Show | 9 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.1200+3174_1200+318 others(12): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116839425 | |||||
| chr12:116839429
|
A | G | 1 | a0001c0001t0017g0213 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1200+3147A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116839429 | ||||||
| chr12:116839486
|
G | C | 5 | a0001c0001t0002g0209a0001c0004t0001g0083a0002c0010t0002g0001others(2): Show | 5 | HG00438.hp1 HG02040.hp1 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.1200+3204G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116839486 | ||||||
| chr12:116839774
|
A | AAGGG | 7 | a0001c0001t0026g0181a0001c0005t0013g0006a0001c0005t0013g0154others(4): Show | 7 | HG01891.hp2 HG02922.hp1 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.1200+3509_1200+351 others(8): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116839774 | |||||
| chr12:116839859
|
A | G | 1 | a0001c0002t0003g0008 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1200+3577A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116839859 | ||||||
| chr12:116839912
|
G | A | 5 | a0001c0001t0002g0034a0001c0001t0002g0103a0001c0001t0002g0104others(2): Show | 5 | HG02615.hp1 HG02622.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1200+3630G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116839912 | ||||||
| chr12:116840148
|
C | T | 1 | a0001c0001t0001g0072 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1200+3866C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116840148 | ||||||
| chr12:116840317
|
A | C | 10 | a0001c0003t0035g0088a0001c0009t0010g0049a0001c0009t0023g0026others(7): Show | 10 | HG01106.hp1 HG02486.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1200+4035A>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116840317 | ||||||
| chr12:116840328
|
A | G | 3 | a0001c0003t0002g0100a0001c0003t0002g0101a0001c0003t0002g0102 | 3 | HG01074.hp2 HG02280.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1200+4046A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116840328 | ||||||
| chr12:116840399
|
C | G | 1 | a0001c0011t0053g0011 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1200+4117C>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116840399 | ||||||
| chr12:116840590
|
G | A | 1 | a0001c0014t0002g0137 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1200+4308G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116840590 | ||||||
| chr12:116840607
|
C | T | 1 | a0001c0001t0002g0209 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1200+4325C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116840607 | ||||||
| chr12:116840616
|
A | G | 9 | a0001c0001t0002g0032a0001c0001t0008g0028a0001c0001t0008g0029others(6): Show | 9 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.1200+4334A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116840616 | ||||||
| chr12:116840829
|
T | C | 6 | a0001c0001t0005g0105a0001c0002t0005g0064a0001c0003t0005g0035others(3): Show | 6 | HG02280.hp1 HG02886.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1200+4547T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116840829 | ||||||
| chr12:116840922
|
C | CTG | 179 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(176): Show | 179 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(176): Show |
intron_variant | MODIFIER | c.1200+4660_1200+466 others(6): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116840922 | |||||
| chr12:116841063
|
A | T | 246 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(243): Show | 246 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(243): Show |
intron_variant | MODIFIER | c.1200+4781A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841063 | ||||||
| chr12:116841214
|
G | A | 1 | a0001c0003t0006g0165 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1200+4932G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841214 | ||||||
| chr12:116841465
|
T | C | 52 | a0001c0001t0001g0178a0001c0001t0002g0209a0001c0001t0004g0095others(49): Show | 52 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.1200+5183T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841465 | ||||||
| chr12:116841522
|
C | T | 36 | a0001c0001t0001g0178a0001c0001t0004g0095a0001c0001t0004g0096others(33): Show | 36 | HG00544.hp1 HG01243.hp1 HG01243.hp2 others(33): Show |
intron_variant | MODIFIER | c.1200+5240C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841522 | ||||||
| chr12:116841523
|
G | A | 1 | a0001c0011t0053g0011 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1200+5241G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841523 | ||||||
| chr12:116841558
|
G | T | 3 | a0001c0005t0030g0051a0001c0005t0030g0052a0001c0005t0070g0050 | 3 | HG01891.hp1 HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1200+5276G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841558 | ||||||
| chr12:116841606
|
G | A | 5 | a0001c0001t0019g0124a0001c0001t0019g0163a0001c0001t0019g0187others(2): Show | 5 | HG00140.hp1 HG01261.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.1200+5324G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841606 | ||||||
| chr12:116841623
|
C | A | 15 | a0001c0001t0002g0209a0001c0001t0019g0124a0001c0001t0019g0163others(12): Show | 15 | HG00140.hp1 HG00438.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1200+5341C>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841623 | ||||||
| chr12:116841760
|
AATATAAA others(33): Show |
A | 4 | a0001c0001t0002g0209a0002c0010t0002g0001a0002c0010t0002g0002others(1): Show | 4 | HG00438.hp1 HG02040.hp1 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.1200+5496_1200+553 others(44): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841760 | |||||
| chr12:116841766
|
AAT | A | 4 | a0001c0004t0052g0015a0001c0007t0025g0009a0001c0007t0025g0056others(1): Show | 4 | HG01884.hp2 HG02145.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1200+5496_1200+549 others(6): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841766 | |||||
| chr12:116841776
|
TATAAATA others(111): Show |
T | 2 | a0001c0001t0005g0105a0001c0003t0021g0038 | 2 | HG02280.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1200+5498_1200+561 others(4): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841776 | |||||
| chr12:116841778
|
T | A | 2 | a0001c0005t0020g0162a0001c0013t0020g0098 | 2 | HG02970.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1200+5496T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841778 | ||||||
| chr12:116841780
|
A | T | 1 | a0001c0005t0020g0162 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1200+5498A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841780 | ||||||
| chr12:116841782
|
TATATATA others(81): Show |
T | 1 | a0001c0009t0051g0016 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1200+5522_1200+560 others(92): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841782 | |||||
| chr12:116841784
|
TATATATA others(3): Show |
T | 1 | a0001c0003t0035g0088 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1200+5512_1200+552 others(14): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841784 | |||||
| chr12:116841784
|
TATATATA others(103): Show |
T | 1 | a0001c0001t0004g0095 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1200+5512_1200+562 others(4): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841784 | |||||
| chr12:116841790
|
TATAAATA others(97): Show |
T | 8 | a0001c0002t0005g0064a0001c0003t0005g0035a0001c0003t0005g0036others(5): Show | 8 | HG01243.hp1 HG02486.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.1200+5512_1200+561 others(4): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841790 | |||||
| chr12:116841792
|
T | A | 6 | a0001c0001t0012g0261a0001c0001t0019g0124a0001c0001t0019g0163others(3): Show | 6 | HG00140.hp1 HG01192.hp1 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.1200+5510T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841792 | ||||||
| chr12:116841792
|
TAAATATA others(93): Show |
T | 22 | a0001c0001t0001g0178a0001c0001t0004g0110a0001c0001t0004g0145others(19): Show | 22 | HG00544.hp1 HG01243.hp2 HG02074.hp1 others(19): Show |
intron_variant | MODIFIER | c.1200+5524_1200+562 others(104): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841792 | |||||
| chr12:116841794
|
A | AAT | 5 | a0001c0001t0019g0124a0001c0001t0019g0163a0001c0001t0019g0187others(2): Show | 5 | HG00140.hp1 HG01261.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.1200+5522_1200+552 others(6): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841794 | |||||
| chr12:116841794
|
A | T | 4 | a0001c0001t0004g0096a0001c0001t0004g0170a0001c0001t0004g0172others(1): Show | 4 | HG01192.hp1 HG02647.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.1200+5512A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841794 | ||||||
| chr12:116841794
|
AATATATA others(95): Show |
A | 9 | a0001c0001t0002g0103a0001c0004t0052g0015a0001c0005t0013g0006others(6): Show | 9 | HG00741.hp1 HG01891.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.1200+5574_1200+567 others(4): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841794 | |||||
| chr12:116841796
|
TATATATA others(91): Show |
T | 2 | a0001c0001t0004g0170a0001c0001t0004g0172 | 2 | HG03831.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1200+5524_1200+562 others(102): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841796 | |||||
| chr12:116841798
|
T | A | 1 | a0001c0001t0004g0096 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1200+5516T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841798 | ||||||
| chr12:116841804
|
TAAATATA others(45): Show |
T | 1 | a0001c0001t0014g0027 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1200+5538_1200+558 others(56): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841804 | |||||
| chr12:116841804
|
TAAATATA others(81): Show |
T | 10 | a0001c0001t0001g0196a0001c0001t0001g0203a0001c0001t0001g0224others(7): Show | 10 | HG00423.hp1 HG00673.hp2 HG00741.hp2 others(7): Show |
intron_variant | MODIFIER | c.1200+5536_1200+562 others(92): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841804 | |||||
| chr12:116841806
|
A | T | 2 | a0001c0002t0018g0047a0001c0014t0002g0137 | 2 | HG02109.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1200+5524A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841806 | ||||||
| chr12:116841806
|
AATATATA others(83): Show |
A | 2 | a0001c0001t0012g0261a0001c0001t0022g0223 | 2 | HG01192.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.1200+5538_1200+562 others(94): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841806 | |||||
| chr12:116841808
|
T | A | 1 | a0001c0002t0018g0047 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1200+5526T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841808 | ||||||
| chr12:116841808
|
TATATATA others(31): Show |
T | 4 | a0001c0001t0011g0099a0001c0001t0011g0160a0001c0002t0011g0097others(1): Show | 4 | HG02809.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1200+5550_1200+558 others(42): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841808 | |||||
| chr12:116841808
|
TATATATA others(43): Show |
T | 7 | a0001c0001t0001g0069a0001c0002t0001g0078a0001c0002t0001g0080others(4): Show | 7 | HG01099.hp2 HG01358.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.1200+5536_1200+558 others(54): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841808 | |||||
| chr12:116841812
|
TATATAAA others(75): Show |
T | 1 | a0001c0001t0045g0114 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1200+5536_1200+561 others(86): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841812 | |||||
| chr12:116841812
|
TATATAAA others(145): Show |
T | 1 | a0001c0014t0002g0137 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1200+5532_1200+568 others(4): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841812 | |||||
| chr12:116841814
|
TATAAAAA others(73): Show |
T | 8 | a0001c0001t0002g0032a0001c0001t0008g0028a0001c0001t0008g0029others(5): Show | 8 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1200+5536_1200+561 others(84): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841814 | |||||
| chr12:116841816
|
TAAAAATA others(33): Show |
T | 3 | a0001c0005t0030g0051a0001c0005t0030g0052a0001c0005t0070g0050 | 3 | HG01891.hp1 HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1200+5538_1200+557 others(44): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841816 | |||||
| chr12:116841818
|
A | T | 142 | a0001c0001t0001g0072a0001c0001t0001g0086a0001c0001t0001g0092others(139): Show | 142 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.1200+5536A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841818 | ||||||
| chr12:116841818
|
AAAATATA others(71): Show |
A | 10 | a0001c0001t0001g0248a0001c0001t0005g0245a0001c0001t0005g0246others(7): Show | 10 | HG01175.hp2 HG02109.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.1200+5538_1200+561 others(82): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841818 | |||||
| chr12:116841819
|
A | T | 1 | a0001c0002t0001g0073 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1200+5537A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841819 | ||||||
| chr12:116841820
|
A | T | 6 | a0001c0002t0005g0149a0001c0002t0005g0151a0001c0002t0033g0150others(3): Show | 6 | HG01106.hp1 HG02572.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1200+5538A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841820 | ||||||
| chr12:116841820
|
AATATATA others(69): Show |
A | 122 | a0001c0001t0001g0072a0001c0001t0001g0086a0001c0001t0001g0092others(119): Show | 122 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.1200+5550_1200+562 others(80): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841820 | |||||
| chr12:116841820
|
AATATATA others(97): Show |
A | 4 | a0001c0002t0065g0093a0001c0009t0023g0026a0001c0011t0023g0007others(1): Show | 4 | HG01884.hp1 HG02486.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1200+5550_1200+565 others(4): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841820 | |||||
| chr12:116841822
|
T | A | 1 | a0001c0005t0020g0162 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1200+5540T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841822 | ||||||
| chr12:116841822
|
T | TATATATA others(3): Show |
1 | a0001c0014t0018g0019 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1200+5549_1200+555 others(14): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841822 | |||||
| chr12:116841822
|
T | TATATATA others(41): Show |
1 | a0001c0006t0006g0057 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1200+5562_1200+560 others(52): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841822 | |||||
| chr12:116841822
|
TATATATA others(5): Show |
T | 1 | a0001c0003t0006g0208 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1200+5562_1200+557 others(16): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841822 | |||||
| chr12:116841828
|
TATATAAA others(59): Show |
T | 3 | a0001c0002t0005g0149a0001c0002t0005g0151a0001c0002t0033g0150 | 3 | HG02922.hp2 NA20129.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1200+5552_1200+561 others(70): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841828 | |||||
| chr12:116841828
|
TATATAAA others(87): Show |
T | 1 | a0001c0002t0001g0073 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1200+5552_1200+564 others(98): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841828 | |||||
| chr12:116841830
|
TATAAATA others(57): Show |
T | 1 | a0001c0001t0002g0034 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1200+5552_1200+561 others(68): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841830 | |||||
| chr12:116841832
|
T | A | 2 | a0001c0006t0031g0067a0001c0016t0032g0044 | 2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1200+5550T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841832 | ||||||
| chr12:116841832
|
TAAATATA others(81): Show |
T | 2 | a0001c0006t0036g0018a0001c0011t0053g0011 | 2 | HG02615.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1200+5564_1200+565 others(92): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841832 | |||||
| chr12:116841834
|
A | T | 2 | a0001c0006t0031g0067a0001c0016t0032g0044 | 2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1200+5552A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841834 | ||||||
| chr12:116841836
|
TATATATA others(3): Show |
T | 1 | a0001c0001t0019g0124 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1200+5566_1200+557 others(14): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841836 | |||||
| chr12:116841836
|
TATATATA others(15): Show |
T | 1 | a0001c0002t0018g0047 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1200+5564_1200+558 others(26): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841836 | |||||
| chr12:116841844
|
TAAATATA others(5): Show |
T | 1 | a0001c0016t0032g0044 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1200+5574_1200+558 others(16): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841844 | |||||
| chr12:116841844
|
TAAATATA others(30): Show |
T | 1 | a0001c0003t0014g0065 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1200+5565_1200+560 others(41): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841844 | |||||
| chr12:116841844
|
TAAATATA others(111): Show |
T | 3 | a0001c0001t0004g0096a0001c0002t0002g0129a0001c0015t0002g0020 | 3 | HG02258.hp1 HG02647.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1200+5564_1200+568 others(4): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841844 | |||||
| chr12:116841846
|
A | T | 2 | a0001c0005t0020g0162a0001c0013t0020g0098 | 2 | HG02970.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1200+5564A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841846 | ||||||
| chr12:116841846
|
AATATATA others(1): Show |
A | 4 | a0001c0001t0019g0187a0001c0001t0056g0220a0001c0001t0057g0188others(1): Show | 4 | HG00140.hp1 HG01261.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.1200+5566_1200+557 others(12): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841846 | |||||
| chr12:116841848
|
TATATATA others(3): Show |
T | 4 | a0001c0001t0002g0209a0002c0010t0002g0001a0002c0010t0002g0002others(1): Show | 4 | HG00438.hp1 HG02040.hp1 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.1200+5574_1200+558 others(14): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841848 | |||||
| chr12:116841848
|
TATATATA others(27): Show |
T | 1 | a0001c0003t0035g0088 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1200+5574_1200+560 others(38): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841848 | |||||
| chr12:116841850
|
TATATAAA others(25): Show |
T | 9 | a0001c0001t0014g0037a0001c0001t0069g0068a0001c0002t0002g0108others(6): Show | 9 | HG01074.hp2 HG01109.hp1 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.1200+5574_1200+560 others(36): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841850 | |||||
| chr12:116841856
|
A | T | 7 | a0001c0001t0011g0099a0001c0001t0011g0160a0001c0002t0011g0097others(4): Show | 7 | HG02451.hp2 HG02572.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1200+5574A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841856 | ||||||
| chr12:116841858
|
A | T | 7 | a0001c0001t0019g0163a0001c0001t0019g0187a0001c0001t0056g0220others(4): Show | 7 | HG00140.hp1 HG01261.hp2 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.1200+5576A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841858 | ||||||
| chr12:116841860
|
T | A | 1 | a0001c0003t0006g0230 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1200+5578T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841860 | ||||||
| chr12:116841868
|
T | A | 2 | a0001c0001t0019g0163a0001c0009t0010g0049 | 2 | HG02735.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1200+5586T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841868 | ||||||
| chr12:116841870
|
A | T | 1 | a0001c0006t0031g0067 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1200+5588A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841870 | ||||||
| chr12:116841871
|
A | T | 1 | a0001c0006t0031g0067 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1200+5589A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841871 | ||||||
| chr12:116841882
|
A | AAT | 4 | a0001c0001t0002g0209a0001c0006t0031g0067a0002c0010t0002g0001others(1): Show | 4 | HG00438.hp1 HG02040.hp1 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.1200+5608_1200+560 others(6): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841882 | |||||
| chr12:116841882
|
A | AATATATA others(59): Show |
1 | a0001c0009t0010g0049 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1200+5621_1200+562 others(70): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841882 | |||||
| chr12:116841882
|
A | AATATATA others(21): Show |
1 | a0003c0017t0006g0060 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1200+5640_1200+566 others(32): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841882 | |||||
| chr12:116841882
|
A | AATATATA others(83): Show |
1 | a0001c0009t0037g0043 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1200+5609_1200+561 others(94): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841882 | |||||
| chr12:116841882
|
A | T | 1 | a0001c0016t0032g0044 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1200+5600A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841882 | ||||||
| chr12:116841883
|
A | T | 1 | a0001c0016t0032g0044 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1200+5601A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841883 | ||||||
| chr12:116841884
|
T | A | 4 | a0001c0001t0019g0124a0001c0001t0019g0187a0001c0001t0056g0220others(1): Show | 4 | HG00140.hp1 HG01261.hp2 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.1200+5602T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841884 | ||||||
| chr12:116841892
|
A | T | 31 | a0001c0001t0001g0069a0001c0001t0002g0209a0001c0001t0011g0099others(28): Show | 31 | HG00140.hp1 HG00438.hp1 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.1200+5610A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841892 | ||||||
| chr12:116841892
|
AAAAT | A | 9 | a0001c0001t0014g0037a0001c0001t0069g0068a0001c0002t0002g0108others(6): Show | 9 | HG01074.hp2 HG01109.hp1 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.1200+5612_1200+561 others(8): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841892 | |||||
| chr12:116841894
|
A | T | 45 | a0001c0001t0001g0069a0001c0001t0001g0178a0001c0001t0001g0196others(42): Show | 45 | HG00140.hp1 HG00544.hp1 HG00741.hp2 others(42): Show |
intron_variant | MODIFIER | c.1200+5612A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841894 | ||||||
| chr12:116841894
|
AAT | A | 3 | a0001c0005t0030g0051a0001c0005t0030g0052a0001c0005t0070g0050 | 3 | HG01891.hp1 HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1200+5624_1200+562 others(6): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841894 | |||||
| chr12:116841896
|
T | A | 28 | a0001c0001t0001g0069a0001c0001t0001g0196a0001c0001t0001g0203others(25): Show | 28 | HG00140.hp1 HG00741.hp2 HG01099.hp2 others(25): Show |
intron_variant | MODIFIER | c.1200+5614T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841896 | ||||||
| chr12:116841896
|
T | TATATATA others(15): Show |
1 | a0001c0014t0018g0019 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1200+5621_1200+562 others(26): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841896 | |||||
| chr12:116841900
|
T | A | 34 | a0001c0001t0001g0178a0001c0001t0004g0110a0001c0001t0004g0145others(31): Show | 34 | HG00544.hp1 HG01243.hp1 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.1200+5618T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841900 | ||||||
| chr12:116841902
|
T | A | 8 | a0001c0001t0002g0032a0001c0001t0008g0028a0001c0001t0008g0029others(5): Show | 8 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1200+5620T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841902 | ||||||
| chr12:116841904
|
T | A | 1 | a0001c0001t0045g0114 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1200+5622T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841904 | ||||||
| chr12:116841908
|
A | T | 9 | a0001c0001t0002g0032a0001c0001t0008g0028a0001c0001t0008g0029others(6): Show | 9 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.1200+5626A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841908 | ||||||
| chr12:116841920
|
A | T | 32 | a0001c0001t0001g0259a0001c0001t0002g0032a0001c0001t0002g0209others(29): Show | 32 | HG00140.hp1 HG00438.hp1 HG01169.hp1 others(29): Show |
intron_variant | MODIFIER | c.1200+5638A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841920 | ||||||
| chr12:116841922
|
A | T | 2 | a0001c0001t0019g0163a0001c0003t0035g0088 | 2 | HG02735.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1200+5640A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841922 | ||||||
| chr12:116841924
|
TATATATA others(5): Show |
T | 1 | a0001c0003t0006g0208 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1200+5666_1200+567 others(16): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841924 | |||||
| chr12:116841934
|
T | A | 1 | a0001c0001t0019g0163 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1200+5652T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841934 | ||||||
| chr12:116841936
|
A | T | 2 | a0001c0001t0019g0163a0001c0002t0001g0073 | 2 | HG02735.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.1200+5654A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841936 | ||||||
| chr12:116841938
|
T | C | 4 | a0001c0001t0019g0124a0001c0001t0019g0187a0001c0001t0056g0220others(1): Show | 4 | HG00140.hp1 HG01261.hp2 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.1200+5656T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841938 | ||||||
| chr12:116841944
|
TATAAATA others(9): Show |
T | 1 | a0001c0002t0049g0004 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1200+5664_1200+567 others(20): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841944 | |||||
| chr12:116841946
|
TAAATATA others(9): Show |
T | 46 | a0001c0001t0001g0178a0001c0001t0001g0224a0001c0001t0002g0031others(43): Show | 46 | HG00423.hp1 HG00544.hp1 HG01169.hp2 others(43): Show |
intron_variant | MODIFIER | c.1200+5666_1200+568 others(20): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841946 | |||||
| chr12:116841946
|
TAAATATA others(15): Show |
T | 2 | a0001c0006t0031g0067a0001c0016t0032g0044 | 2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1200+5666_1200+568 others(26): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841946 | |||||
| chr12:116841948
|
A | T | 5 | a0001c0001t0002g0209a0001c0013t0020g0098a0002c0010t0002g0001others(2): Show | 5 | HG00438.hp1 HG02040.hp1 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.1200+5666A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841948 | ||||||
| chr12:116841950
|
T | A | 8 | a0001c0003t0002g0102a0001c0005t0013g0006a0001c0005t0013g0154others(5): Show | 8 | HG01891.hp2 HG02132.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.1200+5668T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841950 | ||||||
| chr12:116841952
|
T | A | 1 | a0001c0001t0019g0163 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1200+5670T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841952 | ||||||
| chr12:116841952
|
T | TATATATA others(3): Show |
1 | a0001c0005t0020g0162 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1200+5677_1200+567 others(14): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841952 | |||||
| chr12:116841952
|
TATATATA others(9): Show |
T | 1 | a0001c0013t0020g0098 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1200+5672_1200+568 others(20): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841952 | |||||
| chr12:116841953
|
A | G | 4 | a0001c0002t0065g0093a0001c0009t0023g0026a0001c0011t0023g0007others(1): Show | 4 | HG01884.hp1 HG02486.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1200+5671A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841953 | ||||||
| chr12:116841956
|
T | G | 1 | a0001c0003t0035g0088 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1200+5674T>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841956 | ||||||
| chr12:116841956
|
TATAGAGA others(3): Show |
T | 1 | a0001c0009t0010g0049 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1200+5676_1200+568 others(14): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841956 | |||||
| chr12:116841956
|
TATAGAGA others(7): Show |
T | 3 | a0001c0001t0002g0209a0002c0010t0002g0001a0002c0010t0002g0254 | 3 | HG00438.hp1 HG02040.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.1200+5676_1200+568 others(18): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841956 | |||||
| chr12:116841958
|
T | G | 5 | a0001c0003t0035g0088a0001c0003t0042g0229a0001c0006t0006g0057others(2): Show | 5 | HG02818.hp2 HG03654.hp2 HG03834.hp2 others(2): Show |
intron_variant | MODIFIER | c.1200+5676T>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841958 | ||||||
| chr12:116841958
|
TAGAG | T | 190 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(187): Show | 190 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(187): Show |
intron_variant | MODIFIER | c.1200+5701_1200+570 others(8): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841958 | |||||
| chr12:116841960
|
G | T | 9 | a0001c0001t0019g0163a0001c0002t0041g0075a0001c0003t0006g0054others(6): Show | 9 | HG00140.hp2 HG01106.hp1 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.1200+5678G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841960 | ||||||
| chr12:116841962
|
G | T | 4 | a0001c0001t0019g0163a0001c0005t0020g0162a0001c0014t0018g0019others(1): Show | 4 | HG01106.hp1 HG02132.hp2 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.1200+5680G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841962 | ||||||
| chr12:116841963
|
A | C | 1 | a0001c0009t0051g0016 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1200+5681A>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841963 | ||||||
| chr12:116841964
|
G | T | 9 | a0001c0001t0019g0124a0001c0001t0019g0163a0001c0001t0019g0187others(6): Show | 9 | HG00140.hp1 HG01106.hp1 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.1200+5682G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841964 | ||||||
| chr12:116841966
|
G | T | 9 | a0001c0001t0019g0124a0001c0001t0019g0163a0001c0001t0019g0187others(6): Show | 9 | HG00140.hp1 HG01106.hp1 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.1200+5684G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841966 | ||||||
| chr12:116841968
|
G | A | 236 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(233): Show | 236 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(233): Show |
intron_variant | MODIFIER | c.1200+5686G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841968 | ||||||
| chr12:116841968
|
G | T | 5 | a0001c0001t0019g0124a0001c0001t0019g0163a0001c0001t0019g0187others(2): Show | 5 | HG01261.hp2 HG02055.hp2 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.1200+5686G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841968 | ||||||
| chr12:116841970
|
G | T | 5 | a0001c0001t0019g0124a0001c0001t0019g0163a0001c0001t0019g0187others(2): Show | 5 | HG01261.hp2 HG02055.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1200+5688G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841970 | ||||||
| chr12:116841981
|
A | G | 1 | a0001c0014t0002g0137 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1200+5699A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841981 | ||||||
| chr12:116842082
|
C | T | 1 | a0001c0004t0052g0015 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1200+5800C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116842082 | ||||||
| chr12:116842251
|
C | T | 44 | a0001c0001t0002g0032a0001c0001t0002g0133a0001c0001t0002g0175others(41): Show | 44 | HG00408.hp2 HG00609.hp1 HG01106.hp1 others(41): Show |
intron_variant | MODIFIER | c.1200+5969C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116842251 | ||||||
| chr12:116842322
|
G | T | 4 | a0001c0001t0002g0034a0001c0001t0002g0103a0001c0001t0002g0253others(1): Show | 4 | HG02615.hp1 HG02886.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1200+6040G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116842322 | ||||||
| chr12:116842384
|
C | G | 1 | a0001c0001t0008g0041 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1200+6102C>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116842384 | ||||||
| chr12:116842453
|
C | G | 1 | a0001c0014t0018g0019 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1200+6171C>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116842453 | ||||||
| chr12:116842568
|
ATTTG | A | 89 | a0001c0001t0002g0031a0001c0001t0002g0032a0001c0001t0002g0045others(86): Show | 89 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.1200+6307_1200+631 others(8): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116842568 | |||||
| chr12:116842623
|
G | A | 1 | a0001c0002t0067g0042 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1200+6341G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116842623 | ||||||
| chr12:116842698
|
C | A | 3 | a0001c0005t0020g0162a0001c0013t0020g0098a0001c0016t0032g0044 | 3 | HG02630.hp1 HG02970.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1200+6416C>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116842698 | ||||||
| chr12:116842770
|
C | T | 3 | a0001c0005t0030g0051a0001c0005t0030g0052a0001c0005t0070g0050 | 3 | HG01891.hp1 HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1200+6488C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116842770 | ||||||
| chr12:116842899
|
G | A | 1 | a0001c0001t0017g0200 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1201-6415G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116842899 | ||||||
| chr12:116842983
|
T | C | 1 | a0001c0001t0001g0092 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1201-6331T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116842983 | ||||||
| chr12:116843021
|
A | C | 6 | a0001c0001t0008g0028a0001c0001t0008g0029a0001c0001t0008g0040others(3): Show | 6 | HG02572.hp2 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1201-6293A>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116843021 | ||||||
| chr12:116843160
|
A | C | 4 | a0001c0001t0002g0209a0002c0010t0002g0001a0002c0010t0002g0002others(1): Show | 4 | HG00438.hp1 HG02040.hp1 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.1201-6154A>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116843160 | ||||||
| chr12:116843269
|
G | A | 2 | a0001c0001t0001g0211a0001c0001t0001g0244 | 2 | HG00408.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.1201-6045G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116843269 | ||||||
| chr12:116843492
|
C | CA | 159 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(156): Show | 159 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(156): Show |
intron_variant | MODIFIER | c.1201-5799dupA | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116843492 | |||||
| chr12:116843492
|
C | CAA | 39 | a0001c0001t0001g0092a0001c0001t0001g0141a0001c0001t0001g0193others(36): Show | 39 | HG00408.hp1 HG00408.hp2 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.1201-5800_1201-579 others(6): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116843492 | |||||
| chr12:116843492
|
CAAAA | C | 6 | a0001c0001t0008g0028a0001c0001t0008g0029a0001c0001t0008g0040others(3): Show | 6 | HG02572.hp2 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1201-5802_1201-579 others(8): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116843492 | |||||
| chr12:116843512
|
A | C | 4 | a0001c0001t0019g0163a0001c0001t0019g0187a0001c0001t0056g0220others(1): Show | 4 | HG00140.hp1 HG01261.hp2 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.1201-5802A>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116843512 | ||||||
| chr12:116843516
|
C | A | 25 | a0001c0001t0004g0095a0001c0001t0004g0096a0001c0001t0004g0110others(22): Show | 25 | HG00544.hp1 HG00673.hp2 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.1201-5798C>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116843516 | ||||||
| chr12:116843555
|
C | T | 1 | a0001c0004t0052g0015 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1201-5759C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116843555 | ||||||
| chr12:116843644
|
G | A | 1 | a0001c0002t0005g0183 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1201-5670G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116843644 | ||||||
| chr12:116843705
|
TG | T | 257 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(254): Show | 257 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(254): Show |
intron_variant | MODIFIER | c.1201-5605delG | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116843705 | |||||
| chr12:116843758
|
C | G | 2 | a0001c0003t0035g0088a0001c0014t0018g0019 | 2 | HG01106.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1201-5556C>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116843758 | ||||||
| chr12:116844165
|
G | A | 6 | a0001c0001t0001g0190a0001c0001t0001g0256a0001c0001t0001g0257others(3): Show | 6 | HG01192.hp1 HG01257.hp1 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.1201-5149G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116844165 | ||||||
| chr12:116844724
|
G | T | 6 | a0001c0001t0008g0028a0001c0001t0008g0029a0001c0001t0008g0040others(3): Show | 6 | HG02572.hp2 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1201-4590G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116844724 | ||||||
| chr12:116844911
|
C | T | 3 | a0001c0005t0020g0162a0001c0013t0020g0098a0001c0016t0032g0044 | 3 | HG02630.hp1 HG02970.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1201-4403C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116844911 | ||||||
| chr12:116844913
|
T | C | 39 | a0001c0001t0004g0095a0001c0001t0004g0096a0001c0001t0004g0110others(36): Show | 39 | HG00544.hp1 HG00673.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.1201-4401T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116844913 | ||||||
| chr12:116845013
|
T | C | 1 | a0001c0002t0018g0047 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1201-4301T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116845013 | ||||||
| chr12:116845209
|
A | T | 1 | a0001c0009t0051g0016 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1201-4105A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116845209 | ||||||
| chr12:116845222
|
T | G | 3 | a0001c0002t0018g0022a0001c0002t0018g0047a0001c0006t0050g0013 | 3 | HG00741.hp1 HG02109.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.1201-4092T>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116845222 | ||||||
| chr12:116845243
|
CA | C | 8 | a0001c0001t0004g0226a0001c0001t0008g0028a0001c0001t0008g0029others(5): Show | 8 | HG01361.hp1 HG02572.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1201-4055delA | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116845243 | |||||
| chr12:116845243
|
CAAA | C | 98 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(95): Show | 98 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.1201-4057_1201-405 others(7): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116845243 | |||||
| chr12:116845254
|
A | T | 1 | a0001c0009t0051g0016 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1201-4060A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116845254 | ||||||
| chr12:116845256
|
A | T | 3 | a0001c0001t0007g0179a0001c0001t0007g0180a0001c0009t0051g0016 | 3 | HG02976.hp2 HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1201-4058A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116845256 | ||||||
| chr12:116845257
|
AAAT | A | 8 | a0001c0001t0001g0122a0001c0001t0001g0166a0001c0001t0001g0216others(5): Show | 8 | HG01074.hp1 HG01978.hp1 HG02004.hp2 others(5): Show |
intron_variant | MODIFIER | c.1201-4055_1201-405 others(7): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116845257 | |||||
| chr12:116845258
|
A | T | 19 | a0001c0001t0001g0146a0001c0001t0001g0205a0001c0001t0001g0211others(16): Show | 19 | HG00408.hp1 HG01169.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.1201-4056A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116845258 | ||||||
| chr12:116845259
|
AT | A | 27 | a0001c0001t0002g0034a0001c0001t0002g0103a0001c0001t0002g0253others(24): Show | 27 | HG00140.hp1 HG00609.hp1 HG01074.hp2 others(24): Show |
intron_variant | MODIFIER | c.1201-4054delT | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116845259 | ||||||
| chr12:116845259
|
ATAT | A | 24 | a0001c0001t0001g0237a0001c0001t0002g0175a0001c0001t0002g0184others(21): Show | 24 | HG00438.hp2 HG01175.hp2 HG01358.hp2 others(21): Show |
intron_variant | MODIFIER | c.1201-4054_1201-405 others(7): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116845259 | ||||||
| chr12:116845260
|
T | A | 76 | a0001c0001t0002g0023a0001c0001t0002g0031a0001c0001t0002g0032others(73): Show | 76 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.1201-4054T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116845260 | ||||||
| chr12:116845262
|
T | A | 92 | a0001c0001t0002g0023a0001c0001t0002g0031a0001c0001t0002g0032others(89): Show | 92 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.1201-4052T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116845262 | ||||||
| chr12:116845264
|
T | A | 90 | a0001c0001t0002g0023a0001c0001t0002g0034a0001c0001t0002g0103others(87): Show | 90 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.1201-4050T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116845264 | ||||||
| chr12:116845266
|
T | A | 20 | a0001c0001t0002g0175a0001c0001t0002g0184a0001c0001t0002g0189others(17): Show | 20 | HG00438.hp2 HG01175.hp2 HG02071.hp1 others(17): Show |
intron_variant | MODIFIER | c.1201-4048T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116845266 | ||||||
| chr12:116845268
|
T | A | 6 | a0001c0001t0002g0175a0001c0001t0002g0184a0001c0001t0002g0189others(3): Show | 6 | HG00438.hp2 HG02071.hp1 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1201-4046T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116845268 | ||||||
| chr12:116845272
|
T | G | 1 | a0001c0002t0004g0005 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1201-4042T>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116845272 | ||||||
| chr12:116845274
|
T | G | 9 | a0001c0001t0001g0141a0001c0001t0001g0235a0001c0001t0001g0244others(6): Show | 9 | HG01099.hp2 HG01243.hp2 HG01257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1201-4040T>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116845274 | ||||||
| chr12:116845274
|
TAG | T | 12 | a0001c0002t0002g0265a0001c0002t0010g0266a0001c0005t0013g0006others(9): Show | 12 | HG01106.hp1 HG01891.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.1201-4019_1201-401 others(6): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116845274 | |||||
| chr12:116845274
|
TAGAG | T | 87 | a0001c0001t0002g0023a0001c0001t0002g0031a0001c0001t0002g0032others(84): Show | 87 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.1201-4021_1201-401 others(8): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116845274 | |||||
| chr12:116845274
|
TAGAGAG | T | 4 | a0001c0002t0067g0042a0001c0007t0025g0009a0001c0007t0025g0056others(1): Show | 4 | HG01884.hp2 HG02145.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1201-4023_1201-401 others(10): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116845274 | |||||
| chr12:116845276
|
G | T | 104 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(101): Show | 104 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.1201-4038G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116845276 | ||||||
| chr12:116845278
|
G | T | 67 | a0001c0001t0001g0092a0001c0001t0001g0166a0001c0001t0001g0196others(64): Show | 67 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.1201-4036G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116845278 | ||||||
| chr12:116845280
|
G | T | 123 | a0001c0001t0001g0166a0001c0001t0001g0224a0001c0001t0002g0023others(120): Show | 123 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.1201-4034G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116845280 | ||||||
| chr12:116845282
|
G | T | 100 | a0001c0001t0001g0166a0001c0001t0002g0023a0001c0001t0002g0031others(97): Show | 100 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.1201-4032G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116845282 | ||||||
| chr12:116845284
|
G | T | 37 | a0001c0001t0002g0133a0001c0001t0002g0175a0001c0001t0002g0184others(34): Show | 37 | HG00408.hp2 HG00438.hp2 HG01175.hp2 others(34): Show |
intron_variant | MODIFIER | c.1201-4030G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116845284 | ||||||
| chr12:116845337
|
T | A | 1 | a0002c0010t0002g0254 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1201-3977T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116845337 | ||||||
| chr12:116845446
|
A | G | 2 | a0001c0003t0035g0088a0001c0014t0018g0019 | 2 | HG01106.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1201-3868A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116845446 | ||||||
| chr12:116845447
|
A | G | 2 | a0001c0003t0035g0088a0001c0014t0018g0019 | 2 | HG01106.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1201-3867A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116845447 | ||||||
| chr12:116845450
|
T | A | 2 | a0001c0003t0035g0088a0001c0014t0018g0019 | 2 | HG01106.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1201-3864T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116845450 | ||||||
| chr12:116845564
|
A | G | 1 | a0001c0004t0052g0015 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1201-3750A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116845564 | ||||||
| chr12:116845648
|
G | A | 19 | a0001c0001t0005g0105a0001c0001t0005g0245a0001c0001t0005g0246others(16): Show | 19 | HG01175.hp2 HG01243.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.1201-3666G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116845648 | ||||||
| chr12:116845728
|
C | T | 3 | a0001c0009t0023g0026a0001c0011t0023g0007a0001c0011t0039g0012 | 3 | HG02486.hp1 HG02630.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1201-3586C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116845728 | ||||||
| chr12:116845787
|
C | T | 9 | a0001c0005t0013g0006a0001c0005t0013g0154a0001c0005t0030g0051others(6): Show | 9 | HG01891.hp1 HG01891.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.1201-3527C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116845787 | ||||||
| chr12:116845801
|
C | A | 5 | a0001c0001t0019g0124a0001c0001t0019g0163a0001c0001t0019g0187others(2): Show | 5 | HG00140.hp1 HG01261.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.1201-3513C>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116845801 | ||||||
| chr12:116845910
|
G | A | 10 | a0001c0001t0002g0031a0001c0001t0002g0045a0001c0001t0002g0048others(7): Show | 10 | HG01169.hp2 HG01261.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.1201-3404G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116845910 | ||||||
| chr12:116846203
|
C | T | 2 | a0001c0004t0052g0015a0001c0011t0053g0011 | 2 | HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1201-3111C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116846203 | ||||||
| chr12:116846248
|
CATTATTC others(19): Show |
C | 6 | a0001c0001t0005g0105a0001c0002t0005g0064a0001c0003t0005g0035others(3): Show | 6 | HG02280.hp1 HG02886.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1201-3059_1201-303 others(30): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116846248 | |||||
| chr12:116846343
|
G | A | 1 | a0001c0001t0002g0034 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1201-2971G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116846343 | ||||||
| chr12:116846409
|
G | A | 6 | a0001c0001t0001g0224a0001c0002t0001g0073a0001c0002t0001g0074others(3): Show | 6 | HG00423.hp1 HG02135.hp1 HG03834.hp1 others(3): Show |
intron_variant | MODIFIER | c.1201-2905G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116846409 | ||||||
| chr12:116846412
|
C | T | 3 | a0001c0009t0023g0026a0001c0011t0023g0007a0001c0011t0039g0012 | 3 | HG02486.hp1 HG02630.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1201-2902C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116846412 | ||||||
| chr12:116846418
|
A | T | 1 | a0001c0002t0008g0140 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1201-2896A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116846418 | ||||||
| chr12:116846437
|
A | ATTTTTTT others(4): Show |
55 | a0001c0001t0002g0023a0001c0001t0002g0032a0001c0001t0002g0034others(52): Show | 55 | HG00423.hp2 HG00609.hp1 HG01074.hp1 others(52): Show |
intron_variant | MODIFIER | c.1201-2875_1201-286 others(15): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116846437 | |||||
| chr12:116846437
|
A | ATTTTTTT others(5): Show |
128 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0092others(125): Show | 128 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.1201-2876_1201-286 others(16): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116846437 | |||||
| chr12:116846437
|
A | ATTTTTTT others(6): Show |
32 | a0001c0001t0001g0086a0001c0001t0001g0146a0001c0001t0001g0178others(29): Show | 32 | HG00438.hp1 HG00741.hp2 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.1201-2865_1201-286 others(17): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116846437 | |||||
| chr12:116846437
|
A | ATTTTTTT others(8): Show |
1 | a0001c0004t0052g0015 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1201-2865_1201-286 others(19): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116846437 | |||||
| chr12:116846490
|
A | G | 1 | a0001c0001t0003g0157 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1201-2824A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116846490 | ||||||
| chr12:116846498
|
C | G | 3 | a0001c0007t0025g0009a0001c0007t0025g0056a0001c0007t0046g0053 | 3 | HG01884.hp2 HG02145.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1201-2816C>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116846498 | ||||||
| chr12:116846543
|
G | A | 1 | a0001c0012t0001g0123 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1201-2771G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116846543 | ||||||
| chr12:116846566
|
A | G | 5 | a0001c0001t0019g0124a0001c0001t0019g0163a0001c0001t0019g0187others(2): Show | 5 | HG00140.hp1 HG01261.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.1201-2748A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116846566 | ||||||
| chr12:116846707
|
C | T | 1 | a0001c0006t0036g0018 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1201-2607C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116846707 | ||||||
| chr12:116846824
|
C | T | 2 | a0001c0004t0052g0015a0001c0011t0053g0011 | 2 | HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1201-2490C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116846824 | ||||||
| chr12:116846901
|
AT | A | 29 | a0001c0001t0004g0095a0001c0001t0004g0096a0001c0001t0004g0128others(26): Show | 29 | HG00544.hp1 HG00673.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.1201-2392delT | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116846901 | |||||
| chr12:116846901
|
ATT | A | 18 | a0001c0001t0001g0086a0001c0001t0001g0203a0001c0001t0001g0205others(15): Show | 18 | HG00140.hp1 HG00408.hp1 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.1201-2393_1201-239 others(6): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116846901 | |||||
| chr12:116846901
|
ATTT | A | 194 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0092others(191): Show | 194 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(191): Show |
intron_variant | MODIFIER | c.1201-2394_1201-239 others(7): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116846901 | |||||
| chr12:116846946
|
T | C | 1 | a0001c0011t0053g0011 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1201-2368T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116846946 | ||||||
| chr12:116846970
|
G | A | 91 | a0001c0001t0002g0023a0001c0001t0002g0031a0001c0001t0002g0032others(88): Show | 91 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.1201-2344G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116846970 | ||||||
| chr12:116846983
|
A | G | 26 | a0001c0001t0004g0095a0001c0001t0004g0096a0001c0001t0004g0110others(23): Show | 26 | HG00544.hp1 HG00673.hp2 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.1201-2331A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116846983 | ||||||
| chr12:116847001
|
T | C | 1 | a0001c0011t0053g0011 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1201-2313T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116847001 | ||||||
| chr12:116847019
|
C | T | 1 | a0001c0001t0017g0167 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1201-2295C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116847019 | ||||||
| chr12:116847154
|
C | T | 1 | a0001c0009t0051g0016 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1201-2160C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116847154 | ||||||
| chr12:116847298
|
C | T | 1 | a0001c0009t0051g0016 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1201-2016C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116847298 | ||||||
| chr12:116847316
|
C | T | 6 | a0001c0005t0013g0006a0001c0005t0013g0154a0001c0005t0054g0021others(3): Show | 6 | HG01891.hp2 HG02922.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.1201-1998C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116847316 | ||||||
| chr12:116847325
|
C | A | 1 | a0001c0009t0051g0016 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1201-1989C>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116847325 | ||||||
| chr12:116847398
|
A | G | 2 | a0001c0005t0030g0051a0001c0005t0030g0052 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1201-1916A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116847398 | ||||||
| chr12:116847474
|
C | G | 96 | a0001c0001t0001g0141a0001c0001t0001g0193a0001c0001t0001g0215others(93): Show | 96 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.1201-1840C>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116847474 | ||||||
| chr12:116847494
|
T | C | 3 | a0001c0005t0020g0162a0001c0013t0020g0098a0001c0016t0032g0044 | 3 | HG02630.hp1 HG02970.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1201-1820T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116847494 | ||||||
| chr12:116847532
|
C | CT | 98 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(95): Show | 98 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.1201-1770dupT | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116847532 | |||||
| chr12:116847532
|
CT | C | 6 | a0001c0001t0019g0124a0001c0001t0019g0163a0001c0001t0019g0187others(3): Show | 6 | HG00140.hp1 HG01261.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.1201-1770delT | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116847532 | |||||
| chr12:116847604
|
C | T | 1 | a0001c0001t0024g0147 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1201-1710C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116847604 | ||||||
| chr12:116847713
|
G | T | 2 | a0001c0001t0069g0068a0001c0002t0010g0132 | 2 | HG01109.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.1201-1601G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116847713 | ||||||
| chr12:116847839
|
T | A | 215 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(212): Show | 215 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(212): Show |
intron_variant | MODIFIER | c.1201-1475T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116847839 | ||||||
| chr12:116848043
|
G | C | 19 | a0001c0001t0005g0105a0001c0001t0005g0245a0001c0001t0005g0246others(16): Show | 19 | HG01175.hp2 HG01243.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.1201-1271G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116848043 | ||||||
| chr12:116848074
|
T | C | 256 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(253): Show | 256 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(253): Show |
intron_variant | MODIFIER | c.1201-1240T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116848074 | ||||||
| chr12:116848090
|
T | C | 3 | a0001c0001t0002g0175a0001c0001t0002g0184a0001c0001t0014g0156 | 3 | NA18957.hp2 NA19062.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.1201-1224T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116848090 | ||||||
| chr12:116848237
|
A | G | 1 | a0001c0012t0001g0238 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1201-1077A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116848237 | ||||||
| chr12:116848311
|
G | A | 1 | a0001c0009t0051g0016 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1201-1003G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116848311 | ||||||
| chr12:116848323
|
G | A | 26 | a0001c0001t0004g0095a0001c0001t0004g0096a0001c0001t0004g0110others(23): Show | 26 | HG00544.hp1 HG00673.hp2 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.1201-991G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116848323 | ||||||
| chr12:116848574
|
A | G | 18 | a0001c0001t0008g0028a0001c0001t0008g0029a0001c0001t0008g0040others(15): Show | 18 | HG00140.hp1 HG00741.hp1 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.1201-740A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116848574 | ||||||
| chr12:116848579
|
C | T | 12 | a0001c0001t0008g0028a0001c0001t0008g0029a0001c0001t0008g0040others(9): Show | 12 | HG00741.hp1 HG01884.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1201-735C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116848579 | ||||||
| chr12:116848619
|
A | G | 1 | a0001c0002t0004g0268 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1201-695A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116848619 | ||||||
| chr12:116849176
|
C | T | 76 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0086others(73): Show | 76 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.1201-138C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116849176 | ||||||
| chr12:116849254
|
C | T | 1 | a0001c0002t0001g0066 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1201-60C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116849254 | ||||||
| chr12:116849275
|
G | T | 2 | a0001c0001t0002g0209a0002c0010t0002g0254 | 2 | HG00438.hp1 HG02040.hp1 |
intron_variant | MODIFIER | c.1201-39G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116849275 | ||||||
| chr12:116849307
|
C | T | 3 | a0001c0001t0001g0166a0001c0002t0001g0111a0001c0002t0012g0014 | 3 | HG01361.hp1 HG02004.hp2 HG02148.hp2 |
splice_region_variant&intron_variant | LOW | c.1201-7C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116849307 |